WO2009028629A1 - 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
- WO2009028629A1 WO2009028629A1 PCT/JP2008/065454 JP2008065454W WO2009028629A1 WO 2009028629 A1 WO2009028629 A1 WO 2009028629A1 JP 2008065454 W JP2008065454 W JP 2008065454W WO 2009028629 A1 WO2009028629 A1 WO 2009028629A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- heterocyclic compound
- formula
- disclosed
- substituents
- iii
- 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
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/675,663 US8344135B2 (en) | 2007-08-29 | 2008-08-28 | Heterocyclic compound and use thereof |
| EP08828528.3A EP2184285B1 (en) | 2007-08-29 | 2008-08-28 | Heterocyclic compound and use thereof |
| JP2009530185A JP5350247B2 (ja) | 2007-08-29 | 2008-08-28 | 複素環化合物およびその用途 |
| TW097145882A TW201004620A (en) | 2008-07-18 | 2008-11-27 | Heterocyclic compound and use thereof |
| PE2008002012A PE20091259A1 (es) | 2008-07-18 | 2008-12-03 | Compuestos heterociclicos como inhibidores de raf quinasa |
| ARP080105279A AR069567A1 (es) | 2008-07-18 | 2008-12-04 | Compuestos heterociclicos que tienen una fuerte actividad inhibidora de raf y son utiles para el tratamiento preventivo y similares del cancer y sus usos |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007-223284 | 2007-08-29 | ||
| JP2007223284 | 2007-08-29 | ||
| JP2008-187953 | 2008-07-18 | ||
| JP2008187953 | 2008-07-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2009028629A1 true WO2009028629A1 (ja) | 2009-03-05 |
Family
ID=40387343
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2008/065454 Ceased WO2009028629A1 (ja) | 2007-08-29 | 2008-08-28 | 複素環化合物およびその用途 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8344135B2 (ja) |
| EP (1) | EP2184285B1 (ja) |
| JP (1) | JP5350247B2 (ja) |
| WO (1) | WO2009028629A1 (ja) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010064611A1 (ja) * | 2008-12-01 | 2010-06-10 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| 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 |
| US8445509B2 (en) | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
| US8501936B2 (en) | 2009-06-05 | 2013-08-06 | Cephalon, Inc. | Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives |
| JP2016520617A (ja) * | 2013-05-30 | 2016-07-14 | カラ ファーマシューティカルズ インコーポレイテッド | 新規の化合物及びその使用 |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1951060B (zh) | 2004-04-30 | 2011-11-30 | 捷讯研究有限公司 | 处理数据传输的系统和方法 |
| CA2716949A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | N- (6-aminopyridin-3-yl) -3- (sulfonamido) benzamide derivatives as b-raf inhibitors for the treatment of cancer |
| US8394795B2 (en) * | 2008-02-29 | 2013-03-12 | Array Biopharma Inc. | Pyrazole [3, 4-B] pyridine Raf inhibitors |
| WO2009111278A2 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Raf inhibitor compounds and methods of use thereof |
| CA2716947A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Imidazo [4,5-b] pyridine derivatives used as raf inhibitors |
| CN103003264B (zh) | 2010-05-21 | 2014-08-06 | 切米利亚股份公司 | 嘧啶衍生物 |
| PT2580322T (pt) * | 2010-06-09 | 2018-03-01 | Dana Farber Cancer Inst Inc | Uma mutação em mek1 que confere resistência aos inibidores de raf e mek |
| AU2012230229A1 (en) | 2011-03-24 | 2013-10-10 | Noviga Research Ab | Novel pyrimidine derivatives |
| WO2012148792A1 (en) * | 2011-04-26 | 2012-11-01 | Merck Sharp & Dohme Corp. | Heterocyclic compounds as b-raf inhibitors for treatment of cancer |
| US9497220B2 (en) | 2011-10-17 | 2016-11-15 | Blackberry Limited | Dynamically generating perimeters |
| US9161226B2 (en) | 2011-10-17 | 2015-10-13 | Blackberry Limited | Associating services to perimeters |
| US9613219B2 (en) | 2011-11-10 | 2017-04-04 | Blackberry Limited | Managing cross perimeter access |
| US8799227B2 (en) | 2011-11-11 | 2014-08-05 | Blackberry Limited | Presenting metadata from multiple perimeters |
| US9369466B2 (en) | 2012-06-21 | 2016-06-14 | Blackberry Limited | Managing use of network resources |
| GB2508792A (en) * | 2012-09-11 | 2014-06-18 | Rec Modules Pte Ltd | Back contact solar cell cell interconnection arrangements |
| US20140280698A1 (en) * | 2013-03-13 | 2014-09-18 | Qnx Software Systems Limited | Processing a Link on a Device |
| WO2016086026A1 (en) | 2014-11-26 | 2016-06-02 | Kala Pharmaceuticals, Inc. | Crystalline forms of a therapeutic compound and uses thereof |
| CN105884628B (zh) * | 2016-06-06 | 2018-06-29 | 上海工程技术大学 | 2,4-二叔丁基-5-氨基酚的制备方法 |
| WO2020097398A1 (en) * | 2018-11-07 | 2020-05-14 | Dana-Farber Cancer Institute, Inc. | Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof |
| EP3877371A4 (en) * | 2018-11-07 | 2022-07-27 | Dana-Farber Cancer Institute, Inc. | IMIDAZOPYRIDINE DERIVATIVES AND AZA-IMIDAZOPYRIDINE DERIVATIVES USED AS JANUS KINASE 2 INHIBITORS AND ASSOCIATED USES |
| CA3181537A1 (en) | 2020-05-06 | 2021-11-11 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| WO2022140527A1 (en) | 2020-12-23 | 2022-06-30 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| TW202325289A (zh) | 2021-11-09 | 2023-07-01 | 美商雅捷可斯治療公司 | Jak2抑制劑之形式及組合物 |
| TW202334139A (zh) | 2021-11-09 | 2023-09-01 | 美商雅捷可斯治療公司 | 作為jak2抑制劑之6-雜芳氧基苯并咪唑及氮雜苯并咪唑 |
| 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 |
| JP2025534664A (ja) * | 2022-10-12 | 2025-10-17 | メイズ セラピューティクス, インコーポレイテッド | 溶質キャリアファミリー6aメンバー19(slc6a19)の阻害剤及びその使用方法 |
| WO2024189493A1 (en) | 2023-03-10 | 2024-09-19 | Breakpoint Therapeutics Gmbh | Inhibitors of dna polymerase theta |
| CN119119096B (zh) * | 2024-09-09 | 2025-09-16 | 郑州药领医药科技有限公司 | 一种4-((4,4,5,5-四甲基-1,3,2-二氧硼杂环戊烷-2-基)甲基)哌啶-1-甲酸叔丁酯的合成方法 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002044156A2 (en) * | 2000-11-29 | 2002-06-06 | Glaxo Group Limited | Benzimidazole derivatives useful as tie-2 and/or vegfr-2 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 |
| WO2007030377A1 (en) * | 2005-08-30 | 2007-03-15 | Novartis Ag | Substituted benzimidazoles as kinase inhibitors |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US21048A (en) * | 1858-07-27 | holzer | ||
| US4237300A (en) | 1975-12-09 | 1980-12-02 | Merck & Co., Inc. | Certain 6-substituted-2-pyridinamines |
| US4177274A (en) | 1975-12-09 | 1979-12-04 | Merck & Co., Inc. | Substituted imidazo [1,2-a] pyridines |
| US4096264A (en) | 1975-12-09 | 1978-06-20 | Merck & Co., Inc. | Certain substituted imidazo [1,2-a] pyridines |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| SK285357B6 (sk) | 1997-09-26 | 2006-11-03 | Zentaris Gmbh | Zlúčeniny na báze azabenzimidazolu modulujúce funkciu serínovej/treonínovej proteínkinázy |
| EP1158985B1 (en) | 1999-01-13 | 2011-12-28 | Bayer HealthCare LLC | OMEGA-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| US7928239B2 (en) | 1999-01-13 | 2011-04-19 | Bayer Healthcare Llc | Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas |
| EP1140840B1 (en) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| GB0005357D0 (en) | 2000-03-06 | 2000-04-26 | Smithkline Beecham Plc | Compounds |
| DE60103136T2 (de) | 2000-03-06 | 2004-10-28 | Smithkline Beecham Plc, Brentford | Imidazolderivate als Raf-Kinase Inhibitoren |
| EP1318992B1 (en) | 2000-09-21 | 2005-07-27 | Smithkline Beecham Plc | Imidazole derivatives as raf kinase inhibitors |
| GB0112348D0 (en) | 2001-05-19 | 2001-07-11 | Smithkline Beecham Plc | Compounds |
| GB0121488D0 (en) | 2001-09-05 | 2001-10-24 | Smithkline Beecham Plc | Compounds |
| GB0121494D0 (en) | 2001-09-05 | 2001-10-24 | Smithkline Beecham Plc | Compounds |
| JP2005504793A (ja) | 2001-09-05 | 2005-02-17 | スミスクライン ビーチャム パブリック リミテッド カンパニー | Rafキナーゼ阻害剤としてのヘテロサイクルカルボキサミド誘導体 |
| ATE403653T1 (de) | 2001-09-05 | 2008-08-15 | Smithkline Beecham Plc | Pyridin-substituierte furanderivate als raf- kinase inhibitoren |
| US7846959B2 (en) | 2004-05-07 | 2010-12-07 | Exelixis, Inc. | Raf modulators and methods of use |
| KR20060079098A (ko) * | 2004-12-31 | 2006-07-05 | 주식회사 엘지생명과학 | 신규한([1,3]티아졸로[5,4-b]피리딘-2-일)-2-카르복사마이드유도체 |
| WO2006076376A1 (en) | 2005-01-11 | 2006-07-20 | Medicinova, Inc. | Topical treatment of solid tumors and ocular neovascularization |
| US7759342B2 (en) * | 2005-01-13 | 2010-07-20 | Signal Pharmaceuticals, Llc | Methods of treatment and prevention using haloaryl substituted aminopurines |
| KR20070052207A (ko) | 2005-11-16 | 2007-05-21 | 주식회사 엘지생명과학 | 신규한 kdr 억제제 |
| PE20090370A1 (es) * | 2007-06-05 | 2009-04-30 | Takeda Pharmaceutical | Derivados de heterociclo fusionado como inhibidores de quinasa |
| EP2181987B9 (en) | 2007-08-23 | 2014-09-03 | Takeda Pharmaceutical Company Limited | 2-Carbonylaminobenzothiazoles and their use for the prophylaxis and treatment of cancer |
-
2008
- 2008-08-28 EP EP08828528.3A patent/EP2184285B1/en active Active
- 2008-08-28 US US12/675,663 patent/US8344135B2/en not_active Expired - Fee Related
- 2008-08-28 WO PCT/JP2008/065454 patent/WO2009028629A1/ja not_active Ceased
- 2008-08-28 JP JP2009530185A patent/JP5350247B2/ja not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002044156A2 (en) * | 2000-11-29 | 2002-06-06 | Glaxo Group Limited | Benzimidazole derivatives useful as tie-2 and/or vegfr-2 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 |
| WO2007030377A1 (en) * | 2005-08-30 | 2007-03-15 | Novartis Ag | Substituted benzimidazoles as kinase inhibitors |
Cited By (10)
| 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 |
| US8445509B2 (en) | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
| WO2010064611A1 (ja) * | 2008-12-01 | 2010-06-10 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| US8143258B2 (en) | 2008-12-02 | 2012-03-27 | Takeda Pharmaceutical Company Limited | Benzothiazole compounds useful for Raf inhibition |
| US8497274B2 (en) | 2008-12-02 | 2013-07-30 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| US8501936B2 (en) | 2009-06-05 | 2013-08-06 | Cephalon, Inc. | Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives |
| US8633173B2 (en) | 2009-06-05 | 2014-01-21 | Cephalon, Inc | Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives |
| JP2016520617A (ja) * | 2013-05-30 | 2016-07-14 | カラ ファーマシューティカルズ インコーポレイテッド | 新規の化合物及びその使用 |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2184285A4 (en) | 2011-07-20 |
| US20100249119A1 (en) | 2010-09-30 |
| JP5350247B2 (ja) | 2013-11-27 |
| US8344135B2 (en) | 2013-01-01 |
| EP2184285B1 (en) | 2015-11-04 |
| JPWO2009028629A1 (ja) | 2010-12-02 |
| EP2184285A1 (en) | 2010-05-12 |
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