JP2008518900A5 - - Google Patents

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Publication number
JP2008518900A5
JP2008518900A5 JP2007538537A JP2007538537A JP2008518900A5 JP 2008518900 A5 JP2008518900 A5 JP 2008518900A5 JP 2007538537 A JP2007538537 A JP 2007538537A JP 2007538537 A JP2007538537 A JP 2007538537A JP 2008518900 A5 JP2008518900 A5 JP 2008518900A5
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JP
Japan
Prior art keywords
alkyl
compound
formula
aryl
membered
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
JP2007538537A
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English (en)
Japanese (ja)
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JP2008518900A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/IB2005/003297 external-priority patent/WO2006048744A1/en
Publication of JP2008518900A publication Critical patent/JP2008518900A/ja
Publication of JP2008518900A5 publication Critical patent/JP2008518900A5/ja
Withdrawn legal-status Critical Current

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JP2007538537A 2004-11-02 2005-10-21 インダゾール化合物の調製方法 Withdrawn JP2008518900A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US62463504P 2004-11-02 2004-11-02
US71707105P 2005-09-14 2005-09-14
PCT/IB2005/003297 WO2006048744A1 (en) 2004-11-02 2005-10-21 Methods of preparing indazole compounds

Publications (2)

Publication Number Publication Date
JP2008518900A JP2008518900A (ja) 2008-06-05
JP2008518900A5 true JP2008518900A5 (cg-RX-API-DMAC10.html) 2008-11-06

Family

ID=35744929

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007538537A Withdrawn JP2008518900A (ja) 2004-11-02 2005-10-21 インダゾール化合物の調製方法

Country Status (14)

Country Link
US (1) US7232910B2 (cg-RX-API-DMAC10.html)
EP (1) EP1809621A1 (cg-RX-API-DMAC10.html)
JP (1) JP2008518900A (cg-RX-API-DMAC10.html)
KR (1) KR20070058690A (cg-RX-API-DMAC10.html)
AR (1) AR051754A1 (cg-RX-API-DMAC10.html)
AU (1) AU2005300310A1 (cg-RX-API-DMAC10.html)
BR (1) BRPI0518203A2 (cg-RX-API-DMAC10.html)
CA (1) CA2586174A1 (cg-RX-API-DMAC10.html)
IL (1) IL182693A0 (cg-RX-API-DMAC10.html)
MX (1) MX2007005291A (cg-RX-API-DMAC10.html)
NO (1) NO20071619L (cg-RX-API-DMAC10.html)
RU (1) RU2007116107A (cg-RX-API-DMAC10.html)
TW (1) TWI294421B (cg-RX-API-DMAC10.html)
WO (1) WO2006048744A1 (cg-RX-API-DMAC10.html)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2134702B2 (en) * 2007-04-05 2023-08-30 Pfizer Products Inc. Crystalline forms of 6-[2-(methylcarbamoyl)phenylsulfanyl]-3-e-[2-(pyridin-2-yl)ethenyl]indazole suitable for the treatment of abnormal cell growth in mammals
JP5348725B2 (ja) 2007-10-25 2013-11-20 ジェネンテック, インコーポレイテッド チエノピリミジン化合物の製造方法
EP2163544A1 (en) * 2008-09-16 2010-03-17 Pfizer, Inc. Methods of preparing indazole compounds
PE20141317A1 (es) * 2009-01-08 2014-09-26 Merck Patent Gmbh Nuevas formas polimorficas de sal de clorhidrato de 3-(1-{3-[5-(1-metil-piperidin-4-ilmetoxi)-pirimidin-2-il]-bencil}-6-oxo-1,6-dihidro-piridazin-3-il)-benzonitrilo y sus procesos de preparacion
WO2013046133A1 (en) 2011-09-30 2013-04-04 Pfizer Inc. Pharmaceutical compositions of n-methyl-2-[3-((e)-2-pyridin-2-yl-vinyl)-1h-indazol-6-ylsulfanyl]-benzamide
KR20140088556A (ko) 2011-11-11 2014-07-10 화이자 인코포레이티드 만성 골수성 백혈병을 치료하기 위한 n-메틸-2-[3-((e)-2-피리딘-2-일-비닐)-1h-인다졸-6-일설파닐]-벤즈아미드
US9899120B2 (en) 2012-11-02 2018-02-20 Nanotek Instruments, Inc. Graphene oxide-coated graphitic foil and processes for producing same
US10087073B2 (en) 2013-02-14 2018-10-02 Nanotek Instruments, Inc. Nano graphene platelet-reinforced composite heat sinks and process for producing same
EP2792360A1 (en) 2013-04-18 2014-10-22 IP Gesellschaft für Management mbH (1aR,12bS)-8-cyclohexyl-11-fluoro-N-((1-methylcyclopropyl)sulfonyl)-1a-((3-methyl-3,8-diazabicyclo[3.2.1]oct-8-yl)carbonyl)-1,1a,2,2b-tetrahydrocyclopropa[d]indolo[2,1-a][2]benzazepine-5-carboxamide for use in treating HCV
WO2015067224A1 (en) 2013-11-08 2015-05-14 Zentiva, K.S. Salts of 6-[2-(methylcarbamoyl)phenylsulfanyl]-3-e-[2-(pyridin-2-yl)ethanyl] indazole
PT3077397T (pt) * 2013-12-06 2020-01-22 Vertex Pharma Composto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]pirazolo[1,5-a]pirimidin-3-carboxamida útil como inibidor da atr quinase, a sua preparação, diferentes formas sólidas e derivados radiomarcados do mesmo
WO2015119930A1 (en) 2014-02-04 2015-08-13 Pfizer Inc. Combination of a pd-1 antagonist and a vegfr inhibitor for treating cancer
RU2667486C2 (ru) * 2014-03-31 2018-09-20 Сэндзю Фармацевтикал Ко., Лтд. Производное алкинилиндазола и его применение
WO2016032927A1 (en) 2014-08-25 2016-03-03 Pfizer Inc. Combination of a pd-1 antagonist and an alk inhibitor for treating cancer
WO2016108106A1 (en) * 2014-12-29 2016-07-07 Shilpa Medicare Limited An improved process for preparation of axitinib
RU2714233C2 (ru) 2015-02-26 2020-02-13 Мерк Патент Гмбх Ингибиторы pd-1 / pd-l1 для лечения рака
US9580406B2 (en) 2015-04-28 2017-02-28 Signa S.A. De C.V. Processes for the preparation of axitinib
MX390878B (es) 2015-06-16 2025-03-21 Merck Patent Gmbh Usos medicos de antagonista de ligando 1 de muerte programada (pd-l1).
IL265762B2 (en) 2016-10-06 2024-04-01 Merck Patent Gmbh Dosing regimen of avelumab for the treatment of cancer
WO2020128893A1 (en) 2018-12-21 2020-06-25 Pfizer Inc. Combination treatments of cancer comprising a tlr agonist
ES2982700T3 (es) 2019-04-18 2024-10-17 Synthon Bv Proceso para preparar axitinib, proceso para purificar el producto intermedio 2-((3-yodo-1H-indazol-6-il)tio)-n-metilbenzamida, proceso para purificar axitinib a través de la sal HCI de axitinib, forma sólida de la sal HCI de axitinib
CA3253467A1 (en) 2022-03-03 2023-09-07 Pfizer Inc. MULTISPECIFIC ANTIBODIES AND THEIR USES
WO2025157389A1 (en) 2024-01-22 2025-07-31 Iomx Therapeutics Ag Combinations of halogenated heterocyclic kinase inhibitors and vegfr inhibitors

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI262914B (en) * 1999-07-02 2006-10-01 Agouron Pharma Compounds and pharmaceutical compositions for inhibiting protein kinases
CA2517517C (en) * 2003-03-03 2012-12-18 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
KR20050119671A (ko) * 2003-04-03 2005-12-21 화이자 인코포레이티드 Ag013736을 포함하는 제형
WO2006123223A1 (en) 2005-05-19 2006-11-23 Pfizer Inc. Pharmaceutical compostions comprising an amorphous form of a vegf-r inhibitor

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