CL2004000016A1 - 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. - Google Patents
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.Info
- Publication number
- CL2004000016A1 CL2004000016A1 CL200400016A CL2004000016A CL2004000016A1 CL 2004000016 A1 CL2004000016 A1 CL 2004000016A1 CL 200400016 A CL200400016 A CL 200400016A CL 2004000016 A CL2004000016 A CL 2004000016A CL 2004000016 A1 CL2004000016 A1 CL 2004000016A1
- Authority
- CL
- Chile
- Prior art keywords
- compound
- pharmaceutically acceptable
- acceptable salt
- same
- tirosina
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds 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
- C07C229/30—Compounds 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
Abstract
LA PRESENTE INVENCION SE RELACIONA CON UN COMPUESTO DE LA FORMULA (I) DONDE S1 Y S2 SON CADA UNO INDISPENSABLE, HIDROGENO, ALQUILO, ALQUENILO, ALQUINILO, ARALQUILO, ARILO SUSTITUIDO Y S1 Y S2 JUNTOS CON EL NITROGENO AL CUAL ESTAN UNIDOS FORMAN UN HETEROARILO ITROGENADO Y UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, METODO PARA PREPARAR EL COMPUESTO DE FORMULA (I) Y SU DEL COMPUESTO DE FORMULA (I) EN LA PREPARACION DE 3-CIANO QUINOLINAS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44147003P | 2003-01-21 | 2003-01-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2004000016A1 true CL2004000016A1 (es) | 2005-04-15 |
Family
ID=32825162
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL200400016A CL2004000016A1 (es) | 2003-01-21 | 2004-01-05 | 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. |
CL2007001286A CL2007001286A1 (es) | 2003-01-21 | 2007-05-07 | Procedimiento para preparar amidas aromaticas del acido crotonico por formacion delcloruro de acido correspondiente y amidacion posterior. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2007001286A CL2007001286A1 (es) | 2003-01-21 | 2007-05-07 | Procedimiento para preparar amidas aromaticas del acido crotonico por formacion delcloruro de acido correspondiente y amidacion posterior. |
Country Status (15)
Country | Link |
---|---|
US (1) | US7126025B2 (es) |
EP (1) | EP1585479A2 (es) |
CN (1) | CN100537518C (es) |
AR (1) | AR042877A1 (es) |
AU (1) | AU2004207475A1 (es) |
CA (1) | CA2514550A1 (es) |
CL (2) | CL2004000016A1 (es) |
CR (1) | CR7950A (es) |
EC (1) | ECSP055974A (es) |
MX (1) | MXPA05008876A (es) |
NO (1) | NO20053890L (es) |
RU (1) | RU2345984C2 (es) |
SG (1) | SG166678A1 (es) |
TW (1) | TW200418763A (es) |
WO (1) | WO2004066919A2 (es) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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. |
US7432377B2 (en) * | 2004-01-16 | 2008-10-07 | Wyeth | Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof |
DE602005023333D1 (de) | 2004-10-15 | 2010-10-14 | Takeda Pharmaceutical | Kinaseinhibitoren |
ZA200706804B (en) | 2005-02-03 | 2008-10-29 | Gen Hospital Corp | Method for treating gefitinib resistant cancer |
WO2006127205A2 (en) * | 2005-05-25 | 2006-11-30 | Wyeth | Methods of preparing 3-cyano-quinolines and intermediates made thereby |
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 |
AU2006249600A1 (en) * | 2005-05-25 | 2006-11-30 | Wyeth | Methods of synthesizing substituted 3-cyanoquinolines and intermediates thereof |
US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
PE20070763A1 (es) | 2005-11-04 | 2007-08-08 | Wyeth Corp | COMBINACIONES ANTINEOPLASICAS DE UN INHIBIDOR DE mTOR, TRASTUZUMAB Y/O HKI-272 |
EP1948179A1 (en) | 2005-11-11 | 2008-07-30 | Boehringer Ingelheim International GmbH | Quinazoline derivatives for the treatment of cancer diseases |
US20100120717A1 (en) | 2006-10-09 | 2010-05-13 | Brown Jason W | 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 |
ES2531322T3 (es) | 2008-06-17 | 2015-03-13 | Wyeth Llc | Combinaciones antineoplásicas que contienen HKI-272 y vinorelbina |
PL2326329T3 (pl) | 2008-08-04 | 2017-07-31 | Wyeth Llc | Przeciwnowotworowe połączenia 4-anilino-3-cyjanochinolin i kapecytabiny |
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 |
AU2009315603B2 (en) * | 2008-11-17 | 2013-08-01 | Novartis Ag | Enantioselective synthesis of gamma-amino-alpha,beta-unsaturated carboxylic acid derivatives |
WO2010117633A1 (en) | 2009-04-06 | 2010-10-14 | 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 |
HUE044629T2 (hu) | 2009-07-06 | 2019-11-28 | Boehringer Ingelheim Int | Eljárás BIBW2992, annak sói, valamint e hatóanyagot tartalmazó szilárd gyógyászati készítmények szárítására |
EP2498751B1 (en) | 2009-11-09 | 2019-04-03 | Wyeth LLC | Coated drug spheroids and uses thereof for eliminating or reducing conditions such as emesis and diarrhea |
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 |
US9758471B2 (en) | 2014-06-02 | 2017-09-12 | Sun Pharmaceutical Industries Limited | 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 |
BR112020007424A2 (pt) | 2017-10-18 | 2020-12-08 | Jiangsu Hengrui Medicine Co., Ltd. | Métodos de preparação de compostos |
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 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4194050A (en) * | 1976-04-30 | 1980-03-18 | Sumitomo Chemical Company, Limited | Process for producing an enamide |
US4195021A (en) * | 1977-10-26 | 1980-03-25 | Eli Lilly And Company | 1,3-Disubstituted 2-azetidinone antibitotics |
US4193983A (en) * | 1978-05-16 | 1980-03-18 | Syva Company | Labeled liposome particle compositions and immunoassays therewith |
BE897134A (fr) | 1983-06-24 | 1983-12-27 | Solvay | Dienes polysubstitues |
US4478959A (en) * | 1983-09-29 | 1984-10-23 | Air Products And Chemicals, Inc. | Amino and amido divalent metal carboxylates useful as catalysts for polyurethane formulations |
DE3347659A1 (de) * | 1983-12-31 | 1985-07-11 | Bayer Ag, 5090 Leverkusen | Neue lackloesungen auf der basis von hydantoingruppen enthaltenden polymeren |
US4664825A (en) * | 1984-10-25 | 1987-05-12 | The Lubrizol Corporation | Sulfurized compositions and lubricants containing them |
CA2038633A1 (en) | 1990-03-20 | 1991-09-21 | Yoshimi Tsuchiya | Substituted amine derivatives having anti-hyperlipemia activity |
US6002008A (en) | 1997-04-03 | 1999-12-14 | American Cyanamid Company | Substituted 3-cyano quinolines |
UA73073C2 (uk) | 1997-04-03 | 2005-06-15 | Уайт Холдінгз Корпорейшн | Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція |
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. |
-
2004
- 2004-01-05 CL CL200400016A patent/CL2004000016A1/es unknown
- 2004-01-12 TW TW093100676A patent/TW200418763A/zh unknown
- 2004-01-14 AR ARP040100092A patent/AR042877A1/es unknown
- 2004-01-15 US US10/758,187 patent/US7126025B2/en not_active Expired - Fee Related
- 2004-01-16 EP EP04702974A patent/EP1585479A2/en not_active Withdrawn
- 2004-01-16 WO PCT/US2004/001133 patent/WO2004066919A2/en active Application Filing
- 2004-01-16 MX MXPA05008876A patent/MXPA05008876A/es active IP Right Grant
- 2004-01-16 AU AU2004207475A patent/AU2004207475A1/en not_active Abandoned
- 2004-01-16 CN CNB2004800077239A patent/CN100537518C/zh not_active Expired - Fee Related
- 2004-01-16 CA CA002514550A patent/CA2514550A1/en not_active Abandoned
- 2004-01-16 RU RU2005126418/04A patent/RU2345984C2/ru not_active IP Right Cessation
- 2004-01-16 SG SG200704889-5A patent/SG166678A1/en unknown
-
2005
- 2005-08-19 CR CR7950A patent/CR7950A/es not_active Application Discontinuation
- 2005-08-19 NO NO20053890A patent/NO20053890L/no not_active Application Discontinuation
- 2005-08-22 EC EC2005005974A patent/ECSP055974A/es unknown
-
2007
- 2007-05-07 CL CL2007001286A patent/CL2007001286A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
RU2005126418A (ru) | 2006-01-27 |
US7126025B2 (en) | 2006-10-24 |
CN100537518C (zh) | 2009-09-09 |
ECSP055974A (es) | 2006-01-16 |
CA2514550A1 (en) | 2004-08-12 |
WO2004066919A2 (en) | 2004-08-12 |
RU2345984C2 (ru) | 2009-02-10 |
TW200418763A (en) | 2004-10-01 |
CR7950A (es) | 2006-05-30 |
US20040162442A1 (en) | 2004-08-19 |
AU2004207475A1 (en) | 2004-08-12 |
NO20053890D0 (no) | 2005-08-19 |
CN1761644A (zh) | 2006-04-19 |
AR042877A1 (es) | 2005-07-06 |
WO2004066919A3 (en) | 2005-01-27 |
CL2007001286A1 (es) | 2008-01-25 |
EP1585479A2 (en) | 2005-10-19 |
MXPA05008876A (es) | 2005-10-05 |
SG166678A1 (en) | 2010-12-29 |
NO20053890L (no) | 2005-10-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CL2004000016A1 (es) | 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. | |
DE502006006854D1 (de) | Substituierte benzo (d) isoaxol-3-yl-amin-verbindungen als analgetika | |
EA200702497A1 (ru) | Замещенные арилпиразолы для применения против паразитов | |
MX2007007845A (es) | Sulfonilpirrolidinas, metodo para producir las mismas y su uso como medicamento. | |
ATE446962T1 (de) | Thiazolopyridinon-derivate als mch- rezeptorantagonisten | |
NO20075142L (no) | krystallformer av asenapinmaleat | |
BR122013025375B8 (pt) | compostos orgânicos, seus métodos de preparo e uso, bem como composições farmacêuticas | |
EA200500017A1 (ru) | Новые соединения | |
CY1116885T1 (el) | Υποκατεστημενα παραγωγα κυκλοεξυλομεθυλιου | |
EA201000642A1 (ru) | 2'-фтор-2'-дезокситетрагидроуридины в качестве ингибиторов цитидиндеаминазы | |
EA200801608A1 (ru) | Производные бензимидазолонкарбоновой кислоты | |
EP1698335A4 (en) | AGENT FOR PREVENTING AND / OR TREATING DISEASES INVOLVING A MITOCHONDRIAL BENZODIAZEPINE RECEPTOR | |
SI1828177T1 (sl) | Novi antagonisti mch receptorja | |
DK1511761T3 (da) | Fremgangsmåde til fremstilling af cykliske peptider | |
TW200630359A (en) | (S)-(-)-1-(4-fluoroisoquinolin-5-yl)sulfonyl-2-methyl-1,4-homopiperazine hydrochloride dihydrate | |
EA200600621A1 (ru) | Производные тетрагидронафталина, способ их получения и их применение в качестве противовоспалительных средств | |
EA201070424A1 (ru) | Хиназолиндионовые производные, их получение и их применения в терапии | |
EA200701648A1 (ru) | Замещённые пирролы и имидазолы, содержащие их композиции, способ получения и применение | |
EA200601065A1 (ru) | Производные имидазола, способы их получения и применения | |
EA200500899A1 (ru) | Антагонисты аденозиндифосфатного рецептора тромбоцитов | |
DE602007012313D1 (de) | Als a2b-adenosinrezeptorantagonisten geeignete 5-phenyl-6-pyridin-4-yl-1,3-dihydro-2h-imidazoä4,5-büpyridin-2-onderivate | |
EA200700550A1 (ru) | Производные алкилидентетрагидронафталина, способ их получения и их применение в качестве противовоспалительных средств | |
EA200501122A1 (ru) | Замещенные алкиламидопиперидины | |
AR056418A1 (es) | Derivados de bencimidazol como 5-ht6, 5-ht2a, metodo para la obtencion del compuesto y el uso para la fabricacion de un mediicamento | |
EA200702587A1 (ru) | Способ синтеза промежуточных продуктов, предназначенных для получения трициклических бензимидазолов |