ATE414077T1 - Verfahren zur herstellung von 1-ä(benzimidazol-1- yl)chinolin-8-ylüpiperidin-4-ylaminderivaten - Google Patents

Verfahren zur herstellung von 1-ä(benzimidazol-1- yl)chinolin-8-ylüpiperidin-4-ylaminderivaten

Info

Publication number
ATE414077T1
ATE414077T1 AT04736779T AT04736779T ATE414077T1 AT E414077 T1 ATE414077 T1 AT E414077T1 AT 04736779 T AT04736779 T AT 04736779T AT 04736779 T AT04736779 T AT 04736779T AT E414077 T1 ATE414077 T1 AT E414077T1
Authority
AT
Austria
Prior art keywords
ylupiperidine
ylamin
benzimidazole
quinoline
derivatives
Prior art date
Application number
AT04736779T
Other languages
English (en)
Inventor
Norma Jacqueline Tom
David Harold Brown Ripin
Michael James Castaldi
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
Application granted granted Critical
Publication of ATE414077T1 publication Critical patent/ATE414077T1/de

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)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (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)
AT04736779T 2003-06-24 2004-06-14 Verfahren zur herstellung von 1-ä(benzimidazol-1- yl)chinolin-8-ylüpiperidin-4-ylaminderivaten ATE414077T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US48217603P 2003-06-24 2003-06-24

Publications (1)

Publication Number Publication Date
ATE414077T1 true ATE414077T1 (de) 2008-11-15

Family

ID=33539339

Family Applications (1)

Application Number Title Priority Date Filing Date
AT04736779T ATE414077T1 (de) 2003-06-24 2004-06-14 Verfahren zur herstellung von 1-ä(benzimidazol-1- yl)chinolin-8-ylüpiperidin-4-ylaminderivaten

Country Status (24)

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

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GB0411421D0 (en) * 2004-05-21 2004-06-23 Glaxo Group Ltd Novel compounds
WO2006038111A1 (en) * 2004-10-07 2006-04-13 Pfizer Products Inc. Benzoimidazole derivatives useful as antiproliferative agents
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
ATE542813T1 (de) 2008-08-06 2012-02-15 Pfizer 6-substituierte 2- heterocyclylaminopyrazinverbindungen als chk-1- inhibitoren
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
KR101738063B1 (ko) 2012-09-21 2017-05-19 아로그 파마슈티칼스, 인코퍼레이티드 구조적으로 활성인 인산화된 flt3 키나제의 억제 방법
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
TWI599356B (zh) 2012-09-26 2017-09-21 安羅格製藥有限責任公司 抑制突變型c-kit的方法
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
CN108778276A (zh) 2016-11-02 2018-11-09 安罗格制药有限责任公司 用于治疗flt3突变型增殖性疾患相关突变的克莱拉尼
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
CN117447376A (zh) * 2019-12-09 2024-01-26 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
CN118767143A (zh) 2019-12-12 2024-10-15 听治疗有限责任公司 用于预防和治疗听力损失的组合物和方法
CA3186319A1 (en) * 2020-07-20 2022-01-27 Arog Pharmaceuticals, Inc. Crystal forms of crenolanib and methods of use thereof
US11713310B2 (en) 2020-07-20 2023-08-01 Arog Pharmaceuticals, Inc. Crystal forms of crenolanib and methods of use thereof
IL300205A (en) * 2020-08-05 2023-03-01 Massachusetts Gen Hospital Salt-inducible kinase inhibitors
US11524006B2 (en) 2020-09-17 2022-12-13 Arog Pharmaceuticals, Inc. Crenolanib for treating TRK kinase associated proliferative disorders
US20220079934A1 (en) * 2020-09-17 2022-03-17 Arog Pharmaceuticals, Inc. Crenolanib for treating pain
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
WO2022090547A1 (en) 2020-10-30 2022-05-05 Dsm Ip Assets B.V. Production of carotenoids by fermentation
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

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US4897401A (en) * 1987-06-19 1990-01-30 Janssen Pharmaceutical N.V. N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives useful in treating allergic diseases
US5478832A (en) * 1992-05-08 1995-12-26 The Green Cross Corporation Quinoline compounds
HU225960B1 (en) * 1997-02-27 2008-01-28 Takeda Pharmaceutical Amine compounds, their production and use
UA75055C2 (uk) * 1999-11-30 2006-03-15 Пфайзер Продактс Інк. Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі
EP1245390A4 (de) * 1999-12-10 2009-04-01 Fujifilm Corp Tintenstrahldruckkopf und drucker
WO2002022549A1 (en) * 2000-09-14 2002-03-21 Kaneka Corporation Process for the removal of 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
KR20060012033A (ko) 2006-02-06
CA2529032C (en) 2009-12-22
NO20060376L (no) 2006-01-24
ZA200509253B (en) 2007-01-31
CL2004001470A1 (es) 2005-05-13
HK1089170A1 (en) 2006-11-24
JP2007516168A (ja) 2007-06-21
WO2004113322A1 (en) 2004-12-29
US7183414B2 (en) 2007-02-27
KR100787649B1 (ko) 2007-12-21
MXPA05014203A (es) 2006-02-24
RU2323214C2 (ru) 2008-04-27
ES2315663T3 (es) 2009-04-01
AU2004249511A1 (en) 2004-12-29
TW200517393A (en) 2005-06-01
SG161745A1 (en) 2010-06-29
CO5650165A2 (es) 2006-06-30
NZ571898A (en) 2010-01-29
BRPI0411794A (pt) 2006-08-08
AR044849A1 (es) 2005-10-05
CN1809556A (zh) 2006-07-26
TWI294425B (en) 2008-03-11
NZ543714A (en) 2009-06-26
RU2005138367A (ru) 2006-08-10
US20050020625A1 (en) 2005-01-27
CN100404530C (zh) 2008-07-23
US20070088032A1 (en) 2007-04-19
CA2529032A1 (en) 2004-12-29
DK1641780T3 (da) 2009-02-02
IL172064A (en) 2011-01-31
DE602004017731D1 (de) 2008-12-24
AU2004249511B2 (en) 2011-01-20
EP1641780A1 (de) 2006-04-05
KR20070092333A (ko) 2007-09-12
EP1641780B1 (de) 2008-11-12

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