MA31002B1 - Derives de 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine - Google Patents
Derives de 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazineInfo
- Publication number
- MA31002B1 MA31002B1 MA32006A MA32006A MA31002B1 MA 31002 B1 MA31002 B1 MA 31002B1 MA 32006 A MA32006 A MA 32006A MA 32006 A MA32006 A MA 32006A MA 31002 B1 MA31002 B1 MA 31002B1
- Authority
- MA
- Morocco
- Prior art keywords
- alkyl
- imidazo
- tetrahydro
- alkoxy
- halogen
- Prior art date
Links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- Health & Medical Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
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- Heart & Thoracic Surgery (AREA)
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- Pulmonology (AREA)
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- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Dermatology (AREA)
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- Hematology (AREA)
- Anesthesiology (AREA)
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- Vascular Medicine (AREA)
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Abstract
L'INVENTION PORTE SUR DES DÉRIVÉS DE 5,6,7,8-TÉTRAHYDRO-IMIDAZO[1,5-A]PYRAZINE DE FORMULE (1), DANS LAQUELLE X REPRÉSENTE CH2 OU O ; R1 REPRÉSENTE UN GROUPE PHÉNYLE, LEQUEL GROUPE EST INDÉPENDAMMENT MONO-, DI- OU TRI- SUBSTITUÉ, LES SUBSTITUANTS ÉTANT INDÉPENDAMMENT CHOISIS DANS LE GROUPE CONSTITUÉ PAR ALKYLE EN C1-C4, ALCOXY EN C1-C4, HALOGÈNE, CYANO, TRIFLUOROMÉTHOXY ET TRIFLUOROMÉTHYLE ; R2 REPRÉSENTE ALKYLE EN C1-C4, ALCOXY EN C1-C4, ALCÉNYLE EN C2-C4, HALOGÈNE, CYANO, HYDROXYMÉTHYLE, TRIFLUOROMÉTHYLE, C(O)NR5R6 OU CYCLOPROPYLE ; R3 REPRÉSENTE ALKYLE EN C1-C4, ALCOXY EN C1-C4-MÉTHYLE, OU HALOGÈNE ; R4 REPRÉSENTE ALKYLE EN C1-C4 ; R5 REPRÉSENTE HYDROGÈNE OU ALKYLE EN C1-C4 ; ET R6 REPRÉSENTE HYDROGÈNE OU ALKYLE EN C1-C4. L'INVENTION PORTE ÉGALEMENT SUR DES SELS PHARMACEUTIQUEMENT ACCEPTABLES DE TELS COMPOSÉS ; ET SUR L'UTILISATION DE TELS COMPOSÉS EN TANT QUE MÉDICAMENTS, NOTAMMENT EN TANT QU'ANTAGONISTES DU RÉCEPTEUR DE L'OREXINE.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2006055019 | 2006-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31002B1 true MA31002B1 (fr) | 2009-12-01 |
Family
ID=39273168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32006A MA31002B1 (fr) | 2006-12-22 | 2009-06-17 | Derives de 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8188082B2 (fr) |
| EP (1) | EP2125823B1 (fr) |
| JP (1) | JP2010513466A (fr) |
| KR (1) | KR20090106538A (fr) |
| CN (1) | CN101568542B (fr) |
| AT (1) | ATE545647T1 (fr) |
| AU (1) | AU2007337659A1 (fr) |
| BR (1) | BRPI0720522A2 (fr) |
| CA (1) | CA2669561A1 (fr) |
| ES (1) | ES2380391T3 (fr) |
| MA (1) | MA31002B1 (fr) |
| MX (1) | MX2009006553A (fr) |
| NO (1) | NO20092715L (fr) |
| RU (1) | RU2009127842A (fr) |
| WO (1) | WO2008078291A1 (fr) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2380391T3 (es) | 2006-12-22 | 2012-05-11 | Actelion Pharmaceuticals Ltd. | Derivados de 5,6,7,8-tetrahidro-imidazo[1,5-a]pirazina |
| US7775298B2 (en) | 2007-10-29 | 2010-08-17 | Abergeldie Holdings Pty Ltd/Abergeldie Plant Pty Ltd | Drilling assemblies and methods of drilling |
| CN101468988A (zh) * | 2007-12-26 | 2009-07-01 | 上海恒瑞医药有限公司 | 哌嗪类衍生物,其制备方法及其在医药上的应用 |
| US20110105514A1 (en) * | 2008-06-25 | 2011-05-05 | Hamed Aissaoui | 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine compounds |
| ES2585806T3 (es) | 2009-10-23 | 2016-10-10 | Janssen Pharmaceutica N.V. | Octahidropirrolo [3,4-c] pirroles disustituidos como moduladores de receptores de orexina |
| CN102258508A (zh) * | 2011-04-14 | 2011-11-30 | 威海迪素制药有限公司 | 芳基丙烯酸衍生物抗癫痫的用途 |
| US9440982B2 (en) | 2012-02-07 | 2016-09-13 | Eolas Therapeutics, Inc. | Substituted prolines/piperidines as orexin receptor antagonists |
| WO2013119639A1 (fr) | 2012-02-07 | 2013-08-15 | Eolas Therapeutics, Inc. | Pipéridines/prolines substituées en tant qu'antagonistes du récepteur de l'orexine |
| CN103980281B (zh) * | 2014-05-27 | 2016-06-08 | 天津市斯芬克司药物研发有限公司 | 一种咪唑吡嗪化合物及其制备方法 |
| TW201613902A (en) | 2014-08-13 | 2016-04-16 | Eolas Therapeutics Inc | Difluoropyrrolidines as orexin receptor modulators |
| LT3414241T (lt) | 2016-02-12 | 2022-08-25 | Astrazeneca Ab | Halogenu pakeisti piperidinai kaip oreksino receptoriaus moduliatoriai |
| HRP20220642T1 (hr) | 2016-03-10 | 2022-06-24 | Janssen Pharmaceutica Nv | Postupci za liječenje depresije uporabom antagonista receptora oreksina 2 |
| CN105753788A (zh) * | 2016-04-08 | 2016-07-13 | 西南科技大学 | 一种1-取代-2-苯基-4-碘咪唑的制备方法 |
| WO2017194548A1 (fr) | 2016-05-10 | 2017-11-16 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Méthodes et compositions pharmaceutiques pour le traitement de maladies inflammatoires auto-immunes |
| DK3682881T3 (da) | 2017-09-14 | 2026-05-11 | Daiichi Sankyo Co Limited | Forbindelse med cyklisk struktur |
| CN108101930B (zh) * | 2017-12-22 | 2020-10-30 | 武汉大学 | 一类含有苯并噻二唑并噻吩单元的小分子受体材料及其制备方法与应用 |
| AU2019245403B2 (en) * | 2018-03-29 | 2025-02-06 | Board Of Regents, The University Of Texas System | Imidazopiperazine inhibitors of transcription activating proteins |
| WO2019195846A1 (fr) | 2018-04-06 | 2019-10-10 | Board Of Regents, The University Of Texas System | Inhibiteurs d'imidazopipérazinone de protéines d'activation de la transcription |
| GB201908511D0 (en) | 2019-06-13 | 2019-07-31 | Adorx Therapeutics Ltd | Hydroxamate compounds |
| CN116348112A (zh) * | 2020-10-02 | 2023-06-27 | 德州大学系统董事会 | 转录激活蛋白的咪唑并哌嗪抑制剂 |
| JP2023544173A (ja) | 2020-10-02 | 2023-10-20 | ボード オブ レジェンツ,ザ ユニバーシティ オブ テキサス システム | 転写活性化タンパク質のイミダゾピペラジン阻害剤 |
| KR102910851B1 (ko) * | 2021-04-21 | 2026-01-09 | 장춘 진사이언스 파마슈티컬 씨오., 엘티디. | 이미다졸 함유 축합고리계 유도체, 이의 제조방법 및 이의 의약적 용도 |
| EP4574826A4 (fr) * | 2022-10-19 | 2025-12-10 | Changchun Genescience Pharmaceutical Co Ltd | Forme cristalline d'un antagoniste de nk3r, son procédé de préparation et son utilisation |
| WO2025224168A1 (fr) | 2024-04-24 | 2025-10-30 | Idorsia Pharmaceuticals Ltd | Dérivés d'arylsulfone et de sulfanone utilisés en tant que modulateurs du récepteur de l'orexine |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU6011301A (en) * | 2000-03-14 | 2001-09-24 | Actelion Pharmaceuticals Ltd | 1,2,3,4-tetrahydroisoquinoline derivatives |
| CA2408343A1 (fr) | 2000-05-11 | 2002-11-07 | Banyu Pharmaceutical Co., Ltd. | Derives n-acyltetrahydroisoquinoline |
| WO2002051232A2 (fr) | 2000-12-27 | 2002-07-04 | Actelion Pharmaceuticals Ltd. | Nouvelles benzazepines et derives heterocycliques associes |
| GB0124463D0 (en) * | 2001-10-11 | 2001-12-05 | Smithkline Beecham Plc | Compounds |
| MXPA04002269A (es) | 2002-07-09 | 2004-06-29 | Actelion Pharmaceuticals Ltd | Derivados de 7,8,9,10-tetrahidro-6h-azepino,6,7,8,9-tetrahidro-pirido y 2,3-dihidro-2h-pirrolo[2,1-b]-quinazolinona. |
| CA2494636A1 (fr) * | 2002-08-07 | 2004-02-19 | Novartis Ag | Composes organiques servant d'agents pour le traitement d'etats pathologiques induits par l'aldosterone |
| AU2004224156B2 (en) | 2003-03-26 | 2010-08-12 | Actelion Pharmaceuticals Ltd. | Tetrahydroisoquinolyl acetamide derivatives for use as orexin receptor antagonists |
| CA2540196C (fr) * | 2003-09-26 | 2012-03-20 | Actelion Pharmaceuticals Ltd | Derives de pyridine et leur utilisation comme antagonistes de l'urotensine ii |
| JP4094050B2 (ja) | 2004-03-01 | 2008-06-04 | アクテリオン ファーマシューティカルズ リミテッド | 置換1,2,3,4−テトラヒドロイソキノリン誘導体 |
| EP1998774A1 (fr) | 2006-03-15 | 2008-12-10 | Actelion Pharmaceuticals Ltd. | Derives de tetrahydroisoquinoleine pour renforcer la fonction de la memoire |
| ATE496051T1 (de) | 2006-04-26 | 2011-02-15 | Actelion Pharmaceuticals Ltd | Pyrazolotetrahydropyridinderivate als orexinrezeptorantagonisten |
| WO2008026149A1 (fr) * | 2006-08-28 | 2008-03-06 | Actelion Pharmaceuticals Ltd | Dérivés de 1,4,5,6,7,8-hexahydro-1,2,5-triaza-azulène en tant qu'antagonistes de récepteur d'orexine |
| ES2380391T3 (es) | 2006-12-22 | 2012-05-11 | Actelion Pharmaceuticals Ltd. | Derivados de 5,6,7,8-tetrahidro-imidazo[1,5-a]pirazina |
| PE20091010A1 (es) | 2007-10-10 | 2009-08-08 | Actelion Pharmaceuticals Ltd | Derivados de tetrahidroquinolina |
| US20110105514A1 (en) * | 2008-06-25 | 2011-05-05 | Hamed Aissaoui | 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine compounds |
-
2007
- 2007-12-20 ES ES07859469T patent/ES2380391T3/es active Active
- 2007-12-20 AT AT07859469T patent/ATE545647T1/de active
- 2007-12-20 MX MX2009006553A patent/MX2009006553A/es not_active Application Discontinuation
- 2007-12-20 AU AU2007337659A patent/AU2007337659A1/en not_active Abandoned
- 2007-12-20 JP JP2009542373A patent/JP2010513466A/ja active Pending
- 2007-12-20 WO PCT/IB2007/055245 patent/WO2008078291A1/fr not_active Ceased
- 2007-12-20 CA CA002669561A patent/CA2669561A1/fr not_active Abandoned
- 2007-12-20 BR BRPI0720522-8A patent/BRPI0720522A2/pt not_active IP Right Cessation
- 2007-12-20 KR KR1020097015261A patent/KR20090106538A/ko not_active Ceased
- 2007-12-20 RU RU2009127842/04A patent/RU2009127842A/ru not_active Application Discontinuation
- 2007-12-20 US US12/520,693 patent/US8188082B2/en not_active Expired - Fee Related
- 2007-12-20 CN CN2007800478100A patent/CN101568542B/zh not_active Expired - Fee Related
- 2007-12-20 EP EP07859469A patent/EP2125823B1/fr active Active
-
2009
- 2009-06-17 MA MA32006A patent/MA31002B1/fr unknown
- 2009-07-20 NO NO20092715A patent/NO20092715L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ATE545647T1 (de) | 2012-03-15 |
| AU2007337659A1 (en) | 2008-07-03 |
| WO2008078291A1 (fr) | 2008-07-03 |
| KR20090106538A (ko) | 2009-10-09 |
| CN101568542A (zh) | 2009-10-28 |
| BRPI0720522A2 (pt) | 2014-01-07 |
| EP2125823A1 (fr) | 2009-12-02 |
| CA2669561A1 (fr) | 2008-07-03 |
| MX2009006553A (es) | 2009-06-26 |
| JP2010513466A (ja) | 2010-04-30 |
| CN101568542B (zh) | 2013-03-27 |
| RU2009127842A (ru) | 2011-01-27 |
| ES2380391T3 (es) | 2012-05-11 |
| NO20092715L (no) | 2009-07-20 |
| US20100093740A1 (en) | 2010-04-15 |
| EP2125823B1 (fr) | 2012-02-15 |
| US8188082B2 (en) | 2012-05-29 |
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