WO2009025358A1 - 複素環化合物およびその用途 - Google Patents
複素環化合物およびその用途 Download PDFInfo
- Publication number
- WO2009025358A1 WO2009025358A1 PCT/JP2008/065011 JP2008065011W WO2009025358A1 WO 2009025358 A1 WO2009025358 A1 WO 2009025358A1 JP 2008065011 W JP2008065011 W JP 2008065011W WO 2009025358 A1 WO2009025358 A1 WO 2009025358A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- heterocyclic compound
- disclosed
- formulae
- iii
- salt
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
- C07D277/82—Nitrogen atoms
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009529075A JP5270553B2 (ja) | 2007-08-23 | 2008-08-22 | 複素環化合物およびその用途 |
| EP08827923.7A EP2181987B9 (en) | 2007-08-23 | 2008-08-22 | 2-Carbonylaminobenzothiazoles and their use for the prophylaxis and treatment of cancer |
| US12/674,801 US8324395B2 (en) | 2007-08-23 | 2008-08-22 | Heterocyclic compound and use thereof |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007-217633 | 2007-08-23 | ||
| JP2007217633 | 2007-08-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2009025358A1 true WO2009025358A1 (ja) | 2009-02-26 |
Family
ID=40378258
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2008/065011 Ceased WO2009025358A1 (ja) | 2007-08-23 | 2008-08-22 | 複素環化合物およびその用途 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8324395B2 (ja) |
| EP (1) | EP2181987B9 (ja) |
| JP (1) | JP5270553B2 (ja) |
| WO (1) | WO2009025358A1 (ja) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8143258B2 (en) | 2008-12-02 | 2012-03-27 | Takeda Pharmaceutical Company Limited | Benzothiazole compounds useful for Raf inhibition |
| US8304557B2 (en) | 2007-06-05 | 2012-11-06 | Takeda Pharmaceutical Company Limited | Fused heterocycle derivatives and use thereof |
| US8324395B2 (en) | 2007-08-23 | 2012-12-04 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8344135B2 (en) | 2007-08-29 | 2013-01-01 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8445509B2 (en) | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
| US8697874B2 (en) | 2008-12-01 | 2014-04-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| JP2014530194A (ja) * | 2011-09-14 | 2014-11-17 | ニューファーマ, インコーポレイテッド | 特定の化学的実体、組成物、および方法 |
| US10047059B2 (en) | 2012-11-12 | 2018-08-14 | Neupharma, Inc. | Substituted quinoxalines for inhibiting kinase activity |
| US10457641B2 (en) | 2012-09-24 | 2019-10-29 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US10590106B2 (en) | 2012-01-25 | 2020-03-17 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009111279A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Pyrazole [3, 4-b] pyridine raf inhibitors |
| US20110003809A1 (en) * | 2008-02-29 | 2011-01-06 | Array Biopharma Inc. | Imidazo [4,5-b] pyridine derivatives used as raf inhibitors |
| JP2011513332A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | 癌の治療のためのraf阻害剤としてのn−(6−アミノピリジン−3−イル)−3−(スルホンアミド)ベンズアミド誘導体 |
| KR20100122505A (ko) * | 2008-02-29 | 2010-11-22 | 어레이 바이오파마 인크. | Raf 저해물질 화합물 및 이들의 이용 방법 |
| ES2725790T3 (es) | 2011-08-26 | 2019-09-27 | Neupharma Inc | Algunas entidades químicas, composiciones, y métodos |
| WO2013043935A1 (en) | 2011-09-21 | 2013-03-28 | Neupharma, Inc. | Certain chemical entites, compositions, and methods |
| US9249111B2 (en) | 2011-09-30 | 2016-02-02 | Neupharma, Inc. | Substituted quinoxalines as B-RAF kinase inhibitors |
| CN109053630B (zh) * | 2018-08-22 | 2022-04-01 | 中国人民解放军第二军医大学 | 一种苯并噻唑类衍生物及其用途 |
| CN114805120A (zh) * | 2022-05-23 | 2022-07-29 | 江苏瑞达环保科技有限公司 | 一种间氰甲基苯甲酸甲酯的合成工艺 |
| CN115724837B (zh) * | 2022-10-26 | 2024-07-23 | 中国人民解放军海军军医大学 | 一种抑制程序性细胞坏死的苯并噻唑衍生物及其应用 |
Citations (22)
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| US2399026A (en) | 1941-02-06 | 1946-04-23 | Chem Ind Basel | Amides of 2-aminoarylenethiazoles |
| WO1999010325A1 (en) | 1997-08-06 | 1999-03-04 | Glaxo Group Limited | Benzylidene-1,3-dihydro-indol-2-one derivatives as receptor tyrosine kinase inhibitors, particularly of raf kinases |
| WO2000041698A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| WO2000042012A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS |
| WO2001066540A1 (en) | 2000-03-06 | 2001-09-13 | Smithkline Beecham P.L.C. | Imidazol-2-carboxamide derivatives as raf kinase inhibitors |
| WO2001066539A1 (en) | 2000-03-06 | 2001-09-13 | Smithkline Beecham P.L.C. | Imidazol derivatives as raf kinase inhibitors |
| WO2002024680A1 (en) | 2000-09-21 | 2002-03-28 | Smithkline Beecham P.L.C. | Imidazole derivatives as raf kinase inhibitors |
| WO2002044156A2 (en) | 2000-11-29 | 2002-06-06 | Glaxo Group Limited | Benzimidazole derivatives useful as tie-2 and/or vegfr-2 inhibitors |
| WO2002062763A2 (en) | 2001-02-07 | 2002-08-15 | Bayer Corporation | Inhibition of raf kinase using quinolyl isoquinolyl or pyridyl ureas |
| WO2002094808A1 (en) | 2001-05-19 | 2002-11-28 | Smithkline Beecham P.L.C. | Imidazole-2-carboxamide derivatives as raf kinase inhibitors |
| WO2003022838A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham Plc | Pyridine substituted furan derivatives as raf kinase inhibitors |
| WO2003022837A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham P.L.C. | Heterocycle-carboxamide derivatives as raf kinase inhibitors |
| WO2003022833A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham Plc | Pyridylfurans and pyrroles as raf kinase inhibitors |
| WO2003022836A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham Plc | Nitrogen-containing heterocyclic compounds and their use as raf inhibitors |
| WO2003074515A1 (en) * | 2002-03-01 | 2003-09-12 | Smithkline Beecham Corporation | Diamino-pyrimidines and their use as angiogenesis inhibitors |
| WO2003082272A1 (en) | 2002-03-29 | 2003-10-09 | Chiron Corporation | Substituted benzazoles and use thereof as raf kinase inhibitors |
| WO2005032548A1 (en) | 2003-09-29 | 2005-04-14 | Chiron Corporation | Substituted benzazoles and use thereof as inhibitors of raf kinase |
| WO2005037273A1 (en) * | 2003-10-16 | 2005-04-28 | Chiron Corporation | Substituted benzazoles and use thereof as inhibitors of raf kinase |
| WO2005112932A2 (en) | 2004-05-07 | 2005-12-01 | Exelixis, Inc. | Raf modulators and methods of use |
| WO2006076376A1 (en) | 2005-01-11 | 2006-07-20 | Medicinova, Inc. | Topical treatment of solid tumors and ocular neovascularization |
| WO2007030377A1 (en) | 2005-08-30 | 2007-03-15 | Novartis Ag | Substituted benzimidazoles as kinase inhibitors |
| WO2007121484A2 (en) * | 2006-04-19 | 2007-10-25 | Novartis Ag | 6-o-substituted benzoxazole and benzothiazole compounds and methods of inhibiting csf-1r signaling |
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| CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| ES2230719T3 (es) | 1997-09-26 | 2005-05-01 | Zentaris Gmbh | Compuestos basados en azabencimidazol para modular una funcion de proteina-quinasa de serina/treonina. |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
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| WO2009028655A1 (ja) | 2007-08-30 | 2009-03-05 | Takeda Pharmaceutical Company Limited | 複素環化合物およびその用途 |
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-
2008
- 2008-08-22 EP EP08827923.7A patent/EP2181987B9/en active Active
- 2008-08-22 US US12/674,801 patent/US8324395B2/en not_active Expired - Fee Related
- 2008-08-22 WO PCT/JP2008/065011 patent/WO2009025358A1/ja not_active Ceased
- 2008-08-22 JP JP2009529075A patent/JP5270553B2/ja not_active Expired - Fee Related
Patent Citations (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2399026A (en) | 1941-02-06 | 1946-04-23 | Chem Ind Basel | Amides of 2-aminoarylenethiazoles |
| WO1999010325A1 (en) | 1997-08-06 | 1999-03-04 | Glaxo Group Limited | Benzylidene-1,3-dihydro-indol-2-one derivatives as receptor tyrosine kinase inhibitors, particularly of raf kinases |
| WO2000041698A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| WO2000042012A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS |
| WO2001066540A1 (en) | 2000-03-06 | 2001-09-13 | Smithkline Beecham P.L.C. | Imidazol-2-carboxamide derivatives as raf kinase inhibitors |
| WO2001066539A1 (en) | 2000-03-06 | 2001-09-13 | Smithkline Beecham P.L.C. | Imidazol derivatives as raf kinase inhibitors |
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| WO2002094808A1 (en) | 2001-05-19 | 2002-11-28 | Smithkline Beecham P.L.C. | Imidazole-2-carboxamide derivatives as raf kinase inhibitors |
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| WO2003022837A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham P.L.C. | Heterocycle-carboxamide derivatives as raf kinase inhibitors |
| WO2003022833A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham Plc | Pyridylfurans and pyrroles as raf kinase inhibitors |
| WO2003022836A1 (en) | 2001-09-05 | 2003-03-20 | Smithkline Beecham Plc | Nitrogen-containing heterocyclic compounds and their use as raf inhibitors |
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| WO2007030377A1 (en) | 2005-08-30 | 2007-03-15 | Novartis Ag | Substituted benzimidazoles as kinase inhibitors |
| WO2007121484A2 (en) * | 2006-04-19 | 2007-10-25 | Novartis Ag | 6-o-substituted benzoxazole and benzothiazole compounds and methods of inhibiting csf-1r signaling |
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| See also references of EP2181987A4 * |
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Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8304557B2 (en) | 2007-06-05 | 2012-11-06 | Takeda Pharmaceutical Company Limited | Fused heterocycle derivatives and use thereof |
| US8324395B2 (en) | 2007-08-23 | 2012-12-04 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8344135B2 (en) | 2007-08-29 | 2013-01-01 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8445509B2 (en) | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
| US8697874B2 (en) | 2008-12-01 | 2014-04-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8497274B2 (en) | 2008-12-02 | 2013-07-30 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8143258B2 (en) | 2008-12-02 | 2012-03-27 | Takeda Pharmaceutical Company Limited | Benzothiazole compounds useful for Raf inhibition |
| JP2014530194A (ja) * | 2011-09-14 | 2014-11-17 | ニューファーマ, インコーポレイテッド | 特定の化学的実体、組成物、および方法 |
| JP2017082011A (ja) * | 2011-09-14 | 2017-05-18 | ニューファーマ, インコーポレイテッド | 特定の化学的実体、組成物、および方法 |
| US10065932B2 (en) | 2011-09-14 | 2018-09-04 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US10759766B2 (en) | 2011-09-14 | 2020-09-01 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US10590106B2 (en) | 2012-01-25 | 2020-03-17 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US10457641B2 (en) | 2012-09-24 | 2019-10-29 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US10047059B2 (en) | 2012-11-12 | 2018-08-14 | Neupharma, Inc. | Substituted quinoxalines for inhibiting kinase activity |
Also Published As
| Publication number | Publication date |
|---|---|
| US20110172245A1 (en) | 2011-07-14 |
| JPWO2009025358A1 (ja) | 2010-11-25 |
| EP2181987A1 (en) | 2010-05-05 |
| EP2181987B9 (en) | 2014-09-03 |
| EP2181987B1 (en) | 2014-03-05 |
| US8324395B2 (en) | 2012-12-04 |
| EP2181987A4 (en) | 2012-03-07 |
| JP5270553B2 (ja) | 2013-08-21 |
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