WO2006116713A1 - Substituted amide derivatives as protein kinase inhibitors - Google Patents

Substituted amide derivatives as protein kinase inhibitors Download PDF

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Publication number
WO2006116713A1
WO2006116713A1 PCT/US2006/016344 US2006016344W WO2006116713A1 WO 2006116713 A1 WO2006116713 A1 WO 2006116713A1 US 2006016344 W US2006016344 W US 2006016344W WO 2006116713 A1 WO2006116713 A1 WO 2006116713A1
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WO
WIPO (PCT)
Prior art keywords
phenyl
optionally substituted
alkyl
oxo
methyl
Prior art date
Application number
PCT/US2006/016344
Other languages
French (fr)
Inventor
Tae-Seong Kim
David Bauer
Steven Bellon
Alessandro Boezio
Shon Booker
Deborah Choquette
Derin C. D'amico
Noel D'angelo
Celia Dominguez
Ingrid M. Fellows
Julie Germain
Russell Graceffa
Jean-Christophe Harmange
Satoko Hirai
Daniel La
Matthew Lee
Longbin Liu
Mark H. Norman
Michele Potashman
Philip Roveto
Aaron C. Siegmund
Ning Xi
Kevin Yang
Original Assignee
Amgen Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to SI200631479T priority Critical patent/SI1881976T1/en
Priority to CA2605680A priority patent/CA2605680C/en
Application filed by Amgen Inc. filed Critical Amgen Inc.
Priority to EA200702339A priority patent/EA013231B1/en
Priority to JP2008509191A priority patent/JP5463033B2/en
Priority to MX2007013216A priority patent/MX2007013216A/en
Priority to EP06751834A priority patent/EP1881976B1/en
Priority to DK06751834.0T priority patent/DK1881976T3/en
Priority to PL06751834T priority patent/PL1881976T3/en
Priority to ES06751834T priority patent/ES2396219T3/en
Priority to AU2006239216A priority patent/AU2006239216B2/en
Priority to NZ562595A priority patent/NZ562595A/en
Priority to BRPI0608097-9A priority patent/BRPI0608097A2/en
Priority to RS20120566A priority patent/RS52596B/en
Publication of WO2006116713A1 publication Critical patent/WO2006116713A1/en
Priority to IL186526A priority patent/IL186526A/en
Priority to NO20076093A priority patent/NO20076093L/en
Priority to HK08103876.5A priority patent/HK1116161A1/en
Priority to HRP20121069TT priority patent/HRP20121069T1/en

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Definitions

  • This invention is in the field of pharmaceutical agents and specifically relates to compounds, compositions, uses and methods for treating cancer.
  • Protein kinases represent a large family of proteins, which play a central role in the regulation of a wide variety of cellular processes, maintaining control over cellular function.
  • a partial list of such kinases includes abl, Akt, bcr-abl, BIk, Brk, Btk, c-kit, c-Met, c-src, c-fins, CDKl , CDK2, CDK3 , CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDKl 0, cRafl , CSF 1 R, CSK, EGFR, ErbB2, ErbB3, ErbB4, Erk, Fak, fes, FGFRl, FGFR2, FGFR3, FGFR4, FGFR5, Fgr, flt-1, Fps, Frk, Fyn, Hck, IGF-IR, INS-R, Jak, KDR, Lck, Lyn, MEK, ⁇ 38, P
  • ocular neovascularisation such as retinopathies (including diabetic retinopathy), age-related macular degeneration, psoriasis, hemangioblastoma, hemangioma, arteriosclerosis, inflammatory disease, such as a rheumatoid or rheumatic inflammatory disease, especially arthritis (including rheumatoid arthritis), or other chronic inflammatory disorders, such as chronic asthma, arterial or post-transplantational atherosclerosis, endometriosis, and neoplastic diseases, for example so-called solid tumors and liquid tumors (such as leukemias).
  • VEGF Vascular Endothelial Growth Factor
  • VPF Vascular Permeability Factor
  • VEGF is a dimeric, disulfide-linked 46-kDa glycoprotein related to "Platelet-Derived Growth Factor” (PDGF); it is produced by normal cell lines and tumor cell lines; is an endothelial cell-specific mitogen; shows angiogenic activity in in vivo test systems (e.g. rabbit cornea); is chemotactic for endothelial cells and monocytes; and induces plasminogen activators in endothelial cells, which are involved in the proteolytic degradation of extracellular matrix during the formation of capillaries.
  • PDGF Platinum-Derived Growth Factor
  • VEGF vascular endothelial growth factor
  • VEGF receptors are transmembranous receptor tyrosine kinases. They are characterized by an extracellular domain with seven immunoglobulin-like domains and an intracellular tyrosine kinase domain.
  • VEGF receptors e.g. VEGFR- 1 (also known as flt-1), VEGFR-2 (also known as KDR) 5 and VEGFR-3.
  • VEGF vascular endothelium
  • VEGF expression could explain the occurrence of cerebral edema in patients with glioma.
  • Direct evidence of the role of VEGF as a tumor angiogenesis factor in vivo is shown in studies in which VEGF expression or VEGF activity was inhibited. This was achieved with anti-VEGF antibodies, with dominant-negative VEGFR-2 mutants, which inhibited signal transduction, and with antisense-VEGF RNA techniques. All approaches led to a reduction in the growth of glioma cell lines or other tumor cell lines in vivo as a result of inhibited tumor angiogenesis.
  • Angiogenesis is regarded as an absolute prerequisite for tumors, which grow beyond a diameter of about 1-2 mm; up to this limit, oxygen and nutrients may be supplied to the tumor cells by diffusion. Every tumor, regardless of its origin and its cause, is thus dependent on angiogenesis for its growth after it has reached a certain size.
  • VEGF's are unique in that they are the only angiogenic growth factors known to contribute to vascular hyperpermeability and the formation of edema. Indeed, vascular hyperpermeability and edema that is associated with the expression or administration of many other growth factors appears to be mediated via VEGF production. Inflammatory cytokines stimulate VEGF production. Hypoxia results in a marked upregulation of VEGF in numerous tissues, hence situations involving infarct, occlusion, ischemia, anemia, or circulatory impairment typically invoke VEGF/VPF-mediated responses.
  • VEGF-mediated hyperpermeability can significantly contribute to disorders with these etiologic features.
  • regulators of angiogenesis have become an important therapeutic target.
  • the hepatocyte growth factor receptor (“c-Met) is a unique receptor tyrosine kinase shown to be overexpressed in a variety of malignancies.
  • c-Met typically comprises, in its native form, a 190-kDa heterodimeric (a disulfide-linked 50-kDa ⁇ -chain and a 145-kDa ⁇ - chain) membrane-spanning tyrosine kinase protein (Proc. Natl. Acad. Sci. USA, 84:6379-6383 (1987)).
  • c-Met is mainly expressed in epithelial cells and stimulation of c-Met leads to scattering, angiogenesis, proliferation and metastasis. (See Cytokine and Growth Factor Reviews, 13:41-59 (2002)).
  • HGF hepatocyte growth factor
  • SF scatter factor
  • HGF-SF Hepatocyte Growth Factor- Scatter Factor
  • c-Met Receptor Goldberg and Rosen, eds., Birkhauser Verlag-Basel, 67-79 (1993).
  • HGF/SF Hepatocyte Growth Factor- Scatter Factor
  • the biological effect of HGF/SF may depend in part on the target cell.
  • HGF induces a spectrum of biological activities in epithelial cells, including mitogenesis, stimulation of cell motility and promotion of matrix invasion (Biochem. Biophys. Res. Comm., 122:1450-1459 (1984); Proc. Natl. Acad. Sci. U.S.A., 88:415-419 (1991)).
  • HGF can also act as a "scatter factor", an activity that promotes the dissociation of epithelial and vascular endothelial cells (Nature, 327:239-242 (1987); J. Cell Biol., 111:2097-2108 (1990); EMBO J., 10:2867- 2878 (1991); Proc. Natl. Acad. Sci. USA, 90:649-653 (1993)).
  • HGF Hepatocyte Growth Factor-Scatter Factor
  • C-Met Receptor Goldberg and Rosen, eds., Birkhauser Verlag-Basel, 131-165 (1993)
  • HGF and c-Met are expressed at abnormally high levels in a large variety of solid tumors.
  • High levels of HGF and/or c-Met have been observed in liver, breast, pancreas, lung, kidney, bladder, ovary, brain, prostate, gallbladder and myeloma tumors in addition to many others.
  • the role of HGF/c-Met in metastasis has been investigated in mice using cell lines transformed with HGF/c-Met (J. MoI. Med., 74:505-513 (1996)).
  • Overexpression of the c-Met oncogene has also been suggested to play a role in the pathogenesis and progression of thyroid tumors derived from follicular epithelium (Oncogene, 7:2549-2553 (1992)).
  • HGF is a morphogen (Development, 110:1271-1284 (1990); Cell, 66:697-711 (1991)) and a potent angiogenic factor (J. Cell Biol., 119:629-641 (1992)).
  • Angiogenesis can be stimulated by HGF, as well as vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF).
  • HGF vascular endothelial growth factor
  • bFGF basic fibroblast growth factor
  • Angiogenesis the process of sprouting new blood vessels from existing vasculature and arteriogenesis, the remodeling of small vessels into larger conduit vessels are both physiologically important aspects of vascular growth in adult tissues. These processes of vascular growth are required for beneficial processes such as tissue repair, wound healing, recovery from tissue ischemia and menstrual cycling. They are also required for the development of pathological conditions such as the growth of neoplasias, diabetic retinopathy, rheumatoid arthritis, psoriasis, certain forms of macular degeneration, and certain inflammatory pathologies. The inhibition of vascular growth in these contexts has also shown beneficial effects in preclinical animal models.
  • angiogenesis For example, inhibition of angiogenesis by blocking vascular endothelial growth factor or its receptor has resulted in inhibition of tumor growth and in retinopathy. Also, the development of pathological pannus tissue in rheumatoid arthritis involves angiogenesis and might be blocked by inhibitors of angiogenesis.
  • the ability to stimulate vascular growth has potential utility for treatment of ischemia- induced pathologies such as myocardial infarction, coronary artery disease, peripheral vascular disease, and stroke.
  • ischemia- induced pathologies such as myocardial infarction, coronary artery disease, peripheral vascular disease, and stroke.
  • the sprouting of new vessels and/or the expansion of small vessels in ischemic tissues prevents ischemic tissue death and induces tissue repair.
  • Certain diseases are known to be associated with deregulated angiogenesis, for example ocular neovascularization, such as retinopathies (including diabetic retinopathy), age-related macular degeneration, psoriasis, hemangioblastoma, hemangioma, arteriosclerosis, inflammatory disease, such as a rheumatoid or rheumatic inflammatory disease, especially arthritis (including rheumatoid arthritis), or other chronic inflammatory disorders, such as chronic asthma, arterial or post- transplantational atherosclerosis, endometriosis, and neoplastic diseases, for example so-called solid tumors and liquid tumors (such as leukemias). Treatment of malaria and related viral diseases may also be mediated by HGF and cMet.
  • HGF HGF-like growth factor
  • c-Met Elevated levels of HGF and c-Met have also been observed in non-oncological settings, such as hypertension, myocardial infarction and rheumatoid arthritis. It has been observed that levels of HGF increase in the plasma of patients with hepatic failure (Gohda et al., supra) and in the plasma (Hepatol., 13:734-750 (1991)) or serum (J. Biochem., 109:8-13 (1991)) of animals with experimentally induced liver damage. HGF has also been shown to be a mitogen for certain cell types, including melanocytes, renal tubular cells, keratinocytes, certain endothelial cells and cells of epithelial origin (Biochem. Biophys. Res.
  • Metastatic SCC cells overexpress c-Met and have enhanced tumoregenesis and metastasis in vivo [G. Gong et al., Oncogene, 23:6199-6208 (2004)].
  • C-Met is required for tumor cell survival [N. Shinomiya et al., Cancer Research, 64:7962-7970 (2004)].
  • C. Birchmeier et al. Nature Reviews/Molecular Biology 4:915-925 (2003).
  • a compound that reduces the effect of HGF would be a useful compound.
  • Compounds of the current invention have not been previously described as inhibitors of angiogenesis such as for the treatment of cancer.
  • Kirin publication WO 00/43366 describes substituted phenyl compounds.
  • Kirin publication WO 03/000660 describes substituted phenyl compounds.
  • Substituted quinolines are described in US Patent No. 6,143,764.
  • WO 02/32872 describes substituted quinolines.
  • Patent Application WO 00/47212 describes substituted quinazoline derivatives.
  • Patent Application WO 98/37079 describes substituted N-heterocyclic compounds.
  • Kubo et al, Biorg. Med. Chem., 11 :5117-33 (2003) describes phenoxyquinoline derivatives.
  • Patent Application WO 04/46133 published 3 June 2004, describes amino- heterocycles for treating pain.
  • Patent Application WO 03/004472 published 16 January 2003, describes pyrazine-2-carboxamides.
  • JP63145272 published 17 June 1988, describes 4,5- dihydro-6-(4-substituted phenyl)-3(2H)-pyridazinones.
  • Kamel, et al., Egyptian J. of Pharm. Sci., 38:61-69 (1997) describes 4-substituted phenoxyquinolines.
  • Patent Application WO 04/18430 published 4 March 2004, describes quinoline derivatives.
  • Patent Application WO 02/32872 published 25 April 2002, describes urea derivatives.
  • Patent Application WO 04/37784 published 6 May 2004, describes substituted pyrrolidones.
  • Patent Application WO 00/50405 published 31 August 2000, describes quinoline-6-carboxamides.
  • Patent Application WO 04/083235 published 30 September 2004, describes azaheterocyclyl aromatic compounds.
  • T is selected from phenyl, 5-6-membered heteroaryl, or 5-6 membered heterocyclyl;
  • Z is selected from N or CR 7 ;
  • Z 1 is selected from N or CR 7 ;
  • W is a substituted or unsubstituted phenyl, a substituted or unsubstituted benzomorpholinyl, a substituted or unsubstituted 6-membered nitrogen containing heteroaryl; a substituted or unsubstituted c 3-7 cycloalkyl, c h alky and Ci- ⁇ alkynyl;
  • X is selected from O 5 S, S(O), SO 2 , NR 2 and CR 3 R 4 ;
  • W is benzomorpholinyl Y may further include -C(O);
  • R a is selected from H, alkyl, heterocyclyl, aryl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl; wherein R a is optionally substituted;
  • R 1 is a partially unsaturated or saturated ring selected from
  • J is N or CR 4a ;
  • J 2 is O or CR 4a R 4a ;
  • Q is a 1-5 membered saturated or partially unsaturated alkly chain, or a 2-5 membered saturated or partially unsaturated heteroalkyl chain;
  • R is selected from H, alkyl, haloalkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl and R 5 -carbonyl;
  • R 3 and R 4 are each independently selected from H, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, R 6 and alkyl substituted with R 6 ; alternatively R 3 and R 4 , together with the carbon atom they are attached to, form an optionally substituted 3-6 membered ring;
  • R 3a is absent or is selected from H, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, R 6 and alkyl substituted with R 6 ;
  • R 4a is absent or is selected from H, halo, -OR 5 -NR a R 5 , alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, R 6 and alkyl substituted with R 6 ;
  • R 5 is independently selected at each occurrence from H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl, alkylthioalkyl, arylalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl;
  • R 5a is independently selected at each occurrence from H, alkyl, haloalkyl, arylalkyl aminoalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl; or when R 5 and R a , or R 5a and R a is bonded to the same nitrogen atom, R a and R 5 , or R a and R 5a may independently optionally combine to form a heterocyclo ring.
  • the invention also relates to compounds wherein
  • R is selected from
  • R 5a is selected from H, C 1-6 -alkyl, C 1-6 -haloalkyl, phenyl-C 1-6 -alkyl, 5-6 membered heterocyclyl-C ⁇ -alkyl, C 3-6 -cycloalkyl-C 1-6 -alkyl, phenyl, 5-6-membered heterocyclyl, C 2-6 -alkenyl, C 2-6 -alkynyl and C 3-6 -cycloalkyl; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R 8 is independently selected from H, cyano, aminocarbonyl, C 1-3 -alkylaminocarbonyl, C 1-6 - alkyl, C 1-6 -alkoxy, C 1-3 -alkylamino-C 1-3 -alkoxy, 5-6 membered heterocyclyl-C 1-3 -alkoxy, C 4-6 -cycloalkyl-C 1-3 -alkoxy, 5-6 membered heterocyclyl-C 1-3 -(hydroxyalkoxy), C 3-6 - cycloalkyl-C 1-3 -(hydroxyalkoxy), C 1-2 -alkoxy-C 1-3 -alkoxy, phenyloxy-C 1-3 alkoxy, 5-6 membered heterocyclyloxy-C t o-alkoxy, cycloalkyloxy-C 1-3 -alkoxy, 5-6 membered heterocyclyloxy, and C 3-6 -cycloalkyloxy; in conjunction with any of the above or below
  • the invention also relates to compounds wherein
  • R 8 is independently selected from H, methyl, cyano, aminocarbonyl, methylaminocarbonyl, methoxy, dimethylaminopropoxy, 3-(morpholin-4-yl)ethoxy, 3-(pyrrolidin-l-yl)propoxy,
  • R is selected from 6,7-dimethoxy-4-quinolinyl, 6-methoxy-7-(dimethylaminopropoxy)-4- quinolinyl, 6-methoxy-7-(3 -(morpholin-4-yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 - (pyrrolidin-l-yl)propoxy)-4-quinolinyl, 6-methoxy-7-(2-hydroxy-3-(morpholin-4- yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 -(1 ,2,4-triazol- 1 -yl)propoxy)-4-quinolinyl, 6- methoxy-7-(3 -(4-methylpiperazin- 1 -yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 -(piperidin- 4-yl)propoxy)-4-quinolinyl, 6,7-dimethoxy-4
  • the invention also relates to compounds wherein W is selected from substituted or unsubstituted phenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted pyrimidinyl, substituted or unsubstituted pyridazinyl and substituted or unsubstituted pyrazinyl; in conjunction with any of the above or below embodiments.
  • W is selected from substituted or unsubstituted phenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted pyrimidinyl, substituted or unsubstituted pyridazinyl and substituted or unsubstituted pyrazinyl; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • W is substituted or unsubstituted phenyl; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • W is substituted or unsubstituted pyridyl; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein X is O; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • the invention also relates to compounds wherein
  • the invention also relates to compounds wherein p is 1 ; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein R 1 is selected from
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-1O ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and R a R 5a N-C 1-3 alkyl;
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyrid
  • R° is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R Sa R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1 -ylmethyl, pyrrolidin-1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R Sa is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membere
  • R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein
  • R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C 1-2 -alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two R c substituents, two R b substituents or R c together with R b together form an optionally substituted fused phenyl ring; or wherein two R c substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R 1 is selected from
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-Q. 3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-1O heteroaryl, optionally substituted C 3-6 cycloalkyl, and R a R 5a N-C 1-3 alkyl;
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 member
  • the invention also relates to compounds wherein
  • R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C ⁇ -alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two R c substituents, two R substituents or R c together with R b together form an optionally substituted fused phenyl ring; or wherein two R 0 substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein R 1 is selected from
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C ⁇ alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R ⁇ R 3 N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylinethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl,
  • the invention also relates to compounds wherein
  • the invention also relates to compounds wherein R 1 is selected from
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-1O heteroaryl, optionally substituted C 3-6 cycloalkyl, and
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 member
  • R a is selected from H, C 1-6 -alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C 1-6 -alkyl, optionally substituted 5-6 membered heterocyclyl-C 1-6 -alkyl, C 3-6 -cycloalkyl, C 3-6 -cycloalkyl-C 1-6 -alkyl, C 2-6 -alkenyl and C 2-6 -alkynyl; and
  • the invention also relates to compounds wherein
  • the invention also relates to compounds of Formula II
  • T is O or S
  • R 3 and R 4 is each independently selected from H, C 1-2 _alkyl, phenyl, 5-6-membered heterocyclyl, phenyl-C 1-2- alkyl, 5-6-membered heterocyclyl- Ci- 2 -alkyl, C 3-6- cycloalkyl, and Cs- ⁇ .cycloalkyl-Ci-2-alkyl; alternatively R 3 and R 4 , together with the atom they are attached to, form an optionally substituted 4-6 membered ring;
  • D 1 is selected from N or CR 11 ;
  • D 2 is selected from NR 13 , O, or CHR 11 ; provided either D 1 is N or D 2 is NR 13 ; O ring R d including D 1 D 2 forms an optionally substituted optionally benzo-fused 4-7 membered heterocyclic moiety,
  • R 11 is selected from H, halo, C 1-4 -alkyl, C 1-4 -haloalkyl, C 1-4 -hydroxyalkyl, -NH 2 , -OR 12 , alkoxycarbonyl, -CO 2 H, -CONR 3 R 5a , (C 1 -C 3 )alkylamino, diCCrC ⁇ alkylamino, (C 1 - C 3 )hydroxyalkylamino, (C 1 -C 3 )alkylamino-(C 1 -C 3 )alkylamino, C 1-3 -alkoxy-C 1-3 -alkyl, C 1- 3 -alkylamino-C 1-3 -alkyl, C 1-3 -alkylthio-C 1-3 -alkyl, optionally substituted phenyl-Ci- 3 -alkyl, 5-6 membered heterocyclyl-C 1-3 -alkyl, C 3-6 -cycloalkyl
  • R 5a is selected from H, alkyl, haloalkyl, arylalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl;
  • R 12 is selected from H, halo, C 1-2 -alkyl and methoxy;
  • R 13 is selected from H, alkyl, haloalkyl, optionally substituted phenylalkyl, optionally substituted 5-10 membered heterocyclylalkyl, cycloalkylalkyl, optionally substituted phenyl or naphthyl, optionally substituted 5-10 membered heterocyclyl and cycloalkyl.
  • R 9 and R 10 are independently selected from H, cyano, aminocarbonyl, C 1-3 - alkylaminocarbonyl, C 1-3 -alkylamino-C 1-3 -alkoxy, 5-6 membered heterocycryl-Q- 3 - alkoxy, C 4-6 -cycloalkyl-C 1-3 -alkoxy, 5-6 membered heterocyclyl-C 1-3 -(hydroxyalkoxy), C 3- 6 -cycloalkyl-C 1-3 -(hydroxyalkoxy), C 1-2 -alkoxy-C 1-3 -alkoxy, phenyloxy-C 1-3 alkoxy, 5-6 membered heterocyclyloxy-C 1-3 -alkoxy, cycloalkyloxy-C 1-3 -alkoxy, 5-6 membered heterocyclyloxy, and C 3-6 -cycloalkyloxy; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein R 9 is independently selected from H, methyl, cyano, aminocarbonyl, methylaminocarbonyl, methoxy, dimethylaminopropoxy, 3-(rnorpholin-4-yl)ethoxy, 3-(pyrrolidin-l-yl)propoxy, 2-hydroxy-3-(morpholin-4-yl)propoxy, 3-(l,2,4-triazol-l-yl)propoxy, 3-(4- methylpiperazin-l-yl)propoxy, 3-(piperidin-4-yl)propoxy, dimethylaminoethoxy and diethylaminoethoxy; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R 10 is methoxy; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • Z a is CH; wherein Z b is CH; wherein Z c is CF; and wherein Z d is CH; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein Z a is N; Z a is CH; Z° is CH; Z d is CH; and R 2 is H; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein Z a is CH; Z b is N; Z c is CH; Z d is CH; and R 12 is H; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wnercm Z a is CH; Z b is N; Z c is CH; Z d is N; and
  • R 12 is H; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and R a R 5a N-C 1-3 alkyl;
  • R e is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 member
  • R a is selected from H, C 1-6 -alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C 1-6 -alkyl, optionally substituted 5-6 membered heterocyclyl-C 1-6 -alkyl, C 3-6 -cycloalkyl, C 3-6 -cycloalkyl-C 1-6 -alkyl, C 2-6 -alkenyl and C 2 - 6 -alkynyl; and R 5a is selected from H, C 1-6 -alkyl, C 1-6 -haloalkyl, phenyl-C 1-6 -alkyl, 5-6 membered heterocyclyl-C 1-6 -alkyl, C 3-6 -cycloalkyl-C 1-6 -alkyl, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C 2 .
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6
  • R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C 1-2 -alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or two R c substituents, two R b substituents or R c together with R b together form an optionally substituted fused phenyl ring; or two R 0 substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R° is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, ⁇ yrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5
  • the invention also relates to compounds wherein
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 member
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl; and wherein
  • the invention also relates to compounds wherein R e is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl,
  • the invention also relates to compounds wherein
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobuty
  • R is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and R a R 5a N-C 1-3 alkyl;
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R ⁇ R 5 N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered
  • R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-Q.
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-1O heteroaryl, optionally substituted C 3-6 cycloalkyl, and
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobuty
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-1O ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and R a R 5a N-C 1-3 alkyl;
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optional
  • the invention also relates to compounds wherein
  • R b is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C 1-3 alkyl, optionally substituted C 1-6 - alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C 6-10 ary, optionally substituted C 6-10 heteroaryl, optionally substituted C 3-6 cycloalkyl, and R a R 5a N-Ci -3 alkyl;
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optional
  • R c is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R 5a R a N-, R 5a R a N-C 1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 member
  • R a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R 5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-Ci -2 - alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two R c substituents, two R b substituents or R c together with R b together form an optionally substituted fused phenyl ring; or wherein two R° substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein n is 0 or 1; in conjunction with any of the above or below embodiments; T is O; in conjunction with any of the above or below embodiments; and R 3 and R 4 are both H; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R is in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds R is
  • R 8a is C 1-3 alkyl or H; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds wherein
  • R 8a is C 1-3 alkyl or H ; in conjunction with any of the above or below embodiments.
  • the invention also relates to compounds and pharmaceutically acceptable salts and solvates thereof selected from
  • Compounds of the present invention would be useful for, but not limited to, the prevention or treatment of angiogenesis related diseases.
  • the compounds of the invention have kinase inhibitory activity, such as VEGFR/KDR and/or c-Met inhibitory activity.
  • the compounds of the invention are useful in therapy as antineoplasia agents or to minimize deleterious effects of VEGF and/or HGF.
  • neoplasia including cancer and metastasis, including, but not limited to: carcinoma such as cancer of the bladder, breast, colon, kidney, liver, lung (including small cell lung cancer), esophagus, gall-bladder, ovary, pancreas, stomach, cervix, thyroid, prostate, and skin (including squamous cell carcinoma); hematopoietic tumors of lymphoid lineage (including leukemia, acute lymphocitic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell-lymphoma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, hairy cell lymphoma and Burkett's lymphoma); hematopoietic tumors of myeloid lineage (including acute and chronic myelogenous leukemias, myelodysplastic syndrome and promyelocytic leukemia); tumors of me
  • tumors of the central and peripheral nervous system including astrocytoma, neuroblastoma, glioma and schwannomas); and other tumors (including melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid follicular cancer and Kaposi's sarcoma).
  • the compounds are useful for the treatment of neoplasia selected from lung cancer, colon cancer and breast cancer.
  • the compounds also would be useful for treatment of ophthalmological conditions such as corneal graft rejection, ocular neovascularization, retinal neovascularization including neovascularization following injury or infection, diabetic retinopathy, retrolental fibroplasia and neovascular glaucoma; retinal ischemia; vitreous hemorrhage; ulcerative diseases such as gastric ulcer; pathological, but non-malignant, conditions such as hemangiomas, including infantile hemaginomas, angiofibroma of the nasopharynx and avascular necrosis of bone; and disorders of the female reproductive system such as endometriosis.
  • the compounds are also useful for the treatment of edema, and conditions of vascular hyperpermeability.
  • the compounds of the invention are useful in therapy of proliferative diseases. These compounds can be used for the treatment of an inflammatory rheumatoid or rheumatic disease, especially of manifestations at the locomotor apparatus, such as various inflammatory rheumatoid diseases, especially chronic polyarthritis including rheumatoid arthritis, juvenile arthritis or psoriasis arthropathy; paraneoplastic syndrome or tumor-induced inflammatory diseases, turbid effusions, collagenosis, such as systemic Lupus erythematosus, poly-myositis, dermato-myositis, systemic sclerodermia or mixed collagenosis; postinfectious arthritis (where no living pathogenic organism can be found at or in the affected part of the body), seronegative spondylarthritis, such as spondylitis ankylosans; vasculitis, sarcoidosis, or arthrosis; or further any combinations thereof.
  • synovial inflammation for example, synovitis, including any of the particular forms of synovitis, in particular bursal synovitis and purulent synovitis, as far as it is not crystal-induced.
  • synovial inflammation may for example, be consequential to or associated with disease, e.g. arthritis, e.g. osteoarthritis, rheumatoid arthritis or arthritis deformans.
  • the present invention is further applicable to the systemic treatment of inflammation, e.g. inflammatory diseases or conditions, of the joints or locomotor apparatus in the region of the tendon insertions and tendon sheaths.
  • Such inflammation may be, for example, consequential to or associated with disease or further (in a broader sense of the invention) with surgical intervention, including, in particular conditions such as insertion endopathy, myofasciale syndrome and tendomyosis.
  • the present invention is further especially applicable to the treatment of inflammation, e.g. inflammatory disease or condition, of connective tissues including dermatomyositis and myositis.
  • These compounds can be used as active agents against such disease states as arthritis, atherosclerosis, psoriasis, hemangiomas, myocardial angiogenesis, coronary and cerebral collaterals, ischemic limb angiogenesis, wound healing, peptic ulcer Helicobacter related diseases, fractures, cat scratch fever, rubeosis, neovascular glaucoma and retinopathies such as those associated with diabetic retinopathy or macular degeneration.
  • some of these compounds can be used as active agents against solid tumors, malignant ascites, hematopoietic cancers and hyperproliferative disorders such as thyroid hyperplasia (especially Grave's disease), and cysts (such as hypervascularity of ovarian stroma, characteristic of polycystic ovarian syndrome (Stein-Leventhal syndrome)) since such diseases require a proliferation of blood vessel cells for growth and/or metastasis.
  • thyroid hyperplasia especially Grave's disease
  • cysts such as hypervascularity of ovarian stroma, characteristic of polycystic ovarian syndrome (Stein-Leventhal syndrome)
  • some of these compounds can be used as active agents against burns, chronic lung disease, stroke, polyps, anaphylaxis, chronic and allergic inflammation, ovarian hyperstimulation syndrome, brain tumor-associated cerebral edema, high-altitude, trauma or hypoxia induced cerebral or pulmonary edema, ocular and macular edema, ascites, and other diseases where vascular hyperpermeability, effusions, exudates, protein extravasation, or edema is a manifestation of the disease.
  • the compounds will also be useful in treating disorders in which protein extravasation leads to the deposition of fibrin and extracellular matrix, promoting stromal proliferation (e.g. fibrosis, cirrhosis and carpal tunnel syndrome).
  • the compounds of the present invention are also useful in the treatment of ulcers including bacterial, fungal, Mooren ulcers and ulcerative colitis.
  • the compounds of the present invention are also useful in the treatment of conditions wherein undesired angiogenesis, edema, or stromal deposition occurs in viral infections such as Herpes simplex, Herpes Zoster, AIDS, Kaposi's sarcoma, protozoan infections and toxoplasmosis, following trauma, radiation, stroke, endometriosis, ovarian hyperstimulation syndrome, systemic lupus, sarcoidosis, synovitis, Crohn's disease, sickle cell anemia, Lyme disease, pemphigoid, Paget's disease, hyperviscosity syndrome, Osler-Weber-Rendu disease, chronic inflammation, chronic occlusive pulmonary disease, asthma, and inflammatory rheumatoid or rheumatic disease.
  • the compounds are also useful in the reduction of subcutaneous fat and for the treatment
  • the compounds of the present invention are also useful in the treatment of ocular conditions such as ocular and macular edema, ocular neovascular disease, scleritis, radial keratotomy, uveitis, vitritis, myopia, optic pits, chronic retinal detachment, post-laser complications, glaucoma, conjunctivitis, Stargardt's disease and Eales disease in addition to retinopathy and macular degeneration.
  • ocular conditions such as ocular and macular edema, ocular neovascular disease, scleritis, radial keratotomy, uveitis, vitritis, myopia, optic pits, chronic retinal detachment, post-laser complications, glaucoma, conjunctivitis, Stargardt's disease and Eales disease in addition to retinopathy and macular degeneration.
  • the compounds of the present invention are also useful in the treatment of cardiovascular conditions such as atherosclerosis, restenosis, arteriosclerosis, vascular occlusion and carotid obstructive disease.
  • the compounds of the present invention are also useful in the treatment of cancer related indications such as solid tumors, sarcomas (especially Ewing's sarcoma and osteosarcoma), retinoblastoma, rhabdomyosarcomas, neuroblastoma, hematopoietic malignancies, including leukemia and lymphoma, tumor-induced pleural or pericardial effusions, and malignant ascites.
  • cancer related indications such as solid tumors, sarcomas (especially Ewing's sarcoma and osteosarcoma), retinoblastoma, rhabdomyosarcomas, neuroblastoma, hematopoietic malignancies, including leukemia and lymphoma, tumor-induced pleural or pericardial effusions, and malignant ascites.
  • the compounds of the present invention are also useful in the treatment of diabetic conditions such as diabetic retinopathy and microangiopathy.
  • the compounds of the present invention are also useful in the reduction of blood flow in a tumor in a subject.
  • the compounds of the present invention are also useful in the reduction of metastasis of a tumor in a subject.
  • the compounds of this invention may also act as inhibitors of other protein kinases, e.g. tie-2, lck, src, fgf, c-Met, ron, ckit and ret, and thus be effective in the treatment of diseases associated with other protein kinases.
  • other protein kinases e.g. tie-2, lck, src, fgf, c-Met, ron, ckit and ret.
  • these compounds are also useful for veterinary treatment of companion animals, exotic animals and farm animals, including mammals, rodents, and the like. More preferred animals include horses, dogs, and cats.
  • the compounds of the present invention include the pharmaceutically acceptable derivatives thereof.
  • Angiogenesis is defined as any alteration of an existing vascular bed or the formation of new vasculature, which benefits tissue perfasion. This includes the formation of new vessels by sprouting of endothelial cells from existing blood vessels or the remodeling of existing vessels to alter size, maturity, direction or flow properties to improve blood perfasion of tissue.
  • HGF refers to hepatocyte growth factor/scatter factor.
  • HGF hepatocyte growth factor/scatter factor isolated from species other than humans.
  • c-Met refers to the receptor for HGF. This includes purified receptor, fragments of receptor, chemically synthesized fragments of receptor, derivatives or mutated versions of receptor, and fusion proteins comprising the receptor and another protein. "c-Met” as used herein also includes the HGF receptor isolated from a species other than humans. As used herein, “HGF” refers to hepatocyte growth factor/scatter factor.
  • HGF hepatocyte growth factor/scatter factor isolated from species other than humans.
  • c-Met refers to the receptor for HGF. This includes purified receptor, fragments of receptor, chemically synthesized fragments of receptor, derivatives or mutated versions of receptor, and fusion proteins comprising the receptor and another protein. "c-Met” as used herein also includes the HGF receptor isolated from a species other than humans. As used herein, the terms “hepatocyte growth factor” and “HGF” refer to a growth factor typically having a structure with six domains (finger, Kringle 1, Kringle 2, Kringle 3, Kringle 4 and serine protease domains).
  • HGF hepatocyte growth factor
  • HGF hepatocyte growth factor from humans
  • huHGF hepatocyte growth factor from humans
  • rat HGF any non-human mammalian species, and in particular rat HGF.
  • the terms as used herein include mature, pre, pre-pro, and pro forms, purified from a natural source, , chemically synthesized or recombinantly produced.
  • Human HGF is encoded by the cDNA sequence published by Miyazawa et al. (1989), supra, or Nakamura et al. (1989), supra.
  • sequences reported by Miyazawa et al. and Nakamura et al. differ in 14 amino acids. The reason for the differences is not entirely clear; polymorphism or cloning artifacts are among the possibilities. Both sequences are specifically encompassed by the foregoing terms. It will be understood that natural allelic variations exist and can occur among individuals, as demonstrated by one or more amino acid differences in the amino acid sequence of each individual.
  • the terms "hepatocyte growth factor” and "HGF” specifically include the delta 5 huHGF as disclosed by Sel ⁇ et al., supra.
  • HGF receptor and "c-Met” when used herein refer to a cellular receptor for HGF, which typically includes an extracellular domain, a transmembrane domain and an intracellular domain, as well as variants and fragments thereof which retain the ability to bind HGF.
  • HGF receptor and "c-Met” include the polypeptide molecule that comprises the full-length, native amino acid sequence encoded by the gene variously known as pl90.sup.MET. The present definition specifically encompasses soluble forms of HGF receptor, and HGF receptor from natural sources, synthetically produced in vitro or obtained by genetic manipulation including methods of recombinant DNA technology.
  • the HGF receptor variants or fragments preferably share at least about 65% sequence homology, and more preferably at least about 75% sequence homology with any domain of the human c-Met amino acid sequence published in Rodrigues et al., MoI. Cell. Biol., 11:2962-2970 (1991); Park et al., Proc. Natl. Acad. Sci., 84:6379-6383 (1987); or Ponzetto et al., Oncogene, 6:553-
  • agonist and “agonistic” when used herein refer to or describe a molecule which is capable of, directly or indirectly, substantially inducing, promoting or enhancing HGF biological activity or HGF receptor activation.
  • cancer and “cancerous” when used herein refer to or describe the physiological condition in mammals that is typically characterized by unregulated cell growth.
  • cancer examples include but are not limited to, carcinoma, lymphoma, sarcoma, blastoma and leukemia. More particular examples of such cancers include squamous cell carcinoma, lung cancer, pancreatic cancer, cervical cancer, bladder cancer, hepatoma, breast cancer, colon carcinoma, and head and neck cancer. While the term "cancer” as used herein is not limited to any one specific form of the disease, it is believed that the methods of the invention will be particularly effective for cancers which are found to be accompanied by increased levels of
  • HGF HGF or expression of c-Met in the mammal.
  • treating refers to curative therapy, prophylactic therapy, and preventative therapy.
  • mammal refers to any mammal classified as a mammal, including humans, cows, horses, dogs and cats. In a preferred embodiment of the invention, the mammal is a human.
  • nucleic acid ligands Given that elevated levels of c-Met and HGF are observed in hypertension, arteriosclerosis, myocardial infarction, and rheumatoid arthritis, nucleic acid ligands will serve as useful therapeutic agents for these diseases.
  • treatment includes therapeutic treatment as well as prophylactic treatment
  • a “pharmaceutically-acceptable derivative” denotes any salt, ester of a compound of this invention, or any other compound which upon administration to a patient is capable of providing (directly or indirectly) a compound of this invention, or a metabolite or residue thereof, characterized by the ability to inhibit angiogenesis.
  • the phrase "therapeutically-effective" is intended to qualify the amount of each agent, which will achieve the goal of improvement in disorder severity and the frequency of incidence over treatment of each agent by itself, while avoiding adverse side effects typically associated with alternative therapies. For example, effective neoplastic therapeutic agents prolong the survivability of the patient, inhibit the rapidly proliferating cell growth associated with the neoplasm, or effect a regression of the neoplasm.
  • H denotes a single hydrogen atom. This radical may be attached, for example, to an oxygen atom to form a hydroxyl radical.
  • alkyl is used, either alone or within other terms such as “haloalkyl” and “alkylamino", it embraces linear or branched radicals having one to about twelve carbon atoms. More preferred alkyl radicals are “lower alkyl” radicals having one to about six carbon atoms. Examples of such radicals include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isoamyl, hexyl and the like. Even more preferred are lower alkyl radicals having one or two carbon atoms.
  • alkylenyl embraces bridging divalent alkyl radicals such as methylenyl and ethyl enyl.
  • lower alkyl substituted with R 2 does not include an acetal moiety.
  • alkenyl embraces linear or branched radicals having at least one carbon- carbon double bond of two to about twelve carbon atoms. More preferred alkenyl radicals are “lower alkenyl” radicals having two to about six carbon atoms. Most preferred lower alkenyl radicals are radicals having two to about four carbon atoms. Examples of alkenyl radicals include ethenyl, propenyl, allyl, propenyl, butenyl and 4-methylbutenyl.
  • alkenyl and “lower alkenyl” embrace radicals having "cis” and “trans” orientations, or alternatively, "E” and "Z” orientations.
  • alkynyl denotes linear or branched radicals having at least one carbon- carbon triple bond and having two to about twelve carbon atoms. More preferred alkynyl radicals are "lower alkynyl” radicals having two to about six carbon atoms. Most preferred are lower alkynyl radicals having two to about four carbon atoms. Examples of such radicals include propargyl, butynyl, and the like.
  • halo means halogens such as fluorine, chlorine, bromine or iodine atoms.
  • haloalkyl embraces radicals wherein any one or more of the alkyl carbon atoms is substituted with halo as defined above. Specifically embraced are monohaloalkyl, dihaloalkyl and polyhaloalkyl radicals including perhaloalkyl.
  • a monohaloalkyl radical for one example, may have either an iodo, bromo, chloro or fluoro atom within the radical.
  • Dihalo and polyhaloalkyl radicals may have two or more of the same halo atoms or a combination of different halo radicals.
  • “Lower haloalkyl” embraces radicals having 1-6 carbon atoms. Even more preferred are lower haloalkyl radicals having one to three carbon atoms. Examples of haloalkyl radicals include fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl.
  • Perfluoroalkyl means alkyl radicals having all hydrogen atoms replaced with fluoro atoms. Examples include trifluoromethyl and pentafluoroethyl.
  • hydroxyalkyl embraces linear or branched alkyl radicals having one to about ten carbon atoms any one of which may be substituted with one or more hydroxyl radicals. More preferred hydroxyalkyl radicals are "lower hydroxyalkyl” radicals having one to six carbon atoms and one or more hydroxyl radicals. Examples of such radicals include hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxybutyl and hydroxyhexyl. Even more preferred are lower hydroxyalkyl radicals having one to three carbon atoms.
  • alkoxy embraces linear or branched oxy-containing radicals each having alkyl portions of one to about ten carbon atoms. More preferred alkoxy radicals are "lower alkoxy" radicals having one to six carbon atoms. Examples of such radicals include methoxy, ethoxy, propoxy, butoxy and tert-butoxy. Even more preferred are lower alkoxy radicals having one to three carbon atoms. Alkoxy radicals may be further substituted with one or more halo atoms, such as fluoro, chloro or bromo, to provide "haloalkoxy" radicals. Even more preferred are lower haloalkoxy radicals having one to three carbon atoms. Examples of such radicals include fluoromethoxy, chloromethoxy, trifluoromethoxy, trifiuoroethoxy, fluoroethoxy and fluoropropoxy.
  • aryl alone or in combination, means a carbocyclic aromatic system containing one or two rings wherein such rings may be attached together in a fused manner.
  • aryl embraces aromatic radicals such as phenyl, naphthyl, indenyl, tetrahydronaphthyl, and indanyl. More preferred aryl is phenyl.
  • Said "aryl” group may have 1 to 3 substituents such as lower alkyl, hydroxyl, halo, haloalkyl, nitro, cyano, alkoxy and lower alkylamino. Phenyl substituted with -0-CH 2 -O- forms the aryl benzodioxolyl substituent.
  • heterocyclyl embraces saturated, partially saturated and unsaturated heteroatom-containing ring radicals, where the heteroatoms may be selected from nitrogen, sulfur and oxygen. It does not include rings containing -O-O-,-O-S- or -S-S- portions.
  • Said "heterocyclyl” group may have 1 to 3 substiruents such as hydroxyl, Boc, halo, haloalkyl, cyano, lower alkyl, lower aralkyl, oxo, lower alkoxy, amino and lower alkylamino.
  • saturated heterocyclic radicals include saturated 3 to 6-membered heteromonocyclic groups containing 1 to 4 nitrogen atoms [e.g.
  • pyrrolidinyl imidazolidinyl, piperidinyl, pyrrolinyl, piperazinyl]; saturated 3 to 6-membered heteromonocyclic group containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms [e.g. morpholinyl]; saturated 3 to 6- membered heteromonocyclic group containing 1 to 2 sulfur atoms and 1 to 3 nitrogen atoms [e.g., thiazolidinyl].
  • partially saturated heterocyclyl radicals include dihydrothienyl, dihydropyranyl, dihydrofuryl and dihydrothiazolyl.
  • unsaturated heterocyclic radicals also termed "heteroaryl” radicals
  • unsaturated heterocyclic radicals include unsaturated 5 to 6 membered heteromonocyclyl group containing 1 to 4 nitrogen atoms, for example, pyrrolyl, imidazolyl, pyrazolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazolyl [e.g., 4H-l,2,4-triazolyl, IH-1, 2,3 -triazolyl, 2H-1,2,3- triazolyl]; unsaturated 5 ⁇ - to 6-membered heteromonocyclic group containing an oxygen atom, for example, pyranyl, 2-furyl, 3-furyl, etc.; unsaturated 5 to 6-membered heteromonocyclic group containing a sulfur atom, for example, 2-thienyl, 3-thienyl,
  • heterocyclyl also embraces radicals where heterocyclic radicals are fused/condensed with aryl radicals: unsaturated condensed heterocyclic group containing 1 to 5 nitrogen atoms, for example, indolyl, isoindolyl, indolizinyl, benzimidazolyl, quinolyl, isoquinolyl, indazolyl, benzotriazolyl, tetrazolopyridazinyl [e.g., tetrazolo [l,5-b]pyridazinyl]; unsaturated condensed heterocyclic group containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms [e.g.
  • Preferred heterocyclic radicals include five to ten membered fused or unfused radicals.
  • heteroaryl radicals include quinolyl, isoquinolyl, imidazolyl, pyridyl, thienyl, thiazolyl, oxazolyl, furyl, and pyrazinyl.
  • Other preferred heteroaryl radicals are 5- or 6-membered heteroaryl, containing one or two heteroatoms selected from sulfur, nitrogen and oxygen, selected from thienyl, furyl, pyrrolyl, indazolyl, pyrazolyl, oxazolyl, triazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, pyridyl, piperidinyl and pyrazinyl.
  • non-nitrogen containing heteroaryl include pyranyl, 2-furyl, 3- furyl, 2-thienyl, 3-thienyl, benzofuryl, benzothienyl, and the like.
  • partially saturated and saturated heterocyclyl include pyrrolidinyl, imidazolidinyl, piperidinyl, pyrrolinyl, pyrazolidinyl, piperazinyl, morpholinyl, tetrahydropyranyl, thiazolidinyl, dihydrothienyl, 2,3-dihydro-benzo[l,4]dioxanyl, indolinyl, isoindolinyl, dihydrobenzothienyl, dihydrobenzofuryl, isochromanyl, chromanyl, 1,2- dihydroquinolyl, 1,2,3,4-tetrahydro-isoquinolyl, 1,2,3,4-tetraliydro-quinolyl, 2,
  • sulfonyl whether used alone or linked to other terms such as alkylsulfonyl, denotes respectively divalent radicals -SO 2 -.
  • sulfamyl denotes a sulfonyl radical substituted with an amine radical, forming a sulfonamide (-SO 2 NH 2 ).
  • alkylaminosulfonyl includes "N-alkylaminosulfonyl” where sulfamyl radicals are independently substituted with one or two alkyl radical(s). More preferred alkylaminosulfonyl radicals are “lower alkylaminosulfonyl” radicals having one to six carbon atoms. Even more preferred are lower alkylaminosulfonyl radicals having one to three carbon atoms. Examples of such lower alkylaminosulfonyl radicals include N-methylaminosulfonyl, and N-ethylaminosulfonyl.
  • carboxy or “carboxyl”, whether used alone or with other terms, such as “carboxyalkyl”, denotes -CO 2 H.
  • N-alkylaminocarbonyl and N,N-dialkylaminocarbonyl denote aminocarbonyl radicals independently substituted with one or two alkyl radicals, respectively. More preferred are “lower alkylaminocarbonyl” having lower alkyl radicals as described above attached to an aminocarbonyl radical.
  • N-arylaminocarbonyl and “N-alkyl-N-arylaminocarbonyl” denote aminocarbonyl radicals substituted, respectively, with one aryl radical, or one alkyl and one aryl radical.
  • heterocyclylalkylenyl and “heterocyclylalkyl” embrace heterocyclic- substituted alkyl radicals. More preferred heterocyclylalkyl radicals are "5- or 6-membered heteroarylalkyl” radicals having alkyl portions of one to six carbon atoms and a 5- or 6- membered heteroaryl radical. Even more preferred are lower heteroarylalkylenyl radicals having alkyl portions of one to three carbon atoms. Examples include such radicals as pyridylmethyl and thienylmethyl.
  • aralkyl embraces aryl-substituted alkyl radicals.
  • Preferable aralkyl radicals are "lower aralkyl” radicals having aryl radicals attached to alkyl radicals having one to six carbon atoms. Even more preferred are “phenylalkylenyl” attached to alkyl portions having one to three carbon atoms. Examples of such radicals include benzyl, diphenylmethyl and phenylethyl.
  • the aryl in said aralkyl may be additionally substituted with halo, alkyl, alkoxy, halkoalkyl and haloalkoxy.
  • alkylthio embraces radicals containing a linear or branched alkyl radical, of one to ten carbon atoms, attached to a divalent sulfur atom. Even more preferred are lower alkylthio radicals having one to three carbon atoms.
  • An example of “alkylthio” is methylthio, (CH 3 S-).
  • haloalkylthio embraces radicals containing a haloalkyl radical, of one to ten carbon atoms, attached to a divalent sulfur atom. Even more preferred are lower haloalkylthio radicals having one to three carbon atoms. An example of “haloalkylthio” is trifluoromethylthio.
  • alkylamino embraces “N-alkylamino” and "N,N-dialkylamino” where amino groups are independently substituted with one alkyl radical and with two alkyl radicals, respectively. More preferred alkylamino radicals are “lower alkylamino” radicals having one or two alkyl radicals of one to six carbon atoms, attached to a nitrogen atom. Even more preferred are lower alkylamino radicals having one to three carbon atoms. Suitable alkylamino radicals may be mono or dialkylamino such as N-methylamino, N-ethylamino, N 5 N- dimethylamino, N,N-diethylamino and the like.
  • arylamino denotes amino groups, which have been substituted with one or two aryl radicals, such as N-phenylamino.
  • the arylamino radicals may be further substituted on the aryl ring portion of the radical.
  • heteroarylamino denotes amino groups, which have been substituted with one or two heteroaryl radicals, such as N-thienylamino.
  • heteroarylamino radicals may be further substituted on the heteroaryl ring portion of the radical.
  • aralkylamino denotes amino groups, which have been substituted with one or two aralkyl radicals. More preferred are phenyl-Q-Cralkylamino radicals, such as N- benzylamino.
  • the aralkylamino radicals may be further substituted on the aryl ring portion.
  • N-alkyl-N-arylamino and “N-aralkyl-N-alkylamino” denote amino groups, which have been independently substituted with one aralkyl and one alkyl radical, or one aryl and one alkyl radical, respectively, to an amino group.
  • aminoalkyl embraces linear or branched alkyl radicals having one to about ten carbon atoms any one of which may be substituted with one or more amino radicals. More preferred aminoalkyl radicals are "lower aminoalkyl” radicals having one to six carbon atoms and one or more amino radicals. Examples of such radicals include aminomethyl, aminoethyl, aminopropyl, aminobutyl and aminohexyl. Even more preferred are lower aminoalkyl radicals having one to three carbon atoms.
  • alkylaminoalkyl embraces alkyl radicals substituted with alkylamino radicals. More preferred alkylaminoalkyl radicals are "lower alkylaminoalkyl” radicals having alkyl radicals of one to six carbon atoms. Even more preferred are lower alkylaminoalkyl radicals having alkyl radicals of one to three carbon atoms. Suitable alkylaminoalkyl radicals may be mono or dialkyl substituted, such as N-methylaminomethyl, N,N-dimethyl-aminoethyl, N,N-diethylaminomethyl and the like.
  • alkylaminoalkoxy embraces alkoxy radicals substituted with alkylamino radicals. More preferred alkylaminoalkoxy radicals are "lower alkylaminoalkoxy” radicals having alkoxy radicals of one to six carbon atoms. Even more preferred are lower alkylaminoalkoxy radicals having alkyl radicals of one to three carbon atoms. Suitable alkylaminoalkoxy radicals may be mono or dialkyl substituted, such as N-methylaminoethoxy, N,N-dimethylaminoethoxy, N,N-diethylaminoethoxy and the like.
  • alkylaminoalkoxyalkoxy embraces alkoxy radicals substituted with alkylaminoalkoxy radicals. More preferred alkylaminoalkoxyalkoxy radicals are "lower alkylaminoalkoxyalkoxy" radicals having alkoxy radicals of one to six carbon atoms. Even more preferred are lower alkylaminoalkoxyalkoxy radicals having alkyl radicals of one to three carbon atoms.
  • Suitable alkylaminoalkoxyalkoxy radicals may be mono or dialkyl substituted, such as N-methylaminomethoxyethoxy, N-methylaminoethoxyethoxy, N 5 N- dimethylaminoethoxyethoxy, N,N-diethylaminomethoxymethoxy and the like.
  • carboxyalkyl embraces linear or branched alkyl radicals having one to about ten carbon atoms any one of which maybe substituted with one or more carboxy radicals. More preferred carboxyalkyl radicals are "lower carboxyalkyl” radicals having one to six carbon atoms and one carboxy radical. Examples of such radicals include carboxymethyl, carboxypropyl, and the like. Even more preferred are lower carboxyalkyl radicals having one to three CH 2 groups.
  • halosulfonyl embraces sulfonyl radicals substituted with a halogen radical. Examples of such halosulfonyl radicals include chlorosulfonyl and fluorosulfonyl.
  • arylthio embraces aryl radicals of six to ten carbon atoms, attached to a divalent sulfur atom.
  • An example of “arylthio” is phenylthio.
  • aralkylthio embraces aralkyl radicals as described above, attached to a divalent sulfur atom. More preferred are phenyl-C 1 -C 3 -alkylthio radicals. An example of “aralkylthio” is benzylthio.
  • aryloxy embraces optionally substituted aryl radicals, as defined above, attached to an oxygen atom. Examples of such radicals include phenoxy.
  • aralkoxy embraces oxy-containing aralkyl radicals attached through an oxygen atom to other radicals. More preferred aralkoxy radicals are "lower aralkoxy” radicals having optionally substituted phenyl radicals attached to lower alkoxy radical as described above.
  • heteroaryloxy embraces optionally substituted heteroaryl radicals, as defined above, attached to an oxygen atom.
  • heteroarylalkoxy embraces oxy-containing heteroarylalkyl radicals attached through an oxygen atom to other radicals. More preferred heteroarylalkoxy radicals are "lower heteroarylalkoxy” radicals having optionally substituted heteroaryl radicals attached to lower alkoxy radical as described above.
  • cycloalkyl includes saturated carbocyclic groups.
  • Preferred cycloalkyl groups include C 3 -C 6 rings. More preferred compounds include, cyclopentyl, cyclopropyl, and cyclohexyl.
  • cycloalkylalkyl embraces cycloalkyl-s ⁇ bstituted alkyl radicals.
  • Preferable cycloalkylalkyl radicals are "lower cycloalkylalkyl” radicals having cycloalkyl radicals attached to alkyl radicals having one to six carbon atoms. Even more preferred are “5-6- membered cycloalkylalkyl” attached to alkyl portions having one to three carbon atoms. Examples of such radicals include cyclohexylmethyl.
  • the cycloalkyl in said radicals may be additionally substituted with halo, alkyl, alkoxy and hydroxy.
  • cycloalkenyl includes carbocyclic groups having one or more carbon- carbon double bonds including “cycloalkyldienyl” compounds.
  • Preferred cycloalkenyl groups include C 3 -C 6 rings. More preferred compounds include, for example, cyclopentenyl, cyclopentadienyl, cyclohexenyl and cycloheptadienyl.
  • the compounds of the invention are endowed with kinase inhibitory activity, such as KDR and/or c-Met inhibitory activity.
  • the present invention also comprises the use of a compound of the invention, or pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment either acutely or chronically of an angiogenesis mediated disease state, including those described previously.
  • the compounds of the present invention are useful in the manufacture of an anti-cancer medicament.
  • the compounds of the present invention are also useful in the manufacture of a medicament to attenuate or prevent disorders through inhibition of KDR and/or c-Met.
  • the present invention comprises a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formulas I-II in association with a least one pharmaceutically acceptable carrier, adjuvant or diluent.
  • the present invention also comprises a method of treating angiogenesis related disorders in a subject having or susceptible to such disorder, the method comprising treating the subject with a therapeutically effective amount of a compound of Formula I-II.
  • the compounds of the invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more compounds of the invention or other agents.
  • the therapeutic agents can be formulated as separate compositions that are administered at the same time or sequentially at different times, or the therapeutic agents can be given as a single composition.
  • co-therapy in defining use of a compound of the present invention and another pharmaceutical agent, is intended to embrace administration of each agent in a sequential manner in a regimen that will provide beneficial effects of the drug combination, and is intended as well to embrace co-administration of these agents in a substantially simultaneous manner, such as in a single capsule having a fixed ratio of these active agents or in multiple, separate capsules for each agent.
  • administration of compounds of the present invention may be in conjunction with additional therapies known to those skilled in the art in the prevention or treatment of neoplasia, such as with radiation therapy or with cytostatic or cytotoxic agents.
  • Compounds of Formula I may also be administered sequentially with known anticancer or cytotoxic agents when a combination formulation is inappropriate.
  • the invention is not limited in the sequence of administration; compounds of the invention maybe administered either prior to, simultaneous with or after administration of the known anticancer or cytotoxic agent.
  • standard treatment of primary tumors consists of surgical excision followed by either radiation or IV administered chemotherapy.
  • the typical chemotherapy regime consists of either DNA alkylating agents, DNA intercalating agents, CDK inhibitors, or microtubule poisons.
  • the chemotherapy doses used are just below the maximal tolerated dose and therefore dose limiting toxicities typically include, nausea, vomiting, diarrhea, hair loss, neutropenia and the like.
  • antineoplastic agents available in commercial use, in clinical evaluation and in pre-clinical development, which would be selected for treatment of neoplasia by combination drug chemotherapy.
  • Such antineoplastic agents fall into several major categories, namely, antibiotic-type agents, alkylating agents, antimetabolite agents, hormonal agents, immunological agents, interferon-type agents and a category of miscellaneous agents.
  • a first family of antineoplastic agents which may be used in combination with compounds of the present invention, consists of antimetabolite-type/thymidilate synthase inhibitor antineoplastic agents.
  • Suitable antimetabolite antineoplastic agents may be selected from but not limited to the group consisting of 5-FU-fTbrinogen, acanthifolic acid, aminothiadiazole, brequinar sodium, carmofur, Ciba-Geigy CGP-30694, cyclopentyl cytosine, cytarabine phosphate stearate, cytarabine conjugates, Lilly DATHF, Merrel Dow DDFC, dezaguanine, dideoxycytidine, dideoxyguanosine, didox, Yoshitomi DMDC, doxifluridine, Wellcome EHNA, Merck & Co.
  • EX-Ol 5 isopropyl pyrrolizine, Lilly LY-188011, Lilly LY-264618, methobenzaprim, methotrexate, Wellcome MZPES, norspermidine, NCI NSC-127716, NCI NSC-264880, NCI NSC-39661, NCI NSC-612567, Warner-Lambert PALA, pentostatin, piritrexim, plicamycin, Asahi Chemical PL- AC, Takeda TAC-788, thioguanine, tiazofurin, Erbamont TIF, trimetrexate, tyrosine kinase inhibitors, Taiho UFT and uricytin.
  • a second family of antineoplastic agents which may be used in combination with compounds of the present invention, consists of alkylating-type antineoplastic agents.
  • Suitable alkylating-type antineoplastic agents may be selected from but not limited to the group consisting of Shionogi 254-S, aldo-phosphamide analogues, altretamine, anaxirone, Boehringer Mannheim BBR-2207, bestrabucil, budotitane, Wakunaga CA- 102, carboplatin, carmustine, Chinoin-139, Chinoin-153, chlorambucil, cisplatin, cyclophosphamide, American Cyanamid CL-286558, Sanofi CY-233, cyplatate, DegussaD-19-384, Sumimoto DACHP(Myr)2, diphenylspiromustine, diplatinum cytostatic, Erba distamycin derivatives, Chugai DWA- 2114R,
  • a third family of antineoplastic agents which may be used in combination with compounds of the present invention consists of antibiotic-type antineoplastic agents.
  • Suitable antibiotic-type antineoplastic agents may be selected from but not limited to the group consisting of Taiho 4181 -A, aclarubicin, actinomycin D, actinoplanone, Erbamont ADR-456, aeroplysinin derivative, Ajinomoto AN-201-II, Ajinomoto AN-3, Nippon Soda anisomycins, anthracycline, azino-mycin-A, bisucaberin, Bristol-Myers BL-6859, Bristol-Myers BMY- 25067, Bristol-Myers BMY-25551, Bristol-Myers BMY-26605, Bristol-Myers BMY-27557, Bristol-Myers BMY-28438, bleomycin sulfate, bryostatin-1, Taiho C-1027, calichemycin, chrom
  • a fourth family of antineoplastic agents which may be used in combination with compounds of the present invention consists of a miscellaneous family of antineoplastic agents, including tubulin interacting agents, topoisomerase II inhibitors, topoisomerase I inhibitors and hormonal agents, selected from but not limited to the group consisting of ⁇ - carotene, ⁇ -difluoromethyl-arginine, acitretin, Biotec AD-5, Kyorin AHC-52, alstonine, amonafide, amphethinile, amsacrine, Angiostat, ankinomycin, anti-neoplaston AlO, antineoplaston A2, antineoplaston A3, antineoplaston A5, antineoplaston AS2-1, Henkel APD, aphidicolin glycinate, asparaginase, Avarol, baccharin, batracylin, benfluron, benzotript, Ipsen- Beaufour BIM-23015, bisantren
  • the present compounds may also be used in co-therapies with other anti- neoplastic agents, such as acemannan, aclarubicin, aldesleukin, alemtuzumab, alitretinoin, altretamine, amifostine, aminolevulinic acid, amrubicin, amsacrine, anagrelide, anastrozole, ANCER, ancestim, ARGLABIN, arsenic trioxide, BAM 002 (Novelos), bexarotene, bicalutamide, broxuridine, capecitabine, celmoleukin, cetrorelix, cladribine, clotrimazole, cytarabine ocfosfate, DA 3030 (Dong- A), daclizumab, denileukin diftitox, deslorelin, dexrazoxane, dilazep, docetaxel, docosanol,
  • the combination comprises a composition of the present invention in combination with at least one anti-angiogenic agent.
  • Agents are inclusive of, but not limited to, in vitro synthetically prepared chemical compositions, antibodies, antigen binding regions, radionuclides, and combinations and conjugates thereof.
  • An agent can be an agonist, antagonist, allosteric modulator, toxin or, more generally, may act to inhibit or stimulate its target (e.g., receptor or enzyme activation or inhibition), and thereby promote cell death or arrest cell growth.
  • anti-tumor agents include HERCEPTINTM (trastuzumab), which may be used to treat breast cancer and other forms of cancer, and RITUXANTM (rituximab), ZEVALINTM (ibritumomab tiuxetan), and LYMPHOCIDETM (epraruzumab), which maybe used to treat non-Hodgkin's lymphoma and other forms of cancer, GLEEV ACTM which may be used to treat chronic myeloid leukemia and gastrointestinal stromal tumors, and BEXXARTM (iodine 131 tositumomab) which may be used for treatment of non-Hodgkins's lymphoma.
  • anti-angiogenic agents include ERBITUXTM (IMC-C225), KDR (kinase domain receptor) inhibitory agents (e.g., antibodies and antigen binding regions that specifically bind to the kinase domain receptor), anti-VEGF agents (e.g., antibodies or antigen binding regions that specifically bind VEGF, or soluble VEGF receptors or a ligand binding region thereof) such as AVASTINTM or VEGF-TRAPTM, and anti-VEGF receptor agents (e.g., antibodies or antigen binding regions that specifically bind thereto), EGFR inhibitory agents (e.g., antibodies or antigen binding regions that specifically bind thereto) such as ABX-EGF (panirumumab), IRESSATM (gefitinib), TARCEVATM (erlotinib), anti-Angl and anti-Ang2 agents (e.g., antibodies or antigen binding regions specifically binding thereto or to their receptors, e.g., Tie2/Tek), and anti-
  • compositions of the present invention can also include one or more agents (e.g., antibodies, antigen binding regions, or soluble receptors) that specifically bind and inhibit the activity of growth factors, such as antagonists of hepatocyte growth factor (HGF, also known as Scatter Factor), and antibodies or antigen binding regions that specifically bind its receptor "c-met".
  • agents e.g., antibodies, antigen binding regions, or soluble receptors
  • HGF hepatocyte growth factor
  • c-met antibodies or antigen binding regions that specifically bind its receptor "c-met”.
  • anti-angiogenic agents include Campath, IL-8, B-FGF, Tek antagonists (Ceretti et al., US Publication No. 2003/0162712; US Patent No. 6,413,932), anti-TWEAK agents (e.g., specifically binding antibodies or antigen binding regions, or soluble TWEAK receptor antagonists; see, Wiley, US Patent No. 6,727,225), ADAM distintegrin domain to antagonize the binding of integrin to its ligands (Fanslow et al., US Publication No. 2002/0042368), specifically binding anti-eph receptor and/or anti-ephrin antibodies or antigen binding regions (US Patent Nos.
  • anti-PDGF-BB antagonists e.g., specifically binding antibodies or antigen binding regions
  • antibodies or antigen binding regions specifically binding to PDGF-BB ligands
  • PDGFR kinase inhibitory agents e.g., antibodies or antigen binding regions that specifically bind thereto
  • Additional anti-angiogenic/anti-tumor agents include: SD-7784 (Pfizer, USA); cilengitide.(Merck KGaA, Germany, EPO 770622); pegaptanib octasodium, (Gilead Sciences, USA); Alphastatin, (BioActa, UK); M-PGA, (Celgene, USA, US 5712291); ilomastat, (Arriva, USA, US 5892112); emaxan ⁇ b, (Pfizer, USA, US 5792783); vatalanib, (Novartis, Switzerland); 2-methoxyestradiol, (EntreMed, USA); TLC ELL- 12, (Elan, Ireland); anecortave acetate, (Alcon, USA); al ⁇ ha-D148 Mab, (Amgen, USA); CEP-7055,(Cephalon, USA); anti- Vn Mab, (Crucell, Netherlands) DAC:antiangiogenic, (Conju
  • Endostatin (Boston Childrens Hospital, USA); ATN 161, (Attenuon, USA); ANGIOST ATIN, (Boston Childrens Hospital, USA); 2-methoxyestradiol, (Boston Childrens Hospital, USA); ZD 6474, (AstraZeneca, UK); ZD 6126, (Angiogene Pharmaceuticals, UK); PPI 2458, (Praecis, USA); AZD 9935, (AstraZeneca, UK); AZD 2171, (AstraZeneca, UK); vatalanib (pINN), (Novartis, Switzerland and Schering AG, Germany); tissue factor pathway inhibitors, (EntreMed, USA); pegaptanib (Pinn), (Gilead Sciences, USA); xanthorrhizol, (Yonsei University, South Korea); vaccine, gene-based, VEGF-2, (Scripps Clinic and Research Foundation, USA); SPV5.2, (Supratek, Canada); SDX
  • VE-cadherin-2 antagonists (ImClone Systems, USA); Vasostatin, (National Institutes of Health, USA);vaccine, FIk-I, (ImClone Systems, USA); TZ 93, (Tsumura, Japan); TumStatin, (Beth Israel Hospital, USA); truncated soluble FLT 1 (vascular endothelial growth factor receptor 1), (Merck & Co, USA); Tie-2 ligands, (Regeneron, USA); and, thrombospondin 1 inhibitor, (Allegheny Health, Education and Research Foundation, USA).
  • the present compounds may also be used in co-therapies with other antineoplastic agents, such as VEGF antagonists, other kinase inhibitors including p38 inhibitors, KDR inhibitors, EGF inhibitors and CDK inhibitors, TNF inhibitors, metallomatrix proteases inhibitors (MMP), COX-2 inhibitors including celecoxib, NSAID 's, or ⁇ v ⁇ 3 inhibitors.
  • VEGF antagonists such as VEGF antagonists, other kinase inhibitors including p38 inhibitors, KDR inhibitors, EGF inhibitors and CDK inhibitors, TNF inhibitors, metallomatrix proteases inhibitors (MMP), COX-2 inhibitors including celecoxib, NSAID 's, or ⁇ v ⁇ 3 inhibitors.
  • the present invention comprises processes for the preparation of a compound of Formula I-II.
  • pharmaceutically acceptable salts are also included in the family of compounds of Formula I-II.
  • pharmaceutically-acceptable salts embraces salts commonly used to form alkali metal salts and to form addition salts of free acids or free bases. The nature of the salt is not critical, provided that it is pharmaceutically acceptable.
  • Suitable pharmaceutically acceptable acid addition salts of compounds of Formula I-II may be prepared from an inorganic acid or from an organic acid. Examples of such inorganic acids are hydrochloric, hydrobromic, hydroiodic, nitric, carbonic, sulfuric and phosphoric acid.
  • organic acids may be selected from aliphatic, cycloaliphatic, aromatic, arylaliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, example of which are formic, acetic, adipic, butyric, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, mesylic, 4- hydroxybenzoic, phenylacetic, mandelic, embonic (pamoic), methanesulfonic, ethanesulfonic, ethanedisulfonic, benzenesulfonic, pantothenic, 2-hydroxyethanesulfonic, toluenesulfonic, sulfanilic, cyclohexylaminosulfonic, camphoric, camphors
  • Suitable pharmaceutically-acceptable base addition salts of compounds of Formula I-II include metallic salts, such as salts made from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc, or salts made from organic bases including primary, secondary and tertiary amines, substituted amines including cyclic amines, such as caffeine, arginine, diethylamine, N-ethyl piperidine, aistidine, glucamine, isopropylamine, lysine, morpholine, N- ethyl morpholine, piperazine, piperidine, triethylamine, trimethylamine.
  • metallic salts such as salts made from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc
  • organic bases including primary, secondary and tertiary amines, substituted amines including cyclic amines, such as caffeine, arginine, diethylamine, N-ethyl piperidine, aistidine, glucamine, isoprop
  • All of these salts may be prepared by conventional means from the corresponding compound of the invention by reacting, for example, the appropriate acid or base with the compound of Formula I-II.
  • a compound of Formula I-II may also form internal salts.
  • the halo substituted ring R-halo 1 is condensed with an alcohol 2 (where X is O) is heated, preferably in the presence of a catalyst such as DMAP, solvent such as dioxane, and base, such as pyridine to form the ether 3.
  • a catalyst such as DMAP
  • solvent such as dioxane
  • base such as pyridine
  • the reaction is heated above RT, more preferably above 75 0 C 5 even more preferably at about 110 0 C.
  • the nitro compound 3 is reduced to the amine 4 such as by treatment with Fe, HCl and an alcohol such as MeOH, in an appropriate solvent such as THF.
  • the amine 4 is coupled with a carboxylic acid derivative R ⁇ OH, such as a carboxylic acid or anhydride, in the presence of a coupling agent such as HATU, or with PyBOP and base such as DIEA, to yield the desired compounds 5.
  • a carboxylic acid derivative R ⁇ OH such as a carboxylic acid or anhydride
  • a coupling agent such as HATU
  • PyBOP and base such as DIEA
  • compounds of the invention where X is O and R 1 is 2-oxopyrrolyl can be prepared by the method described in Scheme 2.
  • the halo substituted quinoline derivative 6, is condensed with alcohol 7 is heated, preferably in the presence of a catalyst such as DMAP, solvent such as dioxane, and base, such as pyridine to form ether 8.
  • a catalyst such as DMAP
  • solvent such as dioxane
  • base such as pyridine
  • the reaction is heated above RT, more preferably above 75 °C, even more preferably at about 110 °C.
  • the nitro compound 8 is reduced to the amine 9 such as by treatment with Fe, HCl and an alcohol such as MeOH, in an appropriate solvent such as THF.
  • the amine 9 is coupled with a carboxylic acid, in the presence of a coupling agent such as HATU to yield the desired compounds 10.
  • compounds of the invention where R 1 is 2-oxoimidazolyl can be prepared by the method described in Scheme 3.
  • the amine 9 can be activated such as with a chloroformate to form the caarbamate 11.
  • the substituted imidazolidin-2-one is treated with base, such as NaH, in an appropriate solvent such as DMF and added to the carbamate 11 to provide the desired compounds 12.
  • R 1 is 2-oxopyrrolyl
  • the N-protected 2-oxopyrrolidine 13 is alkylated such as by treatment with base, e.g. LDA, in a suitable solvent such as THF, followed by addition of a compound with an appropriate leaving group, such as a halo substituent.
  • the reaction temperature is preferably below RT, preferably at about 0 0 C.
  • the free amine 15 is treated with a chlorformate in the presence of base, such as TEA, to form the active ester 16.
  • Treatment with the ester 16 with an amine yields the desired amides 17.
  • Substituted pyridazines 21 of the invention can be prepared by the method described in Scheme 5. Hydrazines 18 are reacted with oxaldehyde then with 2,2-dimethyl-l,3-dioxane- 4,6-dione followed by acid, such as acetic acid ,and piperidines, to form the diaza butadiene-4- ylidene 19. Cyclization, such as by treatment with base, e.g. sodium methoxide, yields the pyridazine carboxylic acid 20. The reaction is heated at a temperature above RT, preferably at about reflux. Formation of the desired amides 21 from the pyridazine 20 is by the coupling procedure described above, or with PyBOP and base such as DIEA.
  • Substituted pyrimidines 25 of the invention can be prepared by the method described in Scheme 6. Alkylation of the oxo-l,6-dihydropyrimidine ester 22, such as by reaction with the appropriate halide in the presence of base, e.g. K 2 CO 3 , and a solvent such as DMF, provided the substituted pyrimidines 23. De-esterification of 23, such as by treatment with base, e.g. NaOH, provides the carboxylic acid 24, which can be coupled via the methods described above to provide the amides 25.
  • base e.g. K 2 CO 3
  • a solvent such as DMF
  • Substituted oxazolidine acetamides 28 of the invention can be prepared by the method described in Scheme 7.
  • Treatment of the amine 9 with an activated acetyl compound, e.g. chloroacetyl chloride, such as in the presence of base, e.g. NaHCO 3 provides the chloroacetamide 26.
  • the reaction is held at a temperature below RT, preferably at about 0 °C.
  • Imidazolidine acetic acids 31 of the invention can be prepared by the method described in Scheme 8. Alkylation of the imidazolidine 29, such as by treatment with base, e.g. NaH, followed by addition of the appropriate haloacetic acid ester provides the desired substituted imidazolidine 30. De-esterification of 30 such as by treatment with base, e.g. NaOH, provides the desired acetic acid 31, which can be coupled with an amine to provide the acetamides of the invention.
  • pyrrolyl acetic acids 37 of the invention can be prepared by the method described in Scheme 9.
  • Substituted hydroxyl-pyrroles 34 formed such as by Grignard reactions with pyrrolidine-2,5-dione and substituted magnesium bromides, are reduced, such with NaBH 3 CN and acid, e.g. HCl, to provide the pyrrolidones 35.
  • Alkylation of the pyrrolidone such as with treatment with base, e.g. NaH, followed by addition of 2- haloacetates, provides the desired pyrrolidinyl acetates 36.
  • De-esterification of 36 such as by treatment with acid, e.g. HCl, provides the desired pyrrolidinyl acetic acid 37 which can be treated with an amine as described above to provide the acetamides of the invention.
  • compounds of the invention where W is pyridyl can be prepared by the method described in Scheme 10.
  • the halo substituted quinoline derivative 38 is condensed with alcohol 39, preferably in the presence of a catalyst such as DMAP, solvent such as dioxane, and base, such as pyridine to form ether 40.
  • a catalyst such as DMAP
  • solvent such as dioxane
  • base such as pyridine
  • the reaction is heated above RT, more preferably above about 75 °C, even more preferably at about 105 0 C.
  • the halo compound 40 is converted to the amine 41 such as by treatment with LiHMDS, 2- (dicyclohexylphosphino)biphenyl and a palladium catalyst, such as Pd 2 (dba) 3 .
  • the reaction is heated above RT, more preferably at about 65 °C.
  • the amine 41 is coupled with a carboxylic acid, in the presence of a coupling agent such as HBTU
  • the starting compounds defined in Schemes 1-10 may also be present with functional groups in protected form if necessary and/or in the form of salts, provided a salt-forming group is present and the reaction in salt form is possible. If so desired, one compound of Formula I can be converted into another compound of Formula I or a N-oxide thereof; a compound of Formula I can be converted into a salt; a salt of a compound of Formula I can be converted into the free compound or another salt; and/or a mixture of isomeric compounds of Formula I can be separated into the individual isomers.
  • N-Oxides can be obtained in a known matter by reacting a compound of Formula I with hydrogen peroxide, oxone, or a peracid, e.g.
  • mCPBA in an inert solvent, e.g. CH 2 Cl 2 , or a mixture OfH 2 O and an alcohol such as MeOH or EtOH, at a temperature between about -10-35 °C, such as about O °C - RT.
  • an inert solvent e.g. CH 2 Cl 2
  • an alcohol such as MeOH or EtOH
  • the protecting groups may already be present in precursors and should protect the functional groups concerned against unwanted secondary reactions, such as acylations, etherifications, esterifications, oxidations, solvolysis, and similar reactions. It is a characteristic of protecting groups that they lend themselves readily, i.e. without undesired secondary reactions, to removal, typically by solvolysis, reduction, photolysis or also by enzyme activity, for example under conditions analogous to physiological conditions, and that they are not present in the end-products.
  • the specialist knows, or can easily establish, which protecting groups are suitable with the reactions mentioned above and hereinafter.
  • Salts of a compound of Formula I with a salt-forming group may be prepared in a manner known per se. Acid addition salts of compounds of Formula I may thus be obtained by treatment with an acid or with a suitable anion exchange reagent.
  • a salt with two acid molecules for example, a dihalogenide of a compound of Formula I
  • Salts can usually be converted to free compounds, e.g. by treating with suitable basic agents, for example with alkali metal carbonates, alkali metal hydrogen carbonates, or alkali metal hydroxides, typically potassium carbonate or sodium hydroxide.
  • suitable basic agents for example with alkali metal carbonates, alkali metal hydrogen carbonates, or alkali metal hydroxides, typically potassium carbonate or sodium hydroxide.
  • All process steps described here can be carried out under known reaction conditions, preferably under those specifically mentioned, in the absence of or usually in the presence of solvents or diluents, preferably such as are inert to the reagents used and able to dissolve these, in the absence or presence of catalysts, condensing agents or neutralizing agents, for example ion exchangers, typically cation exchangers, for example in the H + form, depending on the type of reaction and/or reactants at reduced, normal, or elevated temperature, for example in the range from about -100 °C to about 190 °C, preferably from about -80 0 C to about 150 °C, for example at about -80 0 C to about 60 °C, at RT, at about -20 °C to about 40 °C or at the boiling point of the solvent used, under atmospheric pressure or in a closed vessel, where appropriate under pressure, and/or in an inert atmosphere, for example under argon or nitrogen.
  • solvents or diluents
  • Salts may be present in all starting compounds and transients, if these contain salt- forming groups. Salts may also be present during the reaction of such compounds, provided the reaction is not thereby disturbed. In certain cases, typically in hydrogenation processes, it is possible to achieve stereoselective reactions, allowing for example easier recovery of individual isomers.
  • the solvents from which those can be selected which are suitable for the reaction in question include for example H 2 O, esters, typically lower alkyl-lower alkanoates, e.g., EtOAc, ethers, typically aliphatic ethers, e.g., Et 2 O, or cyclic ethers, e.g., THF, liquid aromatic hydrocarbons, typically benzene or toluene, alcohols, typically MeOH, EtOH or 1-propanol, IPOH, nitriles, typically CH 3 CN, halogenated hydrocarbons, typically CH 2 Cl 2 , acid amides, typically DMF, bases, typically heterocyclic nitrogen bases, e.g.
  • carboxylic acids typically lower alkanecarboxylic acids, e.g., AcOH
  • carboxylic acid anhydrides typically lower alkane acid anhydrides, e.g., acetic anhydride
  • cyclic linear, or branched hydrocarbons, typically cyclohexane, hexane, or isopentane, or mixtures of these solvents, e.g., aqueous solutions, unless otherwise stated in the description of the process.
  • solvent mixtures may also be used in processing, for example in chromatography.
  • the invention relates also to those forms of the process in which one starts from a compound obtainable at any stage as a transient and carries out the missing steps, or breaks off the process at any stage, or forms a starting material under the reaction conditions, or uses said starting material in the form of a reactive derivative or salt, or produces a compound obtainable by means of the process according to the invention and processes the said compound in situ.
  • the compounds of Formula I are also obtainable in the form of hydrates, or their crystals can include for example the solvent used for crystallization (present as solvates).
  • New starting materials and/or intermediates, as well as processes for the preparation thereof, are likewise the subject of this invention.
  • such starting materials are used and reaction conditions so selected as to enable the preferred compounds to be obtained.
  • optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, e.g., by formation of diastereoisomeric salts, by treatment with an optically active acid or base.
  • appropriate acids are tartaric, diacetyltartaric, dibenzoyltartaric, ditoluoyltartaric, and camphorsulfonic acid and then separation of the mixture of diastereoisomers by crystallization followed by liberation of the optically active bases from these salts.
  • a different process for separation of optical isomers involves the use of a chiral chromatography column optimally chosen to maximize the separation of the enantiomers.
  • Still another available method involves synthesis of covalent diastereoisomeric molecules by reacting compounds of the invention with an optically pure acid in an activated form or an optically pure isocyanate.
  • the synthesized diastereoisomers can be separated by conventional means such as chromatography, distillation, crystallization or sublimation, and then hydrolyzed to deliver the enantiomerically pure compound.
  • the optically active compounds of the invention can likewise be obtained by using optically active starting materials. These isomers may be in the form of a free acid, a free base, an ester or a salt.
  • the compounds of this invention may contain one or more asymmetric centers and thus occur as racemates and racemic mixtures, scalemic mixtures, single enantiomers, individual diastereomers and diastereomeric mixtures. All such isomeric forms of these compounds are expressly included in the present invention.
  • the compounds of this invention may also be represented in multiple tautomeric forms, for example, as illustrated below:
  • the invention expressly includes all tautomeric forms of the compounds described herein.
  • the compounds may also occur in cis- or trans- or E- or Z- double bond isomeric forms. All such isomeric forms of such compounds are expressly included in the present invention. All crystal forms of the compounds described herein are expressly included in the present invention.
  • Substituents on ring moieties may be attached to specific atoms, whereby they are intended to be fixed to that atom, or they may be drawn unattached to a specific atom, whereby they are intended to be attached at any available atom that is not already substituted by an atom other than H (hydrogen).
  • the compounds of this invention may contain heterocyclic ring systems attached to another ring system.
  • Such heterocyclic ring systems may be attached through a carbon atom or a heteroatom in the ring system.
  • a compound of any of the formulas delineated herein maybe synthesized according to any of the processes delineated herein, hi the processes delineated herein, the steps may be performed in an alternate order and may be preceded, or followed, by additional protection/deprotection steps as necessary.
  • the processes may further comprise use of appropriate reaction conditions, including inert solvents, additional reagents, such as bases (e.g., LDA, DIEA, pyridine, K 2 CO 3 , and the like), catalysts, and salt forms of the above.
  • bases e.g., LDA, DIEA, pyridine, K 2 CO 3 , and the like
  • Purification methods include, for example, crystallization, chromatography (liquid and gas phase, and the like), extraction, distillation, trituration, reverse phase HPLC and the like. Reactions conditions such as temperature, duration, pressure, and atmosphere (inert gas, ambient) are known in the art and may be adjusted as appropriate for the reaction.
  • the compounds of this invention may be modified by appending appropriate functionalities to enhance selective biological properties.
  • modifications are known in the art and include those which increase biological penetration into a given biological compartment (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.
  • Step 1 l-methyl-2-phenyl-5-(pyridin-4-yl)-l,2-dihydropyrazol-3-one.
  • thyl isonicotinoylacetate (3.01 g, 16 mmol) and l-methyl-2-phenylhydrazine (2.03 g, 17 mmol) were suspended in water (50 ml) and glacial acetic acid (1.35 ml, 23 mmol) was added.
  • the flask was fitted with a reflux condensor and placed in a preheated oil bath (115 C) and stirred.
  • Step 2 l-methyI-3-oxo-2-phenyI-5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4- carbaldehyde.
  • N 5 N- dimethylformamide 10.0 ml, 130 mmol.
  • the flask was cooled in an ice water bath, and phosphorous oxychloride (4.2 ml, 45 mmol) was added.
  • the reaction was warmed to room temperature and stirred under nitrogen.
  • Step 3 l-methyI-3-oxo-2-phenyl-5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxyIic acid.
  • the crude l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4- carbaldehyde was dissolved in t-BuOH ( ⁇ 70 ml) and 2-methyl-2-butene (25 ml, 236 mmol) was added, followed by sodium chlorite (2.43 g, 27 mmol) in water (30 ml) with ⁇ 5 ml water rinse.
  • potassium phosphate monobasic (10.35 g, 76 mmol) was added as a suspension in water ( ⁇ 70 ml), and the reaction was stirred at room temperature. After 9 hours, the reaction was poured into water (400 ml) and the aqueous phase was then extracted with EtOAc, DCM, and 10:1 DCM / MeOH exhaustively until most of the product had been extracted.
  • Step 4 N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-methyl-3-oxo-2-phenyl- 5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide.
  • Step 1 Methyl l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate.
  • Step 2 Methyl 5-(bromomethyl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxylate.
  • Methyl l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (7.82 g, 31.8 mmol) was dissolved in CHCl 3 (150 ml) and n-bromosuccimide (6.91 g, 38.8 mmol) was added. The reaction was stirred at room temperature, and after 1.5 hours, more NBS (6.23 g, 35.2 mmol) was added.
  • Step 3 Methyl l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH- pyrazole-4-carboxylate.
  • Methyl 5-(bromomethyl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylate (1.266 g, 3.9 mmol) was dissolved in dichlormethane (30 ml) and pyrrolidine (0.40 ml, 4.8 mmol) was added via syringe. The reaction was stirred under nitrogen at room temperature.
  • Step 4 l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH-pyrazole-4- carboxylic acid.
  • Methyl l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH- pyrazole-4-carboxylate (1.182 g, 3.7 mmol) was dissolved in MeOH (17 ml) and sodium hydroxide (4.2 ml, , 1.0 M, 4.2 mmol) and solid sodium hydroxide (282 mg, 7.05 mmol) were added.
  • Step 5 N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-
  • Step 1 Ethyl l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate.
  • dichloromethane 10 niL
  • methyl trifluoromethanesulfonate 1200 mg, 7.3 mmol.
  • the red solution was stirred at room temperature. After 14 h, the mixture was partitioned between dichloromethane and NaHCO 3 (sat). The aqueous was extracted with dichloromethane (2x).
  • Step 2 N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide.
  • a solution of ethyl l-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxylate (260 mg, 1056 ⁇ mol) in MeOH was treated with NaOH (1000 ⁇ l, 5000 ⁇ mol) in H 2 O (3 mL). The mixture was heated to 6O 0 C for 30 min and then cooled to room temperature. Then, the mixture was neutralized with aq.
  • Step 1 Benzyl 5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate.
  • a suspension of 3-methyl-l-phenyl-lH-pyrazol-5-ol (10.0 g, 57 mmol) and calcium hydroxide (8.5 g, 115 mmol) in dry 1,4-dioxane (10OmL) was heated to 50 °C for 20 min. The suspension was chilled to 10 °C and benzyl chloro formate (8.2 ml, 57 mmol) was in dioxane (1OmL) added.
  • Step 2 Benzyl l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylate.
  • benzyl 5 -hydroxy-3 -methyl- 1-phenyl- lH-pyrazole-4-carboxylate 3380 mg, 11 mmol
  • trimethylaluminum (16 niL, 33 mmol, 2M in toluene). Internal temperature reached 27 °C.
  • l,2-epoxy-2-methylpropane 1000 mg, 16 mmol
  • Step 3 l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylic acid.
  • benzyl l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate 300 mg, 789 ⁇ mol
  • MeOH MeOH
  • Pd/C 40mg
  • Step 4 N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide.
  • N-(3-fluoro-4-(7-Methoxyquinolin-4-yloxy)phenyl)-l,2-dimethyl-3-oxo-5-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide A mixture of HATU (458 mg, 1206 ⁇ mol), 1,2- dimethyl-3-oxo-5-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylic acid (140 mg, 603 ⁇ mol), 3- fluoro-4-(7-methoxyquinolin-4-yloxy)benzenamine (258 mg, 908 ⁇ mol), and Triethylamine (254 ⁇ L, 1809 ⁇ mol) in DMF (2 mL) was stirred at 6O 0 C overnight.
  • Step 1 l-(2-(l,3-dioxo-l,3-dihydro-2H-isoindol-2-yl)ethyl)-N-(3-fluoro-4-((7-
  • Step 2 l-(2-aminoethyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide.

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Abstract

Selected compounds are effective for prophylaxis and treatment of diseases, such as HGF mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

Description

SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS
FIELD OF THE INVENTION
This invention is in the field of pharmaceutical agents and specifically relates to compounds, compositions, uses and methods for treating cancer.
BACKGROUND OF THE INVENTION
Protein kinases represent a large family of proteins, which play a central role in the regulation of a wide variety of cellular processes, maintaining control over cellular function. A partial list of such kinases includes abl, Akt, bcr-abl, BIk, Brk, Btk, c-kit, c-Met, c-src, c-fins, CDKl , CDK2, CDK3 , CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDKl 0, cRafl , CSF 1 R, CSK, EGFR, ErbB2, ErbB3, ErbB4, Erk, Fak, fes, FGFRl, FGFR2, FGFR3, FGFR4, FGFR5, Fgr, flt-1, Fps, Frk, Fyn, Hck, IGF-IR, INS-R, Jak, KDR, Lck, Lyn, MEK, ρ38, PDGFR, PIK, PKC, PYK2, ros, tie, tie2, TRK, Yes, and Zap70. Inhibition of such kinases has become an important therapeutic target. Certain diseases are known to be associated with deregulated angiogenesis, for example ocular neovascularisation, such as retinopathies (including diabetic retinopathy), age-related macular degeneration, psoriasis, hemangioblastoma, hemangioma, arteriosclerosis, inflammatory disease, such as a rheumatoid or rheumatic inflammatory disease, especially arthritis (including rheumatoid arthritis), or other chronic inflammatory disorders, such as chronic asthma, arterial or post-transplantational atherosclerosis, endometriosis, and neoplastic diseases, for example so-called solid tumors and liquid tumors (such as leukemias).
At the center of the network regulating the growth and differentiation of the vascular system and its components, both during embryonic development and normal growth, and in a wide number of pathological anomalies and diseases, lies the angiogenic factor known as Vascular Endothelial Growth Factor"(VEGF; originally termed 'Vascular Permeability Factor", VPF), along with its cellular receptors (see G. Breier et al., Trends in Cell Biology, 6:454-456 (1996)).
VEGF is a dimeric, disulfide-linked 46-kDa glycoprotein related to "Platelet-Derived Growth Factor" (PDGF); it is produced by normal cell lines and tumor cell lines; is an endothelial cell-specific mitogen; shows angiogenic activity in in vivo test systems (e.g. rabbit cornea); is chemotactic for endothelial cells and monocytes; and induces plasminogen activators in endothelial cells, which are involved in the proteolytic degradation of extracellular matrix during the formation of capillaries. A number of isoforms of VEGF are known, which show comparable biological activity, but differ in the type of cells that secrete them and in their heparin-binding capacity, m aααiuυn, mwc cue uiu« * family, such as "Placenta Growth Factor"(PlGF) and VEGF-C.
VEGF receptors (VEGFR) are transmembranous receptor tyrosine kinases. They are characterized by an extracellular domain with seven immunoglobulin-like domains and an intracellular tyrosine kinase domain. Various types of VEGF receptor are known, e.g. VEGFR- 1 (also known as flt-1), VEGFR-2 (also known as KDR)5 and VEGFR-3.
A large number of human tumors, especially gliomas and carcinomas, express high levels of VEGF and its receptors. This has led to the hypothesis that the VEGF released by tumor cells stimulates the growth of blood capillaries and the proliferation of tumor endothelium in a paracrine manner and through the improved blood supply, accelerates tumor growth. Increased VEGF expression could explain the occurrence of cerebral edema in patients with glioma. Direct evidence of the role of VEGF as a tumor angiogenesis factor in vivo is shown in studies in which VEGF expression or VEGF activity was inhibited. This was achieved with anti-VEGF antibodies, with dominant-negative VEGFR-2 mutants, which inhibited signal transduction, and with antisense-VEGF RNA techniques. All approaches led to a reduction in the growth of glioma cell lines or other tumor cell lines in vivo as a result of inhibited tumor angiogenesis.
Angiogenesis is regarded as an absolute prerequisite for tumors, which grow beyond a diameter of about 1-2 mm; up to this limit, oxygen and nutrients may be supplied to the tumor cells by diffusion. Every tumor, regardless of its origin and its cause, is thus dependent on angiogenesis for its growth after it has reached a certain size.
Three principal mechanisms play an important part in the activity of angiogenesis inhibitors against tumors: 1) Inhibition of the growth of vessels, especially capillaries, into avascular resting tumors, with the result that there is no net tumor growth owing to the balance that is achieved between cell death and proliferation; 2) Prevention of the migration of tumor cells owing to the absence of blood flow to and from rumors; and 3) Inhibition of endothelial cell proliferation, thus avoiding the paracrine growth-stimulating effect exerted on the surrounding tissue by the endothelial cells which normally line the vessels. See R. Connell and J. Beebe, Exp. Opin. Ther. Patents, 11:77-114 (2001). VEGF's are unique in that they are the only angiogenic growth factors known to contribute to vascular hyperpermeability and the formation of edema. Indeed, vascular hyperpermeability and edema that is associated with the expression or administration of many other growth factors appears to be mediated via VEGF production. Inflammatory cytokines stimulate VEGF production. Hypoxia results in a marked upregulation of VEGF in numerous tissues, hence situations involving infarct, occlusion, ischemia, anemia, or circulatory impairment typically invoke VEGF/VPF-mediated responses. Vascular hyperpermeability, associated edema, altered transendothelial exchange and macromolecular extravasation, which is often accompanied by diapedesis, can result in excessive matrix deposition, aberrant stromal proliferation, fibrosis, etc. Hence, VEGF- mediated hyperpermeability can significantly contribute to disorders with these etiologic features. As such, regulators of angiogenesis have become an important therapeutic target. The hepatocyte growth factor receptor ("c-Met") is a unique receptor tyrosine kinase shown to be overexpressed in a variety of malignancies. c-Met typically comprises, in its native form, a 190-kDa heterodimeric (a disulfide-linked 50-kDa α-chain and a 145-kDa β- chain) membrane-spanning tyrosine kinase protein (Proc. Natl. Acad. Sci. USA, 84:6379-6383 (1987)). c-Met is mainly expressed in epithelial cells and stimulation of c-Met leads to scattering, angiogenesis, proliferation and metastasis. (See Cytokine and Growth Factor Reviews, 13:41-59 (2002)).
The ligand for c-Met is hepatocyte growth factor (also known as scatter factor, HGF and SF). HGF is a heterodimeric protein secreted by cells of mesodermal origin (Nature, 327:239-242 (1987); J. Cell Biol., 111:2097-2108 (1990)).
Various biological activities have been described for HGF through interaction with c- met (Hepatocyte Growth Factor- Scatter Factor (HGF-SF) and the c-Met Receptor, Goldberg and Rosen, eds., Birkhauser Verlag-Basel, 67-79 (1993). The biological effect of HGF/SF may depend in part on the target cell. HGF induces a spectrum of biological activities in epithelial cells, including mitogenesis, stimulation of cell motility and promotion of matrix invasion (Biochem. Biophys. Res. Comm., 122:1450-1459 (1984); Proc. Natl. Acad. Sci. U.S.A., 88:415-419 (1991)). It stimulates the motility and invasiveness of carcinoma cells, the former having been implicated in the migration of cells required for metastasis. HGF can also act as a "scatter factor", an activity that promotes the dissociation of epithelial and vascular endothelial cells (Nature, 327:239-242 (1987); J. Cell Biol., 111:2097-2108 (1990); EMBO J., 10:2867- 2878 (1991); Proc. Natl. Acad. Sci. USA, 90:649-653 (1993)). Therefore, HGF is thought to be important in tumor invasion (Hepatocyte Growth Factor-Scatter Factor (HGF-SF) and the C-Met Receptor, Goldberg and Rosen, eds., Birkhauser Verlag-Basel, 131-165 (1993)).
HGF and c-Met are expressed at abnormally high levels in a large variety of solid tumors. High levels of HGF and/or c-Met have been observed in liver, breast, pancreas, lung, kidney, bladder, ovary, brain, prostate, gallbladder and myeloma tumors in addition to many others. The role of HGF/c-Met in metastasis has been investigated in mice using cell lines transformed with HGF/c-Met (J. MoI. Med., 74:505-513 (1996)). Overexpression of the c-Met oncogene has also been suggested to play a role in the pathogenesis and progression of thyroid tumors derived from follicular epithelium (Oncogene, 7:2549-2553 (1992)). HGF is a morphogen (Development, 110:1271-1284 (1990); Cell, 66:697-711 (1991)) and a potent angiogenic factor (J. Cell Biol., 119:629-641 (1992)).
Recent work on the relationship between inhibition of angiogenesis and the suppression or reversion of tumor progression shows great promise in the treatment of cancer (Nature, 390:404-407 (1997)), especially the use of multiple angiogenesis inhibitors compared to the effect of a single inhibitor. Angiogenesis can be stimulated by HGF, as well as vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF).
Angiogenesis, the process of sprouting new blood vessels from existing vasculature and arteriogenesis, the remodeling of small vessels into larger conduit vessels are both physiologically important aspects of vascular growth in adult tissues. These processes of vascular growth are required for beneficial processes such as tissue repair, wound healing, recovery from tissue ischemia and menstrual cycling. They are also required for the development of pathological conditions such as the growth of neoplasias, diabetic retinopathy, rheumatoid arthritis, psoriasis, certain forms of macular degeneration, and certain inflammatory pathologies. The inhibition of vascular growth in these contexts has also shown beneficial effects in preclinical animal models. For example, inhibition of angiogenesis by blocking vascular endothelial growth factor or its receptor has resulted in inhibition of tumor growth and in retinopathy. Also, the development of pathological pannus tissue in rheumatoid arthritis involves angiogenesis and might be blocked by inhibitors of angiogenesis.
The ability to stimulate vascular growth has potential utility for treatment of ischemia- induced pathologies such as myocardial infarction, coronary artery disease, peripheral vascular disease, and stroke. The sprouting of new vessels and/or the expansion of small vessels in ischemic tissues prevents ischemic tissue death and induces tissue repair. Certain diseases are known to be associated with deregulated angiogenesis, for example ocular neovascularization, such as retinopathies (including diabetic retinopathy), age-related macular degeneration, psoriasis, hemangioblastoma, hemangioma, arteriosclerosis, inflammatory disease, such as a rheumatoid or rheumatic inflammatory disease, especially arthritis (including rheumatoid arthritis), or other chronic inflammatory disorders, such as chronic asthma, arterial or post- transplantational atherosclerosis, endometriosis, and neoplastic diseases, for example so-called solid tumors and liquid tumors (such as leukemias). Treatment of malaria and related viral diseases may also be mediated by HGF and cMet.
Elevated levels of HGF and c-Met have also been observed in non-oncological settings, such as hypertension, myocardial infarction and rheumatoid arthritis. It has been observed that levels of HGF increase in the plasma of patients with hepatic failure (Gohda et al., supra) and in the plasma (Hepatol., 13:734-750 (1991)) or serum (J. Biochem., 109:8-13 (1991)) of animals with experimentally induced liver damage. HGF has also been shown to be a mitogen for certain cell types, including melanocytes, renal tubular cells, keratinocytes, certain endothelial cells and cells of epithelial origin (Biochem. Biophys. Res. Commun., 176:45-51 (1991); Biochem. Biophys. Res. Commun., 174:831-838 (1991); Biochem., 30:9768-9780 (1991); Proc. Natl. Acad. Sci. USA, 88:415-419 (1991)). Both HGF and the c-Met proto- oncogene have been postulated to play a role in microglial reactions to CNS injuries (Oncogene, 8:219-222 (1993)).
Metastatic SCC cells overexpress c-Met and have enhanced tumoregenesis and metastasis in vivo [G. Gong et al., Oncogene, 23:6199-6208 (2004)]. C-Met is required for tumor cell survival [N. Shinomiya et al., Cancer Research, 64:7962-7970 (2004)]. For a general review see C. Birchmeier et al., Nature Reviews/Molecular Biology 4:915-925 (2003). In view of the role of HGF and/or c-Met in potentiating or promoting such diseases or pathological conditions, it would be useful to have a means of substantially reducing or inhibiting one or more of the biological effects of HGF and its receptor. Thus a compound that reduces the effect of HGF would be a useful compound. Compounds of the current invention have not been previously described as inhibitors of angiogenesis such as for the treatment of cancer.
Kirin Japanese patent application JPl 1158149, published 28 November 1997, describes substituted phenyl compounds. Kirin publication WO 00/43366 describes substituted phenyl compounds. Kirin publication WO 03/000660 describes substituted phenyl compounds. Substituted quinolines are described in US Patent No. 6,143,764. WO 02/32872 describes substituted quinolines. Patent Application WO 00/47212 describes substituted quinazoline derivatives. Patent Application WO 98/37079 describes substituted N-heterocyclic compounds. Kubo et al, Biorg. Med. Chem., 11 :5117-33 (2003) describes phenoxyquinoline derivatives. Patent Application WO 04/46133, published 3 June 2004, describes amino- heterocycles for treating pain. Patent Application WO 03/004472, published 16 January 2003, describes pyrazine-2-carboxamides. JP63145272, published 17 June 1988, describes 4,5- dihydro-6-(4-substituted phenyl)-3(2H)-pyridazinones. Kamel, et al., Egyptian J. of Pharm. Sci., 38:61-69 (1997) describes 4-substituted phenoxyquinolines. Patent Application WO 04/18430, published 4 March 2004, describes quinoline derivatives. Patent Application WO 02/32872, published 25 April 2002, describes urea derivatives. Patent Application WO 04/37784, published 6 May 2004, describes substituted pyrrolidones. Patent Application WO 00/50405 published 31 August 2000, describes quinoline-6-carboxamides. Patent Application WO 04/083235, published 30 September 2004, describes azaheterocyclyl aromatic compounds.
Compounds of the current invention have not been described as inhibitors of c-Met such as for the treatment of cancer.
DESCRIPTION OF THE INVENTION A class of compounds useful in treating cancer and angiogenesis is defined by Formula I
R-X-W-Y-R1 I
enantiomers, diastereomers, salts solvates, andN-oxides thereof wherein R is
Figure imgf000007_0001
T is selected from phenyl, 5-6-membered heteroaryl, or 5-6 membered heterocyclyl; Z is selected from N or CR7; Z1 is selected from N or CR7; W is a substituted or unsubstituted phenyl, a substituted or unsubstituted benzomorpholinyl, a substituted or unsubstituted 6-membered nitrogen containing heteroaryl; a substituted or unsubstituted c3-7cycloalkyl, chalky and Ci-βalkynyl; X is selected from O5 S, S(O), SO2, NR2 and CR3R4;
Y is selected from -NRaC(O)-(CR3R4)p-, -NRaC(=S)-(CR3R4)p-, -NRa-(CR3R4)p-, -NRa- (CR3R4)pC(=O)-, -NRa-(CR3R4)pC(=S)-, -NRaS(O)r, -NRaS(=O>(CR3R4)p-,
-C(=O)NRa-(CR3R4)p-, and -NRa-(CR3R4)p-S(=O)r, and where W is benzomorpholinyl Y may further include -C(O); Ra is selected from H, alkyl, heterocyclyl, aryl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl; wherein Ra is optionally substituted; R1 is a partially unsaturated or saturated ring selected from
Figure imgf000008_0001
wherein J is N or CR4a; J2 is O or CR4aR4a;
Q is a 1-5 membered saturated or partially unsaturated alkly chain, or a 2-5 membered saturated or partially unsaturated heteroalkyl chain;
R1 is optionally fused with an optionally substituted phenyl or an optionally substituted 5-6 membered heterocyclyl ring; wherein R1 is optionally substituted with one or more substituents independently selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-6 alkyl, R5(S=O)-C1-6 alky, NR5R5a-(C=O)-C1-6 alky, optionally substituted alkyl, alkenyl hydroxyalkyl, C1-6 alkoxy-Ci-6 alkyl, alkenylalkyl, C1-6 alkylthio-C1-3 alkyl, -C1-6 alkyl-NRa-C(=O)-OR5, • -C1-3 alkyl-NRa-(C=O)-R5, -C1-3 alkyl-C(=O)- C1-3 alkyl, aminoalkyl, hydroxy-substituted aminoalkyl, hydroxy-substituted haloalkyl, (heterocyclo)hydroxyalkyl, haloC1-6-alkyl, azidoalkyl, optionally substituted aryl-C1-6 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-6 alkyl, optionally substituted C1-6-alkyl, optionally substituted C3-7 cycloalkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted 5-10 membered heteroaryl, optionally, optionally substituted C3-6 cycloalkyl, substituted heteroarylalkyl, optionally substituted arylalkyl, and optionally substituted C6-^ aryl;
R is selected from H, alkyl, haloalkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl and R5-carbonyl;
R3 and R4 are each independently selected from H, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, R6 and alkyl substituted with R6; alternatively R3 and R4, together with the carbon atom they are attached to, form an optionally substituted 3-6 membered ring;
R3a is absent or is selected from H, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, R6 and alkyl substituted with R6; R4a is absent or is selected from H, halo, -OR5 -NRaR5, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, R6 and alkyl substituted with R6;
R5 is independently selected at each occurrence from H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl, alkylthioalkyl, arylalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl;
R5a is independently selected at each occurrence from H, alkyl, haloalkyl, arylalkyl aminoalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl; or when R5 and Ra, or R5aand Ra is bonded to the same nitrogen atom, Ra and R5, or Ra and R5a may independently optionally combine to form a heterocyclo ring.
R6 is selected from cyano, -OR2, -SR2, halo, -SO2R2, -C(=O)R2, -SO2NR2R5, -NR5C(=O)OR2, - NR5C(=O)NR5R2, -NR5C(=O)R2, -CO2R2, -C(=O)NR2R5 and -NR2R5;
R7 is selected from H, halo, cyano, -C(=O)NRaR5 and alkyl;
R8 is one or more substituents independently selected at each occurrence from H, cyano, hydroxyl, halo, optionally substituted heterocyclyl, -C(=O)NRaR5, -0C(=0)NRaR5, -
NRaC(=O)OR5, -NRaC(=0)-R5, R5R1N-O2S-, R5O2S-, R5O2SR3N-, R5R3N-, alkyl, aminoalkyl, alkylaminoalkyl, alkoxyalkyl, phenylalkyl, heterocyclylalkyl, alkoxy, haloalkoxy, alkylaminoalkoxy, arylalkoxy, heterocyclylalkoxy, cycloalkylalkoxy, heterocyclyl(hydroxyalkoxy), cycloalkyl(hydroxy alkoxy), aryl(hydroxyalkoxy), alkoxyalkoxy, aryloxyalkoxy, heterocyclyloxyalkoxy, cycloalkyloxyalkoxy, aryloxy, heterocyclyloxy, cycloalkyloxy; aryl and heteroaryl, alternatively where R comprises an NRaR5 moiety Ra and R5, together with the nitrogen atom they are attached to, may optionally form a substituted or unsubstituted 4-6 membered ring;
R8* is one or more substituents independently selected at each occurrence from H, cyano, hydroxyl, halo, optionally substituted heterocyclyl, -NRaC(=0)NRaR5'
NRaC(=NRb)-NR5, NRaC(=S)NRaR5, -OC(=O)NRaR5, -NRaC(=O)OR5, -NRaC(=0)-R5, R5R5N-O2S-, R5O2S-, R5O2SR3N-, R5RaN-, alkyl, aminoalkyl, alkylaminoalkyl, alkoxyalkyl, phenylalkyl, heterocyclylalkyl, alkoxy, haloalkoxy, alkylaminoalkoxy, arylalkoxy, heterocyclylalkoxy, cycloalkylalkoxy, heterocyclyl(hydroxyalkoxy), cycloalkyl(hydroxyalkoxy), aryl(hydroxyalkoxy), alkoxyalkoxy, aryloxyalkoxy, heterocyclyloxyalkoxy, cycloalkyloxyalkoxy, aryloxy, heterocyclyloxy, and cycloalkyloxy; alternatively where R8a comprises an NRaR5 moiety Ra and R5, together with the nitrogen atom they are attached to, may optionally form a substituted or unsubstituted 4-6 membered ring; p is O, 1, 2, or 3; and t is 0, 1 or 2; wherein each alkyl, aryl, heteroaryl, cycloalkyl, alkenyl, alkynyl, heterocyclyl, and alkoxy moiety of any R, R1, R2, R3, R4, R5, R7, R8, R8*, and Ra is optionally independently substituted with one or more groups independently selected at each occurrence from halo, oxo, -NRaR5, -OR5a, -CO2R5, -C(=O)R5, (d-C^alkylamino, -NH-N=NH, (Ci-Ctøalkyl, (Ci-C6)alkynyl, (C3-C6)cycloalkyl, (d-Q^aloalkyl, di(Ci-C6)alkylamino, (C1- C6)alkylamino-(C1-C6)alkyl,
Figure imgf000010_0001
(C1-C6)alkylamino-(C1- C6)alkylamino, phenyl, heterocyclic, heteroaryl, -(CR3R4)palkyl-S(=O)-alkyl, and -(CR3R4)palkyl-S(O)2-alkyl.
The invention also relates to compounds wherein
R is selected from
Figure imgf000010_0002
R8 is independently selected from H, cyano, hydroxy, -C(=O)NRaR5a, 5-6 membered heterocyclyl, -NRaC(=O)-R5a, R5aRaN-O2S-, R5aO2SRaN-5 R5aRaN-, C1-6-alkyl, amino-Ci-6- alkyl, C1-6-alkylamino-C1-6-alkyl, alkoxy-C1-6-alkyl, ρhenyl-C1-6-alkyl, heterocyclyl-C1-6- alkyl, C1-6-alkoxy, halo-C1-6-alkoxy, C1-6-alkylamino-C1-6-alkoxy, aryl-C1-6-alkoxy, 5-6- membered heterocyclyl-C1-6-alkoxy, C3-6-cycloalkyl-C1-6-alkoxy, 5-6-membered heterocyclyl(hydroxyl-C1-6-alkoxy), C3-6-cycloalkyl(hydroxyl-C1-6-alkoxy), phenyl(hydroxyl-C1-6-alkoxy), C1-6-alkoxy-C1-6-alkoxy, phenyloxy-C1-6-alkoxy, 5-6 membered heterocyclyloxy-C^e-alkoxy, C3-6-cycloalkyloxy-C1-6-alkoxy, phenyloxy, 5-6- membered heterocyclyloxy, and C3-6-cycloalkyloxy; Ra is selected from H, C1-6-alkyl, 5-6 membered heterocyclyl, phenyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and
R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C^-alkyl, C3-6-cycloalkyl-C1-6-alkyl, phenyl, 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
R8 is independently selected from H, cyano, aminocarbonyl, C1-3-alkylaminocarbonyl, C1-6- alkyl, C1-6-alkoxy, C1-3-alkylamino-C1-3-alkoxy, 5-6 membered heterocyclyl-C1-3-alkoxy, C4-6-cycloalkyl-C1-3-alkoxy, 5-6 membered heterocyclyl-C1-3-(hydroxyalkoxy), C3-6- cycloalkyl-C1-3-(hydroxyalkoxy), C1-2-alkoxy-C1-3-alkoxy, phenyloxy-C1-3alkoxy, 5-6 membered heterocyclyloxy-Cto-alkoxy, cycloalkyloxy-C1-3-alkoxy, 5-6 membered heterocyclyloxy, and C3-6-cycloalkyloxy; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
R8 is independently selected from H, methyl, cyano, aminocarbonyl, methylaminocarbonyl, methoxy, dimethylaminopropoxy, 3-(morpholin-4-yl)ethoxy, 3-(pyrrolidin-l-yl)propoxy,
2-hydroxy-3-(morpholin-4-yl)propoxy, 3-(l ,2,4-triazol-l -yl)propoxy, 3-(4- methylpiperazin-l-yl)propoxy, 3-(piperidin-4-yl)propoxy, dimethylaminoethoxy and diethylaminoethoxy; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein R is selected from 6,7-dimethoxy-4-quinolinyl, 6-methoxy-7-(dimethylaminopropoxy)-4- quinolinyl, 6-methoxy-7-(3 -(morpholin-4-yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 - (pyrrolidin-l-yl)propoxy)-4-quinolinyl, 6-methoxy-7-(2-hydroxy-3-(morpholin-4- yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 -(1 ,2,4-triazol- 1 -yl)propoxy)-4-quinolinyl, 6- methoxy-7-(3 -(4-methylpiperazin- 1 -yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 -(piperidin- 4-yl)propoxy)-4-quinolinyl, 6,7-dimethoxy-4-quinazolinyl and 6-methoxy-7-
(dimethylaminopropoxy)-4-quinazolinyl; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein W is selected from substituted or unsubstituted phenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted pyrimidinyl, substituted or unsubstituted pyridazinyl and substituted or unsubstituted pyrazinyl; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
W is substituted or unsubstituted phenyl; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
W is substituted or unsubstituted pyridyl; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein X is O; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Y is selected from -NHC(=O)-, -NHC(=O)-(CH2)P-, -NH-(CH2)P-, and -NH-(CH2)PC(=O)-; and wherein p is O or 1 ; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Y is -NHC(=O)-; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein p is 1 ; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein R1 is selected from
Figure imgf000012_0001
Figure imgf000013_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-1O ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-C1-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(-O)OR5a, -C(=0)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Ci-o-alkyl, C3-6-cycloalkyl, Ca-o-cycloalkyl-d-e-alkyl, C2-6-alkenyl and C2-6-alkynyl; and RSa is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycycloρropyl)methyl,, ethylaminomethyl, ρiperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a,
-C(=O)NR5aRa, and -C(=O)R5a ;
R° is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, RSaRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1 -ylmethyl, pyrrolidin-1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein RSa is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl wherein
Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein
R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
R1 is selected from
Figure imgf000015_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-Q.3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-1O heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-C1-3alkyl;
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-Ci.2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=0)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, Ci-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and
C3-6-cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, rnethoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR a, ~C(=O)NR5aRa, and -C(=O)R5a ; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(-O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein
R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C^-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two R substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two R0 substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein R1 is selected from
Figure imgf000017_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C^ alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and
RaR5aN-C1-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R^R3N-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylinethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-Ci-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Q-e-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-Ci-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, Cj-β-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, Co-e-alkynyl and C3-6-cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2 -hydroxy 2- methylbutyl, 2-hydroxy-2-methylρropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, and -C(-O)R5a ; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R53R3N-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)ORSa, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or R° together with Rb together form an optionally substituted fused phenyl ring; or wherein two R° substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein R1 is selected from
Figure imgf000019_0001
wherein
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-1O heteroaryl, optionally substituted C3-6 cycloalkyl, and
RaR5aN-C1-3alkyl;
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and
R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)~, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; or wherein two adjacent R0 substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxyproρyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, and -C(=O)R5a ; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two R° substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds of Formula II
Figure imgf000020_0001
wherein T is O or S;
R3 and R4 is each independently selected from H, C1-2_alkyl, phenyl, 5-6-membered heterocyclyl, phenyl-C1-2-alkyl, 5-6-membered heterocyclyl- Ci-2-alkyl, C3-6-cycloalkyl, and Cs-δ.cycloalkyl-Ci-2-alkyl; alternatively R3 and R4, together with the atom they are attached to, form an optionally substituted 4-6 membered ring;
R9 and R10 is independently selected from H, cyano, hydroxy, -C(=O)NRaR5a, 5-6 membered heterocyclyl, -NRaC(=O)-R5a, R5aRaN-O2S-, R5aO2SRaN-, R5aRaN-, C1-6-alkyl, amino-C1-6- alkyl, Ci-β-alkylarnino-Ci-δ-alkyl, alkoxy-C1-6-alkyl, hydroxy, aryl-C1-6-alkyl, heterocyclyl-C1-6-alkyl, C1-6-alkoxy, halo-C1-6-alkoxy, C1-6-alkylamino-C1-6-alkoxy, aryl- C1-6-alkoxy, 5-6-membered heterocyclyl, -C1-6alkoxy, C3-6-cycloalkyl-C1-6-alkoxy, 5-6- membered heterocyclyl(hydroxyl-C1-6-alkoxy), Cs-e-cycloalky^hydroxyl-Cμδ-alkoxy), phenyl(hydroxyl-C1-6-alkoxy), C1-6-alkoxy-C1-6-alkoxy, phenyloxy-C1-6-alkoxy, 5-6 membered heterocyclyloxy-Q-ό-alkoxy,
Figure imgf000021_0001
phenyloxy, 5-6- membered heterocyclyloxy, and C3-6-cycloalkyloxy; each of Za, Zb, Zc and Zd is independently selected from N or CH; provided no more than 2 of Za, Zb, Zc and Zd are N; n is O, 1, 2 or 3;
D1 is selected from N or CR11;
D2 is selected from NR13, O, or CHR11; provided either D1 is N or D2 is NR13; O ring Rd including D1 D2 forms an optionally substituted optionally benzo-fused 4-7 membered heterocyclic moiety,
R11 is selected from H, halo, C1-4-alkyl, C1-4-haloalkyl, C1-4-hydroxyalkyl, -NH2, -OR12, alkoxycarbonyl, -CO2H, -CONR3R5a, (C1-C3)alkylamino, diCCrC^alkylamino, (C1- C3)hydroxyalkylamino, (C1-C3)alkylamino-(C1-C3)alkylamino, C1-3-alkoxy-C1-3-alkyl, C1- 3-alkylamino-C1-3-alkyl, C1-3-alkylthio-C1-3-alkyl, optionally substituted phenyl-Ci-3-alkyl, 5-6 membered heterocyclyl-C1-3-alkyl, C3-6-cycloalkyl-C1-3-alkyl, optionally substituted phenyl, optionally substituted 5-6 membered heterocyclyl, and C3-6-cycloalkyl; Ra is selected from H, alkyl, heterocyclyl, aryl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl;
R5a is selected from H, alkyl, haloalkyl, arylalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl;
R12 is selected from H, halo, C1-2-alkyl and methoxy; R13 is selected from H, alkyl, haloalkyl, optionally substituted phenylalkyl, optionally substituted 5-10 membered heterocyclylalkyl, cycloalkylalkyl, optionally substituted phenyl or naphthyl, optionally substituted 5-10 membered heterocyclyl and cycloalkyl.
The invention also relates to compounds wherein R9 and R10 are independently selected from H, cyano, aminocarbonyl, C1-3- alkylaminocarbonyl, C1-3-alkylamino-C1-3-alkoxy, 5-6 membered heterocycryl-Q-3- alkoxy, C4-6-cycloalkyl-C1-3-alkoxy, 5-6 membered heterocyclyl-C1-3-(hydroxyalkoxy), C3- 6-cycloalkyl-C1-3-(hydroxyalkoxy), C1-2-alkoxy-C1-3-alkoxy, phenyloxy-C1-3alkoxy, 5-6 membered heterocyclyloxy-C1-3-alkoxy, cycloalkyloxy-C1-3-alkoxy, 5-6 membered heterocyclyloxy, and C3-6-cycloalkyloxy; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein R9 is independently selected from H, methyl, cyano, aminocarbonyl, methylaminocarbonyl, methoxy, dimethylaminopropoxy, 3-(rnorpholin-4-yl)ethoxy, 3-(pyrrolidin-l-yl)propoxy, 2-hydroxy-3-(morpholin-4-yl)propoxy, 3-(l,2,4-triazol-l-yl)propoxy, 3-(4- methylpiperazin-l-yl)propoxy, 3-(piperidin-4-yl)propoxy, dimethylaminoethoxy and diethylaminoethoxy; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
R10 is methoxy; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Za is CH; wherein Zb is CH; wherein Zc is CF; and wherein Zd is CH; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein Za is N; Za is CH; Z° is CH; Zd is CH; and R 2 is H; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein Za is CH; Zb is N; Zc is CH; Zd is CH; and R12 is H; in conjunction with any of the above or below embodiments. The invention also relates to compounds wnercm Za is CH; Zb is N; Zc is CH; Zd is N; and
R12 is H; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Figure imgf000023_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-C1-3alkyl;
Re is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2.6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent R° substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylρropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a,
-C(=O)NR5aRa, and -C(=O)R5a ;
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or two R0 substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Figure imgf000024_0001
wherein R° is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, ρyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted ρhenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl;or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Figure imgf000026_0001
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3.6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, Ci-β-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; or wherein two adjacent R0 substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein Re is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-d^- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Figure imgf000027_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and
RaR5aN-C1-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-I0 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-d-ό-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, ρiperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a,
-C(=O)NR5aRa, and -C(=O)R5a ; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, ρiperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, optionally substituted benzyl, and ; Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Figure imgf000029_0001
R is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-C1-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C^- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, d-β-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3.6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C^-cycloalkyl-d-e-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl;or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, and -C(=O)R5a ;
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R^R5N-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-Q.2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Figure imgf000031_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-1O heteroaryl, optionally substituted C3-6 cycloalkyl, and
RaR5aN-C1-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-1O aryl, nitrile, -C(=0)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Ci-δ-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naplithy, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, and -C(=O)R5a ; Rc is one or more sύbstituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or R° together with R together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Figure imgf000032_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-1O ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-C1-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C^- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aiyl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-Q-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Q-e-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6-alkyl, C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-Cue-alkyl, C^e-cycloalkyl-Q-e-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and
C3-6-cycloalkyl;or wherein two adjacent R° substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 - ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, and -C(=O)R5a ; R° is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Figure imgf000034_0001
Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6- alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-Ci-3alkyl; Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Ci-6-alkyl, C3-6-cycloalkyl,
Figure imgf000034_0002
C2-6-alkenyl and C2-6-alkynyl; and R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl;or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1- ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(=O)OR5a, -C(=O)NR5aR\ and -C(=O)R5a ;
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C]^- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-I0 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl
Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-Ci-2- alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two R° substituents, together form an optionally substituted 3-6 membered spiro ring; in conjunction with any of the above or below embodiments.
The invention also relates to compounds wherein n is 0 or 1; in conjunction with any of the above or below embodiments; T is O; in conjunction with any of the above or below embodiments; and R3 and R4 are both H; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
R is
Figure imgf000036_0001
in conjunction with any of the above or below embodiments.
The invention also relates to compounds R is
Figure imgf000036_0002
R8a is C1-3 alkyl or H; in conjunction with any of the above or below embodiments. The invention also relates to compounds wherein
Figure imgf000036_0003
R8a is C1-3 alkyl or H ; in conjunction with any of the above or below embodiments. The invention also relates to compounds and pharmaceutically acceptable salts and solvates thereof selected from
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin- 4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l- ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((ethyl(methyl)amino)methyl)-l- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide:; N-(4-(6,7-diinethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((dimethylamino)metb.yl)-l-niethyl-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 5-(aminomethyl)-N-(3-fluoro-4-(7-metlioxyquinolin-4-yloxy)plienyl)-l-metliyl-3-oxo-2- phenyl-2, 3 -dihydro- 1 H-pyrazole-4-carboxamide; tert-butyl (4-((3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)carbamoyl)-l-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazol-5-yl)methylcarbamate;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)- 1 -methyl-3 -oxo-2-phenyl-5-(pyrrolidin- 1 - ylmethyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l- ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3 -oxo-2-phenyl- 1 -
((tetrahydrofuran-2-yl)methyl)-2,3-dihydro-lH-pyrazole-4-carboxamide; 5-((ethyl(methyl)amino)methyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
2-benzyl-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-5-(pyridin-4-yl)-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
2-benzyl-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-5-(pyridin-4-yl)-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-(l-phenylethyl)-5-
(pyridin-4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l -methyl-3-oxo-2-(l -phenylethyl)-5-
(pyridin-4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-methoxyqumolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)-
2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)- 2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)- 1 -methyl-3 -oxo-2-phenyl-5-(pyridm-4-yl)-
2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-2-yl)-
2,3-dihydro-lH-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-2-yl)-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(tetraliydro-
2H-pyran-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-meth.yl-3-oxo-2-phenyl-5-(tetrahydro-2H- pyran-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide; 1 -Methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-(2-methyl- 1 ,3-thiazol-4-yl)-
3 -oxo-2-phenyl-2,3 -dihydro-1 H-pyrazole-4-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-methyl-5-(5-methyl-3-isoxazolyl)- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-methyl-5-(5-methyl-3-isoxazolyl)-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolmyl)oxy)phenyl)-l-methyl-5-(5-methyl-3-isoxazolyl)-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 1 -methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolmyl)oxy)-2-pyridinyl)-l-methyl-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-methyl-5-(2-methyl-l,3-thiazol-4- yl)-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)- 1 -methyl-5-(2-methyl- 1 ,3 -thiazol-4- yl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-(6,7-dimethoxyquinolm-4-yloxy)-3-fluorophenyl)-N,l,5-trimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 2-(3-chlorophenyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-ρyrazole-4-carboxamide;
2-(3-chlorophenyl)-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo- 2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3 -fluorophenyl)- 1 ,5-dimethyl-3 -oxo-2-p-tolyl-2,3 - dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-(4-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(5-(6,7-dimethoxyqu.inolin-4-yloxy)pyridine-2-yl)-l,5-dimethyl-3-oxo-2-p-tolyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-(4-fluorophenyl)-l,5-dimethyl-3-oxo-
2,3-dihydro-lH-pyrazole-4-carboxamide; 2-(3-chloroplienyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-methoxyqumolm-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2-p-tolyl-2,3-dihydro-lH- pyrazole-4-carboxamide;
2-(2-chlorophenyl)-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo- 2,3-dihydro-lH-pyrazole-4-carboxamide;
2-(2-cb.lorophenyl)-N-(4-(657-dimethoxyquinolin-4-yloxy)-3-fluoroprienyl)-l,5-dimethyl-3- oxo-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 2-(2-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-2-(4-fluorophenyl)-l ,5-dimethyl-3-oxo-
2,3-dihydro-lH-pyrazole-4-carboxamide; 2-(3 -chlorophenyl)-N-(3 -fluoro-4-(7 -methoxyquinolin-4-yloxy)phenyl)- 1 , 5 -dimethyl-3 -oxo-
2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(6-(6,7-dimethoxyquinolin-4-yloxy)pyridin-3-yl)-l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro- 1 H-pyrazole-4-carboxamide;
N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 2-benzyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 2-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2,3-dihydro-
1 H-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)~ 1 -methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H- pyrazole-4-carboxamide;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyqυ.inolin-4-yloxy)ρhenyl)-5-methyl-3-oxo-l-(2-oxobutyl)-2-phenyl-
2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-l-(3-methyl-2-oxobutyl)-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (R)-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxybutyl)-5-methyl-3 -oxo-
2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -((2R,3R)-3 -hydroxybutan-2-yl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-((2R,3R)-3-hydroxybutan-2-yl)-N-(5-(7-methoxyquinolin-4-yloxy)ρyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
(R)-l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
(S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (R)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolm-4-yloxy)phenyl)-5-methyl-l-((3-methyl-2-oxooxazolidin-5- yl)methyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-(methylamino)propyl)-5- methyl-3 -oxo-2-phenyl-2 ,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(3-chloro-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylbutyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo-
2-phenyl-2,3-dihydro-lH-ρyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-morpholinopropyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-l-(oxazolidin-5-ylmethyl)-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
(S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxybutyl)-5-methyl-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(3-amino-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxy-2-meth.ylpropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-metliyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5-inethyl-
3-oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-l-(2-hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-meth.yl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4~carboxaniide; l-(3-(dimethylammo)-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-
5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
(R)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3-oxo- 2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
(R)-N-(4-(6,7-dimethoxyqumolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridm-2-yl)-l-(2-hydroxy-2-meth.ylpropyl)-5-methyl-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-2-(3-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2- hydroxypropyl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide; (R)-2-(3 -chlorophenyl)- 1 -(2-hydroxypropyl)-N-(5-(7-methoxyqumolin-4-yloxy)pyridin-2-yl)- 5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide;
(R)-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-2-(4-fluorophenyl)- 1 -(2- hydroxypropyl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide l-(2-hydroxy-2-methylpropyl)-N-(5-(l-oxo-7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-Fluoro-4-(7-hydroxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-N-(5-(7-hydroxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(4-(6-Ethyl-7-methoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
N-(3 -Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 ,5-dimethyl-3 -oxo-2-phenyl-2,3 - dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-Methoxyquinolin-4-yloxy)phenyl)-l,2-dimethyl-3-oxo-5-phenyl-2,3-dihydro- lH-pyrazole-4-carboxamide; N-(5-(7-Methoxyquinolin-4-yloxy)pyridin-2-yl)-l,2-dimethyl-3-oxo-5-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamide; N-(4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,2-dimethyl-3-oxo-5-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-Methoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH- ρyrazole-4-carboxamide; (R)-l-(2-Hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-methyl-3-oxo-5- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
(R)-N-(3 -Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxypropyl)-2-methyl-3 -oxo- 5-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide
(S)-N-(3-fluoro-4-(6-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-aminoethyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide l-(2-(l,3-dioxo-l,3-dihydro-2H-isoindol-2-yl)ethyl)-N-(3-fluoro-4-((7-(methyloxy)-4- quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide; l-(2-aminoethyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; 5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-ρhenyl-l-
(phenylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide l-benzyl-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
5-methyl-l-(2-(methyloxy)ethyl)-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo- 2-ρhenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-l-(2-(methyloxy)ethyl)-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(2-hydroxyethyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2- ρhenyl-2, 3 -dihydro- 1 H-pyrazole-4-carboxamide; l-((2R)-2-fluoropropyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (S)-l-(2-(dimethylamino)propyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5- methyl-3 -oxo-2-phenyl-2 ,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-l-(2-(l- pyrrolidinyl)ethyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-((2S)-2-fluoropropyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-
2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-((2S)-2-fluoropropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-((2S)-2-(acetylammo)propyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5- methyl-3 -oxo-2-phenyl-2 ,3 -dihydro-1 H-pyrazole-4-carboxamide; l-((2S)-2-aminopropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)prienyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-((2S)-2-azidopropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-metliyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-qumolinyl)oxy)phenyl)-l-(2-hydroxyethyl)-5-methyl-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3 -oxo-2 -phenyl- 1 -propyl-
2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2R)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2S)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-(2-methylpropyl)-3-oxo-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-l-(2-oxopropyl)-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2,3-dihydroxy-2-methylpropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5- methyl-3 -oxo-2 -phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-((6,7-bis(methyloxy)-4-quinazolinyl)oxy)-3-fluorophenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl- 1 -(2-methyl-2-propen- 1 - yl)-3 -oxo-2-phenyl-2,3-dihydro- 1 H-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2S)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-253-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-niethyl-3-oxo-l-(2- oxopropyl)-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3 -fluorophenyl)- 1 -(2,3 -dihydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-l-(2-methyl-2-propen-
1 -yl)-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-3-oxo-2-phenyl-l-propyl- 2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-3-oxo-2-phenyl-l-(2- propen- 1 -yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)- 1 -oxido-4-quinolmyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2- phenyl-1 -(2-propen-l -yl)-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3 -fluorophenyl)-5-methyl-3 -oxo-2-phenyl- 1 -
(phenylmethyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluoro-N-(5-oxo-l-phenyl-2,5-dihydro-lH-pyrazol-3- yl)benzamide;
4-(6,7-Dimethoxyquinolin-4-yloxy)-N-((l,2-dimethyl-5-oxo-3-phenyl-2,5-dihydro-lH- pyrazol-4-yl)methyl)-3-fluorobenzamide; 4-(6,7-Dimethoxyquinolin-4-yloxy)-N-(2,3 -dimethyl-5-oxo- 1 -phenyl-2,5-dihydro- 1 H-pyrazol-
4-yl)-3-fluorobenzamide 4-(6,7-Dimethoxyquinolin-4-yloxy)-N-((2,3-dimethyl-5-oxo-l-phenyl-2,5-dihydro-lH- pyrazol-4-yl)methyl)-3-fluorobenzamide; l-Benzyl-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l,2-dihydropyrazolo[l,5- a]pyridine-3 -carboxamide;
4-((5-(6,7-Dimethoxyquinolin-4-yloxy)ρyridin-2-ylamino)methyl)-l,5-dimethyl-2-phenyl-l,2- dihydropyrazol-3-one;
N-(3-fluoro-4-(2-(3-methyl-l,2,4-oxadiazol-5-yl)thieno[3,2-b]ρyridin-7-yloxy)phenyl)-l-(2- hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide; N-(3-fluoro-4-((2-(l-methyl-lH-imidazol-5-yl)thieno[3,2-b]pyridin-7-yl)oxy)phenyl)-l-(2- hydroxy-2-methylproρyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide;
N-(3-fluoro-4-((2-(l-methyl-lH-imidazol-5-yl)thieno[3,2-b]pyridin-7-yl)oxy)ρhenyl)-l-((2R)- 2-hydroxypropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)phenyl)-l-(2-liydroxy-2-metliylpropyl)-5- methyl-3-oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(lH-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3 -oxo-2-phenyl-2,3-dihydro- 1 H-pyrazole-4-carboxamide; Methyl(6-((4-(((l-(2-hydroxy-2-methylproρyl)-5-methyl-3-oxo-2-ρhenyl-2,3-dihydro-lH- pyrazol-4-yl)carbonyl)amino)phenyl)oxy)-lH-benzimidazol-2-yl)carbamate; N-(4-(2-(azetidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenyl)-5-methyl-3-oxo-
2-phenyl- 1 -propyl-2,3-dihydro- 1 H-pyrazole-4-carboxamide;
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-metriyl-3-oxo-2-prienyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N-methylthieno[3 ,2-b]pyridine-2-carboxamide;
N-(3-fluoro-4-(2-(l-methylpiperazine-4-carbonyl)thieno[3,2-b]pyridin-7-yloxy)phenyl)-l-(2- liydroxy-2-methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4- carboxamide;
N-(2-(dimethylamino)ethyl)-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2- phenyl-253-dihydro-lH-pyrazole-4-carboxamido)pb.enoxy)thieno[3,2-b]pyridine-2- carboxamide; N-(4-(2-(3 -(dimethylamino)pyrrolidine- 1 -carbonyl)thieno[3 ,2-b]pyridin-7-yloxy)-3 - fluorophenyl)- 1 -(2-hydroxy-2-methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H- ρyrazole-4-carboxamide; 7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N,N-dimethylthieno[3,2-b]pyridine-2-carboxamide; 7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2-carboxamide; N-(2-(dimethylamino)ethyl)-7-(2-fluoro-4-(l-(2-hydroxy-2-methylproρyl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)phenoxy)-N-methylthieno[3,2- b]pyridine-2-carboxamide; 7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N-(2-methoxyethyl)thieno[3,2-b]pyridine-2- carboxamide; N-(4-(2-(azetidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-cyclopropyl-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamido)phenoxy)thieno[3 ,2-b]pyridine-2-carboxamide 7-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dmydro-lH-pyrazole-4- carboxamido)phenoxy)thieno[3,2-b]pyridine-2-carboxamide; N-(3-fluoro-4-(6-(pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)phenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(6-(pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)phenyl)-5-metliyl-3-oxo-2- phenyl- 1 -propyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(6-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyrimidin-4-yl)morpholine-4-carboxamide; N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)plienoxy)pyrimidin-4-yl)morpholine-4-carboxamide; N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidm-4-yl)piperidine- 1 -carboxamide; N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidin-4-yl)-4-methylpiperazine-l-carboxamide; (R)-N-(4-(6-(3-(dirnethylamino)pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)-3- fluorophenyl)-5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamide; (R)-N-(4-(6-aminopyrimidin-4-yloxy)-3 -fluorophenyl)- 1 -(2-hydroxyproρyl)-5-methyl-3 -oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3 -fluoro-4-(2-(pyrrolidine- 1 -carboxamido)pyridin-4-yloxy)phenyl)- 1 ,5-dimethyl-3 -oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(4-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyridin-2-yl)piperidine-l-carboxamide; (R)-N-(4-(2-(3 -(dimethylamino)pyrrolidine- 1 -carboxamido)pyridin-4-yloxy)-3 -fluorophenyl)- l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(2-(pyrrolidine-l-carboxamido)pyridin-4-yloxy)phenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(2-(pyrrolidine- 1 -carboxamido)pyridin-4-yloxy)phenyl)-5-methyl-3 -oxo-2- phenyl- 1 -propyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-ρyrazole-4-carboxamido)-2- fluorophenoxy)pyridm-2-yl)morpholine-4-carboxamide; N-(4-(2-fluoro-4-(l -(2-hydroxy-2-methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H- pyrazole-4-carboxamido)phenoxy)pyridin-2-yl)piperidine-l-carboxamide; 5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)metliyl)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide; N-(4-(hydroxy(7-methoxyquinolin-4-yl)methyl)phenyl)-5-methyl-3-oxo-2-phenyl-l-ρropyl-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l,5-dimethyl-N-(5-((7-(niethyloxy)-4-quinolinyl)oxy)-2-pyrimidinyl)-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)sulfinyl)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)thio)phenyl)-3- oxo-2-phenyl-2 ,3 -dihydro- 1 H-pyrazole-4-carboxamide 5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)thio)phenyl)-3 -oxo-2-phenyl- 1 -propyl-2,3 - dihydro-lH-pyrazole-4-carboxamide 5-methyl-N-(3-((7-(methyloxy)-4-quinolinyl)oxy)propyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
5-methyl-N-(trans-4-((7-(methyloxy)-4-quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-l-propyl- 2,3-dihydro-lH-pyrazole-4-carboxarnide;
5-methyl-N-(cis-4-((7-(methyloxy)-4-quinolinyl)oxy)cyclohexyl)-3 -oxo-2-phenyl- 1 -propyl- 2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(trans-4-((7-(methyloxy)-4- quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide 5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-ρyrimidinyl)-3-oxo-2-phenyl-l-propyl-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-5-methyl-4-((7-((7-(methyloxy)-4-quinolinyl)oxy)-2,3-dihydro-
4H-l,4-benzoxazin-4-yl)carbonyl)-2-phenyl-l,2-dihydro-3H-pyrazol-3-one; l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-3-hydroxy-2-(l-oxoisoindolin-2- yl)propanamide;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluoroplienyl)-2-(l-oxoisoindolin-2-yl)acetainide; N-(4-(6,7-diniethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxo-l,5-diplienyl-l,2- dihydropyridine-3-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6-oxo-l-(phenylmethyl)-
1 , 1 ',2',3 ',6,6'-hexahydro-3 ,4'-bipyridine-5-carboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6-oxo- 1 -(phenylmethyl)- 1,6- dihydro-3,3'-bipyridine-5-carboxamide; N-(5-((657-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridmyl)-6'-oxo- 1 '-(phenylmethyl)- l',6'- dihydro-2,3'-bipyridine-5'-carboxamide N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-2-oxo-l-(phenylmethyl)-5-(2- thienyl)-l,2-dihydro-3-pyridinecarboxamide;
N-(5-((6,7-bis(niethyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-2-oxo-l-(phenylmethyl)-5-(2- pyrazinyl)- 1 ,2-dihydro-3 -pyridinecarboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-2-oxo-l-(phenylmethyl)-
1 ,2-dihydro-3 -pyridinecarboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-bromo-l-(3-methylphenyl)-2- oxo- 1 ,2-dihydro-3 -pyridinecarboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-(l-methyl-lH-pyrazol-4-yl)-2- oxo-1 -phenyl-1 ,2-dihydro-3-pyridinecarboxamide; N-(3-fluoro-4-((6-(methyloxy)-7-((3-(4-morpholinyl)propyl)oxy)-4-quinolinyl)oxy)phenyl)-2- oxo-5-phenyl- 1 -(phenylmethyl)- 1 ,2-dihydro-3 -pyridinecarboxamide;
1 , 1 -dimethylethyl 5-(((5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)amino)carbonyl)- 6-oxo- 1 -(phenylmethyl)- 1 ,3 ' ,6,6 ' -tetrahydro-3 ,4' -bipyridine- 1 ' (2'H)-carboxylate;
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-2-oxo-l-(phenylmethyl)-5-(2- pyrimidinyl)- 1 ,2-dihydro-3 -pyridinecarboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-2-oxo-l-phenyl-5-(lH-pyrazol-
4-yl)- 1 ,2-dihydro-3 -pyridinecarboxamide; 1 -benzyl-5-bromo-N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-2-oxo-l ,2- dihydropyridine-3-carboxamide;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyridin-3-yl)-l,2- dihydropyridine-3-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyrazin-2-yl)-l,2- dihydropyridine-3 -carboxamide; .N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyridin-3-yl)-l}2- dihydropyridine-3 -carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l -phenyl-5-(pyrazin-2-yl)-l ,2- dihydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(thiophen-2-yl)-l,2- dihydropyridine-3 -carboxamide;
5-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-l,2- dihydropyridine-3 -carboxamide; tert-butyl 4-(5-((5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)carbamoyl)-6-oxo-l-phenyl- l,6-dihydropyridin-3-yl)-5,6-dihydropyridine-l(2H)-carboxylate; 5-bromo-N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)prienyl)-2-oxo-l-prienyl-l,2- dihydropyridine-3 -carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(2-methoxyetriylamino)-2-oxo-l - phenyl-l,2-dihydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolm-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-4-(tetrahydro-2H-pyran-4- ylamino)- 1 ,2-dihydropyridine-3 -carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo- 1 -phenyl-4-(phenylamino)- 1 ,2- dihydropyridine-3 -carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(4-methylpiperazin-l-yl)-2-oxo-l- phenyl- 1 ,2-dihydropyridine-3 -carboxamide; N-(5-(6,7-dimethoxyquinolm-4-yloxy)pyridin-2-yl)-4-(methylamino)-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(dimethylamino)-2-oxo-l -phenyl-1 ,2- dihydropyridine-3 -carboxamide; 4-(2-methoxyethylamino)-N-(5-(7-methoxyquinolm-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl- l,2-dihydropyridine-3-carboxamide;
N-(3 -fl"uoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-4-(2-methoxyethylamino)-2-oxo- 1 -phenyl- 1 ,2-dihydropyridine-3 -carboxamide
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-
1 -cyclopentyl-6-oxo-5-(2-oxo- 1 -pyrrolidinyl)- 1 ,6-dihydro-3 -pyridinecarboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)ρyridin-2-yl)-4-(2-methoxyethylamino)-2-oxo- l,2-dihydropyridine-3-carboxamide; 1 -benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(dimethylamino)-2-oxo- 1 ,2- dihydroρyridine-3-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(methylamino)-2-oxo-l,2- dihydropyridine-3 -carboxamide; 1 -benzyl-N-(5-(6,7-diniethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(phenylaniino)- 1 ,2- dihydroρyridine-3-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolm-4-yloxy)pyridin-2-yl)-2-oxo-4-(pyridin-4-ylamino)-
1 ^-dihydropyridine-S-carboxamide;
1 -benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(4-methylpiperazm- 1 -yl)-2- oxo-1 ^-dihydropyridine-S-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(tetrahydro-2H-pyran-4- ylaniino)-l,2-dihydropyridine-3-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(4-
(trifluoromethyl)plienylamino)- 1 ,2-dihydropyridine-3 -carboxamide; 1 -cyclopentyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-6-oxo-5-(2- oxopyrrolidin- 1 -yl)- 1 ,6-dihydropyridine-3 -carboxamide; N-(3 -fluoro-4-(2-(pyrrolidine- 1 -carboxamido)pyridin-4-yloxy)phenyl)-3 -oxo-2-phenyl-2,3 - dihydropyridazine-4-carboxamide;
6-((diethylammo)methyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-3-oxo-2- phenyl-2,3-dihydropyridazine-4-carboxamide;
6-((dimethylamino)methyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-2- phenyl-2,3-dihydropyridazine-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)pb.enyl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide; N-(5-(6,7-dimetb.oxyqumolin-4-yloxy)pyridin-2-yl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide; 2-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-6-methyl-3-oxo-2,3- dihydropyridazine-4-carboxamide;
N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3 -oxo-2-phenyl-2,3 -dihydropyridazine-4- carboxamide;
N-(2-cliloro-4-(6,7-dimethoxyquinolm-4-yloxy)phenyl)-6-metriyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide; (R)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-6-((3-(dimeth.ylamino)pyrrolidin-
1 -yl)methyl)-3 -oxo-2-phenyl-2,3 -dihydropyridazine-4-carboxamide; 3-benzyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxoimidazolidine-l- carboxamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-flvιorophenyl)-5-((dimetliylamino)metliyl)-2-oxo-3- phenyl-tetrahydropyrimidine- 1 (2H)-carboxamide; N-(3 -Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3 -oxo-4-phenylmorpholine-2- carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)- 1 -methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H- pyrazole-4-carboxamide; and
N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-4-phenylmorpholine-2- carboxamide.
INDICATIONS
Compounds of the present invention would be useful for, but not limited to, the prevention or treatment of angiogenesis related diseases. The compounds of the invention have kinase inhibitory activity, such as VEGFR/KDR and/or c-Met inhibitory activity. The compounds of the invention are useful in therapy as antineoplasia agents or to minimize deleterious effects of VEGF and/or HGF.
Compounds of the invention would be useful for the treatment of neoplasia including cancer and metastasis, including, but not limited to: carcinoma such as cancer of the bladder, breast, colon, kidney, liver, lung (including small cell lung cancer), esophagus, gall-bladder, ovary, pancreas, stomach, cervix, thyroid, prostate, and skin (including squamous cell carcinoma); hematopoietic tumors of lymphoid lineage (including leukemia, acute lymphocitic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell-lymphoma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, hairy cell lymphoma and Burkett's lymphoma); hematopoietic tumors of myeloid lineage (including acute and chronic myelogenous leukemias, myelodysplastic syndrome and promyelocytic leukemia); tumors of mesenchymal origin (including fibrosarcoma and rhabdomyosarcoma, and other sarcomas, e.g. soft tissue and bone); tumors of the central and peripheral nervous system (including astrocytoma, neuroblastoma, glioma and schwannomas); and other tumors (including melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid follicular cancer and Kaposi's sarcoma).
Preferably, the compounds are useful for the treatment of neoplasia selected from lung cancer, colon cancer and breast cancer.
The compounds also would be useful for treatment of ophthalmological conditions such as corneal graft rejection, ocular neovascularization, retinal neovascularization including neovascularization following injury or infection, diabetic retinopathy, retrolental fibroplasia and neovascular glaucoma; retinal ischemia; vitreous hemorrhage; ulcerative diseases such as gastric ulcer; pathological, but non-malignant, conditions such as hemangiomas, including infantile hemaginomas, angiofibroma of the nasopharynx and avascular necrosis of bone; and disorders of the female reproductive system such as endometriosis. The compounds are also useful for the treatment of edema, and conditions of vascular hyperpermeability.
The compounds of the invention are useful in therapy of proliferative diseases. These compounds can be used for the treatment of an inflammatory rheumatoid or rheumatic disease, especially of manifestations at the locomotor apparatus, such as various inflammatory rheumatoid diseases, especially chronic polyarthritis including rheumatoid arthritis, juvenile arthritis or psoriasis arthropathy; paraneoplastic syndrome or tumor-induced inflammatory diseases, turbid effusions, collagenosis, such as systemic Lupus erythematosus, poly-myositis, dermato-myositis, systemic sclerodermia or mixed collagenosis; postinfectious arthritis (where no living pathogenic organism can be found at or in the affected part of the body), seronegative spondylarthritis, such as spondylitis ankylosans; vasculitis, sarcoidosis, or arthrosis; or further any combinations thereof. An example of an inflammation related disorder is (a) synovial inflammation, for example, synovitis, including any of the particular forms of synovitis, in particular bursal synovitis and purulent synovitis, as far as it is not crystal-induced. Such synovial inflammation may for example, be consequential to or associated with disease, e.g. arthritis, e.g. osteoarthritis, rheumatoid arthritis or arthritis deformans. The present invention is further applicable to the systemic treatment of inflammation, e.g. inflammatory diseases or conditions, of the joints or locomotor apparatus in the region of the tendon insertions and tendon sheaths. Such inflammation may be, for example, consequential to or associated with disease or further (in a broader sense of the invention) with surgical intervention, including, in particular conditions such as insertion endopathy, myofasciale syndrome and tendomyosis. The present invention is further especially applicable to the treatment of inflammation, e.g. inflammatory disease or condition, of connective tissues including dermatomyositis and myositis.
These compounds can be used as active agents against such disease states as arthritis, atherosclerosis, psoriasis, hemangiomas, myocardial angiogenesis, coronary and cerebral collaterals, ischemic limb angiogenesis, wound healing, peptic ulcer Helicobacter related diseases, fractures, cat scratch fever, rubeosis, neovascular glaucoma and retinopathies such as those associated with diabetic retinopathy or macular degeneration. In addition, some of these compounds can be used as active agents against solid tumors, malignant ascites, hematopoietic cancers and hyperproliferative disorders such as thyroid hyperplasia (especially Grave's disease), and cysts (such as hypervascularity of ovarian stroma, characteristic of polycystic ovarian syndrome (Stein-Leventhal syndrome)) since such diseases require a proliferation of blood vessel cells for growth and/or metastasis. Further, some of these compounds can be used as active agents against burns, chronic lung disease, stroke, polyps, anaphylaxis, chronic and allergic inflammation, ovarian hyperstimulation syndrome, brain tumor-associated cerebral edema, high-altitude, trauma or hypoxia induced cerebral or pulmonary edema, ocular and macular edema, ascites, and other diseases where vascular hyperpermeability, effusions, exudates, protein extravasation, or edema is a manifestation of the disease. The compounds will also be useful in treating disorders in which protein extravasation leads to the deposition of fibrin and extracellular matrix, promoting stromal proliferation (e.g. fibrosis, cirrhosis and carpal tunnel syndrome).
The compounds of the present invention are also useful in the treatment of ulcers including bacterial, fungal, Mooren ulcers and ulcerative colitis. The compounds of the present invention are also useful in the treatment of conditions wherein undesired angiogenesis, edema, or stromal deposition occurs in viral infections such as Herpes simplex, Herpes Zoster, AIDS, Kaposi's sarcoma, protozoan infections and toxoplasmosis, following trauma, radiation, stroke, endometriosis, ovarian hyperstimulation syndrome, systemic lupus, sarcoidosis, synovitis, Crohn's disease, sickle cell anemia, Lyme disease, pemphigoid, Paget's disease, hyperviscosity syndrome, Osler-Weber-Rendu disease, chronic inflammation, chronic occlusive pulmonary disease, asthma, and inflammatory rheumatoid or rheumatic disease. The compounds are also useful in the reduction of subcutaneous fat and for the treatment of obesity.
The compounds of the present invention are also useful in the treatment of ocular conditions such as ocular and macular edema, ocular neovascular disease, scleritis, radial keratotomy, uveitis, vitritis, myopia, optic pits, chronic retinal detachment, post-laser complications, glaucoma, conjunctivitis, Stargardt's disease and Eales disease in addition to retinopathy and macular degeneration.
The compounds of the present invention are also useful in the treatment of cardiovascular conditions such as atherosclerosis, restenosis, arteriosclerosis, vascular occlusion and carotid obstructive disease.
The compounds of the present invention are also useful in the treatment of cancer related indications such as solid tumors, sarcomas (especially Ewing's sarcoma and osteosarcoma), retinoblastoma, rhabdomyosarcomas, neuroblastoma, hematopoietic malignancies, including leukemia and lymphoma, tumor-induced pleural or pericardial effusions, and malignant ascites.
The compounds of the present invention are also useful in the treatment of diabetic conditions such as diabetic retinopathy and microangiopathy. The compounds of the present invention are also useful in the reduction of blood flow in a tumor in a subject.
The compounds of the present invention are also useful in the reduction of metastasis of a tumor in a subject.
The compounds of this invention may also act as inhibitors of other protein kinases, e.g. tie-2, lck, src, fgf, c-Met, ron, ckit and ret, and thus be effective in the treatment of diseases associated with other protein kinases.
Besides being useful for human treatment, these compounds are also useful for veterinary treatment of companion animals, exotic animals and farm animals, including mammals, rodents, and the like. More preferred animals include horses, dogs, and cats. As used herein, the compounds of the present invention include the pharmaceutically acceptable derivatives thereof.
Where the plural form is used for compounds, salts, and the like, this is taken to mean also a single compound, salt and the like.
DEFINITIONS " Angiogenesis" is defined as any alteration of an existing vascular bed or the formation of new vasculature, which benefits tissue perfasion. This includes the formation of new vessels by sprouting of endothelial cells from existing blood vessels or the remodeling of existing vessels to alter size, maturity, direction or flow properties to improve blood perfasion of tissue. As used herein, "HGF" refers to hepatocyte growth factor/scatter factor. This includes purified hepatocyte growth factor/scatter factor, fragments of hepatocyte growth factor/scatter factor, chemically synthesized fragments of hepatocyte growth factor/scatter factor, derivatives or mutated versions of hepatocyte growth factor/scatter factor, and fusion proteins comprising hepatocyte growth factor/scatter factor and another protein. "HGF" as used herein also includes hepatocyte growth factor/scatter factor isolated from species other than humans.
As used herein "c-Met" refers to the receptor for HGF. This includes purified receptor, fragments of receptor, chemically synthesized fragments of receptor, derivatives or mutated versions of receptor, and fusion proteins comprising the receptor and another protein. "c-Met" as used herein also includes the HGF receptor isolated from a species other than humans. As used herein, "HGF" refers to hepatocyte growth factor/scatter factor. This includes purified hepatocyte growth factor/scatter factor, fragments of hepatocyte growth factor/scatter factor, chemically synthesized fragments of hepatocyte growth factor/scatter factor, derivatives or mutated versions of hepatocyte growth factor/scatter factor, and fusion proteins comprising hepatocyte growth factor/scatter factor and another protein. "HGF" as used herein also includes hepatocyte growth factor/scatter factor isolated from species other than humans.
As used herein "c-Met" refers to the receptor for HGF. This includes purified receptor, fragments of receptor, chemically synthesized fragments of receptor, derivatives or mutated versions of receptor, and fusion proteins comprising the receptor and another protein. "c-Met" as used herein also includes the HGF receptor isolated from a species other than humans. As used herein, the terms "hepatocyte growth factor" and "HGF" refer to a growth factor typically having a structure with six domains (finger, Kringle 1, Kringle 2, Kringle 3, Kringle 4 and serine protease domains). Fragments of HGF constitute HGF with fewer domains and variants of HGF may have some of the domains of HGF repeated; both are included if they still retain their respective ability to bind a HGF receptor. The terms "hepatocyte growth factor" and "HGF" include hepatocyte growth factor from humans ("huHGF") and any non-human mammalian species, and in particular rat HGF. The terms as used herein include mature, pre, pre-pro, and pro forms, purified from a natural source, , chemically synthesized or recombinantly produced. Human HGF is encoded by the cDNA sequence published by Miyazawa et al. (1989), supra, or Nakamura et al. (1989), supra. The sequences reported by Miyazawa et al. and Nakamura et al. differ in 14 amino acids. The reason for the differences is not entirely clear; polymorphism or cloning artifacts are among the possibilities. Both sequences are specifically encompassed by the foregoing terms. It will be understood that natural allelic variations exist and can occur among individuals, as demonstrated by one or more amino acid differences in the amino acid sequence of each individual. The terms "hepatocyte growth factor" and "HGF" specifically include the delta 5 huHGF as disclosed by Selά et al., supra.
The terms "HGF receptor" and "c-Met" when used herein refer to a cellular receptor for HGF, which typically includes an extracellular domain, a transmembrane domain and an intracellular domain, as well as variants and fragments thereof which retain the ability to bind HGF. The terms "HGF receptor" and "c-Met" include the polypeptide molecule that comprises the full-length, native amino acid sequence encoded by the gene variously known as pl90.sup.MET. The present definition specifically encompasses soluble forms of HGF receptor, and HGF receptor from natural sources, synthetically produced in vitro or obtained by genetic manipulation including methods of recombinant DNA technology. The HGF receptor variants or fragments preferably share at least about 65% sequence homology, and more preferably at least about 75% sequence homology with any domain of the human c-Met amino acid sequence published in Rodrigues et al., MoI. Cell. Biol., 11:2962-2970 (1991); Park et al., Proc. Natl. Acad. Sci., 84:6379-6383 (1987); or Ponzetto et al., Oncogene, 6:553-
559 (1991).
The terms "agonist" and "agonistic" when used herein refer to or describe a molecule which is capable of, directly or indirectly, substantially inducing, promoting or enhancing HGF biological activity or HGF receptor activation. The terms "cancer" and "cancerous" when used herein refer to or describe the physiological condition in mammals that is typically characterized by unregulated cell growth.
Examples of cancer include but are not limited to, carcinoma, lymphoma, sarcoma, blastoma and leukemia. More particular examples of such cancers include squamous cell carcinoma, lung cancer, pancreatic cancer, cervical cancer, bladder cancer, hepatoma, breast cancer, colon carcinoma, and head and neck cancer. While the term "cancer" as used herein is not limited to any one specific form of the disease, it is believed that the methods of the invention will be particularly effective for cancers which are found to be accompanied by increased levels of
HGF or expression of c-Met in the mammal.
The terms "treating," "treatment," and "therapy" as used herein refer to curative therapy, prophylactic therapy, and preventative therapy.
The term "mammal" as used herein refers to any mammal classified as a mammal, including humans, cows, horses, dogs and cats. In a preferred embodiment of the invention, the mammal is a human.
Given that elevated levels of c-Met and HGF are observed in hypertension, arteriosclerosis, myocardial infarction, and rheumatoid arthritis, nucleic acid ligands will serve as useful therapeutic agents for these diseases.
The term "treatment" includes therapeutic treatment as well as prophylactic treatment
(either preventing the onset of disorders altogether or delaying the onset of a pre-clinically evident stage of disorders in individuals). A "pharmaceutically-acceptable derivative " denotes any salt, ester of a compound of this invention, or any other compound which upon administration to a patient is capable of providing (directly or indirectly) a compound of this invention, or a metabolite or residue thereof, characterized by the ability to inhibit angiogenesis. The phrase "therapeutically-effective" is intended to qualify the amount of each agent, which will achieve the goal of improvement in disorder severity and the frequency of incidence over treatment of each agent by itself, while avoiding adverse side effects typically associated with alternative therapies. For example, effective neoplastic therapeutic agents prolong the survivability of the patient, inhibit the rapidly proliferating cell growth associated with the neoplasm, or effect a regression of the neoplasm.
The term "H" denotes a single hydrogen atom. This radical may be attached, for example, to an oxygen atom to form a hydroxyl radical.
Where the term "alkyl" is used, either alone or within other terms such as "haloalkyl" and "alkylamino", it embraces linear or branched radicals having one to about twelve carbon atoms. More preferred alkyl radicals are "lower alkyl" radicals having one to about six carbon atoms. Examples of such radicals include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isoamyl, hexyl and the like. Even more preferred are lower alkyl radicals having one or two carbon atoms. The term "alkylenyl" embraces bridging divalent alkyl radicals such as methylenyl and ethyl enyl. The term "lower alkyl substituted with R2" does not include an acetal moiety.
The term "alkenyl" embraces linear or branched radicals having at least one carbon- carbon double bond of two to about twelve carbon atoms. More preferred alkenyl radicals are "lower alkenyl" radicals having two to about six carbon atoms. Most preferred lower alkenyl radicals are radicals having two to about four carbon atoms. Examples of alkenyl radicals include ethenyl, propenyl, allyl, propenyl, butenyl and 4-methylbutenyl. The terms "alkenyl" and "lower alkenyl", embrace radicals having "cis" and "trans" orientations, or alternatively, "E" and "Z" orientations.
The term "alkynyl" denotes linear or branched radicals having at least one carbon- carbon triple bond and having two to about twelve carbon atoms. More preferred alkynyl radicals are "lower alkynyl" radicals having two to about six carbon atoms. Most preferred are lower alkynyl radicals having two to about four carbon atoms. Examples of such radicals include propargyl, butynyl, and the like.
The term "halo" means halogens such as fluorine, chlorine, bromine or iodine atoms. The term "haloalkyl" embraces radicals wherein any one or more of the alkyl carbon atoms is substituted with halo as defined above. Specifically embraced are monohaloalkyl, dihaloalkyl and polyhaloalkyl radicals including perhaloalkyl. A monohaloalkyl radical, for one example, may have either an iodo, bromo, chloro or fluoro atom within the radical. Dihalo and polyhaloalkyl radicals may have two or more of the same halo atoms or a combination of different halo radicals. "Lower haloalkyl" embraces radicals having 1-6 carbon atoms. Even more preferred are lower haloalkyl radicals having one to three carbon atoms. Examples of haloalkyl radicals include fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl.
"Perfluoroalkyl" means alkyl radicals having all hydrogen atoms replaced with fluoro atoms. Examples include trifluoromethyl and pentafluoroethyl.
The term "hydroxyalkyl" embraces linear or branched alkyl radicals having one to about ten carbon atoms any one of which may be substituted with one or more hydroxyl radicals. More preferred hydroxyalkyl radicals are "lower hydroxyalkyl" radicals having one to six carbon atoms and one or more hydroxyl radicals. Examples of such radicals include hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxybutyl and hydroxyhexyl. Even more preferred are lower hydroxyalkyl radicals having one to three carbon atoms.
The term "alkoxy" embraces linear or branched oxy-containing radicals each having alkyl portions of one to about ten carbon atoms. More preferred alkoxy radicals are "lower alkoxy" radicals having one to six carbon atoms. Examples of such radicals include methoxy, ethoxy, propoxy, butoxy and tert-butoxy. Even more preferred are lower alkoxy radicals having one to three carbon atoms. Alkoxy radicals may be further substituted with one or more halo atoms, such as fluoro, chloro or bromo, to provide "haloalkoxy" radicals. Even more preferred are lower haloalkoxy radicals having one to three carbon atoms. Examples of such radicals include fluoromethoxy, chloromethoxy, trifluoromethoxy, trifiuoroethoxy, fluoroethoxy and fluoropropoxy.
The term "aryl", alone or in combination, means a carbocyclic aromatic system containing one or two rings wherein such rings may be attached together in a fused manner. The term "aryl" embraces aromatic radicals such as phenyl, naphthyl, indenyl, tetrahydronaphthyl, and indanyl. More preferred aryl is phenyl. Said "aryl" group may have 1 to 3 substituents such as lower alkyl, hydroxyl, halo, haloalkyl, nitro, cyano, alkoxy and lower alkylamino. Phenyl substituted with -0-CH2-O- forms the aryl benzodioxolyl substituent. The term " heterocyclyl" embraces saturated, partially saturated and unsaturated heteroatom-containing ring radicals, where the heteroatoms may be selected from nitrogen, sulfur and oxygen. It does not include rings containing -O-O-,-O-S- or -S-S- portions. Said "heterocyclyl" group may have 1 to 3 substiruents such as hydroxyl, Boc, halo, haloalkyl, cyano, lower alkyl, lower aralkyl, oxo, lower alkoxy, amino and lower alkylamino. Examples of saturated heterocyclic radicals include saturated 3 to 6-membered heteromonocyclic groups containing 1 to 4 nitrogen atoms [e.g. pyrrolidinyl, imidazolidinyl, piperidinyl, pyrrolinyl, piperazinyl]; saturated 3 to 6-membered heteromonocyclic group containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms [e.g. morpholinyl]; saturated 3 to 6- membered heteromonocyclic group containing 1 to 2 sulfur atoms and 1 to 3 nitrogen atoms [e.g., thiazolidinyl]. Examples of partially saturated heterocyclyl radicals include dihydrothienyl, dihydropyranyl, dihydrofuryl and dihydrothiazolyl.
Examples of unsaturated heterocyclic radicals, also termed "heteroaryl" radicals, include unsaturated 5 to 6 membered heteromonocyclyl group containing 1 to 4 nitrogen atoms, for example, pyrrolyl, imidazolyl, pyrazolyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazolyl [e.g., 4H-l,2,4-triazolyl, IH-1, 2,3 -triazolyl, 2H-1,2,3- triazolyl]; unsaturated 5^- to 6-membered heteromonocyclic group containing an oxygen atom, for example, pyranyl, 2-furyl, 3-furyl, etc.; unsaturated 5 to 6-membered heteromonocyclic group containing a sulfur atom, for example, 2-thienyl, 3-thienyl, etc.; unsaturated 5- to 6- membered heteromonocyclic group containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms, for example, oxazolyl, isoxazolyl, oxadiazolyl [e.g., 1 ,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl]; unsaturated 5 to 6-membered heteromonocyclic group containing 1 to 2 sulfur atoms and 1 to 3 nitrogen atoms, for example, thiazolyl, thiadiazolyl [e.g., 1,2,4- thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl]. The term heterocyclyl also embraces radicals where heterocyclic radicals are fused/condensed with aryl radicals: unsaturated condensed heterocyclic group containing 1 to 5 nitrogen atoms, for example, indolyl, isoindolyl, indolizinyl, benzimidazolyl, quinolyl, isoquinolyl, indazolyl, benzotriazolyl, tetrazolopyridazinyl [e.g., tetrazolo [l,5-b]pyridazinyl]; unsaturated condensed heterocyclic group containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms [e.g. benzoxazolyl, benzoxadiazolyl]; unsaturated condensed heterocyclic group containing 1 to 2 sulfur atoms and 1 to 3 nitrogen atoms [e.g., benzothiazolyl, benzothiadiazolyl]; and saturated, partially unsaturated and unsaturated condensed heterocyclic group containing 1 to 2 oxygen or sulfur atoms [e.g. benzofuryl, benzothienyl, 2,3-dihydro- benzo[l,4]dioxinyl and dihydrobenzofuryl]. Preferred heterocyclic radicals include five to ten membered fused or unfused radicals. More preferred examples of heteroaryl radicals include quinolyl, isoquinolyl, imidazolyl, pyridyl, thienyl, thiazolyl, oxazolyl, furyl, and pyrazinyl. Other preferred heteroaryl radicals are 5- or 6-membered heteroaryl, containing one or two heteroatoms selected from sulfur, nitrogen and oxygen, selected from thienyl, furyl, pyrrolyl, indazolyl, pyrazolyl, oxazolyl, triazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, pyridyl, piperidinyl and pyrazinyl.
Particular examples of non-nitrogen containing heteroaryl include pyranyl, 2-furyl, 3- furyl, 2-thienyl, 3-thienyl, benzofuryl, benzothienyl, and the like. Particular examples of partially saturated and saturated heterocyclyl include pyrrolidinyl, imidazolidinyl, piperidinyl, pyrrolinyl, pyrazolidinyl, piperazinyl, morpholinyl, tetrahydropyranyl, thiazolidinyl, dihydrothienyl, 2,3-dihydro-benzo[l,4]dioxanyl, indolinyl, isoindolinyl, dihydrobenzothienyl, dihydrobenzofuryl, isochromanyl, chromanyl, 1,2- dihydroquinolyl, 1,2,3,4-tetrahydro-isoquinolyl, 1,2,3,4-tetraliydro-quinolyl, 2,3,4,4a,9,9a- hexahydro-lH-3-aza-fluorenyl, 5,6,7-trihydro-l,2,4-triazolo[3,4-a]isoquinolyl, 3,4-dihydro- 2H-benzo[l ,4]oxazinyl, benzo[l ,4]dioxanyl, 2,3-dihydro-lH-lλ'-benzo[d]isothiazol-6-yl, dihydropyranyl, dihydrofuryl and dihydrothiazolyl, and the like.
The term "sulfonyl", whether used alone or linked to other terms such as alkylsulfonyl, denotes respectively divalent radicals -SO2-. The terms "sulfamyl," "aminosulfonyl" and "sulfonamidyl," denotes a sulfonyl radical substituted with an amine radical, forming a sulfonamide (-SO2NH2).
The term "alkylaminosulfonyl" includes "N-alkylaminosulfonyl" where sulfamyl radicals are independently substituted with one or two alkyl radical(s). More preferred alkylaminosulfonyl radicals are "lower alkylaminosulfonyl" radicals having one to six carbon atoms. Even more preferred are lower alkylaminosulfonyl radicals having one to three carbon atoms. Examples of such lower alkylaminosulfonyl radicals include N-methylaminosulfonyl, and N-ethylaminosulfonyl.
The terms "carboxy" or "carboxyl", whether used alone or with other terms, such as "carboxyalkyl", denotes -CO2H. The term "carbonyl", whether used alone or with other terms, such as "aminocarbonyl", denotes -(C=O)-.
The term "aminocarbonyl" denotes an amide group of the formula -C(=O)NH2.
The terms "N-alkylaminocarbonyl" and "N,N-dialkylaminocarbonyl" denote aminocarbonyl radicals independently substituted with one or two alkyl radicals, respectively. More preferred are "lower alkylaminocarbonyl" having lower alkyl radicals as described above attached to an aminocarbonyl radical.
The terms "N-arylaminocarbonyl" and "N-alkyl-N-arylaminocarbonyl" denote aminocarbonyl radicals substituted, respectively, with one aryl radical, or one alkyl and one aryl radical. The terms "heterocyclylalkylenyl" and "heterocyclylalkyl" embrace heterocyclic- substituted alkyl radicals. More preferred heterocyclylalkyl radicals are "5- or 6-membered heteroarylalkyl" radicals having alkyl portions of one to six carbon atoms and a 5- or 6- membered heteroaryl radical. Even more preferred are lower heteroarylalkylenyl radicals having alkyl portions of one to three carbon atoms. Examples include such radicals as pyridylmethyl and thienylmethyl.
The term "aralkyl" embraces aryl-substituted alkyl radicals. Preferable aralkyl radicals are "lower aralkyl" radicals having aryl radicals attached to alkyl radicals having one to six carbon atoms. Even more preferred are "phenylalkylenyl" attached to alkyl portions having one to three carbon atoms. Examples of such radicals include benzyl, diphenylmethyl and phenylethyl. The aryl in said aralkyl may be additionally substituted with halo, alkyl, alkoxy, halkoalkyl and haloalkoxy.
The term "alkylthio" embraces radicals containing a linear or branched alkyl radical, of one to ten carbon atoms, attached to a divalent sulfur atom. Even more preferred are lower alkylthio radicals having one to three carbon atoms. An example of "alkylthio" is methylthio, (CH3S-).
The term "haloalkylthio" embraces radicals containing a haloalkyl radical, of one to ten carbon atoms, attached to a divalent sulfur atom. Even more preferred are lower haloalkylthio radicals having one to three carbon atoms. An example of "haloalkylthio" is trifluoromethylthio.
The term "alkylamino" embraces "N-alkylamino" and "N,N-dialkylamino" where amino groups are independently substituted with one alkyl radical and with two alkyl radicals, respectively. More preferred alkylamino radicals are "lower alkylamino" radicals having one or two alkyl radicals of one to six carbon atoms, attached to a nitrogen atom. Even more preferred are lower alkylamino radicals having one to three carbon atoms. Suitable alkylamino radicals may be mono or dialkylamino such as N-methylamino, N-ethylamino, N5N- dimethylamino, N,N-diethylamino and the like.
The term "arylamino" denotes amino groups, which have been substituted with one or two aryl radicals, such as N-phenylamino. The arylamino radicals may be further substituted on the aryl ring portion of the radical.
The term "heteroarylamino" denotes amino groups, which have been substituted with one or two heteroaryl radicals, such as N-thienylamino. The "heteroarylamino" radicals may be further substituted on the heteroaryl ring portion of the radical. The term "aralkylamino" denotes amino groups, which have been substituted with one or two aralkyl radicals. More preferred are phenyl-Q-Cralkylamino radicals, such as N- benzylamino. The aralkylamino radicals may be further substituted on the aryl ring portion.
The terms "N-alkyl-N-arylamino" and "N-aralkyl-N-alkylamino" denote amino groups, which have been independently substituted with one aralkyl and one alkyl radical, or one aryl and one alkyl radical, respectively, to an amino group.
The term "aminoalkyl" embraces linear or branched alkyl radicals having one to about ten carbon atoms any one of which may be substituted with one or more amino radicals. More preferred aminoalkyl radicals are "lower aminoalkyl" radicals having one to six carbon atoms and one or more amino radicals. Examples of such radicals include aminomethyl, aminoethyl, aminopropyl, aminobutyl and aminohexyl. Even more preferred are lower aminoalkyl radicals having one to three carbon atoms.
The term "alkylaminoalkyl" embraces alkyl radicals substituted with alkylamino radicals. More preferred alkylaminoalkyl radicals are "lower alkylaminoalkyl" radicals having alkyl radicals of one to six carbon atoms. Even more preferred are lower alkylaminoalkyl radicals having alkyl radicals of one to three carbon atoms. Suitable alkylaminoalkyl radicals may be mono or dialkyl substituted, such as N-methylaminomethyl, N,N-dimethyl-aminoethyl, N,N-diethylaminomethyl and the like.
The term "alkylaminoalkoxy" embraces alkoxy radicals substituted with alkylamino radicals. More preferred alkylaminoalkoxy radicals are "lower alkylaminoalkoxy" radicals having alkoxy radicals of one to six carbon atoms. Even more preferred are lower alkylaminoalkoxy radicals having alkyl radicals of one to three carbon atoms. Suitable alkylaminoalkoxy radicals may be mono or dialkyl substituted, such as N-methylaminoethoxy, N,N-dimethylaminoethoxy, N,N-diethylaminoethoxy and the like. The term "alkylaminoalkoxyalkoxy" embraces alkoxy radicals substituted with alkylaminoalkoxy radicals. More preferred alkylaminoalkoxyalkoxy radicals are "lower alkylaminoalkoxyalkoxy" radicals having alkoxy radicals of one to six carbon atoms. Even more preferred are lower alkylaminoalkoxyalkoxy radicals having alkyl radicals of one to three carbon atoms. Suitable alkylaminoalkoxyalkoxy radicals may be mono or dialkyl substituted, such as N-methylaminomethoxyethoxy, N-methylaminoethoxyethoxy, N5N- dimethylaminoethoxyethoxy, N,N-diethylaminomethoxymethoxy and the like.
The term "carboxyalkyl" embraces linear or branched alkyl radicals having one to about ten carbon atoms any one of which maybe substituted with one or more carboxy radicals. More preferred carboxyalkyl radicals are "lower carboxyalkyl" radicals having one to six carbon atoms and one carboxy radical. Examples of such radicals include carboxymethyl, carboxypropyl, and the like. Even more preferred are lower carboxyalkyl radicals having one to three CH2 groups.
The term "halosulfonyl" embraces sulfonyl radicals substituted with a halogen radical. Examples of such halosulfonyl radicals include chlorosulfonyl and fluorosulfonyl.
The term "arylthio" embraces aryl radicals of six to ten carbon atoms, attached to a divalent sulfur atom. An example of "arylthio" is phenylthio.
The term "aralkylthio" embraces aralkyl radicals as described above, attached to a divalent sulfur atom. More preferred are phenyl-C1-C3-alkylthio radicals. An example of "aralkylthio" is benzylthio.
The term "aryloxy" embraces optionally substituted aryl radicals, as defined above, attached to an oxygen atom. Examples of such radicals include phenoxy.
The term "aralkoxy" embraces oxy-containing aralkyl radicals attached through an oxygen atom to other radicals. More preferred aralkoxy radicals are "lower aralkoxy" radicals having optionally substituted phenyl radicals attached to lower alkoxy radical as described above.
The term "heteroaryloxy" embraces optionally substituted heteroaryl radicals, as defined above, attached to an oxygen atom.
The term "heteroarylalkoxy" embraces oxy-containing heteroarylalkyl radicals attached through an oxygen atom to other radicals. More preferred heteroarylalkoxy radicals are "lower heteroarylalkoxy" radicals having optionally substituted heteroaryl radicals attached to lower alkoxy radical as described above.
The term "cycloalkyl" includes saturated carbocyclic groups. Preferred cycloalkyl groups include C3-C6 rings. More preferred compounds include, cyclopentyl, cyclopropyl, and cyclohexyl.
The term "cycloalkylalkyl" embraces cycloalkyl-sύbstituted alkyl radicals. Preferable cycloalkylalkyl radicals are "lower cycloalkylalkyl" radicals having cycloalkyl radicals attached to alkyl radicals having one to six carbon atoms. Even more preferred are "5-6- membered cycloalkylalkyl" attached to alkyl portions having one to three carbon atoms. Examples of such radicals include cyclohexylmethyl. The cycloalkyl in said radicals may be additionally substituted with halo, alkyl, alkoxy and hydroxy.
The term "cycloalkenyl" includes carbocyclic groups having one or more carbon- carbon double bonds including "cycloalkyldienyl" compounds. Preferred cycloalkenyl groups include C3-C6 rings. More preferred compounds include, for example, cyclopentenyl, cyclopentadienyl, cyclohexenyl and cycloheptadienyl.
The term "comprising" is meant to be open ended, including the indicated component but not excluding other elements. The term "Formulas I-II" includes any sub formulas.
The compounds of the invention are endowed with kinase inhibitory activity, such as KDR and/or c-Met inhibitory activity.
The present invention also comprises the use of a compound of the invention, or pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment either acutely or chronically of an angiogenesis mediated disease state, including those described previously. The compounds of the present invention are useful in the manufacture of an anti-cancer medicament. The compounds of the present invention are also useful in the manufacture of a medicament to attenuate or prevent disorders through inhibition of KDR and/or c-Met. The present invention comprises a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formulas I-II in association with a least one pharmaceutically acceptable carrier, adjuvant or diluent.
The present invention also comprises a method of treating angiogenesis related disorders in a subject having or susceptible to such disorder, the method comprising treating the subject with a therapeutically effective amount of a compound of Formula I-II.
COMBINATIONS
While the compounds of the invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more compounds of the invention or other agents. When administered as a combination, the therapeutic agents can be formulated as separate compositions that are administered at the same time or sequentially at different times, or the therapeutic agents can be given as a single composition.
The phrase "co-therapy" (or "combination-therapy"), in defining use of a compound of the present invention and another pharmaceutical agent, is intended to embrace administration of each agent in a sequential manner in a regimen that will provide beneficial effects of the drug combination, and is intended as well to embrace co-administration of these agents in a substantially simultaneous manner, such as in a single capsule having a fixed ratio of these active agents or in multiple, separate capsules for each agent. Specifically, the administration of compounds of the present invention may be in conjunction with additional therapies known to those skilled in the art in the prevention or treatment of neoplasia, such as with radiation therapy or with cytostatic or cytotoxic agents.
If formulated as a fixed dose, such combination products employ the compounds of this invention within the accepted dosage ranges. Compounds of Formula I may also be administered sequentially with known anticancer or cytotoxic agents when a combination formulation is inappropriate. The invention is not limited in the sequence of administration; compounds of the invention maybe administered either prior to, simultaneous with or after administration of the known anticancer or cytotoxic agent. Currently, standard treatment of primary tumors consists of surgical excision followed by either radiation or IV administered chemotherapy. The typical chemotherapy regime consists of either DNA alkylating agents, DNA intercalating agents, CDK inhibitors, or microtubule poisons. The chemotherapy doses used are just below the maximal tolerated dose and therefore dose limiting toxicities typically include, nausea, vomiting, diarrhea, hair loss, neutropenia and the like.
There are large numbers of antineoplastic agents available in commercial use, in clinical evaluation and in pre-clinical development, which would be selected for treatment of neoplasia by combination drug chemotherapy. Such antineoplastic agents fall into several major categories, namely, antibiotic-type agents, alkylating agents, antimetabolite agents, hormonal agents, immunological agents, interferon-type agents and a category of miscellaneous agents.
A first family of antineoplastic agents, which may be used in combination with compounds of the present invention, consists of antimetabolite-type/thymidilate synthase inhibitor antineoplastic agents. Suitable antimetabolite antineoplastic agents may be selected from but not limited to the group consisting of 5-FU-fTbrinogen, acanthifolic acid, aminothiadiazole, brequinar sodium, carmofur, Ciba-Geigy CGP-30694, cyclopentyl cytosine, cytarabine phosphate stearate, cytarabine conjugates, Lilly DATHF, Merrel Dow DDFC, dezaguanine, dideoxycytidine, dideoxyguanosine, didox, Yoshitomi DMDC, doxifluridine, Wellcome EHNA, Merck & Co. EX-Ol 5, fazarabine, floxuridine, fludarabine phosphate, 5- fluorouracil, N-(2'-furanidyl)-5-fluorouracil, Daiichi Seiyaku FO-152, isopropyl pyrrolizine, Lilly LY-188011, Lilly LY-264618, methobenzaprim, methotrexate, Wellcome MZPES, norspermidine, NCI NSC-127716, NCI NSC-264880, NCI NSC-39661, NCI NSC-612567, Warner-Lambert PALA, pentostatin, piritrexim, plicamycin, Asahi Chemical PL- AC, Takeda TAC-788, thioguanine, tiazofurin, Erbamont TIF, trimetrexate, tyrosine kinase inhibitors, Taiho UFT and uricytin.
A second family of antineoplastic agents, which may be used in combination with compounds of the present invention, consists of alkylating-type antineoplastic agents. Suitable alkylating-type antineoplastic agents may be selected from but not limited to the group consisting of Shionogi 254-S, aldo-phosphamide analogues, altretamine, anaxirone, Boehringer Mannheim BBR-2207, bestrabucil, budotitane, Wakunaga CA- 102, carboplatin, carmustine, Chinoin-139, Chinoin-153, chlorambucil, cisplatin, cyclophosphamide, American Cyanamid CL-286558, Sanofi CY-233, cyplatate, DegussaD-19-384, Sumimoto DACHP(Myr)2, diphenylspiromustine, diplatinum cytostatic, Erba distamycin derivatives, Chugai DWA- 2114R, ITI E09, elmustine, Erbamont FCE-24517, estramustine phosphate sodium, fotemustine, Unimed G-6-M, Chinoin GYKI- 17230, hepsul-fam, ifosfamide, iproplatin, lomustine, mafosfamide, mitolactol, Nippon Kayaku NK-121, NCI NSC-264395, NCI NSC- 342215, oxaliplatin, Upjohn PCNU, prednimustine, Proter PTT-119, ranimustine, semustine, SmithKline SK&F-101772, Yakult Honsha SN-22, spiromus-tine, Tanabe Seiyaku TA-077, tauromustine, temozolomide, teroxirone, tetraplatin and trimelamol.
A third family of antineoplastic agents which may be used in combination with compounds of the present invention consists of antibiotic-type antineoplastic agents. Suitable antibiotic-type antineoplastic agents may be selected from but not limited to the group consisting of Taiho 4181 -A, aclarubicin, actinomycin D, actinoplanone, Erbamont ADR-456, aeroplysinin derivative, Ajinomoto AN-201-II, Ajinomoto AN-3, Nippon Soda anisomycins, anthracycline, azino-mycin-A, bisucaberin, Bristol-Myers BL-6859, Bristol-Myers BMY- 25067, Bristol-Myers BMY-25551, Bristol-Myers BMY-26605, Bristol-Myers BMY-27557, Bristol-Myers BMY-28438, bleomycin sulfate, bryostatin-1, Taiho C-1027, calichemycin, chromoximycin, dactinomycin, daunorubicin, Kyowa Hakko DC-102, Kyowa Hakko DC-79, Kyowa Hakko DC-88A, Kyowa Hakko DC89-A1, Kyowa Hakko DC92-B, ditrisarubicin B, Shionogi DOB-41, doxorubicin, doxorubicin-fibrinogen, elsamicin-A, epirubicin, erbstatin, esorubicin, esperamicin-Al, esperamicin-Alb, Erbamont FCE-21954, Fujisawa FK-973, fostriecin, Fujisawa FR-900482, glidobactin, gregatin-A, grincamycin, herbimycin, idarubicin, illudins, kazusamycin, kesarirhodins, Kyowa Hakko KM-5539, Kirin Brewery KRN-8602, Kyowa Hakko KT-5432, Kyowa Hakko KT-5594, Kyowa Hakko KT-6149, American Cyanamid LL-D49194, Meiji Seika ME 2303, menogaril, mitomycin, mitoxantrone, SmithKline M-TAG, neoenactin, Nippon Kayaku NK-313, Nippon Kayaku NKT-01 , SRI International NSC-357704, oxalysine, oxaunomycin, peplomycin, pilatin, pirarubicin, porothramycin, pyrindanycin A, Tobishi RA-I, rapamycin, rhizoxin, rodorubicin, sibanomicin, siwenmycin, Sumitomo SM-5887, Snow Brand SN-706, Snow Brand SN-07, sorangicin-A, sparsomycin, SS Pharmaceutical SS-21020, SS Pharmaceutical SS-7313B, SS Pharmaceutical SS-9816B, steffimycin B, Taiho 4181-2, talisomycin, Takeda TAN-868A, terpentecin, thrazine, tricrozarin A, Upjohn U-73975, Kyowa Hakko UCN-10028A, Fujisawa WF-3405, Yoshitomi Y-25024 and zorubicin.
A fourth family of antineoplastic agents which may be used in combination with compounds of the present invention consists of a miscellaneous family of antineoplastic agents, including tubulin interacting agents, topoisomerase II inhibitors, topoisomerase I inhibitors and hormonal agents, selected from but not limited to the group consisting of α- carotene, α-difluoromethyl-arginine, acitretin, Biotec AD-5, Kyorin AHC-52, alstonine, amonafide, amphethinile, amsacrine, Angiostat, ankinomycin, anti-neoplaston AlO, antineoplaston A2, antineoplaston A3, antineoplaston A5, antineoplaston AS2-1, Henkel APD, aphidicolin glycinate, asparaginase, Avarol, baccharin, batracylin, benfluron, benzotript, Ipsen- Beaufour BIM-23015, bisantrene, Bristol-Myers BMY-40481 , Vestar boron- 10, bromofosfamide, Wellcome BW-502, Wellcome BW-773, caracemide, carmethizole hydrochloride, Ajinomoto CDAF, chlorsulfaquinoxalone, Chemes CHX-2053, Chemex CHX- 100, Warner-Lambert CI-921, Warner-Lambert CI-937, Warner-Lambert CI-941, Warner- Lambert CI-958, clanfenur, claviridenone, ICN compound 1259, ICN compound 4711, Contracan, Yakult Honsha CPT-11, crisnatol, curaderm, cytochalasin B, cytarabine, cytocytin, Merz D-609, DABIS maleate, dacarbazine, datelliptinium, didemnin-B, dihaematoporphyrin ether, dihydrolenperone, dinaline, distamycin, Toyo Pharmar DM-341, Toyo Pharmar DM-75, Daiichi Seiyaku DN-9693, docetaxel elliprabin, elliptinium acetate, Tsumura EPMTC, the epothilones, ergotamine, etoposide, etretinate, fenretinide, Fujisawa FR-57704, gallium nitrate, genkwadaphnin, Chugai GLA-43, Glaxo GR-63178, grifolan NMF-5N, hexadecylphosphocholine, Green Cross HO-221, homoharringtonine, hydroxyurea, BTG ICRF-187, ilmofosine, isoglutamine, isotretinoin, Otsuka JI-36, Ramot K-477, Otsuak K- 76COONa, Kureha Chemical K-AM, MECT Corp KI-8110, American Cyanamid L-623, leukoregulin, lonidamine, Lundbeck LU-23-112, Lilly LY-186641, NCI (US) MAP, marycin, Merrel Dow MDL-27048, Medco MEDR-340, merbarone, merocyanlne derivatives, methylanilinoacridine, Molecular Genetics MGI- 136, minactivin, mitonafide, mitoquidone mopidamol, motretinide, Zenyaku Kogyo MST-16, N-(retinoyl)amino acids, Nisshin Flour Milling N-021, N-acylated-dehydroalanines, nafazatrom, Taisho NCU-190, nocodazole derivative, Normosang, NCI NSC-145813, NCI NSC-361456, NCI NSC-604782, NCI NSC- 95580, ocreotide, Ono ONO-112, oquizanocine, Akzo Org-10172, paclitaxel, pancratistatin, pazelliptine, Warner-Lambert PD-111707, Warner-Lambert PD-115934, Warner-Lambert PD- 131141, Pierre Fabre PE-IOOl, ICRT peptide D, piroxantrone, polyhaematoporphyrin, polypreic acid, Efamol porphyrin, probimane, procarbazine, proglumide, Invitron protease nexin I, Tobishi RA-700, razoxane, Sapporo Breweries RBS, restrictin-P, retelliptine, retinoic acid, Rhone-Poulenc RP-49532, Rhone-Poulenc RP-56976, SmithKline SK&F-104864, Sumitomo SM-108, Kuraray SMANCS, SeaPharm SP-10094, spatol, spirocyclopropane derivatives, spirogermanium, Unimed, SS Pharmaceutical SS-554, strypoldinone, Stypoldione, Suntory SUN 0237, Suntory SUN 2071, superoxide dismutase, Toyama T-506, Toyama T-680, taxol, Teijin TEI-0303 , teniposide, thaliblastine, Eastman Kodak TJB-29, tocotrienol, topotecan, Topostin, Teijin TT-82, Kyowa Hakko UCN-01, Kyowa Hakko UCN-1028, ukrain, Eastman Kodak USB-006, vinblastine sulfate, vincristine, vindesine, vinestramide, vinorelbine, vintriptol, vinzolidine, withanolides and Yamanouchi YM-534.
Alternatively, the present compounds may also be used in co-therapies with other anti- neoplastic agents, such as acemannan, aclarubicin, aldesleukin, alemtuzumab, alitretinoin, altretamine, amifostine, aminolevulinic acid, amrubicin, amsacrine, anagrelide, anastrozole, ANCER, ancestim, ARGLABIN, arsenic trioxide, BAM 002 (Novelos), bexarotene, bicalutamide, broxuridine, capecitabine, celmoleukin, cetrorelix, cladribine, clotrimazole, cytarabine ocfosfate, DA 3030 (Dong- A), daclizumab, denileukin diftitox, deslorelin, dexrazoxane, dilazep, docetaxel, docosanol, doxercalciferol, doxifluridine, doxorubicin, bromocriptine, carmustine, cytarabine, fluorouracil, HIT diclofenac, interferon alfa, daunorubicm, doxorubicin, tretinoin, edelfosine, edrecolomab, eflornithine, emitefur, epirubicin, epoetin beta, etoposide phosphate, exemestane, exisulind, fadrozole, filgrastim, finasteride, fludarabine phosphate, formestane, fotemustine, gallium nitrate, gemcitabine, gemtuzumab zogamicin, gimeracil/oteracil/tegafur combination, glycopine, goserelin, heptaplatin, human chorionic gonadotropin, human fetal alpha fetoprotein, ibandronic acid, idarubicin, (imiquimod, interferon alfa, interferon alfa, natural, interferon alfa-2, interferon alfa-2a, interferon alfa-2b, interferon alfa-Nl, interferon alfa-n3, interferon alfacon-1, interferon alpha, natural, interferon beta, interferon beta-la, interferon beta-lb, interferon gamma, natural interferon gamma-la, interferon gamma-lb, interleukin-1 beta, iobenguane, irinotecan, irsogladine, lanreotide, LC 9018 (Yakult), leflunomide, lenograstim, lentinan sulfate, letrozole, leukocyte alpha interferon, leuprorelin, levamisole + fluorouracil, liarozole, lobaplatin, lonidamine, lovastatin, masoprocol, melarsoprol, metoclopramide, mifepristone, miltefosine, mirimostim, mismatched double stranded RNA, mitoguazone, mitolactol, mitoxantrone, molgramostim, nafarelin, naloxone + pentazocine, nartograstim, nedaplatin, nilutamide, noscapine, novel erythropoiesis stimulating protein, NSC 631570 octreotide, oprelvekin, osaterone, oxaliplatin, paclitaxel, pamidronic acid, pegaspargase, peginterferon alfa-2b, pentosan polysulfate sodium, pentostatin, picibanil, pirarubicin, rabbit antithymocyte polyclonal antibody, polyethylene glycol interferon alfa-2a, porfimer sodium, raloxifene, raltitrexed, rasburicase, rhenium Re 186 etidronate, RII retinamide, rituximab, romurtide, samarium (153 Sm) lexidronam, sargramostim, sizofiran, sobuzoxane, sonermin, strontium-89 chloride, suramin, tasonermin, tazarotene, tegafur, temoporfin, temozolomide, teniposide, tetrachlorodecaoxide, thalidomide, thymalfasin, thyrotropin alfa, topotecan, toremifene, tositumomab-iodine 131, trastuzumab, treosulfan, tretinoin, trilostane, trimetrexate, triptorelin, tumor necrosis factor alpha, natural, ubenimex, bladder cancer vaccine, Maruyama vaccine, melanoma lysate vaccine, valrubicin, verteporfin, vinorelbine, VIRULIZIN, zinostatin stimalamer, or zoledronic acid; abarelix; AE 941 (Aeterna), ambamustine, antisense oligonucleotide, bcl-2 (Genta), APC 8015 (Dendreon), cetuximab, decitabine, dexaminoglutethimide, diaziquone, EL 532 (Elan), EM 800 (Endorecherche), eniluracil, etanidazole, fenretinide, filgrastim SDOl (Amgen), fulvestrant, galocitabine, gastrin 17 immunogen, HLA-B7 gene therapy (Vical), granulocyte macrophage colony stimulating factor, histamine dihydrochloride, ibritumomab tiuxetan, ilomastat, IM 862 (Cytran), interleukin-2, iproxifene, LDI 200 (Milkhaus), leridistim, lintuzumab, CA 125 MAb (Biomira), cancer MAb (Japan Pharmaceutical Development), HER-2 and Fc MAb (Medarex), idiotypic 105AD7 MAb (CRC Technology), idiotypic CEA MAb (Trilex), LYM-I -iodine 131 MAb (Techniclone), polymorphic epithelial mucin-yttrium 90 MAb (Antisoma), marimastat, menogaril, mitumomab, motexafm gadolinium, MX 6 (Galderma), nelarabine, nolatrexed, P 30 protein, pegvisomant, pemetrexed, porfiromycin, prinomastat, RL 0903 (Shire), rubitecan, satraplatin, sodium phenylacetate, sparfosic acid, SRL 172 (SR Pharma), SU 5416 (SUGEN), TA 077 (Tanabe), tetrathiomolybdate, thaliblastine, thrombopoietin, tin ethyl etiopurpurin, tirapazamine, cancer vaccine (Biomira), melanoma vaccine (New York University), melanoma vaccine (Sloan Kettering Institute), melanoma oncolysate vaccine (New York Medical College), viral melanoma cell lysates vaccine (Royal Newcastle Hospital), or valspodar. Alternatively, the present compounds may also be used in co-therapies with VEGFR inhibitors including
N-(4-chlorophenyl)-4-(4-pyridinylmethyl)- 1 -phthalazinamine;
4-[4-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]carbonyl]amino]phenoxy]-N-methyl-2- pyridinecarboxamide; N-[2-(diethylamino)ethyl]-5-[(5-fluoro-l,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4- dimethyl- 1 H-pyrrole-3 -carboxamide; 3-[(4-bromo-2,6-difmorophenyl)methoxy]-5-[[[[4-(l- pyrrolidinyl)butyl]amino]carbonyl]amino]-4-isothiazolecarboxainide; N-(4-bromo-2-fluorophenyl)-6-methoxy-7-[(l-methyl-4-piperidinyl)methoxy]-4- quinazolinamine; 3-[5,6,7513-tetraliydro-9-[(l-methylethoxy)methyl]-5-oxo-12H-indeno[2,l-a]pyrrolo[3,4- c]carbazol-12-yl]propyl ester N,N-dimethyl-glycine;
N-[5-[[[5-(l,l -dimethyl ethyl)-2-oxazolyl]methyl]thio] -2-thiazolyl] -4-piperidinecarboxamide; N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[[[2-
(methylsulfonyl)ethyl] amino]methyl] -2-furanyl] -4-quinazolinamine
4-[(4-Methyl-l-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]- phenyl]benzamide
N-(3-chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-4-quinazolinamine iV-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine
N-(3-((((2R)-l-methyl-2-pyrrolidinyl)methyl)oxy)-5-(trifluoromethyl)phenyl)-2-((3-(l,3- oxazol-5-yl)phenyl)amino)-3-pyridinecarboxamide; 2-(((4-fluoroρhenyl)methyl)amino)-N-(3-((((2R)-l-methyl-2-pyrrolidinyl)methyl)oxy)-5-
(trifluoromethyl)phenyl)-3-pyridinecarboxamide; N-[3-(Azetidin-3-ylmethoxy)-5-trifluoromethyl-phenyl]-2-(4-fluoro-benzylamino)- nicotinamide.
6-fluoro-N-(4-(l-methylethyl)phenyl)-2-((4-pyridinylmethyl)amino)-3-pyridinecarboxamide; 2-((4-pyridinylmethyl)amino)-N-(3-(((2S)-2-pyrrolidinylmethyl)oxy)-5-
(trifluoromethyl)phenyl)-3-pyridinecarboxamide; N-(3-(l , 1 -dimethylethyl)-lH-pyrazol-5-yl)-2-((4-pyridinylmethyl)amino)-3- pyridinecarboxamide; N-(3 ,3 -dimethyl-2,3 -dihydro- 1 -benzofuran-6-yl)-2-((4-pyridinylmethyl)amino)-3 - pyridinecarboxamide;
N-(3-((((2S)-l-methyl-2-pyrrolidinyl)methyl)oxy)-5-(trifluoromethyl)phenyl)-2-((4- pyridinylmethyl)amino)-3 -pyridinecarboxamide;
2-((4-pyridinylmethyl)amino)-N-(3 -((2-( 1 -pyrrolidinyl)ethyl)oxy)-4-(trifluoromethyl)phenyl)-
3 -pyridinecarboxamide; N-(3 ,3 -dimethyl-2,3 -dihydro-1 H-indol-6-yl)-2-((4-ρyridinylmethyl)amino)-3 - pyridinecarboxamide; N-(4-(pentafluoroethyl)-3-(((2S)-2-pyrrolidinylmethyl)oxy)ρhenyl)-2-((4- pyridinylmethyl)amino)-3-pyridinecarboxaniide; N-(3-((3-azetidinylmethyl)oxy)-5-(trifluoromethyl)phenyl)-2-((4-pyridinylniethyl)amino)-3- pyridinecarboxamide; N-(3-(4-piperidinyloxy)-5-(trifluoromethyl)phenyl)-2-((2-(3-pyridinyl)ethyl)ammo)-3- pyridinecarboxamide;
N-(4,4-dimethyl-l,2,3,4-tetrahydro-isoquinolin-7-yl)-2-(lH-indazol-6-ylammo)-nicotinamide; 2-(lH-indazol-6-ylamino)-N-[3-(l-methylpyrrolidin-2-ylmethoxy)-5-trifluoromethyl-phenyl]- nicotinamide; N-[I -(2-dimethylamino-acetyl)-3 ,3-dimethyl-2,3-dihydro-l H-indol-6-yl]-2-(l H-indazol-6- ylamino)-nicotinamide; 2-(lH-indazol-6-ylamino)-N-[3-(pyrrolidin-2-ylmethoxy)-5-trifluoromethyl-plienyl]- nicotinamide;
N-(l-acetyl-3,3-dimethyl-253-dihydro-lH-indol-6-yl)-2-(lH-indazol-6-ylamino)-nicotinamide; N-(4,4-dimethyl-l-oxo-l,2,3,4-tetrahydro-isoquinolin-7-yl)-2-(lH-indazol-6-ylamino)- nicotinamide; N-[4-(tert-butyl)-3-(3-piperidylpropyl)phenyl][2-(lH-indazol-6-ylamino)(3- pyridyl)] carboxamide;
N-[5-(tert-butyl)isoxazol-3 -yl] [2-(l H-indazol-6-ylamino)(3-pyridyl)] carboxamide; and N-[4-(tert-butyl)phenyl][2-(lH-indazol-6-ylamino)(3-pyridyl)]carboxamide.
Other compounds described in the following patents and patent applications can be used in combination therapy: US 6,258,812, US 2003/0105091, WO 01/37820, US 6,235,764, WO 01/32651, US 6,630,500, US 6,515,004, US 6,713,485, US 5,521,184, US 5,770,599, US 5,747,498, WO 02/68406, WO 02/66470, WO 02/55501, WO 04/05279, WO 04/07481, WO 04/07458, WO 04/09784, WO 02/59110, WO 99/45009, WO 00/59509, WO 99/61422, US 5,990,141, WO 00/12089 and WO 00/02871.
In some embodiments, the combination comprises a composition of the present invention in combination with at least one anti-angiogenic agent. Agents are inclusive of, but not limited to, in vitro synthetically prepared chemical compositions, antibodies, antigen binding regions, radionuclides, and combinations and conjugates thereof. An agent can be an agonist, antagonist, allosteric modulator, toxin or, more generally, may act to inhibit or stimulate its target (e.g., receptor or enzyme activation or inhibition), and thereby promote cell death or arrest cell growth. Exemplary anti-tumor agents include HERCEPTIN™ (trastuzumab), which may be used to treat breast cancer and other forms of cancer, and RITUXAN™ (rituximab), ZEVALIN™ (ibritumomab tiuxetan), and LYMPHOCIDE™ (epraruzumab), which maybe used to treat non-Hodgkin's lymphoma and other forms of cancer, GLEEV AC™ which may be used to treat chronic myeloid leukemia and gastrointestinal stromal tumors, and BEXXAR™ (iodine 131 tositumomab) which may be used for treatment of non-Hodgkins's lymphoma. Exemplary anti-angiogenic agents include ERBITUX™ (IMC-C225), KDR (kinase domain receptor) inhibitory agents (e.g., antibodies and antigen binding regions that specifically bind to the kinase domain receptor), anti-VEGF agents (e.g., antibodies or antigen binding regions that specifically bind VEGF, or soluble VEGF receptors or a ligand binding region thereof) such as AVASTIN™ or VEGF-TRAP™, and anti-VEGF receptor agents (e.g., antibodies or antigen binding regions that specifically bind thereto), EGFR inhibitory agents (e.g., antibodies or antigen binding regions that specifically bind thereto) such as ABX-EGF (panirumumab), IRESSA™ (gefitinib), TARCEVA™ (erlotinib), anti-Angl and anti-Ang2 agents (e.g., antibodies or antigen binding regions specifically binding thereto or to their receptors, e.g., Tie2/Tek), and anti-Tie2 kinase inhibitory agents (e.g., antibodies or antigen binding regions that specifically bind thereto). The pharmaceutical compositions of the present invention can also include one or more agents (e.g., antibodies, antigen binding regions, or soluble receptors) that specifically bind and inhibit the activity of growth factors, such as antagonists of hepatocyte growth factor (HGF, also known as Scatter Factor), and antibodies or antigen binding regions that specifically bind its receptor "c-met".
Other anti-angiogenic agents include Campath, IL-8, B-FGF, Tek antagonists (Ceretti et al., US Publication No. 2003/0162712; US Patent No. 6,413,932), anti-TWEAK agents (e.g., specifically binding antibodies or antigen binding regions, or soluble TWEAK receptor antagonists; see, Wiley, US Patent No. 6,727,225), ADAM distintegrin domain to antagonize the binding of integrin to its ligands (Fanslow et al., US Publication No. 2002/0042368), specifically binding anti-eph receptor and/or anti-ephrin antibodies or antigen binding regions (US Patent Nos. 5,981,245; 5,728,813; 5,969,110; 6,596,852; 6,232,447; 6,057,124 and patent family members thereof), and anti-PDGF-BB antagonists (e.g., specifically binding antibodies or antigen binding regions) as well as antibodies or antigen binding regions specifically binding to PDGF-BB ligands, and PDGFR kinase inhibitory agents (e.g., antibodies or antigen binding regions that specifically bind thereto).
Additional anti-angiogenic/anti-tumor agents include: SD-7784 (Pfizer, USA); cilengitide.(Merck KGaA, Germany, EPO 770622); pegaptanib octasodium, (Gilead Sciences, USA); Alphastatin, (BioActa, UK); M-PGA, (Celgene, USA, US 5712291); ilomastat, (Arriva, USA, US 5892112); emaxanϊb, (Pfizer, USA, US 5792783); vatalanib, (Novartis, Switzerland); 2-methoxyestradiol, (EntreMed, USA); TLC ELL- 12, (Elan, Ireland); anecortave acetate, (Alcon, USA); alρha-D148 Mab, (Amgen, USA); CEP-7055,(Cephalon, USA); anti- Vn Mab, (Crucell, Netherlands) DAC:antiangiogenic, (ConjuChem, Canada); Angiocidin, (InKine Pharmaceutical, USA); KM-2550, (Kyowa Hakko, Japan); SU-0879, (Pfizer, USA); CGP-79787, (Novartis, Switzerland, EP 970070); ARGENT technology, (Ariad, USA); YIGSR-Stealth, (Johnson & Johnson, USA); fibrinogen-E fragment, (BioActa, UK); angiogenesis inhibitor, (Trigen, UK); TBC-1635, (Encysive Pharmaceuticals, USA); SC-236, (Pfizer, USA); ABT-567, (Abbott, USA); Metastatin, (EntreMed, USA); angiogenesis inhibitor, (Tripep, Sweden); maspin, (Sosei, Japan); 2-methoxyestradiol, (Oncology Sciences Corporation, USA); ER-68203-00, (IVAX, USA); Benefin, (Lane Labs, USA); Tz-93, (Tsumura, Japan); TAN-1120, (Takeda, Japan); FR-111142, (Fujisawa, Japan, JP 02233610); platelet factor 4, (RepliGen, USA, EP 407122); vascular endothelial growth factor antagonist, (Borean, Denmark); cancer therapy, (University of South Carolina, USA); bevacizumab (pINN), (Genentech, USA); angiogenesis inhibitors, (SUGEN, USA); XL 784, (Exelixis, USA); XL 647, (Exelixis, USA); MAb, alpha5beta3 integrin, second generation, (Applied Molecular Evolution, USA and Medlmmune, USA); gene therapy, retinopathy, (Oxford BioMedica, UK); enzastaurin hydrochloride (USAN), (Lilly, USA); CEP 7055, (Cephalon, USA and Sanofi-Synthelabo, France); BC 1, (Genoa Institute of Cancer Research, Italy); angiogenesis inhibitor, (Alchemia, Australia); VEGF antagonist, (Regeneron, USA); rBPI 21 and BPI-derived antiangiogenic, (XOMA, USA); PI 88, (Progen, Australia); cilengitide (pINN), (Merck KGaA, German; Munich Technical University, Germany, Scripps Clinic and Research Foundation, USA); cetuximab (INN), (Aventis, France); AVE 8062, (Ajinomoto, Japan); AS 1404, (Cancer Research Laboratory, New Zealand); SG 292, (Telios, USA);
Endostatin, (Boston Childrens Hospital, USA); ATN 161, (Attenuon, USA); ANGIOST ATIN, (Boston Childrens Hospital, USA); 2-methoxyestradiol, (Boston Childrens Hospital, USA); ZD 6474, (AstraZeneca, UK); ZD 6126, (Angiogene Pharmaceuticals, UK); PPI 2458, (Praecis, USA); AZD 9935, (AstraZeneca, UK); AZD 2171, (AstraZeneca, UK); vatalanib (pINN), (Novartis, Switzerland and Schering AG, Germany); tissue factor pathway inhibitors, (EntreMed, USA); pegaptanib (Pinn), (Gilead Sciences, USA); xanthorrhizol, (Yonsei University, South Korea); vaccine, gene-based, VEGF-2, (Scripps Clinic and Research Foundation, USA); SPV5.2, (Supratek, Canada); SDX 103, (University of California at San Diego, USA); PX 478, (ProlX, USA); METASTATIN, (EntreMed, USA); troponin I, (Harvard University, USA); SU 6668, (SUGEN, USA); OXI 4503, (OXiGENE, USA); o-guanidines, ( Dimensional Pharmaceuticals, USA); motuporamine C, (British Columbia University, Canada); CDP 791, (Celltech Group, UK); atiprimod (pINN), (GlaxoSmithKline, UK); E 7820, (Eisai, Japan); CYC 381, (Harvard University, USA); AE 941, (Aeterna, Canada); vaccine, angiogenesis, (EntreMed, USA); urokinase plasminogen activator inhibitor, (Dendreon, USA); oglufanide (pINN), (Melmotte, USA); HIF- lalfa inhibitors, (Xenova, UK); CEP 5214, (Cephalon, USA); BAY RES 2622, (Bayer, Germany); Angiocidin, (InKine, USA); A6, (Angstrom, USA); KR 31372, (Korea Research Institute of Chemical Technology, South Korea); GW 2286, (GlaxoSmithKline, UK); EHT 0101, (ExonHit, France); CP 868596, (Pfizer, USA); CP 564959, (OSI, USA); CP 547632, (Pfizer, USA); 786034,
(GlaxoSmithKline, UK); KRN 633, (Kirin Brewery, Japan); drug delivery system, intraocular, 2-methoxyestradiol, (EntreMed, USA); anginex, (Maastricht University, Netherlands, and Minnesota University, USA); ABT 510, (Abbott, USA); AAL 993, (Novartis, Switzerland); VEGI, (ProteomTech, USA); tumor necrosis factor-alpha inhibitors, (National Institute on Aging, USA); SU 11248, (Pfizer, USA and SUGEN USA); ABT 518, (Abbott, USA); YH16, (Yantai Rongchang, China); S-3APG , (Boston Childrens Hospital, USA and EntreMed, USA); MAb, KDR, (ImClone Systems, USA); MAb, alpha5 betal, (Protein Design, USA); KDR kinase inhibitor, (Celltech Group, UK, and Johnson & Johnson, USA); GFB 116, (South Florida University, USA and Yale University, USA); CS 706, (Sankyo, Japan); combretastatin A4 prodrug, (Arizona State University, USA); chondroitinase AC, (IBEX, Canada); BAY RES 2690, (Bayer, Germany); AGM 1470, (Harvard University, USA, Takeda, Japan, and TAP, USA); AG 13925, (Agouron, USA); Tetrathiomolybdate, (University of Michigan, USA); GCS 100, (Wayne State University, USA) CV 247, (Ivy Medical, UK); CKD 732, (Chong Kun Dang, South Korea); MAb, vascular endothelium growth factor, (Xenova, UK); irsogladine (INN), (Nippon Shinyaku, Japan); RG 13577, (Aventis, France); WX 360, (Wilex, Germany); squalamine (pINN), (Genaera, USA); RPI 4610, (Sirna, USA); cancer therapy, (Marinova, Australia); heparanase inhibitors, (InSight, Israel); KL 3106, (Kolon, South Korea); Honokiol, (Emory University, USA); ZK CDK, (Schering AG, Germany); ZK Angio, (Schering AG, Germany); ZK 229561, (Novartis, Switzerland, and Schering AG, Germany); XMP 300, (XOMA, USA); VGA 1102, (Taisho, Japan); VEGF receptor modulators, (Pharmacopeia,
USA); VE-cadherin-2 antagonists , (ImClone Systems, USA); Vasostatin, (National Institutes of Health, USA);vaccine, FIk-I, (ImClone Systems, USA); TZ 93, (Tsumura, Japan); TumStatin, (Beth Israel Hospital, USA); truncated soluble FLT 1 (vascular endothelial growth factor receptor 1), (Merck & Co, USA); Tie-2 ligands, (Regeneron, USA); and, thrombospondin 1 inhibitor, (Allegheny Health, Education and Research Foundation, USA).
Alternatively, the present compounds may also be used in co-therapies with other antineoplastic agents, such as VEGF antagonists, other kinase inhibitors including p38 inhibitors, KDR inhibitors, EGF inhibitors and CDK inhibitors, TNF inhibitors, metallomatrix proteases inhibitors (MMP), COX-2 inhibitors including celecoxib, NSAID 's, or αvβ3 inhibitors.
The present invention comprises processes for the preparation of a compound of Formula I-II. Also included in the family of compounds of Formula I-II are the pharmaceutically acceptable salts thereof. The term "pharmaceutically-acceptable salts" embraces salts commonly used to form alkali metal salts and to form addition salts of free acids or free bases. The nature of the salt is not critical, provided that it is pharmaceutically acceptable. Suitable pharmaceutically acceptable acid addition salts of compounds of Formula I-II may be prepared from an inorganic acid or from an organic acid. Examples of such inorganic acids are hydrochloric, hydrobromic, hydroiodic, nitric, carbonic, sulfuric and phosphoric acid. Appropriate organic acids may be selected from aliphatic, cycloaliphatic, aromatic, arylaliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, example of which are formic, acetic, adipic, butyric, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, mesylic, 4- hydroxybenzoic, phenylacetic, mandelic, embonic (pamoic), methanesulfonic, ethanesulfonic, ethanedisulfonic, benzenesulfonic, pantothenic, 2-hydroxyethanesulfonic, toluenesulfonic, sulfanilic, cyclohexylaminosulfonic, camphoric, camphorsulfonic, digluconic, cyclopentanepropionic, dodecylsulfonic, glucoheptanoic, glycerophosphonic, heptanoic, hexanoic, 2-hydroxy-ethanesulfonic, nicotinic, 2-naphthalenesulfonic, oxalic, palmoic, pectinic, persulfuric, 2-phenylpropionic, picric, pivalic propionic, succinic, tartaric, thiocyanic, mesylic, undecanoic, stearic, algenic, β-hydroxybutyric, salicylic, galactaric and galacturonic acid. Suitable pharmaceutically-acceptable base addition salts of compounds of Formula I-II include metallic salts, such as salts made from aluminum, calcium, lithium, magnesium, potassium, sodium and zinc, or salts made from organic bases including primary, secondary and tertiary amines, substituted amines including cyclic amines, such as caffeine, arginine, diethylamine, N-ethyl piperidine, aistidine, glucamine, isopropylamine, lysine, morpholine, N- ethyl morpholine, piperazine, piperidine, triethylamine, trimethylamine. All of these salts may be prepared by conventional means from the corresponding compound of the invention by reacting, for example, the appropriate acid or base with the compound of Formula I-II. When a basic group and an acid group are present in the same molecule, a compound of Formula I-II may also form internal salts.
GENERAL SYNTHETIC PROCEDURES
The compounds of the invention can be synthesized according to the following procedures of Schemes 1-10, wherein the substituents are as defined for Formulas I-II, above, except where further noted.
The following abbreviations are used throughout the specification:
HOAc acetic acid
MeCN, CH3CN acetonitrile NH3 ammonia NH4Cl ammonium chloride Ar argon HBTA O-benzotriazol-l-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate HATU O-(7-azabenzotriazol- 1 -yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate PyBop benzotriazol- 1 -yl-oxy-tripyrrolidino-phosphonium hexafluorophosphate
Pd2(dba)3 bis(dibenzylideneacetone) palladium
BINAP 2,2'-bis(diphenylphosphino)-l ,1 '-binaphthyl
TEAC bis(tetra-ethylammonium)carbonate
BBr3 boron tribromide
BSA bovine serum albumin
Br2 bromine
BOC butyloxycarbonyl
Cs2CO3 cesium carbonate
CHCl3 chloroform
CDCl3 chloroform deuterated
Cu copper
CuI copper(I) iodide
Et2O diethyl ether
DBU 1 ,8-diazabicyclo[5 A0]undec-7-ene
DIBAL diisobutylaluminum hydride
DIAD diisopropyl azodicarboxylate T7US2006/016344
DIEA diisopropylethylamine
DMF dimethylformamide
DMAP 4-diniethylaminopyridine
DMSO dimethylsulfoxide
EDC, EDCI 1 -(3 -dimethylaminopropyl)-3 -ethylcarbodiimide hydrochloride dppa diphenylphosphoryl azide
EtOAc ethyl acetate
FBS fetal bovine serum g gram h hour
HBr hydrobromic acid
HCl hydrochloric acid
HOBt 1-hydroxybenzotriazole hydrate
H2 hydrogen
H2O2 hydrogen peroxide
Fe iron
LiHMDS lithium bis(trimethylsilyl)-amide
LDA Lithium diisopropylamide
MCPBA meta-chloroperbenzoic acid
MgSO4 magnesium sulfate
MeOH, CH3OH - methanol
MeI methyl iodide
CH2Cl2, DCM methylene chloride
NMP N-methylpyrrolidinone
ML, ml milliliter
N2 nitrogen
Pd/C palladium on carbon
Pd(OAc)2 palladium acetate
Pd(OH)2 palladium hydroxide
Pd(PPh3)4 palladium tetrakis triphenylphosphine
Pd(dppf)Cl2 l,l-bis(diphenylphosphino)ferrocene palladium chloride
PBS phosphate buffered saline
POCl3 phosphorous oxychloride
K2CO3 potassium carbonate T7US2006/016344
KOH potassium hydroxide
RT room temperature
NaHCO3 sodium bicarbonate
NaBH4 sodium borohydride
NaBH3CN sodium cyanoborohydride
NaOtBu sodium tert-butoxide
NaOH sodium hydroxide
NaClO2 sodium chlorite
NaCl sodium chloride
NaHPO4 sodium biphospate
NaH sodium hydride
NaI sodium iodide
Na2SO4 sodium sulfate
TBTU O-benzotriazol- 1 -yl-N,N,N ' ,N ' -tetramethyluronium tetrafluoroborate
THF tetrahydrofuran
Et3N, TEA triethylamine
TFA trifluoroacetic acid
P(t-bu)3 tri(tert-butyl)phosphine
H2O water
Scheme 1
R-halo - HX-W-NO2 -^ R_χ_W-NO2-^ R.χ.w.NH2 2 base 3
4 HATU | R1-OH
R-X-W-Y-R1
5
Substituted compounds 5, where Y is -NH-C(=O)-, can be prepared by the process outlined in Scheme 1. The halo substituted ring R-halo 1, is condensed with an alcohol 2 (where X is O) is heated, preferably in the presence of a catalyst such as DMAP, solvent such as dioxane, and base, such as pyridine to form the ether 3. Preferably the reaction is heated above RT, more preferably above 75 0C5 even more preferably at about 110 0C. The nitro compound 3 is reduced to the amine 4 such as by treatment with Fe, HCl and an alcohol such as MeOH, in an appropriate solvent such as THF. The amine 4 is coupled with a carboxylic acid derivative R^OH, such as a carboxylic acid or anhydride, in the presence of a coupling agent such as HATU, or with PyBOP and base such as DIEA, to yield the desired compounds 5.
Scheme 2
Figure imgf000079_0001
Alternatively, compounds of the invention where X is O and R1 is 2-oxopyrrolyl can be prepared by the method described in Scheme 2. The halo substituted quinoline derivative 6, is condensed with alcohol 7 is heated, preferably in the presence of a catalyst such as DMAP, solvent such as dioxane, and base, such as pyridine to form ether 8. Preferably the reaction is heated above RT, more preferably above 75 °C, even more preferably at about 110 °C. The nitro compound 8 is reduced to the amine 9 such as by treatment with Fe, HCl and an alcohol such as MeOH, in an appropriate solvent such as THF. The amine 9 is coupled with a carboxylic acid, in the presence of a coupling agent such as HATU to yield the desired compounds 10.
Scheme 3
Figure imgf000080_0001
12
Alternatively, compounds of the invention where R1 is 2-oxoimidazolyl can be prepared by the method described in Scheme 3. The amine 9 can be activated such as with a chloroformate to form the caarbamate 11. The substituted imidazolidin-2-one is treated with base, such as NaH, in an appropriate solvent such as DMF and added to the carbamate 11 to provide the desired compounds 12.
US2006/016344
Scheme 4
Figure imgf000081_0001
Compounds of the invention where R1 is 2-oxopyrrolyl can be prepared by the method described in Scheme 4. The N-protected 2-oxopyrrolidine 13 is alkylated such as by treatment with base, e.g. LDA, in a suitable solvent such as THF, followed by addition of a compound with an appropriate leaving group, such as a halo substituent. The reaction temperature is preferably below RT, preferably at about 0 0C. Following deprotection, such as by treatment with TFA, where the amine is protected with a BOC group, the free amine 15 is treated with a chlorformate in the presence of base, such as TEA, to form the active ester 16. Treatment with the ester 16 with an amine yields the desired amides 17.
Scheme 5
Figure imgf000082_0001
21
Substituted pyridazines 21 of the invention can be prepared by the method described in Scheme 5. Hydrazines 18 are reacted with oxaldehyde then with 2,2-dimethyl-l,3-dioxane- 4,6-dione followed by acid, such as acetic acid ,and piperidines, to form the diaza butadiene-4- ylidene 19. Cyclization, such as by treatment with base, e.g. sodium methoxide, yields the pyridazine carboxylic acid 20. The reaction is heated at a temperature above RT, preferably at about reflux. Formation of the desired amides 21 from the pyridazine 20 is by the coupling procedure described above, or with PyBOP and base such as DIEA.
Scheme 6
Figure imgf000083_0001
24
25
Substituted pyrimidines 25 of the invention can be prepared by the method described in Scheme 6. Alkylation of the oxo-l,6-dihydropyrimidine ester 22, such as by reaction with the appropriate halide in the presence of base, e.g. K2CO3, and a solvent such as DMF, provided the substituted pyrimidines 23. De-esterification of 23, such as by treatment with base, e.g. NaOH, provides the carboxylic acid 24, which can be coupled via the methods described above to provide the amides 25.
T7US2006/016344
Scheme 7
Figure imgf000084_0001
Substituted oxazolidine acetamides 28 of the invention can be prepared by the method described in Scheme 7. Treatment of the amine 9 with an activated acetyl compound, e.g. chloroacetyl chloride, such as in the presence of base, e.g. NaHCO3, provides the chloroacetamide 26. The reaction is held at a temperature below RT, preferably at about 0 °C. Treatment of the acetamide 26 with an amino-alcohol, at a temperature above RT, preferably above 50 °C, more preferably at about 80 0C, provides the substituted acetamide 27. Cyclization of the acetamide 27, such as by treatment with l-(2,5-dioxopyrrolidine-l- carbonyl)pyrrolidine-2,5-dione and DBU, yields the desired oxazoldine acetamides 28.
Scheme 8
Figure imgf000084_0002
Imidazolidine acetic acids 31 of the invention can be prepared by the method described in Scheme 8. Alkylation of the imidazolidine 29, such as by treatment with base, e.g. NaH, followed by addition of the appropriate haloacetic acid ester provides the desired substituted imidazolidine 30. De-esterification of 30 such as by treatment with base, e.g. NaOH, provides the desired acetic acid 31, which can be coupled with an amine to provide the acetamides of the invention. Scheme 9
Figure imgf000085_0001
Br CO,Bu-f Base
Figure imgf000085_0002
37
36
Similarly, pyrrolyl acetic acids 37 of the invention can be prepared by the method described in Scheme 9. Substituted hydroxyl-pyrroles 34, formed such as by Grignard reactions with pyrrolidine-2,5-dione and substituted magnesium bromides, are reduced, such with NaBH3CN and acid, e.g. HCl, to provide the pyrrolidones 35. Alkylation of the pyrrolidone, such as with treatment with base, e.g. NaH, followed by addition of 2- haloacetates, provides the desired pyrrolidinyl acetates 36. De-esterification of 36, such as by treatment with acid, e.g. HCl, provides the desired pyrrolidinyl acetic acid 37 which can be treated with an amine as described above to provide the acetamides of the invention.
Scheme 10
Figure imgf000086_0001
42
Alternatively, compounds of the invention where W is pyridyl can be prepared by the method described in Scheme 10. The halo substituted quinoline derivative 38, is condensed with alcohol 39, preferably in the presence of a catalyst such as DMAP, solvent such as dioxane, and base, such as pyridine to form ether 40. Preferably the reaction is heated above RT, more preferably above about 75 °C, even more preferably at about 105 0C. The halo compound 40 is converted to the amine 41 such as by treatment with LiHMDS, 2- (dicyclohexylphosphino)biphenyl and a palladium catalyst, such as Pd2(dba)3. Preferably the reaction is heated above RT, more preferably at about 65 °C. The amine 41 is coupled with a carboxylic acid, in the presence of a coupling agent such as HBTU to yield the desired compounds 42.
The starting compounds defined in Schemes 1-10 may also be present with functional groups in protected form if necessary and/or in the form of salts, provided a salt-forming group is present and the reaction in salt form is possible. If so desired, one compound of Formula I can be converted into another compound of Formula I or a N-oxide thereof; a compound of Formula I can be converted into a salt; a salt of a compound of Formula I can be converted into the free compound or another salt; and/or a mixture of isomeric compounds of Formula I can be separated into the individual isomers. N-Oxides can be obtained in a known matter by reacting a compound of Formula I with hydrogen peroxide, oxone, or a peracid, e.g. mCPBA, in an inert solvent, e.g. CH2Cl2, or a mixture OfH2O and an alcohol such as MeOH or EtOH, at a temperature between about -10-35 °C, such as about O °C - RT. If one or more other functional groups, for example carboxy, hydroxy, amino, or mercapto, are or need to be protected in a compound of Formula I or in the preparation of compounds of Formula I, because they should not take part in the reaction, these are such groups as are usually used in the synthesis of peptide compounds, and also of cephalosporins and penicillins, as well as nucleic acid derivatives and sugars. The protecting groups may already be present in precursors and should protect the functional groups concerned against unwanted secondary reactions, such as acylations, etherifications, esterifications, oxidations, solvolysis, and similar reactions. It is a characteristic of protecting groups that they lend themselves readily, i.e. without undesired secondary reactions, to removal, typically by solvolysis, reduction, photolysis or also by enzyme activity, for example under conditions analogous to physiological conditions, and that they are not present in the end-products. The specialist knows, or can easily establish, which protecting groups are suitable with the reactions mentioned above and hereinafter.
The protection of such functional groups by such protecting groups, the protecting groups themselves, and their removal reactions are described for example in standard reference works, such as J.F.W. McOmie, "Protective Groups in Organic Chemistry", Plenum Press, London and New York (1973), in T.W. Greene, "Protective Groups in Organic Synthesis", Wiley, New York (1981), in "The Peptides", Volume 3, E. Gross and J. Meienhofer editors, Academic Press, London and New York (1981), in "Methoden der Organischen Chemie" (Methods of Organic Chemistry), Houben Weyl, 41 edition, Volume 15/1, Georg Thieme Verlag, Stuttgart (1974), in H.-D. Jakubke and H. Jescheit, "Aminosauren, Peptide, Proteine" (Amino acids, Peptides, Proteins), Verlag Chemie, Weinheim, Deerfield Beach, and Basel (1982), and in Jochen Lehmann, "Chemie der Kohlenhydrate: Monosaccharide und Derivate" (Chemistry of Carbohydrates: Monosaccharides and Derivatives), Georg Thieme Verlag, Stuttgart (1974). In the additional process steps, carried out as desired, functional groups of the starting compounds which should not take part in the reaction may be present in unprotected form or may be protected for example by one or more of the protecting groups mentioned above under "protecting groups". The protecting groups are then wholly or partly removed according to one of the methods described there. Salts of a compound of Formula I with a salt-forming group may be prepared in a manner known per se. Acid addition salts of compounds of Formula I may thus be obtained by treatment with an acid or with a suitable anion exchange reagent. A salt with two acid molecules (for example, a dihalogenide of a compound of Formula I) may also be converted into a salt with one acid molecule per compound (for example, a monohalogenide); this may be done by heating to a melt, or for example by heating as a solid under a high vacuum at elevated temperature, for example from 130 to 170 0C, one molecule of the acid being expelled per molecule of a compound of Formula I.
Salts can usually be converted to free compounds, e.g. by treating with suitable basic agents, for example with alkali metal carbonates, alkali metal hydrogen carbonates, or alkali metal hydroxides, typically potassium carbonate or sodium hydroxide.
All process steps described here can be carried out under known reaction conditions, preferably under those specifically mentioned, in the absence of or usually in the presence of solvents or diluents, preferably such as are inert to the reagents used and able to dissolve these, in the absence or presence of catalysts, condensing agents or neutralizing agents, for example ion exchangers, typically cation exchangers, for example in the H+ form, depending on the type of reaction and/or reactants at reduced, normal, or elevated temperature, for example in the range from about -100 °C to about 190 °C, preferably from about -80 0C to about 150 °C, for example at about -80 0C to about 60 °C, at RT, at about -20 °C to about 40 °C or at the boiling point of the solvent used, under atmospheric pressure or in a closed vessel, where appropriate under pressure, and/or in an inert atmosphere, for example under argon or nitrogen.
Salts may be present in all starting compounds and transients, if these contain salt- forming groups. Salts may also be present during the reaction of such compounds, provided the reaction is not thereby disturbed. In certain cases, typically in hydrogenation processes, it is possible to achieve stereoselective reactions, allowing for example easier recovery of individual isomers.
The solvents from which those can be selected which are suitable for the reaction in question include for example H2O, esters, typically lower alkyl-lower alkanoates, e.g., EtOAc, ethers, typically aliphatic ethers, e.g., Et2O, or cyclic ethers, e.g., THF, liquid aromatic hydrocarbons, typically benzene or toluene, alcohols, typically MeOH, EtOH or 1-propanol, IPOH, nitriles, typically CH3CN, halogenated hydrocarbons, typically CH2Cl2, acid amides, typically DMF, bases, typically heterocyclic nitrogen bases, e.g. pyridine, carboxylic acids, typically lower alkanecarboxylic acids, e.g., AcOH, carboxylic acid anhydrides, typically lower alkane acid anhydrides, e.g., acetic anhydride, cyclic, linear, or branched hydrocarbons, typically cyclohexane, hexane, or isopentane, or mixtures of these solvents, e.g., aqueous solutions, unless otherwise stated in the description of the process. Such solvent mixtures may also be used in processing, for example in chromatography.
The invention relates also to those forms of the process in which one starts from a compound obtainable at any stage as a transient and carries out the missing steps, or breaks off the process at any stage, or forms a starting material under the reaction conditions, or uses said starting material in the form of a reactive derivative or salt, or produces a compound obtainable by means of the process according to the invention and processes the said compound in situ. In the preferred embodiment, one starts from those starting materials, which lead to the compounds described above as preferred.
The compounds of Formula I, including their salts, are also obtainable in the form of hydrates, or their crystals can include for example the solvent used for crystallization (present as solvates).
New starting materials and/or intermediates, as well as processes for the preparation thereof, are likewise the subject of this invention. In the preferred embodiment, such starting materials are used and reaction conditions so selected as to enable the preferred compounds to be obtained.
Starting materials of the invention, are known, are commercially available, or can be synthesized in analogy to or according to methods that are known in the art. In the preparation of starting materials, existing functional groups, which do not participate in the reaction, should, if necessary, be protected. Preferred protecting groups, their introduction and their removal are described above or in the examples.
All remaining starting materials are known, capable of being prepared according to known processes, or commercially obtainable; in particular, they can be prepared using processes as described in the examples.
Compounds of the present invention can possess, in general, one or more asymmetric carbon atoms and are thus capable of existing in the form of optical isomers as well as in the form of racemic or non-racemic mixtures thereof. The optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, e.g., by formation of diastereoisomeric salts, by treatment with an optically active acid or base. Examples of appropriate acids are tartaric, diacetyltartaric, dibenzoyltartaric, ditoluoyltartaric, and camphorsulfonic acid and then separation of the mixture of diastereoisomers by crystallization followed by liberation of the optically active bases from these salts. A different process for separation of optical isomers involves the use of a chiral chromatography column optimally chosen to maximize the separation of the enantiomers. Still another available method involves synthesis of covalent diastereoisomeric molecules by reacting compounds of the invention with an optically pure acid in an activated form or an optically pure isocyanate. The synthesized diastereoisomers can be separated by conventional means such as chromatography, distillation, crystallization or sublimation, and then hydrolyzed to deliver the enantiomerically pure compound. The optically active compounds of the invention can likewise be obtained by using optically active starting materials. These isomers may be in the form of a free acid, a free base, an ester or a salt.
The compounds of this invention may contain one or more asymmetric centers and thus occur as racemates and racemic mixtures, scalemic mixtures, single enantiomers, individual diastereomers and diastereomeric mixtures. All such isomeric forms of these compounds are expressly included in the present invention.
The compounds of this invention may also be represented in multiple tautomeric forms, for example, as illustrated below:
Figure imgf000090_0001
The invention expressly includes all tautomeric forms of the compounds described herein.
The compounds may also occur in cis- or trans- or E- or Z- double bond isomeric forms. All such isomeric forms of such compounds are expressly included in the present invention. All crystal forms of the compounds described herein are expressly included in the present invention.
Substituents on ring moieties (e.g., phenyl, thienyl, etc.) may be attached to specific atoms, whereby they are intended to be fixed to that atom, or they may be drawn unattached to a specific atom, whereby they are intended to be attached at any available atom that is not already substituted by an atom other than H (hydrogen).
The compounds of this invention may contain heterocyclic ring systems attached to another ring system. Such heterocyclic ring systems may be attached through a carbon atom or a heteroatom in the ring system.
Alternatively, a compound of any of the formulas delineated herein maybe synthesized according to any of the processes delineated herein, hi the processes delineated herein, the steps may be performed in an alternate order and may be preceded, or followed, by additional protection/deprotection steps as necessary. The processes may further comprise use of appropriate reaction conditions, including inert solvents, additional reagents, such as bases (e.g., LDA, DIEA, pyridine, K2CO3, and the like), catalysts, and salt forms of the above. The intermediates may be isolated or carried on in situ, with or without purification. Purification methods are known in the art and include, for example, crystallization, chromatography (liquid and gas phase, and the like), extraction, distillation, trituration, reverse phase HPLC and the like. Reactions conditions such as temperature, duration, pressure, and atmosphere (inert gas, ambient) are known in the art and may be adjusted as appropriate for the reaction.
As can be appreciated by the skilled artisan, the above synthetic schemes are not intended to comprise a comprehensive list of all means by which the compounds described and claimed in this application may be synthesized. Further methods will be evident to those of ordinary skill in the art. Additionally, the various synthetic steps described above may be performed in an alternate sequence or order to give the desired compounds. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing the inhibitor compounds described herein are known in the art and include, for example, those such as described in R. Larock, "Comprehensive Organic Transformations", VCH Publishers (1989); T.W. Greene and P.G.M. Wuts, "Protective Groups in Organic Synthesis", 3rd edition, John Wiley and Sons (1999); L. Fieser and M. Fieser, "Fieser and Fieser's Reagents for Organic Synthesis", John Wiley and Sons (1994); A. Katritzky and A. Pozharski, "Handbook of Heterocyclic Chemistry", 2nd edition (2001); M. Bodanszky, A. Bodanszky, "The Practice of Peptide Synthesis", Springer- Verlag, Berlin Heidelberg (1984); J. Seyden-Penne, "Reductions by the Alumino- and Borohydrides in Organic Synthesis", 2nd edition, Wiley- VCH, (1997); and L. Paquette, editor, "Encyclopedia of Reagents for Organic Synthesis", John Wiley and Sons (1995). The compounds of this invention may be modified by appending appropriate functionalities to enhance selective biological properties. Such modifications are known in the art and include those which increase biological penetration into a given biological compartment (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.
These detailed descriptions fall within the scope, and serve to exemplify, the above- described General Synthetic Procedures, which form part of the invention. These detailed descriptions are presented for illustrative purposes only and are not intended as a restriction on the scope of the invention. Unless otherwise noted, all materials were obtained from commercial suppliers and used without further purification. Anhydrous solvents such as DMF, THF, CH2Cl2 and toluene were obtained from the Aldrich Chemical Company, EMD among others.
Example 1
Figure imgf000092_0001
NaCIO2,
KH2PO4, f-BuOH, H2O
Figure imgf000092_0002
Figure imgf000092_0003
Step 1: l-methyl-2-phenyl-5-(pyridin-4-yl)-l,2-dihydropyrazol-3-one. thyl isonicotinoylacetate (3.01 g, 16 mmol) and l-methyl-2-phenylhydrazine (2.03 g, 17 mmol) were suspended in water (50 ml) and glacial acetic acid (1.35 ml, 23 mmol) was added. The flask was fitted with a reflux condensor and placed in a preheated oil bath (115 C) and stirred. After 4 hours, the reaction cooled to room temperature and extracted with EtOAc (2 x 100 ml; 50 ml), 10:1 DCM / MeOH (110 ml), and EtOAc again. The organic phases were combined, dried over sodium sulfate, filtered, and concentrated. The crude material was purified on silica gel (DCM -> 20:1 -> 10:1 DCM / MeOH -> 10:1 -> 4:1 DCM / 2 N ammonia in MeOH). Fractions with product collected, concentrated, and repurified on silica gel using DCM -> 20:1 JJUM / MeUM -> 5: 1 DCM / 2 N ammonia in MeOH). The fractions with product were collected and concentrated to give l-methyl-2-phenyl-5-(pyridin-4-yl)-l,2-dihydropyrazol-3- one (3.31 g, 70% purity, 9.2 mmol, 59%). MS (ESI pos. ion) m/z: 252 (MH+). Calc'd exact mass for C15H13N3O: 251.
Figure imgf000093_0001
Step 2 : l-methyI-3-oxo-2-phenyI-5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4- carbaldehyde. To a 25 ml round-bottom flask with stirbar was added N5N- dimethylformamide (10.0 ml, 130 mmol). The flask was cooled in an ice water bath, and phosphorous oxychloride (4.2 ml, 45 mmol) was added. The reaction was wanned to room temperature and stirred under nitrogen. After 50 minutes, this was transferred, first via syringe and then pipette, to a solution of l-methyl-2-phenyl-5-(pyridin-4-yl)-l,2-dihydropyrazol-3-one (3.31 g, 13 mmol) in DMF (18 ml). The flask was placed in a preheated oil bath (120 C), stirred for 12 minutes, and then cooled to room temperature. The reaction was poured into a aqueous solution of 5 N NaOH (40 ml) and diluted with ice water (-75 ml). More ice and water were added. The aqueous phase was extracted with chloroform and the organic extracts were dried over sodium sulfate, filtered, and concentrated. DMF present, so the crude material was diluted with chloroform and washed with water. The aqueous extractions were extracted with chloroform, and the organic layers were combined, dried over sodium sulfate, filtered, and concentrated to give the crude product. MS (ESI pos. ion) m/z: 280 (MH+). Calc'd exact mass for C16H13N3O2: 279. Material taken to next step without further purification.
Figure imgf000093_0002
Step 3: l-methyI-3-oxo-2-phenyl-5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxyIic acid. The crude l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4- carbaldehyde was dissolved in t-BuOH (~ 70 ml) and 2-methyl-2-butene (25 ml, 236 mmol) was added, followed by sodium chlorite (2.43 g, 27 mmol) in water (30 ml) with ~ 5 ml water rinse. Then, potassium phosphate monobasic (10.35 g, 76 mmol) was added as a suspension in water (~ 70 ml), and the reaction was stirred at room temperature. After 9 hours, the reaction was poured into water (400 ml) and the aqueous phase was then extracted with EtOAc, DCM, and 10:1 DCM / MeOH exhaustively until most of the product had been extracted. The organic extracts were combined, dried over sodium sulfate, filtered, and concentrated to give desired 1 -methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)-2,3-dihydro- 1 H-pyrazole-4-carboxylic acid (1.98 g, 6.7 mmol, 52% yield over two steps). MS (ESI pos. ion) m/z: 296 (MH+). Calc'd exact mass for C16H13N3O3: 295.
Figure imgf000094_0001
Step 4. N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-methyl-3-oxo-2-phenyl- 5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide. 4-(6,7-dimethoxyquinolin-4- yloxy)-3-fluorobenzenamine (628.9 mg, 2.001 mmol) and l-methyl-3-oxo-2-phenyl-5- (pyridin-4-yl)-2,3-dihydro-l H-pyrazole-4-carboxylic acid (520 mg, 1.76 mmol) (1.679 g of a -30% by weight solution of acid in DMF) was dissolved in DCM (20 ml) and HATU (1.042 g, 2.740 mmol) was added. The reaction was stirred under nitrogen at room temperature overnight, and then filtered. The filtered solid was washed with dichloromethane, and the filtrate was concentrated and purified on silica gel (DCM -> 50:1 -> 25:1 -> 10:1 DCM / MeOH). The fractions with product were collected, concentrated, and purified on silica gel (30:1 -> 20:1 -> 10:1 DCM / MeOH). Fractions with product collected, concentrated, and purified again on silica gel (25: 1 -> 20: 1 DCM / MeOH). Fractions with pure product collected and concentrated to give desired N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3- fluorophenyl)- 1 -methyl-3 -oxo-2-phenyl-5-(pyridin-4-yl)-2,3 -dihydro- 1 H-pyrazole-4- carboxamide (225.9 mg, 0.382 mmol, 22% yield). MS (ESI pos. ion) m/z: 592 (MH+). Calc'd exact mass for C33H26FN5O5: 591. 1H NMR (400 MHz, CDCl3): 10.96 (s, IH), 8.88 (d, J = 4.0 Hz, 2H), 8.48 (d, J - 6.0 Hz, IH), 7.83 (d, J = 12 Hz, IH), 7.65 - 7.47 (m, 8H), 7.41 (s, IH), 7.30 (d, J = 10.0 Hz, IH), 7.16 (t, J = 8.0 Hz, IH), 6.40 (d, J = 5.2 Hz, IH), 4.05 (s, 6H), 3.20 (s, 3H). Example 2
Figure imgf000095_0001
Figure imgf000095_0002
Step 1: Methyl l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate.
2,3-dimethyl-5-oxo-l-phenyl-2,5-dihydro-lH-pyrazole-4-carboxylic acid (7.55 g, 33 mmol) was dissolved in dichlormethane (145 ml) and oxalyl chloride (4.1 ml, 46 mmol) was added via syringe over about 10 minutes, resulting in vigorous bubbling. After stirring at room temperature for about 30 minutes, the reaction was cautiously quenched with MeOH (100 ml). The methanol was added slowly at first as vigorous gas evolution was observed. The reaction was stirred at room temperature for 1 hour, concentrated, and then partitioned between dichlormethane (125 ml) and saturated sodium bicarbonate (125 ml). More dichlormethane and saturated sodium bicarbonate were added, and the layers of the biphasic, homogeneous solution were separated. The aqueous phase was extracted with dichlormethane (3 x 100 ml), and the organic phases were collected, dried over sodium sulfate, filtered, and concentrated to give desired methyl l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (7.82 g, 79% purity by HPLC, 25 mmol, 77% yield). MS (ESI pos. ion) m/z: 247 (MH+). Calc'd exact mass for C13H14N2O3: 246.
Figure imgf000096_0001
Step 2: Methyl 5-(bromomethyl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxylate. Methyl l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (7.82 g, 31.8 mmol) was dissolved in CHCl3 (150 ml) and n-bromosuccimide (6.91 g, 38.8 mmol) was added. The reaction was stirred at room temperature, and after 1.5 hours, more NBS (6.23 g, 35.2 mmol) was added. After another hour of stirring, the reaction was filtered, and the solid was washed with chloroform. The filtrate was concentrated, treated with dichlormethane, and refϊltered. The filtrate was again concentrated, and filtered through silica gel (~ 3 inches, dichlormethane/MeOH). The fractions with product collected, concentrated, and purified on silica gel (dichlormethane / MeOH) to give the desired methyl 5-
(bromomethyl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (4.11 g, 82% purity, 10.4 mmol, 33% yield). MS (ESI pos. ion) m/z: 325, 327 (MH+). Calc'd exact mass for C13H13Br790N2O3: 324. Calc'd exact mass for C13H13Br81 0N2O3: 326.
Figure imgf000096_0002
Step 3: Methyl l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH- pyrazole-4-carboxylate. Methyl 5-(bromomethyl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylate (1.266 g, 3.9 mmol) was dissolved in dichlormethane (30 ml) and pyrrolidine (0.40 ml, 4.8 mmol) was added via syringe. The reaction was stirred under nitrogen at room temperature. After about 20 minutes, more pyrrolidine (0.090 ml, 1.1 mmol) was added, and stirring was continued for 3.5 hours. The reaction was concentrated and purified on silica gel (dichlormethane, MeOH, 2 N ammonia in MeOH) to give the desired methyl 1 -methyl-3 -oxo-2-phenyl-5-(pyrrolidin- 1 -ylmethyl)-2,3-dihydro- 1 H-pyrazole-4- carboxylate (1.182 g, 70% purity by HPLC, 2.62 mmol, 67% yield). MS (ESI pos. ion) m/z: 316 (MH+). Calc'd exact mass for C17H21N3O3: 315.
Figure imgf000097_0001
Step 4: l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH-pyrazole-4- carboxylic acid. Methyl l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH- pyrazole-4-carboxylate (1.182 g, 3.7 mmol) was dissolved in MeOH (17 ml) and sodium hydroxide (4.2 ml, , 1.0 M, 4.2 mmol) and solid sodium hydroxide (282 mg, 7.05 mmol) were added. The reaction was stirred at room temperature for 3 hours, and then stirred at 9O0C for 1 hour. The reaction was then cooled to room temperature and treated with aq.lO % HCl to lower the pH to around 2. The reaction was concentrated, treated with 1 :1 dichlormethane / MeOH, and filtered. The filtrate was concentrated to give the desired methyl l-methyl-3-oxo- 2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxylate (1.342 g, 77% purity by HPLC, 3.43 mmol, 93% yield). MS (ESI pos. ion) m/z: 302 (MH+). Calc'd exact mass for C16H19N3O3: 301.
Figure imgf000097_0002
Step 5: N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-
(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide. 5-(7-methoxy-quinolin- 4-yloxy)pyridin-2-amine (549 mg, 2.05 mmol) and l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l- ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxylic acid (696 mg, 2.31 mmol) were suspended in dichlormethane (10 ml) and N-ethyl-N-isopropylpropan-2-amine (0.70 ml, 4.0 mmol), DMF (0.5 ml) and more dichlormethane (5 ml) were added. Finally, HATU (1.004 g, 2.641 mmol) was added, and the reaction was stirred under nitrogen at room temperature. After stirring for 2.5 weeks, the reaction was filtered and the solid was washed with DCM and MeOH. The filtrate was concentrated and purified on silica gel (~ 3 inches, dichlormethane, MeOH , 2 N ammonia in MeOH) to give the desired N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l- methyl-3-oxo-2-phenyl-5-(pyrrolidin-l-ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide (90.6 mg, 0.165 mmol, 8%). MS (ESI pos. ion) m/z: 551 (MH+). Calc'd exact mass for C31H30N6O4: 550. 1H NMR (400 MHz, CDCl3): 11.44 (s, IH), 8.61 (d, J = 6.0 Hz, IH), 8.38 (d, J = 9.2 Hz, IH), 8.30 - 8.21 (m, 2H), 7.62 - 7.37 (m, 7H), 7.24 (d, J = 8.0 Hz, IH), 6.43 (d, J = 6.4 Hz, IH), 4.35 (s, 2H), 3.98 (s, 3H), 3.57 (s, 3H), 2.73 (s, 4H), 1.84 (s, 4H).
Example 3
Figure imgf000098_0001
N-(4-(657-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((ethyl(methyl)amino)methyl)-l- methyl-3-oxo-2-phenyl-2,3-dihydro-lH^yrazole-4-carboxamide: MS (ESI pos. ion) m/z 586 (MH+) Calc'd exact mass for C32H32FN5O5 585. IH NMR (300 MHz, CDCl3) 11.08 (s, 1 H). 8.49 (d, J=5.26 Hz, 1 H) 7.93 (d, =12.42 Hz, 1 H); 7.68 - 7.25 (m, 8 H), 7.18 (t, J=I 7.25 Hz, 1 H) 6.43 (d, =6.14 Hz, 1 H) 4.21 (s, 2 H) 4.06 (s, 3 H) 3.57 (s, 3 H) 2.62 (q, J=7.16 Hz, 2 H) 2.36 (s, 3 H) 1.14 (t, =7.09 Hz, 3 H).
Example 4
Figure imgf000098_0002
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((dimethylamino)methyl)-l- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z 572 (MH+) Calc'd exact mass for C31H30FN5O5 571.6. IH NMR (300 MHz, CDCl3) 11.06 (1 H, s), 8.49 (1 H, d, =5.3 Hz), 7.93 (1 H, d, =12.4 Hz), 7.66 - 7.28 (8 H, m), 7.18 (1 H, t, =8.8 Hz), 6.44 (2 H, d, =5.5 Hz), 4.16 (2 H, s), 4.11-3.99 (6 H, m), 3.56 (3 H, s), 2.41 (6 H, s). Example 5
Figure imgf000099_0001
5-(aminomethyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 514 (MH+). Calc'd exact mass for C28H24FN5O4: 513. 1H NMR (400 MHz, CDCl3): 10.93 (s, IH), 8.61 (d, J = 5.5 Hz, IH), 8.29 (d, J = 8.0 Hz, IH), 7.93 (d, J = 13.0 H, IH), 7.62 - 7.48 (m, 3H), 7.44 (s, IH), 7.39 (d, J = 8.0 Hz, 2H), 7.35-7.16 (m, 3H), 6.43 (d, J = 5.0 Hz, IH), 4.30 (s, 2H), 3.98 (s, 3H), 3.51 (s, 3H), 2.0 (br s, 3H).
Figure imgf000099_0002
tert-butyl (4-((3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl) carbamoyl)- 1 -methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazol-5-yl)methylcarbamate: MS (ESI pos. ion) m/z: 614 (MH+). Calc'd exact mass for C33H32FN5O6: 613.
Example 7
Figure imgf000099_0003
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l- ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 551 (MH+). Calc'd exact mass for C31H30N6O4: 550. 1H NMR (400 MHz, CDCl3) 11.44 (s, IH)5 8.61 (d, J = 5.0 Hz, IH), 8.38 (d, J = 9.0 Hz, IH), 8.28-8.22 (m, 2H), 7.56 (t, J = 7.0 Hz, 2H), 7.53-7.45 (m, 2H), 7.41 (dt, J = 8.0 Hz, 2.0 Hz, 3H), 7.26-7.21 (m, IH), 6.43 (d, J = 5.0 Hz, IH), 4.35 (s, 2H), 3.98 (s, 3H), 3.57 (s, 3H), 2.78 - 2.69 (m, 4H), 1.89 - 1.81 (m, 4H).
Example 8
Figure imgf000100_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyI-3-oxo-2-phenyl-5- (pyrrolidin-l-ylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 568 (MH+). Calc'd exact mass for C32H30FN5O4: 567. 1H NMR (400 MHz, CDCl3): 11.06 (s, IH), 8.60 (d, J = 5.0 Hz, IH), 8.28 (d, J = 9.0 Hz, IH), 7.93 (d, J = 12.0 Hz, IH), 7.59 (t, J - 8.0 Hz, 2H), 7.51 (d, J = 7.0 Hz, IH), 7.40 (t, J = 9.0 Hz, 3H), 7.33 - 7.21 (m, 2H), 7.17 (t, J = 8.0 Hz, IH), 6.41 (d, J = 5.0 Hz, IH), 4.35 (s, 2H), 3.98 (s, 3H), 3.58 (s, 3H), 2.75 - 2.70 (m, 4H), 1.86 - 1.81 (m, 4H). Example 9
Figure imgf000100_0002
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3-oxo-2-phenyl-l- ((tetrahydrofuran-2-yl)methyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 569 (MH+). Calc'd exact mass for C32H29FN4O5: 568; 1H NMR (400 MHz, CDCl3): 10.94 (s, IH), 8.76 (d, J = 7.0 Hz, IH), 8.46 (d, J = 9.0 Hz, IH), 8.07 (d, J = 12.0 Hz, IH), 7.79 - 7.76 (m, IH), 7.64 7.59 (m, 3H), 7.48 (d, J = 9.0 Hz, 2H), 7.41 - 7.31 (m, 2H), 7.30 - 7.24 (m, IH), 6.80 (d, J = 7.0 Hz, IH), 4.09 (s, 3H), 4.08 - 4.01 (m, IH), 3.87 (dd, J = 15.0 Hz, 3.5 Hz, IH), 3.75 - 3.64 (m, 3H), 2.51 (s, 3H), 2.01 - 1.91 (m, IH), 1.84 (quintet, J = 6.0 Hz, 2H), 1.56 - 1.47 (m, IH).
Example 10
Figure imgf000101_0001
5-((ethyl(methyl)amino)methyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 556 (MH+). Calc'd exact mass for C31H30FN5O4: 555. 1H NMR (400 MHz, CDCl3): 11.06 (s, IH), 8.59 (d, J = 5.0 Hz, IH), 8.28 (d, J = 9.0 Hz, IH), 7.92 (d, J = 12.0 Hz, IH), 7.59 (t, J = 7.0 Hz, 2H), 7.53 - 7.48 (m, IH), 7.43 - 7.36 (m, 3H), 7.31 (d, J = 9.0 Hz, IH), 7.23 (d, J = 10.0 Hz, IH), 7.17 (t, J = 9.0 Hz, IH), 6.41 (d, J = 5.0 Hz, IH), 4.22 (s, 2H), 3.98 (s, 3H), 3.58 (s, 3H), 2.63 (quartet, J = 7.0 Hz, 2H), 2.37 (s, 3H), 1.15 (t, J = 7.0 Hz, 3H).
Example 11
Figure imgf000101_0002
2-benzyl-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-5-(pyridin-4-yl)-2,3- dihydro-lH-pyrazole-4-carboxamide MS (ESI pos. ion) m/z 559 (MH+). Calc'd exact mass for C32H26N6O4 558.
Example 12
Figure imgf000101_0003
2-benzyl-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-5-(pyridin-4- yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z 576 (MH+). Calc'd exact mass for C33H26FN5O4 575.
Example 13
Figure imgf000102_0001
(S)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-(l-phenylethyl)-5- (pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 573 (MH+). Calc'd exact mass for C33H28N6O4: 572. 1H NMR (400 MHz, CDCl3): 11.52 (s, IH), 8.98 (d, J = 6.0 Hz, 2H), 8.84 (d, J = 6.0 Hz, IH), 8.41 (d, J = 9.0 Hz, IH), 8.37 (d, J = 3.0 Hz5 IH), 8.31 (d, J = 9.0 Hz, IH), 7.81 (d, J = 5.0 Hz, 2H), 7.78 (d, J = 2.0 Hz, IH), 7.60 (dd, J - 9.0 Hz, 2.0 Hz, IH), 7.50 - 7.38 (m, 6H), 6.76 (d, J = 7.0 Hz, IH), 6.17 (quartet, J = 8.0 Hz, IH), 4.08 (s, 3H), 3.13 (s, 3H), 2.02 (d, J = 7.0 Hz, 3H).
Example 14
Figure imgf000102_0002
(S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-(l-phenylethyl)- 5-(pyridin-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 590 (MH+). Calc'd exact mass for C34H28FN5O4: 589.
Example 15
Figure imgf000102_0003
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass for C31H24N6O4: 544.
Example 16
Figure imgf000103_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4- yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 562 (MH+). Calc'd exact mass for C32H24FN5O4: 561.
Example 17
Figure imgf000103_0002
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4- yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 575 (MH+). Calc'd exact mass for C32H26N6O5: 574.
Example 18
Figure imgf000103_0003
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 510 (MH+). Calc'd exact mass for C29H27N5O4: 509. 1HNMR (300 MHz, CDCl3): 0.81 (t, 3H), 1.54 (m, 2H), 2.82 (s, 3H), 3.75 (m, 2H), 4.0 (s, 3H), 6.45 (d, IH), 7.31 (d, 2H), 7.41-7.52 (m, 6H), 8.30 (d, 2H), 8.40 (d, IH), 8.60 (d, IH).
Example 19
Figure imgf000104_0001
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-3-yl)-
2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass for C31H24N6O4: 544. 1HNMR (300 MHz, CDCl3): 3.42 (s, 3H), 3.89 (s, 3H), 4.37-4.49 (m, IH), 5.22 (s, IH), 6.34 (d, J=5.26 Hz, IH), 7.15 (dd, J=9.21, 2.48 Hz, IH), 7.20 (s, 2H), 7.28-7.50 (m, 7H), 8.15 (d, J=6.14 Hz, IH), 8.17 (s, IH), 8.29 (d, J=9.06 Hz, IH), 8.52 (d, J=5.26, IH), 11.55 (s, IH).
Example 20
Figure imgf000104_0002
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-2- yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 562 (MH+). Calc'd exact mass for C32H24FN5O4: 561. 1HNMR (300 MHz, CDCl3): 2.80 (s, IH)5 3.34 (s, 3H), 3.96 (s, 3H), 6.39 (d, J=5.12 Hz, IH), 7.11-7.32 (m, 4H), 7.40-7.64 (m, 6H), 7.79-8.01 (m, 3H), 8.25 (d, J-9.21 Hz, IH), 8.57 (d, J=5.26 Hz, IH), 8.80 (d, J=4.53 Hz, IH), 11.12 (s, IH).
Example 21
Figure imgf000104_0003
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-2-yl)- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass for C31H24N6O4: 544. 1HNMR (SOO MHZ5 CDCI3): 3.24 (s, 3H), 3.88 (s, 3H), 6.32 (d, J=5.26 Hz, IH), 7.13 (dd, J=9.13, 2.41 Hz, IH), 7.20 (s, IH), 7.31-7.53 (m, 7H), 7.80-7.90 (m, 2H), 8.10-8.23 (m, 3H), 8.50 (d, J=5.26 Hz5 IH)5 8.72 (d, J=4.82 Hz, IH)5 11.39 (s, IH).
Example 22
Figure imgf000105_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5- (tetrahydro-2H-pyran-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 569 (MH+). Calc'd exact mass for C32H29FN4O5: 568. 1HNMR (SOO MHZ5 CDCI3): 1.83 (d, J=10.96 Hz, 2H)5 2.33 (qd, J=12.57, 4.38 Hz, 2H), 3.49 (s, 3H), 3.63 (t, J=I 1.03 Hz, 2H), 3.96 (s, 3H), 4.15 (dd, J=I 1.40, 3.80 Hz, 2H)5 4.47-4.60 (m, IH), 5.29 (s, IH)5 6.40 (dd, J=5.19, 0.80 Hz5 IH)5 7.14-7.42 (m, 4H), 7.46-7.60 (m, 3H)5 7.92 (dd, J=12.50, 2.27 Hz, IH), 8.27 (d, J=9.21 Hz, IH), 8.59 (d, J=5.26 Hz5 IH)5 11.25 (s, IH).
Example 23
Figure imgf000105_0002
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(tetrahydro- 2H-pyran-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 552 (MH+). Calc'd exact mass for C31H29N5O5: 551. 1HNMR (SOO MHZ5 CDCI3): 1.76 (d, J=10.67 Hz5 2H)5 2.19-2.35 (m, 2H), 3.42 (s, 3H), 3.50-3.60 (m, 2H), 3.89 (s, 3H), 4.07 (dd, J=I 1.55, 3.80 Hz, 2H)5 4.37-4.49 (m, IH), 5.22 (s, IH)5 6.34 (d, J=5.26 Hz5 IH)5 7.15 (dd, J=9.215 2.48 Hz, IH)5 7.28-7.50 (m, 5H)5 8.15 (d, J=6.14 Hz, IH)5 8.17 (s, IH)5 8.29 (d, J=9.06 Hz, IH), 8.52 (d, J=5.26 Hz5 IH)5 11.55 (s, IH). Example 24
Figure imgf000106_0001
l-Methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-(2-methyl-l,3-thiazol-4- yl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 565 (MH+). Calc'd exact mass for C30H24N6O4S : 564. 1H NMR (400 MHz, DMSO-J6) 11.51 (s, 1 H), 8.62 (d, .7=5.18 Hz, 1 H), 8.32 - 8.36 (m, 2 H), 8.29 (d, J-9.09 Hz, 1 H), 8.22 (d, .7=9.09 Hz, 1 H), 7.77 (dd, .7=9.16, 2.84 Hz, 1 H), 7.61 - 7.68 (m, 2 H), 7.53 - 7.60 (m, 3 H), 7.42 (d, J=2.40 Hz, 1 H), 7.30 (dd, J=9.09, 2.40 Hz, 1 H), 6.53 (d, .7=5.18 Hz, 1 H), 3.94 (s, 3 H), 3.28 - 3.33 (m, 3 H), 2.78 (s, 3 H):
Example 25
Figure imgf000106_0002
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-methyl-5-(5-methyl-3- isoxazolyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 579 (MH+). Calc'd exact mass for C31H26N6O6: 578.
Example 26
Figure imgf000106_0003
l-methyl-5-(5-methyl-3-isoxazolyl)-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 549 (MH+). Calc'd exact mass for C30H24N6O5: 548.
Example 27
Figure imgf000107_0001
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-methyl-5-(5-methyl-3- isoxazolyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 566 (MH+). Calc'd exact mass for C31H24FN5O5: 565.
Example 28
Figure imgf000107_0002
l-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 546 (MH+). Calc'd exact mass for C3oH23N704: 545.
Example 29
Figure imgf000107_0003
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 563.2 (MH+). Calc'd exact mass for C31H23FN6O4: 562. Example 30
Figure imgf000108_0001
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-methyl-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 576 (MH+). CaIc' d exact mass for C31H25N7O5 : 575. 1H NMR (400 MHz, DMSO-J6) 11.28 (s, 1 H), 9.11 (d, J=I.14 Hz, 1 H), 8.87 - 8.90 (m, 1 H), 8.85 (d, J=2.53 Hz, 1 H), 8.48 (d, J=5.31 Hz, 1 H), 8.34 (d, J=2.91 Hz, 1 H), 8.22 (d, J=9.09 Hz, 1 H), 7.74 (dd, J=8.97, 2.91 Hz, 1 H), 7.64 - 7.69 (m, 2 H), 7.57 - 7.63 (m, 3 H), 7.52 (s, 1 H), 7.40 (s, 1 H), 6.52 (d, J=5.31 Hz, 1 H), 3.94 (d, J=5.31 Hz, 6 H), 3.30 (s, 3H).
Example 31
Figure imgf000108_0002
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-methyl-5-(2-methyl-l,3- thiazol-4-yl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 595 (MH+). Calc'd exact mass for C31H26N6O5S: 594.
Example 32
Figure imgf000108_0003
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-methyl-5-(2-methyl-l,3-thiazol- 4-yl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 582 (MH+). Calc'd exact mass for C31H24FN5O4S: 581. Example 33
Figure imgf000109_0001
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-N,l55-triinethyl-3-oxo-2-phenyl- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z 543 (MH+) CaIc' d exact mass for C30H27FN4O5 543. IH NMR (300 MHz, CDCl3) 8.28 (1 H, d, 5.3 Hz), 7.56 (1 H, s), 7.33 - 7.53 (4 H, m), 7.24 - 7.10 (5 H, m), 6.26 (1 H, d, =5.4 Hz), 4.06 (6 H, s), 3.52 (3 H, s), 3.22 (3 H, s), 2.54 (3 H, s).
Example 34
Figure imgf000109_0002
2-(3-chlorophenyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 563 (MH+). Calc'd exact mass for C29H24ClFN4O5: 562.
Example 35
Figure imgf000109_0003
2-(3-chlorophenyl)-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dιmethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 546 (MH+). Calc'd exact mass for C28H24ClN5O5: 545. Example 36
Figure imgf000110_0001
N-(4-(6,7-dimethoxyquinolin-4-yIoxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2-p-tolyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C30H27FN4O5: 542. 1H NMR (400 MHz, DMSO-J6) 11-00 (s, 1 H), 8.48 (d, J=5.31 Hz, 1 H), 7.98 (dd, J=13.20, 2.21 Hz, 1 H), 7.53 (s, 1 H)5 7.29 - 7.45 (m, 7 H), 6.47 (d, J=5.43 Hz, 1 H), 3.95 (s, 6 H), 3.35 (s, 3 H), 2.70 (s, 3 H), 2.40 (s, 3 H).
Example 37
Figure imgf000110_0002
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-(4-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 547 (MH+). Calc'd exact mass for C29H24F2N4O5: 546. 1H NMR (400 MHz, DMSO-^6) 10.94 (s, 1 H), 8.48 (d, J=5.18 Hz, 1 H), 7.98 (dd, J=13.07, 2.34 Hz, 1 H), 7.32 - 7.55 (m, 8 H), 6.47 (d, J=5.05 Hz, 1 H)5 3.95 (s, 6 H)5 3.37 (s, 3 H), 2.70 (s, 3 H). Example 38
Figure imgf000110_0003
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridine-2-yl)-l,5-dimethyl-3-oxo-2-p-tolyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 526 (MH+). Calc'd exact mass for C29H27N5O5: 525.
Example 39
Figure imgf000111_0001
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-(4-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 530 (MH+). Calc'd exact mass for C28H24FN5O5: 529.
Example 40
Figure imgf000111_0002
2-(3-chlorophenyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 516 (MH+). Calc'd exact mass for C27H22ClN5O4: 515. 1H NMR (400 MHz, DMSO-J6) H -15 (s, 1 H), 8.62 (d, J=5.30 Hz, 1 H), 8.32 - 8.39 (m, 2 H), 8.22 (d, J=9.22 Hz, 1 H), 7.81 (dd, J=8.97, 3.03 Hz, 1 H), 7.57 - 7.66 (m, 3 H), 7.41 - 7.46 (m, 2 H), 7.30 (dd, J=9.16, 2.59 Hz, 1 H), 6.54 (d, J=5.18 Hz, 1 H), 3.94 (s, 3 H), 3.40 (s, 3 H), 2.73 (s, 3 H). Example 41
Figure imgf000112_0001
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2-p-tolyl-2,3-dihydro- lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 496 (MH+). Calc'd exact mass for C28H25N5O4: 495. 1H NMR (400 MHz, DMSO-J6) H -29 (s, 1 H), 8.62 (d, J=4.93 Hz, 1 H), 8.30 - 8.40 (m, 2 H), 8.22 (d, J=9.22 Hz, 1 H), 7.80 (d, J=9.60 Hz, 1 H), 7.26 - 7.46 (m, 6 H), 6.53 (d, J=4.93 Hz, 1 H), 3.94 (s, 3 H), 3.35 (s, 3 H), 2.71 (s, 3 H), 2.40 (s, 3 H).
Example 42
Figure imgf000112_0002
2-(2-chlorophenyl)-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 546 (MH+). Calc'd exact mass for C28H24ClN5O5: 545.
Example 43
Figure imgf000112_0003
2-(2-chlorophenyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 563 (MH+). Calc'd exact mass for C29H24ClFN4O5: 562.
I ll Example 44
Figure imgf000113_0001
2-(2-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 533 (MH+). Calc'd exact mass for C28H22ClFN4O4: 532. 1H NMR (400 MHz, DMSO-J6) 10.88 (s, 1 H), 8.61 (d, .7=5.18 Hz, 1 H), 8.23 (d, J=9.09 Hz, 1 H), 7.99 (dd, J=13.07, 1.71 Hz, 1 H), 7.77 (d, J=7.71 Hz, 1 H), 7.55 - 7.72 (m, 3 H), 7.37 - 7.47 (m, 2 H), 7.26 - 7.38 (m, 2 H), 6.48 (d, J=5.18 Hz, 1 H), 3.94 (s, 3 H), 3.34 (s, 3 H), 2.71 (s, 3 H).
Example 45
Figure imgf000113_0002
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-2-(4-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 517 (MH+). Calc'd exact mass for C28H22F2N4O4: 516. 1H NMR (400 MHz, DMSO-^6) 10.95 (s, 1 H), 8.61 (d, J=5.18 Hz, 1 H), 8.23 (d, J=9.09 Hz, 1 H), 7.99 (dd, .7=12.88, 1.89 Hz, 1 H), 7.27 - 7.57 (m, 8 H), 6.48 (d, .7=5.18 Hz, 1 H), 3.94 (s, 3 H), 3.36 (s, 3 H), 2.70 (s, 3 H).
Example 46
Figure imgf000113_0003
2-(3-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yIoxy)phenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 533 (MH+). Calc'd exact mass for C28H22ClFN4O4: 532. 1H NMR (400 MHz, DMSO-J6) 10.85 (s, 1 H), 8.62 (d, J=5.18 Hz, 1 H), 8.24 (d, J=9.09 Hz, 1 H), 7.99 (dd, J=13.01, 2.40 Hz, 1 H), 7.57 - 7.66 (m, 3 H), 7.29 - 7.47 (m, 5 H), 6.49 (d, J=5.05 Hz, 1 H), 3.95 (s, 3 H), 3.41 (s, 3 H), 2.72 (s, 3 H).
Example 47
Figure imgf000114_0001
N-(6-(6,7-dimethoxyquinolin-4-yloxy)pyridin-3-yl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 512 (MH+). Calc'd exact mass for C28 H25N5O5: 511 IH NMR (400 MHz, DMSO-J6) 10.86 (s,l H), 8.56 (d, J=5.05 Hz, 1 H), 8.50 (d, J-2.65 Hz, 1 H), 8.27 (dd, J=2.9, 5.81 Hz, IH), 7.7-7.38 (3m, 7 H).7.31 (d, J=8.72 Hz, 1 H), 6.84 (d, J=5.18 Hz, IH), 3.95 (s, 3 H), 3.89 (s, 3 H), 3.38 (s, 3H), 2.71 (s, 3 H).
Example 48
Figure imgf000114_0002
N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass for C29 H25ClN4O5: 544 IH NMR (400 MHz, CDCl3) 11.12 (s, 1 H), 8.70 (d, J=8.79 Hz, 1 H), 8.50 (d, J=5.37 Hz, IH), 7.43 - 7.63 (m, 5 H), 7.38 (d, J=7.32 Hz, 2H), 7.11 (dd, J=9.28, 1.95 Hz, 1 H), 6.55 (d, J=3.91 Hz, 1 H), 4.07 (s, 3 H), 4.04 (s, 3 H), 3.48 (s, 1 H), 3.37 (s, 3 H), 2.81 (s, 3 H) 2006/016344
Example 49
Figure imgf000115_0001
2-benzyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C30H27FN4O5 542 IH NMR (400 MHz, CDCl3) 10.98 (s, 1 H), 8.50 (d, J=5.37 Hz, 1 H), 7.97 (d, J=12.70 Hz, IH), 7.61 (s, 1 H), 7.53 (s, 1 H), 7.42 - 7.29 (m, 4 H), 7.24 - 7.15 (m, 3 H), 6.49 (s, 1 H), 5.18 (s, 2 H), 4.07 (s, 6 H), 3.40 (s, 3 H), 2.67 (s, 3H)
Example 50
Figure imgf000115_0002
2-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 526 (MH+). Calc'd exact mass for C29 H27 N5 O5: 525 IH NMR (400 MHz, CDCl3) 11.43 (s, 1 H), 8.51 (d, J=5.37 Hz, IH,), 8.40 (d, J=8.79 Hz, 1 H), 8.29 (s, 1 H), 7.67 - 7.12 (m, 8 H), 6.53 - 6.44 (m, 1 H), 5.18 (s, 2 H), 4.07 (s, 3 H), 3.40 (s, 6 H), 2.66 (s, 3 H) Example 51
Figure imgf000115_0003
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamide.
Figure imgf000116_0001
Step 1: Ethyl l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate. To a solution of ethyl 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (1000 mg, 5.0 mmol) in dichloromethane (10 niL) was added methyl trifluoromethanesulfonate (1200 mg, 7.3 mmol). The red solution was stirred at room temperature. After 14 h, the mixture was partitioned between dichloromethane and NaHCO3 (sat). The aqueous was extracted with dichloromethane (2x). The combined organic was dried over Na2SO4, concentrated and purified on silica. The product was triturated with EtOAc-hexane-CHCl3 to give the pure product as crystals (260 mg, 21%). Calc'd for C12H12N2O3, 232.08; MS (ESI pos. ion) m/z: 233 (MH+). 1H NMR (400 MHz, CHLOROFORM-d): 1.36 (t, J=7.04 Hz, 3 H), 3.39 (s, 3 H), 4.32 (q, J=7.17 Hz, 2 H), 7.32 (d, J=7.43 Hz, 2 H), 7.42 (t, J-7.34 Hz, 1 H), 7.50 (t, J=7.73 Hz, 2 H), 7.99 (s, 1 H).
Figure imgf000116_0002
Step 2 : N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide. A solution of ethyl l-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxylate (260 mg, 1056 μmol) in MeOH was treated with NaOH (1000 μl, 5000 μmol) in H2O (3 mL). The mixture was heated to 6O0C for 30 min and then cooled to room temperature. Then, the mixture was neutralized with aq. HCl (5 N, 1.1 mL) and concentrated to dryness. The residue was further dried with (azeotrope distillation with toluene, 3 x 5 mL). The resulting carboxylic acid was mixed with 5-(7-methoxyquinolin-4- yloxy)pyridm-2-amine (282 mg, 1054 μmol), Et3N (500 μl, 3587 μmol), and HATU (401 mg, 1054 μmol) in DMF (4 mL) - dichloromethane (5 mL) and was stirred at 6O0C for 2 h. Upon cooling to room temperature, the mixture was diluted with EtOAc containing 10% MeOH (30 mL) and washed with H2O. The organic layer was dried over Na2SO4, concentrated, and eluded on silica (1-10% 2N NH3-MeOH in CHCl3). The product was further purified on preparative HPLC to afford a white powder (100 mg, 20%). 006/016344
Calc'd for C26H21N5O4: 467.16; MS (ESI pos. ion) m/z: 468 (MH+). 1H NMR (400 MHz, DMSOd6) 3.49 (s, 3 H) 3.95 (s, 3 H) 6.55 (d, J 5.1, 1 H) 7.30 (dd, J 2.0, 9.0, 1 H) 7.42 (s, 1 H) 7.59 (s, 17 H) 7.50- 7.60 (m, 5 H), 7.84 (dd, J 2.8, 9.2, IH), 8.22 (d, J 9.2, IH), 8.34 - 8.38 (m, 2 H) 8.62 (d, J 5.3, 1 H) 8.69 (s, 1 H) 10.86 (s, 1 H).
Example 52
Figure imgf000117_0001
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide
Figure imgf000117_0002
Step 1: Benzyl 5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate. A suspension of 3-methyl-l-phenyl-lH-pyrazol-5-ol (10.0 g, 57 mmol) and calcium hydroxide (8.5 g, 115 mmol) in dry 1,4-dioxane (10OmL) was heated to 50 °C for 20 min. The suspension was chilled to 10 °C and benzyl chloro formate (8.2 ml, 57 mmol) was in dioxane (1OmL) added. The resultant was heated to 90 °C for 3h, cooled to 25 °C and then, chilled (00C) 1 M HCl (200 mL) was added. The mixture was stirred at 25 0C overnight. A solid collected by filtration was washed with cold EtOH (2x25mL) and ether (5OmL), dried at 80°C (sand bath) exposed to air for 4h to give the title compound (14.Og, 79% yield) as an off-white solid. MS (ESI pos. ion) m/z: 309 (MH+). Calc'd exact mass for C18H16N2O3 308.
Figure imgf000118_0001
Step 2: Benzyl l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylate. To a stirring suspension of benzyl 5 -hydroxy-3 -methyl- 1-phenyl- lH-pyrazole-4-carboxylate (3380 mg, 11 mmol) in chlorobenzene (3OmL) at 10 °C under nitrogen was added trimethylaluminum (16 niL, 33 mmol, 2M in toluene). Internal temperature reached 27 °C. At 250C, l,2-epoxy-2-methylpropane (1000 mg, 16 mmol) was added. The reaction mixture was stirred for 3 h at 25°C, and then diluted with THF (50OmL). The resultant was chilled to 10°C, and sodium sulfate decahydrate (2g) was added. After lhr, another 2g of sodium sulfate decahydrate added. After 2h, the gel was filtered through a bed of celite and washed with EtOAc (3xl00mL). The filtrate was then washed with aq. IM HCl (5OmL) and brine. The organic layer was dried over MgSO4. and concentrated. The residue was purified on 12Og silica chromatography (30>90% EtOAc/hex). To give the title compound (1.1 Ig, 27% yield) as an amorphous solid. MS (ESI pos. ion) m/z: 381 (MH+). Calc'd exact mass for C22H24N2O4380.
Figure imgf000118_0002
Step 3 : l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylic acid. To a stirring solution of benzyl l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (300 mg, 789 μmol) in MeOH (1OmL) was purged with argon for lOmin. To this solution was added Pd/C (40mg), and the mixture was stirred for 3h under balloon of hydrogen. Reaction was monitored by LCMS. The reaction mixture was filtered through a bed of celite and concentrated under reduced pressure to give the title compound (220 mg, 96.1% yield) as an off-white solid. MS (ESI pos. ion) m/z: 291 (MH+). Calc'd exact mass for C15H18N2O4290.
Figure imgf000118_0003
Step 4 : N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide. To a stirring solution of l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxylic acid (104 mg, 358 μmol) and diisopropylethylamine (62 μl, 358 μmol) in DMF (ImL) was added HATU (136 mg, 358 μmol) and stirred at 37 °C under nitrogen for 15min. To this was added 3-fluoro-4-(7-methoxyquinolin-4-yloxy)benzenamine (98 mg, 344 μmol) and stirred overnight at 37 0C. The reaction mixture was diluted with dichloromethane (1OmL) and washed with IM NaOH (2OmL), and extracted with dichloromethane (3x5mL). Combined organics layer was washed with brine and then dried with MgSO4. Residual DMF was removed with repeated azeotroping with toluene (4x5mL) under reduced pressure. The residue was purified on 12g silica (10>30% of 6% 2M NH3 in MeOH/DCM). Final material was lyophilized from 50% ACN/water to give the title compound (155mg, 74% yield) as a white fluffy solid. MS (ESI pos. ion) m/z: 587 (MH+). Calc'd exact mass for C32H31FN4O6 587. 1H NMR (400 MHz, CHLOROFORM-d) 10.88 (1 H, s), 8.47 (1 H, d, J=5.3 Hz), 7.92 (1 H, dd, J=I 2.5, 2.0 Hz)5 7.59 (1 H, s), 7.54 (2 H, t, J=7.7 Hz), 7.40 - 7.49 (2 H, m), 7.30 (3 H, d, J=7.8 Hz)5 7.17 (1 H, t, J=8.7 Hz), 6.45 (1 H, d, J=5.3 Hz)5 4.06 (3 H5 s), 4.05 (3 H5 s), 3.88 (2 H, s), 2.89 (3 H5 s), 2.01 (1 H5 s), 1.15 (6 H, s)
Example 53
Figure imgf000119_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3-oxo-l-(2-oxobutyl)-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 555 (MH+). Calc'd exact mass for C31H27FN4O5: 554. 1H NMR (400 MHz5 CHLOROFORM-d) 10.86 (1 H5 s), 8.60 (1 H, d, J-5.3 Hz)5 8.28 (1 H, d, J=9.2 Hz), 7.65 - 8.00 (2 H5 m), 7.41 - 7.58 (4 H5 m)5 7.28 - 7.35 (3 H5 m), 7.23 (1 H5 dd, J=9.2, 2.3 Hz)5 7.17 (1 H5 1, J=8.7 Hz)5 6.44 (1 H, d5 J=5.3 Hz)5 4.51 (2 H5 s)5 3.97 (3 H5 s), 2.68 (3 H5 s), 2.26 (2 H5 q5 J=7.2 Hz)5 1.01 (3 H, t, J=7.2 Hz).
Example 54 T7US2006/016344
Figure imgf000120_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-l-(3-methyl-2-oxobutyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 569 (MH+). Calc'd exact mass for C32H29FN4O5: 568. 1H NMR (400 MHz5 CHLOROFORM-d) 10.88 (1 H, s), 8.59 (1 H, d, J=5.3 Hz), 8.21 - 8.30 (2 H, m), 7.97 - 8.03 (1 H, m), 7.87 - 7.95 (2 H, m), 7.71 (1 H5 1, J=7.4 Hz), 7.44 - 7.57 (3 H5 m), 7.41 (1 H5 d, J=2.2 Hz)5 7.26 - 7.34 (3 H5 m), 7.23 (1 H, dd, J=9.25 2.3 Hz), 7.17 (1 H5 1, J=8.7 Hz)5 6.42 (1 H, d, J=5.3 Hz)5 4.58 (2 H5 s), 3.97 (3 H5 s), 2.67 (3 H5 s), 2.38 - 2.52 (1 H5 m), 2.26 (3 H5 s), 0.96 (6 H5 d, J=6.8 Hz).
Example 55
Figure imgf000120_0002
(R)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxybutyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 557 (MH+). Calc'd exact mass for C31H29FN4O5: 556. 1H NMR (400 MHz5 CHLOROFORM-d) 10.90 (1 H5 s), 8.50 (1 H5 d, J=5.3 Hz), 8.30 (1 H5 d, J=9.2 Hz)5 7.95 (1 H5 dd, J=12.55 2.0 Hz)5 7.39 - 7.53 (3 H, m), 7.36 (1 H5 d, J=2.2 Hz)5 7.11 - 7.31 (6 H5 m), 6.42 (3 H5 d5 J=5.3 Hz)5 3.95 (3 H5 s), 3.79 - 3.90 (1 H5 m). 3.70 (1 H5 dd5 J=1.6 Hz)5 3.56 - 3.66 (1 H5 m), 2.85 (3 H5 s), 1.60 - 1.82 (1 H5 m)5 1.27 - 1.43 (2 H5 m), 0.83 (3 H5 1, J=7.3 Hz)
Example 56
Figure imgf000120_0003
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-((2R,3R)-3-hydroxybutan-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 557 (MH+). Calc'd exact mass for C31H29FN4O5: 556. 1H NMR (400 MHz, CHLOROFORM- d) 10.94 (1 H, s), 8.54 (1 H, d, J=5.1 Hz)5 8.27 (1 H, d, J=9.0 Hz), 7.90 (1 H, dd, J=12.3, 2.0 Hz), 7.43 - 7.57 (3 H, m), 7.37 - 7.40 (1 H, m), 7.31 (2 H, d, J=7.6 Hz), 7.25 - 7.28 (1 H, m), 7.23 (1 H, dd, J=9.2, 2.2 Hz), 7.16 (1 H, t, J=8.7 Hz), 6.40 (1 H, d, J=5.1 Hz), 3.77 - 4.05 (6 H, m), 2.89 (3 H, s), 1.63 - 1.91 (2 H, m), 1.50 (3 H, d, J=7.0 Hz), 1.11 (3 H, d, J=6.3 Hz)
Example 57
Figure imgf000121_0001
l-((2R,3R)-3-hydroxybutan-2-yl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 540 (MH+). Calc'd exact mass for C30H29N5O5: 539. 1H NMR (400 MHz, CHLOROFORM- d) 11.30 (1 H, s), 8.59 (1 H, d, J=5.3 Hz), 8.36 (1 H, d, J=9.0 Hz), 8.21 - 8.26 (2 H, m), 7.43 - 7.56 (4 H, m), 7.41 (1 H, d, J=2.5 Hz), 7.30 - 7.35 (2 H, m), 7.23 (1 H, dd, J=9.2, 2.5 Hz), 6.42 (I H, d, J=5.3 Hz), 3.97 - 4.05 (1 H, m), 3.97 (3 H5 s), 3.84 - 3.93 (1 H5 m), 3.49 (1 H, s), 2.90 (3 H5 s), 1.50 (3 H, d, J=7.2 Hz)5 1.12 (3 H5 d5 J=6.3 Hz)
Example 58
Figure imgf000121_0002
(S)-l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 554 (MH+). Calc'd exact mass for C31H31N5O5: 553. 1H NMR (400 MHz, DMSO-d6) 11.29 (1 H5 S)5 8.63 (1 H, d, J=5.1 Hz)5 8.37 (1 H, d, J=9.0 Hz)5 8.32 (1 H, d, J=2.9 Hz)5 8.22 (1 H5 d5 J=9.2 Hz), 7.80 (1 H, dd, J=9.0, 2.9 Hz)5 7.60 (2 H5 t, J=7.5 Hz), 7.51 (1 H5 1, J=7.3 Hz)5 7.40 - 7.47 (3 H5 m), 7.30 (1 H, dd, J=9.2, 2.5 Hz), 6.54 (1 H5 d, J=5.3 Hz), 5.10 (1 H5 d, J=5.9 Hz)5 3.87 - 3.98 (4 H, m), 3.71 (1 H, d)5 3.10 - 3.21 (1 H5 m), 2.76 (3 H, s), 1.33 - 1.46 (1 H5 m), 0.64 (3 H5 d, J=6.8 Hz)5 0.58 (3 H, d, J=6.8 Hz) Example 59
Figure imgf000122_0001
(R)-l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 554 (MH+). Calc'd exact mass for C31H31N5O5: 553. 1H NMR (400 MHz, DMSO-d6) 11.30 (1 H, s), 8.63 (1 H, d, J=5.1 Hz), 8.37 (1 H, d, J=9.0 Hz), 8.33 (1 H, d, J=2.7 Hz), 8.22 (1 H, d, J=9.2 Hz), 7.80 (1 H, dd, J=9.1, 2.8 Hz), 7.60 (2 H, t, J=7.5 Hz), 7.51 (1 H, t, J=7.3 Hz), 7.39 - 7.47 (3 H, m), 7.30 (1 H, dd, J=9.2, 2.5 Hz), 6.54 (1 H, d, J=5.1 Hz), 5.11 (1 H, d, J=5.9 Hz), 3.85 - 3.97 (4 H, m), 3.71 (2 H, s), 3.10 - 3.21 (2 H, m), 2.76 (3 H, s), 1.32 - 1.47 (1 H, m), 0.64 (3 H, d, J=6.7 Hz), 0.58 (3 H, d, J=6.8 Hz)
Example 60
Figure imgf000122_0002
(S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 571 (MH+). Calc'd exact mass for C32H31FN4O5: 570. 1H NMR (400 MHz, CHLOROFORM- d) 10.93 (1 H, s), 8.47 (1 H, d, J=5.3 Hz), 8.31 (1 H, d, J=9.2 Hz), 7.89 - 8.03 (1 H, m), 7.39 - 7.50 (3 H, m), 7.34 (1 H, d, J=2.0 Hz), 7.19 - 7.31 (3 H, m), 7.08 (2 H, d, J=7.2 Hz), 6.45 (1 H, d, J=5.3 Hz), 3.95 (3 H, s), 3.86 (1 H, dd, J=14.9 Hz), 3.64 - 3.77 (1 H, m), 3.44 - 3.48 (4 H, m), 3.33 - 3.42 (1 H, m), 2.82 (9 H, s), 1.46 - 1.61 (3 H, m), 0.80 (3 H, d, J=6.7 Hz), 0.72 (3 H, d, J=6.8 Hz)
Example 61
Figure imgf000122_0003
(R)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 571 (MH+). Calc'd exact mass for C32H3iFN4O5: 570. 1H NMR (400 MHz5 CHLOROFORM- d) 0.73 (d, J=6.85 Hz, 3 H) 0.81 (d, J=6.85 Hz, 3 H) 1.43 - 1.65 (m, 1 H) 2.83 (s, 3 H) 3.39 - 3.45 (m, 1 H) 3.94 (s, 3 H) 7.05 (d, J=7.04 Hz, 2 H) 7.20 - 7.28 (m, 3 H) 7.34 (d, J=2.35 Hz, 1 H) 7.38 - 7.46 (m, 3 H) 7.97 (dd, J=12.42, 1.66 Hz, 1 H) 8.31 (d, 1=9.19 Hz, 1 H) 8.47 (d, J=5.28 Hz, 1 H) 10.93 (s, 1 H)
Example 62
Figure imgf000123_0001
N-(3-fluoro-4-(7-methoxyqumolin-4-yloxy)phenyl)-5-methyl-l-((3-methyI-2- oxooxazoUdm-5-yl)methyI)-3-oxo-2φhenyl-2^-dmydro-lH-pyrazole-4-carboxaim^e: MS (ESI pos. ion) m/z: 598 (MH+). Calc'd exact mass for C32H28FN5O6: 597. 1H NMR (400
MHz, CHLOROFORM-d) 10.77 (1 H, s), 8.61 (1 H, d, J=5.7 Hz), 8.28 (1 H, d, J=9.2 Hz), 7.91 (1 H, dd, J=12.3, 2.2 Hz), 7.68 (1 H, d, J=2.0 Hz), 7.58 (2 H, t, J=7.6 Hz), 7.48 (1 H, t, J=7.5 Hz), 7.38 (2 H, d, J=7.4 Hz), 7.33 (1 H, d, J=8.8 Hz), 7.23 - 7.30 (1 H, m), 7.17 (1 H, t, J=8.6 Hz), 6.49 (1 H, d, J=5.5 Hz), 4.42 - 4.55 (1 H, m), 4.14 (1 H, dd, JhISJ, 8.4 Hz), 4.04 (3 H, s), 3.91 (1 H, dd, J=15.7, 3.3 Hz), 3.52 (1 H, t, J=8.9 Hz), 3.06 (1 H, dd, J=9.2, 5.9 Hz), 2.77 - 2.93 (6 H, m), 2.67 (4 H, s)
Example 63
Figure imgf000123_0002
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-(methylamino)propyl)- 5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 609 (MH+). Calc'd exact mass for C31H30FN5O5: 608. 1H NMR (400 MHz, DMSO-dβ) 11.00 (1 H, s), 8.62 (1 H, d, J=5.3 Hz), 8.23 (1 H, d, J=9.2 Hz), 7.97 (1 H, s), 7.59 (2 H, t, J=7.5 Hz), 7.26 - 7.54 (7 H, m), 6.49 (1 H, d, J=5.1 Hz), 5.15 (1 H, s), 3.79 - 4.00 (5 H, m), 3.35 - 3.59 (3 H, m), 2.75 (3 H, s), 2.29 (2 H, d, J=5.5 Hz)5 2.07 (3 H, s), 0.99 - 1.16 (1 H, m)
Example 64
Figure imgf000124_0001
l-(3-chloro-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 577 (MH+). Calc'd exact mass for C30H26ClFN4O5: 576
Example 65
Figure imgf000124_0002
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylbutyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 571 (MH+). Calc'd exact mass for C32H31FN4O5: 570. 1H NMR (400 MHz, DMSO-d6) 10.90 (1 H, s)5 8.63 (1 H, d, J=5.1 Hz), 8.24 (1 H, d, J-9.0 Hz), 7.99 (1 H5 dd, J-13.0, 2.2 Hz), 7.64 (1 H, s)5 7.59 (2 H515 J=7.5 Hz), 7.51 (1 H, t, J=7.4 Hz)5 7.41 - 7.47 (4 H5 m), 7.36 - 7.41 (1 H, m), 7.32 (1 H5 dd, J-9.1, 2.4 Hz), 6.50 (1 H5 d, J=5.3 Hz)5 4.55 - 4.65 (1 H, m), 4.30 (1 H5 dd, J=16.0, 9.2 Hz), 4.02 (1 H, dd, J=15.95 2.6 Hz), 3.95 (3 H, s), 3.43 (1 H, t, J=9.1 Hz)5 3.07 (1 H5 dd, J=9.4, 5.5 Hz)5 2.76 (3 H, s)
Example 66
Figure imgf000124_0003
l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 554 T/US2006/016344
(MH+). Calc'd exact mass for C31H31N5O5: 553. 1H NMR (400 MHz, DMS0-d6) 11.30 (1 H, s), 8.63 (1 H, d, J=5.3 Hz), 8.30 - 8.42 (2 H, m), 8.22 (1 H, d, J=9.2 Hz), 7.81 (1 H, dd, J=9.1, 2.8 Hz), 7.60 (2 H, t, J=7.5 Hz), 7.51 (1 H, t, J=7.3 Hz)5 7.39 - 7.47 (3 H, m), 7.30 (1 H5 dd, J=9.2, 2.5 Hz), 6.54 (1 H, d, J=5.3 Hz)5 5.11 (1 H5 d, J=5.7 Hz), 3.86 - 3.98 (4 H, m), 3.66 - 3.75 (1 H, m), 3.09 - 3.20 (1 H5 m), 2.76 (3 H, s)5 1.34 - 1.45 (1 H5 m)5 0.64 (3 H, d, J=6.7 Hz)5 0.58 (3 H, d, J=6.7 Hz)
Example 67
Figure imgf000125_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 571 (MH+). Calc'd exact mass for C32H31FN4O5: 570.
Example 68
Figure imgf000125_0002
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-morpholinopropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 628 (MH+). Calc'd exact mass for C34H34FN5O6: 627.
Example 69
Figure imgf000125_0003
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-l-(oxazolidin-5-ylmethyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 584 (MH+). Calc'd exact mass for C31H26FN5O6: 583. 1H NMR (400 MHz, DMS0-d6) 11.30 (1 H, s), 8.63 (1 H5 d, J=5.3 Hz), 8.30 - 8.42 (2 H, m), 8.22 (1 H, d, J=9.2 Hz), 7.81 (1 H, dd, J=9.1, 2.8 Hz), 7.60 (2 H, t, J=7.5 Hz), 7.51 (1 H, t, J=7.3 Hz), 7.39 - 7.47 (3 H, m), 7.30 (1 H, dd, J=9.2, 2.5 Hz), 6.54 (1 H, d, J=5.3 Hz), 5.11 (1 H, d, J=5.7 Hz), 3.86 - 3.98 (4 H, m), 3.66 - 3.75 (1 H, m), 3.09 - 3.20 (1 H, m), 2.76 (3 H, s), 1.34 - 1.45 (1 H, m), 0.64 (3 H, d, J=6.7 Hz), 0.58 (3 H, d, J=6.7 Hz)
Example 70
Figure imgf000126_0001
(S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxybutyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 557 (MH+). Calc'd exact mass for C31H29FN4O5: 556.
Example 71
Figure imgf000127_0001
l-(3-amino-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5- methyl-3-oxo~2-phenyl-2,3-dmydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 558 (MH+). Calc'd exact mass for C30H28FN5O5: 557. 1H NMR (400 MHz, DMSO-d6) 10.93 (1 H, s), 8.55 (1 H, d, J=5.3 Hz), 8.16 (1 H, d, J=9.0 Hz), 7.92 (1 H, dd, J=12.9, 2.3 Hz), 7.51 (2 H, t, J=7.5 Hz), 7.43 (1 H, t, J=7.4 Hz), 7.32 - 7.38 (4 H, m). 7.21 - 7.31 (2 H, m), 6.42 (1 H, d, J=5.1 Hz), 5.05 (1 H, s), 3.81 - 3.90 (4 H, m), 3.69 - 3.77 (1 H, m), 2.67 - 2.72 (3 H, m), 2.23 - 2.31 (2 H, m) Example 72
Figure imgf000127_0002
l-(2-hydroxy-2-methylpropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 540 (MH+). Calc'd exact mass for C30H29N5O5: 539. 1H NMR (400 MHz, CHLOROFORM-d) 11.23 (1 H, s), 8.58 (1 H, d, J=5.1 Hz), 8.37 (1 H, d, J-8.8 Hz), 8.20 - 8.27 (2 H, m), 7.50 (3 H, d, J=7.8 Hz), 7.38 - 7.44 (2 H, m), 7.26 - 7.34 (2 H, m), 7.23 (1 H, d, J=8.8 Hz), 6.43 (1 H, d, J=4.9 Hz), 3.97 (3 H, s), 3.88 (2 H, s), 2.88 (3 H, s), 2.51 (1 H, s), 1.14 (6 H, s)
Example 73
Figure imgf000127_0003
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 557 (MH+). Calc'd exact mass for C3JH29N4O5: 556. 1H NMR (400 MHz, CHLOROFORM-
US d) 10.88 (1 H, s). 8.56 (1 H, d, J=5.3 Hz), 8.27 (1 H, d, J=9.2 Hz), 7.92 (1 H, dd, J=12.5, 2.0 Hz), 7.54 (2 H, t, J=7.6 Hz), 7.38 - 7.49 (2 H, m), 7.29 (3 H, d, J=8.0 Hz), 7.23 (1 H, dd, J=9.2, 2.3 Hz), 7.17 (1 H, t, J=8.7 Hz), 6.42 (1 H, d, J=5.3 Hz), 3.97 (3 H, s), 3.88 (2 H, s), 2.89 (3 H, s), 1.82 (I H, s), 1.15 (6 H, s)
Example 74
Figure imgf000128_0001
(i?)-l-(2-hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo- 2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 526 (MH+). Calc'd exact mass for C29H27N5O5: 525. 1H NMR (400 MHz, CHLOROFORM-d) 11.20 (1 H, s), 8.55 (1 H5 d, J=5.3 Hz), 8.37 (1 H, d, J=9.0 Hz), 8.21 - 8.28 (2 H, m), 7.46 - 7.56 (3 H, m), 7.37 - 7.45 (2 H, m), 7.21 - 7.31 (4 H, m), 6.45 (1 H, d, J-5.3 Hz), 3.89 - 4.01 (4 H, m), 3.78 - 3.88 (1 H, m), 3.66 (1 H, dd, J=14.8, 2.2 Hz), 2.83 (3 H, s), 1.08 (3 H, d, J=6.1 Hz)
Example 75
Figure imgf000128_0002
l-(3-(dimethylamino)-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4- yloxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS
(ESI pos. ion) m/z: 586 (MH+). Calc'd exact mass for C32H32FN5O5: 585. 1H NMR (400 MHz, CHLOROFORM-d) 10.88 (1 H, s), 8.58 (1 H, s), 8.23 - 8.33 (1 H, m), 7.85 - 7.97 (1 H, m), 7.11 - 7.61 (11 H, m), 6.37 - 6.46 (1 H, m), 3.97 (3 H, s), 3.79 (4 H, s), 3.48 (1 H, s), 2.87 (3 H, s), 2.11 - 2.20 (7 H, m), 1.92 - 2.02 (2 H, m).
Example 76
Figure imgf000128_0003
(R)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C30H27FN4O5: 542. 1H NMR (400 MHz, CHLOROFORM-d) 10.89 (1 H, s), 8.48 (1 H, d, J=S.3 Hz), 8.29 (1 H, d, J=9.2 Hz), 7.95 (1 H, dd, J=12.4, 1.7 Hz), 7.38 - 7.51 (1 H, m), 7.35 (1 H, d, J=2.0 Hz), 7.17 - 7.29 (3 H, m), 7.14 (2 H, d, J=7.6 Hz), 6.42 (1 H, d, J=5.3 Hz), 3.97 - 4.08 (1 H, m), 3.95 (3 H, s), 3.78 - 3.92 (2 H, m), 3.64 (1 H, d, J=12.9 Hz), 2.84 (3 H, s), 1.17 - 1.27 (4 H, m), 1.09 (3 H, d, J=5.9 Hz).
Example 77
Figure imgf000129_0001
(R)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxypropyl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 573 (MH+). Calc'd exact mass for C31H29FN4O6: 572. 1H NMR (400 MHz, CHLOROFORM-d) 10.88 (1 H, s), 8.45 (1 H, d, J=5.5 Hz), 7.93 (1 H, dd, J=12.5, 2.3 Hz), 7.60 (1 H, s), 7.53 (2 H, t, J-7.5 Hz), 7.45 (1 H, t, J=7.4 Hz), 7.41 (1 H, s), 7.27 - 7.33 (3 H, m), 7.19 (1 H, t, J=8.6 Hz), 6.46 (1 H, d, J=5.3 Hz), 4.07 (3 H, s), 4.04 (3 H, s), 3.79 - 3.96 (2 H, m), 3.63 - 3.74 (1 H, m), 2.86 (3 H, s), 1.10 (3 H5 d, J=6Λ Hz)
Example 78
Figure imgf000129_0002
l-(2-hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 526 (MH+).
Calc'd exact mass for C29H27N5O5: 525. 1H NMR (400 MHz, DMSO-d6) 11.27 (1 H5 s), 8.62 (1 H, d, J=5.3 Hz), 8.36 (1 H, d, J=9.0 Hz), 8.32 (1 H5 d, J=2.7 Hz), 8.22 (1 H, d, J=9.0 Hz)5 7.80 (1 H, dd, J=9.0, 2.9 Hz), 7.59 (2 H5 1, J=7.5 Hz)5 7.51 (1 H, t, J=7.4 Hz), 7.39 - 7.45 (4 H5 m), 7.30 (1 H, dd, J=9.15 2.4 Hz)5 6.54 (1 H5 d5 J=5.3 Hz), 5.08 (1 H5 d, J=5.3 Hz)5 3.94 (3 H5 s), 3.88 (1 H5 dd, J=15.25 8.9 Hz)5 3.55 - 3.69 (2 H5 m), 2.77 (3 H, s) Example 79
Figure imgf000130_0001
iV-(5-(6,7-dimethoxyquiiioliii-4-yloxy)pyridin-2-yl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 570 (MH+). Calc'd exact mass for C31H31N5O6: 569. IH NMR (400 MHz, DMSO-J6) 11.25 (s, 1 H), 8.49 (d, J=5.2 Hz, 1 H)5 8.36 (d, J=9.0 Hz, 1 H), 8.32 (d, J=2.7 Hz, 1 H), 7.79 (dd, J=9.0, 3.0 Hz, 1 H), 7.66 - 7.29 (m, 7 H), 6.54 (d, J=5.2 Hz, 1 H), 4.85 (s, 1 H), 3.95 (s, 3 H), 3.94 (s, 3 H), 3.86 (s, 2 H), 2.81 (s, 3 H), 0.96 (s, 6 H). Example 80
Figure imgf000130_0002
(R)-2-(3-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2- hydroxypropyl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 577 (MH+). Calc'd exact mass for C30H26ClFN4O5: 576. Example 81
Figure imgf000130_0003
(R)-2-(3-chlorophenyl)-l-(2-hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2- yl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 560 (MH+). Calc'd exact mass for C29H26ClN5O5: 559. Example 82
Figure imgf000131_0001
(2?)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-2-(4-fluorophenyl)-l-(2- hydroxypropyl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 561 (MH+). Calc'd exact mass for C30H26F2N4O5: 560.
Example 83
Figure imgf000131_0002
l-(2-hydroxy-2-methylpropyl)-N-(5-(l-oxo-7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: A mixture of m-CPBA (151 mg, 675 μmol) and l-(2-hydroxy-2-methylpropyl)-N-(5-(7-methoxyquinolin-4- yloxy)pyridin-2-yl)-5-metliyl-3-oxo-2-phenyl-2,3-diriydro-lH-pyrazole-4-carboxamide (280 mg, 519 μmol) in dichloromethane (10 mL) was stirred at room temperature for 14 h. More m- CPBA (151 mg, 675 μmol) was added, and the mixture was stirred for 24 h. The product fraction was purified from preparative HPLC to give the title compound as a white solid (25 mg, 8.7%). Calc'd for C30H29N5O6, 555; MS (ESI pos. ion) m/z: 556 (MH+). 1HNMR (400 MHz, CDCl3): 11.3 (IH, s), 8.60 (IH, d, J 6.7), 8.42 (IH, d, J 9.0), 8.32 (IH, d, J 9.4), 8.23 (IH, s), 8.00 (IH, s), 7.54-7.50 (3H, m), 7.44-7.40 (2H, m), 7.30 (2H, m), 6.52 (IH, d, J 7.1), 4.06 (3H, s), 3.88 (2H, s), 2.87 (3H, s), 1.15 (6H, s). US2006/016344
Example 84
Figure imgf000132_0001
N-(3-Fluoro-4-(7-hydroxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: Calc'd for C30H27FN4O5: 542; MS (ESI pos. ion) m/z: 543 (MH+). 1HNMR (400 MHz, DMSO-d6): 10.95 (IH, s, NH), 10.39 (IH, s, OH), 8.56 (IH, d, J5.4), 8.18 (IH5 d, J 7.2), 7.96 (IH, d, J 7.9), 7.58 - 7.22 (8H, m), 6.42 (IH, d, J4.0), 5.75 (IH, s), 4.83 (IH, s, OH), 3.87 (2H, s, CH2), 2.80 (3H, s), 0.96 (6H, s).
Example 85
Figure imgf000132_0002
l-(2-hydroxy-2-methylpropyl)-N-(5-(7-hydroxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: Calc'd for 029H27N5O5: 525; MS (ESI pos. ion) m/z: 526 (MH+).
Example 86
Figure imgf000132_0003
N-(4-(6-Ethyl-7-methoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2-phenyl- 2,3-dihydro-lH-pyrazole-4-carboxamide: Calc'd for C3OH27FN4O4: 526; MS (ESI pos. ion) m/z: 527 (MH+). 1HNMR (400 MHz, CDCl3): 10.88 (IH), 8.54 (IH, d, J = 5.1), 8.09 (IH, s), 7.92 (IH, dd, J 2.0, 13.8), 7.57 (2H5 1, J 7.5), 7.48 (IH, t, J 7.2), 7.37 (2H, m5), 7.32 (IH5 d), 7.17 (IH, t, J 8.8), 6.39 (IH, d, 4.9), 3.99 (3H, s), 3.38 (3H, s), 2.84 (2H, m) 2.81 (3H5 s), 1.32 (3H, t, J 7.5).
Example 87
Figure imgf000133_0001
N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: Calc'd for C28H23FN4O4: 498; MS (ESI pos. ion) m/z: 499 (MH+). 1HNMR (400 MHz, CDCl3): 10.88 (IH), 8.58 (IH, d, J = 5.7), 8.27 (IH, d, J = 9.2), 7.92 (IH, dd, J 2.1, 12.5), 7.57 (2H, t, J 7.8), 7.48 (IH, t, J 7.4), 7.41 (ds, J 2.4), 7.37 (2H, J 7.6), 7.29 (IH, d), 7.22 (IH, dd, J 2.4, 9.2), 7.17 (2H, t, J 8.6), 6.41 (IH, d, 5.3), 3.97 (3H, s), 3.38 (3H, s), 2.80 (3H, s).
Example 88
Figure imgf000133_0002
N-(3-fluoro-4-(7-Methoxyquinolin-4-yloxy)phenyl)-l,2-dimethyl-3-oxo-5-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: A mixture of HATU (458 mg, 1206 μmol), 1,2- dimethyl-3-oxo-5-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylic acid (140 mg, 603 μmol), 3- fluoro-4-(7-methoxyquinolin-4-yloxy)benzenamine (258 mg, 908 μmol), and Triethylamine (254 μL, 1809 μmol) in DMF (2 mL) was stirred at 6O0C overnight. The mixture was diluted with EtOAc (10 mL). The mixture was transferred to a separatory funnel with EtOAc (20 mL) and was washed with NaOH (IN, 10 mL), H2O (2x10 mL), NaHCO3 (sat), NaCl (sat), and dried over Na2SO4. The residue after concentration was purified on silica gel and the product was triturated with EtOAc-hexane (1 :2) to afford a pink solid (106 mg, 35%). Calc'd for C28H23FN4O4: 498; MS (ESI pos. ion) m/z: 499 (MH+). 1HNMR (CDCl3, 400 MHz): 11.04 (IH, s), 8.56 (IH, d, J 5.3), 7.88 (IH, d, J 14.7), 7.55-7.40 (5H, m), 7.47 (IH, s), 7.35 (IH, d), 7.22 (IH, d, J9.1), 7.13 (IH, t, J 8.8), 6.36 (IH, d, J 5.3), 3.96 (3H, s), 3.62 (3H, s), 3.41 (3H, s). Example 89
Figure imgf000134_0001
N-(5-(7-Methoxyquinolin-4-yloxy)pyridin-2-yl)-l,2-dimethyl-3-oxo-5-phenyl-2,3-dihydro- lH-pyrazole-4-carboxamide: Calc'd for C27H23N5O4: 481; MS (ESI pos. ion) m/z: 482 (MH+). 1HNMR (CDCl3, 400 MHz): 11.46 (IH, s), 8.58 (IH, d, J 5.3), 8.30 (IH, d, J 9.0), 8.25-8.21 (2H, m), 7.56-7.40 (7H), 7.22 (IH, dd, J 2.3, 9.0), 6.39 (IH, d, J 5.3), 3.97 (3H, s), 3.62 (3H, s), 3.40 (3H, s).
Example 90
Figure imgf000134_0002
N-(4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,2-dimethyl-3-oxo-5-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: Calc'd for C27H23N5O4: 528; MS (ESI pos. ion) m/z: 529(MH+). 1HNMR (CDCL3, 400 MHz): 11.05 (IH, s), 8.46 (IH, d, J 5.2), 7.88 (IH, dd, J 2.2, 12.5), 7.53-7.58 (4H, m), 7.47-7.49 (2H, m), 7.40 (IH, s), 7.32 (IH, d, 8), 7.14 (IH, t, J 8.7), 6.39 (IH, d, J 5.1), 4. 05 (3H, s), 4.04 (3H, s), 3.62 (3H, s), 3.41 (3H, s).
Example 91
Figure imgf000134_0003
N-(5-(7-Methoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro- lH-pyrazole-4-carboxamide: Calc'd for C27H23N5O4: 481; MS (ESI pos. ion) m/z: 482 (MH+). 1H NMR (CDCl3, 400 MHz): 11.27 (IH, s), 8.60 (IH, d, J 5.1), 8.38 (IH, d, J 9.0), 8.23 (2H, m), 7.53 (3H, m), 7.47 (IH, m), 7.41 (IH, d), 7.37 (2H, d, J 7.4), 7.23 (IH, dd, J 2.4, 9.7), 6.42 (IH, d, J 5.1), 3.97 (3H,s), 3.37 (3H,s), 2.80 (3H, s). 2006/016344
Example 92
Figure imgf000135_0001
(R)-l-(2-Hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-methyl-3-oxo- 5-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: CaIc' d for C29H27N5O5: 525; MS (ESI pos. ion) m/z: 526 (MH+). 1HNMR (CDCl3, 400 MHz): 11.28 (lH,s), 8.53 (IH, d, J 5.1), 8.24- 8.21 (3H, m), 7.49-7.39 (7H, m), 7.22 IH, bd, J 9.2), 6.38 (IH, d, J5.1), 4.7 (IH, b), 3.96 (4H, bs), 3.75 (2H, m). 3.63 (3H, s), 1.04 (3H, d, J6.3).
Example 93
Figure imgf000135_0002
("R)-N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-2-methyl-3- oxo-5-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: CaIc' d for C3oH27FN405: 542; MS (ESI pos. ion) m/z: 543 (MH+). 1HNMR (CDCl3, 400 MHz): 11.05 (IH, s), 8.55 (IH, d, J 5.3), 8.26 (IH, d, J 9.2), 7.86 (IH, d, J 12.5), 7.53-7.45 (5H, m), 7.39 (IH, d, J 2.3), 7.32 (IH, d, J 9.7), 7.77 (IH, dd, J 9.2, 2.6), 7.14 (IH, t, J 8.8), 6.37 (IH, J 5.3), 3.96 (3H, s), 3.90 (IH, m), 3.76 (2H, d, J 6.0), 3.62 (3H, s), 1.94 (IH, d, J 4.3), 1.04 (3H, d, J 6.2).
Example 94
Figure imgf000135_0003
(S)-N-(3-fluoro-4-(6-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C30H27FN4O5: 542. 1HNMR (SOO MHZ5 CDCI3): 1.01 (d, J-5.85 Hz, 3H), 2.72-2.79 (m, 3H), 3.55 (d, J=12.28 Hz, IH), 3.69-3.93 (m, 3H), 6.44 (d, J=4.53 Hz, IH), 7.02 (d, J=6.72 Hz, 2H), 7.04 (s, 2H), 7.27-7.40 (m, 4H), 7.56 (d, J=2.78 Hz, IH), 7.78-7.91 (m, 2H), 8.31 (d, J=5.26 Hz, IH), 10.80 (s, IH).
Example 95
Figure imgf000136_0001
l-(2-aminoethyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy) phenyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide
Figure imgf000136_0002
Step 1: l-(2-(l,3-dioxo-l,3-dihydro-2H-isoindol-2-yl)ethyl)-N-(3-fluoro-4-((7-
(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole- 4-carboxamide. To a solution of N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2- hydroxyethyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide (0.20 g, 0.38 mmol) and phthalimide (0.11 g, 0.76 mmol) in 10 mL Of CH2Cl2 was added triphenyl phosphine (0.13 ml, 0.57 mmol), followed by diethyl azodicarboxylate (0.089 ml, 0.57 mmol) via a syringe. The reaction mixture was stirred at RT for 16 hours. The resulting solution was concentrated in vacuo, and the residue was purified by silica gel chromatography (EtOAc to 10% MeOH/EtOAc) to give the title compound as a light yellow solid (0.22 g, 88% yield). MS (ESI pos. ion) m/z: 658 (MH+). Calc'd exact mass for C37H28FN5O6: 657. IH NMR (300 MHz, MeOH) 8.53 (1 H, d, J=5.5 Hz), 8.28 (1 H, d, J=9.0 Hz), 7.80 - 7.91 (5 H, m), 7.50 (1 H5 s), 7.48 (2 H, d, J=3.0 Hz), 7.26 - 7.36 (6 H, m), 6.49 (1 H5 dd, J=5.4, 1.0 Hz)5 4.27 (2 H, t, J=5.5 Hz), 3.97 (3 H, s), 3.74 (2 H5 1, J=5.5 Hz), 2.68 (3 H5 s).
Figure imgf000137_0001
Step 2: l-(2-aminoethyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide. To a solution of l-(2- (l,3-dioxoisoindolin-2-yl)ethyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide (0.20 g, 0.30 mmol) in 1:1 H2O/EtOH was added hydrazine (0.049 g, 1.5 mmol). The reaction was heated to 5O0C for 8 hours and then cooled to RT. The reaction mixture was then diluted with 20 mL of satd. NaHCO3 aq. solution and 60 mL of EtOAc. The organic phase was separated and washed with 30 mL of brine, dried over Na2SO4 and concentrated in vacuo. The residue was washed with 20% hexane in EtOAc to give the title compound as a light yellow solid (0.13 g, 81% yield). MS (ESI pos. ion) m/z: 528 (MH+). Calc'd exact mass for C29H26FN5O4: 527. IH NMR (300 MHz, MeOH) 8.54 (1 H, d, J=5.5 Hz), 8.30 (1 H5 d, J=9.2 Hz), 7.93 - 7.97 (1 H, m), 7.54 - 7.66 (3 H5 m)5 7.44 - 7.51 (2 H5 m), 7.27 - 7.38 (4 H5 m), 6.50 (1 H, dd, J=5.5, 0.9 Hz)5 3.92 - 4.02 (5 H, m), 2.83 (3 H, s), 2.68 (2 H5 15 J=6.7 Hz).
Example 96
Figure imgf000137_0002
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-l- (phenylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 558 (MH+). Calc'd exact mass for C33H27N5O4: 557. IH NMR (300 MHz, CHLOROFORM-d) 11.40 (1 H, s), 8.80 (1 H, d, J=6.4 Hz), 8.49 (1 H, d, J=9.2 Hz), 8.39 (1 H, d, J=9.4 Hz), 8.27 (1 H, d, J=2.6 Hz), 7.95 (1 H, d, J=2.1 Hz), 7.41 - 7.58 (5 H, m), 7.31 (1 H, d, J=2.3 Hz), 7.23 - 7.30 (4 H, m), 6.86 - 6.91 (1 H, m), 6.85 (1 H, s), 6.73 (1 H, d, J=6.6 Hz), 4.98 (2 H, s), 4.07 (3 H, s), 2.84 (3 H, s).
Example 97
Figure imgf000138_0001
l-benzyl-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 575 (MH+). Calc'd exact mass for C34H27FN4O4: 574. IH NMR (300 MHz, CHLOROFORM-d) 11.02 (1 H, s), 8.78 (1 H, s), 8.41 (1 H, d, J=9.4 Hz), 8.03 (1 H, dd, J=12.5, 1.8 Hz), 7.89 (1 H, s), 7.20 - 7.54 (11 H, m), 6.80 - 6.91 (2 H, m), 6.75 (1 H, s), 4.99 (2 H, s), 4.06 (3 H, s), 2.85 (3 H, s).
Example 98
Figure imgf000138_0002
5-methyl-l-(2-(methyloxy)ethyl)-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 526 (MH+). Calc'd exact mass for C29H27N5O5: 525. IH NMR (300 MHz, MeOH) 8.81 (1 H, d, J=6.8 Hz), 8.46 - 8.59 (2 H, m), 8.34 (1 H, d, J=2.4 Hz), 7.84 (1 H, dd, J=9.2, 2.8 Hz), 7.43 - 7.64 (7 H, m), 7.00 (1 H, d, J=6.8 Hz), 4.06 - 4.15 (5 H, m), 3.25 - 3.40 (5 H, m), 2.82 (3 H, s). 16344
Example 99
Figure imgf000139_0001
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-l-(2-(methyloxy)ethyl)- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C30H27FN4O5: 542. IH NMR (300 MHz, CHLOROFORM-d) 10.90 (1 H, s), 8.59 (1 H, d, J=5.3 Hz)5 8.27 (1 H, d, J=9.2 Hz), 7.93 (1 H, dd, J-12.5, 2.4 Hz), 7.52 - 7.59 (1 H, m), 7.14 - 7.48 (8 H, m), 6.41 (1 H, dd, J=5.3, 0.9 Hz), 3.94 - 4.02 (5 H, m), 3.34 (2 H, t, J=5.0 Hz), 3.25 (3 H, s), 2.83 (3 H, s).
Example 100
Figure imgf000139_0002
l-(2-hydroxyethyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 512 (MH+). Calc'd exact mass for C28H25N5O5: 511. IH NMR (300 MHz, MeOH) 8.81 (1 H, d, J=6.8 Hz), 8.44 - 8.58 (2 H, m), 8.33 (1 H, s), 7.83 (1 H, d, J=9.0 Hz), 7.43 - 7.64 (7 H, m), 7.00 (1 H, d, J=6.6 Hz), 4.08 (3 H, s), 4.03 (2 H, t, J=4.4 Hz), 3.51 (2 H, t, J=4.3 Hz), 2.84 (3 H, s).
Example 101
Figure imgf000139_0003
l-((2R)-2-fluoropropyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 528 (MH+). Calc'd exact mass for C29H26FN5O4: 527. Example 102
Figure imgf000140_0001
(S)-l-(2-(dimethylamino)propyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxainide: MS (ESI pos. ion) m/z: 570 (MH+). Calc'd exact mass for C32H32FN5O4: 569. IH NMR (300 MHz, MeOH) 8.82 (1 H, d, J=6.6 Hz), 8.53 (1 H, d, J=9.2 Hz), 8.01 (1 H5 dd, J=12.8, 2.3 Hz)5 7.35 - 7.68 (9 H, m), 6.99 (1 H, dd, J=6.8, 0.9 Hz)5 4.27 - 4.45 (2 H, m), 4.08 (3 H, s), 3.42 - 3.54 (1 H, m), 2.87 (3 H5 s), 2.67 (6 H5 s), 1.23 (3 H, d5 J=6.8 Hz).
Example 103
Figure imgf000140_0002
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-l-(2-(l- pyrrolidinyl)ethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 582 (MH+). Calc'd exact mass for C33H32FN5O4: 581. IH NMR (300 MHz5 MeOH) 8.82 (1 H5 d, J=6.8 Hz), 8.55 (1 H, d, J=9.2 Hz)5 8.02 (1 H5 dd, J=12.75 1.8 Hz), 7.37 - 7.68 (9 H, m), 7.00 (1 H5 d, J=6.6 Hz)5 4.27 - 4.38 (2 H5 m), 4.09 (3 H5 s), 3.21 - 3.34 (6 H, m), 2.87 (3 H5 s), 2.01 (4H, m).
Example 104
Figure imgf000140_0003
l-((2S)-2-fluoropropyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 528 (MH+). Calc'd exact mass for C29H26FN5O4: 527. IH NMR (300 MHz, MeOH) 8.81 (1 H5 d, J=6.8 Hz), 8.44 - 8.58 (2 H, m), 8.34 (1 H, d, J=2.6 Hz), 7.83 (1 H, dd, J=9.1, 2.9 Hz), 7.41 - 7.64 (7 H, m). 7.00 (1 H, d, J=6.8 Hz), 4.09 (3H, s), 3.88 - 4.12 (1 H, m), 3.35 (2 H, m), 2.77 - 2.85 (3 H, m), 1.13 - 1.33 (3 H, m).
Example 105
Figure imgf000141_0001
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-((2S)-2-fluoropropyl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass for C30H26F2N4O4: 544. Example 106
Figure imgf000141_0002
l-((2S)-2-(acetylamino)propyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 584 (MH+). Calc'd exact mass for C32H30FN5O5: 583. IH NMR (300 MHz, MeOH) 8.83 (1 H, d, J-6.6 Hz), 8.57 (1 H, d, J=9.4 Hz), 8.04 (1 H, dd, J=12.9, 1.8 Hz), 7.39 - 7.66 (9 H, m), 7.00 (1 H, dd, J=6.8, 1.1 Hz), 4.10 (3H, s), 3.83 - 4.11 (3 H, m), 2.80 (3 H, s), 1.84 (3 H, s), 0.98 (3 H, d, J=6.4 Hz).
Example 107
Figure imgf000141_0003
l-((2S)-2-aminopropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 542 US2006/016344
(MH+). Calc'd exact mass for C30H28FN5O4: 541. IH NMR (300 MHz, MeOH) 8.83 (1 H5 d, J=6.8 Hz), 8.55 (1 H, d, J=9.2 Hz), 8.04 (1 H, dds J=12.8, 1.7 Hz), 7.39 - 7.69 (9 H, m), 6.99 (1 H, dd, J=6.6, 0.9 Hz), 4.06 - 4.31 (2 H, m), 4.09 (3H, s), 3.28 - 3.41 (1 H, m), 2.86 (3 H, s), 1.14 (3 H, d, J=6.6 Hz). "
Example 108
Figure imgf000142_0001
l-((2S)-2-azidopropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 568 (MH+). Calc'd exact mass for C30H26FN7O4: 567. IH NMR (300 MHz, CHLOROFORM-d) 10.84 (1 H, s), 8.59 (1 H, d, J=5.3 Hz), 8.27 (1 H, d, J=9.2 Hz), 7.92 (1 H, dd, J=12.6, 2.4 Hz), 7.53 - 7.60 (2 H, m), 7.14 - 7.50 (7 H, m), 6.41 (1 H, dd, J=5.3, 0.9 Hz), 3.96 (3 H, s), 3.56 - 3.84 (3 H, m), 2.85 (3 H, s), 1.15 (3 H, d, J-6.6 Hz).
Example 109
Figure imgf000142_0002
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-(2-hydroxyethyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 529 (MH+). Calc'd exact mass for C29H25FN4O5: 528.
Example 110
Figure imgf000142_0003
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-l- propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 527 (MH+). T/US2006/016344
Calc'd exact mass for C30H27FN4O4: 526. IH NMR (400 MHz, CHLOROFORM-d) 10.91 (1 H, s), 8.59 (1 H, d, J=5.3 Hz), 8.27 (1 H, d, J=9.0 Hz), 7.91 - 7.93 (2 H5 d, J=2.0 Hz), 7.41 - 7.58 (4 H, m), 7.14 - 7.38 (4 H, m), 6.42 (1 H, d, J=5.3 Hz), 3.96 (3 H, s), 3.76 (2 H, t, J=7.2 Hz), 2.80 (3 H, s), 1.45 - 1.56 (2 H, m, J=IA, 7.4, 7.4, 7.4, 7.4 Hz), 0.80 (3 H, t, J=7.4 Hz).
Example 111
Figure imgf000143_0001
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2R)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 573 (MH+). Calc'd exact mass for C31H29FN4O6: 572.
Example 112
Figure imgf000143_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2S)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 573 (MH+). Calc'd exact mass for C3iH29FN4O6: 572.
Example 113
Figure imgf000143_0003
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-(2-methylpropyl)-3-oxo- 2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 524 (MH+). Calc'd exact mass for C30H29N5O4: 523. IH NMR (400 MHz, CHLOROFORM-d) 11.28 (1 H, T/US2006/016344 s), 8.60 (1 H5 d, J=5.3 Hz), 8.37 (1 H, d, J=8.8 Hz), 8.24 (1 H5 d, J=6.1 Hz)5 8.23 (1 H5 s), 7.41 - 7.56 (5 H5 m)5 7.35 (2 H5 d, J=8.0 Hz), 7.23 (1 H5 dd, J=9.2, 2.3 Hz)5 6.43 (1 H, d, J=5.3 Hz), 3.97 (3 H5 s)5 3.64 (2 H5 d, J=7.4 Hz)5 2.81 (3 H5 s),1.84 (1 H5 dt, J=13.8, 6.9 Hz)5 0.77 (6 H, d, J=6.7 Hz).
Example 114
Figure imgf000144_0001
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-l-propyl- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 510 (MH+). Calc'd exact mass for C29H27N5O4: 509. IH NMR (400 MHz5 CHLOROFORM-d) 11.29 (1 H, s), 8.61 (1 H5 d, J=5.5 Hz)5 8.38 (1 H, d, J=9.0 Hz), 8.22 - 8.27 (2 H5 m), 7.32 - 7.57 (7 H, m), 7.22 - 7.30 (1 H5 m), 6.46 (1 H, d, J=5.5 Hz), 3.98 (3 H, s), 3.76 (2 H5 1, J=7.2 Hz)5 2.79 - 2.83 (3 H5 m), 1.42 - 1.56 (2 H, m, J=7.4, 7.4, 7.4, 7.4 Hz)5 0.70 - 0.86 (3 H5 1, J=7.4 Hz).
Example 115
Figure imgf000145_0001
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-l-(2-oxopropyI)- 2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 541 (MH+). Calc'd exact mass for C30H25FN4O5: 540. IH NMR (300 MHz, CHLOROFORM-d) 10.86 (1 H, s), 8.60 (1 H, d, J=5.3 Hz), 8.28 (1 H, d, J=9.2 Hz), 7.92 (1 H, dd, J=12.5, 2.4 Hz), 7.41 - 7.59 (4 H, m), 7.14 - 7.33 (4 H, m), 6.42 (1 H, dd, J=5.3, 0.9 Hz), 4.52 (2 H, s), 3.97 (3 H, s), 2.63 - 2.72 (3 H, s), 2.04 - 2.10 (3 H, s)
Example 116
Figure imgf000145_0002
l-(2,3-dihydroxy-2-methylpropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy) phenyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 573 (MH+). Calc'd exact mass for C31H29FN4O6: 572. IH NMR (400 MHz, CHLOROFORM-d) 10.85 (1 H, s), 8.56 (1 H, d, J=5.3 Hz), 8.27 (1 H, d, J=9.2 Hz), 7.90 (1 H, dd, J=12.5, 1.6 Hz), 7.54 (2 H, t, J=7.7 Hz), 7.38 - 7.47 (2 H, m), 7.14 - 7.32 (5 H, m), 6.42 (1 H, d, J=5.3 Hz), 4.09 - 4.19 (1 H, m), 3.96 (3 H, s), 3.86 (1 H, d, J=15.7 Hz), 3.34 (2 H, s), 2.89 (3 H, s), 1.07 (3 H, s).
Example 117
Figure imgf000145_0003
16344
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C28H25FN4O5: 542.
Example 118
Figure imgf000146_0001
N-(4-((6,7-bis(methyloxy)-4-quinazolinyl)oxy)-3-fluorophenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 588 (MH+). Calc'd exact mass for C31H30FN5O6: 587.
Example 119
Figure imgf000146_0002
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-l-(2-methyl-2-propen- l-yl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 539 (MH+). Calc'd exact mass for C31H27FN4O4: 538.
Example 120
Figure imgf000146_0003
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2S)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 573 (MH+). Calc'd exact mass for C31H29FN4O6: 572. T7US2006/016344
Example 121
Figure imgf000147_0001
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-l-(2- oxopropyl)-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 571 (MH+). Calc'd exact mass for C31H27FN4O6: 570.
Example 122
Figure imgf000147_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-(2,3-dihydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS
(ESI pos. ion) m/z: 603 (MH+). Calc'd exact mass for C32H31FN4O7: 602.
Example 123
Figure imgf000147_0003
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-l-(2-methyl-2- propen-l-yl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 569 (MH+). Calc'd exact mass for C32H29FN4O5: 568. IH NMR (400 MHz, MeOH) 10.16 (2 H, s), 7.73 (2 H5 d, J=5.7 Hz), 7.24 (2 H, s), 7.21 (1 H, d, J=I .6 Hz), 6.94 (2 H, s), 6.80 - 6.90 (8 H, m), 6.58 - 6.71 (13 H, m), 5.86 (2 H, d, J=5.5 Hz)5 4.13 - 4.19 (17 H, m), 3.65 - 3.72 (8 H, m), 3.30 (15 H5 d, J=1.8 Hz), 2.57 - 2.60 (6 H, m), 2.27 (1 H, s), 1.99 - 2.14 (13 H5 m), 0.84 (8 H5 s) Example 124
Figure imgf000148_0001
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-3-oxo-2-phenyl-l- propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 540 (MH+). Calc'd exact mass for C3oH29FNs05: 539.
Example 125
Figure imgf000148_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 515 (MH+). Calc'd exact mass for C28H23FN4O5: 514.
Example 126
Figure imgf000148_0003
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-3-oxo-2-phenyl-l-(2- propen-l-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 538 (MH+). Calc'd exact mass for C30H27N5O5: 537. Example 127
Figure imgf000149_0001
N-(4-((6,7-bis(methyloxy)-l-oxido-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2- phenyl-l-(2-propen-l-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 571 (MH+). Calc'd exact mass for C31H27FN4O6: 570. IH NMR (400 MHz, MeOH) 8.36 (1 H, d, J=I. Q Hz), 7.90 - 7.97 (2 H, m), 7.68 (1 H, s), 7.53 - 7.62 (3 H, m), 7.42 (2 H, d, J=7.2 Hz), 7.30 - 7.37 (2 H, m), 6.59 (1 H, d, J=6.8 Hz), 5.69 (1 H, dd, J=I 1.2, 5.9 Hz), 5.21 (1 H, d, J=10.4 Hz), 4.93 (1 H, d, J=YIl Hz), 4.48 (2 H, d, J=4.9 Hz), 4.01 - 4.11 (6 H, m), 2.77 (3 H, s).
Example 128
Figure imgf000149_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2-phenyl-l- (phenylmethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 605 (MH+). Calc'd exact mass for C35H29FN4O5: 604.
Example 129
Figure imgf000149_0003
4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluoro-N-(5-oxo-l-phenyl-2,5-dihydro-lH-pyrazol- 3-yl)benzamide: Calc'd for C27H21FN4O5: 500; MS (ESI pos. ion) m/z: 501 (MH+) US2006/016344
1HNMR (DMSO-d6, 400 MHz): 8.54 (IH, d, J 5.2), 7.88 (IH, dd, J 11.6, 1.6), 7.71 (IH, d, J 8.4), 7.59-7.54 (3H, m), 7.48 - 7.37 (4H, m), 7.13 (IH, t, J 7.3), 6.56 (IH, d, J5.1), 3.96 (6H, s).
Example 130
Figure imgf000150_0001
4-(6,7-Dimethoxyquinolin-4-yloxy)-N-((l,2-dimethyl-5-oxo-3-phenyl-2,5-dihydro-lH- pyrazol-4-yl)methyl)-3-fluorobenzamide: CaIc' d for C30H27FN4O5: 542; MS (ESI pos. ion) m/z: 543 (MH+)
1HNMR (CDCl3, 400 MHz): 8.51 (2H, m), 7.81 (IH, dd, J 1.8, 10.8), 7.71 (IH, d, J 8.3), 7.57- 7.48 (5H, m), 7.44 (IH, s), 7.28 (IH, t, J 8.0), 6.42 (IH, d, J5.3), 4.46 (d, 2H, d, J 4.9), 4.06 (6H, s), 3.48 (3H, s), 3.14 (3H, s).
Example 131
Figure imgf000150_0002
4-(6,7-Dimethoxyquinolin-4-yloxy)-N-(2,3-dimethyl-5-oxo-l-phenyl-2,5-dihydro-lH- pyrazol-4-yl)-3-fluorobenzamide: Calc'd for C29H25FN4O5: 528; MS (ESI pos. ion) m/z:
529 (MH+).
1HNMR (CDCl3, 400 MHz): 9.20 (IH, b), 8.56 (IH, d, J5.3), 7.86 (IH, J ), 7.76 (IH, d, J) 7.57
(IH, s), 7.50-7.44 (3H, m), 7.40 (2H, d, J 7.4), 7.34 (IH, t, J7.2), 7.28 (IH, m), 6.56 (IH, d, J
4.9), 4.07 (3H, s), 4.06 (3H, s), 3.12 (3H, s), 2.30 (3H, s). Example 132
Figure imgf000150_0003
4-(6,7-Dimethoxyquinolin-4-yloxy)-N-((2,3-dimethyl-5-oxo-l-phenyl-2,5-dihydro-lH- pyrazol-4-yl)methyl)-3-fluorobenzamide: Calc'd for C30H27FN4O5: 542; MS (ESI pos. ion) m/z: 543 (MH+). 1HNMR (CDCl3, 400 MHz): 8.49 (IH, d, J 5.3), 8.12 (IH, t, NH), 7.80 (IH, dd, J 1.7, 10.6), 7.67 (IH, d), 7.54 (IH, s), 7.48 (2H, t, J 8.0), 7.43 (IH, s), 7.38 (2H, d J 7.6), 7.33 (IH, t, J 7.3), 7.25 (IH, m), 6.40 (IH, d, 5.3), 4.44 (2H, d, J 5.1), 4.05 (6H, s), 3.11 (3H, s), 2.38 (3H, s).
Example 133
Figure imgf000151_0001
l-Benzyl-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l,2-dihydropyrazolo[l,5- a]pyridine-3-carboxamide: A mixture of HATU (760 mg, 2.0 mmol), crude l-benzyl-2-oxo- l,2-dihydropyrazolo[l,5-a]pyridine-3-carboxylic acid (268 mg, 1.0 mmol), 5-(7- methoxyquinolin-4-yloxy)pyridin-2-amine (220 mg, 1.0 mmol), and triethylamine (2000 μl, 14 mmol) in DMF (3 mL) plus CHCL3 (3 mL) was stirred at 6O0C for 4 days. Then, the mixture was diluted with EtOAc (10 mL) and H2O (5 mL). The organic layer was washed with NaOH (1 N), H2O, NaHCO3, and dried over Na2SO4. The organic residue was purified on silica and further purified by trituration with EtOAc in ether (5%), resulting a light green powder. Calc'd for C30H23N5O4: 517; MS (ESI pos. ion) m/z: 518
1HNMR (CDCl3, 400 MHz): 10.96 (IH, s), 8.62 (IH, d, J 5.3), 8.48 (IH, d, J 9.0), 8.29-8.25 (2H, m), 7.73 (IH, d, J6.8), 7.55-7.53 (IH, dd, J2.7, 9.0), 7.48-7.43 (2H, m), 7.40-7.34 (3H, m), 7.29-7.23 (3H, m), 6.74 (IH, t, J7.1), 6.46 (IH, d J5.3), 5.48 (2 H, s), 3.98 (3H, s).
Example 134
Figure imgf000151_0002
4-((5-(6,7-Dimethoxyquinolin-4-yloxy)pyridin-2-ylamino)methyl)-l,5-dimethyl-2-phenyl- 1 ,2-dihy dropyr azol-3-one Calc'd for C28H27N5O4: 497; MS (ESI pos. ion) m/z: 498. 1HNMR (400 MHz, CDCl3): 8.48 (IH, d, J 5.1), 8.06 (IH, s), 7.57 (IH, s), 7.47 (2H, t, J 7.2), 7.42 (3H, m), 7.33-7.22 (2H, m), 6.56 (IH3 d, J 9.0), 6.43 (IH, d, J 5.3), 5.56 (IH, s, NH), 4.36 (2H5 d, J 5.5, NCH2), 4.06 (6H, d), 3.08 (3H. s), 2.36 (3H, s).
Example 135
Figure imgf000152_0001
Figure imgf000152_0002
Step 1: Thiophen-3-amine. A 200-mL flask equipped with a reflux condenser and a magnetic stirbar was charged with methyl 3-aminothiophene-2-carboxylate (20.00 g, 127.2 mmol) and suspended in 2 N NaOH (140 mL, 2 equiv), then was heated to reflux for 4 h. The flask was removed from the oil bath and immersed in an ice/water bath and neutralized to pH 5 by the addition of cone. HCl (about 20 mL). The mixture was extracted with EtOAc (2x100 mL), and the combined organic extracts were washed with sat'd brine (100 mL) then dried over Na2SO4. The organic layer was dried, filtered and concentrated to a brown oil. The oil was dried under vacuum and dissolved in 1-propanol (60 mL, 5 vol), and treated with oxalic acid (11.1 g, 1.0 equiv). The resulting slurry was stirred at 40 deg C (oil bath) for 45 min, then the precipitate was isolated by vacuum filtration and washed with cold 1-propanol. The light brown solid (6.9 g, 30% y) was dried under vacuum. The product was isolated as the likely oxalate salt (30% yield). The product was used as is in the next step.
Figure imgf000153_0001
Step 2: 2,2-dimethyl-5-((thiophen-3-ylamino)methylene)-l,3-dioxane-4,6-dione. A 200- mL, rb flask equipped with a magnetic stirbar and a reflux condenser was charged with 3- aminothiophene oxalate (6.9 g, 36 mmol) and triethoxymethane (61 ml, 365 mmol) under N2. After stirring for 15 min, 2,2-dimethyl-l,3-dioxane-4,6-dione (5.3 g, 36 mmol) was added in one portion to the light brown slurry, and the mixture was heated to 85 deg C in an oil bath overnight. The next day, a dark precipitate had formed and the mixture was cooled to ambient temp. The mixture was then cooled in an ice bath and the mixture was vacuum filtered through paper. The brown-red solids were washed with MTBE, air dried, then dried under vacuum to yield 2,2-dimethyl-5-((thiophen-3-ylamino)methylene)-l,3-dioxane-4,6-dione (6.73 g, 73% yield).
Figure imgf000153_0002
Step 3: thieno[3,2-b]pyridin-7-ol. A 200-mL rb flask was charged with 2,2-dimethyl-5- ((thiophen-3-ylamino)methylene)-l,3-dioxane-4,6-dione (6.73 g, 26.6 mmol) and diphenyl ether (25 mL) and heated to about 200 deg C for about 30-45 min and the mixture was allowed to cool to rt overnight. The mixture was scraped down with a spatula and diluted with MTBE. The mixture was filtered through paper and washed with MTBE. The brown solid was air dried to yield thieno[3,2-b]pyridin-7-ol.
Figure imgf000154_0001
Step 4: 7-chlorothieno[3,2-b]pyridine. A 2-L, 3-neck, rb flask equipped with a mechanical overhead stirrer, a 250-mL addition funnel, and a thermocouple w/N2-inlet adapter was charged with thieno[3,2-b]pyridin-7-ol (144 g, 952 mmol), chloroform (700 mL) and anhydrous N,N-dimethylformamide (100 ml, 1297 mmol). The heterogeneous mixture was cooled in an ice bath with stirring, then oxalyl dichloride (166 ml, 1905 mmol) was added dropwise via the addition funnel. Towards the end of the addition, the exotherm had diminished so the remaining reagent was added more quickly, which resulted in rapid off- gassing and the eruption of a portion of the contents out of the vessel. Upon complete addition, the mixture was allowed to stir out for 2 h, at which point LC-MS analysis indicated only about 10% conversion to the desired product (71556-13-A). The ice bath was removed, and the mixture was heated to reflux with a mantle. The heterogeneous mixture quickly turned homogeneous upon reaching temperature, and LC-MS indicated complete conversion after 1 h @ reflux (71556-13 -B). After standing at ambient temp over the weekend, an orange solid had formed from the dark brown supernate. The mixture was cooled in an ice bath, then diluted with MTBE (800 mL), resulting in the exothermic precipitation of copious amounts of a dense, mustard-brown solid. The solid was isolated by vacuum filtration and washed with MTBE until the filtrate was colorless to yield the solid and a cloudy, bright orange filtrate. The solid product was then carefully partitioned between DCM (1 L) and sat'd aq. NaHCO3 (1 L). The phases were mixed and the light brown aqueous layer was back extracted with DCM (500 mL). The combined organic layers were washed with sat'd brine, then dried over anhydrous Na2SO4. MTBE (500 mL) was added, then concentrated by about 200 mL, then hexane (500 mL) was added to form a dark brown precipitate. The mixture was further concentrated by 100 mL, then cooled in an ice bath. The mixture was then filtered and washed with hexane/MTBE (200 mL). The filtrate was then concentrated to dryness to yield the title compound as a light brown oil that crystallized to a dark rust colored, oily solid (97.7 g, 60.5% yield).
Figure imgf000155_0001
Step 5: lithium 7-chlorothieno[3,2-b]pyridine-2-carboxylate. A solution of 7- chlorothieno[352-b]ρyridine (40 g, 0.236 mol) in THF (400 niL) was cooled to -78 deg C, dropwise added butyl lithium (1.5 M in hexanes, 103.8 mL, 0.259 mol). After stirring for 1 h, the mixture was quenched with CO2 fgas with the formation of precipitate. The mixture was allowed to warm to rt , diluted with Et20 and filtered slowly. The filter cake was washed with ether and dried under vacuum. The crude mixture was dissolved in methanol and stirred with activated carbon and filtered through a pad of celite and the volume concentrated. The solution was triturated with ether and the solid collected and further triturated with isopropanol to provide the title compound: MS (ESI pos. ion) m/z: 214 (its corresponding acid form). Calc'd exact mass for C31H27FN6O5S: 214.
Figure imgf000155_0002
Step 6: (lZ)-N'-(((7-chlorothieno[3,2-b]pyridin-2-yl)carbonyl)oxy)ethanimidamide. A 100 mL round bottom flask was charged with lithium 7-chlorothieno[3 ,2-b]pyridine-2- carboxylate (0.500 g, 2.28 mmol), methylene chloride (15 ml), and 6 drops of DMF. Oxalyl chloride (0.248 ml, 2.85 mmol) was added dropwise, and the reaction mixture was stirred at room temperature for 3 hours then concentrated in vacuo to yield 7-chlorothieno[3,2- b]pyridine-2-carbonyl chloride as a brown solid. This material was suspended in chloroform (5 mL). N'-hydroxyacetamidine (0.186 g, 2.50 mmol), triethylamine (0.347 ml, 2.50 mmol), and chloroform (15 mL) were stirred together in a 50 mL flask to form a slurry, which was slowly added to the 7-chlorothieno[3,2-b]pyridine-2-carbonyl chloride suspension, then stirred for 1.5 hours at room temperature. The reaction mixture was diluted with chloroform (50 mL) and washed with water (50 mL), sat. aq. NaHCO3 (50 mL) and brine (50 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo. The resulting brown solid was triturated with toluene, and the precipitate collected to obtain the title compound (0.282 g, 46% yield) as a tan solid.
Figure imgf000155_0003
Step 7: 7-chloro-2-(3-methyl-l,2,4-oxadiazol-5-yl)thieno[3,2-b]pyridine. A 50 niL round bottom flask with a reflux condenser was charged with (lZ)-N'-(((7-chlorothieno[3,2- b]pyridin-2-yl)carbonyl)oxy)ethanimidamide (0.282 g, 1.04 mmol) and toluene (10 ml) and heated to 110 °C and stirred for 18 hours. LC/MS analysis indicated a mixture of the product and 7-chlorothieno[3,2-b]pyridine-2-carboxylic acid. The reaction was diluted with chloroform (30 niL) and washed with water (30 mL), sat. aq. NaHCO3 (30 niL), and brine (30 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo to yield 7- chloro-2-(3-methyl-l,2,4-oxadiazol-5-yl)thieno[3,2-b]pyridine (0.1128 g, 43% yield) as a light yellow solid, which was used without further purification.
Figure imgf000156_0001
Step 8: 3-fluoro-4-(2-(3-methyl-l,2,4-oxadiazol-5-yl)thieno[3,2-b]pyridin-7- yloxy)benzenamine. A 15 mL sealed tube was charged with 7-chloro-2-(3 -methyl- 1,2,4- oxadiazol-5-yl)thieno[3,2-b]pyridine (0.113 g, 0.449 mmol), 4-amino-2-fluorophenol (0.071 g, 0.56 mmol), cesium carbonate (0.512 g, 1.57 mmol), and DMF (2.00 ml) and sealed. The reaction mixture was stirred at 90 0C for 18 hours, allowed to cool to room temperature, then diluted with chloroform (50 mL) and washed with water (50 mL), sat. aq. NaHCO3 (50 mL), and brine (50 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo to yield a black solid. The product was purified by silica gel chromatography eluting with 3% methanol in methylene chloride to yield 3-fluoro-4-(2-(3-methyl-l,2,4-oxadiazol-5- yl)thieno[3,2-b]pyridin-7-yloxy)benzenamine (0.074 g, 48% yield) as a yellow solid.
Figure imgf000156_0002
Step 9: N-(3-fluoro-4-(2-(3-methyl-l,2,4-oxadiazol-5-yl)thieno[3,2-b]pyridin-7- yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamide. A 16 mm sealed tube was charged with 3-fluoro-4-(2-(3-methyl- l,2,4-oxadiazol-5-yl)thieno[3,2-b]pyridin-7-yloxy)benzenamine (0.0740 g, 0.22 mmol), l-(2- hydroxy-2-methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxylic acid (0.094 g, 0.32 mmol), EDC (0.062 g, 0.32 mmol), HOBT (0.033 g, 0.22 mmol), Hunig's 2006/016344
Base (0.13 ml, 0.76 mmol), and DMF (1.00 ml), sealed, and stirred at room temperature for 18 hours. LC/MS analysis indicated the presence of remaining 3 -fluoro-4-(2-(3 -methyl- 1,2,4- oxadiazol-5-yl)thieno[3,2-b]pyridin-7-yloxy)benzenamine, so additional l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-253-dihydro-lH-pyrazole-4-carboxylic acid (0.031 g, 0.11 mmol) was added and the reaction mixture was stirred at 50 °C for 8 hours. The flask was allowed to cool to room temperature, the mixture was diluted with chloroform (25 mL), then washed with water (25 mL), sat. aq. NaHCO3 (25 mL), and brine (25 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo to yield a tan oil. The product was purified by silica gel chromatography eluting with 3% methanol in methylene chloride. The isolated yellow solid was triturated with EtOAc to yield N-(3 -fluoro-4-(2-(3 -methyl- 1 ,2,4- oxadiazol-5-yl)thieno[3,2-b]pyridin-7-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide (0.035 g, 26% yield). MS (ESI pos. ion) m/z: 615 (MH+). Calc'd exact mass for C8H4C1NO2S: 614. 1H NMR (400 MHz, DMSO-J6) 11.00 (s, 1 H), 8.68 (d, J=5.31 Hz, 1 H), 8.49 (s, 1 H), 7.96 - 8.04 (m, 1 H), 7.43 - 7.60 (m, 4 H), 7.35 (d, J=8.21 Hz, 3 H), 6.89 (d, J=5.31 Hz, 1 H), 4.84 (s, 1 H), 3.87 (s, 2 H), 2.80 (s, 3 H), 2.46 (s, 3 H), 0.96 (s, 6 H).
Example 136
Figure imgf000157_0001
N-(3-fluoro-4-((2-(l-methyl-lH-imidazol-5-yl)thieno[3,2-b]pyridin-7-yl)oxy)phenyl)-l-(2- hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyI-2,3-dihydro-lH-pyrazoIe-4- carboxamide: MS (ESI pos. ion) m/z: 613 (MH+). Calc'd exact mass for C32H29FN6O4S : 612. 1H NMR (400 MHz, DMSO-J6) 10.97 (s, 1 H), 8.52 (d, J=5.43 Hz, 1 H), 7.99 (dd, J=13.14, 2.15 Hz, 1 H), 7.87 (s, 1 H), 7.78 (s, 1 H), 7.56 (t, J=7.71 Hz, 2 H), 7.40 - 7.50 (m, 3 H), 7.35 (d, J=7.83 Hz, 3 H), 6.65 (d, J=5.43 Hz, 1 H), 4.85 (s, 1 H), 3.90 (s, 3 H), 3.82 - 3.88 (m, 2 H), 2.79 (s, 3 H), 0.96 (s, 6 H). 6 016344
Example 137
Figure imgf000158_0001
N-(3-fluoro-4-((2-(l-methyl-lH-imidazol-5-yl)thieno[3,2-b]pyridin-7-yl)oxy)phenyl)-l- ((2R)-2-hydroxypropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide: MS (ESI pos. ion) m/z: 599 (MH+). Calc'd exact mass for C31H27FN6O4S: 598.
Example 138
Figure imgf000158_0002
N-(3-fluoro-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)phenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 517 (MH+). Calc'd exact mass for C27H25FN6O4: 516. 1H NMR (400 MHz, DMSO-J6) 12.27 (s, 1 H), 10.91 (s, 1 H), 8.30 (s, 1 H), 7.88 (dd, J=12.88, 2.27 Hz, 1 H), 7.56 (t, J=7.77 Hz, 2 H), 7.50 (d, J-3.41 Hz, 1 H), 7.46 (t, 1 H), 7.32 - 7.39 (m, 3 H), 7.24 - 7.31 (m, 1 H), 6.58 (d, J=3.41 Hz, 1 H), 4.83 (s, 1 H), 3.86 (s, 2 H), 2.80 (s, 3 H), 0.96 (s, 6 H).
Example 139
Figure imgf000158_0003
N-(3-fluoro-4-(lH-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)- 5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 516 (MH+). Calc'd exact mass for C28H26FN5O4 : 515. 1H NMR (400 MHz, DMSO-J6) 11.77 (s, 1 H), 10.92 (s, 1 H), 8.07 (d, J=5.43 Hz, 1 H), 7.88 - 7.97 (m, 1 H), 7.56 (t, J=7.77 . 2006/016344
Hz, 2 H)5 7.24 - 7.41 (m, 6 H), 6.37 (d, J=5.43 Hz, 1 H), 6.24 (s, 1 H), 4.84 (s, 1 H), 3.86 (s, 2 H), 2.79 (s, 3 H), 0.96 (s, 6 H).
Example 140
Figure imgf000159_0001
Methyl (6-((4-(((l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazol-4-yl)carbonyl)amino)phenyl)oxy)-lH-benzimidazol-2-yl)carbamate
MS (ESI pos. ion) m/z: 571 (MH+). CaIc' d exact mass for C30H30N6O6 : 570. 1H NMR (400 MHz, DMSO-J6) 10.66 (s, 1 H), 7.51 - 7.61 (m, 4 H), 7.40 - 7.48 (m, 1 H), 7.29 - 7.39 (m, 3 H), 7.01 (d, J=I.89 Hz, 1 H), 6.88 - 6.95 (m, 2 H), 6.79 (dd, J=8.53, 2.34 Hz, 1 H), 4.80 (s, 1 H), 3.84 (s, 2 H), 3.74 (s, 3 H), 2.78 (s, 3 H), 0.95 (s, 6 H).
Example 141
Figure imgf000159_0002
N-(4-(2-(azetidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenyl)-5-methyl-3- oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4-carboxamide
Figure imgf000159_0003
Azetidin-l-yl(7-chlorothieno[3,2-b]pyridin-2-yl)methanone
A 50 mL round bottom flask was charged with lithium 7-chlorothieno[3,2-b]pyridine-2- carboxylate (0.500 g, 2.28 mmol), methylene chloride (15 ml), and 12 drops of DMF. Oxalyl chloride (0.298 ml, 3.42 mmol) was added dropwise, and the mixture was stirred at room temperature for 3 hours and concentrated to yield a tan solid. This was redissolved in methylene chloride (15 ml). Azetidine hydrochloride (0.426 g, 4.55 mmol) was added in one portion and Hunig's Base (1.59 ml, 9.11 mmol) was added dropwise. This mixture was stirred at room temperature overnight, then diluted with methylene chloride (15 mL) and washed with , 006/016344 water (25 mL), sat. NaHCO3 (25 mL), and brine (25 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo to yield azetidin-l-yl(7-chlorothieno[3,2-b]pyridin- 2-yl)methanone (0.58 g, 100% yield) as a tan solid.
Figure imgf000160_0001
N-(4-(2-(azetidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenyl)-5-methyl-3- oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 586 (MH+). Calc'd exact mass for C31H28FN5O4S: 585. 1H NMR (400 MHz, DMSO-J6) 10.96 (s, 1 H), 8.60 (d, J=5.56 Hz, 1 H), 7.98 (d, J=14.53 Hz, 1 H), 7.91 (s, 1 H), 7.60 (t, J=7.52 Hz, 2 H), 7.42 - 7.55 (m, 4 H), 7.35 (d, J=9.22 Hz, 1 H), 6.77 (d, J-5.18 Hz, 1 H), 4.63 (t, J-7.20 Hz, 2 H), 4.12 (t, J=7.64 Hz, 2 H), 3.83 (t, J=7.33 Hz, 2 H), 2.75 (s, 3 H), 2.31 - 2.40 (m, 2 H), 1.35 - 1.45 (m, 2 H), 0.69 (t, J=I.39 Hz, 3 H)
Example 142
Figure imgf000160_0002
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N-methylthieno[3,2-b]pyridine-2-carboxamide: MS (ESI pos. ion) m/z: 590 (MH+). Calc'd exact mass for C30H28FN5O5S: 589. 1H NMR (400 MHz, DMSO-J6) 10.99 (s, 1 H), 8.95 (d, J=4.80 Hz, 1 H), 8.58 (d, J=5.43 Hz, 1 H), 8.21 (s, 1 H), 7.99 (dd, J=13.14, 2.27 Hz, 1 H), 7.57 (t, J=7.83 Hz, 2 H), 7.44 - 7.51 (m, 2 H), 7.36 (d, J=7.58 Hz, 3 H), 6.76 (d, J=5.31 Hz, 1 H), 4.86 (s, 1 H), 3.87 (s, 2 H), 2.85 (d, J=4.67 Hz, 3 H), 2.80 (s, 3 H), 0.97 (s, 6 H). Example 143
Figure imgf000161_0001
N-(3-fluoro-4-(2-(l-methylpiperazine-4-carbonyl)thieno[3,2-b]pyridin-7-yloxy)phenyl)-l- (2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide: MS (ESI pos. ion) m/z: 659 (MH+). Calc'd exact mass for C34H35FN6O5S: 658. 1H NMR (400 MHz5 DMSO-J6) 10.98 (s, 1 H), 8.59 (d, J=5.30 Hz, 1 H), 7.98 (dd, J=13.07, 2.21 Hz, 1 H), 7.84 (s, 1 H), 7.56 (t, J=7.71 Hz, 2 H), 7.42 - 7.51 (m, 2 H), 7.35 (d, J=7.45 Hz, 3 H), 6.76 (d, J=5.43 Hz, 1 H), 4.84 (s, 1 H), 3.86 (s, 2 H), 3.67 (bs, 4 H), 2.79 (s, 3 H), 2.37 (bs, 4 H), 2.21 (s, 3 H), 0.96 (s, 6 H)
Example 144
Figure imgf000161_0002
N-(2-(dimethylamino)ethyl)-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo- 2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2- carboxamide: MS (ESI pos. ion) m/z: 647 (MH+). Calc'd exact mass for C33H35FN6O5S: 646.
Example 145
Figure imgf000161_0003
N-(4-(2-(3-(dimethylamino)pyrrolidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3- fluorophenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- T/US2006/016344 pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 673 (MH+). Calc'd exact mass for C35H37FN6O5S: 672.
Example 146
Figure imgf000162_0001
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N,N-dimethylthieno[3,2-b]pyridine-2-carboxamide:
MS (ESI pos. ion) m/z: 604 (MH+). Calc'd exact mass for C31H30FN5O5S: 603. 1H NMR (400 MHz, DMSO-J6) 10.98 (s, 1 H), 8.58 (d, J=5.43 Hz, 1 H), 7.98 (dd, J=13.07, 1.96 Hz, 1 H), 7.94 (s, 1 H), 7.56 (t, J=7.71 Hz, 2 H), 7.43 - 7.51 (m, 2 H), 7.35 (d, J=8.08 Hz, 3 H), 6.76 (d, J=5.43 Hz, 1 H), 4.85 (s, 1 H), 3.86 (s, 2 H), 3.23 - 3.30 (m, 3 H), 3.06 (s, 3 H), 2.79 (s, 3 H), 0.96 (s, 6 H).
Example 147
Figure imgf000162_0002
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2-carboxamide: MS (ESI pos. ion) m/z: 576 (MH+). Calc'd exact mass for C29H26FN5O5S: 575. 1H NMR (400 MHz, DMSO-J6) 10.98 (s, 1 H), 8.58 (d, J=5.30 Hz, 1 H), 8.42 (s, 1 H)5 8.26 (s, 1 H), 7.95 - 8.01 (m, 1 H), 7.86 (s, 1 H), 7.56 (t, J=7.64 Hz, 2 H), 7.43 - 7.51 (m, 2 H), 7.35 (d, J=7.83 Hz, 3 H), 6.75 (d, J=5.43 Hz, 1 H), 5.76 (s, 1 H), 3.86 (s, 2 H), 2.79 (s, 3 H), 0.96 (s, 6 H).
Example 148
Figure imgf000162_0003
6 016344
N-(2-(dimethylamino)ethyl)-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo- 2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)phenoxy)-N-methylthieno[3,2- b]pyridine-2-carboxamide: MS (ESI pos. ion) m/z: 661 (MH+). Calc'd exact mass for C34H37FN6O5S: 660.
Example 149
Figure imgf000163_0001
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N-(2-methoxyethyl)thieno[3,2-b]pyridine-2- carboxamide: MS (ESI pos. ion) m/z: 634 (MH+). Calc'd exact mass for C32H32FN5O6S: 633.
Example 150
Figure imgf000163_0002
N-(4-(2-(azetidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenyl)-l-(2- hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide: MS (ESI pos. ion) m/z: 616 (MH+). Calc'd exact mass for C32H30FN5O5S: 615.
Example 151
Figure imgf000163_0003
N-cyclopropyl-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2-carboxamide: MS (ESI pos. ion) m/z: 616 (MH+). Calc'd exact mass for C32H30FN5O5S: 615. IH NMR (400 MHz, DMSO-J6) 10.98 (s, 1 H), 8.93 (d, J=4.04 Hz, 1 H), 8.57 (d, J=5.31 Hz, 1 H), 8.22 (s, 1 H), 7.94 - 8.01 (m, 2 H), 7.56 (t, J=7.83 Hz, 2 H), 7.43 - 7.50 (m, 2 H), 7.35 (d, J=7.83 Hz, 3 H), 6.75 (d, J=5.43 Hz, 1 H), 4.84 (s, 1 H), 3.87 (s, 2 H), 2.79 (s, 3 H), 0.96 (s, 6 H), 0.72 - 0.78 (m, 2 H), 0.60 - 0.66 (m, 2 H)
Example 152
Figure imgf000164_0001
7-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido) phenoxy)thieno[3,2-b]pyridine-2-carboxamide: MS (ESI pos. ion) m/z: 546 (MH+). Calc'd exact mass for C28H24FN5O4S: 545.
Example 153
Figure imgf000164_0002
Figure imgf000164_0003
N-(3-fluoro-4-(6-(pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)phenyl)-l-(2-hydroxy-2- methyIpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide
163
Figure imgf000165_0001
Step 1: 4-chloro-6-(2-fluoro-4-nitrophenoxy)pyrimidine. 6,6-dichloropyrimidine (1.000 g, 7 mmol) was dissolved in N,N-dimethylformamide (5 ml, 7 mmol), then 2-fluoro-4- nitrophenol (1 g, 7 mmol) was added into the mixture. Then Cesium Carbonate (2g, 10 mmol) was added into the mixture with stirring. The mixture was stirred at ambient temperature under nitrogen overnight. The progress of the reaction was monitored by LC/MS, which had confirmed completion. Then diluted the mixture with water was stirred an additional 3 hours. The precipitate was collected by filtration and washed with hexanes. The solid was dried in a reduced-pressure oven overnight to give the desired product 4-chloro-6-(2-fluoro-4- nitrophenoxy)pyrimidine (1.500 g, 6 mmol, 83% yield) as a yellow solid. MS (ESI pos. ion) m/z: 270 (MH+). Calc'd exact mass for C10H5ClFN3O3: 269. 1HNMR (SOO MHZ5 CDCI3): 7.14 (s, IH), 7.43 (s, IH), 8.14 (s, 2H), 8.55 (s, IH).
Figure imgf000165_0002
Step 2: N-(6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-yl)pyrrolidine-l-carboxamide. 4- chloro-6-(2-fluoro-4-nitrophenoxy)pyrimidine (0.300 g, 1 mmol) was mixed with ammonium hydroxide (3 ml, 77 mmol) in a microwave vial. The resulting mixture was capped, and then placed into a CEM microwave for 10 minutes at 90 0C, while 40 Watts of energy was supplied via Powermax. The mixture was diluted with water and stirred an additional 20 minutes. The precipitate was collected by filtration and washed with hexanes. The solid was dried in a reduced-pressure oven overnight to give desired product 6-(2-fluoro-4- nitrophenoxy)pyrimidin-4-amine (0.120 g, 0.5 mmol, 43% yield) as yellow solid, which was carried into the next step of the synthesis as crude material.
6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-amine (0.550 g, 2.2 mmol) was dissolved in tetrahydrofuran (10 ml). Then triethylamine (0.61 ml, 4.4 mmol) was added to the mixture with stirring. Then phenyl chloroformate (0.55 ml, 4.4 mmol) was added slowly to the mixture. The mixture was stirred at ambient temperature for 1.5 hours. Then pyrrolidine (1.8 ml, 22 mmol) was added to the mixture, and the mixture was stirred an additional 30 minutes. The mixture was diluted with sat. ammonium chloride and dichloromethane and stirred an additional 10 minutes. The organic layer was collected by extracting with dichloromethane (3 x 10 ml). Combined organic layer was dried over sodium sulfate, filtered, and concentrated in- vacuo. The crude was purified by chromatography (Amino-Propyl silica gel column) in a gradient of 1-5% MeOH/ dichloromethane to give an oil. The oil was recrystallized from dichloromethane/hexanes to give the desired product N-(6-(2-fluoro-4- nitrophenoxy)pyrimidin-4-yl)pyrrolidine-l-carboxamide (0.330 g, 0.95 mmol, 43% yield) as a yellow solid. MS (ESI pos. ion) m/z: 348 (MH+). Calc'd exact mass for C15H14FN5O4: 347. INMR (300 MHz, CDCl3): 1.94 (s, 4H), 3.37-3.49 (m, 4H), 5.23 (s, IH), 7.09-7.21 (m, IH),
7.29-7.38 (m, IH), 7.99-8.09 (m, 2H), 8.25 (d, J=0.73 Hz, IH).
Figure imgf000166_0001
Step 3: N-(6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl)pyrrolidine-l-carboxamide. N-
(6-(2-fluoro-4-nitrophenoxy)pyrimidin-4-yl)pyrrolidine-l-carboxamide (0.320 g, 0.921 mmol) was dissolved in a mixture of 3:1 ethanol/water (8 ml). Then iron (0.276 g, 4.95 mmol) and ammonium chloride (0.0281 g, 0.525 mmol) was added to the mixture with stirring. The mixture was placed in a pre-heated oil bath (80 0C) for 1 hour. The oil bath was removed to allow the mixture to cool to ambient temperature. The mixture was filtered through a filter diskette. The flask was rinsed with methanol (3 x 10 ml) and filtered through diskette. Combined organic solution was concentrated in- vacuo. Then water was added to the mixture with stirring. The precipitate was collected by filtration and washed with hexanes. The solid was dried in a reduced-pressure oven to give the desired product N-(6-(4-amino-2- fluorophenoxy)pyrimidin-4-yl)pyrrolidine-l-carboxamide (0.240 g, 0.756 mmol, 82% yield) as a yellow solid. MS (ESI pos. ion) m/z: 318 (MH+). Calc'd exact mass for C15H16FN5O2: 317. 1HNMR (300 MHz, CDCl3): 1.91-2.05 (s, 4H), 3.41-3.54 (t, 4H), 6.41-6.52 (m, 2H), 6.92-7.01 (t, IH), 7.21 (s, IH), 7.63 (s, IH), 8.36 (s, IH).
Figure imgf000166_0002
2006/016344
Step 4: N-(3-flouro-4-(6-(pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)phenyl)-l-(2- hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide. l-(2-hydroxy-2-methylpropyl)5-methyl-3-oxo-2-phenyl-2,3-d.ihydro-lH- ρyrazole-4-carboxylic acid (0.230 g, 0.792 mmol) was dissolved in dichloromethane (10 ml). Then DMF (0.5 ml) was added to the mixture while stirring. Then N-(6-(4-amino~2- fluorophenoxy)pyrimidin-4-yl)pyrrolidine-l-carboxamide (0.277 g, 0.871 mmol), along with TEA (0.33 ml, 2.38 mmol) was added to the mixture and stirred 5 minutes at ambient temperature. Then HATU (0.301 g, 0.792 mmol) was added into the mixture in one portion. The resulting mixture was allowed to stir under inert atmosphere for 3 hours. The reaction was monitored by LC/MS, which confirmed completion. The mixture was diluted with dichloromethane and water and with 4:1 dichloromethane /methanol (3 x 20 ml). Combined organic layer was dried over sodium sulfate, filtered, and concentrated in- vacuo. The crude was purified by chromatography (Amino-Propyl silica gel column, in a gradient of 1-5% MeOH/ dichloromethane to give an oil. The oil was recrystallized from dichloromethane/hexanes to give the desired product N-(3-flouro-4-(6-(pyrrolidine-l - carboxamido)pyrimidin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide (0.330 g, 0.56 mmol, 70% yield) as a white solid. MS (ESI pos. ion) m/z: 590 (MH+). Calc'd exact mass for C30H32FN7O5: 589. 1HNMR (300 MHz, CDCl3): 1.05 (s, 6H), 1.91 (s, 4H), 2.21 (s, IH), 2.78 (s, 3H), 3.40 (s, 4H), 3.78 (s, 2H), 7.01-7.22 (m, 4H), 7.31-7.48 (m, 2H), 7.59 (s, IH), 7.79 (dd, J=12.42, 2.19 Hz, IH), 8.26 (s, IH), 10.75 (s, IH).
Example 154
Figure imgf000167_0001
N-(3-fluoro-4-(6-(pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)phenyl)-5-methyl-3-oxo- 2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 560 (MH+). Calc'd exact mass for C29H30FN7O4: 559. 1HNMR (SOO MHZ5 CDCI3): 0.80 (t, J=7.38 Hz, 3H), 1.61 (s, 4H), 1.99 (s, 4H), 2.80 (s, 3H), 3.49 (s, 4H), 3.74 (t, J=7.16 Hz, 2H), 7.11 (t, J=8.55 Hz, IH), 7.34 (s, IH), 7.37 (d, J=I.32 Hz, IH), 7.47 (d, J=7.31 Hz, IH), 7.55 (t, J=7.38 Hz, 2H), 7.69 (s, IH), 7.86 (dd, J= 12.42, 2.34 Hz, IH), 8.35 (s, IH), 10.81 (s, IH). Example 155
Figure imgf000168_0001
N-(6-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyrimidin-4-yl)morpholine-4-carboxamide: MS (ESI pos. ion) m/z: 532 (MH+). Calc'd exact mass for C27H26FN7O4: 531. 1HNMR (SOO MHZ5 CDCI3): 2.71 (S, 2H), 3.28 (s, 2H), 3.37-3.46 (m, 3H), 4.05 (q, J-7.06 Hz, 4H), 7.05 (d, J=8.48 Hz, 2H), 7.16-7.21 (m, 2H), 7.26-7.31 (m, 2H), 7.36-7.51 (m, 2H), 8.35 (s, IH), 10.81 (s, IH).
Example 156
Figure imgf000168_0002
N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidin-4-yl)morpholine-4-carboxamide: MS (ESI pos. ion) m/z: 576 (MH+). Calc'd exact mass for C29H30FN7O5: 575. 1NMR (SOO MHZ5 CDCB): 0.80 (s, 3H), 1.26 (s, IH), 1.62 (s, 4H), 2.80 (s, 4H)5 3.53 (s, 5H), 3.75 (s, 3H), 7.11 (s, IH), 7.26 (s, 2H), 7.55 (s, 5H)5 7.84 (s, IH), 8.36 (s, IH)5 10.83 (s, IH).
Example 157
Figure imgf000168_0003
N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidin-4-yl)piperidine-l-carboxamide: MS (ESI pos. ion) m/z: 574 (MH+). Calc'd exact mass for C30H32FN7O4: 573. 1NMR (300 MHz, CDC13): 0.80 (t, J=7.45 Hz5 3H)5 1.38-1.59 (m, 2H)5 1.65 (s, 8H)5 2.80 (s, 3H)5 3.49 (d, J= 5.26 Hz5 4H)5 3.74 (t, J= 7.31, 2H), 7.11 (t, J=8.55 Hz, IH), 7.23-7.29 (m, IH), 7.41-7.62 (m, 4H), 7.86 (dd, J=12.50, 2.27 Hz, IH), 8.35 (s, IH), 10.81 (s, IH).
Example 158
Figure imgf000169_0001
N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidin-4-yl)-4-methylpiperazine-l-carboxamide: MS (ESI pos. ion) m/z: 589 (MH+). Calc'd exact mass for C30H33FN8O4: 588. 1NMR (SOO MHZ5 CDCIS): 0.79 (t, J=7.38 Hz, 3H), 1.43-1.56 (m, J=7.31 Hz, 2H), 2.35 (s, 3H), 2.48 (s, 4H), 2.80 (s, 3H), 3.57 (s, 4H), 3.75 (t, J=7.31 Hz, 2H), 5.28-5.34 (m, IH), 7.11 (t, J=8.55 Hz, IH), 7.22-7.30 (m, 2H), 7.32-7.62 (m, 3H), 7.86 (dd, J=12.42, 2.34 Hz, IH), 8.35 (s, IH), 10.83 (s, IH).
Example 159
Figure imgf000169_0002
(R)-N-(4-(6-(3-(dimethylamino)pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)-3- fluorophenyl)-5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamide: MS (ESI pos. ion) m/z: 603 (MH+). Calc'd exact mass for C31H35FN8O4: 602. 1NMR (300 MHz, CDC13): 0.79 (t, J=7.45 Hz, 3H), 1.43-1.56 (m, 2H), 2.25-2.32 (m, 6H), 2.79 (s, 4H), 3.24 (s, IH), 3.47 (s, 3H), 3.62-3.80 (m, 4H), 5.30 (s, IH), 7.11 (t, J=8.55, IH), 7.32-7.38 (m, 2H), 7.43-7.56 (m, 3H), 7.58 (s, IH), 7.83 (s, IH), 8.34 (s, IH), 10.83 (s, IH). 16344
Example 160
Figure imgf000170_0001
(R)-N-(4-(6-aminopyrimidin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 479 (MH+). Calc'd exact mass for C24H23FN6O4: 478. 1NMR (SOO MHZ5 CDCB): 0.98 (d, J=5.99 Hz, 3H), 2.72 (s, 3H), 3.45-3.58 (m, IH), 3.67-3.85 (m, 2H), 4.96 (s, 2H), 5.23 (s, IH), 5.78 (s, IH), 7.00-7.20 (m, 3H), 7.31-7.49 (m, 3H), 7.76 (dd, J=12.50, 2.12 Hz, IH), 8.14 (s, IH)5 10.75 (s, IH). Example 161
TEA
Figure imgf000170_0003
Figure imgf000170_0002
Figure imgf000170_0004
Figure imgf000170_0005
N-(3-fluoro-4-(2-(pyrrolidine-l-carboxamido)pyridin-4-yloxy)phenyl)-l,5-dimethyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide
Figure imgf000171_0001
Step 1: 4-(2-fluoro-4-nitrophenoxy)pyridin-2-amine. 4-chloropyridin-2-amine (0.500 g, 3.9 mmol) was added to a microwave vial, along with l-niethyl-2-pyrrolidinone (1 ml, 10 mmol). The mixture was stirred into a homogeneous mixture, then 2-fluoro-4-nitrophenol (1.2 g, 7.8 mmol) was added to the mixture. After 2 minutes of stirring, cone. HCl (4 drops) was added to the mixture. The capped vial was placed into a CEM microwave for 25 minutes at 140 0C, while 60 Watts of power was supplied via Powermax. The mixture was transferred to a round bottomed flask, and warm ethyl acetate was added with stirring. Then cone. HCl was added dropwise into the mixture to form HCl salt. The precipitate was collected by filtration and washed with hexanes to give desired product 4-(2-fluoro-4-nitrophenoxy)pyridin-2-amine (0.480 g, 1.9 mmol, 50% yield) as a beige solid. MS (ESI pos. ion) m/z: 250 (MH+). Calc'd exact mass for C11H8ClFN3O3: 249. 1HNMR (300 MHz, CD3OD): 1.17 (t, J=7.31 Hz, IH), 3.02 (m, IH), 6.19 (d, J=2.19 Hz, IH), 6.59 (dd, J=7.23, 2.41 Hz, IH), 7.48-7.57 (m, IH), 7.71-7.79 (m, IH), 8.08-8.23 (m, 2H).
Figure imgf000171_0002
Step 2: N-(4-(2-fluoro-4-nitrophenoxy)pyridin-2-yl)pyrrolidine-l-carboxamide. 4-(2- fluoro-4-nitrophenoxy)pyridin-2-amine(0.150 g, 0.60 mmol) was dissolved in THF (10 ml). Then triethylamine (0.17 ml, 1.2 mmol) was added to the mixture while stirring. Then phenyl chloroformate (0.15 ml, 1.2 mmol) was added to the mixture dropwise. The mixture was stirred at ambient temperature for 1.5 hours. Then pyrrolidine (0.50 ml, 6.0 mmol) was added to the mixture and stirred an additional 30 minutes. The mixture was diluted with sat. ammonium chloride (10 ml) and dichloromethane (10 ml) and stirred 10 minutes and was collected by extracted with dichloromethane (3 x 10 ml). The organic layer was dried over sodium sulfate, filtered, and concentrated in- vacuo. The crude was purified by chromatography (Amino-Propyl silica gel column) in a gradient of 1-5% MeOH/ dichloromethane to give the desired product N-(4-(2-fluoro-4-nitrophenoxy)pyridin-2- yl)pyrrolidine-l-carboxamide (0.184 g, 0.53 mmol, 88% yield) as tan oil. MS (ESI pos. ion) m/z: 347 (MH+). Calc'd exact mass for C16H15FN4O4: 346. 1HNMR (SOO MHZ5 CDCI3 ): 1.96 (s, 4H), 3.44 (t, J=6.65 Hz, 4H), 6.81-6.96 (m, 2H)5 8.06-8.18 (m, 4H).
Figure imgf000172_0001
Step 3: N-(4-(4-amino-2-fluorophenoxy)pyridin-2-yl)pyrrolidine-l-carboxamide. N-(4- (2-fluoro-4-nitrophenoxy)pyridin-2-yl)pyrrolidme- 1 -carboxamide (0.180 g, 0.52 mmol) was dissolved in a mixture of 3:1 ethanol/water (4 ml) with stirring. Then iron (0.160 g, 2.8 mmol) and ammonium chloride (0.016 g, 0.30 mmol) was added to the mixture. The mixture was placed in a pre-heated oil-bath (80 0C) for 1 hour. The oil bath was removed, and the mixture was allowed to cool to ambient temperature. The mixture was filtered through filter diskette. The flask was rinsed with methanol (3 x 10 ml), and the combined filtrate was evaporated in- vacuo. The residue was diluted with dichloromethane and IN NaOH (2 ml). The organic were extracted with dichloromethane (3 x 10 ml), dried over sodium sulfate, filtered and concentrated in vacuo, to give the desired product N-(4-(4-amino-2-fluorophenoxy)pyridin-2- yl)pyrrolidine-l -carboxamide (0.125 g, 0.4 mmol, 76 % yield) as a tan oil. MS (ESI pos. ion) m/z: 317 (MH+). Calc'd exact mass for C16H17FN4O2: 316. 1HNMR (SOO MHZ5 CDCI3): 1.96 (s, 4H)5 3.44 (s5 4H)5 6.52 (d, J=3.07 Hz, 2H)5 6.96 (s5 IH)5 7.26 (s, 1 H), 7.67 (s, IH), 8.01 (d, J=5.70 Hz5 IH).
Figure imgf000172_0002
Step 4: N-(3-fluoro-4-(2-(pyrroUdine-l-carboxamido)pyridin-4-yloxy)phenyl)-l,5- dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide. The title compound was prepared following the previously described procedure. MS (ESI pos. ion) m/z: 531 (MH+). Calc'd exact mass for C28H27FN6O4: 530. 1HNMR (SOO MHZ5 CDCI3): 1.70 (S, IH), 1.88 (s, 4H), 2.69-2.75 (m, 3H), 3.29 (s, 3H)5 3.37 (t, J=6.58 Hz, 4H), 6.41 (dd, J=5.70, 2.34, IH)5 6.92 (s, IH)5 7.02 (t5 J=8.70, IH), 7.17 (ddd, J=8.84, 2.34, 1.24 Hz, IH), 7.26-7.32 (m, 2H)5 7.37-7.52 (m, 2H), 7.67 (d, J=2.34, IH), 7.80 (dd, J=12.575 2.34, IH)5 7.94 (d, J=5.85, IH), 10.75 (s, IH). Example 162
Figure imgf000173_0001
N-(4-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyridin-2-yl)piperidine-l-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass for C29H29FN6O4: 544. 1HNMR (SOO MHZ5 CDCI3): 1.61 (S, 5H), 1.74 (s, IH), 2.79 (s, 3H), 3.37 (s, 3H), 3.45 (d, J=5.46 Hz, 4H), 6.49 (td, J=6.36, 1.79 Hz, IH), 7.09 (t, J=8.76 Hz, IH), 7.34-7.39 (m, 2H), 7.44-7.66 (m, 4H), 7.86 (dd, J=12.43, 2.26 Hz, IH), 7.95-8.04 (m, IH), 10.81 (s, IH).
Example 163
Figure imgf000173_0002
CR)-N-(4-(2-(3-(dimethylamino)pyrrolidine-l-carboxamido)pyridm-4-yloxy)-3- fluorophenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 574 (MH+). Calc'd exact mass for C30H32FN7O4: 573. 1HNMR (SOO MHz, CDCl3): 1.62 (s, 5H), 2.27 (s, 5H), 2.79 (s, 3H), 3.20 (t, J=9.14 Hz, IH), 3.37 (s, 2H), 3.41 (dd, J=10.17, 3.20 Hz, IH)5 3.65 (s, IH)5 6.49 (dd, J=5.84, 2.26 Hz5 IH)5 6.97 (s, IH)5 7.09 (t, J=8.76 Hz5 IH)5 7.21-7.25 (m, IH)5 7.34-7.39 (m, 2H), 7.44-7.59 (m, IH)5 7.72 (d5 J=2.07 Hz5 IH)5 7.87 (dd, J-12.62, 2.26, Hz, IH), 8.02 (d, J=5.84 Hz, IH), 10.81 (s, IH).
Example 164
Figure imgf000173_0003
N-(3-fluoro-4-(2-(pyrrolidine-l-carboxamido)pyridin-4-yloxy)phenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 589 (MH+). Calc'd exact mass for C31H33FN6O5: 588. 1HNMR (SOO MHz, CDCl3): 1.12 (s, 6H), 1.95 (s, 4H), 2.20 (s, IH), 2.86 (s, 3H), 3.38-3.53 (m, 4H), 3.86 (s, 2H), 5.30 (s, 2H), 6.48 (dd, J=5.55, 2.05 Hz, IH), 7.01-7.13 (m, 2H), 7.19-7.32 (m, IH), 7.39- 7.57 (m, 3H), 7.73 (d, J=2.05 Hz, IH), 7.87 (dd, J=12.50, 2.12 Hz, IH), 8.00 (d, J=5.70 Hz, IH), 10.82 (s, IH).
Example 165
Figure imgf000174_0001
N-(3-fluoro-4-(2-(pyrrolidine-l-carboxamido)pyridin-4-yloxy)phenyl)-5-methyl-3-oxo-2- phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 559 (MH+). Calc'd exact mass for C30H31FN6O4: 558. 1HNMR (SOO MHZ5 CDCI3): 0.80 (t, J=7.45 Hz, 3H), 1.58 (s, 2H), 1.95 (s, 4H), 2.80 (s, 3H), 3.41-3.48 (m, 4H), 3.72-3.78 (m, 2H), 6.96 (s, IH), 7.09 (s, IH), 7.33-7.38 (m, 2H), 7.46 (s, IH), 7.52-7.59 (m, IH), 7.74 (d, J=2.19 Hz, IH), 8.02 (d, J=5.85 Hz, IH), 10.82 (s, IH).
Example 166
Figure imgf000174_0002
N-(4-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyridin-2-yl)morpholine-4-carboxamide: MS (ESI pos. ion) m/z: 547 (MH+). Calc'd exact mass for C28H27FN6O5: 546. 1HNMR (SOO MHZ5 CDCI3): 2.79 (S, 3H), 3.37 (s, 3H), 3.43-3.52 (m, 4H), 3.66-3.76 (m, 4H), 6.51 (dd, J=5.85, 2.19 Hz, IH), 7.09 (t, J=8.70 Hz, IH), 7.20-7.25 (m, IH), 7.33-7.40 (m, 2H), 7.44-7.64 (m, 4H), 7.88 (dd, J=12.57, 2.48 Hz, IH), 8.02 (d, j=5.70 Hz, IH)5 10.83 (s, IH). 6 016344
Example 167
Figure imgf000175_0001
N-(4-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro- lH-pyrazole-4-carboxamido)phenoxy)pyridin-2-yl)piperidine-l-carboxamide: MS (ESI pos. ion) m/z: 603 (MH+). CaIc' d exact mass for C32H35FN6O5: 602. 1HNMR (SOO MHZ, CDCl3): 1.12 (s, 6H), 1.61 (s, 6H), 2.28 (s, IH), 2.86 (s, 3H), 3.44 (d, J=4.97 Hz, 4H), 3.86 (s, 2H), 5.30 (s, IH), 6.46 (dd, J=5.77, 2.12 Hz, IH), 7.08 (t, J=8.70 Hz, IH), 7.21 (d, J=1.02 Hz, IH), 7.27 (t, J=8.18 Hz, IH), 7.40-7.57 (m, 3H), 7.65 (d, J=1.90 Hz, IH), 7.87 (dd, J=12.64, 2.27 Hz, IH), 8.00 (d, J=5.85 Hz, IH), 10.82 (s, IH).
Example 168
Figure imgf000175_0002
Figure imgf000175_0003
44
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)methyl)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide
Figure imgf000176_0001
Step 1: 7-methoxy-4-(phenylthio)quinoline. In a 25 mL sealed tube under N2> were dissolved 4-chloro-7-methoxyquinoline (1.00 g, 5.16 mmol), thiophenol (0.528 ml, 5.16 mmol) and cesium carbonate (2.52 g, 7.75 mmol) in 5 mL of DMSO then heated at 100 0C. After 2h, the crude reaction mixture was directly purified by MPLC (ISCO, dichloromethane:MeOH 100:0 to 90:10) to afford 7-methoxy-4-(phenylthio)quinoline (1.32 g, 95.6% yield) as an off- white solid. MS (ESI pos. ion) m/z: 268 (MH+). Calc'd exact mass for C16H13NOS: 267. 1H NMR (400 MHz, CDCl3): 8.49 (d, J=4.93 Hz, 1 H), 8.13 (d, J=9.22 Hz, 1 H), 7.56 - 7.62 (m, 2 H), 7.45 - 7.53 (m, 4 H), 7.23 - 7.29 (m, 1 H), 6.68 (d, J=4.93 Hz, 1 H), 3.98 (s, 3 H).
Figure imgf000176_0002
Step 2. 7-methoxy-4-(phenylsulfinyl)quinoline. In a 50 mL round bottom flask under N2) was dissolved 7-methoxy-4-(phenylthio)quinoline (1.38 g, 5.16 mmol) in 50 mL of dichloromethane then cooled to -78 0C. Solid rø-CPBA (77%) (1.25 g, 7.23 mmol) was added potionwise to the reaction, and the mixture was warmed slowly over 3 h to rt. After 3 h, the reaction mixture was diluted with dichloromethane and then neutralized with aqueous NaHCO3 (sat.). The aqueous phase was extracted three times with dichloromethane, and then the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude mixture was purified by MPLC (ISCO. DCM:MeOH 100:0 to 90: 10) to afford 7-methoxy-4- (phenylsulfinyl)quinoline (1.37 g, 93.7% yield) as an off-white foam. MS (ESI pos. ion) m/z: 284 (MH+). Calc'd exact mass for C16H13NO2S: 283.
Figure imgf000176_0003
Step 3. (4-bromophenyl)(7-methoxyquinolin-4-yl)methanol. hi a 100 mL round bottom flask under N2, was dissolved 7-methoxy-4-(phenylsulfinyl)quinoline (650 mg, 2.29 mmol) in 10 mL of THF and then the solution was cooled to -78 0C and treated with PhMgBr (3M in Et2O) (1.50 mL, 4.59 mmol). The reaction mixture was then warmed to rt. After 30 min, the mixture was cooled again to -78 0C, and solid 4-bromobenzaldehyde (1.27 g, 6.88 mmol) was added. Then, the reaction mixture was warmed to rt. After 2h the reaction mixture was neutralized with aqueous NH4Cl (sat.). The aqueous phase was extracted three times with dichloromethane, and then the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude mixture was purified by MPLC (ISCO dichloromethane:MeOH 100:0 to 90:10) to afford (4-bromophenyl)(7-methoxyquinolm-4- yl)methanol (540 mg, 68.4% yield) as a yellow solid. MS (ESI pos. ion) m/z: 345 (M2H+). Calc'd exact mass for C17Hi4BrNO2: 343. 1H NMR (400 MHz, CDCl3) 8.83 (d, J=4.42 Hz, 1 H)5 7.81 (d, J=9.35 Hz, 1 H)5 7.53 (d, J=4.42 Hz5 1 H)5 7.44 - 7.49 (m, 3 H)5 7.25 (d5 J=8.34 Hz, 2 H)5 7.14 (dd, J=9.28, 2.59 Hz, 1 H)5 6.43 (s, 1 H)5 3.93 (s, 3 H).
Figure imgf000177_0001
Step 4: (4-aminophenyl)(7-methoxyquinolin-4-yl)methanol. hi a 25 mL sealed tube under N2, were dissolved Pd2(dba)3 (84 mg, 92 μmol), t-Bu3P (IM in PIiMe) (92 μl, 92 μmol), (4- bromophenyl)(7-methoxyquinolin-4-yl)methaiiol (316 mg, 918 μmol) and LiHMDS (IM in THF) (2.75 mL, 2.75 mmol) in 3.5 mL of toluene and the solution was then heated at 80 0C. After 3h, the crude reaction mixture was neutralized by adding 5 drops of MeOH and then directly purified by MPLC (ISCO5 dichloromethane:MeOH 100:0 to 90:10) to afford (4- aminophenyl)(7-methoxyquinolin-4-yl)methanol (140 mg, 54% yield). MS (ESI pos. ion) m/z: 281 (MH+). Calc'd exact mass forC17H16N202: 280.
Figure imgf000177_0002
Step 5 : N-(4-((S)-hydroxy(7-(methyIoxy)-4-quinolinyl)methyl)phenyl)-5-methyl-3-oxo-2- phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4-carboxamide. In a 10 mL sealed tube under N2, were dissolved HATU (250 mg, 658 μmol), (4-aminophenyl)(7-methoxyquinolin-4- yl)methanol (123 mg, 439 μmol), 5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH- pyrazole-4-carboxylic acid (143 mg, 548 μmol) and K2CO3 (182 mg, 1316 μmol) in 2 mL of DMF at rt. After 1O h, the reaction mixture was heated at 600C for 3h and then diluted with dichloromethane, and treated with aqueous NaOH (IN). The aqueous phase was extracted with dichloromethane, and then the organic layer was dried over Na2SO4, filtered and concentrated 006/016344 under reduced pressure. The crude mixture was purified by MPLC (ISCO, dichloromethane:MeOH 100:0 to 90:10) to afford N-(4-(hydroxy(7-methoxyquinolin-4- yl)methyl)ρhenyl)-5-methyl-3 -oxo-2-phenyl-l -propyl-2,3 -dihydro- 1 H-pyrazole-4- carboxamide (208 mg, 90.7% yield) as an off-white solid. MS (ESI pos. ion) m/z: 523 (MH+). Calc'd exact mass for C31H30N4O4: 522. 1H NMR (400 MHz, DMSO-J6) 10.67 (s, 1 H), 8.83 (d, J=4.55 Hz, 1 H), 8.05 (d, J=9.35 Hz, 1 H), 7.53 - 7.61 (m, 3 H), 7.46 - 7.52 (m, 3 H), 7.36 - 7.44 (m, 3 H), 7.31 (d, J=8.59 Hz, 2 H), 7.16 (dd, J=9.16, 2.72 Hz, 1 H), 6.32 (d, J=4.42 Hz, 1 H), 6.15 (d, J=4.29 Hz, 1 H), 3.88 (s, 3 H), 3.79 (t, J=7.20 Hz, 2 H), 2.71 (s, 3 H), 1.33 - 1.41 (m, 2 H)5 0.66 (t, J=7.39 Hz, 3 H).
Figure imgf000178_0001
Step 6: 5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)methyl)phenyl)-3-oxo-2-phenyl-l- propyl-2,3-dihydro-lH-pyrazole-4-carboxamide. In a 25 mL round bottom flask was dissolved N-(4-(hydroxy(7 -methoxyquinolin-4-yl)methyl)phenyl)-5-methyl-3-oxo-2-phenyl-l- propyl-2,3 -dihydro- lH-pyrazole-4-carboxamide (104 mg, 199 μmol) in 4 mL of formic acid and the resultant was then treated with zinc dust (325 mg, 4975 μmol) and heated at 60 0C. After 6h the reaction mixture was diluted with ethyl acetate, filtered over Celite and neutralized with aqueous NaHCO3 (sat.). The aqueous phase was extracted with ethyl acetate, and then the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude mixture was purified by MPLC (ISCO, dichloromethane: 1% NH4OH in MeOH, 100:0 to 90: 10) to afford N-(4-((7-methoxyquinolin-4-yl)methyl)phenyl)-5-methyl-3- oxo-2 -phenyl- 1 -propyl-2,3 -dihydro- lH-pyrazole-4-carboxamide (25 mg, 25% yield) as an off- white solid. MS (ESI pos. ion) m/z: 507 (MH+). Calc'd exact mass for C31H30N4O3: 506. 1H NMR (400 MHz, DMSO-J6) 10.65 (s, 1 H), 8.74 (d, J=4.42 Hz, 1 H), 8.10 (d, J=9.22 Hz, 1 H), 7.57 (t, J=7.52 Hz, 2 H), 7.46 - 7.52 (m, 3 H), 7.35 - 7.44 (m, 3 H), 7.14 - 7.28 (m, 4 H), 4.38 (s, 2 H), 3.90 (s, 3 H), 3.79 (t, J=7.14 Hz, 2 H), 2.72 (s, 3 H), 1.32 - 1.41 (m, 2 H), 0.66 (t, J=7.39 Hz, 3 H). 6 016344
Example 169
Figure imgf000179_0001
N-(4-(hydroxy(7-methoxyquinolin-4-yl)methyl)phenyl)-5-methyl-3-oxo-2-phenyl-l- propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 523 (MH+). Calc'd exact mass for C31H30N4O4: 522. 1H NMR (400 MHz, DMSO-J6) 10.67 (s, 1 H), 8.83 (d, J-4.55 Hz, 1 H), 8.05 (d, J=9.35 Hz, 1 H), 7.53 - 7.61 (m, 3 H), 7.46 - 7.52 (m, 3 H), 7.36 - 7.44 (m, 3 H), 7.31 (d, J=8.59 Hz, 2 H), 7.16 (dd, J=9.16, 2.72 Hz, 1 H), 6.32 (d, J=4.42 Hz, 1 H), 6.15 (d, J=4.29 Hz, 1 H), 3.88 (s, 3 H)5 3.79 (t, J=7.20 Hz, 2 H), 2.71 (s, 3 H), 1.33 - 1.41 (m, 2 H), 0.66 (t, J-7.39 Hz, 3 H).
Example 170
Figure imgf000179_0002
l,5-dimethyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyrimidinyl)-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 483 (MH+). Calc'd exact mass forC26H22N6O4: 482.
Example 171
Figure imgf000179_0003
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)sulfinyl)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 541 (MH+). Calc'd exact mass for C30H28N4O4S: 540. 1H NMR (400 MHz, DMSO-J6 + CDCl3) 10.90 (s, 1 H), 9.06 (d, J=4.55 Hz, 1 H), 8.02 (d, J=9.09 Hz, 1 H), 7.97 (d, J=4.42 Hz, 1 H), 7.65 - 7.74 (m, 4 H), 7.55 (t, J=7.58 Hz, 2 H), 7.44 - 7.51 (m, 2 H), 7.37 (d, J=7.45 Hz, 2 H), 7.28 (dd, J=9.16, 2.46 Hz, 1 H), 3.90 (s, 3 H), 3.79 (t, J=I 26 Hz, 2 H), 2.70 (s, 3 H), 1.32 - 1.44 (m, 2 H), 0.67 (t, J=7.39 Hz, 3 H).
Example 172
Figure imgf000180_0001
l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)thio)phenyl)- 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 555 (MH+). Calc'd exact mass for C31H30N4O4S: 554.
Example 173
Figure imgf000180_0002
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)thio)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 525 (MH+). Calc'd exact mass for C30H28N4O3S: 524. 1H NMR (400 MHz, DMSO-4): 10.96 (s, 1 H), 8.53 (d, J=4.80 Hz, 1 H), 8.07 (d, J=9.22 Hz, 1 H), 7.79 (d, J=8.46 Hz, 2 H), 7.55 - 7.63 (m, 4 H), 7.52 (t, J=7.20 Hz, 1 H), 7.37 - 7.47 (m, 3 H), 7.32 (dd, J=9.09, 2.27 Hz, 1 H), 6.61 (d, J=4.80 Hz, 1 H), 3.93 (s, 3 H), 3.83 (t, J=7.07 Hz, 2 H), 2.75 (s, 3 H), 1.31 - 1.47 (m, 2 H), 0.69 (t, J=7.39 Hz, 3 H).
Example 174
Figure imgf000180_0003
5-methyl-N-(3-((7-(methyloxy)-4-quinolinyl)oxy)propyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 475 (MH+). Calc'd exact mass forC27H30N4O4: 474. Example 175
Figure imgf000181_0001
5-methyl-N-(trans-4-((7-(methyloxy)-4-quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-l- propyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 515 (MH+). Calc'd exact mass for C30H34N4O4: 514. 1H NMR (400 MHz, DMSO-4) 8.61 (d, J=5.31 Hz, 1 H), 8.56 (d, J=7.83 Hz, 1 H), 8.03 (d, J=9.09 Hz, 1 H), 7.56 (t, J=7.64 Hz, 2 H), 7.47 (t, J=7.20 Hz, 1 H), 7.38 (d, J=7.58 Hz, 2 H), 7.30 (d, J=2.40 Hz, 1 H), 7.11 - 7.21 (m, 1 H), 6.96 (d, J=5.31 Hz, 1 H), 4.66 - 4.78 (m, 1 H), 3.89 (s, 3 H), 3.81 - 3.95 (m, 1 H), 3.74 (t, J=7.20 Hz, 2 H), 2.68 (s, 3 H), 2.11 (d, J=10.11 Hz, 2 H), 1.99 (d, J=12.25 Hz, 2 H), 1.60 - 1.75 (m, 2 H), 1.40 - 1.52 (m, 2 H), 1.29 - 1.39 (m, 2 H), 0.66 (t, J=7.45 Hz, 3 H).
Example 176
Figure imgf000181_0002
5-methyl-N-(cis-4-((7-(methyloxy)-4-quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-l-propyl- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) ni/z: 515 (MH+). Calc'd exact mass forC30H34N4O4: 514.
Example 177
Figure imgf000181_0003
l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(trans-4-((7-(methyloxy)-4-quinolinyl)oxy) cyclohexyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 545 (MH+). Calc'd exact mass forC3 ^36N4O5: 544. 1H NMR (400 MHz, DMSO-J6): 8.61 (d, J=5.18 Hz, 1 H), 8.58 (d, J=7.83 Hz, 1 H), 8.03 (d, J=8.97 Hz, 1 H), 7.53 (t, J-7.71 Hz, 2 H), 7.41 (t, J=7.26 Hz, 1 H), 7.26 - 7.31 (m, 3 H), 7.17 (dd, J=9.16, 2.46 Hz, 1 H), 6.96 16344
(d, J=5.56 Hz5 1 H)5 4.77 (s, 1 H)5 4.68 - 4.78 (m, 1 H), 3.89 (s, 3 H), 3.85 - 3.92 (m, 1 H), 3.78 (s, 2 H), 2.73 (s, 3 H)5 2.12 (d, J=13.64 Hz5 2 H), 1.99 (d, J=13.52 Hz, 2 H)5 1.61 - 1.75 (m, 2 H)5 1.37 - 1.52 (m, 2 H)5 0.93 (s, 6 H).
Example 178
Figure imgf000182_0001
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 508 (MH+). Calc'd exact mass for C30H29N5O3: 507.
Example 179
Figure imgf000182_0002
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyrimidinyl)-3-oxo-2-phenyl-l-propyl- 2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 511 (MH+). Calc'd exact mass forC28H26N6O4: 510. 1H NMR (400 MHz, DMSO-J6+ CDCl3) 11.45 (s, 1 H), 8.74 (s, 2 H), 8.63 (d, J=4.93 Hz, 1 H)5 8.23 (d, J=9.22 Hz5 1 H)5 7.60 (t, J=7.20 Hz, 2 H), 7.48 - 7.55 (m, 1 H), 7.40 - 7.47 (m, 3 H), 7.31 (d, J=8.46 Hz, 1 H)5 6.65 (d, J=5.05 Hz5 1 H)5 3.94 (s, 3 H), 3.83 (t, J=6.51 Hz, 2 H), 2.75 (s, 3 H)5 1.34 - 1.48 (m, 2 H)5 0.70 (t, J=7.14 Hz5 3 H).
Example 180
Figure imgf000182_0003
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-l-(2-hydroxy-2-methylpropyl)- 5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 556 (MH+). Calc'd exact mass for C31H30FN5O4: 555. 16344
Example 181
Figure imgf000183_0001
l-(2-hydroxy-2-methylpropyl)-5-methyl-4-((7-((7-(methyloxy)-4-quinolinyl)oxy)-2,3- dihydro-4H-l,4-benzoxazin-4-yl)carbonyl)-2-phenyl-l,2-dihydro-3H-pyrazol-3-one
MS (ESI pos. ion) m/z: 581 (MH+). Calc'd exact mass for C33H32N4O6: 580. 1H NMR (400 MHz, DMSO-J6) 8.58 (d, J=5.18 Hz, 1 H), 8.17 (d, J=9.09 Hz, 1 H), 7.76 (d, J=10.86 Hz, 1 H), 7.51 (t, J=7.77 Hz, 2 H), 7.40 (d, J=2.53 Hz, 1 H), 7.37 (t, J=7.45 Hz, 1 H), 7.28 (dd, J=9.22, 2.53 Hz, 1 H), 7.23 (d, J=7.33 Hz, 2 H), 6.82 (d, J=2.78 Hz, 1 H), 6.70 (dd, J=9.03, 2.59 Hz, 1 H), 6.47 (d, J=5.31 Hz, 1 H), 4.80 (s, 1 H), 4.31 (t, J=4.36 Hz, 2 H), 3.93 (s, 3 H), 3.89-3.96 (m, 2 H), 3.75 (s, 2 H), 2.54 (s, 3 H), 0.95 (s, 6 H).
Example 182
Figure imgf000183_0002
l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)amino) phenyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide: MS (ESI pos. ion) m/z: 538 (MH+). Calc'd exact mass for C31H31N5O4: 537.
Example 183
Figure imgf000183_0003
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-3-hydroxy-2-(l-oxoisoindolin-2- yl)propanamide: MS (ESI pos. ion) m/z: 518 (MH+). Calc'd exact mass for C28H24FN3O6: 517. 1H NMR (400 MHz, CHLOROFORM-d) 9.74 (1 H, s), 8.44 (1 H, d, J-5.3 Hz), 7.75 - 7.84 (2 H, m), 7.53 - 7.61 (2 H, m), 7.42 - 7.51 (2 H, m), 7.40 (1 H, s), 7.18 (1 H, t, J=8.6 Hz), 6 016344
6.35 (1 H5 d, J=5.3 Hz), 5.30 (3 H, s), 5.21 (1 H, t, J=5.4 Hz), 4.76 (2 H, s), 4.27 - 4.36 (1 H, m), 4.19 - 4.27 (1 H, m), 4.04 (6 H, s).
Example 184
Figure imgf000184_0001
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-(l-oxoisoindolin-2-yl)acetamide: MS (ESI pos. ion) m/z: 488 (MH+). Calc'd exact mass for C27H22FN3O5: 487. 1H NMR (400 MHz, CHLOROFORM-d) 9.26 (1 H, s), 8.46 (1 H, dd, J=5.3, 0.8 Hz), 7.90 (1 H, d, J=8.0 Hz), 7.76 (1 H, d, J=12.1 Hz), 7.62 (1 H, t, J=7.5 Hz), 7.47 - 7.58 (3 H, m). 7.41 (1 H, s), 7.24 (1 H, s), 7.17 (1 H, t, J=8.4 Hz), 6.36 (1 H, d, JhS. \ Hz), 4.67 (2 H, s), 4.46 (2 H, s), 4.04 (6 H, s). Example 185
HO.n.OH
Cu(OAc)2, sieves
Figure imgf000184_0002
pyridine, DCM
Figure imgf000184_0003
Figure imgf000184_0004
Figure imgf000184_0005
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxo-l,5-diphenyl-l,2- dihydropyridine-3-carboxamide
Figure imgf000185_0001
Step 1: methyl 54>romo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylate: A round bottom flask was charged with methyl 5-bromo-2-oxo-l,2-dihydropyridine-3-carboxylate (0.500 g, 2.2 mmol), phenylboronic acid (0.66 g, 5.4 mmol), and copper(II) acetate (0.78 g, 4.3 mmol). Dichloromethane (25 mL) was added, followed by 4A molecular sieves (500 mg, activated) and pyridine (0.70 mL, 8.6 mmol). The reaction mixture was stirred overnight at room temperature in the presence of air. The reaction mixture was diluted with dichloromethane and filtered through a small pad of Celite, washing well with dichloromethane. The filtrate was concentrated under vacuum. The remaining residue was purified by silica gel chromatography (1% methanol/dichloromethane) to give methyl 5- bromo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylate as a yellow foam/oil (0.655 g, 1.9 mmol, 89% yield). MS (ESI pos. ion) m/z: 309 (MH+). Calc'd exact mass for C13H10BrNO3: 308.
Figure imgf000185_0002
Step 2: 5-bromo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylic acid. Methyl 5-bromo- 2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylate (0.554 g, 1.80 mmol) was dissolved in dioxane (10.5 mL) then diluted with water (3.5 mL). 2N aqueous sodium hydroxide solution (0.944 ml, 1.89 mmol) was slowly added to the mixture. The reaction mixture was stirred at room temperature overnight, then concentrated under vacuum to remove the dioxane followed by dilution with water. This aqueous layer was acidified with IN aqueous hydrochloric acid (1.89 mL, 1.89 mmol). A precipitate formed was collected on a glass frit, and washed with minimal water. The solid was dissolved in dichloromethane and then dried over sodium sulfate. This mixture was filtered, and the filtrate was concentrated under vacuum. The remaining residue was dried under high vacuum to afford 5-bromo-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxylic acid as a yellow solid (0.458 g, 1.56 mmol, 86.6% yield). MS (ESI pos. ion) m/z: 295 (MH+). Calc'd exact mass for C12H8BrNO3: 294. T/US2006/016344
Figure imgf000186_0001
Step 3 : 5-bromo-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxo-l-phenyl- l,2-dihydropyridine-3-carboxamide. 5-Bromo-2-oxo-l-phenyl-l,2-dihydropyridine-3- carboxylic acid (0.458 g, 1.6 mmol), 4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorobenzenamine (0.49 g, 1.6 mmol), EDC (0.45 g, 2.3 mmol), and HOAt (0.21 g, 1.6 mmol) were added to a reaction flask then suspended in N, N-dimethylformamide (7.0 mL). iV,N-diisopropylethylamine (0.95 ml, 5.5 mmol) was added to the reaction mixture and stirring was continued at room temperature overnight. The reaction mixture was diluted with ethyl acetate and water and then extracted with ethyl acetate. A precipitate formed between the layers. The aqueous layer was filtered and the precipitate collected. The filtered aqueous layer was extracted with ethyl acetate (Ix). The combined ethyl acetate layers were washed with brine and then dried over sodium sulfate. The precipitate was dissolved in dichloromethane and also dried over sodium sulfate. All of the organic layers were combined and concentrated under vacuum. The remaining residue was purified by silica gel chromatography (1% methanol/dichloromethane to 2% methanol /dichloromethane) to give 5-bromo-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3- fluorophenyl)-2-oxo-l -phenyl- l,2-dihydropyridine-3-carboxamide as a yellow solid (0.846 g, 1.4 mmol, 92% yield). MS (ESI pos. ion) m/z: 590 (MH+). Calc'd exact mass for C29H21BrFN3O5: 589.
Figure imgf000186_0002
Step 4: N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxo-l,5-diphenyl-l,2- dihydropyridine-3-carboxamide. 5-Bromo-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3- fluorophenyl)-2-oxo-l-phenyl-l,2-dihydro-pyridine-3-carboxamide (0.075 g, 0.13 mmol) was suspended in DMF (1.5 mL) and then was added a solution of potassium carbonate (0.053 g, 0.38 mmol) in water (0.5 mL), phenylboronic acid (0.015 g, 0.13 mmol) and PdCl2(dρpf)2 (0.0093 g, 0.013 mmol). The reaction mixture was heated at 8O0C for 6 hours. The reaction , 006/016344 mixture was diluted with ethyl acetate and water then extracted with ethyl acetate. The organic layer was washed with brine then dried over sodium sulfate and concentrated under vacuum. The remaining residue was purified by silica gel chromatography (1% methanol/ dichloromethane to 2% methanol /dichloromethane) to give N-(4-(6,7-dimethoxyquinolin-4- yloxy)-3-fiuorophenyl)-2-oxo-l,5-diphenyl-l,2-dihydropyridine-3-carboxamide as a light yellow solid (0.069 g, 0.12 mmol, 92% yield). MS (ESI pos. ion) m/z: 588 (MH+). Calc'd exact mass for C35H26FN3O5 : 587. 1HNMR (400 MHz, DMS(W6) 12.19 (s, 1 H), 8.87 (d, J=2.91 Hz, 1 H), 8.40 - 8.55 (m, 2 H), 8.09 (dd, J=12.82, 2.34 Hz, 1 H), 7.75 (d, J=7.33 Hz, 2 H), 7.16 - 7.67 (m, 12 H)3 6.49 (d, J=5.05 Hz, 1 H), 3.95 (s, 6 H). Example 186
Figure imgf000187_0001
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6-oxo-l-(phenylmethyl)- l,1^2S3\6,6'4iexahydro-3,4'4)ipyridme-5-carboxainide: MS (ESI pos. ion) m/z: 590 (MH+). Calc'd exact mass for C34H31N5O5 : 589. 1H NMR (400 MHz, DMSO-J6) 12.63 (s, 1 H), 8.64 (s, 1 H), 8.49 (d, J=5.05 Hz, 1 H), 8.32 - 8.45 (m, 3 H), 7.86 (d, J=8.34 Hz, 1 H), 7.54 (s, 1 H), 7.26 - 7.45 (m, 6 H), 6.55 (d, J=5.05 Hz, 1 H), 6.23 (s, 1 H), 5.34 (s, 2 H), 3.94 (d, J=4.29 Hz, 6 H), 3.37 (s, 3 H), 2.91 (t, J=4.42 Hz, 2 H), 2.29 (s, 2 H).
Example 187
Figure imgf000187_0002
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6-oxo-l-(phenylmethyl)-l,6- dihydro-3,3'-bipyridine-5-carboxamide: MS (ESI pos. ion) m/z: 586 (MH+). Calc'd exact mass for C34H27N5O5 : 585. 1H NMR (400 MHz, DMSO-^6) 12.57 (s, 1 H), 8.96 (d, J=2.53 Hz, 1 H), 8.94 (d, J=I.89 Hz, 1 H), 8.84 (d, J=2.65 Hz, 1 H), 8.58 - 8.62 (m, 1 H), 8.50 (d, J=5.18 Hz, 1 H), 8.43 (d, J=8.97 Hz, 1 H), 8.40 (d, J=2.78 Hz, 1 H), 8.10 - 8.16 (m, 1 H), 7.87 (dd, J=9.09, 2.78 Hz, 1 H), 7.46 - 7.56 (m, 4 H), 7.36 - 7.44 (m, 3 H), 7.29 - 7.35 (m, 1 H), 6.56 (d, J=5.31 Hz, 1 H), 5.40 (s, 2 H), 3.95 (d, J=4.04 Hz, 6 H). 2006/016344
Example 188
Figure imgf000188_0001
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6'-oxo-ll-(phenylmethyl)-l',6'- dihydro-2,3'-bipyridine-5'-carboxamide: MS (ESI pos. ion) m/z: 586 (MH+). Calc'd exact mass for C34H27N5O5 : 585. 1R NMR (400 MHz, DMSO-J6) 12.54 (s, 1 H), 9.27 (d, J=2.78 Hz5 1 H), 9.19 (d, J=2.78 Hz, 1 H), 8.68 (d, J=AAl Hz, 1 H), 8.50 (d, J-5.18 Hz, 1 H), 8.44 (d, J=8.97 Hz, 1 H), 8.40 (d, J=2.91 Hz, 1 H), 7.97 - 8.02 (m, 1 H), 7.90 - 7.96 (m, 1 H), 7.88 (dd, J=8.97, 2.91 Hz, 1 H), 7.54 (s, 1 H), 7.45 - 7.49 (m, 2 H), 7.36 - 7.43 (m, 4 H), 7.29 - 7.35 (m, 1 H), 6.56 (d, J=5.18 Hz, 1 H), 5.45 (s, 2 H), 3.95 (d, J=3.66 Hz, 6 H).
Example 189
Figure imgf000188_0002
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-2-oxo-l-(phenylmethyl)-5-(2- thienyl)-l,2-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 591 (MH+). Calc'd exact mass for C33H26N4O5S: 590. 1H NMR (400 MHz5 DMSO-J6) 12.54 (s, 1 H), 8.82 (s, 1 H), 8.71 (s, 1 H), 8.50 (d, J=4.80 Hz, 1 H), 8.36 - 8.45 (m, 2 H), 7.87 (d, J-9.85 Hz, 1 H), 7.59 (d, J=A.&0 Hz, 1 H), 7.54 (s, 1 H), 7.48 - 7.52 (m, 1 H), 7.43 - 7.48 (m, 2 H), 7.35 - 7.43 (m, 3 H), 7.28 - 7.36 (m, 1 H), 7.14 - 7.20 (m, 1 H), 6.56 (d, J=5.43 Hz, 1 H), 5.39 (s, 2 H), 3.95 (d, J=4.67 Hz, 6 H).
Example 190
Figure imgf000188_0003
2006/016344
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-2-oxo-l-(phenylmethyl)-5-(2- pyrazinyl)-l,2-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 587 (MH+). Calc'd exact mass for C33H26N6O5: 586. 1H NMR (400 MHz, DMSO-J6) 12.46 (s, 1 H)5 9.32 (d, J=2.65 Hz, 1 H), 9.30 (d, J-1.39 Hz, 1 H), 9.26 (d, J=2.65 Hz, 1 H), 8.73 (dd, J=2.40, 1.64 Hz, 1 H), 8.63 (d, J=2.40 Hz, 1 H), 8.49 (d, J=5.18 Hz, 1 H), 8.43 (d, J=9.09 Hz, 1 H), 8.40 (d, J=2.78 Hz, 1 H), 7.88 (dd, J=8.97, 2.91 Hz, 1 H), 7.54 (s, 1 H), 7.46 - 7.52 (m, 2 H), 7.36 - 7.43 (m, 3 H), 7.29 - 7.36 (m, 1 H), 6.55 (d, J=5.18 Hz, 1 H), 5.44 (s, 2 H), 3.95 (d, J=3.92 Hz, 6 H).
Example 191
Figure imgf000189_0001
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-2-oxo-l-
(phenylmethyl)-l,2-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 523.2 (MH+). Calc'd exact mass for C33H26N6O5: 586. 1H NMR (400 MHz, DMSO-J6) 12.74 (s, 1 H), 8.49 (d, J=5.18 Hz, 1 H), 8.36 - 8.44 (m, 3 H), 8.22 (s, 1 H), 7.85 (dd, J=8.97, 2.78 Hz, 1 H), 7.54 (s, 1 H), 7.27 - 7.43 (m, 6 H), 6.54 (d, J=5.18 Hz, 1 H), 5.27 (s, 2 H), 3.95 (d, J=4.29 Hz, 6 H), 2.20 (s, 3 H).
Example 192
Figure imgf000189_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-bromo-l-(3- methylphenyl)-2-oxo-l,2-dihydro-3-pyridinecarboxamide: MS (ESl pos. ion) m/z: 605 (MH+). Calc'd exact mass for C30H23BrFN3O5: 604. 1H NMR (400 MHz, DMSO-J6) 12.00 (s, 1 H), 8.53 (d, J=2.78 Hz, 1 H), 8.46 - 8.51 (m, 2 H), 8.04 (dd, J=12.88, 2.40 Hz, 1 H), 7.53 - 7.58 (m, 1 H), 7.53 (s, 1 H), 7.42 - 7.50 (m, 2 H), 7.41 (s, 1 H), 7.31 - 7.39 (m, 3 H), 6.48 (d, J=4.93 Hz, 1 H), 3.95 (d, J=2.02 Hz, 6 H), 2.39 (s, 3 H). Example 193
Figure imgf000190_0001
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-(l-methyl-lH-pyrazol-4- yl)-2-oxo-l-phenyl-l,2-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 592 (MH+). Calc'd exact mass for C33H26FN5O5: 591. 1HNMR (400 MHz, DMS(W6) 12.28 (s, 1 H), 8.76 (d, J=2.53 Hz, 1 H), 8.49 (d, J=5.31 Hz, 1 H), 8.42 (d, J=2.53 Hz, 1 H), 8.26 (s, 1 H), 8.08 (d, J=12.76 Hz, 1 H), 7.93 (s, 1 H), 7.52 - 7.64 (m, 7 H), 7.46 (t, J=8.65 Hz, 1 H), 7.41 (s, 1 H), 6.51 (d, J=4.93 Hz, 1 H), 3.95 (s, 6 H), 3.86 (s, 3 H).
Example 194
Figure imgf000190_0002
N-(3-fluoro-4-((6-(methyloxy)-7-((3-(4-morpholinyl)propyl)oxy)-4-quinolinyl) oxy)phenyl)-2-oxo-5-phenyl-l-(phenylmethyl)-l,2-dihydro-3-pyridinecarboxamide: MS
(ESI pos. ion) m/z: 715 (MH+). Calc'd exact mass for C42H39FN4O6: 714.
Example 195
Figure imgf000190_0003
1 , 1 -dimethylethyl 5-(((5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)amino)carbonyl)- 6-oxo-l-(phenylmethyl)-l,3',6,6'-tetrahydro-3,4'-bipyridine-l '(2'H)-carboxylate: MS (ESI pos. ion) m/z: 690 (MH+). Calc'd exact mass for C39H39N5O7: 689. Example 196
Figure imgf000191_0001
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-2-oxo-l-(phenylmethyl)-5-(2- pyrimidinyl)-l,2-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 604 (MH+). CaIc' d exact mass for C34H26FN5O5: 603.
Example 197
Figure imgf000191_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-2-oxo-l-phenyl-5-(lH- pyrazol-4-yl)-l,2-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 578 (MH+). Calc'd exact mass for C32H24FN5O5: 577.
Example 198
Figure imgf000191_0003
l-benzyl-5-bromo-N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy) phenyl)-2-oxo-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 622 (MH+). Calc'd exact mass for C30H23BrClN3O5: 621. IH NMR (400 MHz, CDCl3) 12.34 (s, 1 H), 8.66 - 8.72 (m, 2 H5), 8.53 (d, J=5.37 Hz, 1 H), 7.66 (d, J=2.93 Hz, 1 H), 7.52 (s, 1 H), 7. 49 - 7.29 (m, 7 H), 7.12 - 7.18 (m, 1 H), 6.55 (d, J=5.37 Hz, 1 H), 5.29 (d, J=4.88 Hz, 2 H), 4.06 (s, 6 H) Example 199
Figure imgf000192_0001
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyridin-3-yl)-l,2- dihydropyridme-3-carboxamide: MS (ESI pos. ion) m/z: 542 (MH+). Calc'd exact mass for C32H23N5O4 541. IH NMR (400 MHz, CDCl3) 12.44 (s, 1 H), 9.03 (d, J=2.78 Hz, 1 H), 8.83 (d, J=0.51 Hz5 IH), 8.70 - 8.64 (m, 1 H), 8.63 (d, J=5.43 Hz, 1 H), 8.51 (d, J=9.09 Hz, 1 H), 8.28 -8.23 (m, 2H), 7.93 (d, J=2.91 Hz, 1 H), 7.91 - 7.88 (m, 1 H), 7.65-7.39 (3m, 8 H), 7.25 (d, J=2.53 Hz5 1 H), 6.47 (d, J=5.43 Hz, 1 H), 3.99 (s, 3 H)
Example 200
Figure imgf000192_0002
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyrazin-2-yl)-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C31H22N6O4 542 IH NMR (400 MHz, CDCl3) 12.36 (s, 1 H), 9.37 (d, J=2.78 Hz, 1 H), 9.08 (s, 1 H), 8.69 - 8.60 (m, 2 H), 8.59 - 8.50 (m, 2 H), 8.52 (d, J=8.97 Hz, 1 H)5 8.28 -8.23 (m, 2 H), 7.66 - 7.42 (3 m, 7 H), 7.24 (d, J=2.27 Hz, 1 H)5 6.46 (d, J=5.31 Hz5 1 H), 3.99 (s, 3 H).
Example 201
Figure imgf000192_0003
N-(5-(6,7-dimethoxyquinolin-4-yIoxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyridin-3-yl)-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z 572 (MH+). Calc'd exact mass for C33H25N5O5 571
Example 202
Figure imgf000193_0001
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyrazin-2-yl)-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z 573 (MH+). Calc'd exact mass for C32H24N6O5 572.
Example 203
Figure imgf000193_0002
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(thiophen-2-yl)-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z 577 (MH+). Calc'd exact mass for C32H24N4O5S 576.
Example 204
Figure imgf000193_0003
5-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z 585 (MH+). Calc'd exact mass for C35H28N4O5 584
Example 205
Figure imgf000194_0001
tert-butyl 4-(5-((5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)carbamoyl)-6-oxo-l- phenyl-l,6-dihydropyridin-3-yl)-5,6-dihydropyridine-l(2H)-carboxylate:
MS (ESI pos. ion) m/z 676 (MH+). Calc'd exact mass for C38H37N5O7 675
Example 206
Figure imgf000194_0002
5-bromo-N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 607 (MH+). Calc'd exact mass for C29 H21BrClN3O5: 606 IH NMR (400 MHz, CDCl3) 12.12 (s, 1 H), 8.79 (d, J=2.44 Hz, 1 H), 8.66 (d, J=8.79 Hz, IH), 8.52 (d, J=4.88 Hz5 1 H), 7.78 (d, J=2.93 Hz, 1 H), 7.67 - 7.31 (m, 8 H), 7.07 - 7.21 (m, 1 H), 6.54 (d, J=4.88 Hz, 1 H), 4.05 (s, 3 H), 4.04 (s, 3 H)
Example 207
Figure imgf000195_0001
Figure imgf000195_0002
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(2-methoxyethylamino)-2-oxo-l- phenyl-l,2-dihydropyridine-3-carboxamide
Figure imgf000195_0003
Step 1: 2-fluoro-4-iodonicotinic acid. To a stirred solution of 2-fluoro-4-iodopyridine-3- carboxaldehyde (10.Og5 39.8 rnmol) in tert-butanol (350 mL) and water (100 niL) at room temperature were added 2-methyl-2-butene (42.1 ml, 398 mmol), sodium phosphate, monobasic, monohydrate (60.5 g, 438 mmol) and sodium chlorite (18.0 g, 199 mmol). The reaction mixture was stirred at room temperature for 75 min. The reaction mixture was diluted with dichloromethane and a 6M aqueous solution of hydrochloric acid was added until pH ~2. T/US2006/016344
The water layer was extracted with dichloromethane. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. Purification by MPLC (CH2Cl2MeOH+ 1% AcOH: 100/0 to 80/20) afforded 2-fluoro-4-iodonicotinic acid (10.63 g, 39.8 mmol, 100% yield). MS (ESI pos. ion) m/z: 268 (MH+). Calc'd exact mass for C6H3FINO2: 267.
Figure imgf000196_0001
Step 2: 2-hydroxy-4-iodonicotinic acid. A suspension of 2-fluoro-4-iodonicotinic acid (896 mg, 3356 μmol) in 6M hydrochloric acid (13423 μl, 80540 μmol) was heated at 100 0C. After 5 min, the reaction became a solution, and then a precipitate appeared. The reaction mixture was stirred 60 min at 100 0C and then cooled to room temperature. Filtration afforded 2- hydroxy-4-iodonicotinic acid (710 mg, 2679 μmol, 80% yield). MS (ESI pos. ion) m/z: 248
(M+H-H2O). Calc'd exact mass for C6H4INO3: 265.
Figure imgf000196_0002
Step 3: methyl 2-hydroxy-4-iodonicotinate. Thionyl chloride (3.81 ml, 52.2 mmol) was added to a suspension of 2-hydroxy-4-iodonicotinic acid (3.46 g, 13.1 mmol) in dichloromethane (12 mL) in a pressure vessel at room temperature. The reaction mixture was then heated at 75 0C for 3h. An aliquot was taken and hydrolyzed with methanol. LCMS analysis showed the derived methyl ester seen as major compound. The reaction mixture was cooled to room temperature and was concentrated in vacuo to give 2-hydroxy-4-iodonicotinoyl chloride. 2-hydroxy-4-iodonicotinoyl chloride in MeOH (100 mL) was stirred at room temperature for 2h. Concentration in vacuo of the reaction mixture afforded methyl 2-hydroxy- 4-iodonicotinate (3.64g, 13.1 mmol, quantitative yield). MS (ESI pos. ion) m/z: 280 (MH+). Calc'd exact mass for C7H6INO3: 279.
Figure imgf000196_0003
Step 4: methyl 4-iodo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylate. Methyl 2- hydroxy-4-iodonicotinate (123 mg, 441 μmol), phenylboronic acid (161 mg, 1322 μmol), copper acetate (160 mg, 882 μmol) were combined. Dichloroethane (6 mL) was added followed by molecular sieves 4A activated (490 mg) and pyridine (143 μl, 1763 μmol). The reaction mixture was stirred at 55 0C for 3 h. LCMS analysis of an aliquot showed the reaction was complete. The reaction mixture was diluted with dichloromethane and filtered through a pad of celite (rinsing with dichloromethane). The filtrate was concentrated in vacuo and purification by MPLC (ISCO, CH2Cl2MeOH: 100/0 to 97.5/2.5) afforded methyl 4-iodo-2- oxo-l-phenyl-l,2-dihydropyridine-3-carboxylate (142 mg, 400 μmol, 91% yield). MS (ESI pos. ion) m/z: 356 (MH+). Calc'd exact mass for C13H10INO3: 355.
Figure imgf000197_0001
Step 5: 4-iodo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylic acid. To a stirred solution of methyl 4-iodo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxylate (2.34 g, 6.59 mmol) in dioxane (39 mL) was added water (12 mL) followed by sodium hydroxide 6M solution (4.39 ml, 26.4 mmol). The reaction mixture was heated at 50 0C for 4h. LCMS analysis of an aliquot showed the reaction was complete. The reaction mixture was cooled to room temperature and concentrated in vacuo. Water was added, and the pH was adjusted to ~3 with 6M aqueous hydrochloric acid solution. The solid formed was isolated by filtration and was dried under high vacuum overnight to give 4-iodo-2-oxo-l -phenyl- l,2-dihydropyridine-3- carboxylic acid (1.79 g, 5.25 mmol, 80% yield), which was used without further purification. MS (ESI pos. ion) m/z: 364 (M+Na). Calc'd exact mass for C12H8INO3: 341.
Figure imgf000197_0002
Step 6: N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-iodo-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide. To a stirred solution of 4-iodo-2-oxo-l -phenyl- 1,2- dihydropyridine-3 -carboxylic acid (132 mg, 387 μmol) in CH2Cl2 (3.9 mL) in a pressure vessel at room temperature was added thionyl chloride (113 μl, 1548 μmol). The reaction mixture was heated at 75 0C and stirred for Ih. An aliquot was taken, hydrolized with methanol and analyzed by LCMS: the reaction was done. The reaction mixture was concentrated in vacuo. 4- iodo-2-oxo-l-phenyl-l,2-dihydropyridine-3-carbonyl chloride was used in the next step without further purification. To a solution of 4-iodo-2-oxo-l -phenyl- l,2-dihydropyridine-3-carbonyl chloride (139 mg, 387 μmol) in dichloromethane (4 mL) at room temperature was added diisopropylethylamine (202 μl, 1160 μmol) followed by 5-(6,7-dimethoxyquinolin-4- yloxy)pyridin-2-amine (115 mg, 387 μmol). The reaction mixture was stirred at room temperature for 2h. An aliquot was taken and analyzed by LCMS: reaction was done. The reaction mixture was diluted with methanol and directly adsorbed on silica. Purification by MPLC (CH2Cl2/MeOH: 100/0 to 96/4) afforded N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin- 2-yl)-4-iodo-2-oxo-l-phenyl-l,2-dihydropyridme-3-carboxamide (162 mg, 261 μmol, 68% yield for two steps). MS (ESI pos. ion) m/z: 621 (MH+). Calc'd exact mass for C2SH20IN4O5: 620.
Figure imgf000198_0001
Step 7: N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(2-methoxyethylamino)-2- oxo-l-phenyI-l,2-dihydropyridine-3-carboxamide. 2-methoxyethylamine (137 μl, 1573 μmol) was added to a suspension of N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4- iodo-2-oxo-l -phenyl- l,2-dihydropyridine-3-carboxamide (122 mg, 197 μmol) in iso-propanol (1 mL). The reaction mixture was heated at 100°C for 80 min. An aliquot was taken and analyzed by LCMS: The reaction was done. The reaction mixture was diluted with dichloromethane. The crude was adsorbed on silica and purified by MPLC (CH2Cl2/Me0H: 100/0 to 95/5) to afford the title compound N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2- yl)-4-(2-methoxyethylamino)-2-oxo-l-phenyl-l,2-dihydropyridine-3-carboxamide (84 mg, 148 μmol, 75% yield). MS (ESI pos. ion) m/z: 568 (MH+). Calc'd exact mass for C31H29N5O6: 567. IH NMR (400 MHz, DMSO-J6) 13.28 (s, 1 H), 10.80 - 10.71 (m, 1 H), 8.49 (d, J=5.2 Hz5 1 H), 8.34 (d, J=9.1 Hz, 1 H), 8.30 (d, J=2.8 Hz, 1 H), 7.79 (dd, J=9.2, 3.1 Hz, 1 H), 7.73 (d, J=7.8 Hz, 1 H), 7.58 - 7.37 (m, 7 H), 6.53 (d, J=5.2 Hz, 1 H), 6.32 (d, J=8.1 Hz, 1 H), 3.95 (s, 3 H), 3.94 (s, 3 H), 3.64 - 3.54 (m, 4 H), 3.34 (s, 3 H). US2006/016344
Example 208
Figure imgf000199_0001
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-4-(tetrahydro-2H- pyran-4-ylamino)-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 594 (MH+). Calc'd exact mass for C33H31N5O6: 593.
Example 209
Figure imgf000199_0002
iV-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridm-2-yl)-2-oxo-l-phenyl-4-(phenylamino)-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 586 (MH+). Calc'd exact mass for C34H27N5O5: 585. IH NMR (400 MHz, DMSO-J6) 13.33 (s, 1 H), 12.37 (s, 1 H), 8.50 (d, J=5.2 Hz, 1 H), 8.38 (d, J=9.1 Hz, 1 H), 8.35 (d, J=2.8 Hz, 1 H), 7.82 (dd, J=9.1, 3.0 Hz, 1 H), 7.72 (d, J=7.8 Hz, 1 H), 7.59 - 7.33 (m, 12 H), 6.56 (d, J=5.3 Hz, 1 H), 6.18 (d, J=7.8 Hz, 1 H), 3.95 (s, 3 H) 3.94 (s, 3 H).
Example 210
Figure imgf000199_0003
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(4-methylpiperazin-l-yl)-2-oxo-l- phenyl-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 593 (MH+). Calc'd exact mass for C33H32N6O5: 592. IH NMR (400 MHz5 DMSO-J6) 11.74 (s, 1 H), 8.48 (d, J=5.3 Hz, 1 H), 8.37 (d, J=9.0 Hz, 1 H), 8.30 (d, J=2.9 Hz, 1 H), 7.79 (dd, J=9.1, 2.9 Hz, 1 H), 7.61 (d, J=8.1 Hz3 1 H), 7.56 - 7.48 (m, 3 H), 7.47 - 7.37 (m, 4 H), 6.51 (d, J=5.3 Hz, 1 H), 6.45 (d, J=8.1 Hz, 1 H), 3.95 (s, 3 H), 3.94 (s, 3 H), 3.47 - 3.41 (m, 4 H), 2.46 - 2.37 (m, 4 H), 2.21 (s, 3 H).
Example 211
Figure imgf000200_0001
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(methylamino)-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 524 (MH+). Calc'd exact mass for C29H25N5O5: 523.
Example 212
Figure imgf000200_0002
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(dimethylamino)-2-oxo-l-phenyl- l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 538 (MH+). Calc'd exact mass for C3OH27N5O5: 537.
Example 213
Figure imgf000200_0003
4-(2-methoxyethylamino)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl- l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z 538 (MH+). Calc'd exact mass for C30H27N5O5 537. 006/016344
Example 214
Figure imgf000201_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-4-(2-methoxyethylamino)-2-oxo-l- phenyl-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z 555 (MH+). Calc'd exact mass for C31H27FN4O5 554
Example 215
Figure imgf000201_0002
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-cyclopentyl-6-oxo-5-(2- oxo-l-pyrrolidinyl)-l,6-dihydro-3-pyridinecarboxamide: MS (ESI pos. ion) m/z: 617 (MH+). Calc'd exact mass for C30H21BrFN4O5: 616
Example 216
Figure imgf000201_0003
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(2-methoxyethylamino)-2- oxo-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 582 (MH+). Calc'd exact mass for C32H31N5O6: 581. IH NMR (400 MHz, DMSO-^6) 13.45 (s, 1 H) 10.58 (s, 1 H) 8.49 (d, J=5.13 Hz, 1 H) 8.33 (dd, J=5.90, 2.82 Hz, 2 H) 7.89 (d, J=7.69 Hz, 1 H) 7.79 (dd, J=9.10, 2.69 Hz, 1 H) 7.54 (s, 1 H) 7.41 (s, 1 H) 7.26 - 7.39 (m, 5 H) 6.52 (d, J=5.13 Hz, 1 H) 6.26 (d, J=7.69 Hz, 1 H) 5.10 (s, 2 H) 3.94 (d, J=3.33 Hz, 6 H) 3.48 - 3.59 (m, 4 H) 3.32 (s, 3 H) 006/016344
Example 217
Figure imgf000202_0001
l-benzyl-N-(5-(6,7-dimethoxyqumolin-4-yloxy)pyridin-2-yl)-4-(dimethylamino)-2-oxo-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 552 (MH+). Calc'd exact mass for C31H29N5O5: 551.
Example 218
Figure imgf000202_0002
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(methylamino)-2-oxo-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 538 (MH+). Calc'd exact mass for
C30H27N5O5: 537.
Example 219
Figure imgf000202_0003
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(phenylamino)-l,2- dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 600 (MH+). Calc'd exact mass for C35H29N5O5: 599. 2006/016344
Example 220
Figure imgf000203_0001
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(pyridin-4-ylamino)- l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 601 (MH+). Calc'd exact mass for C34H28N6O5: 600. IHNMR (400 MHz, DMSO-J6) 13.48 (s, 1 H) 12.46 (s, 1 H) 8.45 - 8.57 (m, 3 H) 8.34 (d, J=12.05 Hz, 2 H) 8.02 (d, 1 H) 7.83 (s, 1 H) 7.52 (s, 1 H) 7.32 - 7.42 (m, 7 H) 6.50 - 6.60 (m, 2 H) 3.93 (s, 3 H) 3.92 (s, 3 H)
Example 221
Figure imgf000203_0002
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(4-methylpiperazin-l-yl)-2- oxo-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 607 (MH+). Calc'd exact mass for C34H34N6O5: 606.
Example 222
Figure imgf000203_0003
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(tetrahydro-2H- pyran-4-ylamino)-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 608 (MH+). Calc'd exact mass for C34H33N5O6: 607. IH NMR (400 MHz, DMSO-J6) 13.47 (s, 1 H) 10.66 (d, J=7.58 Hz, 2 H) 8.50 (d, J=5.18 Hz, 1 H) 8.31 - 8.36 (m, 1 H) 7.89 (d, J=I. S3 Hz, 006/016344
1 H) 7.78 (dd, J=8.97, 3.03 Hz, 1 H) 7.55 (s, 1 H) 7.42 (s, 1 H) 7.26 - 7.40 (m, 5 H) 6.53 (d, J=5.18 Hz, 1 H) 6.36 (d, J=7.83 Hz, 1 H) 5.11 (s, 2 H) 3.95 (d, J=4.04 Hz, 6 H) 3.86 (d, .M 1.49 Hz, 3 H) 3.45 - 3.55 (m, 3 H) 1.89 - 1.99 (m, 2 H) 1.44 - 1.57 (m, 2 H)
Example 223
Figure imgf000204_0001
l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(4-(trifluoromethyl) phenylamino)-l,2-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 668 (MH+). Calc'd exact mass for C36H28F3N5O5: 667. IH NMR (400 MHz, DMSO-4) □ ppm 13.59 (s, 2 H) 12.42 (s, 1 H) 8.82 (d, J=6.44 Hz, 1 H) 8.49 (d, J=2.91 Hz, 1 H) 8.44 (d, J=9.09 Hz, 1 H) 7.77 (s, 1 H) 7.29 - 7.42 (m, 5 H) 7.00 (d, J=6.44 Hz, 1 H) 5.18 (s, 2 H) 4.05 (s, 3 H) 4.03 (s, 3 H)
Example 224
Figure imgf000204_0002
l-cyclopentyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-6-oxo-5-(2- oxopyrrolidin-l-yl)-l,6-dihydropyridine-3-carboxamide: MS (ESI pos. ion) m/z: 587 (MH+). Calc'd exact mass for C32H31FN4O6: 586.
Example 225
Figure imgf000204_0003
N-(3-fluoro-4-(2-(pyrrolidine-l-carboxamido)pyridin-4-yloxy)phenyl)-3-oxo-2-phenyl- 2,3-dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 515 (MH+). Calc'd exact mass for C27H23FN6O4: 514. 1HNMR (300 MHz, CDCl3): 1.23 (s, IH), 1.52 (s, 4H), 2.98- 3.08 (m, 5H), 6.10 (s, IH), 6.11 (d, J=4.11 Hz5 IH), 6.61 (s, IH)5 6.73 (t, J=8.61 Hz, IH)5 6.84 (s, IH)5 6.91 (s, IH), 7.09 (d, J=6.65 Hz, IH)5 7.15 (q, J=7.96 Hz5 2H)5 7.29 (s, IH)5 7.49 (d, J=12.13 Hz5 IH), 7.61 (d, J=5.67 Hz, IH), 7.80 (d, J=3.91 Hz5 IH), 7.97 (d, J=4.11 Hz, IH), 11.39 (s, lH).
Example 226
Figure imgf000205_0001
6-((diethylamino)methyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-3-oxo-2- phenyl-2,3-dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 598 (MH+). Calc'd exact mass for C33H32FN5O5: 597. 1HNMR (300 MHz, CDCl3): 11.99 (s, IH), 8.61 (s, 2H), 8.04 (s, IH)5 7.82 (s, IH), 7.57 (m, 4H), 7.26 (s, 3H), 6.61 (s, IH)5 4.10 (d, J=6.1 Hz5 9H)5 3.82 (s, 2H), 3.16 (s, IH), 2.79 (s, 4H)5 1.81 (s, IH)5 1.27 (s, IH). Example 227
Figure imgf000205_0002
6-((dimethylamino)methyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-2- phenyl-2,3-dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 540 (MH+). Calc'd exact mass for C30H26FN5O4: 539. 1HNMR (300 MHz, CDCl3): 1.71 (s, IH)5 1.75 (ddd, J=6.4, 3.5, 3.3 Hz, 3H), 2.30 (s, 2H)5 3.03-3.13 (m, J=6.5, 3.6, 3.3, 3.3, Hz5 3H)5 3.51 (s, IH)5 3.93 (s, 2H), 6.70-6.75 (m, 2H)5 7.20 (m5 2H)5 7.33-7.54 (m, 6H)5 7.80 (d, IH)5 8.45 (d, IH)5 8.52 (s, IH), 11.85 (s, IH). Example 228
Figure imgf000206_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 497 (MH+). Calc'd exact mass for C28H21FN4O4: 496. 1HNMR (300 MHz, CDCl3): 2.54 (s, 3H), 3.96 (s, 4H), 6.40 (s, IH), 7.24 (s, 2H), 7.40 (s, 2H), 7.55 (s, 4H), 7.96 (s, IH), 8.29 (s, 2H), 8.59 (s, IH), 12.01 (s, IH).
Example 229
Figure imgf000206_0002
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 510 (MH+). Calc'd exact mass for C28H23N5O5: 509. 1HNMR (SOO MHZ5 CDCI3): 2.55 (s, 3H), 4.06 (d, J=I.2 Hz, 6H), 6.49 (d, J=5.3 Hz, IH), 6.82 (s, IH), 7.45-7.64 (m, 7H), 8.29-8.33 (m, IH), 8.46 (d, J=8.9 Hz, IH), 8.52 (d, J=5.3 Hz, IH), 12.37 (s, IH).
Example 230
Figure imgf000206_0003
2-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-6-methyl-3-oxo-2,3- dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 524 (MH+). Calc'd exact mass for C29H25N5O5: 523. 1HNMR (SOO MHZ5 CDCI3): 2.48 (s, 3H)5 4.06 (s, 6H)5 5.30 (s, 2H)5 5.42 (s, 2H)5 6.46 (d, J=5.3 Hz, IH)5 7.35 (d5 J=6.7 Hz5 2H)5 7.43-7.61 (m, 3H)5 8.17 (s, IH)5 8.34 (s, IH)5 8.44 (d, J=8.9 Hz5 IH)5 8.52 (d, J=5.1 Hz5 IH)5 12.50 (s, IH). 6 016344
Example 231
Figure imgf000207_0001
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-2-phenyl-2,3-dihydropyridazine -4-carboxamide: MS (ESI pos. ion) m/z: 483 (MH+). Calc'd exact mass for C27H19FN4O4: 482. 1HNMR (300 MHz, CDCl3): 3.97 (s, 3H)5 5.30 (s, IH), 6.41 (d, J=4.1 Hz, IH), 7.19-7.28 (m, 3H), 7.58 (s, 3H), 7.96 (d, J=I 1.8 Hz, IH), 8.24 (d, J=2.9 Hz, 2H), 8.28 (s, IH), 8.42 (d, J=3.9 Hz, IH), 8.60 (d, J=5.0 Hz, IH), 11.89 (s, IH).
Example 232
Figure imgf000207_0002
N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z: 543 (MH+). Calc'd exact mass for C29H23ClN4O5 542. IH NMR (400 MHz, CDCl3) 12.24 (s, 1 H), 8.68 (d, J-9.28 Hz, 1 H,), 8.53 (d, J=5.37 Hz, 1 H), 8.32 (s, 1 H), 7.73-7.40 (m, 7 H), 7.30 (s, IH), 7.17 (d, JM7.81, IH), 6.57 (d, J=4.40 Hz, 1 H,), 4.07 (s, 3 H), 4.05 (s, 3 H), 2.54 (s, 3 H5) Example 233
Figure imgf000207_0003
16344
(R)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-6-((3-(dimethylamino) pyrrolidin-l-yl)methyl)-3-oxo-2-phenyl-2,3-dihydropyridazine-4-carboxamide: MS (ESI pos. ion) m/z 639 (MH+). Calc'd exact mass for C35H35FN6O5 638.
Example 234
Figure imgf000208_0001
3-benzyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxoimidazolidine-l- carboxamide: MS (ESI pos. ion) m/z: 517 (MH+). Calc'd exact mass for C28H25FN4O5: 516.
Example 235
Figure imgf000208_0002
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((dimethylamino)methyl)-2-oxo- 3-phenyl-tetrahydropyrimidine-l(2H)-carboxamide: MS (ESI pos. ion) m/z: 574 (MH+). Calc'd exact mass for C31H32FN5O5: 573.
Example 236
Figure imgf000209_0001
Figure imgf000209_0002
Step 1: Ethyl 7-methyl-4-oxo-4H-pyrido[l,2-a]pyriniidine-3-carboxyIate. A mixture of diethyl 2-(ethoxymethylene)malonate (0.60 g, 3 mmol), 5-methylpyridin-2-amine (0.20 g, 2 mmol), DBU (0.1 ml, 0.9 mmol) in acetonitrile (2 g, 49 mmol) was heated under Microwave (CEM) at 1500C (150 W) for 20 min. The resultant was diluted with dichloromthane and water, and the organic layer was dried over sodium sulfate. The organic solution was concentrated, and the residue was crystallized in dichloromethane and diethyl ether to give the title compound as a pale yellow solid (0.25 g, 58 %): MS (ESI pos. ion) m/z: 233 (MH+). Calc'd exact mass for Ci2H12N2O3: 232.
Figure imgf000209_0003
Steps 2 and 3: N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-7-methyI-4-oxo-4H- pyrido[l,2-a]pyrimidine-3-carboxamide. To a suspension of ethyl 7-methyl-4-oxo-4H- pyrido[l,2-a]pyrimidine-3-carboxylate (0.11 g, 0.47 mmol) in ethanol was added 1 N NaOH 006/016344 solution (3 mL, 3mmol) at RT. The reaction mixture was stirred for 16 at RT. The resultant was concentrated, and the residue was diluted with water. The aqueous solution was washed with diethyl ether and then acidified with 2N HCl solution and extracted with dichloromethane. The organic solution was dried over magnesium sulfate and concentrated to give a yellow solid (0.090 g, 93%): MS (ESI pos. ion) m/z: 205 (MH+). Calc'd exact mass for C10H8N2O3: 204. A mixture of 3-fluoro-4-(7-methoxyquinolin-4-yloxy)benzenamine (0.08 g, 0.3 mmol), 7- methyl-4-oxo-4H-pyrido[l,2-a]pyrimidine-3-carboxylic acid (0.08 g, 0.4 mmol), HATU (0.4 g, 0.8 mmol) in dichlormethane was stirred for 16 h. Then, the mixture was diluted with dichloromethane and aq. NaHCO3 solution. The organic layer was separated, dried over Na2SO4 and concentrated. The residue was purified by ISCO (0-5 % MeOH in EtOAc) to give the title compound as a yellow solid (0.032 g, 24 %): MS (ESI pos. ion) m/z: 471 (MH+), Calc'd exact mass for C26H19FN4O4: 470; 1HNMR (400 MHz, CDCl3): 11.4 (s, IH), 9.4 (s, IH), 9.1 (s, IH), 8.6 (d, J= 6 Hz, IH), 8.3 (d, J= 9 Hz, IH), 8.0 (dd, J= 3, 12 Hz, IH), 7.9 (m, 2H), 7.5 (m, IH), 7.4 (d, J- 3 Hz, IH), 7.0-7.3 (m, 2H), 6.4 (d, J= 3 Hz, IH), 3.98 (s, 3H), 2.57 (s, 3H).
Example 237
Figure imgf000210_0001
Figure imgf000210_0002
T/US2006/016344
Step 1: 4-Phenylmorpholin-3-one. A 250-mL flask was charged with 2-anilinoethanol (9.17 ml, 73.2 mmol), 9 mL dry EtOH, an overhead stirrer, a calibrated pH probe, and 27 niL water. An addition funnel was charged with 10 N sodium hydroxide solution (45.4 ml, 454 mmol). The solution was heated to 41 °C, and treated with chloracetyl chloride (17.5 ml, 220 mmol) via a syringe pump over 1 h. The sodium hydroxide solution was simultaneously added to the stirring solution so that the pH was maintained between 12 and 12.5. After the addition was complete, the solution was cooled to 0 °C and stirred for 1 h. The solids were collected and washed with water (2 X 60 mL cold water). The solids were dried at 50 0C at 0.2 mm Hg for 36 h to afford 4-phenylmorpholin-3-one (8.10 g, 62.5% yield). 1H NMR (400 MHz, CHLOROFORM-d) 3.75 - 3.80 (m, 2 H) 4.02 - 4.06 (m, 2 H) 4.35 (s, 2 H) 7.27 - 7.36 (m, 3 H) 7.39 - 7.46 (m, 2 H). 13C NMR (101 MHz, CHLOROFORM-d) 49.69 (s, 1 C) 64.14 (s, 1 C) 68.57 (s, 1 C) 125.48 (s, 2 C) 127.15 (s, 1 C) 129.30 (s, 2 C) 141.31 (s, 1 C) 166.59 (s, 1 C).
Figure imgf000211_0001
Step 2: Lithium 3-oxo-4-phenylmorpholine-2-carboxylate. A dry 100 mL Schlenk-type flask was fitted with a nitrogen/vacuum line and charged with 2-bromo-l ,3,5-tri-tert- butylbenzene (0.521 g, 1.601 mmol), 20 mL dry THF, and a stirbar. The solution was cooled to -78 0C and treated with 2.5M butyllithium (0.582 ml, 1.456 mmol). The reaction was stirred for 15min and treated with 4-phenylmorpholin-3-one ( 0.258 g, 1.456 mmol) dissolved in 2 mL dry THF dropwise over 5 min. The reaction was stirred for 2 h at -78 0C. The side arm compartment of the Schlenk-type flask was charged with ~lg dry ice. The system was sealed, and the dry ice was allowed to sublime into the solution. After 30 min, a nitrogen needle was fitted to the flask, and a solid was noted in the solution. The cooling bath was removed, which caused the solids to bubble (presumably dry ice). The solution was allowed to warm to RT overnight. The solution was diluted with 40 mL water and extracted with dichloromethane (2x10 mL). The water was concentrated in vacuo and dried at 60 °C and 0.15 irnnHg to afford lithium 3-oxo-4-phenylmorpholine-2-carboxylate (0.200 g, 60.5% yield). 1H NMR (400 MHz, D2O) 3.72 (t, J=5.23 Hz, 2 H), 3.99 (dt, J=12.10, 5.29 Hz, 1 H), 4.08 (dt, J=12.15, 5.22 Hz, 1 H), 4.61 (s, 1 H), 7.24 - 7.28 (m, 2 H), 7.32 (tt, 1 H), 7.38 - 7.44 (m, 2 H).
Figure imgf000211_0002
006/016344
Step 3 : N-(3-Fluoro-4-(7-methoxy quinolin-4-yloxy)phenyl)-3-oxo-4-phenylmorpholine-2- carboxamide. A dry, 10 mL schlenk-type flask was charged with a stirbar, lithium 3-oxo-4- phenylmorpholine-2-carboxylate (0.096 g, 0.42 rnmol), triethylammonium hydrochloride (0.058 g, 0.42 mmol), 3H-[l,2,3]triazolo[4,5-b]pyridin-3-ol (0.072 g, 0.53 mmol), and evacuated. The flask was back-filled with nitrogen and treated with 2 mL dry TΗF and 1 mL dry NMP. To the stirring solution was added Si-DCC (0.55 g, 0.53 mmol) followed by3- fluoro-4-(7-methoxyquinolin-4-yloxy)benzenamine (0.100 g, 0.35 mmol). The reaction was stirred for 3 d at RT, and then 60 0C for 24 h. The slurry was filtered through a 0.22 μm frit, and the TΗF removed. The crude was purified by ΗPLC (Waters Spherisorb S5 column (PN PSS830195, 20 X 250 mm, 60 A pore, 5 μm particle size)) to afford the title compound (0.026 g, 15.2% yield) 1H NMR (400 MHz5 Chloroform-d) 3.74 (ddd, J-12.32, 3.72, 3.52 Hz, 1 H), 3.95 - 4.03 (m, 4 H), 4.23 (dt, J=12.42, 3.91 Hz, 1 H), 4.27 - 4.38 (m, 1 H), 5.06 (s, 1 H), 6.37 (dd, J=5.23, 1.12 Hz, 1 H), 7.20 (t, J=8.56 Hz, 1 H), 7.24 (dd, J=9.15, 2.49 Hz, 1 H), 7.27 (ddd, J=8.83, 2.47, 1.12 Hz, 1 H), 7.32 - 7.41 (m, 3 H), 7.43 (d, J=2.45 Hz, 1 H), 7.46 - 7.51 (m, 2 H), 7.81 (dd, J=12.03, 2.35 Hz, 1 H), 8.26 (d, J=9.19 Hz, 1 H), 8.59 (d, J=5.18 Hz, 1 H), 9.66 (br. s., 1 H). MS (ESI pos. ion) m/z = 488, calc'd for C27H22FN3O5 487.
Example 238
Figure imgf000212_0001
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamide
Figure imgf000212_0002
Step 1: Ethyl l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate. To a solution of ethyl 3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxylate (1000 mg, 5.0 mmol) in dichloromethane (10 mL) was added methyl trifluoromethanesulfonate (1200 mg, 7.3 rnmol). The red solution was stirred at room temperature. After 14 h, the mixture was partitioned between dichloromethane and NaHCO3 (sat). The aqueous was extracted with dichloromethane (2x). The combined organic was dried over Na2SO4, concentrated and purified on silica. The product was triturated with EtOAc-hexane-CHCl3 to give the pure product as crystals (260 mg, 21%). Calc'd for C12H12N2O3, 232.08; MS (ESI pos. ion) m/z: 233 (MH+). 1H NMR (400 MHz, CHLOROFORM-d): 1.36 (t, J=7.04 Hz, 3 H), 3.39 (s, 3 H), 4.32 (q, J=7.17 Hz, 2 H), 7.32 (d, J=7.43 Hz, 2 H), 7.42 (t, J=7.34 Hz, 1 H), 7.50 (t, J=7.73 Hz, 2 H), 7.99 (s, 1 H).
Figure imgf000213_0001
Step 2 : N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamide. A solution of ethyl l-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxylate (260 mg, 1056 μmol) in MeOH was treated with NaOH (1000 μl, 5000 μmol) in H2O (3 mL). The mixture was heated to 60 0C for 30 min and then cooled to room temperature. Then, the mixture was neutralized with aq. HCl (5 N, 1.1 mL) and concentrated to dryness. The residue was further dried with (azeotrope distillation with toluene, 3 x 5 mL). The resulting carboxylic acid was mixed with 5-(7-methoxyquinolin-4- yloxy)ρyridin-2-amine (282 mg, 1054 μmol), Et3N (500 μl, 3587 μmol), and HATU (401 mg, 1054 μmol) in DMF (4 mL) - dichloromethane (5 mL) and was stirred at 60 0C for 2 h. Upon cooling to room temperature, the mixture was diluted with EtOAc containing 10% MeOH (30 mL) and washed with H2O. The organic layer was dried over Na2SO4, concentrated, and eluded on silica (1-10% 2N NH3-MeOH in CHCl3). The product was further purified on preparative HPLC to afford a white powder (100 mg, 20%). Calc'd for C26H21N5O4: 467.16; MS (ESI pos. ion) m/z: 468 (MH+). 1H NMR (400 MHz, DMSO-d6) 3.49 (s, 3 H) 3.95 (s, 3 H) 6.55 (d, J 5.1, 1 H) 7.30 (dd, J 2.0, 9.0, 1 H) 7.42 (s, 1 H) 7.59 (s, 17 H) 7.50- 7.60 (m, 5 H), 7.84 (dd, J 2.8, 9.2, IH), 8.22 (d, J 9.2, IH), 8.34 - 8.38 (m, 2 H) 8.62 (d, J 5.3, 1 H) 8.69 (s, 1 H) 10.86 (s, 1 H). Example 239
Figure imgf000214_0001
Figure imgf000214_0002
Step l: 4-Phenylmorpholin-3-one. A 250-mL flask was charged with 2-anilinoethanol (9.17 ml, 73.2 mmol), 9 rnL dry EtOH, an overhead stirrer, a calibrated pH probe, and 27 mL water. An addition funnel was charged with ION sodium hydroxide solution (45.4 ml, 454 mmol). The solution was heated to 41 °C, and treated with chloracetyl chloride (17.5 ml, 220 mmol) via a syringe pump over 1 h. The sodium hydroxide solution was simultaneously added to the stirring solution so that the pH was maintained between 12 and 12.5. After the addition was complete, the solution was cooled to 0 °C and stirred for 1 h. The solids were collected and washed with water (2 X 60 mL cold water). The solids were dried at 50 °C at 0.2 mm Hg for 36 h to afford 4-phenylmorpholin-3-one (8.10 g, 62.5% yield). 1H NMR (400 MHz, CHLOROFORM-d) 3.75 - 3.80 (m, 2 H) 4.02 - 4.06 (m, 2 H) 4.35 (s, 2 H) 7.27 - 7.36 (m, 3 H) 7.39 - 7.46 (m, 2 H). 13C NMR (101 MHz, CHLOROFORM-d) 49.69 (s, 1 C) 64.14 (s, 1 C) 68.57 (s, 1 C) 125.48 (s, 2 C) 127.15 (s, 1 C) 129.30 (s, 2 C) 141.31 (s, 1 C) 166.59 (s, 1 C).
Figure imgf000214_0003
Step 2: Lithium 3-oxo-4-phenylmorpholine-2-carboxylate. A dry 100 mL Schlenk-type flask was fitted with a nitrogen/vacuum line and charged with 2-bromo-l,3,5-tri-tert- 44 butylbenzene (0.521 g, 1.601 mmol), 20 mL dry THF, and a stirbar. The solution was cooled to -78 °C and treated with 2.5M butyllithium (0.582 ml, 1.456 mmol). The reaction was stirred for 15min and treated with 4-phenylmorpholin-3-one ( 0.258 g, 1.456 mmol) dissolved in 2 mL dry THF dropwise over 5 min. The reaction was stirred for 2 h at -78 °C. The side arm compartment of the Schlenk-type flask was charged with ~lg dry ice. The system was sealed, and the dry ice was allowed to sublime into the solution. After 30 min, a nitrogen needle was fitted to the flask, and a solid was noted in the solution. The cooling bath was removed, which caused the solids to bubble (presumably dry ice). The solution was allowed to warm to RT overnight. The solution was diluted with 40 mL water and extracted with dichloromethane (2x10 mL). The water was concentrated in vacuo and dried at 60 0C and 0.15 mmHg to afford lithium 3-oxo-4-phenylmorpholine-2-carboxylate (0.200 g, 60.5% yield). 1H NMR (400 MHz, D2O) 3.72 (t, J=5.23 Hz, 2 H), 3.99 (dt, J=12.10, 5.29 Hz, 1 H), 4.08 (dt, J=12.15, 5.22 Hz, 1 H), 4.61 (s, 1 H), 7.24 - 7.28 (m, 2 H), 7.32 (tt, 1 H), 7.38 - 7.44 (m, 2 H).
Figure imgf000215_0001
Step 3 : N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-4-phenylmorpholine-2- carboxamide. A dry, 10 mL schlenk-type flask was charged with a stirbar, lithium 3-oxo-4- phenylmorpholine-2-carboxylate (0.096 g, 0.42 mmol), triethylammonium hydrochloride (0.058 g, 0.42 mmol), 3H-[l,2,3]triazolo[4,5-b]pyridin-3-ol (0.072 g, 0.53 mmol), and evacuated. The flask was back-filled with nitrogen and treated with 2 mL dry THF and 1 mL dry NMP. To the stirring solution was added Si-DCC (0.55 g, 0.53 mmol) followed by3- fluoro-4-(7-methoxyquinolin-4-yloxy)benzenamine (0.100 g, 0.35 mmol). The reaction was stirred for 3 d at RT, and then 60 °C for 24 h. The slurry was filtered through a 0.22 μm frit, and the THF removed. The crude was purified by HPLC (Waters Spherisorb S5 column (PN PSS830195, 20 X 250 mm, 60 A pore, 5 μm particle size)) to afford the title compound (0.026 g, 15.2% yield) 1H NMR (400 MHz, Chloroform-d) 3.74 (ddd, J=I 2.32, 3.72, 3.52 Hz, 1 H), 3.95 - 4.03 (m, 4 H), 4.23 (dt, J=12.42, 3.91 Hz, 1 H), 4.27 - 4.38 (m, 1 H), 5.06 (s, 1 H), 6.37 (dd, J=5.23, 1.12 Hz, 1 H), 7.20 (t, J-8.56 Hz, 1 H), 7.24 (dd, J=9.15, 2.49 Hz, 1 H), 7.27 (ddd, J=8.83, 2.47, 1.12 Hz, 1 H), 7.32 - 7.41 (m, 3 H), 7.43 (d, J=2.45 Hz, 1 H), 7.46 - 7.51 (m, 2 H), 7.81 (dd, J=12.03, 2.35 Hz, 1 H), 8.26 (d, J=9.19 Hz, 1 H), 8.59 (d, J=5.18 Hz, 1 H), 9.66 (br. s., 1 H). MS (ESI pos. ion) m/z = 488, calc'd for C27H22FN3O5 487. The following additional compounds can also be made using the methodology generally set forth above:
Figure imgf000216_0001
Figure imgf000217_0001
Figure imgf000218_0001
Figure imgf000219_0001
Although the pharmacological properties of the compounds of Formulas I-II vary with structural change, in general, activity possessed by compounds of Formulas I-II may be demonstrated in vivo. The pharmacological properties of the compounds of this invention may be confirmed by a number of pharmacological in vitro assays. The exemplified pharmacological assays, which follow have been carried out with the compounds according to the invention and their salts. Compounds of the present invention showed inhibition of c-Met kinase at doses less than 2 μM.
BIOLOGICAL TESTING The efficacy of the compounds of the invention as inhibitors of HGF related activity is demonstrated as follows. c-Met receptor assay Cloning, Expression and Purification of c-Met Kinase Domain
A PCR product covering residues 1058-1365 of c-Met (c-Met kinase domain) is generated from Human Liver QuickClone™ cDNA (Invitrogen) using forward primer 5 '- ATTGACGGATCCATGCTAAATCCAGAGCTGGTCCAGGCA-S' (SEQ ID NO. 1) and reverse primer 5'-ACAACAGAATTCAATACGGAGCGACACATTTTACGTT-S' (SEQ ID NO. 2). The PCR product is cloned into a modified pFastBacl expression vector (harboring the gene for S. japonicum glutathione S-transferase immediately upstream of the multiple cloning site) using standard molecular biological techniques. The GST-c-Met kinase domain fusion (GST-Met) gene is transposed into full-length baculovirus DNA using the BacToBac™ system (Invitrogen). High5 cells are infected with the recombinant baculovirus for 72 h at 27°C. The infected cells are harvested by centrifugation and the pellet is stored at -80°C. The pellet is resuspended in buffer A (50 mM HEPES, pH 8.0, 0.25 M NaCl, 10 mM 2- mercaptoethanol, 10% (w/v) glycerol, 0.5 % (v/v) protease inhibitor cocktail (Sigma P8340), stirred at 4°C to homogeneity, and the cells are disrupted by microfluidization (Microfluidics) at 10,000 psi. The resulting lysate is centrifuged at 50,000 x g for 90 min at 4 °C, and the supernatant is adsorbed onto 10 mL of glutathione sepharose™ 4B (Amersham) by batch method. The slurry is rocked gently overnight at 4°C. The glutathione resin is harvested by centrifugation and washed three times with 40 mL buffer A by batch method. The resin is washed three times with buffer B (buffer A adjusted to 0.1 M NaCl, less protease inhibitors). The protein is eluted with buffer B containing 25 mM reduced glutathione. Eluted fractions are analyzed by SDS-PAGE and concentrated to <10 mL (-10 mg/mL total protein). The concentrated protein is separated by Superdex™ 200 (Amersham) size exclusion 6 016344 chromatography in buffer C (25 mM Tris, pH 7.5, 0.1 M NaCl, 10 mM 2-mercaptoethanol, 10% glycerol). The fractions are analyzed by SDS-PAGE and the appropriate fractions are pooled and concentrated to ~1 mg/mL. The protein is aliquotted and stored at -8O0C. Alternative purification of human GST-cMET from Baculovirus cells Baculovirus cells are broken in 5x (volume/weight) of Lysis Buffer (50 mM HEPES, pH 8.0, 0.25 M NaCl, 5 mM mercaptoethanol, 10% glycerol plus Complete Protease Inhibitors (Roche (#10019600), 1 tablet per 50 mL buffer). The lysed cell suspension is centrifuged at 100,000 x g (29,300 rpm) in a Beckman ultracentrifuge Ti45 rotor for 1 h. The supernatant is incubated with 10 ml of Glutathione Sepharose 4B from Amersham Biosciences (#27-4574- 01). Incubation is carried out overnight in a cold room (approximately 8°C). The resin and supernatant is poured into an appropriately sized disposable column and the flow through supernatant was collected. The resin is washed with 10 column volumes (100 mL) of Lysis Buffer. The GST-cMET is eluted with 45 mL of 10 mM Glutathione (Sigma #G-4251) in Lysis Buffer. The elution is collected as 15 mL fractions. Aliquots of the elution fractions are run on SDS PAGE (12% Tris Glycine gel, Invitrogen, #EC6005BOX). The gel is stained with 0.25% Coomassie Blue stain. Fractions with GST-cMET are concentrated with a Vivaspin 20 mL Concentrator (#VS2002; 10,00 MW cutoff) to a final volume less than 2.0 ml. The concentrated GST-cMET solution is applied to a Superdex 75 16/60 column (Amersham Biosciences #17-1068-01) equilibrated with 25 mM Tris, pH 7.5, 100 mM NaCl, 10 mM mercaptoethanol, 10% glycerol. The GST-cMET is eluted with an isocratic run of the above buffer, with the eluent collected in 1.0 mL fractions. Fractions with significant OD28O readings are run on another 12% Tris Glycine gel. The peak tubes with GST-cMET are pooled and the OD28O is read with the column buffer listed above as the blank buffer.
Phosphorylation of the purified GST-cMET is performed by incubating the protein for 3 h at RT with the following:
Final concentration a) 10O mM ATP (Sigma #A7699) 25 mM b) 1.0 M MgCl2 (Sigma #M-0250) 10O mM c) 200 mM Sodium Orthovanadate (Sigma #S-6508) 15 mM d) 1.0 M Tris-HCl, pH 7.00 (in house) 5O mM e) H2O f) GST-cMET 0.2 - 0.5 mg/mL 44
After incubation, the solution is concentrated in a Vivaspin 20 ml Concentrator to a volume less than 2.00 ml. The solution is applied to the same Superdex 75 16/60 column used above after re-equilibration. The GST-cMET is eluted as described above. The elution fractions corresponding to the first eluted peak on the chromatogram are run on a 12% Tris Glycine gel, as above, to identify the fractions with GST-cMET. Fractions are pooled and the OD28O is read with the column buffer used as the blank.
A Kinase reaction Buffer is prepared as follows:
Per I L
60 mM HEPES PH 7.4 1 M stock 16.7 X 6O mL
50 mM NaCl 5 M stock 100 X 1O mL
20 mM MgCl2 1 M stock 50 X 2O mL
5 mM MnCl2 1 M stock 200 X 5 mL
When the assay is carried out, freshly add:
2 mM DTT 1 M stock 500 X
0.05 % BSA 5 % stock 100 X
0.1 mM Na3OV4 0.1 M stock 1000 X
The HTRF buffer contains:
50 mM Tris-HCl (PH 7.5), 100 mM NaCl, 0.1 % BSA, 0.05 % Tween 20,5mM EDTA
Fresh add SA-APC (PJ25S Phycolink Streptavidin-Allophycocyanin Conjugate, Prozyme Inc.) and Eu-PT66 ( Eu-Wl 024 labeled anti-phosphorotyrosine antibody PT66, AD0069, Lot 168465, Perkin-Elmer Inc.) to reach the final concentration:
0.1 nM final Eu-PT66
H nM final SA-APC
Methods: 1. Dilute GST-cMet (P) enzyme in kinase buffer as follows:
Prepare 8 nM GST-cMet (P) working solution (7.32 μM to 8 nM, 915 X, 10 μL to 9.15 mL). In a 96 well clear plate [Costar # 3365] add 100 μL in eleven columns, in one column add 100 μL kinase reaction buffer alone. 2. Assay plate preparation:
Use Biomek FX to transfer 10 μL 8 nM GST-cMet (P) enzyme, 48.4 μL kinase reaction buffer, 1.6 μL compound (in DMSO) (Start concentration at 10 mM, 1 mM and 0.1 mM, sequential dilution 1 :3 to reach 10 test points) in a 96 well costar clear plate [Costar # 3365], mix several times. Then incubate the plate at RT for 30 min.
3. Prepare Gastrin and ATP working solution in kinase reaction buffer as follows: Prepare 4 μM Gastrin and 16 μM ATP working solution
Per 1O mL Gastrin 4 μM stock (500 μM to 4 μM, 125 X) 80 μL
ATP 16 μM stock (1000 μM to 16 μM, 62.5 X) 160 μL
Use Biomek FX to add 20 μl ATP and Gastrin working solution to the assay plate to start reaction, incubate the plate at RT for 1 h.
4. Transfer 5 μL reaction product at the end of 1 h into 80 μL HTRF buffer in black plate [Costar # 3356], read on Discover after 30 min incubation.
Assay condition summary:
KM ATP * 6 μM
[ATP] 4 μM
KM Gastrin/p(EY) 3.8 μM
[gastrin] l μM
[enzyme] I nM
KM ATP, KM gastrin for various enzymes were determined by HTRF/33P labeling and HTRF methods.
Examples 1-28, 30, 33-34, 36-37, and 39-48 exhibited activity with IC50 values less than 0.5 μM. c-Met cell-based autophosphorylation assay Human PC3 and mouse CT26 cells are available obtained from ATCC. The cells were cultured in a growth medium containing RPMI 1640, penicillin/streptomycin/glutamine (IX) and 5% FBS. 2 x 104 cells in medium were plated per well in a 96 well plate and incubated at 37 °C overnight. The cells were serum-starved by replacing the growth media with basic medium (DMEM low glucose + 0.1 BSA, 120 μL per well) at 37 °C for 16 h. Compounds (either 1 mM and 0.2 niM) in 100% DMSO were serially diluted (1 :3) 3333 fold on a 96 well plate, diluting 1:3 with DMSO from column 1 to 11 (columns 6 and 12 receive no compound). Compound samples (2.4 μL per well) were diluted with basic medium (240 μL) in a 96 well plate. The cells were washed once with basic medium (GIBCO, DMEM 11885-076) then compound solution was added (100 μL). The cells were incubated at 37 °C for I h. A (2 mg/mL) solution of CHO-HGF (7.5 μL) was diluted with 30 mL basic medium to provide a final concentration of 500 ng/mL. This HGF-containing media (120 μL) was transferred to a 96 well plate. Compounds (1.2 μL) was added to the HGF-containing media and mixed well. The mixture of media/HGF/compound (100 μL) was added to the cells (final HGF concentration - 250 ng/mL) then incubated at 37 °C for 10 min. A cell lysate buffer (20 mL) was prepared containing 1% Triton X-100, 50 mM Tris pH 8.0, 100 mM NaCl, Protease inhibitor (Sigma, #P-8340) 200 μL, Roche Protease inhibitor (Complete, # 1-697-498) 2 tablets, Phosphatase Inhibitor II (Sigma, #P-5726) 200 μL, and a sodium vanadate solution (containing 900 μL PBS, 100 μL 300 mM NaVO3, 6 μL H2O2 (30% stock) and stirred at RT for 15 min) (90 μL). The cells were washed once with ice cold IX PBS (GIBCO, #14190- 136), then lysis buffer (60 μL) was added and the cells were incubated on ice for 20 min.
The IGEN assay was performed as follows: Dynabeads M-280 streptavidin beads were pre-incubated with biotinylated anti-human HGFR (240 μL anti-human-HGFR (R&D system, BAF527 or BAF328) @ 100 μg/mL + 360 μL Beads (IGEN #10029 + 5.4 μL buffer - PBS/ 1% BS A/0.1 % Tween20) by rotating for 30 min at RT. Antibody beads (25 μL) were transferred to a 96 well plate. Cell lysate solution (25 μL) was transferred added and the plate was shaken at RT for 1 h. Anti-phosphotyrosine 4G10 (Upstate 05-321) (19.7 μL antibody + 6 mL IX PBS) (12.5 μL) was added to each well, then incubated for 1 h at RT. Anti-mouse IgG ORI- Tag (ORIGEN #110087) (24 μL Antibody + 6 mL buffer) (12.5 μL) was added to each well, then incubated at RT for 30 min. IX PBS (175 μL) was added to each well and the electrochemiluminescence was read by an IGEN M8. Raw data was analyzed using a A- parameter fit equation in XLFit. IC50 values are then determined using Grafit software. Examples 2, 4, 6-8, 11, 13, 15-21, 23-26, 36-37, 39, 41, and 43-44 exhibited activity in PC3 cells with IC50 values less than 1.0 μM. Examples 2, 4, 6-8, 11-13, 15-21, 23-26, 36-37, 41, and 43-44 exhibited activity in CT26 cells with IC50 values less than 1.0 μM. HUVEC Proliferation Assay
Human Umbilical Vein Endothelial cells are purchased from Clonetics, Inc., as cryopreserved cells harvested from a pool of donors. These cells, at passage 1, are thawed and expanded in EBM-2 complete medium, until passage 2 or 3. The cells are trypsinized, washed in DMEM + 10% FBS + antibiotics, and spun at 1000 rpm for 10 min. Prior to centrifugation of the cells, a small amount is collected for a cell count. After centrifugation, the medium is discarded, and the cells are resuspended in the appropriate volume of DMEM + 10% FBS + antibiotics to achieve a concentration of 3 x 105 cells/mL. Another cell count is performed to confirm the cell concentration. The cells are diluted to 3 x 104 cells/mL in DMEM + 10% FBS + antibiotics, and 100 μL of cells are added to a 96-well plate. The cells are incubated at 37 °C for 22 h.
Prior to the completion of the incubation period, compound dilutions are prepared. Five-point, five-fold serial dilutions are prepared in DMSO, at concentrations 400-fold greater than the final concentrations desired. 2.5 μL of each compound dilution are diluted further in a total of 1 mL DMEM + 10% FBS + antibiotics (40Ox dilution). Medium containing 0.25% DMSO is also prepared for the 0 μM compound sample. At the 22 h timepoint, the medium is removed from the cells, and 100 μL of each compound dilution is added. The cells are incubated at 37 0C for 2-3 h. During the compound pre-incubation period, the growth factors are diluted to the appropriate concentrations. Solutions of DMEM + 10% FBS + antibiotics, containing either VEGF or bFGF at the following concentrations: 50, 10, 2, 0.4, 0.08, and 0 ng/mL are prepared. For the compound-treated cells, solutions of VEGF at 550 ng/mL or bFGF at 220 ng/mL for 50 ng/mL or 20 ng/mL final concentrations, respectively, are prepared since 10 μL of each will be added to the cells (110 μL final volume). At the appropriate time after adding the compounds, the growth factors are added. VEGF is added to one set of plates, while bFGF is added to another set of plates. For the growth factor control curves, the media on wells B4-G6 of plates 1 and 2 are replaced with media containing VEGF or bFGF at the varying concentrations (50-0 ng/mL). The cells are incubated at 37 °C for an additional 72 h. At the completion of the 72 h incubation period, the medium is removed, and the cells are washed twice with PBS. After the second wash with PBS, the plates are tapped gently to remove excess PBS, and the cells are placed at -70 °C for at least 30 min. The cells are thawed and analyzed using the CyQuant fluorescent dye (Molecular Probes C-7026), following the manufacturer's recommendations. The plates are read on a Victor/Wallac 1420 workstation at 485 nm/530 ran (excitation/emission). Raw data are collected and analyzed using a 4-parameter fit equation in XLFit. IC50 values are then determined. Rat Corneal Neovascularization Micropocket Model
In Life Aspects: Female Sprague Dawley rats weighing approximately 250 g were randomized into one of five treatment groups. Pretreatment with the vehicle or compound was administered orally, 24 h prior to surgery and continued once a day for seven additional days. On the day of surgery, the rats were temporarily anesthetized in an Isofluorane gas chamber (delivering 2.5 L/min oxygen + 5% Isofluorane). An othoscope was then placed inside the mouth of the animal to visualize the vocal cords. A tip-blunted wire was advanced in between the vocal cords and used as a guide for the placement of an endotracheal Teflon tube (Small Parts Inc. TFE-standard Wall R-SWTT-18). A volume-controlled ventilator (Harvard Apparatus, Inc. Model 683) was connected to the endotracheal tube to deliver a mixture of oxygen and 3% Isofluorane. Upon achieving deep anesthesia, the whiskers were cut short and the eye areas and eyes gently washed with Betadine soap and rinsed with sterile saline. The corneas were irrigated with one to two drops of Proparacaine HCl ophthalmic topical anesthetic solution (0.5%) (Bausch and Lomb Pharmaceuticals, Tampa FL). The rat was then positioned under the dissecting microscope and the corneal surface brought into focus. A vertical incision was made on the midline of the cornea using a diamond blade knife. A pocket was created by using fine scissors to separate the connective tissue layers of the stroma, tunneling towards the limbus of the eye. The distance between the apex of the pocket and the limbus was approximately 1.5 mm. After the pocket had been made, the soaked nitrocellulose disk filter (German Sciences, Ann Arbor MI.) was inserted under the lip of the pocket. This surgical procedure was performed on both eyes. rHu-bFGF soaked disks were placed into the right eye, and the rHu-VEGF soaked disks were placed into the left eye. Vehicle soaked disks were placed in both eyes. The disk was pushed into position at the desired distance from the limbal vessels. Ophthalmic antibiotic ointment was applied to the eye to prevent drying and infection. After seven days, the rats were euthanized by CO2 asphyxiation, and the eyes enucleated. The retinal hemisphere of the eye was windowed to facilitate fixation, and the eye placed into formalin overnight. Post Mortem Aspects: After 24 h in fixative, the corneal region of interest was dissected out from the eye, using fine forceps and a razorblade. The retinal hemisphere was trimmed off and the lens extracted and discarded. The corneal dome was bisected and the superfluous cornea trimmed off. The iris, conjunctiva and associated limbal glands were then 6 016344 carefully teased away. Final cuts were made to generate a square 3 x 3 mm containing the disk, the limbus, and the entire zone of neovascularization.
Gross Image Recording: The corneal specimens were digitally photographed using a
Sony CatsEye DKC5000 camera (A.G. Heinz, Irvine CA) mounted on a Nikon SMZ-U stereo microscope (A.G. Heinz). The corneas were submerged in distilled water and photographed via trans-illumination at approximately 5.0 diameters magnification.
Image analysis: Numerical endpoints were generated using digital micrographs collected from the whole mount corneas after trimming and were used for image analysis on the Metamorph image analysis system (Universal Imaging Corporation, West Chester PA). Three measurements were taken: Disk placement distance from the limbus, number of vessels intersecting a 2.0 mm perpendicular line at the midpoint of the disk placement distance, and percent blood vessel area of the diffusion determined by thresholding.
General Formulations:
0.1% BSA in PBS vehicle: 0.025 g of BSA was added to 25.0 mL of sterile IX phosphate buffered saline, gently shaken until fully dissolved, and filtered at 0.2 μM. Individual 1.0 mL samples were aliquoted into 25 single-use vials, and stored at -20 °C until use. For the rHu- bFGF disks, a vial of this 0.1% BSA solution was allowed to thaw at room temperature. Once thawed, 10 μL of a 100 mM stock solution of DTT was added to the 1 ml BSA vial to yield a final concentration of 1 mM DTT in 0.1% BSA. rHu-VEGF Dilutions: Prior to the disk implant surgery, 23.8 μL of the 0.1% BSA vehicle above was added to a 10 μg rHu-VEGF lyophilized vial yielding a final concentration of 10 μM. rHu-bFGF: Stock concentration of 180 ng/μL: R&D rHu- bFGF: Added 139 μL of the appropriate vehicle above to the 25 μg vial lyophilized vial. 13.3 μL of the [180 ng/μL] stock vial and added 26.6 μL of vehicle to yield a final concentration of 3.75 μM concentration.
Nitro-cellulose disk preparation: The tip of a 20-gauge needle was cut off square and beveled with emery paper to create a punch. This tip was then used to cut out = 0.5 mm diameter disks from a nitrocellulose filter paper sheet (Gelman Sciences). Prepared disks were then placed into Eppendorf microfuge tubes containing solutions of either 0.1% BSA in PBS vehicle, 10 μM rHu-VEGF (R&D Systems, Minneapolis, MN), or 3.75 μM rHu-bFGF (R&D
Systems, Minneapolis, MN) and allowed to soak for 45-60 min before use. Each nitrocellulose filter disk absorbs approximately 0.1 μL of solution.
In the rat micropocket assay, compounds of the present invention will inhibit angiogenesis at a dose of less than 50 mg/kg/day. Tumor model
A431 cells (ATCC) are expanded in culture, harvested and injected subcutaneously into 5-8 week old female nude mice (CDl nu/nu, Charles River Labs) (n = 5-15). Subsequent administration of compound by oral gavage (10 - 200 mpk/dose) begins anywhere from day 0 to day 29 post tumor cell challenge and generally continues either once or twice a day for the duration of the experiment. Progression of tumor growth is followed by three dimensional caliper measurements and recorded as a function of time. Initial statistical analysis is done by repeated measures analysis of variance (RMANOVA), followed by Scheffe post hoc testing for multiple comparisons. Vehicle alone (Ora-Plus, pH 2.0) is the negative control. Compounds of the present invention will be active at doses less than 150 mpk.
Tumor models
Human glioma tumor cells (U87MG cells, ATCC) are expanded in culture, harvested and injected subcutaneously into 5-8 week old female nude mice (CDl nu/nu, Charles River Labs) (n=l 0). Subsequent administration of compound by oral gavage or by IP (10-100 mpk/dose) begins anywhere from day 0 to day 29 post tumor cell challenge and generally continues either once or twice a day for the duration of the experiment. Progression of tumor growth is followed by three dimensional caliper measurements and recorded as a function of time. Initial statistical analysis is done by repeated measures analysis of variance (RMANOVA), followed by Scheffe post hoc testing for multiple comparisons. Vehicle alone (captisol, or the like) is the negative control. Compounds of the present invention will be active at 150 mpk.
Human gastric adenocarcinoma tumor cells (MKN45 cells, ATCC) are expanded in culture, harvested and injected subcutaneously into 5-8 week old female nude mice (CDl nu/nu, Charles River Labs) (n=10). Subsequent administration of compound by oral gavage or by IP (10-100 mpk/dose) begins anywhere from day 0 to day 29 post tumor cell challenge and generally continues either once or twice a day for the duration of the experiment. Progression of tumor growth is followed by three dimensional caliper measurements and recorded as a function of time. Initial statistical analysis is done by repeated measures analysis of variance (RMANOVA), followed by Scheffe post hoc testing for multiple comparisons. Vehicle alone (captisol, or the like) is the negative control. Compounds of the present invention will be active at 150 mpk.
FORMULATIONS
Also embraced within this invention is a class of pharmaceutical compositions comprising the active compounds of Formula I-II in association with one or more non-toxic, pharmaceutically-acceptable carriers and/or diluents and/or adjuvants (collectively referred to herein as "carrier" materials) and, if desired, other active ingredients. The active compounds of the present invention may be administered by any suitable route, preferably in the form of a pharmaceutical composition adapted to such a route, and in a dose effective for the treatment intended. The compounds and compositions of the present invention may, for example, be administered orally, mucosally, topically, rectally, pulmonarily such as by inhalation spray, or parentally including intravascularly, intravenously, intraperitoneally, subcutaneously, intramuscularly intrasternally and infusion techniques, in dosage unit formulations containing conventional pharmaceutically acceptable carriers, adjuvants, and vehicles.
The pharmaceutically active compounds of this invention can be processed in accordance with conventional methods of pharmacy to produce medicinal agents for administration to patients, including humans and other mammals.
For oral administration, the pharmaceutical composition may be in the form of, for example, a tablet, capsule, suspension or liquid. The pharmaceutical composition is preferably made in the form of a dosage unit containing a particular amount of the active ingredient. Examples of such dosage units are tablets or capsules. For example, these may contain an amount of active ingredient from about 1 to 2000 mg, preferably from about 1 to 500 mg. A suitable daily dose for a human or other mammal may vary widely depending on the condition of the patient and other factors, but, once again, can be determined using routine methods.
The amount of compounds which are administered and the dosage regimen for treating a disease condition with the compounds and/or compositions of this invention depends on a variety of factors, including the age, weight, sex and medical condition of the subject, the type of disease, the severity of the disease, the route and frequency of administration, and the particular compound employed. Thus, the dosage regimen may vary widely, but can be determined routinely using standard methods. A daily dose of about 0.01 to 500 mg/kg, preferably between about 0.01 and about 50 mg/kg, and more preferably about 0.01 and about 30 mg/kg body weight may be appropriate. The daily dose can be administered in one to four doses per day.
For therapeutic purposes, the active compounds of this invention are ordinarily combined with one or more adjuvants appropriate to the indicated route of administration. If administered per os, the compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkaiioic acids, cellulose alkyl esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulfuric acids, gelatin, acacia gum, sodium alginate, polyvinylpyrrolidone, and/or polyvinyl alcohol, and then tableted or encapsulated for convenient administration. Such capsules or tablets may contain a controlled- release formulation as may be provided in a dispersion of active compound in hydroxypropylmethyl cellulose.
In the case of psoriasis and other skin conditions, it may be preferable to apply a topical preparation of compounds of this invention to the affected area two to four times a day. Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin {e.g., liniments, lotions, ointments, creams, or pastes) and drops suitable for administration to the eye, ear, or nose. A suitable topical dose of active ingredient of a compound of the invention is 0.1 mg to 150 mg administered one to four, preferably one or two times daily. For topical administration, the active ingredient may comprise from 0.001 % to 10% w/w, e.g. , from 1 % to 2% by weight of the formulation, although it may comprise as much as 10% w/w, but preferably not more than 5% w/w, and more preferably from 0.1% to 1% of the formulation.
When formulated in an ointment, the active ingredients may be employed with either paraffmic or a water-miscible ointment base. Alternatively, the active ingredients may be formulated in a cream with an oil-in- water cream base. If desired, the aqueous phase of the cream base may include, for example at least 30% w/w of a polyhydric alcohol such as propylene glycol, butane- 1, 3 -diol, mannitol, sorbitol, glycerol, polyethylene glycol and mixtures thereof. The topical formulation may desirably include a compound, which enhances absorption or penetration of the active ingredient through the skin or other affected areas. Examples of such dermal penetration enhancers include DMSO and related analogs.
The compounds of this invention can also be administered by a transdermal device. Preferably transdermal administration will be accomplished using a patch either of the reservoir and porous membrane type or of a solid matrix variety. In either case, the active agent is delivered continuously from the reservoir or microcapsules through a membrane into the active agent permeable adhesive, which is in contact with the skin or mucosa of the recipient. If the active agent is absorbed through the skin, a controlled and predetermined flow of the active agent is administered to the recipient, hi the case of microcapsules, the encapsulating agent may also function as the membrane.
The oily phase of the emulsions of this invention may be constituted from known ingredients in a known manner. While the phase may comprise merely an emulsifier, it may comprise a mixture of at least one emulsifier with a fat or an oil or with both a fat and an oil. Preferably, a hydrophilic emulsifier is included together with a lipophilic emulsifier, which acts as a stabilizer. It is also preferred to include both an oil and a fat. Together, the emulsifier(s) with or without stabilizer(s) make-up the so-called emulsifying wax, and the wax together with the oil and fat make up the so-called emulsifying ointment base, which forms the oily dispersed phase of the cream formulations. Emulsifiers and emulsion stabilizers suitable for use in the formulation of the present invention include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate, sodium lauryl sulfate, glyceryl distearate alone or with a wax, or other materials well known in the art.
The choice of suitable oils or fats for the formulation is based on achieving the desired cosmetic properties, since the solubility of the active compound in most oils likely to be used in pharmaceutical emulsion formulations is very low. Thus, the cream should preferably be a non-greasy, non-staining and washable product with suitable consistency to avoid leakage from tubes or other containers. Straight or branched chain, mono- or dibasic alkyl esters such as di- isoadipate, isocetyl stearate, propylene glycol diester of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl stearate, 2-ethylhexyl palmitate or a blend of branched chain esters may be used. These may be used alone or in combination depending on the properties required. Alternatively, high melting point lipids such as white soft paraffin and/or liquid paraffin or other mineral oils can be used.
Formulations suitable for topical administration to the eye also include eye drops wherein the active ingredients are dissolved or suspended in suitable carrier, especially an aqueous solvent for the active ingredients. The active ingredients are preferably present in such formulations in a concentration of 0.5 to 20%, advantageously 0.5 to 10% and particularly about 1.5% w/w.
Formulations for parenteral administration may be in the form of aqueous or nonaqueous isotonic sterile injection solutions or suspensions. These solutions and suspensions may be prepared from sterile powders or granules using one or more of the carriers or diluents mentioned for use in the formulations for oral administration or by using other suitable dispersing or wetting agents and suspending agents. The compounds may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, tragacanth gum, and/or various buffers. Other adjuvants and modes of administration are well and widely known in the pharmaceutical art. The active ingredient may also be administered by injection as a composition with suitable carriers including saline, dextrose, or water, or with cyclodextrin (ie. Captisol), cosolvent solubilization (ie. propylene glycol) or micellar solubilization (ie. Tween 80).
The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example as a solution in 1,3- butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed, including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of iηjectables. For pulmonary administration, the pharmaceutical composition may be administered in the form of an aerosol or with an inhaler including dry powder aerosol.
Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable non-irritating excipient such as cocoa butter and polyethylene glycols that are solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum and release the drug.
The pharmaceutical compositions maybe subjected to conventional pharmaceutical operations such as sterilization and/or may contain conventional adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers etc. Tablets and pills can additionally be prepared with enteric coatings. Such compositions may also comprise adjuvants, such as wetting, sweetening, flavoring, and perfuming agents.
The foregoing is merely illustrative of the invention and is not intended to limit the invention to the disclosed compounds. Variations and changes, which are obvious to one skilled in the art are intended to be within the scope and nature of the invention, which are defined, in the appended claims. From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.
No unacceptable toxological effects are expected when compounds of the present invention are administered in accordance with the present invention.
All mentioned references, patents, applications and publications, are hereby incorporated by reference in their entirety, as if here written.

Claims

WHAT IS CLAIMED IS:
1. A compound of formula I
R-X-W-Y-R1 I
enantiomers, diastereomers, salts solvates, and N-oxides thereof wherein R is
Figure imgf000233_0001
T is selected from phenyl, 5-6-membered heteroaryl, or 5-6 membered heterocyclyl; Z is selected from N or CR7;
Z1 is selected from N or CR7; W is an substituted or unsubstituted phenyl, a substituted or unsubstituted benzomorpholinyl, a substituted or unsubstituted 6-membered nitrogen containing heteroaryl; a substituted or unsubstituted c3-7cycloalkyl, chalky and crόalkynyl; X is selected from O, S, S(=O), SO2, NR2 and CR3R4;
Y is selected from -NRaC(=O)-(CR3R4)p-, -NRaC(=S)-(CR3R4)p-, -NRa-(CR3R4)p-5 -NRa- (CR3R4)pC(=O)-, -NRa-(CR3R4)pC(=S)-, -NRaS(=O)r, -NRaS(=O)t-(CR3R4)p-, -C(=O)NRa-(CR3R4)p-, and -NRa-(CR3R4)p-S(=O)r, and where W is benzomorpholinyl Y may further include -C(=O); Ra is selected from H, alkyl, heterocyclyl, aryl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl; wherein Ra is optionally substituted; R1 is a partially unsaturated or saturated ring selected from
Figure imgf000233_0002
wherein J is N or CR4a; J2 is O or CR4aR4a;
Q is a 1-5 membered saturated or partially unsaturated alkly chain, or a 2-5 membered saturated or partially unsaturated heteroalkyl chain; R1 is optionally fused with an optionally substituted phenyl or an optionally substituted 5-6 membered heterocyclyl ring; wherein R1 is optionally substituted with one or more substituents independently selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-6 alkyl, R5(S=O)-C1-6 alky, NR5R^-(C=O)-C1 -6 alky, optionally substituted alkyl, alkenyl hydroxyalkyl, C1-6 alkoxy-C1-6 alkyl, alkenylalkyl, C1-6 alkylthio-C1-3 alkyl, -C1-6 alkyl-NRa-C(=O)-OR5, • -C1-3 alkyl-NRa-(C=O)-R5, -C1-3 alkyl-C(=O)- C1-3 alkyl, aminoalkyl, hydroxy- substituted aminoalkyl, hydroxy-substituted haloalkyl, (heterocyclo)hydroxyalkyl, haloC1-6-alkyl, azidoalkyl, optionally substituted aryl-C1-6 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-6 alkyl, optionally substituted C1-6-alkyl, optionally substituted C3-7 cycloalkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted 5-10 membered heteroaryl, optionally, optionaolly substituted C3-6 cycloalkyl, substituted heteroarylalkyl, optionally substituted arylalkyl, and optionally substituted C6-I0 aryl; R2 is selected from H, alkyl, haloalkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl and R5-carbonyl; R3 and R4 are each independently selected from H, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, R6 and alkyl substituted with R6; alternatively R3 and R4, together with the carbon atom they are attached to, form an optionally substituted 3-6 membered ring;
R3a is absent or is selected from H, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, R6 and alkyl substituted with R6; R4a is absent or is selected from H, halo, -OR5 -NRaR5, alkyl, aryl, heterocyclyl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, R6 and alkyl substituted with R6; R5 is independently selected at each occurrence from H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl, alkylthioalkyl, arylalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl; R5a is independently selected at each occurrence from H, alkyl, haloalkyl, arylalkyl aminoalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl; or when R5 and Ra, or R5aand Ra are bonded to the same nitrogen atom, Ra and R5, or Ra and R5a may independently optionally combine to form a heterocyclo ring.
R6 is selected from cyano, -OR2, -SR2, halo, -SO2R2, -C(=O)R2, -SO2NR2R5, -NR5C(=O)OR2, - NR5C(^O)NR5R2, -NR5C(=O)R2, -CO2R2, -C(O)NR2R5 and -NR2R5;
R7 is selected from H, halo, cyano, -C(=O)NRaR5 and alkyl; R8 is one or more substituents independently selected at each occurrence from H, cyano, hydroxyl, halo, optionally substituted heterocyclyl, -C(=O)NRaR5, - OC(=O)NRaR5, -NRaC(=O)OR5, -NRaC(=O)-R5, R5RaN-O2S-, R5O2S-, R5O2SR3N-, R5RaN-, alkyl, aminoalkyl, alkylaminoalkyl, alkoxyalkyl, phenylalkyl, heterocyclylalkyl, alkoxy, haloalkoxy, alkylaminoalkoxy, arylalkoxy, heterocyclylalkoxy, cycloalkylalkoxy, heterocyclyl(hydroxyalkoxy), cycloalkyl(hydroxyalkoxy), aryl(hydroxyalkoxy), alkoxyalkoxy, aryloxyalkoxy, heterocyclyloxyalkoxy, cycloalkyloxyalkoxy, aryloxy, heterocyclyloxy, cycloalkyloxy; aryl and heteroaryl, alternatively where R8 comprises an NRaR5 moiety Ra and R5, together with the nitrogen atom they are attached to, may optionally form a substituted or unsubstituted 4-
6 membered ring;
R8* is one or more substituents independently selected at each occurrence from H, cyano, hydroxyl, halo, optionally substituted heterocyclyl, -NRaC(=0)NRaR5' NRaC(=NRb)-NR5, NRaC(=S)NRaR5, -0C(-0)NRaR5, -NRaC(=O)OR5, -
NRaC(=0)-R5, R5RaN-O2S-, R5O2S-, R5O2SRaN-, R5RaN-, alkyl, aminoalkyl, alkylaminoalkyl, alkoxyalkyl, phenylalkyl, heterocyclylalkyl, alkoxy, haloalkoxy, alkylaminoalkoxy, arylalkoxy, heterocyclylalkoxy, cycloalkylalkoxy, heterocyclyl(hydroxyalkoxy), cycloalkyl(hydroxyalkoxy), aryl(hydroxyalkoxy), alkoxyalkoxy, aryloxyalkoxy, heterocyclyloxyalkoxy, cycloalkyloxyalkoxy, aryloxy, heterocyclyloxy, and cycloalkyloxy; alternatively where R8a comprises an NRaR5 moiety Ra and R5, together with the nitrogen atom they are attached to, may optionally form a substituted or unsubstituted 4-6 membered ring; p is O, 1, 2, or 3; and t is O, 1 or 2; wherein each alkyl, aryl, heteroaryl, cycloalkyl, alkenyl, alkynyl, heterocyclyl, and alkoxy moiety of any R, R1, R2, R3, R4, R5, R7, R8, R8*, and Ra is optionally independently substituted with one or more groups independently selected at each occurrence from halo, oxo, -NRaR5, -OR5a, -CO2R5, -C(=O)R5, (Q-C^alkylamino, -NH-N=NH5 (Ci-C6)alkyl, (C1-C6)alkynyl, (C3-C6)cycloalkyl, (d-C^haloalkyl, di(C1-C6)alkylamino, (C1- C6)alkylamino-(C1-C6)alkyl, (CrC6)hydroxyalkylamino, (C1-C6)alkylamino-(C1- C6)alkylamino, phenyl, heterocyclic, heteroaryl, ~(CR3R4)palkyl-S(=O)-alkyl, and -(CR3R4)palkyl-S(O)2-alkyl.
2. Compound of Claim 1, wherein R is selected from
Figure imgf000236_0001
wherein R8 is independently selected at each occurrence from H, cyano, hydroxy, - C(=O)NRaR5a, 5-6 membered heterocyclyl, -NRaC(=O)-R5a, R5aRaN-O2S-, R5aO2SRaN-5 R5aRaN-, C1-6-alkyl, amino-C1-6- alkyl, C1-6-alkylamino-C1-6-alkyl, alkoxy-C1-6-alkyl, phenyl-C1-6-alkyl, heterocyclyl-C1-6- alkyl, C1-6-alkoxy, halo-C1-6-alkoxy, C1-6-alkylammo-C1-6-alkoxy, aryl-C1-6-alkoxy, 5-6- membered heterocyclyl-C1-6-alkoxy, C^ό-cycloalkyl-d-e-alkoxy, 5-6-membered heterocyclyl(hydroxyl-C1-6-alkoxy), C3-6-cycloalkyl(hydroxyl-C1-6-alkoxy), phenyl(hydroxyl-C1-6-alkoxy), C1-6-alkoxy-C1-6-alkoxy, phenyloxy-C1-6-alkoxy, 5-6 membered heterocyclyloxy-C1-6-alkoxy, Cs-β-cycloalkyloxy-Q-e-alkoxy, phenyloxy, 5-6- membered heterocyclyloxy, and Q-e-cycloalkyloxy; wherein Ra is selected from H, C1-6-alkyl, 5-6 membered heterocyclyl, phenyl, phenyl-C1-6- alkyl, 5-6 membered heterocyclyl-Ci-e-alkyl, C3-6-cycloalkyl, C^e-cycloalkyl-Ci-e-alkyl,
C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C^-alkyl, C3-6-CyClOaUCyI-C1 -6-alkyl, phenyl, 5-6-membered heterocyclyl, C2- 6-alkenyl, C2-6-alkynyl and C3-6-cycloalkyl; and pharmaceutically acceptable salts thereof.
3. Compound of Claim 1 wherein R is independently selected at each occurrence from H, cyano, aminocarbonyl, C1-3-alkylaminocarbonyl, C1-6-alkyl, C1-6-alkoxy, C1-3-alkylamino- C1-3-alkoxy, 5-6 membered heterocyclyl-C1-3-alkoxy, C4-6-cycloalkyl-C1-3-alkoxy, 5-6 membered heterocyclyl-C1-3-(hydroxyalkoxy), C3-6-cycloalkyl-C1-3-(hydroxyalkoxy), C1-2- alkoxy-C1-3-alkoxy, phenyloxy-C1-3alkoxy, 5-6 membered heterocyclyloxy-C1-3-alkoxy, cycloalkyloxy-C1-3-alkoxy, 5-6 membered heterocyclyloxy, and C3-6~cycloalkyloxy; and pharmaceutically acceptable salts thereof.
4. Compound of Claim 1 wherein R8 is independently selected from H, methyl, cyano, heterocyclic, heteroaryl, aminocarbonyl, methylaminocarbonyl, methoxy, dimethylaminopropoxy, 3-(morpholin-4-yl)propoxy, 3-(pyrrolidin-l-yl)propoxy, 2-hydroxy-3- (morpholin-4-yl)propoxy, 3-(l,2,4-triazol-l-yl)propoxy, 3-(4-methylpiperazin-l-yl)propoxy, 3- (piperidin-4-yl)propoxy, dimethylaminoethoxy and diethylaminoethoxy; and pharmaceutically acceptable salts thereof.
5. Compound of Claim 1 wherein R is selected from 6,7-dimethoxy-4-quinolinyl, 7- methoxy-4 quinonlinyl, 6-methoxy-7-(dimethylaminopropoxy)-4-quinolinyl, 6-methoxy-7-(3- (morpholin-4-yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 -(pyrrolidin- 1 -yl)propoxy)-4- quinolinyl, 6-methoxy-7-(2-hydroxy-3 -(morpholin-4-yl)propoxy)-4-quinolinyl, 6-methoxy-7- (3-(l,2,4-triazol-l-yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3-(4-methylpiperazin-l- yl)propoxy)-4-quinolinyl, 6-methoxy-7-(3 -(piperidin-4-yl)propoxy)-4-quinolinyl, 6,7- dimethoxy-4-quinazolinyl and 6-methoxy-7-(dimethylaminopropoxy)-4-quinazolinyl; and pharmaceutically acceptable salts thereof.
6. Compound of Claim 1 wherein W is selected from substituted or unsubstituted phenyl, substituted or unsubstiruted pyridyl, substituted or unsubstiruted pyrimidinyl, substituted or unsubstiruted pyridazinyl and substituted or unsubstiruted pyrazinyl; and pharmaceutically acceptable salts thereof.
7. Compound of Claim 1 wherein W is substituted or unsubstiruted phenyl; and pharmaceutically acceptable salts thereof.
8. Compound of Claim 1 wherein W is substituted or unsubstiruted pyridyl; and pharmaceutically acceptable salts thereof.
9. Compound of Claim 1 wherein X is O; and pharmaceutically acceptable salts thereof.
10. Compound of Claim 1 wherein Y is selected from -NHC(=O)-, -NHCC=O)-(CH2)P-. -NH-(CH2)p-, and -NH-(CH2)pC(=O)-; and wherein p is 0 or 1; and pharmaceutically acceptable salts thereof.
11. Compound of Claim 1 wherein Y is -NHC(=O)-; and pharmaceutically acceptable salts thereof.
12. Compound of Claim 1 wherein p is 1 ; and pharmaceutically acceptable salts thereof.
13. Compound of Claim 1 wherein R1 is selected from
Figure imgf000238_0001
Figure imgf000239_0001
Figure imgf000239_0003
Figure imgf000239_0002
wherein Rb is independently selected at each occurrence from H, optionally substituted arylalkyl, optionally substituted 5-6-membered heterocyclyl-Ci-3 alkyl, optionally substituted Q-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-C1-3alkyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Ci-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-Ci-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, Ci-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered
Figure imgf000239_0004
RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent R0 substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
14. Compound of Claim 13 wherein
Rb is selected from H, optionally substituted benzyl, C1-3 alkylaryl, C1-3 alkylheteroaryl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, methoxymethyl,, -(C1-6)alkyl,2-hydroxy 2- methylbutyl, 2-hydroxy-2-methylpropyl, 2-hydroxypropyl, 1-(1- hydroxycyclopropyl)methyl,, ethylaminomethyl, piperidin- 1 -ymiethyl, pyrrolidin- 1 - ylmethyl, pyridyl, thienyl, optionally substituted phenyl, 1-naphthy, nitrile, -C(^O)OR5*1, -C(=0)NRSaRa, and -C(=O)R5a ;
Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec- butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered
Figure imgf000240_0001
optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; C6-10 aryl, nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents bound to the same atom, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts solvates and N-Oxides thereof.
15. Compound of Claim 1 wherein R1 is selected from
Figure imgf000241_0001
wherein Rb is independently selected at each occurrence from H, optionally substituted phenyl- C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substitutedC6-10heteroaryl,, optionally substituted C3-6 cycloalkyl, 2-oxo-propyl, 2-fluoropropyl 2-azidopropyl, and RaR5aN-C1-3alkyl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, -C1-3 alkyl-NRa-C(=O)-OR5, optionally substituted C6-io aryl; nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents bound to the same atom, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts solvates and N-Oxodes thereof.
16. A Compound of Claim 15 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, 3-hydroxypropyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl,2-oxopropyl, 2-azidopropyl,, 2-fluoropropyl,, 2- hydroxypropyl, , 2-hydroxy-3-aminoproply,.2-methoxypropyl,, 2-aminoproply,, 1(1- hydroxycycloproplyl)methyl, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1-naphthyl; wherein R° is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted heteroaryl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6- membered heterocyclyl; or wherein two Rc substituents, two R substituents or Rc together with R together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
17. Compound of Claim 1 wherein R1 is selected from
Figure imgf000242_0001
Figure imgf000243_0001
wherein Rb is independently selected at each occurrence from H, optionally substituted phenyl- C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 aryl, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl, and RaR5aN-Ci-3alkyl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted Ci-6-alkyl, optionally substituted 5-6 membered heterocyclyl, -C1-3 alkyl-NRa-C(=O)-OR5, optionally substituted C6-10 aryl; nitrile, -C(=O)OR5a, -C(=O)NR5aRa, -C(=O)R5a and optionally substituted heteroraryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-Ci-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
18. Compound of Claim 17 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, methylaminomethyl, ethylaminomethyl, piperidin- 1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1- naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-l-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two R substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
19. Compound of Claim 1 wherein R1 is selected from
Figure imgf000244_0001
wherein Rb is independently selected at each occurrence from H, optionally substituted phenyl- C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, and RaR5aN-C1-3alkyl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R58R21N-C1 -3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-Ci-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted
Ci-6-alkyl, optionally substituted 5-6 membered heterocyclyl, -C1-3 alkyl-NRa-C(=O)-OR5, optionally substituted Cβ-.o aryU and optionally substituted heteroraryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-Ci-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent R° substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
20. Compound of Claim 19 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, methylaminomethyl, ethylaminomethyl, piperidin- 1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1- naphthyl; wherein R0 is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with R together form an optionally substituted fused phenyl ring; or wherein two R° substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
21. Compound of Claim 1,
Figure imgf000245_0001
enantiomers, diastereomers, salts, solvates and N-Oxides thereof wherein T is O or S; wherein R3 and R4 is each independently selected from H, C1-2-alkyl, phenyl, 5-6-membered heterocyclyl, phenyl-C1-2-alkyl, 5-6-membered heterocyclyl- d-2-alkyl, C3-6.cycloalkyl, and C3-6-cycloalkyl-C1-2-alkyl; alternatively R3 and R4, together with the atom they are attached to, form an optionally substituted 3-6 membered ring; wherein R9 and R10 is independently selected from H, cyano, hydroxy, -C(=O)NRaR5a, 5-6 membered heterocyclyl, -NRaC(=O)-R5a, R5aRaN-O2S-, R5aO2SRaN-, R5aRaN-, C1-6-alkyl, amino-Ci-6- alkyl, C1-6-alkylamino-C1-6-alkyl, alkoxy-C1-6-alkyl, hydroxy, aryl-C1-6-alkyl, heterocyclyl-C!. 6-alkyl, C1-6-alkoxy, halo-C1-6-alkoxy, C1-6-alkylamino-C1-6-alkoxy, aryl-C1-6-alkoxy, 5-6- membered heterocyclyl, -C1-6alkoxy, C3-6-cycloalkyl-C1-6-alkoxy, 5-6-membered heterocyclyl(hydroxyl-C1-6-alkoxy), C3-6-cycloalkyl(hydroxyl-C1-6-alkoxy), phenyl(hydroxyl- C1-6-alkoxy), Ci-6-alkoxy-C1-6-alkoxy, phenyloxy-C1-6-alkoxy, 5-6 membered heterocyclyloxy- C1-6-alkoxy, C3-6-cycloalkyloxy-C1-6-alkoxy, phenyloxy, 5-6-membered heterocyclyloxy, and C3-6-cycloalkyloxy; wherein each of Za, Zb, Zc and Zd is independently selected from N or CH; provided no more than 2 of Za, Zb, Zc and Zd are N; wherein n is 0, 1 , 2 or 3 ; wherein D1 is selected from N or CR11; wherein D2 is selected from NR13, O5 or CHR11; provided either D1 is N or D2 is NR13;
O wherein ring Rd including D1 D2 forms an optionally substituted optionally benzo-fused 4-7 membered heterocyclic moiety, wherein R11 is selected from H, halo, Ci-4-alkyl, C1-4-haloalkyl, C1-4-hydroxyalkyl, -NH2, -
OR12, alkoxycarbonyl, -CO2H, -CONR3R5a, (C1-C3)alkylamino, di(C1-C6)alkylamino, (C1- C3)hydroxyalkylamino, (C1-C3)alkylamino-(C1-C3)alkylamino, Q-3-alkoxy-Q-ralkyl, C1-3- alkylamino-C1-3-alkyl, Ct-ralkylthio-Q-ralkyl, optionally substituted phenyl-C1-3-alkyl, 5-
6 membered heterocyclyl-C1-3-alkyl, C3-6-cycloalkyl-C1-3-alkyl, optionally substituted phenyl, optionally substituted 5-6 membered heterocyclyl, and C3-6-cycloalkyl; wherein Ra is selected from H, alkyl, heterocyclyl, aryl, arylalkyl, heterocyclylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl and alkynyl; wherein R5a is selected from H, alkyl, haloalkyl, arylalkyl, heterocyclylalkyl, cycloalkylalkyl, aryl, heterocyclyl, alkenyl, alkynyl and cycloalkyl; wherein R12 is selected from H, halo, C1-2-alkyl and methoxy; wherein R13 is selected from H, alkyl, haloalkyl, optionally substituted phenylalkyl, optionally substituted 5-10 membered heterocyclylalkyl, cycloalkylalkyl, optionally substituted phenyl or naphthyl, optionally substituted 5-10 membered heterocyclyl and cycloalkyl; and pharmaceutically acceptable salts thereof.
22. Compound of Claim 21 wherein R9 and R10 are independently selected from H, cyano, aminocarbonyl, Ci-ralkylaminocarbonyl, C1-3-alkylamino-C1-3-alkoxy, 5-6 membered heterocyclyl, -C1-3-alkoxy, hydroxy C4-6-cycloalkyl-C1-3-alkoxy, 5-6 membered heterocyclyl-
Figure imgf000247_0002
C3-6-cycloalkyl-C1-3-(hydroxyalkoxy),
Figure imgf000247_0001
phenyloxy-C1-3alkoxy, 5-6 membered heterocyclyloxy-C1-3-alkoxy, cycloalkyloxy-C1-3-alkoxy, 5-6 membered heterocyclyloxy, and C3-6-cycloalkyloxy; and pharmaceutically acceptable salts solvates and N-Oxides thereof.
23. Compound of Claim 21 wherein R9 is independently selected from H, methyl, cyano, aminocarbonyl, methylaminocarbonyl, methoxy, hydroxy, dimethylaminopropoxy, 3- (morpholin-4-yl)propoxy, 3-(pyrrolidin-l-yl)propoxy, 2-hydroxy-3-(morpholin-4-yl)propoxy, 3-(l,2,4-triazol-l-yl)propoxy, 3-(4-methylpiperazin-l-yl)propoxy, 3-(piperidin-4-yl)propoxy, dimethylaminoethoxy, 1-morpholinyl, 1-piperazinyl, 4-methylpiperazinyl, pyrolidinyl,, 3- aminopyrolidnyl, diethylaminoethoxy; and pharmaceutically acceptable salts thereof.
24. Compound of Claim 21 wherein R10 is H or alkoxy; and
R9 isalkoxy; or heterocyclyl and pharmaceutically acceptable salts solvates and N- Oxides thereof.
25. Compound of Claim 21 wherein Za is CH; wherein Zb is CH; wherein Ze is CF; and wherein Zd is CH; and pharmaceutically acceptable salts thereof.
26. Compound of Claim 21 wherein Za is N; wherein Za is CH; wherein Zc is CH; wherein Zd is CH; and wherein R12 is H; and pharmaceutically acceptable salts thereof.
27. Compound of Claim 21 wherein Za is CH; wherein Zb is N; wherein Zc is CH; wherein Zd is CH; and wherein R12 is H; and pharmaceutically acceptable salts thereof.
28. Compound of Claim 15 wherein Za is CH; wherein Zb is N; wherein Zc is CH; wherein Z is N; and wherein R is H; and pharmaceutically acceptable salts thereof.
Figure imgf000248_0001
wherein Rb is selected from H, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6-10 aryl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-,
R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6-10 aryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-Ci-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent R substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
30. Compound of Claim 29 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, methylaminomethyl, ethylaminomethyl, piperidin- 1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1- naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-Q-ralkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two R0 substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents bound to the same atom, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
Figure imgf000249_0001
substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6-io aryl; wherein two R° groups bound the same atome my combine to form a C3-6 spiro ring wherein Ra is selected from H, C^-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-Ci-β-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two R0 substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
32. Compound of Claim 31 wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6- membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or R° together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
33. Compound of Claim 21 wherein Rd is
Figure imgf000250_0001
wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-d-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6-Io aryl; wherein two Rc groups bound to the same atom may combine to form a C3-6 spiro ring; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
34. Compound of Claim 31 wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-Ci-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6- membered heterocyclyl; or wherein two Rc substituents, together form an optionally substituted fused phenyl ring; or wherein two Rc substituents bound to the same atom my combine tp form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
Figure imgf000251_0001
35. Compound of Claim 21 wherein R is Rb ; wherein Rb is selected from H, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6-1O aryl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6- 10 aryl; wherein two Rc groups bound to the same atom may combine to form a C3-6 spiro ring; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-CyClOaUCyI-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, Ci-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(==O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents bound to the same atome may combine to form an optionally substituted C3-6 spiro ring; and pharmaceutically acceptable salts thereof.
36. Compound of Claim 33 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, methylaminomethyl, etliylaminomethyl, piperidin- 1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1- naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin- 1 -ylmethyl, pyrrolidin- 1 -ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
37. Compound of Claim 21 wherein Rd is
Figure imgf000252_0001
Rc wherein Rb is independently selected at each occurrence from H, optionally substituted phenyl- C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 aryl, optionally substituted C6-10 heteroaryl, optionally substituted C3-6 cycloalkyl,and RaR5aN-C1-3alkyl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, -C1-3 alkyl-NRa-C(=O)-OR5, optionally substituted C6-10 aryl; and optionally substituted heteroraryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, ρhenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, Cs-β-cycloalkyl-Ci-e-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent R together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
38. Compound of Claim 35 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, 3-hydroxypropyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl,2-oxopropyl, 2-azidopropyl,, 2-fluoropropyl,, 2- hydroxypropyl, , 2-hydroxy-3-aminoproply,.2-methoxypropyl,, 2-aminoproply,, 1(1- hydroxycycloproplyl)methyl, ethylaminomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1-naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted heteroaryl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6- membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
39. Compound of Claim 21 wherein Rd is
Figure imgf000253_0001
wherein Rb is selected from H, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl- C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6-10 aryl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, and optionally substituted C6- lo aryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-Ci-6-alkyl, 5-6 membered heterocyclyl-Ci-δ-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
40. Compound of Claim 37 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, methylaminomethyl, ethylaminomethyl, piperidin- 1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1- naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two R° substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
Figure imgf000255_0001
41. Compound of Claim 21 wherein Rd is Rc; wherein Rb is independently selected at each occurrence from H, optionally substituted phenyl- C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, optionally substituted C3-6 cycloalkyl, optionally substituted C3- 6cycloalkyl-C1-3alkyl, and RaR5aN-C1-3alkyl; wherein Rc is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, -C1-3 alkyl-NRa-C(=O)-OR5, optionally substituted C6-10 aryl; and optionally substituted heteroraryl, nitrile, C(=O)OR5' C(=O)NR5aRa', C(=O)R5; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-C1-6- alkyl, C2.6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent RQ substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
42. Compound of Claim 39 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, methylaminomethyl, ethylaminomethyl, piperidin- 1-ylmethyl, pyrrolidin-1-ylmethyl, pyridyl, thienyl, optionally substituted phenyl, and 1- naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted thienyl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6-membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
Figure imgf000256_0001
43. Compound of Claim 15 wherein Rd is Rc; wherein Rb is independently selected at each occurrence from H, optionally substituted phenyl- C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted C6-10 ary, and RaR5aN-C1-3alkyl; wherein R° is one or more substituents selected from H, halo, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, C1-3 alkoxy-C1-3 alkyl, C1-3 alkylthio-C1-3 alkyl, optionally substituted phenyl-C1-3 alkyl, optionally substituted 5-6-membered heterocyclyl-C1-3 alkyl, optionally substituted C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, -C1-3 alkyl-NRa-C(=O)-OR5, optionally substituted C6-K) aryl; and optionally substituted heteroraryl; wherein Ra is selected from H, C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl, optionally substituted phenyl, optionally substituted phenyl-C1-6-alkyl, optionally substituted 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl, C3-6-cycloalkyl-Cμ6- alkyl, C2-6-alkenyl and C2-6-alkynyl; and wherein R5a is selected from H, C1-6-alkyl, C1-6-haloalkyl, phenyl-C1-6-alkyl, 5-6 membered heterocyclyl-C1-6-alkyl, C3-6-cycloalkyl-C1-6-alkyl, RaC(=O)-, optionally substituted phenyl, optionally substituted 5-6-membered heterocyclyl, C2-6-alkenyl, C2-6-alkynyl and C3-6- cycloalkyl; or wherein two adjacent Rc substituents, two adjacent Rb substituents or Rc together with an adjacent Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted spiro ring; and pharmaceutically acceptable salts thereof.
44. Compound of Claim 41 wherein Rb is selected from H, optionally substituted benzyl, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, hydroxymethyl, methoxymethyl, methoxyethyl, 2-hydroxy-2-methylpropyl, ethylaminomethyl, optionally substituted heterorayrl, optionally substituted phenyl, and 1-naphthyl; wherein Rc is one or more substituents selected from H, methyl, isopropyl, tert-butyl, bromo, fluoro, hydroxyl, R5aRaN-, R5aRaN-C1-3 alkyl, methoxymethyl, methoxyethyl, methylthiomethyl, piperidin-1-ylmethyl, pyrrolidin-1-ylmethyl, optionally substituted phenyl, optionally substituted heteroaryl, and optionally substituted benzyl; wherein Ra is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenyl, and phenylmethyl; and wherein R5a is selected from H, methyl, ethyl, isopropyl, butyl, sec-butyl, isobutyl, phenylmethyl, optionally substituted 5-6 membered heterocyclyl-C1-2-alkyl, optionally substituted phenyl, and optionally substituted 5-6- membered heterocyclyl; or wherein two Rc substituents, two Rb substituents or Rc together with Rb together form an optionally substituted fused phenyl ring; or wherein two Rc substituents, together form an optionally substituted 3-6 membered spiro ring; and pharmaceutically acceptable salts thereof.
45. Compound of Claim 21 wherein T is O; and pharmaceutically acceptable salts thereof
46. Compound of Claim 21 wherein n is 0 or 1 ; and pharmaceutically acceptable salts thereof
47. Compound of Claim 21 wherein R3 and R4 are both H; and pharmaceutically acceptable salts thereof
48. Compound of Claim 1 wherein R is
Figure imgf000258_0001
wherein R8a is C1-3 alkyl or H ; and pharmaceutically acceptable salts thereof.
49. Compound of Claim 1 wherein R is
Figure imgf000258_0002
R8 N or
Figure imgf000258_0003
: wherein R8a is C1-3 alkyl or H ; and pharmaceutically acceptable salts thereof.
50. Compound of Claim 1 wherein R is
Figure imgf000258_0004
; and pharmaceutically acceptable salts thereof.
51. Compound of Claim 1 and pharmaceutically acceptable salts and solvates thereof selected from N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-
4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyrrolidin-l- ylmethyl)-2,3-dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((ethyl(methyl)amino)methyl)-l- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide:;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((dimethylamino)methyl)-l-methyl- 3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
5-(aminomethyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; tert-butyl (4-((3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)carbamoyl)- 1 -niethyl-3 -oxo-2- ρhenyl-2,3-dihydro-lH-pyrazol-5-yl)methylcarbamate; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(ρyrrolidin-l- ylmethyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -methyl-3 -oxo-2-phenyl-5-(pyrrolidin- 1 - ylmethyl)-2,3~dihydro-lH-pyrazole-4-carboxamide; N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)ρhenyl)-5-methyl-3 -oxo-2-phenyl- 1 -
((tetraliydrofuran-2-yl)methyl)-2,3-dihydro-lH-pyrazole-4-carboxamide; 5-((ethyl(methyl)amino)methyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l -methyl- 3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
2-benzyl-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-5-(pyridin-4-yl)-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 2-benzyl-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -methyl-3 -oxo-5-(pyridin-4-yl)-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)- 1 -methyl-3 -oxo-2-( 1 -phenylethyl)-5-
(pyridin-4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-(l-phenylethyl)-5-
(pyridin-4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)- 2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)-
2,3-dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(6,7-dimethoxyqumolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-4-yl)-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-2-yl)-
2,3-dihydro-lH-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(pyridin-2-yl)-
2,3-dihydro- 1 H-pyrazole-4-carboxamide;
N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -methyl-3 -oxo-2-phenyl-5-(tetrahydro- , 2H-pyran-4-yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-5-(tetrahydro-2H- pyran-4-yl)-2,3-dihydro-lH-pyrazole-4-carboxamide; 1 -Methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-(2-methyl- 1 ,3 -thiazol-4-yl)-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolmyl)oxy)-2-pyridinyl)-l-methyl-5-(5-methyl-3-isoxazolyl)-
3-0X0-2 -phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-methyl-5-(5-methyl-3-isoxazolyl)-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-ρyridinyl)-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyI)-l-methyl-5-(5-methyl-3-isoxazolyl)-
3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)- 1 -methyl-3 -oxo-2-phenyl-5-(2- pyrazinyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-methyl-3-oxo-2-phenyl-5-(2- pyrazinyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-((6,7-bis(methyloxy)-4-qumolinyl)oxy)-2-pyridinyl)-l-methyl-5-(2-methyl-l,3-thiazol-4- yl)-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)- 1 -methyl-5-(2-methyl- 1 ,3-thiazol-4- yl)-3 -oxo-2-phenyl -2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-N,l,5-trimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
2-(3-chlorophenyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro-lH-ρyrazole-4-carboxamide;
2-(3-chlorophenyl)-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3 -fluorophenyl)- 1 ,5-dimethyl-3 -oxo-2-p-tolyl-2,3 - dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-(657-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-(4-fluorophenyl)-l,5-dimethyl-3- oxo-2, 3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridine-2-yl)- 1 ,5-dimethyl-3 -oxo-2-p-tolyl-2,3 - dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-(4-fluorophenyl)- 1 ,5-dimethyl-3-oxo-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 2-(3-chlorophenyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)- 1 ,5-dimethyl-3 -oxo-2-p-tolyl-2,3 -dihydro- 1 H- pyrazole-4-carboxamide; 2-(2-chlorophenyl)-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 2-(2-chlorophenyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3- oxo-2,3-dihydro- 1 H-pyrazole-4-carboxamide; 2-(2-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-2-(4-fluorophenyl)-l,5-dimethyl-3-oxo- 2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
2-(3-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(6-(6,7-dimethoxyquinolin-4-yloxy)pyridin-3 -yl)- 1 ,5-dimethyl-3 -oxo-2-phenyl-2,3 -dihydro-
1 H-pyrazole-4-carboxamide; N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-l ,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 2-benzyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
2-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l,5-dimethyl-3-oxo-2,3-dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-l-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamide;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3-oxo-l-(2-oxobutyl)-2-phenyl-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl- 1 -(3 -methyl-2-oxobutyl)-3 -oxo-
2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxybutyl)-5-methyl-3 -oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-((2R,3R)-3-hydroxybutan-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-((2R,3R)-3-hydroxybutan-2-yl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (S)-N-(3-fluoro-4-(7-methoxyquinolm-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-l-((3-methyl-2-oxooxazolidin-5- yl)methyl)-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-(methylamino)propyl)-5- methyl-3 -oxo-2-phenyl-2,3-dihydro- 1 H-pyrazole-4-carboxamide; l-(3-chloro-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxy-2-methylbutyl)-5-methyl-3 - oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(2-hydroxy-3-methylbutyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo- 2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-methylbutyl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-3-morpholinopropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-l-(oxazolidm-5-ylmethyl)-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (S)-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxybutyl)-5-methyl-3 -oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(3-amino-2-hydroxypropyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-l H-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)- 1 -(2-hydroxypropyl)-N-(5-(7-methoxyquinolm-4-yloxy)pyridin-2-yl)-5-methyl-3 -oxo-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(3-(dimethylaniino)-2-h.ydroxypropyl)-N-(3-fluoro-4-(7-niethoxyquinolin-4-yloxy)phenyl)-
5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxypropyl)-5-methyl-3 -oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (R)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluoroprienyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxypropyl)-N-(5-(7-metlioxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-
3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (R)-2-(3-chlorophenyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2- hydroxypropyl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide; (R)-2-(3-chlorophenyl)-l-(2-hydroxypropyl)-N-(5-(7-metrioxyqumolin-4-yloxy)pyridin-2-yl)-
5-methyl-3 -oxo-2,3-dihydro- 1 H-pyrazole-4-carboxamide; (R)-N-(3 -fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-2-(4-fluorophenyl)- 1 -(2- hydroxypropyl)-5-methyl-3-oxo-2,3-dihydro-lH-pyrazole-4-carboxamide l-(2-hydroxy-2-metliylpropyl)-N-(5-(l-oxo-7-methoxyquinolin-4-yloxy)pyridin-2-yl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3 -Fluoro-4-(7-hydroxyquinolin-4-yloxy)phenyl)- 1 -(2-hydroxy-2-methylpropyl)-5-methyl-
3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-N-(5-(7-hydroxyquinolin-4-yloxy)pyridin-2-yl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-(6-Ethyl-7-methoxyquinolin-4-yloxy)-3-fluorophenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
N-(3 -fluoro-4-(7-Methoxyquinolin-4-yloxy)phenyl)- 1 ,2-dimethyl-3 -oxo-5-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-(7-Methoxyquinolin-4-yloxy)pyridin-2-yl)-l,2-dimethyl-3-oxo-5-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamide; N-(4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-l,2-dimethyl-3-oxo-5-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(5-(7-Methoxyquinolin-4-yloxy)pyridin-2-yl)- 1 ,5-dimethyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H- pyrazole-4-carboxamide; (R)-l-(2-Hydroxypropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-methyl-3-oxo-5- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; (R)-N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-2-metliyl-3-oxo-
5-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide (S)-N-(3-fluoro-4-(6-methoxyquinolin-4-yloxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3-oxo-
2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
1 -(2-aminoethyl)-N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3 -oxo-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide
1 -(2-(1 ,3-dioxo-l ,3-dihydro-2H-isoindol-2-yl)ethyl)-N-(3-fluoro-4-((7-(methyloxy)-4- quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide;
1 -(2-aminoethyl)-N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3 -oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-l-
(phenylmethyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide l-benzyl-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-l-(2-(methyloxy)ethyl)-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-l-(2-(methyloxy)ethyl)-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxyethyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-((2R)-2-fluoropropyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; (S)-l-(2-(dimethylamino)propyl)-N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-l-(2-(l- pyrrolidinyl)ethyl)-2,3-dihydro-lH-pyrazole-4-carboxamide; l-((2S)-2-fluoropropyl)-5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-3-oxo-
2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-((2S)-2-fluoroproρyl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-((2S)-2-(acetylamino)propyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; l-((2S)-2-aminopropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)plienyl)-5-metliyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-((2S)-2-azidopropyl)-N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-(2-hydroxyethyl)-5-methyl-3-oxo- 2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-2-phenyl-l-propyl-
2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-((2R)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l -((2S)-2-hydroxypropyl)-5- methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-l-(2-methylpropyl)-3-oxo-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
5-methyl-N-(5-((7-(methyloxy)-4-quinolmyl)oxy)-2-pyridinyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-3-oxo-l-(2-oxopropyl)-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 1 -(2,3 -dihydroxy-2-methylpropyl)-N-(3 -fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5 - methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-l-(2-hydroxypropyl)-5-methyl-3- oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinazolinyl)oxy)-3 -fluorophenyl)- 1 -(2-hydroxy-2- methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)oxy)phenyl)-5-methyl-l-(2-methyl-2-propen-l- yl)-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3 -fluorophenyl)- 1 -((2S)-2-hydroxypropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-l-(2- oxopropyl)-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-l-(2,3-dihydroxy-2- methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-ρyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluoroρhenyl)-5-methyl-l-(2-methyl-2-propen-
1 -yl)-3-oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-3-oxo-2-phenyl- 1 -propyl-
2,3-dihydro- 1 H-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-3-oxo-2-phenyl-l-(2- propen- 1 -yl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-((6,7-bis(methyloxy)-l-oxido-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2- phenyl- 1 -(2-propen- 1 -yl)-2,3-dihydro- 1 H-pyrazole-4-carboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-methyl-3-oxo-2-phenyl-l-
(phenylmethyl)-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 4-(6,7-Dimethoxyquinolin-4-yloxy)-3-fluoro-N-(5-oxo-l-phenyl-2,5-dihydro-lH-pyrazol-3- yl)benzamide; 4-(6,7-Dimethoxyquinolin-4-yloxy)-N-((l,2-dimethyl-5-oxo-3-phenyl-2,5-dihydro-lH- pyrazol-4-yl)methyl)-3-fluorobenzarnide;
4-(6,7-Dimethoxyquinolin-4-yloxy)-N-(2,3-dimethyl-5-oxo-l-phenyl-2,5-dihydro-lH-pyrazol- 4-yl)-3-fluorobenzamide
4-(6,7-Dimethoxyquϊnolin-4-yloxy)-N-((2,3-dimethyl-5-oxo-l-phenyl-2,5-dihydro-lH- pyrazol-4-yl)methyl)-3-fluorobenzamide; l-Benzyl-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l,2-dihydropyrazolo[l,5- a]pyridine-3 -carboxamide; 4-((5-(6,7-Dimethoxyquinolin-4-yloxy)pyridin-2-ylamino)methyl)-l,5-dimethyl-2-phenyl-l,2- dihydropyrazol-3 -one; N-(3 -fluoro-4-(2-(3 -methyl- 1 ,2,4-oxadiazol-5-yl)thieno[3 ,2-b]pyridin-7-yloxy)ρhenyl)- 1 -(2- hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide; N-(3 -fluoro-4-((2-( 1 -methyl- 1 H-imidazol-5-yl)thieno[3 ,2-b]pyridin-7-yl)oxy)phenyl)- 1 -(2- hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4- carboxamide; N-(3-fluoro-4-((2-(l-methyl-lH-imidazol-5-yl)thieno[3,2-b]ρyridin-7-yl)oxy)phenyl)-l-((2R)-
2-hydroxypropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; ,
N-(3-fluoro-4-(7H-pyrrolo[2,3-d]pyrimidm-4-yloxy)phenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo~2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3 -fluoro-4-(l H-pyrrolo[2,3 -b]ρyridin-4-yloxy)phenyl)- 1 -(2-hydroxy-2-methylpropyl)-5 - methyl-3 -oxo-2-phenyl-2,3-dihydro- 1 H-pyrazole-4-carboxamide; Metriyl(6-((4-(((l-(2-hydroxy-2-methylpropyl)-5-rnethyl-3-oxo-2-plienyl-2,3-dihydro-lH- pyrazol-4-yl)carbonyl)amino)phenyl)oxy)-lH-benzimidazol-2-yl)carbamate; N-(4-(2-(azetidine-l-carbonyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorophenyl)-5-methyl-3-oxo-
2-phenyl- 1 -propyl-2, 3 -dihydro- 1 H-pyrazole-4-carboxamide;
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-prienyl-2,3-diliydro-lH- pyrazole-4-carboxamido)phenoxy)-N-methylthieno[3,2-b]pyridine-2-carboxamide;
N-(3-fluoro-4-(2-(l-methylpiperazine-4-carbonyl)thieno[3,2-b]pyridin-7-yloxy)pb.enyl)-l-(2- hydroxy-2-methylpropyl)-5-methyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4- carboxamide;
N-(2-(dimethylamino)ethyl)-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2- carboxamide; N-(4-(2-(3-(dimethylamino)pyrrolidine-l-carbonyl)thieno[3,2-b]pyridm-7-yloxy)-3- fluorophenyl)-l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-
1 H-pyrazole-4-carboxamide; 7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N,N-dimethylthieno[3,2-b]pyridine-2-carboxamide;
7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2-carboxamide; N-(2-(dimethylamino)ethyl)-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2- phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)phenoxy)-N-methylthieno[3,2- b]pyridine-2-carboxamide; 7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)-N-(2-methoxyethyl)thieno[3,2-b]pyridine-2- carboxamide;
N-(4-(2-(azetidine- 1 -carbonyl)thieno[3 ,2-b]pyridin-7-yloxy)-3 -fluorophenyl)- 1 -(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-cyclopropyl-7-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3- dihydro-lH-pyrazole-4-carboxamido)phenoxy)thieno[3,2-b]pyridine-2-carboxamide 7-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)thieno [3 ,2-b]pyridine-2-carboxamide;
N-(3 -fluoro-4-(6-(pyrrolidine- 1 -carboxamido)pyrimidin-4-yloxy)phenyl)- 1 -(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(6-(pyrrolidine-l-carboxamido)pyrimidin-4-yloxy)phenyl)-5-methyl-3-oxo-2- phenyl- 1 -propyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(6-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyrimidin-4-yl)morpholine-4-carboxamide; N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidin-4-yl)morpholine-4-carboxamide;
N-(6-(2-fluoro-4-(5-methyl-3 -oxo-2-phenyl- 1 -propyl-2,3 -dihydro- 1 H-pyrazole-4- carboxamido)phenoxy)pyrimidin-4-yl)piperidine- 1 -carboxamide; N-(6-(2-fluoro-4-(5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamido)phenoxy)pyrimidm-4-yl)-4-methylpiperazine-l-carboxamide; (R)-N-(4-(6-(3-(dimethylarnino)pyrrolidme-l-carboxamido)pyrimidm-4-yloxy)-3- fluorophenyl)-5-methyl-3-oxo-2-phenyl-l-propyl-2,3-dihydro-lH-pyrazole-4- carboxamide; (R)-N-(4-(6-aminopyrimidin-4-yloxy)-3-fluorophenyl)-l-(2-hydroxypropyl)-5-methyl-3-oxo-
2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-(2-(pyrrolidme-l-carboxamido)pyridin-4-yloxy)phenyl)-l,5-dimethyl-3-oxo-2- phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(4-( 1 , 5 -dimethyl-3 -oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamido)-2- fluorophenoxy)pyridin-2-yl)piperidine- 1 -carboxamide;
(R)-N-(4-(2-(3-(dimethylamino)pyrrolidme-l-carboxamido)pyridin-4-yloxy)-3-fluorophenyl)- l,5-dimethyl-3-oxo-2-ρhenyl-2,3-dihydro-lH-pyrazole-4-carboxamide;
N-(3-fluoro-4-(2-(pyrrolidme-l-carboxamido)pyridin-4-yloxy)phenyl)-l-(2-hydroxy-2- methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; N-(3-fluoro-4-(2-(pyrrolidine-l-carboxamido)pyridin-4-yloxy)phenyl)-5-methyl-3-oxo-2- phenyl- 1 -propyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(4-(l,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamido)-2- fluorophenoxy)pyridin-2-yl)morpholme-4-carboxamide;
N-(4-(2-fluoro-4-(l-(2-hydroxy-2-methylpropyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydro-lH- pyrazole-4-carboxamido)phenoxy)pyridin-2-yl)piperidine-l-carboxamide; 5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)methyl)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; N-(4-(hydroxy(7-methoxyquinolin-4-yl)methyl)phenyl)-5-methyl-3-oxo-2-phenyl-l-propyl-
2,3-dihydro-lH-pyrazole-4-carboxamide; l,5-dimethyl-N-(5-((7-(methyloxy)-4-quinolmyl)oxy)-2-pyrimidinyl)-3-oxo-2-phenyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)sulflnyl)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)thio)phenyl)-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)thio)phenyl)-3 -oxo-2-phenyl- 1 -propyl-2,3 - dihydro- 1 H-pyrazole-4-carboxamide
5-methyl-N-(3-((7-(methyloxy)-4-quinolinyl)oxy)propyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-N-(trans-4-((7-(methyloxy)-4-quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-l-propyl-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-N-(cis-4-((7-(methyloxy)-4-quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-l-propyl-
2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(trans-4-((7-(methyloxy)-4- quinolinyl)oxy)cyclohexyl)-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide
5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-3-oxo-2-phenyl-l-propyl-2,3- dihydro- 1 H-pyrazole-4-carboxamide; 5-methyl-N-(5-((7-(methyloxy)-4-quinolinyl)oxy)-2-pyrimidinyl)-3-oxo-2-phenyl-l-propyl-
2,3 -dihydro- 1 H-pyrazole-4-carboxamide; N-(3-fluoro-4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-l-(2-hydroxy-2-methylpropyl)-5- methyl-3-oxo-2-phenyl-2,3-dihydro-lH-pyrazole-4-carboxamide; l-(2-hydroxy-2-methylpropyl)-5-methyl-4-((7-((7-(methyloxy)-4-quinolinyl)oxy)-2,3-dihydro-
4H- 1 ,4-benzoxazin-4-yl)carbonyl)-2-phenyl- 1 ,2-dihydro-3H-pyrazol-3 -one; l-(2-hydroxy-2-methylpropyl)-5-methyl-N-(4-((7-(methyloxy)-4-quinolinyl)amino)phenyl)-3- oxo-2-phenyl-2,3 -dihydro- 1 H-pyrazole-4-carboxamide;
N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-3-hydroxy-2-(l-oxoisoindolm-2- yl)propanamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-(l-oxoisoindolin-2-yl)acetamide; N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-2-oxo-l,5-diphenyl-l,2- dihydropyridine-3 -carboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6-oxo-l-(phenylmethyl)-
1 ,1 ',2',3',6,6'-hexaliydro-3,4'-bipyridine-5-carboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-6-oxo- 1 -(phenylmethyl)- 1 ,6- dihydro-3,3'-bipyridme-5-carboxamide; N-(5-((6,7-bis(methyloxy)-4-qumolinyl)oxy)-2-pyridinyl)-6'-oxo-r-(phenylnietliyl)-r,6'- dihydro-2,3'-bipyridine-5'-carboxamide
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-2-oxo-l-(phenylmetliyl)-5-(2- thienyl)- 1 ,2-dihydro-3 -pyridinecarboxamide;
N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-2-oxo-l-(phenylmethyl)-5-(2- pyrazinyl)- 1 ,2-dihydro-3 -pyridinecarboxamide; N-(5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)-5-methyl-2-oxo-l-(phenylmethyl)-
1 ,2-dihydro-3-pyridinecarboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-bromo-l-(3-methylphenyl)-2- oxo- 1 ,2-dihydro-3-pyridinecarboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-5-(l-methyl-lH-pyrazol-4-yl)-2- oxo- 1 -phenyl- 1 ,2-dihydro-3 -pyridinecarboxamide;
N-(3-fluoro-4-((6-(methyloxy)-7-((3-(4-morpholinyl)propyl)oxy)-4-qumolinyl)oxy)phenyl)-2- oxo-5-phenyl-l -(phenylmethyl)- 1 ,2-dihydro-3-pyridinecarboxamide;
1 , 1 -dimethylethyl 5-(((5-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-2-pyridinyl)amino)carbonyl)-
6-oxo- 1 -(phenylmethyl)- 1 ,3 ' ,6,6 ' -tetrahydro-3 ,4 ' -bipyridine- 1 ' (2 'H)-carboxylate; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-2-oxo-l-(phenylmethyl)-5-(2- pyrimidinyl)- 1 ,2-dihydro-3 -pyridinecarboxamide; N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)-2-oxo- 1 -phenyl-5-(l H-pyrazol-
4-yl)- 1 ,2-dihydro-3 -pyridinecarboxamide; l-benzyl-5-bromo-N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-2-oxo-l,2- dihydropyridine-3 -carboxamide;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyridin-3-yl)-l,2- dihydropyridine-3 -carboxamide;
N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyrazin-2-yl)-l,2- dihydropyridine-3 -carboxamide;
.N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyridin-3-yl)-l,2- dihydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(pyrazin-2-yl)-l,2- dihydropyridine-3 -carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-5-(thiophen-2-yl)-l,2- dihydropyridine-3-carboxamide; 5-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide; tert-butyl 4-(5-((5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)carbamoyl)-6-oxo-l-phenyl-
1 ,6-dihydropyridin-3-yl)-5,6-dihydropyridine-l (2H)-carboxylate; 5-bromo-N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)plienyl)-2-oxo-l-plienyl-l,2- dihydropyridine-3-carboxamide;
N-(5-(6,7-dimethoxyqumolin-4-yloxy)pyridin-2-yl)-4-(2-methoxyethylamino)-2-oxo-l- phenyl-l,2-dihydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-4-(tetrahydro-2H-pyran-4- ylamino)-l,2-dihydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl-4-(phenylamino)-l,2- diliydropyridine-3-carboxamide; N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(4-methylpiperazin-l-yl)-2-oxo-l- phenyl- 1 ,2-dihydropyridine-3 -carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(methylamino)-2-oxo- 1 -phenyl- 1 ,2- dihydropyridine-3-carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(dimethylamino)-2-oxo-l-phenyl-l,2- dihydropyridine-3-carboxamide; 4-(2-methoxyethylamino)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-l-phenyl- l,2-dihydropyridine-3-carboxamide; N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-4-(2-methoxyethylamino)-2-oxo-l-phenyl-
1 ,2-dihydropyridine-3 -carboxamide
N-(4-((6,7-bis(methyloxy)-4-quinolinyl)oxy)-3-fluorophenyl)- 1 -cyclopentyl-6-oxo-5-(2-oxo-l -pyrrolidinyl)-l ,6-dihydro-3-pyridinecarboxamide l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(2-methoxyethylamino)-2-oxo- 1 ,2~dihydropyridine-3 -carboxamide;
1 -benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(dimethylamino)-2-oxo- 1 ,2- dihydropyridine-3 -carboxamide; 1 -benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(methylamino)-2-oxo- 1 ,2- dihydroρyridine-3-carboxamide; 1 -benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(phenylamino)- 1 ,2- dihydropyridine-3-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(pyridm-4-ylamino)- l,2-dihydropyridine-3-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-4-(4-methylpiperazin-l-yl)-2- oxo- 1 ,2-dihydropyridine-3 -carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-2-oxo-4-(tetrahydro-2H-pyran-4- ylamino)-l,2-dihydropyridine-3-carboxamide; l-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridm-2-yl)-2-oxo-4-(4- (trifluorometh.yl)phenylamino)-l ^-dihydropyridine-S-carboxaniide; l-cyclopentyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-6-oxo-5-(2- oxopyrrolidin-1 -yl)-l ,6-dihydropyridme-3-carboxaniide; N-(3 -fluoro-4-(2-(pyrrolidine- 1 -carboxamido)pyridin-4-yloxy)phenyl)-3 -oxo-2-phenyl-2,3 - diliydropyridazine-4-carboxamide; 6-((diethylamino)methyl)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluoroplienyl)-3-oxo-2- phenyl-2,3-dihydropyridazine-4-carboxaniide; 6-((dimethylamino)methyl)-N-(3-fluoro-4-(7-meth.oxyquinolin-4-yloxy)phenyl)-3-oxo-2- phenyl-2,3-dihydropyridazine-4-carboxamide;
N-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide;
N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-6-methyl-3-oxo-2-phenyl-2,3- dihydropyridazine-4-carboxamide; 2-benzyl-N-(5-(6,7-dimethoxyquinolin-4-yloxy)pyridin-2-yl)-6-methyl-3-oxo-2,3- dihydropyridazine-4-carboxamide; N-(3-fluoro-4-(7-inethoxyquinolin-4-yloxy)phenyl)-3-oxo-2-phenyl-2,3-dihydropyridazine-4- carboxamide; N-(2-chloro-4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-6-methyl-3-oxo-2-plienyl-2,3- dihydropyridazine-4-carboxamide;
(R)-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3-fluorophenyl)-6-((3-(dimethylamino)pyrrolidin- l-yl)methyl)-3-oxo-2-phenyl-2,3-dihydropyridazine-4-carboxamide;
3 -benzyl-N-(4-(6,7-dimethoxyquinolin-4-yloxy)-3 -fluorophenyl)-2-oxoimidazolidine- 1 - carboxamide; N-(4-(6,7-diinethoxyquinolin-4-yloxy)-3-fluorophenyl)-5-((dimetliylamino)methyl)-2-oxo-3- phenyl-tetrahydropyrimidine- 1 (2H)-carboxamide; N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-4-phenylmorpholine-2- carboxamide; N-(5-(7-methoxyquinolin-4-yloxy)pyridm-2-yl)- 1 -methyl-3-oxo-2-phenyl-2,3 -dihydro- 1 H- pyrazole-4-carboxamide; N-(3-Fluoro-4-(7-methoxyquinolin-4-yloxy)phenyl)-3-oxo-4-phenylmorpholine-2- carboxamide;
Figure imgf000273_0001
Figure imgf000274_0001
Figure imgf000275_0001
Figure imgf000276_0001
52. A pharmaceutical composition comprising a pharmaceutically-acceptable carrier and a compound as in any of Claims 1-49.
53. A method of treating cancer in a subject, said method comprising administering an effective amount of a compound as in any of Claims 1 -49.
54. The method of Claim 50 comprising a combination with a compound selected from antibiotic-type agents, alkylating agents, antimetabolite agents, hormonal agents, immunological agents, interferon-type agents and miscellaneous agents.
55. A method of reducing tumor size in a subject, said method comprising administering an effective amount of a compound as in any of Claims 1-49.
56. A method of treating HGF mediated disorders in a subject, said method comprising administering an effective amount of a compound as in any of Claims 1-49.
57. A method of reducing metastasis in a tumor in a subject, said method comprising administering an effective amount of a compound as in any of Claims 1-49.
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Cited By (106)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2023926A1 (en) * 2006-05-19 2009-02-18 Bayer HealthCare AG Pyridonecarboxamide derivatives useful in treating hyper-proliferative and angiogenesis disorders
EP2038272A2 (en) * 2006-06-30 2009-03-25 Sunesis Pharmaceuticals, Inc. Pyridinonyl pdk1 inhibitors
WO2008103277A3 (en) * 2007-02-16 2009-04-16 Amgen Inc Nitrogen-containing heterocyclyl ketones and their use as c-met inhibitors
WO2009054544A1 (en) * 2007-10-26 2009-04-30 Eisai R & D Management Co., Ltd. Ampa receptor antagonists for parkinson's disease and movement disorders
JP2009539878A (en) * 2006-06-08 2009-11-19 アレイ バイオファーマ、インコーポレイテッド Quinoline compounds and methods of use
WO2009140549A1 (en) * 2008-05-14 2009-11-19 Amgen Inc. Combinations vegf(r) inhibitors and hepatocyte growth factor (c-met) inhibitors for the treatment of cancer
WO2008041053A3 (en) * 2005-05-20 2009-12-23 Methylgene, Inc. Inhibitors of vegf receptor and hgf receptor signaling
US7642266B2 (en) * 2005-10-06 2010-01-05 Schering Corporation Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors
US7687522B2 (en) 2006-12-20 2010-03-30 Amgen Inc. Substituted pyridines and pyrimidines and their use in treatment of cancer
WO2010039248A1 (en) * 2008-10-01 2010-04-08 Ludwig Institute For Cancer Research Methods for the treatment of cancer
US7723330B2 (en) 2006-03-07 2010-05-25 Array Biopharma Inc. Heterobicyclic pyrazole compounds and methods of use
US7737149B2 (en) 2006-12-21 2010-06-15 Astrazeneca Ab N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof
US7772247B2 (en) 2004-07-30 2010-08-10 Methylgene Inc. Substituted thieno[3,2-d]pyridines as inhibitors of the VEGF receptor and HGF receptor
US7790729B2 (en) 2005-05-20 2010-09-07 Methylgene Inc. Inhibitors of VEGF receptor and HGF receptor signaling
WO2010111063A1 (en) 2009-03-21 2010-09-30 Ning Xi Amino ester derivatives, salts thereof and methods of use
US7851489B2 (en) 2006-11-08 2010-12-14 Bristol-Myers Squibb Company Pyridinone compounds
US7880004B2 (en) 2005-09-15 2011-02-01 Bristol-Myers Squibb Company Met kinase inhibitors
WO2011028995A1 (en) * 2009-09-03 2011-03-10 Allergan, Inc. Compounds as tyrosine kinase modulators
US7915287B2 (en) 2006-12-20 2011-03-29 Amgen Inc. Substituted heterocycles and methods of use
WO2011051958A1 (en) 2009-10-30 2011-05-05 E.I. Du Pont De Nemours And Company Fungicidal pyrazolones
JP2011105735A (en) * 2008-03-05 2011-06-02 Methylgene Inc Inhibitor of protein tyrosine kinase activity
EP2336123A2 (en) * 2008-10-14 2011-06-22 Neopharm Co., Ltd. Heterocyclic compound as protein kinase inhibitor
EP2340244A1 (en) * 2008-10-14 2011-07-06 Ning Xi Compounds and methods of use
WO2011080341A1 (en) 2010-01-04 2011-07-07 Enantia, S.L. Process for the preparation of rivaroxaban and intermediates thereof
EP2344479A2 (en) * 2008-09-23 2011-07-20 Georgetown University 1,2-benzisothiazolinone and isoindolinone derivatives
US7998984B2 (en) 2006-05-08 2011-08-16 Astrazeneca Ab 2-pyridone derivatives for the treatment of disease or condition in which inhibition of neutrophil elastase activity is beneficial
US8003662B2 (en) 2006-01-30 2011-08-23 Array Biopharma, Inc. Heterobicyclic thiophene compounds and methods of use
EP2373636A1 (en) * 2008-12-05 2011-10-12 Merck Sharp & Dohme Corp. Inhibitors of phosphoinositide dependent kinase 1 (pdk1)
CN102212062A (en) * 2010-04-02 2011-10-12 东莞市长安东阳光新药研发有限公司 Derivative of amino ester, salt thereof and using method
US8063073B2 (en) 2003-09-18 2011-11-22 Astrazeneca Ab 2-pyridone derivatives as neutrophil elastase inhibitors and their use
WO2011161217A2 (en) 2010-06-23 2011-12-29 Palacký University in Olomouc Targeting of vegfr2
US8114881B2 (en) 2006-05-08 2012-02-14 Astrazeneca Ab 2-pyrazinone derivatives for the treatment of disease or condition in which inhibition of neutrophil elastase activity is beneficial
US8124768B2 (en) 2008-01-23 2012-02-28 Bristol-Myers Squibb Company 4-pyridinone compounds and their use for cancer
US8133899B2 (en) 2008-08-20 2012-03-13 Pfizer Inc. Pyrrolo[2,3-d]pyrimidine compounds
WO2012044577A1 (en) 2010-09-27 2012-04-05 Exelixis, Inc. Dual inhibitors of met and vegf for the treatment of castration resistant prostate cancer and osteoblastic bone metastases
US8232296B2 (en) 2009-02-20 2012-07-31 Astrazeneca Ab Salt 628
WO2012118632A1 (en) * 2011-02-28 2012-09-07 Ning Xi Substituted quinoline compounds and methods of use
USRE43878E1 (en) 2008-07-24 2012-12-25 Eli Lilly And Company Amidophenoxyindazoles useful as inhibitors of c-Met
US8338455B2 (en) 2006-12-20 2012-12-25 Amgen Inc. Compounds and methods of use
WO2013022519A1 (en) 2011-08-10 2013-02-14 Merck Patent Gmbh Pyrido-pyrimidine derivatives
US8410088B2 (en) 2011-04-13 2013-04-02 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US8436024B2 (en) 2009-10-02 2013-05-07 Astrazeneca Ab 2-pyridone compounds
US8466284B2 (en) 2007-11-06 2013-06-18 Astra Zeneca Ab Some 2-pyrazinone derivatives and their use as inhibitors of neutrophile elastase
US8471005B2 (en) 2008-12-19 2013-06-25 Cephalon, Inc. Pyrrolotriazines as ALK and JAK2 inhibitors
US20130252957A1 (en) * 2009-04-27 2013-09-26 Elan Pharmaceuticals, Inc. Pyridinone antagonists of alpha-4 integrins
US8569319B2 (en) 2010-04-29 2013-10-29 Deciphera Pharmaceuticals, LLS Pyridone amides and analogs exhibiting anti-cancer and anti-proliferative activities
WO2014000713A1 (en) 2012-06-29 2014-01-03 Zhejiang Beta Pharma Incorporation NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
WO2014001247A1 (en) 2012-06-26 2014-01-03 Bayer Pharma Aktiengesellschaft N-[4-(Quinolin-4-yloxy)cyclohexyl(methyl)](hetero)arylcarboxamides as androgen receptor antagonists, production and use thereof as medicinal products
WO2014022117A1 (en) 2012-07-28 2014-02-06 Calitor Sciences, Llc Substituted pyrazolone compounds and methods of use
US8691507B2 (en) 2010-09-10 2014-04-08 Epizyme, Inc. Inhibitors of human EZH2 and methods of use thereof
WO2014194975A1 (en) 2013-06-06 2014-12-11 Merck Patent Gmbh A quinoline inhibitor of the macrophage stimulating 1 receptor mst1 r
WO2015012298A1 (en) 2013-07-24 2015-01-29 小野薬品工業株式会社 Quinoline derivative
US8969347B2 (en) 2008-06-03 2015-03-03 Intermune, Inc. Compounds and methods for treating inflammatory and fibrotic disorders
US8999982B2 (en) 2010-08-28 2015-04-07 Lead Discovery Center Gmbh Pharmaceutically active compounds as Axl inhibitors
CN104507930A (en) * 2012-06-29 2015-04-08 贝达药业股份有限公司 Novel fused pyridine derivatives useful as c-Met tyrosine kinase inhibitors
US9006242B2 (en) 2012-10-15 2015-04-14 Epizyme, Inc. Substituted benzene compounds
US20150141463A1 (en) * 2012-07-28 2015-05-21 Calitor Sciences, Llc Substituted pyrazolone compounds and methods of use
US9175331B2 (en) 2010-09-10 2015-11-03 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
US9359379B2 (en) 2012-10-02 2016-06-07 Intermune, Inc. Anti-fibrotic pyridinones
US9376422B2 (en) 2011-04-13 2016-06-28 Epizyme, Inc. Dihidropyridin-2-one benzamine compounds
US9394283B2 (en) 2012-04-13 2016-07-19 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US9428472B2 (en) 2011-08-16 2016-08-30 Georgetown University Methods of treating bacterial infections with 1,2-benzisothiazolinone and isoindolinone derivatives
US9527816B2 (en) 2005-05-10 2016-12-27 Intermune, Inc. Method of modulating stress-activated protein kinase system
WO2017012539A1 (en) * 2015-07-20 2017-01-26 Betta Pharmaceuticals Co.,Ltd Crystalline form of fused pyridine derivative's maleate and uses thereof
US20170157111A1 (en) * 2008-12-10 2017-06-08 The General Hospital Corporation Hif inhibitors and use thereof
US9815850B2 (en) 2016-02-05 2017-11-14 Denali Therapeutics Inc. Compounds, compositions and methods
US9913856B2 (en) 2011-08-30 2018-03-13 Astex Pharmaceuticals, Inc. Drug formulations
US9926367B2 (en) 2006-04-07 2018-03-27 Aerpio Therapeutics, Inc. Antibodies that bind human protein tyrosine phosphatase beta (HPTPbeta) and uses thereof
US9949956B2 (en) 2009-07-06 2018-04-24 Aerpio Therapeutics, Inc. Compounds, compositions, and methods for preventing metastasis of cancer cells
EP3299369A4 (en) * 2015-05-21 2018-05-02 Shanghai Institute of Materia Medica, Chinese Academy of Sciences Pyrido-azaheterecydic compound and preparation method and use thereof
US9994560B2 (en) 2014-03-14 2018-06-12 Aerpio Therapeutics, Inc. HPTP-β inhibitors
WO2018139527A1 (en) 2017-01-26 2018-08-02 小野薬品工業株式会社 Ethane-sulfonate salt of quinoline derivative
US10040782B2 (en) 2013-10-16 2018-08-07 Epizyme, Inc. Hydrochloride salt form for EZH2 inhibition
US10150811B2 (en) 2011-10-13 2018-12-11 Aerpio Therapeutics, Inc. Methods for treating vascular leak syndrome and cancer
WO2019016071A1 (en) 2017-07-18 2019-01-24 Bayer Pharma Aktiengesellschaft Substituted pyrrolopyridine-derivatives
US10208034B2 (en) 2014-12-25 2019-02-19 Ono Pharmaceutical Co., Ltd. Quinoline derivative
US10220048B2 (en) 2013-03-15 2019-03-05 Aerpio Therapeutics, Inc. Compositions and methods for treating ocular diseases
US10221192B2 (en) 2009-09-03 2019-03-05 Allergan, Inc. Compounds as tyrosine kinase modulators
WO2019048988A1 (en) 2017-09-08 2019-03-14 Pi Industries Ltd. Novel fungidal heterocyclic compounds
WO2019048989A1 (en) 2017-09-08 2019-03-14 Pi Industries Ltd. Novel fungicidal heterocyclic compounds
US10233195B2 (en) 2014-04-02 2019-03-19 Intermune, Inc. Anti-fibrotic pyridinones
US10273227B2 (en) 2017-04-27 2019-04-30 Astrazeneca Ab C5-anilinoquinazoline compounds and their use in treating cancer
US10329357B2 (en) 2011-10-13 2019-06-25 Aerpio Therapeutics, Inc. Treatment of ocular disease
US10420764B2 (en) 2012-12-21 2019-09-24 Astrazeneca Ab Pharmaceutical formulation of N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-YL]-4-[(3R,5S)-3 ,5-dimethylpiperazin-1-YL] benzamide
US10456415B2 (en) 2005-09-29 2019-10-29 Astex Pharmaceuticals, Inc. Oligonucleotide analogues incorporating 5-aza-cytosine therein
US10463650B2 (en) 2006-06-27 2019-11-05 Aerpio Pharmaceuticals, Inc. Human protein tyrosine phosphatase inhibitors and methods of use
US10485764B2 (en) 2015-07-02 2019-11-26 Otsuka Pharmaceutical Co., Ltd. Lyophilized pharmaceutical compositions
US10519190B2 (en) 2017-08-03 2019-12-31 Otsuka Pharmaceutical Co., Ltd. Drug compound and purification methods thereof
CN111295380A (en) * 2018-06-01 2020-06-16 杭州阿诺生物医药科技有限公司 High-activity CSF1R inhibitor compound
WO2020120257A1 (en) 2018-12-11 2020-06-18 Bayer Aktiengesellschaft Substituted pyrrolopyridine-derivatives
WO2021023888A1 (en) * 2019-08-08 2021-02-11 B.C.I. Pharma Isoquinoline derivatives as protein kinase inhibitors
JP2021512055A (en) * 2018-01-17 2021-05-13 南京薬捷安康生物科技有限公司 TAM Family Kinase / and CSF1R Kinase Inhibitors and Their Applications
US11072618B2 (en) 2016-12-09 2021-07-27 Denali Therapeutics Inc. Compounds, compositions and methods
WO2021249913A1 (en) 2020-06-09 2021-12-16 Bayer Aktiengesellschaft 2'-(quinolin-3-yl)-5',6'-dihydrospiro[azetidine-3,4'-pyrrolo[1,2-b]pyrazole]-1-carboxylate derivatives and related compounds as map4k1 (hpk1) inhibitors for the treatment of cancer
US20220073496A1 (en) * 2018-08-24 2022-03-10 Nanjing Transthera Biosciences Co., Ltd. Novel quinoline derivative inhibitor
EP3778586A4 (en) * 2018-04-13 2022-03-16 East China University of Science and Technology Quinazoline compound serving as egfr triple mutation inhibitor and applications thereof
US11326212B2 (en) 2010-06-23 2022-05-10 British Columbia Cancer Agency Branch Biomarkers for non-hodgkin lymphomas and uses thereof
WO2022167627A1 (en) 2021-02-05 2022-08-11 Bayer Aktiengesellschaft Map4k1 inhibitors
RU2802283C2 (en) * 2018-08-24 2023-08-24 Транстера Сайенсиз (Наньцзин), Инк. New inhibitor based on a quinoline derivative
US11826363B2 (en) 2017-10-13 2023-11-28 Ono Pharmaceutical Co., Ltd. Therapeutic agent for solid cancers, which comprises Axl inhibitor as active ingredient
US11873298B2 (en) 2017-10-24 2024-01-16 Janssen Pharmaceutica Nv Compounds and uses thereof
US11970486B2 (en) 2016-10-24 2024-04-30 Janssen Pharmaceutica Nv Compounds and uses thereof
US11999750B2 (en) 2022-01-12 2024-06-04 Denali Therapeutics Inc. Crystalline forms of (S)-5-benzyl-N-(5-methyl-4-oxo-2,3,4,5-tetrahydropyrido [3,2-B][1,4]oxazepin-3-yl)-4H-1,2,4-triazole-3-carboxamide
US12018015B2 (en) 2021-06-18 2024-06-25 Aligos Therapeutics, Inc. Methods and compositions for targeting PD-L1
US12037346B2 (en) 2021-04-13 2024-07-16 Nuvalent, Inc. Amino-substituted heteroaryls for treating cancers with EGFR mutations
US12098146B2 (en) 2019-01-24 2024-09-24 Janssen Pharmaceutica Nv Compounds and uses thereof

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1933839A (en) * 2004-01-23 2007-03-21 安进公司 Compounds and methods of use
WO2008035209A2 (en) * 2006-05-30 2008-03-27 Methylgene Inc. Inhibitors of protein tyrosine kinase activity
MY156536A (en) * 2007-08-29 2016-02-26 Methylgene Inc Inhibitors of protein tyrosine kinase activity
EP2183255A4 (en) * 2007-08-29 2011-06-15 Methylgene Inc Processes and intermediates for preparing fused heterocyclic kinase inhibitors
ES2417009T3 (en) * 2007-10-29 2013-08-05 Amgen, Inc Benzomorpholine derivatives and methods of use
ES2531396T3 (en) 2008-01-23 2015-03-13 Bristol Myers Squibb Co Process to prepare pyridinone compounds
WO2011035332A1 (en) * 2009-09-21 2011-03-24 Chemocentryx, Inc. Pyrrolidinone carboxamide derivatives as chemerin-r ( chemr23 ) modulators
SG184883A1 (en) * 2010-04-16 2012-11-29 Methylgene Inc Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disorders
EP3450432A1 (en) 2010-05-17 2019-03-06 Incozen Therapeutics Pvt. Ltd. Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued - 3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of protein kinases
US20130225581A1 (en) * 2010-07-16 2013-08-29 Kyowa Hakko Kirin Co., Ltd Nitrogen-containing aromatic heterocyclic derivative
EP2680844B1 (en) 2011-03-04 2016-10-19 GlaxoSmithKline Intellectual Property Development Limited Amino-quinolines as kinase inhibitors
TWI547494B (en) 2011-08-18 2016-09-01 葛蘭素史克智慧財產發展有限公司 Amino quinazolines as kinase inhibitors
RU2014125230A (en) * 2011-11-22 2015-12-27 ДЕСИФЕРА ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи Pyridonamides and their analogues demonstrating anticancer and antiproliferative activity
CN102643268B (en) * 2011-12-30 2014-05-21 沈阳药科大学 Quinoline and cinnoline compound and application thereof
CN103319468B (en) * 2012-03-21 2016-07-13 广东东阳光药业有限公司 The spiral shell dicyclic compound replaced and using method and purposes
KR20140144726A (en) 2012-03-30 2014-12-19 리젠 파마슈티컬스 소시에떼 아노님 Novel 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5-disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of c-met protein kinases
CN103420986A (en) * 2012-05-18 2013-12-04 广东东阳光药业有限公司 Compound replacing quinoidines as well as using method and application of compound
CN103565653B (en) * 2012-07-16 2017-01-25 广东东阳光药业有限公司 Substituted pyrazolone compound as well as using method and application of pyrazolone compound
TWI570116B (en) * 2012-08-03 2017-02-11 習寧 Substituted pyrazolone compounds and methods of use
KR101350006B1 (en) * 2012-09-06 2014-02-13 씨제이제일제당 (주) Protein kinase inhibitors comprising pyridone derivatives
AR092530A1 (en) 2012-09-13 2015-04-22 Glaxosmithkline Llc AMINO-QUINOLINE COMPOSITE, PHARMACEUTICAL COMPOSITION THAT INCLUDES IT AND USE OF THIS COMPOUND FOR THE PREPARATION OF A MEDICINAL PRODUCT
TWI592417B (en) 2012-09-13 2017-07-21 葛蘭素史克智慧財產發展有限公司 Prodrugs of amino quinazoline kinase inhibitor
CA2900652C (en) 2013-02-15 2021-05-04 Kala Pharmaceuticals, Inc. Therapeutic compounds and uses thereof
WO2014130612A1 (en) 2013-02-20 2014-08-28 Kala Pharmaceuticals, Inc. Therapeutic compounds and uses thereof
US9688688B2 (en) 2013-02-20 2017-06-27 Kala Pharmaceuticals, Inc. Crystalline forms of 4-((4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolin-7-yl)oxy)-1-(2-oxa-7-azaspiro[3.5]nonan-7-yl)butan-1-one and uses thereof
CA2902132C (en) 2013-02-21 2020-09-22 Glaxosmithkline Intellectual Property Development Limited Quinazolines as kinase inhibitors
MX355330B (en) 2013-11-01 2018-04-16 Kala Pharmaceuticals Inc CRYSTALLINE FORMS OF THERAPEUTIC COMPOUNDS and USES THEREOF.
US9890173B2 (en) 2013-11-01 2018-02-13 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
CN104974162B (en) * 2014-04-09 2018-09-14 广东东阳光药业有限公司 Bicyclic pyrazolone compounds and its application method and purposes
US20150299219A1 (en) * 2014-04-22 2015-10-22 Calitor Sciences, Llc Bicyclic pyrazolone compounds and methods of use
HUE049856T2 (en) * 2015-04-14 2020-10-28 Qurient Co Ltd Quinoline derivatives as tam rtk inhibitors
CN106632253B (en) * 2015-11-02 2019-03-22 广东东阳光药业有限公司 The crystal form and its pharmaceutical composition and purposes of a kind of substituted quinoline compound
CN106632254B (en) * 2015-11-02 2019-03-01 广东东阳光药业有限公司 The crystal form and its pharmaceutical composition and purposes of a kind of substituted quinoline compound
JP6921818B2 (en) * 2015-11-14 2021-08-18 サンシャイン・レイク・ファーマ・カンパニー・リミテッドＳｕｎｓｈｉｎｅ Ｌａｋｅ Ｐｈａｒｍａ Ｃｏ．，Ｌｔｄ． Crystal form of substituted quinoline compound and its pharmaceutical composition
US9695150B2 (en) * 2015-11-14 2017-07-04 Calitor Sciences, Llc Crystalline form of a substituted quinoline compound and pharmaceutical compositions thereof
CN107286140A (en) * 2016-04-12 2017-10-24 上海医药工业研究院 Substituted aromatic amines base heteroaromatic class compound and its application as antineoplastic
WO2017198196A1 (en) * 2016-05-18 2017-11-23 王子厚 Quinoline derivative having anti-tumor activity
EP3509423A4 (en) 2016-09-08 2020-05-13 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
CN109688818A (en) 2016-09-08 2019-04-26 卡拉制药公司 Crystal form of therapeutic compounds and application thereof
EP3509422A4 (en) 2016-09-08 2020-05-20 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
AU2019237715B2 (en) 2018-03-08 2021-01-28 Wellmarker Bio Co., Ltd. Thienopyridine derivatives and pharmaceutical composition comprising same
BR112020019191A2 (en) * 2018-03-23 2021-01-05 Yumanity Therapeutics, Inc. COMPOUNDS AND THEIR USES
CN110511218A (en) * 2018-05-21 2019-11-29 中国科学院上海药物研究所 A kind of and ring pyrazolone Carbox amide and preparation method thereof, pharmaceutical composition and purposes
CN108727386A (en) * 2018-07-16 2018-11-02 广州医科大学 A kind of Pyrazolopyrimidines and its preparation method and application
CN111303024B (en) * 2018-12-12 2023-03-28 安徽中科拓苒药物科学研究有限公司 Quinoline-structured pan-KIT kinase inhibitor and application thereof
US20220289679A1 (en) * 2019-07-29 2022-09-15 Takeda Pharmaceutical Company Limited Heterocyclic compound
WO2021026100A1 (en) * 2019-08-02 2021-02-11 Amgen Inc. Pyridine derivatives as kif18a inhibitors
CN112771053A (en) 2019-09-06 2021-05-07 伟迈可生物有限公司 Biomarker-based therapeutic compositions
CN112625026B (en) * 2019-09-24 2022-09-09 药捷安康(南京)科技股份有限公司 Quinoline derivatives of TAM family kinase inhibitors
CA3155924A1 (en) * 2019-09-26 2021-04-01 Exelixis, Inc. Pyridone compounds and methods of use in the modulation of a protein kinase
CN113121429B (en) * 2020-01-15 2024-04-26 鲁南制药集团股份有限公司 C-Met kinase inhibitor and preparation method and application thereof
AU2021226747A1 (en) * 2020-02-24 2022-09-01 Exelixis, Inc. Compounds and methods of use
CN111440174B (en) * 2020-04-02 2021-07-09 广州医科大学 Pyridine amide compound and preparation method and application thereof
TW202315628A (en) * 2021-06-24 2023-04-16 南韓商Ｌｇ化學股份有限公司 Novel pyridine derivative compound as ron inhibitor
CN113999205B (en) * 2021-12-13 2023-09-15 辽宁大学 Pyridine compound containing triazolone amide and imidazolone amide structures and application thereof
CN117362275A (en) * 2022-06-29 2024-01-09 广州百霆医药科技有限公司 Tyrosine protein kinase inhibitor and application thereof
CN116283920B (en) * 2023-03-31 2024-04-16 贵州医科大学 2, 4-disubstituted pyridine compound and application thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000050405A1 (en) 1999-02-24 2000-08-31 Astrazeneca Ab Quinoline derivatives as tyrosine kinase inhibitors
WO2002032872A1 (en) 2000-10-20 2002-04-25 Eisai Co., Ltd. Nitrogenous aromatic ring compounds
WO2004018430A1 (en) 2002-08-23 2004-03-04 Kirin Beer Kabushiki Kaisha COMPOUND HAVING TGFß INHIBITORY ACTIVITY AND MEDICINAL COMPOSITION CONTAINING THE SAME
EP1411046A1 (en) 2001-06-22 2004-04-21 Kirin Beer Kabushiki Kaisha QUINOLINE DERIVATIVE AND QUINAZOLINE DERIVATIVE INHIBITING SELF&minus;PHOSPHORYLATION OF HEPATOCYTUS PROLIFERATOR RECEPTOR&comma; AND MEDICINAL COMPOSITION CONTAINING THE SAME
WO2004037784A2 (en) 2002-10-21 2004-05-06 Irm Llc Pyrrolidones with anti-hiv activity
WO2004083235A2 (en) 2003-03-19 2004-09-30 Exelixis Inc. Tie-2 modulators and methods of use
WO2005005389A2 (en) 2003-07-07 2005-01-20 Merck Patent Gmbh Malonamide derivatives
WO2005117867A2 (en) * 2004-04-23 2005-12-15 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
WO2006004636A2 (en) * 2004-06-28 2006-01-12 Bristol-Myers Squibb Company Fused heterocyclic kinase inhibitors

Family Cites Families (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3755332A (en) * 1971-07-01 1973-08-28 Ciba Geigy Corp Substituted 4 indazolaminoquinolines
DE2948434A1 (en) * 1979-12-01 1981-06-11 Hoechst Ag, 6000 Frankfurt 1-PIPERIDINSULFONYL UREA AND METHOD FOR THE PRODUCTION THEREOF
JPS63145272A (en) 1986-12-09 1988-06-17 Morishita Seiyaku Kk 4,5-dihydro-6-(4-substituted phenyl)-3(2h)-pyridazinone derivative
US4916135A (en) * 1989-05-08 1990-04-10 Hoechst Roussel Pharmaceuticals Inc. N-heteroaryl-4-quinolinamines
GB9323290D0 (en) * 1992-12-10 1994-01-05 Zeneca Ltd Quinazoline derivatives
JPH08193070A (en) * 1995-01-11 1996-07-30 Mitsubishi Chem Corp 2-imidazolidinone derivative,herbicide containing it as effective component,and its intermediate
WO1996023774A1 (en) 1995-01-31 1996-08-08 Zenyaku Kogyo Kabushiki Kaisha Thioquinoline derivatives
GB9505651D0 (en) 1995-03-21 1995-05-10 Agrevo Uk Ltd AgrEvo UK Limited
GB9505702D0 (en) 1995-03-21 1995-05-10 Agrevo Uk Ltd Fungicidal compounds
GB9514265D0 (en) 1995-07-13 1995-09-13 Wellcome Found Hetrocyclic compounds
EP0860433B1 (en) 1995-11-07 2002-07-03 Kirin Beer Kabushiki Kaisha Quinoline derivatives and quinazoline derivatives inhibiting autophosphorylation of growth factor receptor originating in platelet and pharmaceutical compositions containing the same
CN1168138A (en) * 1995-11-14 1997-12-17 法玛西雅厄普约翰公司 Aryl and heteroaryl purine compounds
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
GB9603095D0 (en) * 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
DE19614718A1 (en) * 1996-04-15 1997-10-16 Hoechst Schering Agrevo Gmbh Substituted pyridines / pyrimidines, processes for their preparation and their use as pesticides
KR20000075615A (en) 1997-02-19 2000-12-26 벌렉스 래보라토리즈, 인크. N-Heterocyclic Derivatives as NOS Inhibitors
JP4194678B2 (en) 1997-11-28 2008-12-10 キリンファーマ株式会社 Quinoline derivative and pharmaceutical composition containing the same
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
EP1073640B1 (en) 1998-04-23 2005-04-13 Takeda Pharmaceutical Company Limited Naphthalene derivatives, their production and use
CA2333392A1 (en) 1998-05-28 1999-12-02 Parker Hughes Institute Quinazolines for treating brain tumor
EP1105378B1 (en) * 1998-08-21 2005-03-30 Parker Hughes Institute Quinazoline derivatives
NZ513006A (en) * 1999-01-22 2003-10-31 Kirin Brewery Quinoline derivatives and quinazoline derivatives
KR100838617B1 (en) 1999-02-10 2008-06-16 아스트라제네카 아베 Quinazoline derivatives as angiogenesis inhibitors
US6258820B1 (en) 1999-03-19 2001-07-10 Parker Hughes Institute Synthesis and anti-tumor activity of 6,7-dialkoxy-4-phenylamino-quinazolines
HUP0200803A3 (en) 1999-04-12 2002-12-28 Aventis Pharma Ltd West Mallin Substituted bicyclic heteroaryl compounds as integrin antagonists, pharmaceutical compositions containing them and the intermediates
JP2003509497A (en) 1999-09-21 2003-03-11 アストラゼネカ アクチボラグ Quinazoline compounds and pharmaceutical compositions containing them
HUP0300850A2 (en) 2000-03-17 2003-07-28 Bristol-Myers Squibb Pharma Company Cyclic betha-amino acid derivatives as inhibitors of matrix metalloproteases and tnf-alpha and pharmaceutical compositions containing them and their use
ATE260272T1 (en) 2000-03-17 2004-03-15 Bristol Myers Squibb Pharma Co BETA-AMINO ACID DERIVATIVES FOR USE AS MATRIX METALLOPROTEASES AND TNA-ALPHA INHIBITORS
WO2002000005A1 (en) 2000-06-21 2002-01-03 Alexion Pharmaceuticals, Inc. Libraries displaying human antibody fragments with hybrid complementarity determining regions
WO2002022606A1 (en) 2000-09-15 2002-03-21 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
AU2001292138A1 (en) 2000-10-13 2002-04-22 Astrazeneca Ab Quinazoline derivatives with anti-tumour activity
ES2360205T3 (en) * 2001-03-02 2011-06-01 Agennix Ag THREE HYBRID TEST SYSTEM.
CA2441492C (en) 2001-03-23 2011-08-09 Bayer Corporation Rho-kinase inhibitors
ES2296926T3 (en) 2001-06-06 2008-05-01 Aventis Pharma Limited TETRAHYDROISOQUINOLINAS REPLACED FOR USE IN THE TREATMENT OF INFLAMMATORY DISEASES.
SE0102439D0 (en) 2001-07-05 2001-07-05 Astrazeneca Ab New compounds
WO2002000004A2 (en) 2001-07-05 2002-01-03 Telefonaktiebolaget Lm Ericsson (Publ) Detrimental latch-up avoidans in digital circuits
HUP0401646A2 (en) 2001-11-03 2004-12-28 Astrazeneca Ab, Quinazoline derivatives as antitumor agents, process for their preparation and pharmaceutical compositions containing them
GB0126433D0 (en) 2001-11-03 2002-01-02 Astrazeneca Ab Compounds
CN101607958A (en) 2002-02-01 2009-12-23 阿斯特拉曾尼卡有限公司 Quinazoline compound
US6818772B2 (en) * 2002-02-22 2004-11-16 Abbott Laboratories Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor
US7645878B2 (en) 2002-03-22 2010-01-12 Bayer Healthcare Llc Process for preparing quinazoline Rho-kinase inhibitors and intermediates thereof
NZ535985A (en) 2002-03-29 2007-04-27 Chiron Corp Substituted benzazoles and use thereof as RAF kinase inhibitors
WO2004030672A1 (en) 2002-10-02 2004-04-15 Merck Patent Gmbh Use of 4 amino-quinazolines as anti cancer agents
TW200418466A (en) 2002-11-06 2004-10-01 Smithkline Beecham Corp Chemical compounds
TW200500341A (en) * 2002-11-12 2005-01-01 Astrazeneca Ab Novel compounds
GB0226724D0 (en) 2002-11-15 2002-12-24 Merck Sharp & Dohme Therapeutic agents
US7265122B2 (en) 2003-02-28 2007-09-04 Encysive Pharmaceuticals, Inc. Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists
US7531553B2 (en) 2003-03-21 2009-05-12 Amgen Inc. Heterocyclic compounds and methods of use
GB0310401D0 (en) 2003-05-07 2003-06-11 Astrazeneca Ab Therapeutic agent
CA2536788A1 (en) 2003-08-29 2005-03-10 Pfizer Inc. Naphthalene carboxamides and their derivatives useful as new anti-angiogenic agents
ATE517091T1 (en) 2003-09-26 2011-08-15 Exelixis Inc C-MET MODULATORS AND METHODS OF USE
US7691866B2 (en) 2003-10-16 2010-04-06 Novartis Vaccines And Diagnostics, Inc. 2,6-disubstituted quinazolines, quinoxalines, quinolines and isoquinolines and methods of their use as inhibitors of Raf kinase
CA2553433A1 (en) * 2004-01-23 2005-08-11 Amgen Inc. Quinoline quinazoline pyridine and pyrimidine compounds and their use in the treatment of inflammation angiogenesis and cancer
CN1933839A (en) 2004-01-23 2007-03-21 安进公司 Compounds and methods of use
EP1724268A4 (en) 2004-02-20 2010-04-21 Kirin Pharma Kk Compound having tgf-beta inhibitory activity and pharmaceutical composition containing same
US7523317B2 (en) 2004-04-29 2009-04-21 International Business Machines Corporation Computer grid access management system

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000050405A1 (en) 1999-02-24 2000-08-31 Astrazeneca Ab Quinoline derivatives as tyrosine kinase inhibitors
WO2002032872A1 (en) 2000-10-20 2002-04-25 Eisai Co., Ltd. Nitrogenous aromatic ring compounds
EP1415987A1 (en) 2000-10-20 2004-05-06 Eisai Co., Ltd. Nitrogenous aromatic ring compounds
EP1411046A1 (en) 2001-06-22 2004-04-21 Kirin Beer Kabushiki Kaisha QUINOLINE DERIVATIVE AND QUINAZOLINE DERIVATIVE INHIBITING SELF&minus;PHOSPHORYLATION OF HEPATOCYTUS PROLIFERATOR RECEPTOR&comma; AND MEDICINAL COMPOSITION CONTAINING THE SAME
WO2004018430A1 (en) 2002-08-23 2004-03-04 Kirin Beer Kabushiki Kaisha COMPOUND HAVING TGFß INHIBITORY ACTIVITY AND MEDICINAL COMPOSITION CONTAINING THE SAME
WO2004037784A2 (en) 2002-10-21 2004-05-06 Irm Llc Pyrrolidones with anti-hiv activity
WO2004083235A2 (en) 2003-03-19 2004-09-30 Exelixis Inc. Tie-2 modulators and methods of use
WO2005005389A2 (en) 2003-07-07 2005-01-20 Merck Patent Gmbh Malonamide derivatives
WO2005117867A2 (en) * 2004-04-23 2005-12-15 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
WO2006004636A2 (en) * 2004-06-28 2006-01-12 Bristol-Myers Squibb Company Fused heterocyclic kinase inhibitors

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
R. CONNELL, J. BEEBE, EXP. OPIN. THER. PATENTS, vol. 11, 2001, pages 77 - 114
SCI., vol. 38, 1997, pages 61 - 69

Cited By (236)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8063073B2 (en) 2003-09-18 2011-11-22 Astrazeneca Ab 2-pyridone derivatives as neutrophil elastase inhibitors and their use
US8501784B2 (en) 2003-09-18 2013-08-06 Astrazeneca Ab 2-pyridone derivatives as neutrophil elastase inhibitors and their use
US8470850B2 (en) 2004-07-30 2013-06-25 Methylgene Inc. Inhibitors of VEGF receptor and HGF receptor signalling
US7772247B2 (en) 2004-07-30 2010-08-10 Methylgene Inc. Substituted thieno[3,2-d]pyridines as inhibitors of the VEGF receptor and HGF receptor
US9527816B2 (en) 2005-05-10 2016-12-27 Intermune, Inc. Method of modulating stress-activated protein kinase system
US10010536B2 (en) 2005-05-10 2018-07-03 Intermune, Inc. Method of modulating stress-activated protein kinase system
US7790729B2 (en) 2005-05-20 2010-09-07 Methylgene Inc. Inhibitors of VEGF receptor and HGF receptor signaling
US8093264B2 (en) 2005-05-20 2012-01-10 Methylgene Inc. Fused heterocycles as inhibitors of VEGF receptor and HGF receptor signaling
AU2006343808B2 (en) * 2005-05-20 2012-03-29 Mirati Therapeutics, Inc. Inhibitors of VEGF receptor and HGF receptor signaling
US8329726B2 (en) 2005-05-20 2012-12-11 Methylgene Inc. Inhibitors of VEGF receptor and HGF receptor signaling
WO2008041053A3 (en) * 2005-05-20 2009-12-23 Methylgene, Inc. Inhibitors of vegf receptor and hgf receptor signaling
US7880004B2 (en) 2005-09-15 2011-02-01 Bristol-Myers Squibb Company Met kinase inhibitors
US10933079B2 (en) 2005-09-29 2021-03-02 Astex Pharmaceuticals, Inc. Oligonucleotide analogues incorporating 5-aza-cytosine therein
US10456415B2 (en) 2005-09-29 2019-10-29 Astex Pharmaceuticals, Inc. Oligonucleotide analogues incorporating 5-aza-cytosine therein
US7642266B2 (en) * 2005-10-06 2010-01-05 Schering Corporation Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors
US8003662B2 (en) 2006-01-30 2011-08-23 Array Biopharma, Inc. Heterobicyclic thiophene compounds and methods of use
US7723330B2 (en) 2006-03-07 2010-05-25 Array Biopharma Inc. Heterobicyclic pyrazole compounds and methods of use
US9926367B2 (en) 2006-04-07 2018-03-27 Aerpio Therapeutics, Inc. Antibodies that bind human protein tyrosine phosphatase beta (HPTPbeta) and uses thereof
US11814425B2 (en) 2006-04-07 2023-11-14 Eye Point Pharmaceuticals, Inc. Antibodies that bind human protein tyrosine phosphatase beta (HPTPbeta) and uses thereof
US8114881B2 (en) 2006-05-08 2012-02-14 Astrazeneca Ab 2-pyrazinone derivatives for the treatment of disease or condition in which inhibition of neutrophil elastase activity is beneficial
US7998984B2 (en) 2006-05-08 2011-08-16 Astrazeneca Ab 2-pyridone derivatives for the treatment of disease or condition in which inhibition of neutrophil elastase activity is beneficial
EP2023926A1 (en) * 2006-05-19 2009-02-18 Bayer HealthCare AG Pyridonecarboxamide derivatives useful in treating hyper-proliferative and angiogenesis disorders
EP2023926A4 (en) * 2006-05-19 2010-08-04 Bayer Schering Pharma Ag Pyridonecarboxamide derivatives useful in treating hyper-proliferative and angiogenesis disorders
JP2009539878A (en) * 2006-06-08 2009-11-19 アレイ バイオファーマ、インコーポレイテッド Quinoline compounds and methods of use
US10463650B2 (en) 2006-06-27 2019-11-05 Aerpio Pharmaceuticals, Inc. Human protein tyrosine phosphatase inhibitors and methods of use
US9873693B2 (en) 2006-06-30 2018-01-23 Sunesis Pharmaceuticals, Inc. Methods of treatment using pyridinonyl PDK1 inhibitors
EP2038272A2 (en) * 2006-06-30 2009-03-25 Sunesis Pharmaceuticals, Inc. Pyridinonyl pdk1 inhibitors
US8778977B2 (en) 2006-06-30 2014-07-15 Sunesis Pharmaceuticals, Inc. Pyridinonyl PDK1 inhibitors
EP2038272A4 (en) * 2006-06-30 2011-01-05 Sunesis Pharmaceuticals Inc Pyridinonyl pdk1 inhibitors
US7851489B2 (en) 2006-11-08 2010-12-14 Bristol-Myers Squibb Company Pyridinone compounds
US8536200B2 (en) 2006-11-08 2013-09-17 Bristol-Myers Squibb Company Pyridinone compounds
US7915287B2 (en) 2006-12-20 2011-03-29 Amgen Inc. Substituted heterocycles and methods of use
US8338455B2 (en) 2006-12-20 2012-12-25 Amgen Inc. Compounds and methods of use
US7687522B2 (en) 2006-12-20 2010-03-30 Amgen Inc. Substituted pyridines and pyrimidines and their use in treatment of cancer
EP2125780B1 (en) * 2006-12-20 2012-08-29 Amgen Inc. Substituted heterocycles and methods of use
US7737149B2 (en) 2006-12-21 2010-06-15 Astrazeneca Ab N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof
US10301267B2 (en) 2006-12-21 2019-05-28 Astrazeneca Ab Compounds
US8604022B2 (en) 2006-12-21 2013-12-10 Astrazeneca Ab N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(3,4-dimethylpiperazin-1-yl)benzamide and salts thereof
US8129391B2 (en) 2006-12-21 2012-03-06 Astrazeneca Ab N-[5-[2-(3,5-Dimethoxyphenyl)ethyl]-1H-pyrazol-3-yl]-4-(3,4-dimethylpiperazin-1-yl)benzamide and salts thereof
US9688640B2 (en) 2006-12-21 2017-06-27 Astrazeneca Ab Methods of treating cancer with a pyrazole derivative
JP2010519204A (en) * 2007-02-16 2010-06-03 アムジエン・インコーポレーテツド Nitrogen-containing heterocyclic ketones and their use as c-Met inhibitors
US8314087B2 (en) 2007-02-16 2012-11-20 Amgen Inc. Nitrogen-containing heterocyclyl ketones and methods of use
AU2008219166B2 (en) * 2007-02-16 2013-05-16 Amgen Inc. Nitrogen-containing heterocyclyl ketones and their use as c-Met inhibitors
WO2008103277A3 (en) * 2007-02-16 2009-04-16 Amgen Inc Nitrogen-containing heterocyclyl ketones and their use as c-met inhibitors
WO2009054544A1 (en) * 2007-10-26 2009-04-30 Eisai R & D Management Co., Ltd. Ampa receptor antagonists for parkinson's disease and movement disorders
US8466284B2 (en) 2007-11-06 2013-06-18 Astra Zeneca Ab Some 2-pyrazinone derivatives and their use as inhibitors of neutrophile elastase
US8124768B2 (en) 2008-01-23 2012-02-28 Bristol-Myers Squibb Company 4-pyridinone compounds and their use for cancer
US8258118B2 (en) 2008-01-23 2012-09-04 Bristol-Myers Squibb Company 4-pyridinone compounds and their use for cancer
US8759522B2 (en) 2008-03-05 2014-06-24 Methylgene Inc. Inhibitors of protein tyrosine kinase activity
US8729268B2 (en) 2008-03-05 2014-05-20 Methylgene Inc. Inhibitors of protein tyrosine kinase activity
JP2011105735A (en) * 2008-03-05 2011-06-02 Methylgene Inc Inhibitor of protein tyrosine kinase activity
WO2009140549A1 (en) * 2008-05-14 2009-11-19 Amgen Inc. Combinations vegf(r) inhibitors and hepatocyte growth factor (c-met) inhibitors for the treatment of cancer
JP2011520908A (en) * 2008-05-14 2011-07-21 アムジエン・インコーポレーテツド Combinations of VEGF (R) inhibitors and hepatocyte growth factor (C-MET) inhibitors for the treatment of cancer
US8969347B2 (en) 2008-06-03 2015-03-03 Intermune, Inc. Compounds and methods for treating inflammatory and fibrotic disorders
USRE47142E1 (en) 2008-06-03 2018-11-27 Intermune, Inc. Compounds and methods for treating inflammatory and fibrotic disorders
US9290450B2 (en) 2008-06-03 2016-03-22 Intermune, Inc. Compounds and methods for treating inflammatory and fibrotic disorders
USRE43878E1 (en) 2008-07-24 2012-12-25 Eli Lilly And Company Amidophenoxyindazoles useful as inhibitors of c-Met
US8133899B2 (en) 2008-08-20 2012-03-13 Pfizer Inc. Pyrrolo[2,3-d]pyrimidine compounds
US8987283B2 (en) 2008-08-20 2015-03-24 Zoetis Llc Pyrrolo[2,3-D]pyrimidine compounds
US9161939B2 (en) 2008-08-20 2015-10-20 Zoetis Services Llc Pyrrolo[2,3-d]pyrimidine compounds
EP2344479A2 (en) * 2008-09-23 2011-07-20 Georgetown University 1,2-benzisothiazolinone and isoindolinone derivatives
EP2344479A4 (en) * 2008-09-23 2012-05-30 Univ Georgetown 1,2-benzisothiazolinone and isoindolinone derivatives
US9040715B2 (en) 2008-09-23 2015-05-26 Georgetown University 1,2-benzisothiazolinone and isoindolinone derivatives
JP2012504606A (en) * 2008-10-01 2012-02-23 ラディック インスティテュート フォー キャンサー リサーチ How to treat cancer
WO2010039248A1 (en) * 2008-10-01 2010-04-08 Ludwig Institute For Cancer Research Methods for the treatment of cancer
EP2532657A3 (en) * 2008-10-14 2013-01-23 Sunshine Lake Pharma Co., Ltd Compounds and methods of use
US8957102B2 (en) * 2008-10-14 2015-02-17 Neopharm Co., Ltd. Heterocyclic compound as protein kinase inhibitor
US8426585B2 (en) 2008-10-14 2013-04-23 Ning Xi Compounds comprising a spiro-ring
JP2012505874A (en) * 2008-10-14 2012-03-08 ネオファーム カンパニー， リミテッド Heterocyclic compounds as protein kinases
JP2012505888A (en) * 2008-10-14 2012-03-08 クイ ニング Compounds and methods of use
EP2336123A4 (en) * 2008-10-14 2012-05-02 Neopharm Co Ltd Heterocyclic compound as protein kinase inhibitor
US8293897B2 (en) 2008-10-14 2012-10-23 Ning Xi Compounds comprising a spiro-ring and methods of use
EP2340244A4 (en) * 2008-10-14 2012-07-25 Ning Xi Compounds and methods of use
US20110183983A1 (en) * 2008-10-14 2011-07-28 Neopharm Co., Ltd. Heterocyclic compound as protein kinase inhibitor
JP2015120733A (en) * 2008-10-14 2015-07-02 クイ ニング Compound and use method
EP2340244A1 (en) * 2008-10-14 2011-07-06 Ning Xi Compounds and methods of use
EP2336123A2 (en) * 2008-10-14 2011-06-22 Neopharm Co., Ltd. Heterocyclic compound as protein kinase inhibitor
EP2373636A1 (en) * 2008-12-05 2011-10-12 Merck Sharp & Dohme Corp. Inhibitors of phosphoinositide dependent kinase 1 (pdk1)
EP2373636A4 (en) * 2008-12-05 2012-10-17 Merck Sharp & Dohme Inhibitors of phosphoinositide dependent kinase 1 (pdk1)
US20170157111A1 (en) * 2008-12-10 2017-06-08 The General Hospital Corporation Hif inhibitors and use thereof
US10881656B2 (en) * 2008-12-10 2021-01-05 The General Hospital Corporation HIF inhibitors and use thereof
US8471005B2 (en) 2008-12-19 2013-06-25 Cephalon, Inc. Pyrrolotriazines as ALK and JAK2 inhibitors
US8232296B2 (en) 2009-02-20 2012-07-31 Astrazeneca Ab Salt 628
AU2010229147B2 (en) * 2009-03-21 2012-07-05 Sunshine Lake Pharma Co., Ltd. Amino ester derivatives, salts thereof and methods of use
EP2408300A4 (en) * 2009-03-21 2012-12-12 Sunshine Lake Pharma Co Ltd Amino ester derivatives, salts thereof and methods of use
EP2408300A1 (en) * 2009-03-21 2012-01-25 Sunshine Lake Pharma Co., Ltd Amino ester derivatives, salts thereof and methods of use
JP2012521348A (en) * 2009-03-21 2012-09-13 クイ ニング Amino ester derivatives, salts thereof, and methods of use
WO2010111063A1 (en) 2009-03-21 2010-09-30 Ning Xi Amino ester derivatives, salts thereof and methods of use
US20130252957A1 (en) * 2009-04-27 2013-09-26 Elan Pharmaceuticals, Inc. Pyridinone antagonists of alpha-4 integrins
US9949956B2 (en) 2009-07-06 2018-04-24 Aerpio Therapeutics, Inc. Compounds, compositions, and methods for preventing metastasis of cancer cells
US8614234B2 (en) 2009-09-03 2013-12-24 Allergan, Inc. Compounds as tyrosine kinase modulators
US9725433B2 (en) 2009-09-03 2017-08-08 Allergan, Inc. Compounds as tyrosine kinase modulators
WO2011028995A1 (en) * 2009-09-03 2011-03-10 Allergan, Inc. Compounds as tyrosine kinase modulators
AU2010289353B2 (en) * 2009-09-03 2016-12-08 Allergan, Inc. Compounds as tyrosine kinase modulators
US9328103B2 (en) 2009-09-03 2016-05-03 Allergan, Inc. Compounds as tyrosine kinase modulators
US10221192B2 (en) 2009-09-03 2019-03-05 Allergan, Inc. Compounds as tyrosine kinase modulators
CN102686577A (en) * 2009-09-03 2012-09-19 阿勒根公司 Compounds as tyrosine kinase modulators
US9475801B2 (en) 2009-09-03 2016-10-25 Allergan, Inc. Compounds as tyrosine kinase modulators
US8436024B2 (en) 2009-10-02 2013-05-07 Astrazeneca Ab 2-pyridone compounds
WO2011051958A1 (en) 2009-10-30 2011-05-05 E.I. Du Pont De Nemours And Company Fungicidal pyrazolones
WO2011080341A1 (en) 2010-01-04 2011-07-07 Enantia, S.L. Process for the preparation of rivaroxaban and intermediates thereof
CN102212062A (en) * 2010-04-02 2011-10-12 东莞市长安东阳光新药研发有限公司 Derivative of amino ester, salt thereof and using method
US8569319B2 (en) 2010-04-29 2013-10-29 Deciphera Pharmaceuticals, LLS Pyridone amides and analogs exhibiting anti-cancer and anti-proliferative activities
US11326212B2 (en) 2010-06-23 2022-05-10 British Columbia Cancer Agency Branch Biomarkers for non-hodgkin lymphomas and uses thereof
WO2011161217A2 (en) 2010-06-23 2011-12-29 Palacký University in Olomouc Targeting of vegfr2
US8999982B2 (en) 2010-08-28 2015-04-07 Lead Discovery Center Gmbh Pharmaceutically active compounds as Axl inhibitors
US9333217B2 (en) 2010-09-10 2016-05-10 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
US8691507B2 (en) 2010-09-10 2014-04-08 Epizyme, Inc. Inhibitors of human EZH2 and methods of use thereof
US9175331B2 (en) 2010-09-10 2015-11-03 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
US8895245B2 (en) 2010-09-10 2014-11-25 Epizyme, Inc. Inhibitors of human EZH2 and methods of use thereof
US9949999B2 (en) 2010-09-10 2018-04-24 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
US9334527B2 (en) 2010-09-10 2016-05-10 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
WO2012044577A1 (en) 2010-09-27 2012-04-05 Exelixis, Inc. Dual inhibitors of met and vegf for the treatment of castration resistant prostate cancer and osteoblastic bone metastases
WO2012118632A1 (en) * 2011-02-28 2012-09-07 Ning Xi Substituted quinoline compounds and methods of use
US8410088B2 (en) 2011-04-13 2013-04-02 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US9549931B2 (en) 2011-04-13 2017-01-24 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US9855275B2 (en) 2011-04-13 2018-01-02 Epizyme, Inc. Aryl-or heteroaryl-substituted benzene compounds
US9376422B2 (en) 2011-04-13 2016-06-28 Epizyme, Inc. Dihidropyridin-2-one benzamine compounds
US10155002B2 (en) 2011-04-13 2018-12-18 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US9522152B2 (en) 2011-04-13 2016-12-20 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US10420775B2 (en) 2011-04-13 2019-09-24 Epizyme, Inc. Aryl-or heteroaryl-substituted benzene compounds
US8765732B2 (en) 2011-04-13 2014-07-01 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US9090562B2 (en) 2011-04-13 2015-07-28 Epizyme, Inc. Aryl- or heteroaryl-substituted benzene compounds
US11052093B2 (en) 2011-04-13 2021-07-06 Epizyme, Inc. Aryl-or heteroaryl-substituted benzene compounds
WO2013022519A1 (en) 2011-08-10 2013-02-14 Merck Patent Gmbh Pyrido-pyrimidine derivatives
US9283225B2 (en) 2011-08-10 2016-03-15 Merck Patent Gmbh Pyrido-pyrimidine derivatives
US9428472B2 (en) 2011-08-16 2016-08-30 Georgetown University Methods of treating bacterial infections with 1,2-benzisothiazolinone and isoindolinone derivatives
US10517886B2 (en) 2011-08-30 2019-12-31 Astex Pharmaceuticals, Inc. Drug formulations
US9913856B2 (en) 2011-08-30 2018-03-13 Astex Pharmaceuticals, Inc. Drug formulations
US10815300B2 (en) 2011-10-13 2020-10-27 Aerpio Pharmaceuticals, Inc. Methods for treating vascular leak syndrome and cancer
US10150811B2 (en) 2011-10-13 2018-12-11 Aerpio Therapeutics, Inc. Methods for treating vascular leak syndrome and cancer
US10329357B2 (en) 2011-10-13 2019-06-25 Aerpio Therapeutics, Inc. Treatment of ocular disease
US12043664B2 (en) 2011-10-13 2024-07-23 EyePoint Pharmaceuticals, Inc. Methods for treating vascular leak syndrome and cancer
US10245269B2 (en) 2012-04-13 2019-04-02 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US9394283B2 (en) 2012-04-13 2016-07-19 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US10821113B2 (en) 2012-04-13 2020-11-03 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US9872862B2 (en) 2012-04-13 2018-01-23 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US11491163B2 (en) 2012-04-13 2022-11-08 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
WO2014001247A1 (en) 2012-06-26 2014-01-03 Bayer Pharma Aktiengesellschaft N-[4-(Quinolin-4-yloxy)cyclohexyl(methyl)](hetero)arylcarboxamides as androgen receptor antagonists, production and use thereof as medicinal products
US9428460B2 (en) 2012-06-26 2016-08-30 Bayer Pharma Aktiengesellschaft N-[4-(quinolin-4-yloxy)cyclohexyl(methyl)](hetero)arylcarboxamides as androgen receptor antagonists, production and use thereof as medicinal products
KR20170017015A (en) * 2012-06-29 2017-02-14 베타 파머수티컬 컴퍼니 리미티드 NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
KR20150031320A (en) * 2012-06-29 2015-03-23 베타 파머수티컬 컴퍼니 리미티드 NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
KR101770545B1 (en) 2012-06-29 2017-08-22 베타 파머수티컬 컴퍼니 리미티드 NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
EP2867223A4 (en) * 2012-06-29 2016-01-06 Betta Pharmaceuticals Co Ltd NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
CN104507930A (en) * 2012-06-29 2015-04-08 贝达药业股份有限公司 Novel fused pyridine derivatives useful as c-Met tyrosine kinase inhibitors
AU2013283993B2 (en) * 2012-06-29 2016-07-07 Betta Pharmaceuticals Co., Ltd Novel fused pyridine derivatives useful as c-Met tyrosine kinase inhibitors
WO2014000713A1 (en) 2012-06-29 2014-01-03 Zhejiang Beta Pharma Incorporation NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
US9617257B2 (en) 2012-06-29 2017-04-11 Betta Pharmaceuticals Co., Ltd Fused pyridine derivatives useful as c-Met tyrosine kinase inhibitors
KR101726522B1 (en) 2012-06-29 2017-04-12 베타 파머수티컬 컴퍼니 리미티드 NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
KR101726555B1 (en) 2012-06-29 2017-04-12 베타 파머수티컬 컴퍼니 리미티드 NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS
EP2879677A4 (en) * 2012-07-28 2016-06-01 Calitor Sciences Llc Substituted pyrazolone compounds and methods of use
WO2014022116A2 (en) 2012-07-28 2014-02-06 Calitor Sciences, Llc Substituted pyrazolone compounds and methods of use
WO2014022117A1 (en) 2012-07-28 2014-02-06 Calitor Sciences, Llc Substituted pyrazolone compounds and methods of use
US20150141463A1 (en) * 2012-07-28 2015-05-21 Calitor Sciences, Llc Substituted pyrazolone compounds and methods of use
AU2013296897B2 (en) * 2012-07-28 2015-09-17 Beijing Findcure Biosciences Ltd. Substituted pyrazolone compounds and methods of use
EP2879676A4 (en) * 2012-07-28 2015-12-09 Calitor Sciences Llc Substituted pyrazolone compounds and methods of use
US9326975B2 (en) * 2012-07-28 2016-05-03 Sunshine Lake Pharma Co., Ltd Substituted pyrazolone compounds and methods of use
US10898474B2 (en) 2012-10-02 2021-01-26 Intermune, Inc. Anti-fibrotic pyridinones
US10376497B2 (en) 2012-10-02 2019-08-13 Intermune, Inc. Anti-fibrotic pyridinones
US9359379B2 (en) 2012-10-02 2016-06-07 Intermune, Inc. Anti-fibrotic pyridinones
US9675593B2 (en) 2012-10-02 2017-06-13 Intermune, Inc. Anti-fibrotic pyridinones
US9006242B2 (en) 2012-10-15 2015-04-14 Epizyme, Inc. Substituted benzene compounds
US10098888B2 (en) 2012-10-15 2018-10-16 Epizyme, Inc. Substituted benzene compounds
US9089575B2 (en) 2012-10-15 2015-07-28 Epizyme, Inc. Substituted benzene compounds
US11642348B2 (en) 2012-10-15 2023-05-09 Epizyme, Inc. Substituted benzene compounds
US10092572B2 (en) 2012-10-15 2018-10-09 Epizyme, Inc. Substituted benzene compounds
US9532992B2 (en) 2012-10-15 2017-01-03 Epizyme, Inc. Substituted benzene compounds
US10420764B2 (en) 2012-12-21 2019-09-24 Astrazeneca Ab Pharmaceutical formulation of N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-YL]-4-[(3R,5S)-3 ,5-dimethylpiperazin-1-YL] benzamide
US10220048B2 (en) 2013-03-15 2019-03-05 Aerpio Therapeutics, Inc. Compositions and methods for treating ocular diseases
US9481668B2 (en) 2013-06-06 2016-11-01 Merck Patent Gmbh Quinoline inhibitor of the macrophage stimulating 1 receptor MSTR1
JP2016520627A (en) * 2013-06-06 2016-07-14 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ Quinoline inhibitor of 1 receptor MSTR1 that stimulates macrophages
WO2014194975A1 (en) 2013-06-06 2014-12-11 Merck Patent Gmbh A quinoline inhibitor of the macrophage stimulating 1 receptor mst1 r
TWI649308B (en) * 2013-07-24 2019-02-01 小野藥品工業股份有限公司 Quinoline derivative
WO2015012298A1 (en) 2013-07-24 2015-01-29 小野薬品工業株式会社 Quinoline derivative
KR102251609B1 (en) 2013-07-24 2021-05-13 오노 야꾸힝 고교 가부시키가이샤 Quinoline derivative
US10208022B2 (en) 2013-07-24 2019-02-19 Ono Pharmaceutical Co., Ltd. Quinoline derivative
US10501442B2 (en) 2013-07-24 2019-12-10 Ono Pharmaceuticals Co., Ltd. Quinoline derivative
JP2018024691A (en) * 2013-07-24 2018-02-15 小野薬品工業株式会社 Quinoline derivative
US10676462B2 (en) 2013-07-24 2020-06-09 Ono Pharmaceutical Co., Ltd. Quinoline derivative
CN105408312A (en) * 2013-07-24 2016-03-16 小野药品工业株式会社 Quinoline derivative
US9573935B2 (en) 2013-07-24 2017-02-21 Ono Pharmaceutical Co., Ltd. Quinoline derivative
EP3415501A1 (en) 2013-07-24 2018-12-19 ONO Pharmaceutical Co., Ltd. Quinoline derivative
KR20160033707A (en) 2013-07-24 2016-03-28 오노 야꾸힝 고교 가부시키가이샤 Quinoline derivative
JPWO2015012298A1 (en) * 2013-07-24 2017-03-02 小野薬品工業株式会社 Quinoline derivatives
US9994549B2 (en) 2013-07-24 2018-06-12 Ono Pharmaceutical Co., Ltd. Quinoline derivative
US10710987B2 (en) 2013-10-16 2020-07-14 Epizyme, Inc. Hydrochloride salt form for EZH2 inhibition
US10040782B2 (en) 2013-10-16 2018-08-07 Epizyme, Inc. Hydrochloride salt form for EZH2 inhibition
US9994560B2 (en) 2014-03-14 2018-06-12 Aerpio Therapeutics, Inc. HPTP-β inhibitors
US10858354B2 (en) 2014-03-14 2020-12-08 Aerpio Pharmaceuticals, Inc. HPTP-Beta inhibitors
US10544161B2 (en) 2014-04-02 2020-01-28 Intermune, Inc. Anti-fibrotic pyridinones
US10233195B2 (en) 2014-04-02 2019-03-19 Intermune, Inc. Anti-fibrotic pyridinones
US10208034B2 (en) 2014-12-25 2019-02-19 Ono Pharmaceutical Co., Ltd. Quinoline derivative
EP3299369A4 (en) * 2015-05-21 2018-05-02 Shanghai Institute of Materia Medica, Chinese Academy of Sciences Pyrido-azaheterecydic compound and preparation method and use thereof
US10710996B2 (en) 2015-05-21 2020-07-14 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Pyrido-azaheterecydic compound and preparation method and use thereof
US10485764B2 (en) 2015-07-02 2019-11-26 Otsuka Pharmaceutical Co., Ltd. Lyophilized pharmaceutical compositions
RU2712280C2 (en) * 2015-07-20 2020-01-28 Бетта Фармасьютикалз Ко., Лтд Crystalline form of maleate of condensed pyridine derivative and methods for use thereof
US10577364B2 (en) 2015-07-20 2020-03-03 Betta Pharmaceuticals Co., Ltd Crystalline form of fused pyridine derivative's maleate and uses thereof
AU2016297395B2 (en) * 2015-07-20 2019-01-17 Betta Pharmaceuticals Co., Ltd Crystalline form of fused pyridine derivative's maleate and uses thereof
WO2017012539A1 (en) * 2015-07-20 2017-01-26 Betta Pharmaceuticals Co.,Ltd Crystalline form of fused pyridine derivative's maleate and uses thereof
US9896458B2 (en) 2016-02-05 2018-02-20 Denali Therapeutics Inc. Compounds, compositions and methods
US10131676B2 (en) 2016-02-05 2018-11-20 Denali Therapeutics Inc. Compounds, compositions and methods
US9815850B2 (en) 2016-02-05 2017-11-14 Denali Therapeutics Inc. Compounds, compositions and methods
US10604535B2 (en) 2016-02-05 2020-03-31 Denali Therapeutics Inc. Compounds, compositions and methods
US11970486B2 (en) 2016-10-24 2024-04-30 Janssen Pharmaceutica Nv Compounds and uses thereof
US11072618B2 (en) 2016-12-09 2021-07-27 Denali Therapeutics Inc. Compounds, compositions and methods
WO2018139527A1 (en) 2017-01-26 2018-08-02 小野薬品工業株式会社 Ethane-sulfonate salt of quinoline derivative
US10836747B2 (en) 2017-01-26 2020-11-17 Ono Pharmaceutical Co., Ltd. Ethane-sulfonate salt of quinoline derivative
KR20190111035A (en) 2017-01-26 2019-10-01 오노 야꾸힝 고교 가부시키가이샤 Ethanesulfonate of Quinoline Derivatives
US10273227B2 (en) 2017-04-27 2019-04-30 Astrazeneca Ab C5-anilinoquinazoline compounds and their use in treating cancer
US10829479B2 (en) 2017-04-27 2020-11-10 Astrazeneca Ab C5-anilinoquinazoline compounds and their use in treating cancer
WO2019016071A1 (en) 2017-07-18 2019-01-24 Bayer Pharma Aktiengesellschaft Substituted pyrrolopyridine-derivatives
US10519190B2 (en) 2017-08-03 2019-12-31 Otsuka Pharmaceutical Co., Ltd. Drug compound and purification methods thereof
WO2019048989A1 (en) 2017-09-08 2019-03-14 Pi Industries Ltd. Novel fungicidal heterocyclic compounds
WO2019048988A1 (en) 2017-09-08 2019-03-14 Pi Industries Ltd. Novel fungidal heterocyclic compounds
US11826363B2 (en) 2017-10-13 2023-11-28 Ono Pharmaceutical Co., Ltd. Therapeutic agent for solid cancers, which comprises Axl inhibitor as active ingredient
US11873298B2 (en) 2017-10-24 2024-01-16 Janssen Pharmaceutica Nv Compounds and uses thereof
JP2021512055A (en) * 2018-01-17 2021-05-13 南京薬捷安康生物科技有限公司 TAM Family Kinase / and CSF1R Kinase Inhibitors and Their Applications
JP7282397B2 (en) 2018-01-17 2023-05-29 薬捷安康（南京）科技股▲分▼有限公司 TAM family kinase/and CSF1R kinase inhibitor and use thereof
EP3778586A4 (en) * 2018-04-13 2022-03-16 East China University of Science and Technology Quinazoline compound serving as egfr triple mutation inhibitor and applications thereof
JP2021520418A (en) * 2018-06-01 2021-08-19 アドレイ・ノーティ・バイオファーマ・カンパニー・リミテッド Highly active CSF1R inhibitor compound
CN111295380B (en) * 2018-06-01 2020-11-20 杭州阿诺生物医药科技有限公司 High-activity CSF1R inhibitor compound
JP7090958B2 (en) 2018-06-01 2022-06-27 アドレイ・ノーティ・バイオファーマ・カンパニー・リミテッド Highly active CSF1R inhibitor compound
CN111295380A (en) * 2018-06-01 2020-06-16 杭州阿诺生物医药科技有限公司 High-activity CSF1R inhibitor compound
US11591328B2 (en) 2018-06-01 2023-02-28 Xiamen Biotime Biotechnology Co., Ltd. Highly active CSF1R inhibitor compound
EP3842425A4 (en) * 2018-08-24 2022-05-18 Nanjing Transthera Biosciences Co., Ltd. Novel quinoline derivative inhibitor
RU2802283C2 (en) * 2018-08-24 2023-08-24 Транстера Сайенсиз (Наньцзин), Инк. New inhibitor based on a quinoline derivative
US20220073496A1 (en) * 2018-08-24 2022-03-10 Nanjing Transthera Biosciences Co., Ltd. Novel quinoline derivative inhibitor
WO2020120257A1 (en) 2018-12-11 2020-06-18 Bayer Aktiengesellschaft Substituted pyrrolopyridine-derivatives
US12098146B2 (en) 2019-01-24 2024-09-24 Janssen Pharmaceutica Nv Compounds and uses thereof
CN114391009A (en) * 2019-08-08 2022-04-22 Bci制药公司 Quinoline derivatives as protein kinase inhibitors
WO2021023888A1 (en) * 2019-08-08 2021-02-11 B.C.I. Pharma Isoquinoline derivatives as protein kinase inhibitors
WO2021249913A1 (en) 2020-06-09 2021-12-16 Bayer Aktiengesellschaft 2'-(quinolin-3-yl)-5',6'-dihydrospiro[azetidine-3,4'-pyrrolo[1,2-b]pyrazole]-1-carboxylate derivatives and related compounds as map4k1 (hpk1) inhibitors for the treatment of cancer
WO2022167627A1 (en) 2021-02-05 2022-08-11 Bayer Aktiengesellschaft Map4k1 inhibitors
US12037346B2 (en) 2021-04-13 2024-07-16 Nuvalent, Inc. Amino-substituted heteroaryls for treating cancers with EGFR mutations
US12018015B2 (en) 2021-06-18 2024-06-25 Aligos Therapeutics, Inc. Methods and compositions for targeting PD-L1
US11999750B2 (en) 2022-01-12 2024-06-04 Denali Therapeutics Inc. Crystalline forms of (S)-5-benzyl-N-(5-methyl-4-oxo-2,3,4,5-tetrahydropyrido [3,2-B][1,4]oxazepin-3-yl)-4H-1,2,4-triazole-3-carboxamide

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AU2006239216A1 (en) 2006-11-02
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PL1881976T3 (en) 2013-03-29
CN101248059A (en) 2008-08-20
MX2007013216A (en) 2007-12-12
EA013231B1 (en) 2010-04-30
CY1113324T1 (en) 2016-06-22
US20080312232A1 (en) 2008-12-18
GT200600181A (en) 2007-05-08
PE20061436A1 (en) 2007-02-08
US7858623B2 (en) 2010-12-28
IL186526A0 (en) 2008-01-20
US8685983B2 (en) 2014-04-01
HK1116161A1 (en) 2008-12-19
US20120070413A1 (en) 2012-03-22
IL186526A (en) 2012-10-31
TWI378094B (en) 2012-12-01
CA2605680C (en) 2012-10-16
SI1881976T1 (en) 2013-01-31
US20110118252A1 (en) 2011-05-19
ZA200708775B (en) 2008-06-25
PT1881976E (en) 2012-11-21
UA93375C2 (en) 2011-02-10
DK1881976T3 (en) 2013-02-04

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