GT200600213A - Metodos para sintetizar 3-cianoquinolinas sustituidas y sus intermediarios - Google Patents
Metodos para sintetizar 3-cianoquinolinas sustituidas y sus intermediariosInfo
- Publication number
- GT200600213A GT200600213A GT200600213A GT200600213A GT200600213A GT 200600213 A GT200600213 A GT 200600213A GT 200600213 A GT200600213 A GT 200600213A GT 200600213 A GT200600213 A GT 200600213A GT 200600213 A GT200600213 A GT 200600213A
- Authority
- GT
- Guatemala
- Prior art keywords
- methods
- syntheize
- cianoquinolins
- intermediaries
- substituted
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000011031 large-scale manufacturing process Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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 chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Quinoline Compounds (AREA)
Abstract
LA INVENCIÓN SE REFIERE A MÉTODOS PARA PRODUCIR 3-CIANOQUINOLINAS SUSTITUIDAS, QUE INCLUYEN LOS COMPUESTOS DE ACUERDO CON LA SIGUIENTE FÓRMULA (IV), DICHOS MÉTODOS SON ADECUADOS PARA LA PRODUCCIÓN A GRAN ESCALA, ADEMÁS EVITA EL USO DE SEPARACIONES CROMATOGRÁFICAS, Y SE OBTIENE UN PRODUCTO ESTABLE DE PUREZA ELEVADA, EN FORMA MÁS EFICIENTE QUE EN LA TÉCNICA ANTERIOR.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68439105P | 2005-05-25 | 2005-05-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GT200600213A true GT200600213A (es) | 2007-01-12 |
Family
ID=37037465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GT200600213A GT200600213A (es) | 2005-05-25 | 2006-05-22 | Metodos para sintetizar 3-cianoquinolinas sustituidas y sus intermediarios |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US20060270668A1 (es) |
| EP (1) | EP1883631A1 (es) |
| JP (1) | JP2008545688A (es) |
| KR (1) | KR20080016671A (es) |
| CN (1) | CN101203494A (es) |
| AR (1) | AR053872A1 (es) |
| AU (1) | AU2006249600A1 (es) |
| BR (1) | BRPI0610147A2 (es) |
| CA (1) | CA2609186A1 (es) |
| CR (1) | CR9544A (es) |
| GT (1) | GT200600213A (es) |
| IL (1) | IL187532A0 (es) |
| NO (1) | NO20076067L (es) |
| PA (1) | PA8676201A1 (es) |
| PE (1) | PE20061417A1 (es) |
| RU (1) | RU2007143161A (es) |
| TW (1) | TW200716557A (es) |
| WO (1) | WO2006127207A1 (es) |
| ZA (1) | ZA200710148B (es) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ528216A (en) * | 2001-02-24 | 2006-12-22 | Boehringer Ingelheim Pharma | Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions |
| US7407955B2 (en) | 2002-08-21 | 2008-08-05 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions |
| US7501426B2 (en) | 2004-02-18 | 2009-03-10 | Boehringer Ingelheim International Gmbh | 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions |
| DE102004054054A1 (de) | 2004-11-05 | 2006-05-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine |
| ZA200706804B (en) | 2005-02-03 | 2008-10-29 | Gen Hospital Corp | Method for treating gefitinib resistant cancer |
| DE102005035891A1 (de) * | 2005-07-30 | 2007-02-08 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
| WO2007056118A1 (en) | 2005-11-04 | 2007-05-18 | Wyeth | Antineoplastic combinations with mtor inhibitor, herceptin, and/or hki-272 |
| CA2833706C (en) | 2005-11-11 | 2014-10-21 | Boehringer Ingelheim International Gmbh | Quinazoline derivatives for the treatment of cancer diseases |
| NZ573360A (en) | 2006-05-04 | 2012-08-31 | Boehringer Ingelheim Int | Polymorphic forms of 1-[(4-methyl-quinazolin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-(R)-amino-piperidin-1-yl)-xanthine |
| EP1852108A1 (en) | 2006-05-04 | 2007-11-07 | Boehringer Ingelheim Pharma GmbH & Co.KG | DPP IV inhibitor formulations |
| PE20080251A1 (es) | 2006-05-04 | 2008-04-25 | Boehringer Ingelheim Int | Usos de inhibidores de dpp iv |
| AU2013202912B2 (en) * | 2007-06-08 | 2016-10-27 | Firmenich Incorporated | Modulation of chemosensory receptors and ligands associated therewith |
| AU2016225895B2 (en) * | 2007-10-17 | 2018-02-08 | 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 |
| AU2013203571B2 (en) * | 2007-10-17 | 2016-06-16 | 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 |
| 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 |
| JP2009215259A (ja) * | 2008-03-12 | 2009-09-24 | Ube Ind Ltd | 3−ハロゲノ−4−ヒドロカルビルオキシニトロベンゼン化合物の製造方法 |
| PE20140960A1 (es) | 2008-04-03 | 2014-08-15 | Boehringer Ingelheim Int | Formulaciones que comprenden un inhibidor de dpp4 |
| WO2009151910A2 (en) * | 2008-05-25 | 2009-12-17 | Wyeth | Combination product of receptor tyrosine kinase inhibitor and fatty acid synthase inhibitor for treating cancer |
| EP2915532B1 (en) | 2008-06-17 | 2016-10-19 | Wyeth LLC | Antineoplastic combinations containing hki-272 and vinorelbine |
| WO2010014666A2 (en) | 2008-07-31 | 2010-02-04 | Senomyx, Inc. | Processes and intermediates for making sweet taste enhancers |
| CN115990181A (zh) | 2008-08-04 | 2023-04-21 | 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 |
| UY32030A (es) | 2008-08-06 | 2010-03-26 | Boehringer Ingelheim Int | "tratamiento para diabetes en pacientes inapropiados para terapia con metformina" |
| KR20200118243A (ko) | 2008-08-06 | 2020-10-14 | 베링거 인겔하임 인터내셔날 게엠베하 | 메트포르민 요법이 부적합한 환자에서의 당뇨병 치료 |
| AU2009290911A1 (en) | 2008-09-10 | 2010-03-18 | Boehringer Ingelheim International Gmbh | Combination therapy for the treatment of diabetes and related conditions |
| US20200155558A1 (en) | 2018-11-20 | 2020-05-21 | Boehringer Ingelheim International Gmbh | Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral antidiabetic drug |
| CN101723854A (zh) * | 2008-10-24 | 2010-06-09 | 上海特化医药科技有限公司 | 6-取代氨基-3-氰基喹啉类化合物的制备方法及其中间体 |
| MX2011006713A (es) | 2008-12-23 | 2011-07-13 | Boehringer Ingelheim Int | Formas salinas de compuesto organico. |
| AR074990A1 (es) | 2009-01-07 | 2011-03-02 | Boehringer Ingelheim Int | Tratamiento de diabetes en pacientes con un control glucemico inadecuado a pesar de la terapia con metformina |
| CA2755789C (en) | 2009-04-06 | 2016-01-19 | Wyeth Llc | Treatment regimen utilizing neratinib for breast cancer |
| HRP20191005T1 (hr) | 2009-07-06 | 2019-08-23 | Boehringer Ingelheim International Gmbh | Postupak sušenja bibw2992, njegovih soli i čvrstih farmaceutskih formulacija koje sadrže taj djelatni sastojak |
| AU2010323068B2 (en) | 2009-11-27 | 2015-09-03 | Boehringer Ingelheim International Gmbh | Treatment of genotyped diabetic patients with DPP-IV inhibitors such as linagliptin |
| KR101927068B1 (ko) | 2010-05-05 | 2018-12-10 | 베링거 인겔하임 인터내셔날 게엠베하 | 체중 감소 치료에 후속하는 dpp-4 억제제에 의한 순차적 병용 요법 |
| WO2011161161A1 (en) | 2010-06-24 | 2011-12-29 | Boehringer Ingelheim International Gmbh | Diabetes therapy |
| US9034883B2 (en) | 2010-11-15 | 2015-05-19 | Boehringer Ingelheim International Gmbh | Vasoprotective and cardioprotective antidiabetic therapy |
| WO2012122058A2 (en) | 2011-03-04 | 2012-09-13 | Newgen Therapeutics, Inc. | Alkyne substituted quinazoline compound and methods of use |
| CN102718749A (zh) * | 2011-03-30 | 2012-10-10 | 北京德众万全药物技术开发有限公司 | 抗肿瘤药物诺那替尼的制备方法 |
| CN102718679B (zh) * | 2011-03-30 | 2016-06-08 | 北京万全阳光医药科技有限公司 | 一种诺那替尼关键中间体的制备方法 |
| WO2012155339A1 (zh) | 2011-05-17 | 2012-11-22 | 江苏康缘药业股份有限公司 | 4-苯胺-6-丁烯酰胺-7-烷醚喹唑啉衍生物及其制备方法和用途 |
| WO2013010964A1 (en) | 2011-07-15 | 2013-01-24 | Boehringer Ingelheim International Gmbh | Substituted quinazolines, the preparation thereof and the use thereof in pharmaceutical compositions |
| US9555001B2 (en) | 2012-03-07 | 2017-01-31 | Boehringer Ingelheim International Gmbh | Pharmaceutical composition and uses thereof |
| EP2849754B1 (en) | 2012-05-14 | 2022-09-14 | Boehringer Ingelheim International GmbH | Linagliptin, a xanthine derivative as dpp-4 inhibitor, for use in the treatment of sirs and/or sepsis |
| EP2849755A1 (en) | 2012-05-14 | 2015-03-25 | Boehringer Ingelheim International GmbH | A xanthine derivative as dpp -4 inhibitor for use in the treatment of podocytes related disorders and/or nephrotic syndrome |
| WO2013174767A1 (en) | 2012-05-24 | 2013-11-28 | Boehringer Ingelheim International Gmbh | A xanthine derivative as dpp -4 inhibitor for use in modifying food intake and regulating food preference |
| RU2666534C2 (ru) | 2012-08-06 | 2018-09-11 | Сеномикс, Инк. | Модификатор сладкого вкуса и аромата |
| CN103588755B (zh) * | 2012-08-17 | 2016-06-22 | 正大天晴药业集团股份有限公司 | Neratinib的制备方法 |
| HK1217092A1 (zh) | 2013-02-15 | 2016-12-23 | Kala Pharmaceuticals, Inc. | 治疗性化合物及其用途 |
| JO3155B1 (ar) | 2013-02-19 | 2017-09-20 | Senomyx Inc | معدِّل نكهة حلوة |
| AU2014219024B2 (en) | 2013-02-20 | 2018-04-05 | KALA BIO, Inc. | Therapeutic compounds and uses thereof |
| US9688688B2 (en) | 2013-02-20 | 2017-06-27 | Kala Pharmaceuticals, Inc. | Crystalline forms of 4-((4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolin-7-yl)oxy)-1-(2-oxa-7-azaspiro[3.5]nonan-7-yl)butan-1-one and uses thereof |
| CN103265530A (zh) * | 2013-06-14 | 2013-08-28 | 苏州明锐医药科技有限公司 | 来那替尼的制备方法 |
| KR20160099084A (ko) | 2013-11-01 | 2016-08-19 | 칼라 파마슈티컬스, 인크. | 치료 화합물의 결정질 형태 및 그의 용도 |
| US9890173B2 (en) | 2013-11-01 | 2018-02-13 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
| 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 |
| ES2950384T3 (es) | 2014-02-28 | 2023-10-09 | Boehringer Ingelheim Int | Uso médico de un inhibidor de DPP-4 |
| CN105367552A (zh) | 2015-01-09 | 2016-03-02 | 苏州晶云药物科技有限公司 | 来那替尼马来酸盐的新晶型及其制备方法 |
| CN105461689B (zh) * | 2015-05-19 | 2018-12-04 | 上海麦步医药科技有限公司 | 一种表皮生长因子受体(egfr)抑制剂来那替尼的新型制备方法 |
| CN105085485B (zh) * | 2015-08-21 | 2017-08-29 | 哈尔滨珍宝制药有限公司 | 一种来那替尼的制备方法 |
| CN105330646B (zh) * | 2015-12-04 | 2019-05-24 | 上海勋和医药科技有限公司 | 一种抗肿瘤药马来酸来那替尼的制备方法 |
| JP2019517542A (ja) | 2016-06-10 | 2019-06-24 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | リナグリプチンおよびメトホルミンの組合せ |
| CN105949176B (zh) * | 2016-06-24 | 2018-10-26 | 浙江海正药业股份有限公司 | 一种来那替尼的纯化方法 |
| EP3475269A1 (en) | 2016-06-27 | 2019-05-01 | Pliva Hrvatska D.O.O. | Solid state forms of neratinib and salts thereof |
| CN106220560A (zh) * | 2016-07-27 | 2016-12-14 | 华侨大学 | 一种多取代喹啉衍生物的制备方法 |
| CA3036340A1 (en) | 2016-09-08 | 2018-03-15 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
| MX2019002629A (es) | 2016-09-08 | 2019-10-07 | Kala Pharmaceuticals Inc | Formas cristalinas de compuestos terapéuticos y usos de los mismos. |
| US10253036B2 (en) | 2016-09-08 | 2019-04-09 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
| CN111344280B (zh) * | 2017-11-20 | 2022-08-12 | 苏州韬略生物科技股份有限公司 | (e)-n-(3-氰基-7-乙氧基-4-((4-苯氧基苯基)氨基)喹啉-6-基)-4-(二甲基氨基) 丁-2-烯酰胺马来酸盐及晶型 |
| CN108285421A (zh) * | 2018-01-26 | 2018-07-17 | 黑龙江鑫创生物科技开发有限公司 | 一种微通道反应器合成拉帕替尼中间体的方法 |
| CN110357854A (zh) * | 2018-03-26 | 2019-10-22 | 江苏创诺制药有限公司 | 一种来那替尼的制备方法 |
| CN108373467A (zh) * | 2018-04-27 | 2018-08-07 | 江苏创诺制药有限公司 | 来那替尼游离碱晶型及制备方法 |
| JP7453210B2 (ja) | 2018-08-07 | 2024-03-19 | フィルメニッヒ インコーポレイテッド | 5-置換4-アミノ-1H-ベンゾ[c][1,2,6]チアジアジン2,2-ジオキシド並びにその配合物及び使用 |
| CN109320686B (zh) * | 2018-08-29 | 2021-06-08 | 华南理工大学 | 一种聚异脲类聚合物及其制备方法和应用 |
| 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 |
| CN111875539B (zh) * | 2020-07-15 | 2022-06-21 | 苏中药业集团股份有限公司 | 一种egfr类分子靶向抗肿瘤药物的制备方法 |
| CN111848582A (zh) * | 2020-08-19 | 2020-10-30 | 重庆医科大学 | 制备表皮生长因子受体抑制剂来那替尼有关物质的方法 |
| CN111848581B (zh) * | 2020-08-19 | 2021-08-10 | 昆明学院 | 3-氰基-4-苯胺基-6-氨基喹啉衍生物的制备方法 |
| KR102713340B1 (ko) * | 2022-11-08 | 2024-10-02 | 경희대학교 산학협력단 | 고리화첨가 반응과 고리축소 반응의 연속 반응을 이용한 피롤로[1,2-a]퀴놀린의 제조방법 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| US6297258B1 (en) * | 1998-09-29 | 2001-10-02 | American Cyanamid Company | Substituted 3-cyanoquinolines |
| ES2211175T3 (es) * | 1998-09-29 | 2004-07-01 | Wyeth Holdings Corporation | Inhibidores de proteinas de tipo tirosina quinasas a base de 3-cianoquinolinas sustituidas. |
| US6288082B1 (en) * | 1998-09-29 | 2001-09-11 | American Cyanamid Company | Substituted 3-cyanoquinolines |
| US6384051B1 (en) * | 2000-03-13 | 2002-05-07 | American Cyanamid Company | Method of treating or inhibiting colonic polyps |
| UA77200C2 (en) * | 2001-08-07 | 2006-11-15 | Wyeth Corp | Antineoplastic combination of cci-779 and bkb-569 |
| CN101050189A (zh) * | 2002-02-05 | 2007-10-10 | 惠氏公司 | N-酰基-2-氨基-4-烷氧基-5-硝基苯甲酸类化合物的合成方法 |
| 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. |
| CN1835923A (zh) * | 2003-08-19 | 2006-09-20 | 惠氏控股公司 | 制备4-氨基-3-喹啉腈的方法 |
| UA85394C2 (ru) * | 2003-09-15 | 2009-01-26 | Вайет | Замещенные хинолины в качестве ингибиторов ферментов протеинтирозиновых киназ |
| US7399865B2 (en) * | 2003-09-15 | 2008-07-15 | Wyeth | Protein tyrosine kinase enzyme inhibitors |
| US7365203B2 (en) * | 2003-09-15 | 2008-04-29 | Wyeth | Process for the synthesis of 6-amino-4-(3-chloro-4-fluoro-phenylamino)-7-ethoxy-quinoline-3-carbonitrile |
| EP1711467A2 (en) * | 2004-01-16 | 2006-10-18 | Wyeth | Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof |
-
2006
- 2006-04-28 RU RU2007143161/04A patent/RU2007143161A/ru unknown
- 2006-04-28 JP JP2008513498A patent/JP2008545688A/ja not_active Withdrawn
- 2006-04-28 CN CNA2006800220965A patent/CN101203494A/zh active Pending
- 2006-04-28 KR KR1020077030160A patent/KR20080016671A/ko not_active Withdrawn
- 2006-04-28 AU AU2006249600A patent/AU2006249600A1/en not_active Abandoned
- 2006-04-28 BR BRPI0610147-0A patent/BRPI0610147A2/pt not_active IP Right Cessation
- 2006-04-28 CA CA002609186A patent/CA2609186A1/en not_active Abandoned
- 2006-04-28 TW TW095115306A patent/TW200716557A/zh unknown
- 2006-04-28 WO PCT/US2006/016215 patent/WO2006127207A1/en not_active Ceased
- 2006-04-28 EP EP06769913A patent/EP1883631A1/en not_active Withdrawn
- 2006-05-18 AR ARP060102010A patent/AR053872A1/es unknown
- 2006-05-22 PE PE2006000534A patent/PE20061417A1/es not_active Application Discontinuation
- 2006-05-22 GT GT200600213A patent/GT200600213A/es unknown
- 2006-05-25 PA PA20068676201A patent/PA8676201A1/es unknown
- 2006-05-25 US US11/439,984 patent/US20060270668A1/en not_active Abandoned
-
2007
- 2007-11-20 IL IL187532A patent/IL187532A0/en unknown
- 2007-11-23 CR CR9544A patent/CR9544A/es unknown
- 2007-11-26 ZA ZA200710148A patent/ZA200710148B/xx unknown
- 2007-11-26 NO NO20076067A patent/NO20076067L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US20060270668A1 (en) | 2006-11-30 |
| KR20080016671A (ko) | 2008-02-21 |
| NO20076067L (no) | 2007-12-21 |
| AR053872A1 (es) | 2007-05-23 |
| ZA200710148B (en) | 2008-09-25 |
| IL187532A0 (en) | 2008-03-20 |
| BRPI0610147A2 (pt) | 2010-06-01 |
| CN101203494A (zh) | 2008-06-18 |
| PE20061417A1 (es) | 2007-01-20 |
| CR9544A (es) | 2008-03-07 |
| RU2007143161A (ru) | 2009-07-10 |
| WO2006127207A1 (en) | 2006-11-30 |
| PA8676201A1 (es) | 2009-03-31 |
| EP1883631A1 (en) | 2008-02-06 |
| AU2006249600A1 (en) | 2006-11-30 |
| TW200716557A (en) | 2007-05-01 |
| CA2609186A1 (en) | 2006-11-30 |
| JP2008545688A (ja) | 2008-12-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GT200600213A (es) | Metodos para sintetizar 3-cianoquinolinas sustituidas y sus intermediarios | |
| CR11827A (es) | Activadores de glucoquinasa | |
| AR050254A1 (es) | Intermediarios y procesos para preparar dichos intermediarios utiles en la fabricacion de pirrolotriazinas | |
| SV2010003502A (es) | Fungicidas novedosos | |
| MX2007007189A (es) | Prodrogas de compuestos de 2,4-pirimidindiamina y sus usos. | |
| ECSP099327A (es) | Nuevos derivados de 1,4-benzotiepina-1,1-dióxido sustituidos con radicales bencilo, método para su preparación, productos farmacéuticos que comprenden estos compuestos y su uso | |
| CY1109471T1 (el) | Μεθοδοι και μεσα για την παραγωγη υαλουρονανης | |
| ECSP088145A (es) | Derivados bicíclicos como inhibidores de la cinasa p38 | |
| SG10201811715YA (en) | Intermediates and methods for the synthesis of halichondrin b analogs | |
| UY31674A1 (es) | Derivado heterocíclico fusionado y su uso | |
| CO6321254A2 (es) | Pirimidin -5-carboxamidas sustituidas 281 | |
| UY28800A1 (es) | 5,6-dialquil-7-amino-triazolopirimidinas, procedimientos para su preparación y el uso de las mismas para combatir hongos nocivos | |
| ECSP109942A (es) | Nuevos herbicidas | |
| MX2010001413A (es) | Nuevos herbicidas. | |
| AR064165A1 (es) | Un procedimiento para la preparacion de capecitabina e intermediarios utilizables en dicho procedimiento | |
| SV2008002542A (es) | Formas solidas cristalinas de tigeciclina y metodos para preparar los mismos ref. 01142.0379-00267 (am101946sv) | |
| CL2009001686A1 (es) | Procedimiento de preparacion de agomelatina; y los compuestos intermediarios considerados. | |
| MX2010002245A (es) | Derivados de ariloxiacetamida bi o triciclicos, saturados e insaturados y su uso como fungicidas. | |
| GT200500296A (es) | Sintesis asimetrica de derivados del dehidrobenzofurano | |
| CY1111954T1 (el) | Παραγωγα τετραϋδροναφθαλινιου, μεθοδοι για την παραγωγη αυτων και η χρηση αυτων ως αντιφλεγμονωδη | |
| ECSP088151A (es) | Diazepinoquinolinas, sintesis de las mismas, e intermediarios para obtenerlas | |
| CR11273A (es) | Derivados-2-ona disustituidos en 3, su preparacion y su aplicacion en terapeutica | |
| CR8360A (es) | 1,3 dimetilbutilcarboxanilidas | |
| CR8074A (es) | Triazolopyrimidinas | |
| ECSP088251A (es) | Diazepinoquinolinas, sintesis de las mismas, e intermediarios para obtenerlas |