NO20053890L - Syntese av 4-amino-2-butenolklorider og anvendelse derav for fremstilling av 3-cyanokinoliner - Google Patents

Syntese av 4-amino-2-butenolklorider og anvendelse derav for fremstilling av 3-cyanokinoliner

Info

Publication number
NO20053890L
NO20053890L NO20053890A NO20053890A NO20053890L NO 20053890 L NO20053890 L NO 20053890L NO 20053890 A NO20053890 A NO 20053890A NO 20053890 A NO20053890 A NO 20053890A NO 20053890 L NO20053890 L NO 20053890L
Authority
NO
Norway
Prior art keywords
preparation
cyanoquinolines
butenol
chlorides
synthesis
Prior art date
Application number
NO20053890A
Other languages
English (en)
Other versions
NO20053890D0 (no
Inventor
Jr John Leo Considine
Sylvain Daigneault
Warren Chew
Silvio Iera
Scott Mason Duncan
Jianxin Ren
Original Assignee
Wyeth Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=32825162&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20053890(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of NO20053890D0 publication Critical patent/NO20053890D0/no
Publication of NO20053890L publication Critical patent/NO20053890L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/02Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/30Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and unsaturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Quinoline Compounds (AREA)
  • Steroid Compounds (AREA)

Abstract

Det beskrives en forbindelse med formel (I): hvor S1 og S2 hver uavhengig er hydrogen, alkyl, alkenyl, alkynyl, aralkyl, substituert eller usubstituert aryl, og hvor S1 og S2 sammen med det nitrogen som de er tilknyttet, danner en nitrogenholdig heteroaryl, og et farmasøytisk akseptabelt salt derav; en fremgangsmåte for fremstilling av forbindelsen med formel (I) og anvendelse av forbindelsen med formel (I) ved fremstillingen av 3-cyanokinoliner.
NO20053890A 2003-01-21 2005-08-19 Syntese av 4-amino-2-butenolklorider og anvendelse derav for fremstilling av 3-cyanokinoliner NO20053890L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US44147003P 2003-01-21 2003-01-21
PCT/US2004/001133 WO2004066919A2 (en) 2003-01-21 2004-01-16 Synthesis of 4amino-2-butenoyl chlorides and their use in the preparation of 3-cyano quinolines

Publications (2)

Publication Number Publication Date
NO20053890D0 NO20053890D0 (no) 2005-08-19
NO20053890L true NO20053890L (no) 2005-10-20

Family

ID=32825162

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20053890A NO20053890L (no) 2003-01-21 2005-08-19 Syntese av 4-amino-2-butenolklorider og anvendelse derav for fremstilling av 3-cyanokinoliner

Country Status (15)

Country Link
US (1) US7126025B2 (no)
EP (1) EP1585479A2 (no)
CN (1) CN100537518C (no)
AR (1) AR042877A1 (no)
AU (1) AU2004207475A1 (no)
CA (1) CA2514550A1 (no)
CL (2) CL2004000016A1 (no)
CR (1) CR7950A (no)
EC (1) ECSP055974A (no)
MX (1) MXPA05008876A (no)
NO (1) NO20053890L (no)
RU (1) RU2345984C2 (no)
SG (1) SG166678A1 (no)
TW (1) TW200418763A (no)
WO (1) WO2004066919A2 (no)

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EP1778669A2 (en) 2004-08-18 2007-05-02 Takeda San Diego, Inc. Kinase inhibitors
ATE479687T1 (de) 2004-10-15 2010-09-15 Takeda Pharmaceutical Kinaseinhibitoren
ES2364495T3 (es) 2005-02-03 2011-09-05 The General Hospital Corporation Método para tratar cáncer resistente a gefitinib.
BRPI0610147A2 (pt) * 2005-05-25 2010-06-01 Wyeth Corp método para preparar e sintetizar 3-cianoquinolinas substituìdas e 4-amino-3-cianoquinolinas
CN101180273A (zh) * 2005-05-25 2008-05-14 惠氏公司 合成6-烷基氨基喹啉衍生物的方法
CA2608394A1 (en) * 2005-05-25 2006-11-30 Wyeth Methods of preparing 3-cyano-quinolines and intermediates made thereby
US8119655B2 (en) 2005-10-07 2012-02-21 Takeda Pharmaceutical Company Limited Kinase inhibitors
JP2009514870A (ja) 2005-11-04 2009-04-09 ワイス mTORインヒビター、ハーセプチン、および/またはHKI−272の抗悪性腫瘍性組み合わせ
CA2833706C (en) 2005-11-11 2014-10-21 Boehringer Ingelheim International Gmbh Quinazoline derivatives for the treatment of cancer diseases
SG158147A1 (en) 2006-10-09 2010-01-29 Takeda Pharmaceutical Kinase inhibitors
US8022216B2 (en) 2007-10-17 2011-09-20 Wyeth Llc Maleate salts of (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide and crystalline forms thereof
ES2692769T3 (es) 2008-06-17 2018-12-05 Wyeth Llc Combinaciones antineoplásicas que contienen HKI-272 y vinorelbina
CN105147713A (zh) 2008-08-04 2015-12-16 惠氏有限责任公司 4-苯胺基-3-氰基喹啉和卡培他滨的抗肿瘤组合
WO2010048477A2 (en) * 2008-10-24 2010-04-29 Wyeth Llc Improved process for preparation of coupled products from 4-amino-3-cyanoquinolines using stabilized intermediates
US8288566B2 (en) * 2008-11-17 2012-10-16 Novartis Ag Enantioselective synthesis of γ-amino-αβ-unsaturated carboxylic acid derivatives
SG174382A1 (en) 2009-04-06 2011-11-28 Wyeth Llc Treatment regimen utilizing neratinib for breast cancer
US8779192B2 (en) * 2009-05-14 2014-07-15 Kolon Life Science, Inc. Process of preparing an alkylamine derivative
PL2451445T3 (pl) 2009-07-06 2019-09-30 Boehringer Ingelheim International Gmbh Sposób suszenia BIBW2992, jego soli i stałych preparatów farmaceutycznych zawierających tę substancję czynną
CN102724962B (zh) 2009-11-09 2017-05-17 惠氏有限责任公司 包衣药物球状体及其用于消除或减少病症比如呕吐和腹泻的用途
CN102731395B (zh) * 2011-04-15 2015-02-04 中国科学院上海药物研究所 抗肿瘤药物来那替尼的中间体及其制备与应用
US9242965B2 (en) 2013-12-31 2016-01-26 Boehringer Ingelheim International Gmbh Process for the manufacture of (E)-4-N,N-dialkylamino crotonic acid in HX salt form and use thereof for synthesis of EGFR tyrosine kinase inhibitors
CN104926669A (zh) * 2014-03-18 2015-09-23 江苏豪森医药集团连云港宏创医药有限公司 反式-4-二甲基胺基巴豆酸盐酸盐的制备方法
EP3148977A4 (en) 2014-06-02 2018-01-31 Sun Pharmaceutical Industries Ltd Process for the preparation of 4-dimethylaminocrotonic acid
CN105439879B (zh) * 2014-08-07 2018-08-10 天津法莫西医药科技有限公司 一种反式-4-二甲胺基巴豆酸盐酸盐的制备方法
CN105669479B (zh) * 2015-12-31 2018-04-13 重庆威鹏药业有限公司 一锅法制备高纯度反式‑4‑二甲基胺基巴豆酸盐酸盐的方法
CN108290867B (zh) * 2016-04-28 2022-02-08 江苏恒瑞医药股份有限公司 一种制备酪氨酸激酶抑制剂及其衍生物的方法
TWI691495B (zh) 2017-10-18 2020-04-21 大陸商江蘇恒瑞醫藥股份有限公司 一種酪胺酸激酶抑制劑及其中間體的製備方法
CN111217850B (zh) * 2019-01-31 2023-05-26 微宏先进材料公司 硅基酯类化合物制备方法、硅基酯类化合物、包含其的电解液及二次电池
CN112679473B (zh) * 2019-10-18 2024-03-05 四川科伦药物研究院有限公司 来那替尼中间体晶体、制备方法及其用途

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US6002008A (en) 1997-04-03 1999-12-14 American Cyanamid Company Substituted 3-cyano quinolines
UA77200C2 (en) * 2001-08-07 2006-11-15 Wyeth Corp Antineoplastic combination of cci-779 and bkb-569
CL2004000016A1 (es) 2003-01-21 2005-04-15 Wyeth Corp Compuesto derivado de cloruro de 4-amino-2-butenoilo o una sal farmaceuticamente aceptable del mismo; procedimiento para preparar dicho compuesto, util como intermediario en la sintesis de compuestos inhibidores de proteina quinasa tirosina.

Also Published As

Publication number Publication date
SG166678A1 (en) 2010-12-29
WO2004066919A2 (en) 2004-08-12
US20040162442A1 (en) 2004-08-19
AU2004207475A1 (en) 2004-08-12
CR7950A (es) 2006-05-30
CA2514550A1 (en) 2004-08-12
EP1585479A2 (en) 2005-10-19
TW200418763A (en) 2004-10-01
RU2345984C2 (ru) 2009-02-10
CL2004000016A1 (es) 2005-04-15
CN1761644A (zh) 2006-04-19
US7126025B2 (en) 2006-10-24
CL2007001286A1 (es) 2008-01-25
MXPA05008876A (es) 2005-10-05
WO2004066919A3 (en) 2005-01-27
CN100537518C (zh) 2009-09-09
RU2005126418A (ru) 2006-01-27
NO20053890D0 (no) 2005-08-19
AR042877A1 (es) 2005-07-06
ECSP055974A (es) 2006-01-16

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