HRP20020700A2 - Aryl fused azapolycyclic compounds - Google Patents
Aryl fused azapolycyclic compounds Download PDFInfo
- Publication number
- HRP20020700A2 HRP20020700A2 HRP20020700A HRP20020700A2 HR P20020700 A2 HRP20020700 A2 HR P20020700A2 HR P20020700 A HRP20020700 A HR P20020700A HR P20020700 A2 HRP20020700 A2 HR P20020700A2
- Authority
- HR
- Croatia
- Prior art keywords
- dodeca2
- pentadeca2
- alkyl
- 8tetraene
- 5triene
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 322
- 125000003118 aryl group Chemical group 0.000 title claims description 27
- 238000000034 method Methods 0.000 claims description 126
- 239000000203 mixture Substances 0.000 claims description 93
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 74
- 229920006395 saturated elastomer Polymers 0.000 claims description 66
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 63
- 229910052739 hydrogen Inorganic materials 0.000 claims description 61
- 239000001257 hydrogen Substances 0.000 claims description 57
- 125000000217 alkyl group Chemical group 0.000 claims description 53
- 150000003839 salts Chemical class 0.000 claims description 49
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 48
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 39
- -1 hydroxy, nitro, amino Chemical group 0.000 claims description 39
- 125000001153 fluoro group Chemical group F* 0.000 claims description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims description 23
- 206010012335 Dependence Diseases 0.000 claims description 22
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 20
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 20
- 150000002367 halogens Chemical group 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 241000124008 Mammalia Species 0.000 claims description 19
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 230000009467 reduction Effects 0.000 claims description 18
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims description 17
- 125000001072 heteroaryl group Chemical group 0.000 claims description 17
- 229960002715 nicotine Drugs 0.000 claims description 17
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims description 17
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 17
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- 125000005605 benzo group Chemical group 0.000 claims description 15
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- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 claims description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 13
- 239000001301 oxygen Substances 0.000 claims description 13
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 12
- 241000208125 Nicotiana Species 0.000 claims description 12
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 12
- 125000002619 bicyclic group Chemical group 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 229910052717 sulfur Chemical group 0.000 claims description 12
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 11
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 11
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- 125000003342 alkenyl group Chemical group 0.000 claims description 11
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 11
- 239000011737 fluorine Chemical group 0.000 claims description 11
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
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- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 claims description 10
- QIADRDVMZCRSEO-UHFFFAOYSA-N 6-chloro-10-fluoro-5,14-diazatetracyclo[10.3.1.02,11.04,9]hexadeca-2(11),3,5,7,9-pentaene Chemical compound ClC1=CC=C2C(F)=C(C3CNCC4C3)C4=CC2=N1 QIADRDVMZCRSEO-UHFFFAOYSA-N 0.000 claims description 9
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 9
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 9
- 230000007000 age related cognitive decline Effects 0.000 claims description 9
- 239000011593 sulfur Chemical group 0.000 claims description 9
- SMACJRJUIUCUKX-UHFFFAOYSA-N 5,14diazatetracyclo[10.3.1.02,11.04,9]hexadeca-2(11),3,7,9-tetraen-6-one Chemical compound C1C2C3=CC4=NC(O)=CC=C4C=C3C1CNC2 SMACJRJUIUCUKX-UHFFFAOYSA-N 0.000 claims description 8
- CAONSCPWSFMLMS-UHFFFAOYSA-N 6-methoxy-5,14-diazatetracyclo[10.3.1.02,11.04,9]hexadeca-2(11),3,5,7,9-pentaene Chemical compound C1C2C3=CC4=NC(OC)=CC=C4C=C3C1CNC2 CAONSCPWSFMLMS-UHFFFAOYSA-N 0.000 claims description 8
- 208000024827 Alzheimer disease Diseases 0.000 claims description 8
- 125000002950 monocyclic group Chemical group 0.000 claims description 8
- MQWQCNHPYKVXNY-UHFFFAOYSA-N 3-fluoro-10-aza-tricyclo[6.3.1.02,7]-dodeca-2(7),3,5-triene Chemical compound C1NCC2CC1C1=C2C=CC=C1F MQWQCNHPYKVXNY-UHFFFAOYSA-N 0.000 claims description 7
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- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 7
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- 206010020651 Hyperkinesia Diseases 0.000 claims description 7
- 208000000269 Hyperkinesis Diseases 0.000 claims description 7
- 206010020772 Hypertension Diseases 0.000 claims description 7
- 206010061218 Inflammation Diseases 0.000 claims description 7
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- 208000019695 Migraine disease Diseases 0.000 claims description 7
- 208000005314 Multi-Infarct Dementia Diseases 0.000 claims description 7
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- 208000016620 Tourette disease Diseases 0.000 claims description 7
- 208000025865 Ulcer Diseases 0.000 claims description 7
- 201000006704 Ulcerative Colitis Diseases 0.000 claims description 7
- 201000004810 Vascular dementia Diseases 0.000 claims description 7
- 206010047139 Vasoconstriction Diseases 0.000 claims description 7
- 208000003554 absence epilepsy Diseases 0.000 claims description 7
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- 230000036506 anxiety Effects 0.000 claims description 7
- 206010003119 arrhythmia Diseases 0.000 claims description 7
- 229940125717 barbiturate Drugs 0.000 claims description 7
- 229940049706 benzodiazepine Drugs 0.000 claims description 7
- 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 claims description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
- 239000013043 chemical agent Substances 0.000 claims description 7
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- 230000004054 inflammatory process Effects 0.000 claims description 7
- 208000002551 irritable bowel syndrome Diseases 0.000 claims description 7
- 235000020824 obesity Nutrition 0.000 claims description 7
- 229940005483 opioid analgesics Drugs 0.000 claims description 7
- 208000019906 panic disease Diseases 0.000 claims description 7
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- 201000002212 progressive supranuclear palsy Diseases 0.000 claims description 7
- 201000000980 schizophrenia Diseases 0.000 claims description 7
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- 230000001148 spastic effect Effects 0.000 claims description 7
- 235000019505 tobacco product Nutrition 0.000 claims description 7
- 231100000397 ulcer Toxicity 0.000 claims description 7
- JQSHBVHOMNKWFT-UHFFFAOYSA-N varenicline Chemical compound C12=CC3=NC=CN=C3C=C2C2CC1CNC2 JQSHBVHOMNKWFT-UHFFFAOYSA-N 0.000 claims description 7
- 230000025033 vasoconstriction Effects 0.000 claims description 7
- RGTBLCLLSZPOKR-UHFFFAOYSA-N 5-methyl-1,2,4-oxadiazole Chemical compound CC1=NC=NO1 RGTBLCLLSZPOKR-UHFFFAOYSA-N 0.000 claims description 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 6
- MUAAOAJMVIAASD-UHFFFAOYSA-N chembl198032 Chemical compound C1NCC2CC1C1=C2C=C2N=CN(C)C2=C1 MUAAOAJMVIAASD-UHFFFAOYSA-N 0.000 claims description 6
- SLRAKVICRDZWAA-UHFFFAOYSA-N chembl198035 Chemical compound C1NCC2CC1C1=C2C=C2N=CN(CCCC)C2=C1 SLRAKVICRDZWAA-UHFFFAOYSA-N 0.000 claims description 6
- SOBKRFVVZYOGEO-UHFFFAOYSA-N chembl198333 Chemical compound C1NCC2CC1C1=C2C=C2N=C(C)N(C)C2=C1 SOBKRFVVZYOGEO-UHFFFAOYSA-N 0.000 claims description 6
- ZMRZCVHPEQNWCW-UHFFFAOYSA-N chembl199046 Chemical compound C1NCC2CC1C1=C2C=C2N=C(C)N(CC(C)(C)C)C2=C1 ZMRZCVHPEQNWCW-UHFFFAOYSA-N 0.000 claims description 6
- SPWVDDOSSYRJLM-UHFFFAOYSA-N chembl199096 Chemical compound C1NCC2CC1C1=C2C=C2N=C(C)N(CCC)C2=C1 SPWVDDOSSYRJLM-UHFFFAOYSA-N 0.000 claims description 6
- WBYFNWHZLPPQST-UHFFFAOYSA-N chembl199152 Chemical compound C1NCC2CC1C1=C2C=C2N=CN(CCC)C2=C1 WBYFNWHZLPPQST-UHFFFAOYSA-N 0.000 claims description 6
- NHGOODNSLHNEAP-UHFFFAOYSA-N chembl436110 Chemical compound C1C(C2=CC=3N=C4)CNCC1C2=CC=3N4C1=CC=CC=C1 NHGOODNSLHNEAP-UHFFFAOYSA-N 0.000 claims description 6
- 210000004211 gastric acid Anatomy 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- VSKYGZMZVGNBGR-UHFFFAOYSA-N 4,5-dinitro-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-triene Chemical compound C1NCC2CC1C1=C2C=C([N+](=O)[O-])C([N+]([O-])=O)=C1 VSKYGZMZVGNBGR-UHFFFAOYSA-N 0.000 claims description 5
- 208000019888 Circadian rhythm sleep disease Diseases 0.000 claims description 5
- 208000001456 Jet Lag Syndrome Diseases 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 208000033915 jet lag type circadian rhythm sleep disease Diseases 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000000453 2,2,2-trichloroethyl group Chemical group [H]C([H])(*)C(Cl)(Cl)Cl 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 2
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- GZAHUQFGFBFMCD-UHFFFAOYSA-N chembl198278 Chemical compound C1NCC2CC1C1=C2C=C2N=C(C)C(C)=NC2=C1 GZAHUQFGFBFMCD-UHFFFAOYSA-N 0.000 claims description 2
- NNQXNMIUYWOMIR-UHFFFAOYSA-N chembl198444 Chemical compound C1NCC2CC1C1=C2C=C2N=C(C)NC2=C1 NNQXNMIUYWOMIR-UHFFFAOYSA-N 0.000 claims description 2
- SPAMUHJHVULSFR-UHFFFAOYSA-N chembl198490 Chemical compound C12=CC=3NC=NC=3C=C2C2CC1CNC2 SPAMUHJHVULSFR-UHFFFAOYSA-N 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004043 oxo group Chemical group O=* 0.000 claims description 2
- 150000003457 sulfones Chemical class 0.000 claims description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
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- 238000004458 analytical method Methods 0.000 description 16
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- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
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- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
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- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- FTVLMFQEYACZNP-UHFFFAOYSA-N trimethylsilyl trifluoromethanesulfonate Chemical compound C[Si](C)(C)OS(=O)(=O)C(F)(F)F FTVLMFQEYACZNP-UHFFFAOYSA-N 0.000 description 1
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
- MGTXXLCYXLMYIM-UHFFFAOYSA-K trisodium triperiodate Chemical compound I(=O)(=O)(=O)[O-].[Na+].[Na+].[Na+].I(=O)(=O)(=O)[O-].I(=O)(=O)(=O)[O-] MGTXXLCYXLMYIM-UHFFFAOYSA-K 0.000 description 1
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Classifications
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
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- C07—ORGANIC CHEMISTRY
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- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/514,002 US6605610B1 (en) | 1997-12-31 | 2000-02-25 | Aryl fused azapolycyclic compounds |
PCT/IB2001/000153 WO2001062736A1 (en) | 2000-02-25 | 2001-02-08 | Aryl fused azapolycyclic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20020700A2 true HRP20020700A2 (en) | 2004-12-31 |
Family
ID=24045406
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HRP20020700 HRP20020700A2 (en) | 2000-02-25 | 2002-08-26 | Aryl fused azapolycyclic compounds |
Country Status (40)
Country | Link |
---|---|
US (3) | US6605610B1 (zh) |
EP (2) | EP1259489B1 (zh) |
JP (1) | JP2003524002A (zh) |
KR (1) | KR100537976B1 (zh) |
CN (1) | CN1263745C (zh) |
AP (1) | AP1860A (zh) |
AT (2) | ATE328872T1 (zh) |
AU (2) | AU784081B2 (zh) |
BG (1) | BG65891B1 (zh) |
BR (1) | BR0108610A (zh) |
CA (1) | CA2401229C (zh) |
CR (1) | CR6726A (zh) |
CU (1) | CU23148A3 (zh) |
CY (1) | CY1105301T1 (zh) |
CZ (1) | CZ303203B6 (zh) |
DE (2) | DE60120366T2 (zh) |
DK (2) | DK1619192T3 (zh) |
DZ (1) | DZ3328A1 (zh) |
EA (1) | EA005316B1 (zh) |
EE (1) | EE200200475A (zh) |
ES (2) | ES2336800T3 (zh) |
GE (1) | GEP20053454B (zh) |
HK (1) | HK1050894A1 (zh) |
HR (1) | HRP20020700A2 (zh) |
HU (1) | HU229482B1 (zh) |
IL (2) | IL150639A0 (zh) |
IS (1) | IS2293B (zh) |
MA (1) | MA26875A1 (zh) |
MX (1) | MXPA02008311A (zh) |
NO (1) | NO323608B1 (zh) |
NZ (1) | NZ519973A (zh) |
OA (1) | OA12181A (zh) |
PL (1) | PL365163A1 (zh) |
PT (1) | PT1259489E (zh) |
RS (1) | RS51123B (zh) |
SI (1) | SI1259489T1 (zh) |
SK (1) | SK12042002A3 (zh) |
UA (1) | UA74813C2 (zh) |
WO (1) | WO2001062736A1 (zh) |
ZA (1) | ZA200206768B (zh) |
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BR0208992A (pt) * | 2001-04-20 | 2004-04-27 | Pfizer Prod Inc | Processo para a preparação de indenos 1,3-substituìdos e compostos azapolicìclicos fundidos com arila |
CN1568184A (zh) * | 2001-10-31 | 2005-01-19 | 辉瑞产品公司 | 烟碱乙酰胆碱受体激动剂在治疗多动腿综合征中的用途 |
JP2005510568A (ja) * | 2001-11-30 | 2005-04-21 | ファイザー・プロダクツ・インク | アリール基が結合したアザポリサイクリック化合物 |
NZ532435A (en) * | 2001-11-30 | 2005-04-29 | Pfizer Prod Inc | Pharmaceutical compositions of 5,7,14-triazatetracyclo [10.3.1.0(2,11).0(4,9)]-hexadeca-2(11)3,5,7,9-pentaene |
NZ537003A (en) | 2002-07-18 | 2008-03-28 | Cytos Biotechnology Ag | Hapten-carrier conjugates comprising virus like particles and uses thereof |
EP2174714B1 (en) * | 2002-10-22 | 2013-04-17 | EMD Millipore Corporation | Apparatus with a composite structure for sample preparation |
PL377292A1 (pl) * | 2002-11-25 | 2006-01-23 | Pfizer Products Inc. | Ulepszony sposób wytwarzania 1,3-podstawionych indenów |
BRPI0406670A (pt) * | 2003-01-15 | 2005-12-20 | Pfizer Prod Inc | Processo para a preparação de lactamas policìclicas fundidos com arila |
WO2004103372A1 (en) * | 2003-05-20 | 2004-12-02 | Pfizer Products Inc. | Pharmaceutical compositions of varenicline |
DK1638971T3 (da) * | 2003-06-04 | 2008-10-27 | Pfizer Prod Inc | Fremstilling af substitueret Quinoxaliner fra dianilinen med 2,3-dihydroxy-1,4-dioxan |
MXPA06000892A (es) * | 2003-07-21 | 2006-03-30 | Pfizer Prod Inc | Compuestos azapoliciclicos arilo fusionados. |
US8580842B2 (en) * | 2003-09-30 | 2013-11-12 | Abbott Gmbh & Co. Kg | Heteroaryl-substituted 1,3-dihydroindol-2-one derivatives and medicaments containing them |
ES2368916T3 (es) | 2003-10-14 | 2011-11-23 | Xenoport, Inc. | Forma cristalina de un análogo del ácido gamma-aminobutírico. |
CA2549638A1 (en) * | 2003-12-23 | 2005-07-14 | Pfizer Products Inc. | Therapeutic combination for cognition enhancement and psychotic disorders |
WO2006006071A1 (en) * | 2004-07-07 | 2006-01-19 | Pfizer Products Inc. | Resolution of an aryl-fused azapolycyclic compound |
KR20070098942A (ko) * | 2005-02-24 | 2007-10-05 | 화이자 프로덕츠 인코포레이티드 | 고순도의 치환된 퀴녹살린의 제조 방법 |
KR20090007568A (ko) * | 2006-04-24 | 2009-01-19 | 화이자 프로덕츠 인코포레이티드 | 약물 전달 장치용 비대칭 막 |
EP2086977A2 (en) * | 2006-11-09 | 2009-08-12 | Pfizer Products Inc. | Polymorphs of nicotinic intermediates |
US8486979B2 (en) * | 2006-12-12 | 2013-07-16 | Abbvie Inc. | 1,2,4 oxadiazole compounds and methods of use thereof |
US20080167286A1 (en) | 2006-12-12 | 2008-07-10 | Abbott Laboratories | Pharmaceutical compositions and their methods of use |
UY30846A1 (es) | 2006-12-30 | 2008-07-31 | Abbott Gmbh & Amp | Derivados de oxindol sustituidos, medicamentos que los comprenden y uso de los mismos |
US20090062257A1 (en) * | 2007-08-29 | 2009-03-05 | Protia, Llc | Deuterium-enriched varenicline |
WO2009034431A2 (en) | 2007-09-10 | 2009-03-19 | Pfizer Inc. | Controlled-release dosage forms for varenicline |
WO2009065872A2 (en) * | 2007-11-20 | 2009-05-28 | Medichem, S.A. | Improved processes for the synthesis of varenicline l-tartrate |
NZ586651A (en) * | 2007-12-07 | 2012-06-29 | Abbott Gmbh & Co Kg | 5-halogen-substituted oxindole derivatives and use thereof for treating vasopressine-dependent diseases |
CN102026995B (zh) | 2007-12-07 | 2014-10-29 | Abbvie德国有限责任两合公司 | 5,6-二取代的羟吲哚衍生物和其用途 |
US8703775B2 (en) * | 2007-12-07 | 2014-04-22 | AbbVie Deutschland GmbH & Co. KG | Amidomethyl-substituted oxindole derivatives and the use thereof for the treatment of vasopressin-dependent illnesses |
US8703774B2 (en) * | 2007-12-07 | 2014-04-22 | AbbVie Deutschland GmbH & Co. KG | Carbamate-substituted oxindole derivatives and use thereof for the treatment of vasopressin-dependent diseases |
US8383657B2 (en) | 2007-12-21 | 2013-02-26 | Abbott Laboratories | Thiazolylidine urea and amide derivatives and methods of use thereof |
JP2011516489A (ja) | 2008-03-31 | 2011-05-26 | ユニバーシティ・オブ・サウス・フロリダ | 疾患誘発性運動失調症および非運動失調性平衡異常の治療法 |
CA2709774C (en) * | 2008-05-22 | 2012-10-02 | Teva Pharmaceutical Industries Ltd. | Varenicline tosylate, an intermediate in the preparation process of varenicline l-tartrate |
US20090318695A1 (en) * | 2008-06-19 | 2009-12-24 | Vinod Kumar Kansal | Processes for the preparation of varenicline and intermediates thereof |
US20100010221A1 (en) * | 2008-07-10 | 2010-01-14 | Revital Lifshitz-Liron | Processes for purifying varenicline l-tartrate salt and preparing crystalline forms of varenicline l-tartrate salt |
US8314235B2 (en) * | 2008-09-01 | 2012-11-20 | Actavis Group Ptc Ehf | Process for preparing varenicline, varenicline intermediates, pharmaceutically acceptable salts thereof |
BRPI1008020A2 (pt) * | 2009-02-11 | 2016-03-15 | Sunovion Pharmaceuticals Inc | antagonistas e agonistas inversos h3 da histamina e métodos de uso dos mesmos |
EP2435080A2 (en) | 2009-05-29 | 2012-04-04 | Abbott Laboratories | Pharmaceutical compositions for the treatment of pain |
RU2012102052A (ru) * | 2009-06-22 | 2013-11-20 | Тева Фармасьютикал Индастриз Лтд. | Твердые формы солей варениклина и способы их получения |
KR20180101268A (ko) | 2017-03-03 | 2018-09-12 | 주식회사 씨티씨바이오 | 바레니클린 또는 이의 약학적으로 허용가능한 염의 포접 복합체를 포함하는 구강 투여용 제제 |
US20230116114A1 (en) * | 2020-01-03 | 2023-04-13 | Blue Oak Pharmaceuticals, Inc. | Compounds and compositions for treating cns disorders |
CN115322105A (zh) * | 2021-05-11 | 2022-11-11 | 江苏润安制药有限公司 | 一种合成艾拉莫德关键中间体的方法 |
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US3471503A (en) | 1967-05-05 | 1969-10-07 | Mcneilab Inc | 1,2,3,5,6,7-hexahydro-4-phenethyl-2,6-methano-4h-4- benzazonin-12-ols |
NZ504482A (en) * | 1997-12-31 | 2003-01-31 | Pfizer Prod Inc | Aryl fused azapolycyclic compounds and pharmaceuticals thereof which bind to neuronal nicotinic acetylcholine specific recpetor sites and are useful for modulating cholinergic function |
EP0955301A3 (en) | 1998-04-27 | 2001-04-18 | Pfizer Products Inc. | 7-aza-bicyclo[2.2.1]-heptane derivatives, their preparation and use according to their affinity for neuronal nicotinic acetylcholine receptors |
IL138917A0 (en) | 1998-04-29 | 2001-11-25 | Pfizer Prod Inc | Aryl fused azapolycyclic compounds |
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FR2788982B1 (fr) * | 1999-02-02 | 2002-08-02 | Synthelabo | Compositions pharmaceutiques contenant de la nicotine et leur application dans le sevrage tabagique |
IL137937A0 (en) * | 1999-08-27 | 2001-10-31 | Pfizer Prod Inc | A pharmaceutical composition for the prevention and treatment of nicotine addiction in a mammal |
EP1372692A4 (en) * | 2001-03-19 | 2005-10-26 | Sloan Kettering Inst Cancer | ASYMMETRIC SYNTHESIS OF (S, S, R) - (-) - ACTINONE AND ITS ANALOG AND USES THEREOF |
MXPA06000892A (es) * | 2003-07-21 | 2006-03-30 | Pfizer Prod Inc | Compuestos azapoliciclicos arilo fusionados. |
US8123947B2 (en) | 2007-10-22 | 2012-02-28 | Baxter International Inc. | Priming and air removal systems and methods for dialysis |
-
2000
- 2000-02-25 US US09/514,002 patent/US6605610B1/en not_active Expired - Fee Related
-
2001
- 2001-02-08 CA CA002401229A patent/CA2401229C/en not_active Expired - Fee Related
- 2001-02-08 DZ DZ013328A patent/DZ3328A1/fr active
- 2001-02-08 BR BR0108610-3A patent/BR0108610A/pt not_active Application Discontinuation
- 2001-02-08 HU HU0204580A patent/HU229482B1/hu not_active IP Right Cessation
- 2001-02-08 JP JP2001562518A patent/JP2003524002A/ja active Pending
- 2001-02-08 CN CNB018055737A patent/CN1263745C/zh not_active Expired - Fee Related
- 2001-02-08 IL IL15063901A patent/IL150639A0/xx active IP Right Grant
- 2001-02-08 PT PT01953630T patent/PT1259489E/pt unknown
- 2001-02-08 DK DK05106835.1T patent/DK1619192T3/da active
- 2001-02-08 CZ CZ20022778A patent/CZ303203B6/cs not_active IP Right Cessation
- 2001-02-08 RS YUP-596/02A patent/RS51123B/sr unknown
- 2001-02-08 KR KR10-2002-7011140A patent/KR100537976B1/ko not_active IP Right Cessation
- 2001-02-08 WO PCT/IB2001/000153 patent/WO2001062736A1/en active IP Right Grant
- 2001-02-08 EP EP01953630A patent/EP1259489B1/en not_active Expired - Lifetime
- 2001-02-08 AP APAP/P/2002/002604A patent/AP1860A/en active
- 2001-02-08 EP EP05106835A patent/EP1619192B1/en not_active Expired - Lifetime
- 2001-02-08 ES ES05106835T patent/ES2336800T3/es not_active Expired - Lifetime
- 2001-02-08 OA OA1200200256A patent/OA12181A/en unknown
- 2001-02-08 DE DE60120366T patent/DE60120366T2/de not_active Expired - Lifetime
- 2001-02-08 NZ NZ519973A patent/NZ519973A/en not_active IP Right Cessation
- 2001-02-08 SK SK1204-2002A patent/SK12042002A3/sk not_active Application Discontinuation
- 2001-02-08 AT AT01953630T patent/ATE328872T1/de active
- 2001-02-08 SI SI200130584T patent/SI1259489T1/sl unknown
- 2001-02-08 MX MXPA02008311A patent/MXPA02008311A/es active IP Right Grant
- 2001-02-08 AU AU28748/01A patent/AU784081B2/en not_active Ceased
- 2001-02-08 PL PL01365163A patent/PL365163A1/xx not_active Application Discontinuation
- 2001-02-08 EA EA200200716A patent/EA005316B1/ru not_active IP Right Cessation
- 2001-02-08 ES ES01953630T patent/ES2263640T3/es not_active Expired - Lifetime
- 2001-02-08 DE DE60140965T patent/DE60140965D1/de not_active Expired - Lifetime
- 2001-02-08 DK DK01953630T patent/DK1259489T3/da active
- 2001-02-08 EE EEP200200475A patent/EE200200475A/xx unknown
- 2001-02-08 AT AT05106835T patent/ATE453643T1/de not_active IP Right Cessation
- 2001-02-08 GE GE4911A patent/GEP20053454B/en unknown
- 2001-08-02 UA UA2002075792A patent/UA74813C2/uk unknown
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2002
- 2002-07-05 IS IS6459A patent/IS2293B/is unknown
- 2002-07-05 BG BG106908A patent/BG65891B1/bg unknown
- 2002-07-08 IL IL150639A patent/IL150639A/en not_active IP Right Cessation
- 2002-08-09 CR CR6726A patent/CR6726A/es unknown
- 2002-08-13 MA MA26775A patent/MA26875A1/fr unknown
- 2002-08-21 CU CU177A patent/CU23148A3/es not_active IP Right Cessation
- 2002-08-22 ZA ZA200206768A patent/ZA200206768B/xx unknown
- 2002-08-23 NO NO20024042A patent/NO323608B1/no not_active IP Right Cessation
- 2002-08-26 HR HRP20020700 patent/HRP20020700A2/hr not_active Application Discontinuation
-
2003
- 2003-01-03 US US10/336,508 patent/US7205300B2/en not_active Expired - Fee Related
- 2003-01-03 US US10/336,532 patent/US7144882B2/en not_active Expired - Fee Related
- 2003-04-29 HK HK03103024A patent/HK1050894A1/xx not_active IP Right Cessation
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2005
- 2005-11-18 AU AU2005234671A patent/AU2005234671B2/en not_active Ceased
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