JP2008518900A5 - - Google Patents

Download PDF

Info

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
Authority
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Withdrawn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
Other languages
English (en)
Japanese (ja)
Other versions
JP2008518900A (ja
Filing date
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Withdrawn legal-status Critical Current

Links

JP2007538537A 2004-11-02 2005-10-21 インダゾール化合物の調製方法 Withdrawn JP2008518900A (ja)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 (enExample) 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JP2007538537A Withdrawn JP2008518900A (ja) 2004-11-02 2005-10-21 インダゾール化合物の調製方法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 (enExample)
EP (1) EP1809621A1 (enExample)
JP (1) JP2008518900A (enExample)
KR (1) KR20070058690A (enExample)
AR (1) AR051754A1 (enExample)
AU (1) AU2005300310A1 (enExample)
BR (1) BRPI0518203A2 (enExample)
CA (1) CA2586174A1 (enExample)
IL (1) IL182693A0 (enExample)
MX (1) MX2007005291A (enExample)
NO (1) NO20071619L (enExample)
RU (1) RU2007116107A (enExample)
TW (1) TWI294421B (enExample)
WO (1) WO2006048744A1 (enExample)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101679356A (zh) 2007-04-05 2010-03-24 辉瑞产品公司 适用于治疗哺乳动物异常细胞生长的6-[2-(甲基-氨甲酰基)苯基硫基]-3-e-[2-(吡啶-2-基)乙烯基]吲唑的晶型
WO2009055730A1 (en) 2007-10-25 2009-04-30 Genentech, Inc. Process for making thienopyrimidine compounds
EP2163544A1 (en) * 2008-09-16 2010-03-17 Pfizer, Inc. Methods of preparing indazole compounds
CA2949515C (en) 2009-01-08 2018-10-23 Axel Becker Polymorphic forms of 3-(1-{3-[5-(1-methyl-piperidin-4-ylmethoxy)-pyrimidin-2-yl]-benzyl}-6-oxo-1,6-dihydro-pyridazin-3-yl)-benzonitrile hydrochloride salt and processes of manufacturing thereof
TW201531309A (zh) 2011-09-30 2015-08-16 Pfizer N-甲基-2-〔3-((e)-2-吡啶-2-基-乙烯基)-1h-吲唑-6-基硫烷基〕苯甲醯胺之藥學組成物
JP2014533262A (ja) 2011-11-11 2014-12-11 ファイザー・インク 慢性骨髄性白血病を治療するためのn−メチル−2−[3−((e)−2−ピリジン−2−イル−ビニル)−1h−インダゾール−6−イルスルファニル]−ベンズアミド
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
HUE046727T2 (hu) * 2013-12-06 2020-03-30 Vertex Pharma Az ATR-kináz inhibitoraként használható vegyület, 2-amino-6-fluoro-N-[5-fluoro-piridin-3-IL]-pirazolo-[1,5-A]-pirimidin-3-karboxamid, ennek elõállítása, különbözõ szilárd formái és ezek radioaktív nyomjelzett származékai
US10570202B2 (en) 2014-02-04 2020-02-25 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
US10695426B2 (en) 2014-08-25 2020-06-30 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
KR20170132171A (ko) 2015-02-26 2017-12-01 메르크 파텐트 게엠베하 암 치료를 위한 pd­1 / pd­l1 저해제
US9580406B2 (en) 2015-04-28 2017-02-28 Signa S.A. De C.V. Processes for the preparation of axitinib
RU2766890C2 (ru) 2015-06-16 2022-03-16 Мерк Патент Гмбх Комбинированные способы лечения антагонистами pd-l1
BR112019006504A2 (pt) 2016-10-06 2019-06-25 Pfizer Inc. regime de dosagem de avelumabe para o tratamento de câncer
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
IL315262A (en) 2022-03-03 2024-10-01 Pfizer Multiple specific antibodies related to IL-4, IL-13 and/or TSLP 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
KR101099281B1 (ko) * 2003-03-03 2011-12-26 어레이 바이오파마 인크. p38 억제제 및 그의 사용 방법
KR20050119671A (ko) * 2003-04-03 2005-12-21 화이자 인코포레이티드 Ag013736을 포함하는 제형
US20080274192A1 (en) 2005-05-19 2008-11-06 Pfizer Inc. Pharmaceutical Compositions Comprising an Amorphous Form of a Vegf-R-Inhibitor

Similar Documents

Publication Publication Date Title
JP6722200B2 (ja) 複素環化合物の合成
JP2008523069A5 (enExample)
JP2005519932A5 (enExample)
CN106536516B (zh) 用于制备吡啶化合物的方法
JP2008517983A5 (enExample)
ES2657676T3 (es) Proceso para la preparación de derivados de l-alanina protegidos
RU2018131134A (ru) ЗАМЕЩЕННЫЕ ПИРАЗОЛО[1,5-a]ПИРИМИДИНОВЫЕ СОЕДИНЕНИЯ КАК ИНГИБИТОРЫ ТРК КИНАЗЫ
CA2587528A1 (en) Method for preparing n-phenylpyrazole-1-carboxamides
JP2010539166A5 (enExample)
RU2012116526A (ru) Способы получения производных пиримидина, применимых в качестве ингибиторов протеинкиназы
JP2005505618A5 (enExample)
JP2015518892A5 (enExample)
JP2006523193A5 (enExample)
JP2017522276A5 (enExample)
CA2558195A1 (en) 11-hydroxy-5h-pyrrolo[2,1-c][1,4]benzodiazepin-5-one derivatives as key intermediates for the preparation of c2 substituted pyrrolobenzodiazepines
JP2001510154A5 (enExample)
JP2009536620A5 (enExample)
JP2006509842A5 (enExample)
JP2013518111A5 (enExample)
JP2020502116A5 (enExample)
JP2004523478A5 (enExample)
RU2016138800A (ru) Новый способ получения производных триазина, пиримидина и пиридина
JP2005504790A5 (enExample)
JP2006511498A5 (enExample)
JP2011500796A (ja) 新規前駆体