MXPA05014203A - Procedimientos para la preparacion de derivados de benzoimidazol. - Google Patents

Procedimientos para la preparacion de derivados de benzoimidazol.

Info

Publication number
MXPA05014203A
MXPA05014203A MXPA05014203A MXPA05014203A MXPA05014203A MX PA05014203 A MXPA05014203 A MX PA05014203A MX PA05014203 A MXPA05014203 A MX PA05014203A MX PA05014203 A MXPA05014203 A MX PA05014203A MX PA05014203 A MXPA05014203 A MX PA05014203A
Authority
MX
Mexico
Prior art keywords
benzoimidazole
quinolin
piperidin
processes
preparation
Prior art date
Application number
MXPA05014203A
Other languages
English (en)
Inventor
David Harold Brown Ripin
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 MXPA05014203A publication Critical patent/MXPA05014203A/es

Links

Classifications

    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (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)
  • Epoxy Compounds (AREA)

Abstract

La presente invencion se refiere a un procedimiento para preparar un compuesto de formula l (ver formula (I)) o una sal, profarmaco, hidrato o solvato farmaceuticamente aceptable del mismo en el que R1, R2, R3 y R4 son como se definen en el presente documento; el compuesto de formula I es util en el tratamiento del crecimiento celular anormal, tal como cancer, en mamiferos.
MXPA05014203A 2003-06-24 2004-06-14 Procedimientos para la preparacion de derivados de benzoimidazol. MXPA05014203A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US48217603P 2003-06-24 2003-06-24
PCT/IB2004/001983 WO2004113322A1 (en) 2003-06-24 2004-06-14 Processes for the preparation of 1-[(benzoimidazole-1yl) quinolin-8-yl] piperidin-4-ylamine derivatives

Publications (1)

Publication Number Publication Date
MXPA05014203A true MXPA05014203A (es) 2006-02-24

Family

ID=33539339

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA05014203A MXPA05014203A (es) 2003-06-24 2004-06-14 Procedimientos para la preparacion de derivados de benzoimidazol.

Country Status (25)

Country Link
US (2) US7183414B2 (es)
EP (1) EP1641780B1 (es)
JP (1) JP2007516168A (es)
KR (2) KR20070092333A (es)
CN (1) CN100404530C (es)
AR (1) AR044849A1 (es)
AT (1) ATE414077T1 (es)
AU (1) AU2004249511B2 (es)
BR (1) BRPI0411794A (es)
CA (1) CA2529032C (es)
CL (1) CL2004001470A1 (es)
CO (1) CO5650165A2 (es)
DE (1) DE602004017731D1 (es)
DK (1) DK1641780T3 (es)
ES (1) ES2315663T3 (es)
HK (1) HK1089170A1 (es)
IL (1) IL172064A (es)
MX (1) MXPA05014203A (es)
NO (1) NO20060376L (es)
NZ (2) NZ543714A (es)
RU (1) RU2323214C2 (es)
SG (1) SG161745A1 (es)
TW (1) TWI294425B (es)
WO (1) WO2004113322A1 (es)
ZA (1) ZA200509253B (es)

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GB0411421D0 (en) * 2004-05-21 2004-06-23 Glaxo Group Ltd Novel compounds
JP2008515872A (ja) * 2004-10-07 2008-05-15 ファイザー・プロダクツ・インク 抗増殖剤として有用なベンゾイミダゾール誘導体
KR20080013886A (ko) * 2005-04-05 2008-02-13 파마코페이아, 인코포레이티드 면역억제용 퓨린 및 이미다조피리딘 유도체
US7504513B2 (en) 2006-02-27 2009-03-17 Hoffman-La Roche Inc. Thiazolyl-benzimidazoles
WO2010016005A1 (en) 2008-08-06 2010-02-11 Pfizer Inc. 6 substituted 2-heterocyclylamino pyrazine compounds as chk-1 inhibitors
CA2745596A1 (en) 2008-12-18 2010-10-28 F. Hoffmann-La Roche Ag Thiazolyl-benzimidazoles
CN101993416B (zh) * 2009-08-27 2013-09-11 中国科学院上海药物研究所 喹啉类化合物、其制备方法、包含该化合物的药物组合物及该化合物的用途
JP6407504B2 (ja) 2012-09-21 2018-10-17 アログ・ファーマシューティカルズ・インコーポレイテッドArog Pharmaceuticals,Inc. 恒常的に活性であるリン酸化型flt3キナーゼの阻害方法
JP6042157B2 (ja) 2012-09-26 2016-12-14 アログ・ファーマシューティカルズ・リミテッド・ライアビリティ・カンパニーArog Pharmaceuticals,LLC 変異型c−kitの阻害方法
US11642340B2 (en) 2012-09-26 2023-05-09 Arog Pharmaceuticals, Inc. Method of inhibiting mutant C-KIT
US10835525B2 (en) 2012-09-26 2020-11-17 Arog Pharmaceuticals, Inc. Method of inhibiting mutant C-KIT
BR112015016282A2 (pt) 2013-01-07 2017-07-11 Arog Pharmaceuticals Inc crenolanibe para tratamento de distúrbios proliferativos de flt3 mutado
US10463658B2 (en) 2013-10-25 2019-11-05 Videra Pharmaceuticals, Llc Method of inhibiting FLT3 kinase
EA201991078A1 (ru) 2016-11-02 2019-11-29 Креноланиб для лечения пролиферативных расстройств, связанных с мутацией flt3
CN107382983B (zh) * 2017-08-24 2020-08-07 扬州市三药制药有限公司 一种治疗白血病药物的合成方法
CN107382984B (zh) * 2017-08-24 2020-07-10 扬州市三药制药有限公司 一种治疗白血病药物的制备方法
CN110840893A (zh) 2018-12-13 2020-02-28 安罗格制药有限责任公司 含克莱拉尼的药物组合物及其用途
CN109678849A (zh) * 2019-01-16 2019-04-26 北京悦康科创医药科技股份有限公司 一种抗癌药物的制备方法
US11471451B2 (en) 2019-08-19 2022-10-18 Arog Pharmaceuticals, Inc. Uses of crenolanib
CN114702428B (zh) * 2019-12-09 2023-11-28 苏州恩华生物医药科技有限公司 连双环结构sigma-1受体抑制剂
WO2022019998A1 (en) * 2020-07-20 2022-01-27 Arog Pharmaceuticals, Inc. Crystal forms of crenolanib and methods of use thereof
US20220079934A1 (en) * 2020-09-17 2022-03-17 Arog Pharmaceuticals, Inc. Crenolanib for treating pain
US11524006B2 (en) 2020-09-17 2022-12-13 Arog Pharmaceuticals, Inc. Crenolanib for treating TRK kinase associated proliferative disorders
US11969420B2 (en) 2020-10-30 2024-04-30 Arog Pharmaceuticals, Inc. Combination therapy of crenolanib and apoptosis pathway agents for the treatment of proliferative disorders
CN113683594B (zh) * 2021-09-07 2022-12-27 曲靖师范学院 一种喹啉-苯并咪唑盐类化合物及其合成方法和应用
JP2023063189A (ja) 2021-10-22 2023-05-09 アログ・ファーマシューティカルズ・インコーポレイテッド 以前の治療に対して再発性/不応性のflt3突然変異増殖性障害を治療するためのクレノラニブ

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69839305T2 (de) * 1997-02-27 2009-04-09 Takeda Pharmaceutical Co. Ltd. Aminderivate, ihre herstellung und verwendung als inhibitoren der produktion von amyloid-beta
UA75055C2 (uk) * 1999-11-30 2006-03-15 Пфайзер Продактс Інк. Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі
EP1245390A4 (en) * 1999-12-10 2009-04-01 Fujifilm Corp INK JET HEAD AND PRINTER
EP1321454A4 (en) * 2000-09-14 2005-11-02 Kaneka Corp PROCESS FOR EXTRACTING NITROBENZENESULFONYL
PA8580301A1 (es) * 2002-08-28 2005-05-24 Pfizer Prod Inc Nuevos derivados de benzoimidazol utiles como agentes antiproliferativos

Also Published As

Publication number Publication date
CN1809556A (zh) 2006-07-26
CL2004001470A1 (es) 2005-05-13
AR044849A1 (es) 2005-10-05
KR20060012033A (ko) 2006-02-06
KR20070092333A (ko) 2007-09-12
CA2529032C (en) 2009-12-22
EP1641780B1 (en) 2008-11-12
US7183414B2 (en) 2007-02-27
EP1641780A1 (en) 2006-04-05
ZA200509253B (en) 2007-01-31
SG161745A1 (en) 2010-06-29
CA2529032A1 (en) 2004-12-29
DK1641780T3 (da) 2009-02-02
ATE414077T1 (de) 2008-11-15
NZ571898A (en) 2010-01-29
RU2323214C2 (ru) 2008-04-27
WO2004113322A1 (en) 2004-12-29
NZ543714A (en) 2009-06-26
DE602004017731D1 (de) 2008-12-24
IL172064A (en) 2011-01-31
BRPI0411794A (pt) 2006-08-08
US20070088032A1 (en) 2007-04-19
HK1089170A1 (en) 2006-11-24
TWI294425B (en) 2008-03-11
AU2004249511A1 (en) 2004-12-29
KR100787649B1 (ko) 2007-12-21
AU2004249511B2 (en) 2011-01-20
NO20060376L (no) 2006-01-24
JP2007516168A (ja) 2007-06-21
CN100404530C (zh) 2008-07-23
US20050020625A1 (en) 2005-01-27
RU2005138367A (ru) 2006-08-10
ES2315663T3 (es) 2009-04-01
CO5650165A2 (es) 2006-06-30
TW200517393A (en) 2005-06-01

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