BR0001486A - Processos e intermediários para preparar compostos anticancerìgenos - Google Patents

Processos e intermediários para preparar compostos anticancerìgenos

Info

Publication number
BR0001486A
BR0001486A BR0001486-9A BR0001486A BR0001486A BR 0001486 A BR0001486 A BR 0001486A BR 0001486 A BR0001486 A BR 0001486A BR 0001486 A BR0001486 A BR 0001486A
Authority
BR
Brazil
Prior art keywords
compounds
intermediates
processes
preparing
anticancer compounds
Prior art date
Application number
BR0001486-9A
Other languages
English (en)
Other versions
BRPI0001486B1 (pt
BRPI0001486B8 (pt
Inventor
Richard Shelton Lehner
Timothy Norris
Dinos Paul Santafianos
Original Assignee
Pfizer Prod 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
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of BR0001486A publication Critical patent/BR0001486A/pt
Publication of BRPI0001486B1 publication Critical patent/BRPI0001486B1/pt
Publication of BRPI0001486B8 publication Critical patent/BRPI0001486B8/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94Nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B15/00Obtaining copper
    • C22B15/0002Preliminary treatment
    • C22B15/0004Preliminary treatment without modification of the copper constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B15/00Obtaining copper
    • C22B15/0063Hydrometallurgy
    • C22B15/0065Leaching or slurrying
    • C22B15/0067Leaching or slurrying with acids or salts thereof
    • C22B15/0071Leaching or slurrying with acids or salts thereof containing sulfur
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Metallurgy (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Steroid Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Patente de Invenção: <B>"PROCESSOS E INTERMEDIáRIOS PARA PREPARAR COMPOSTOS ANTICANCERìGENOS"<D>. A presente invenção refere-se a métodos e intermediários para preparação de compostos de fórmula <MU>1<MV> e os sais farmaceuticamente aceitáveis e solvatos resultantes, bem como a compostos estruturalmente relacionados, em que R¹, R² e R^ 15^ são como aqui definidos. Os compostos precedentes são úteis no tratamento de distúrbios hiperproliferativas, tais como cânceres, em mamíferos.
BRPI0001486A 1999-03-31 2000-03-27 processos e intermediários para preparar compostos anticancerígenos BRPI0001486B8 (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12707299P 1999-03-31 1999-03-31

Publications (3)

Publication Number Publication Date
BR0001486A true BR0001486A (pt) 2001-05-02
BRPI0001486B1 BRPI0001486B1 (pt) 2019-01-29
BRPI0001486B8 BRPI0001486B8 (pt) 2021-05-25

Family

ID=22428179

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0001486A BRPI0001486B8 (pt) 1999-03-31 2000-03-27 processos e intermediários para preparar compostos anticancerígenos

Country Status (50)

Country Link
US (1) US6476040B1 (pt)
EP (1) EP1044969B1 (pt)
JP (2) JP3420549B2 (pt)
KR (2) KR100430210B1 (pt)
CN (2) CN100351242C (pt)
AP (2) AP1655A (pt)
AR (1) AR018705A1 (pt)
AT (1) ATE348098T1 (pt)
AU (2) AU781402B2 (pt)
BG (1) BG65194B1 (pt)
BR (1) BRPI0001486B8 (pt)
CA (2) CA2302965C (pt)
CO (1) CO5160273A1 (pt)
CR (1) CR6165A (pt)
CZ (1) CZ299426B6 (pt)
DE (1) DE60032275T2 (pt)
DK (1) DK1044969T3 (pt)
DZ (1) DZ3030A1 (pt)
EA (3) EA005892B1 (pt)
EE (1) EE04589B1 (pt)
EG (1) EG22506A (pt)
ES (1) ES2278578T3 (pt)
GE (1) GEP20022653B (pt)
GT (1) GT200000037A (pt)
HK (1) HK1029790A1 (pt)
HR (1) HRP20000182B1 (pt)
HU (1) HU227698B1 (pt)
ID (1) ID25427A (pt)
IL (2) IL135245A0 (pt)
IS (1) IS2468B (pt)
MA (1) MA25087A1 (pt)
MY (1) MY136270A (pt)
NO (2) NO321952B1 (pt)
NZ (2) NZ503683A (pt)
OA (1) OA11335A (pt)
PA (1) PA8491901A1 (pt)
PE (1) PE20001599A1 (pt)
PL (1) PL339330A1 (pt)
PT (1) PT1044969E (pt)
RS (1) RS49836B (pt)
SG (2) SG121687A1 (pt)
SK (1) SK287339B6 (pt)
SV (1) SV2002000047A (pt)
TN (1) TNSN00064A1 (pt)
TR (1) TR200000837A2 (pt)
TW (1) TW553939B (pt)
UA (2) UA70928C2 (pt)
UY (1) UY26086A1 (pt)
YU (1) YU13200A (pt)
ZA (1) ZA200001586B (pt)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6706721B1 (en) 1998-04-29 2004-03-16 Osi Pharmaceuticals, Inc. N-(3-ethynylphenylamino)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine mesylate anhydrate and monohydrate
US7087613B2 (en) 1999-11-11 2006-08-08 Osi Pharmaceuticals, Inc. Treating abnormal cell growth with a stable polymorph of N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine hydrochloride
UA74803C2 (uk) 1999-11-11 2006-02-15 Осі Фармасьютікалз, Інк. Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування
KR100589032B1 (ko) 2000-10-20 2006-06-14 에자이 가부시키가이샤 질소 함유 방향환 유도체
EP1408980A4 (en) 2001-06-21 2004-10-20 Ariad Pharma Inc NEW QUINAZOLINES AND THEIR USE
US7078409B2 (en) 2002-03-28 2006-07-18 Beta Pharma, Inc. Fused quinazoline derivatives useful as tyrosine kinase inhibitors
JP4703183B2 (ja) 2002-07-15 2011-06-15 シンフォニー エボルーション, インク. 受容体型キナーゼモジュレーターおよびその使用方法
US7148231B2 (en) 2003-02-17 2006-12-12 Hoffmann-La Roche Inc. [6,7-Bis(2-methoxy-ethoxy)-quinazolin-4-yl]-(3-ethynyl-phenyl)amine hydrochloride polymorph
JPWO2004080462A1 (ja) 2003-03-10 2006-06-08 エーザイ株式会社 c−Kitキナーゼ阻害剤
US8309562B2 (en) * 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
CA2531327A1 (en) 2003-07-03 2005-01-13 Myriad Genetics, Inc. Compounds and therapeutical use thereof
PL1667991T3 (pl) 2003-09-16 2008-12-31 Astrazeneca Ab Pochodne chinazoliny jako inhibitory kinazy tyrozynowej
ATE517091T1 (de) 2003-09-26 2011-08-15 Exelixis Inc C-met-modulatoren und verwendungsverfahren
JP4303726B2 (ja) 2003-11-11 2009-07-29 エーザイ・アール・アンド・ディー・マネジメント株式会社 ウレア誘導体およびその製造方法
KR20080095915A (ko) * 2004-05-06 2008-10-29 워너-램버트 캄파니 엘엘씨 4-페닐아미노-퀴나졸린-6-일-아미드
WO2006030826A1 (ja) 2004-09-17 2006-03-23 Eisai R & D Management Co., Ltd. 医薬組成物
US8258145B2 (en) 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
CA2592900A1 (en) 2005-01-03 2006-07-13 Myriad Genetics Inc. Nitrogen containing bicyclic compounds and therapeutical use thereof
US7625911B2 (en) * 2005-01-12 2009-12-01 Mai De Ltd. Amorphous form of erlotinib hydrochloride and its solid amorphous dispersion
JPWO2006090930A1 (ja) 2005-02-28 2008-07-24 エーザイ・アール・アンド・ディー・マネジメント株式会社 スルホンアミド化合物の新規併用
WO2007015569A1 (ja) * 2005-08-01 2007-02-08 Eisai R & D Management Co., Ltd. 血管新生阻害物質の効果を予測する方法
US9006240B2 (en) 2005-08-02 2015-04-14 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
US20090053236A1 (en) * 2005-11-07 2009-02-26 Eisai R & D Management Co., Ltd. USE OF COMBINATION OF ANTI-ANGIOGENIC SUBSTANCE AND c-kit KINASE INHIBITOR
WO2007061130A1 (ja) * 2005-11-22 2007-05-31 Eisai R & D Management Co., Ltd. 多発性骨髄腫に対する抗腫瘍剤
ES2556173T3 (es) * 2006-05-18 2016-01-13 Eisai R&D Management Co., Ltd. Agente antitumoral para un cáncer de tiroides
JPWO2008001956A1 (ja) * 2006-06-29 2009-12-03 エーザイ・アール・アンド・ディー・マネジメント株式会社 肝線維症治療剤
EP2054393A1 (en) 2006-07-28 2009-05-06 Synthon B.V. Crystalline erlotinib
JP5368096B2 (ja) 2006-08-28 2013-12-18 エーザイ・アール・アンド・ディー・マネジメント株式会社 未分化型胃癌に対する抗腫瘍剤
US8372856B2 (en) 2006-10-27 2013-02-12 Synthon Bv Hydrates of erlotinib hydrochloride
AU2008205847A1 (en) 2007-01-19 2008-07-24 Eisai R & D Management Co., Ltd. Composition for treatment of pancreatic cancer
CA2676796C (en) 2007-01-29 2016-02-23 Eisai R & D Management Co., Ltd. Composition for treatment of undifferentiated gastric cancer
PT2170844T (pt) * 2007-02-21 2016-08-05 Natco Pharma Ltd Novos polimorfos de cloridrato de erlotinib e método de preparação
CA2682013C (en) 2007-04-04 2015-06-30 Cipla Limited Process for preparation of erlotinib and its pharmaceutically acceptable salts
WO2009002538A2 (en) * 2007-06-25 2008-12-31 Plus Chemicals S.A. Amorphous erlotinib, processes for the preparation thereof, and processes to prepare additional forms of erlotinib
WO2009007984A2 (en) 2007-07-11 2009-01-15 Hetero Drugs Limited An improved process for erlotinib hydrochloride
WO2009025875A1 (en) * 2007-08-23 2009-02-26 Plus Chemicals Sa Stable formulations of crystalline erlotinib hcl
US20090124642A1 (en) * 2007-08-23 2009-05-14 Augusto Canavesi Crystalline forms of Erlotinib HCI and formulations thereof
US20090076042A1 (en) * 2007-09-15 2009-03-19 Protia, Llc Deuterium-enriched erlotinib
US8952035B2 (en) 2007-11-09 2015-02-10 Eisai R&D Management Co., Ltd. Combination of anti-angiogenic substance and anti-tumor platinum complex
AU2009210098B2 (en) * 2008-01-29 2013-06-13 Eisai R & D Management Co., Ltd. Combined use of angiogenesis inhibitor and taxane
JP2011516426A (ja) * 2008-03-28 2011-05-26 コンサート ファーマシューティカルズ インコーポレイテッド キナゾリン誘導体および治療方法
CA2730226A1 (en) * 2008-07-07 2010-01-14 Plus Chemicals Sa Crystalline forms of erlotinib base and erlotinib hcl
KR101132937B1 (ko) 2008-10-01 2012-04-06 주식회사종근당 N-(3-에티닐페닐)-6,7-비스(2-메톡시에톡시)-4-퀴나졸린아민 납실레이트 염
WO2010040212A1 (en) * 2008-10-08 2010-04-15 Apotex Pharmachem Inc. Processes for the preparation of erlotinib hydrochloride
EA026425B1 (ru) 2009-01-16 2017-04-28 Экселиксис, Инк. Малатная соль n-(4-{[6,7-бис(метилокси)хинолин-4-ил]окси}фенил)-n'-(4-фторфенил)циклопропан-1,1-дикарбоксамида и ее кристаллические формы для лечения рака
WO2010109443A1 (en) 2009-03-26 2010-09-30 Ranbaxy Laboratories Limited Process for the preparation of erlotinib or its pharmaceutically acceptable salts thereof
UA108618C2 (uk) 2009-08-07 2015-05-25 Застосування c-met-модуляторів в комбінації з темозоломідом та/або променевою терапією для лікування раку
US20120302749A1 (en) 2009-11-12 2012-11-29 Ranbaxy Laboratories Limited Processes for the preparation of erlotinib hydrochloride form a and erlotinib hydrochloride form b
WO2011068404A2 (en) 2009-12-02 2011-06-09 Ultimorphix Technologies B.V. Administration of n-(3-ethynylphenylamino)-6,7-bis(2- methoxyethoxy)-4-quinazolinamine mesylate salt by inhalation
BR112012032462A2 (pt) 2010-06-25 2016-11-08 Eisai R&D Man Co Ltd agente antitumoral empregando compostos que, em combinação, têm efeito inibidor de quinase.
US8952022B2 (en) 2010-07-23 2015-02-10 Generics [Uk] Limited Pure erlotinib
IT1402029B1 (it) * 2010-10-14 2013-08-28 Italiana Sint Spa Procedimento per la preparazione di erlotinib
BR112013021941B1 (pt) 2011-04-18 2022-11-16 Eisai R & D Management Co., Ltd Agente terapêutico para tumor
US9945862B2 (en) 2011-06-03 2018-04-17 Eisai R&D Management Co., Ltd. Biomarkers for predicting and assessing responsiveness of thyroid and kidney cancer subjects to lenvatinib compounds
CN102267952B (zh) * 2011-06-21 2013-12-11 天津市汉康医药生物技术有限公司 喹唑啉类化合物、其制备方法和用途
CN103420924B (zh) * 2012-05-25 2016-08-31 浙江九洲药业股份有限公司 一种盐酸埃罗替尼晶型a的制备方法
US9593083B2 (en) 2012-09-04 2017-03-14 Shilpa Medicare Limited Crystalline erlotinib hydrochloride process
KR20150098605A (ko) 2012-12-21 2015-08-28 에자이 알앤드디 매니지먼트 가부시키가이샤 퀴놀린 유도체의 비정질 형태 및 그의 제조방법
WO2014118737A1 (en) 2013-01-31 2014-08-07 Ranbaxy Laboratories Limited Erlotinib salts
CA2912219C (en) 2013-05-14 2021-11-16 Eisai R&D Management Co., Ltd. Biomarkers for predicting and assessing responsiveness of endometrial cancer subjects to lenvatinib compounds
CN103333124B (zh) * 2013-05-28 2015-03-25 埃斯特维华义制药有限公司 一种制备盐酸厄洛替尼晶型f的方法
PT3524595T (pt) 2014-08-28 2022-09-19 Eisai R&D Man Co Ltd Derivado de quinolina altamente puro e método para produção do mesmo
CA2908441A1 (en) 2014-10-28 2016-04-28 Cerbios-Pharma Sa Process for the preparation of erlotinib
HUE064614T2 (hu) 2015-02-25 2024-04-28 Eisai R&D Man Co Ltd Eljárás egy kinolin-származék keserû ízének elnyomására
CA2978226A1 (en) 2015-03-04 2016-09-09 Merck Sharpe & Dohme Corp. Combination of a pd-1 antagonist and a vegfr/fgfr/ret tyrosine kinase inhibitor for treating cancer
WO2016204193A1 (ja) 2015-06-16 2016-12-22 株式会社PRISM Pharma 抗がん剤
CN105884653A (zh) * 2016-06-08 2016-08-24 浙江汇能生物股份有限公司 一种埃罗替尼衍生物及其制备方法
CN106279585A (zh) * 2016-08-26 2017-01-04 宁波圣达精工智能科技有限公司 一种阻燃智能密集书架的制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4747498A (en) * 1986-06-27 1988-05-31 Sunbeam Plastics Corporation Safety dispensing closure-container package
AU661533B2 (en) 1992-01-20 1995-07-27 Astrazeneca Ab Quinazoline derivatives
JP2657760B2 (ja) * 1992-07-15 1997-09-24 小野薬品工業株式会社 4−アミノキナゾリン誘導体およびそれを含有する医薬品
DE69522717T2 (de) * 1995-03-30 2002-02-14 Pfizer Inc., New York Chinazolinderivate
US5747498A (en) * 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
KR19990082463A (ko) 1996-02-13 1999-11-25 돈 리사 로얄 혈관 내피 성장 인자 억제제로서의 퀴나졸린유도체
ATE211134T1 (de) 1996-03-05 2002-01-15 4-anilinochinazolin derivate
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
US6225499B1 (en) 1997-07-14 2001-05-01 Catalytica Pharmaceuticals, Inc. Process for preparing aminoarylacetylenes
ATE295839T1 (de) 1998-04-29 2005-06-15 Osi Pharm Inc N-(3-ethinylphenylamino)-6,7-bis(2-methoxyethox )-4-chinazolinamin-mesylat-anhydrat und -monohydrat

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Publication number Publication date
IS2468B (is) 2008-12-15
HK1029790A1 (en) 2001-04-12
PE20001599A1 (es) 2001-01-18
HRP20000182B1 (en) 2007-10-31
IL168036A (en) 2006-12-10
HU0001353D0 (en) 2000-06-28
HUP0001353A3 (en) 2002-01-28
EP1044969B1 (en) 2006-12-13
GT200000037A (es) 2001-09-21
NO321952B1 (no) 2006-07-24
SG115536A1 (en) 2005-10-28
GEP20022653B (en) 2002-03-25
EA200000274A2 (ru) 2000-10-30
HRP20000182A2 (en) 2001-04-30
DZ3030A1 (fr) 2004-03-27
SK287339B6 (sk) 2010-07-07
AP2000001778A0 (en) 2000-03-31
AU2262000A (en) 2000-10-05
ATE348098T1 (de) 2007-01-15
NO20054715L (no) 2000-10-02
TR200000837A2 (tr) 2000-11-21
EA200201245A1 (ru) 2003-04-24
NZ512818A (en) 2003-01-31
EA004654B1 (ru) 2004-06-24
YU13200A (sh) 2002-10-18
JP4074509B2 (ja) 2008-04-09
CO5160273A1 (es) 2002-05-30
CA2302965C (en) 2004-02-17
AU2005201494A1 (en) 2005-05-05
AU781402B2 (en) 2005-05-19
DE60032275D1 (de) 2007-01-25
ZA200001586B (en) 2001-10-01
JP3420549B2 (ja) 2003-06-23
NO20001648D0 (no) 2000-03-30
EG22506A (en) 2003-03-31
EP1044969A2 (en) 2000-10-18
CZ299426B6 (cs) 2008-07-23
ID25427A (id) 2000-10-05
PL339330A1 (en) 2000-10-09
NZ503683A (en) 2001-09-28
CN1699350A (zh) 2005-11-23
CN1276370A (zh) 2000-12-13
BRPI0001486B1 (pt) 2019-01-29
BG104278A (en) 2001-08-31
EA005561B1 (ru) 2005-04-28
OA11335A (en) 2003-12-10
EA200201244A1 (ru) 2003-04-24
PT1044969E (pt) 2007-05-31
CA2427221C (en) 2008-09-16
IS5411A (is) 2000-10-02
PA8491901A1 (es) 2001-12-14
CZ20001155A3 (cs) 2001-03-14
KR100430209B1 (ko) 2004-05-03
NO20001648L (no) 2000-10-02
EA005892B1 (ru) 2005-06-30
SV2002000047A (es) 2002-01-23
SG121687A1 (en) 2006-05-26
SK4442000A3 (en) 2000-10-09
BRPI0001486B8 (pt) 2021-05-25
CR6165A (es) 2008-10-10
JP2003176274A (ja) 2003-06-24
KR100430210B1 (ko) 2004-05-03
CA2302965A1 (en) 2000-09-30
MY136270A (en) 2008-09-30
UA70928C2 (uk) 2004-11-15
CN100351242C (zh) 2007-11-28
TW553939B (en) 2003-09-21
EE200000255A (et) 2000-12-15
ES2278578T3 (es) 2007-08-16
EA200000274A3 (ru) 2003-02-27
HU227698B1 (en) 2011-12-28
CN1215061C (zh) 2005-08-17
DK1044969T3 (da) 2007-04-23
IL135245A0 (en) 2001-05-20
KR20020084903A (ko) 2002-11-13
BG65194B1 (bg) 2007-06-29
CA2427221A1 (en) 2000-09-30
NO324745B1 (no) 2007-12-03
TNSN00064A1 (fr) 2005-11-10
UA80955C2 (en) 2007-11-26
JP2000290262A (ja) 2000-10-17
EP1044969A3 (en) 2000-11-29
DE60032275T2 (de) 2007-07-12
KR20010014658A (ko) 2001-02-26
UY26086A1 (es) 2000-10-31
AR018705A1 (es) 2001-11-28
RS49836B (sr) 2008-08-07
AU2005201494B2 (en) 2008-02-07
HUP0001353A2 (hu) 2001-05-28
AP1655A (en) 2006-09-01
US6476040B1 (en) 2002-11-05
MA25087A1 (fr) 2000-10-01
EE04589B1 (et) 2006-02-15
AP1265A (en) 2004-03-26

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