PE20050691A1 - Proceso para preparar carboxamidas 2-aminotiazol-5-aromaticas como inhibidores de la cinasa - Google Patents
Proceso para preparar carboxamidas 2-aminotiazol-5-aromaticas como inhibidores de la cinasaInfo
- Publication number
- PE20050691A1 PE20050691A1 PE2005000128A PE2005000128A PE20050691A1 PE 20050691 A1 PE20050691 A1 PE 20050691A1 PE 2005000128 A PE2005000128 A PE 2005000128A PE 2005000128 A PE2005000128 A PE 2005000128A PE 20050691 A1 PE20050691 A1 PE 20050691A1
- Authority
- PE
- Peru
- Prior art keywords
- kinase inhibitors
- ilamino
- methylpyrimidin
- piperazin
- thiazol
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- 150000003857 carboxamides Chemical class 0.000 title 1
- -1 2-CHLORO-6-METHYLPHENYL Chemical class 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- GGNIKGLUPSHSBV-UHFFFAOYSA-N thiazole-5-carboxamide Chemical compound NC(=O)C1=CN=CS1 GGNIKGLUPSHSBV-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000004682 monohydrates Chemical class 0.000 abstract 1
- 230000000771 oncological effect Effects 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
- C07C237/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Virology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
REFERIDA A UN COMPUESTO DE FORMULA I DONDE L ES ALQUILENO, OPCIONALMENTE SUSTITUIDO; Ar ES ARILO, HETEROARILO; R2 ES H, ALQUILO ALQUENILO, ENTRE OTROS; R3 ES H, CIANO, HALOGENO, ENTRE OTROS; R4 ES H, ALQUILO, ARILO, ENTRE OTROS; R5 ES H, HETEROARILO, ARILO, ENTRE OTROS; m ES 0-1. TAMBIEN REFERIDO A PROCESOS DE PREPARACION DE SUS PREFERIDOS: MONOHIDRATO DE CRISTALINO DE N-(2-CLORO-6-METILFENIL)-2-(6-(4-(3-HIDROXIETIL)PIPERAZIN-1-IL)-2-METILPIRIMIDIN-4-ILAMINO)TIAZOL-5-CARBOXAMIDA; SOLVATO DE N-BUTANOL CRISTALINO DE N-(2-CLORO-6-METILFENIL)-2-(6-(4-(3-HIDROXIETIL)PIPERAZIN-1-IL)-2-METILPIRIMIDIN-4-ILAMINO)TIAZOL-5-CARBOXAMIDA Y FORMA PURA T1H1-7 CRISTALINA DE N-(2-CLORO-6-METILFENIL)-2-(6-(4-(3-HIDROXIETIL)PIPERAZIN-1-IL)-2-METILPIRIMIDIN-4-ILAMINO)TIAZOL-5-CARBOXAMIDA; ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE CINASAS UTILES EN EL TRATAMIENTO DE TRASTORNOS INMUNOLOGICOS Y ONCOLOGICOS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54249004P | 2004-02-06 | 2004-02-06 | |
| US62493704P | 2004-11-04 | 2004-11-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20050691A1 true PE20050691A1 (es) | 2005-09-25 |
Family
ID=34864498
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2005000128A PE20050691A1 (es) | 2004-02-06 | 2005-02-04 | Proceso para preparar carboxamidas 2-aminotiazol-5-aromaticas como inhibidores de la cinasa |
Country Status (26)
| Country | Link |
|---|---|
| EP (1) | EP1711481B2 (es) |
| JP (2) | JP5148115B2 (es) |
| KR (2) | KR20120097424A (es) |
| AR (1) | AR047533A1 (es) |
| AT (1) | ATE453630T1 (es) |
| AU (1) | AU2005212405B2 (es) |
| BR (1) | BRPI0507476B8 (es) |
| CA (1) | CA2555291C (es) |
| CY (1) | CY1109907T1 (es) |
| DE (1) | DE602005018601D1 (es) |
| DK (1) | DK1711481T4 (es) |
| ES (1) | ES2337272T5 (es) |
| GE (1) | GEP20094804B (es) |
| HR (1) | HRP20100166T4 (es) |
| IL (1) | IL177280A (es) |
| IN (1) | IN2014DN06567A (es) |
| NO (1) | NO338049B1 (es) |
| NZ (1) | NZ548613A (es) |
| PE (1) | PE20050691A1 (es) |
| PL (1) | PL1711481T5 (es) |
| PT (1) | PT1711481E (es) |
| RU (1) | RU2382039C2 (es) |
| SI (1) | SI1711481T2 (es) |
| TW (1) | TWI338004B (es) |
| WO (1) | WO2005077945A2 (es) |
| ZA (1) | ZA200606242B (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005502643A (ja) | 2001-08-10 | 2005-01-27 | ノバルティス アクチエンゲゼルシャフト | 白血病処置のための単独またはsti571と組み合せたc−srcインヒビターの使用 |
| US7151113B2 (en) | 2003-05-01 | 2006-12-19 | Bristol Myers Squibb Company | Pyrazole-amine compounds useful as kinase inhibitors |
| TWI338004B (en) * | 2004-02-06 | 2011-03-01 | Bristol Myers Squibb Co | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
| US7652146B2 (en) | 2004-02-06 | 2010-01-26 | Bristol-Myers Squibb Company | Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitors |
| TW200600513A (en) | 2004-06-30 | 2006-01-01 | Bristol Myers Squibb Co | A method for preparing pyrrolotriazine compounds |
| EP1885339B1 (en) * | 2005-05-05 | 2015-07-29 | Bristol-Myers Squibb Holdings Ireland | Formulations of a src/abl inhibitor |
| EP1919885B1 (en) | 2005-08-05 | 2010-04-28 | Brystol-Myers Squibb Company | Preparation of 2-amino-thiazole-5-carboxylic-acid derivatives |
| EP1937270A1 (en) * | 2005-09-21 | 2008-07-02 | Brystol-Myers Squibb Company | Oral administration of n-(2-chloro-6-methylphenyl)-2-[[6-4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-1,3-thiazole-5-carboxamide and salts thereof |
| US20070219370A1 (en) * | 2006-03-15 | 2007-09-20 | Bristol-Myers Squibb Company | Process for preparing n-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino] -5-thiazolecarboxamide and related metabolites thereof |
| KR101433629B1 (ko) | 2006-09-11 | 2014-08-27 | 쿠리스 인코퍼레이션 | 아연 결합 부분을 함유한 티로신 키나아제 억제제 |
| AR062927A1 (es) | 2006-10-11 | 2008-12-17 | Bayer Healthcare Ag | 4- [4-( [ [ 4- cloro-3-( trifluorometil) fenil) carbamoil] amino] -3- fluorofenoxi) -n- metilpiridin-2- carboxamida monohidratada |
| JP5528807B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
| WO2008044041A1 (en) | 2006-10-12 | 2008-04-17 | Astex Therapeutics Limited | Pharmaceutical combinations |
| EP1992344A1 (en) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation |
| EP2207777A2 (en) | 2007-10-23 | 2010-07-21 | Teva Pharmaceutical Industries Ltd. | Polymorphs of dasatinib and process for preparation thereof |
| WO2010062715A2 (en) * | 2008-11-03 | 2010-06-03 | Teva Pharmaceutical Industries Ltd. | Polymorphs of dasatinib and process for preparation thereof |
| WO2010067374A2 (en) * | 2008-12-08 | 2010-06-17 | Hetero Research Foundation | Polymorphs of dasatinib |
| CA2759269A1 (en) * | 2009-05-05 | 2010-11-11 | Merck Sharp & Dohme Corp. | P38 kinase inhibiting agents |
| CN101812060B (zh) * | 2010-02-02 | 2011-08-17 | 南京卡文迪许生物工程技术有限公司 | 一种简捷制备高纯度达沙替尼的新方法以及中间体化合物 |
| EP2359813A1 (en) | 2010-02-04 | 2011-08-24 | Ratiopharm GmbH | Pharmaceutical composition comprising N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazolecarboxamid |
| CN102250084A (zh) * | 2010-02-08 | 2011-11-23 | 南京卡文迪许生物工程技术有限公司 | 达沙替尼多晶型物及其制备方法和药用组合物 |
| JP5589097B2 (ja) * | 2010-02-08 | 2014-09-10 | 南京▲か▼文迪許生物工程技術有限公司 | ダサチニブ多結晶体、並びにその調製方法及び薬物組成物 |
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| AU2013276138B2 (en) | 2012-06-15 | 2017-02-23 | Basf Se | Multicomponent crystals comprising Dasatinib and selected cocrystal formers |
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| US9365526B2 (en) | 2012-12-31 | 2016-06-14 | Sun Pharmaceutical Industries Limited | Process for the preparation of dasatinib and its intermediates |
| CN103319476B (zh) * | 2013-06-13 | 2015-12-02 | 济南德爱医药技术有限公司 | 一种激酶抑制剂 |
| MX2016001096A (es) * | 2013-07-25 | 2016-04-25 | Basf Se | Sales de dasatinib en forma amorfa. |
| KR20160023879A (ko) * | 2013-07-25 | 2016-03-03 | 바스프 에스이 | 결정질 형태의 다사티닙 염 |
| CN104341410A (zh) * | 2013-08-09 | 2015-02-11 | 上海科胜药物研发有限公司 | 一种达沙替尼新晶型及其制备方法 |
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| IN2013MU03610A (es) | 2013-12-18 | 2015-04-24 | Dharmesh Mahendrabhai Shah | |
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| AU2015200822A1 (en) | 2014-03-11 | 2015-10-01 | Cerbios-Pharma Sa | Process and intermediates for the preparation of dasatinib |
| RU2567537C1 (ru) * | 2014-04-23 | 2015-11-10 | Олег Ростиславович Михайлов | Кристаллическая безводная дельта-модификация n-(2-хлор-6-метилфенил)-2-[[6-[4-(2-гидроксиэтил)-1-пиперазинил]-2-метил-4-пиримидинил]амино]-5-тиазолкарбоксамида, способ ее получения и фармацевтическая композиция на ее основе |
| HU231013B1 (hu) * | 2014-05-26 | 2019-11-28 | Egis Gyógyszergyár Zrt. | Dasatinib sók |
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| GB201608587D0 (en) | 2016-05-16 | 2016-06-29 | Univ Dundee | Treatment of opiod tolerance |
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| JP6597727B2 (ja) | 2017-05-11 | 2019-10-30 | 東洋インキScホールディングス株式会社 | 表面保護用粘着剤および粘着シート |
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| HUP0202708A3 (en) * | 1999-04-15 | 2004-12-28 | Bristol Myers Squibb Co | Cyclic protein tyrosine kinase inhibitors, pharmaceutical compositions containing them and their use |
| US7169771B2 (en) * | 2003-02-06 | 2007-01-30 | Bristol-Myers Squibb Company | Thiazolyl-based compounds useful as kinase inhibitors |
| AU2005209231B8 (en) * | 2004-01-21 | 2011-07-28 | Emory University | Compositions and methods of use for tyrosine kinase inhibitors to treat pathogenic infection |
| TWI338004B (en) * | 2004-02-06 | 2011-03-01 | Bristol Myers Squibb Co | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
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