CA2586176A1 - Methods for preparing indazole compounds - Google Patents

Methods for preparing indazole compounds Download PDF

Info

Publication number
CA2586176A1
CA2586176A1 CA002586176A CA2586176A CA2586176A1 CA 2586176 A1 CA2586176 A1 CA 2586176A1 CA 002586176 A CA002586176 A CA 002586176A CA 2586176 A CA2586176 A CA 2586176A CA 2586176 A1 CA2586176 A1 CA 2586176A1
Authority
CA
Canada
Prior art keywords
formula
compound
alkyl
aryl
substituted
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.)
Abandoned
Application number
CA002586176A
Other languages
English (en)
French (fr)
Inventor
Srinivasan Babu
Raymond Dagnino Jr.
Michael Allen Ouellette
Bing Shi
Qingping Tian
Scott Edward Zook
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Inc
Original Assignee
Srinivasan Babu
Raymond Dagnino Jr.
Michael Allen Ouellette
Bing Shi
Qingping Tian
Scott Edward Zook
Pfizer 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 Srinivasan Babu, Raymond Dagnino Jr., Michael Allen Ouellette, Bing Shi, Qingping Tian, Scott Edward Zook, Pfizer Inc. filed Critical Srinivasan Babu
Publication of CA2586176A1 publication Critical patent/CA2586176A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/4161,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
CA002586176A 2004-11-02 2005-10-21 Methods for preparing indazole compounds Abandoned CA2586176A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US62457504P 2004-11-02 2004-11-02
US60/624,575 2004-11-02
PCT/IB2005/003300 WO2006048745A1 (en) 2004-11-02 2005-10-21 Methods for preparing indazole compounds

Publications (1)

Publication Number Publication Date
CA2586176A1 true CA2586176A1 (en) 2006-05-11

Family

ID=35528034

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002586176A Abandoned CA2586176A1 (en) 2004-11-02 2005-10-21 Methods for preparing indazole compounds

Country Status (15)

Country Link
EP (1) EP1809625A1 (pt)
JP (1) JP2008518901A (pt)
KR (1) KR20070058689A (pt)
CN (1) CN101044138A (pt)
AR (1) AR051753A1 (pt)
AU (1) AU2005300311A1 (pt)
BR (1) BRPI0517921A (pt)
CA (1) CA2586176A1 (pt)
IL (1) IL182096A0 (pt)
MX (1) MX2007003603A (pt)
NO (1) NO20072747L (pt)
RU (1) RU2007114112A (pt)
TW (1) TW200614990A (pt)
WO (1) WO2006048745A1 (pt)
ZA (1) ZA200702317B (pt)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2073803B1 (en) 2006-10-12 2018-09-19 Astex Therapeutics Limited Pharmaceutical combinations
EP2073807A1 (en) 2006-10-12 2009-07-01 Astex Therapeutics Limited Pharmaceutical combinations
RU2518898C2 (ru) 2007-04-05 2014-06-10 Пфайзер Продактс Инк. Кристаллические формы 6-[2-(метилкарбамоил)фенилсульфанил]-3-е-[2-(пиридин-2-ил)этенил]индазола, пригодные для лечения аномального роста клеток у млекопитаюших
US8354528B2 (en) 2007-10-25 2013-01-15 Genentech, Inc. Process for making thienopyrimidine compounds
EP2163544A1 (en) * 2008-09-16 2010-03-17 Pfizer, Inc. Methods of preparing indazole compounds
KR20140069297A (ko) 2011-09-30 2014-06-09 화이자 인코포레이티드 N-메틸-2-[3-((e)-2-피리딘-2-일-비닐)-1h-인다졸-6-일-설파닐]-벤즈아미드의 약학 조성물
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
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
CN103387565B (zh) * 2013-07-29 2014-10-29 苏州明锐医药科技有限公司 阿西替尼的制备方法
CN103570696B (zh) * 2013-11-06 2016-02-24 湖南欧亚生物有限公司 一种阿西替尼中间体的制备方法以及在制备阿西替尼中的应用
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
EP3102605B1 (en) 2014-02-04 2018-11-14 Pfizer Inc Combination of a pd-1 antagonist and a vegfr inhibitor for treating cancer
EP3127900B1 (en) * 2014-03-31 2017-10-18 Senju Pharmaceutical Co., Ltd. Alkynyl indazole derivative and use thereof
CN104072484B (zh) * 2014-07-07 2016-07-06 渤海大学 氮-(4-(芳巯基)-1氢-吲唑-3-基)-1-(芳杂环取代)甲基亚胺类化合物及其药学上可接受的盐及其制备方法和应用
CA2955676A1 (en) 2014-08-25 2016-03-03 Pfizer Inc. Combination of a pd-1 antagonist and an alk inhibitor for treating cancer
US10118890B2 (en) 2014-10-10 2018-11-06 The Research Foundation For The State University Of New York Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration
SG11201706918YA (en) 2015-02-26 2017-09-28 Merck Patent Gmbh Pd-1 / pd-l1 inhibitors for the treatment of cancer
US9580406B2 (en) 2015-04-28 2017-02-28 Signa S.A. De C.V. Processes for the preparation of axitinib
MX2017016324A (es) 2015-06-16 2018-03-02 Merck Patent Gmbh Tratamientos de combinacion de antagonista de ligando 1 de muerte programada (pd-l1).
AU2017339856A1 (en) 2016-10-06 2019-05-23 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
EA202192731A1 (ru) 2019-04-18 2022-02-04 Синтон Б.В. СПОСОБ ПОЛУЧЕНИЯ АКСИТИНИБА, СПОСОБ ОЧИСТКИ ПРОМЕЖУТОЧНОГО СОЕДИНЕНИЯ 2-((3-ЙОД-1H-ИНДАЗОЛ-6-ИЛ)ТИО)-N-МЕТИЛБЕНЗАМИДА, СПОСОБ ОЧИСТКИ АКСИТИНИБА ЧЕРЕЗ HCl СОЛЬ АКСИТИНИБА, ТВЕРДАЯ ФОРМА HCl СОЛИ АКСИТИНИБА
CN112209861A (zh) * 2019-07-11 2021-01-12 鲁南制药集团股份有限公司 一种阿昔替尼中间体化合物及其制备方法
CN112442010B (zh) * 2019-08-30 2023-10-03 润佳(苏州)医药科技有限公司 一类前药化合物及其在治疗癌症方面的应用
CN111440102B (zh) * 2020-04-26 2022-02-15 大连凯飞化学股份有限公司 一种二硫代二苯甲酰胺类化合物的制备方法
US20240117030A1 (en) 2022-03-03 2024-04-11 Pfizer Inc. Multispecific antibodies and uses thereof
CN114591338B (zh) * 2022-03-31 2023-05-09 苏州欧康维视生物科技有限公司 一种Syk和VEGFR2双靶点抑制剂的制备方法及其用途

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20010306A1 (es) * 1999-07-02 2001-03-29 Agouron Pharma Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
JP3814285B2 (ja) * 2002-12-19 2006-08-23 ファイザー・インク 眼疾患の治療に有用なプロテインキナーゼ阻害剤としての2−(1h−インダゾール−6−イルアミノ)−ベンズアミド化合物
US7521447B2 (en) * 2003-03-03 2009-04-21 Array Biopharma Inc. P38 inhibitors and methods of use thereof
JPWO2005094823A1 (ja) * 2004-03-30 2007-08-16 協和醗酵工業株式会社 Flt−3阻害剤

Also Published As

Publication number Publication date
AR051753A1 (es) 2007-02-07
TW200614990A (en) 2006-05-16
BRPI0517921A (pt) 2008-10-21
WO2006048745A1 (en) 2006-05-11
AU2005300311A1 (en) 2006-05-11
JP2008518901A (ja) 2008-06-05
ZA200702317B (en) 2008-09-25
NO20072747L (no) 2007-07-31
EP1809625A1 (en) 2007-07-25
RU2007114112A (ru) 2008-12-10
CN101044138A (zh) 2007-09-26
KR20070058689A (ko) 2007-06-08
IL182096A0 (en) 2007-07-24
MX2007003603A (es) 2007-05-21

Similar Documents

Publication Publication Date Title
CA2586176A1 (en) Methods for preparing indazole compounds
CN101094836A (zh) 制备吲唑化合物的方法
US7232910B2 (en) Methods of preparing indazole compounds
TWI658042B (zh) 雜環化合物的合成
CA2698245C (en) Process and intermediates for preparing integrase inhibitors
CN109678791B (zh) 1-(2,4-二氟苯)-2,2-二氟-2-(5-取代吡啶-2-基)乙酮及制备方法
US20070203196A1 (en) Methods of preparing indazole compounds
KR20180038460A (ko) 세포독성 벤조다이아제핀 유도체의 제조 방법
EP4249077A1 (en) Novel acridinium salt and method for producing same
AP1299A (en) Process for the production of quinazolines.
JP2015044856A (ja) ビフェニルイミダゾール化合物の調製方法
JP4656604B2 (ja) イノシン誘導体及びその製造方法
WO2008074474A1 (en) Substituted 4-hydroxypyridines
WO2016004899A1 (en) Process for making tetracyclic heterocycle compounds
AU2005300241A2 (en) Methods for preparing indazole compounds
JP7315805B1 (ja) 単環ピリジン誘導体の合成中間体の製造方法
JP2009508898A (ja) 1’−ヒドロキシ−2’−置換シクロヘキシルアゼチジン−2−オン化合物の調製方法
EP2163544A1 (en) Methods of preparing indazole compounds
WO2014126954A1 (en) Regioselective synthesis of substituted pyrimidines
JP2023099776A (ja) 単環ピリジン誘導体の合成中間体の製造方法
CN112135820A (zh) 制备二氨基嘧啶衍生物或其酸加成盐的新方法
JPH0812670A (ja) 新規なピロリジン誘導体
CA2584617A1 (en) Process for producing benzo[c]phenanthridine derivative
JP2007055960A (ja) 1−デオキシガラクトノジリマイシンの製造方法、合成中間体およびその製造方法
JPWO2003042189A1 (ja) 1−h−1,2,4−トリアゾール−3−カルボン酸エステルの製造法

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued