MA39164A1 - Forme de sel cristalline de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone comme antagoniste des récepteurs à l'oréxine - Google Patents
Forme de sel cristalline de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone comme antagoniste des récepteurs à l'oréxineInfo
- Publication number
- MA39164A1 MA39164A1 MA39164A MA39164A MA39164A1 MA 39164 A1 MA39164 A1 MA 39164A1 MA 39164 A MA39164 A MA 39164A MA 39164 A MA39164 A MA 39164A MA 39164 A1 MA39164 A1 MA 39164A1
- Authority
- MA
- Morocco
- Prior art keywords
- methylpyrrolidin
- methanone
- triazol
- imidazol
- benzo
- Prior art date
Links
- -1 (S) - (2- (6-Chloro-7-methyl-1H-benzo [d] imidazol-2-yl) -2-methylpyrrolidin-1-yl) Chemical group 0.000 title abstract 2
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 title abstract 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 title 1
- 239000004472 Lysine Substances 0.000 title 1
- 239000005557 antagonist Substances 0.000 title 1
- RRNLUZWHLGBTDE-ZDUSSCGKSA-N ClC=1C=CC2=C(NC(=N2)[C@]2(N(CCC2)Cl)C)C=1C Chemical compound ClC=1C=CC2=C(NC(=N2)[C@]2(N(CCC2)Cl)C)C=1C RRNLUZWHLGBTDE-ZDUSSCGKSA-N 0.000 abstract 1
- 102000002512 Orexin Human genes 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 108060005714 orexin Proteins 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La présente invention concerne une forme cristalline de chlorhydrate de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone, des procédés de préparation associés, des compositions pharmaceutiques contenant ladite forme cristalline et son utilisation comme médicament, particulièrement comme antagoniste des récepteurs à l'oréxine.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB2013060595 | 2013-12-03 | ||
| PCT/IB2014/066509 WO2015083071A1 (fr) | 2013-12-03 | 2014-12-02 | Forme de sel cristalline de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone comme antagoniste des récepteurs à l'oréxine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA39164A1 true MA39164A1 (fr) | 2017-08-31 |
| MA39164B1 MA39164B1 (fr) | 2019-03-29 |
Family
ID=52282787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA39164A MA39164B1 (fr) | 2013-12-03 | 2014-12-02 | Forme de sel cristalline de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone comme antagoniste des récepteurs à l'oréxine |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US9790208B2 (fr) |
| EP (1) | EP3077390B1 (fr) |
| JP (1) | JP6091716B2 (fr) |
| KR (1) | KR101839716B1 (fr) |
| CN (1) | CN105793258B (fr) |
| AU (1) | AU2014358743B2 (fr) |
| CA (1) | CA2929720C (fr) |
| CL (1) | CL2016001348A1 (fr) |
| CY (1) | CY1119687T1 (fr) |
| DK (1) | DK3077390T3 (fr) |
| EA (1) | EA030109B1 (fr) |
| ES (1) | ES2651508T3 (fr) |
| HR (1) | HRP20171772T1 (fr) |
| HU (1) | HUE034656T2 (fr) |
| IL (1) | IL245922B (fr) |
| LT (1) | LT3077390T (fr) |
| MA (1) | MA39164B1 (fr) |
| MX (1) | MX362701B (fr) |
| MY (1) | MY176244A (fr) |
| NO (1) | NO3077390T3 (fr) |
| NZ (1) | NZ721493A (fr) |
| PH (1) | PH12016500989B1 (fr) |
| PL (1) | PL3077390T3 (fr) |
| PT (1) | PT3077390T (fr) |
| SA (1) | SA516371248B1 (fr) |
| SG (1) | SG11201604541WA (fr) |
| SI (1) | SI3077390T1 (fr) |
| TW (1) | TWI636982B (fr) |
| UA (1) | UA119151C2 (fr) |
| WO (1) | WO2015083071A1 (fr) |
| ZA (1) | ZA201604501B (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101689093B1 (ko) | 2012-06-04 | 2016-12-22 | 액테리온 파마슈티칼 리미티드 | 벤즈이미다졸-프롤린 유도체 |
| WO2015083070A1 (fr) * | 2013-12-03 | 2015-06-11 | Actelion Pharmaceuticals Ltd | Forme cristalline de (s)-(2-(6-chloro-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone et utilisation de celle-ci en tant qu'antagonistes des recepteurs de l'orexine |
| UA119151C2 (uk) * | 2013-12-03 | 2019-05-10 | Ідорсія Фармасьютікалз Лтд | КРИСТАЛІЧНА СОЛЬОВА ФОРМА (S)-(2-(6-ХЛОР-7-МЕТИЛ-1H-БЕНЗО[d]ІМІДАЗОЛ-2-ІЛ)-2-МЕТИЛПІРОЛІДИН-1-ІЛ)(5-МЕТОКСИ-2-(2H-1,2,3-ТРИАЗОЛ-2-ІЛ)ФЕНІЛ)МЕТАНОНУ ЯК АНТАГОНІСТ ОРЕКСИНОВОГО РЕЦЕПТОРА |
| MX366642B (es) | 2013-12-04 | 2019-07-17 | Idorsia Pharmaceuticals Ltd | Uso de derivados de bencimidazol-prolina. |
| RS62357B1 (sr) | 2017-05-03 | 2021-10-29 | Idorsia Pharmaceuticals Ltd | Dobijanje derivata 2-([1,2,3]triazol-2-il)-benzojeve kiseline |
| PH12022552763A1 (en) | 2020-04-19 | 2024-03-25 | Idorsia Pharmaceuticals Ltd | Medical use of daridorexant |
| WO2023160004A1 (fr) * | 2022-02-25 | 2023-08-31 | 南京知和医药科技有限公司 | Composé à cycle fusionné ayant une activité analgésique, son procédé de préparation et son utilisation |
| CN118724879B (zh) * | 2023-12-19 | 2025-02-11 | 南京知和医药科技有限公司 | 一种氘代稠环化合物及其制备方法与用途 |
| ES3038762A1 (es) | 2024-04-12 | 2025-10-14 | Moehs Iberica Sl | Procedimiento de síntesis de ácido 5-metoxi-2-(2H-1,2,3-triazol-2yl)benzoico, sal sódica de dicho ácido como intermedio de síntesis y uso del ácido o de su sal en la preparación de daridorexant y ciertos intermedios en la síntesis del mismo |
| WO2025253419A1 (fr) * | 2024-06-06 | 2025-12-11 | Msn Laboratories Private Limited, R&D Center | Formes à l'état solide de chlorhydrate de (s)-(2-(5-chloro-4-méthyl-1h-benzo[d]imidazol-2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone et leurs procédés de préparation |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3282927A (en) | 1964-05-21 | 1966-11-01 | Bristol Myers Co | 5-phenyl-4-thiazolylpenicillins |
| WO2001096302A1 (fr) | 2000-06-16 | 2001-12-20 | Smithkline Beecham P.L.C. | Piperidines utiles en tant qu'antagonistes du recepteur d'orexine |
| US20030055037A1 (en) | 2000-10-06 | 2003-03-20 | Delombaert Stephane | Benzimidazole and indole derivatives as CRF receptor modulators |
| AU2002224885A1 (en) | 2000-11-28 | 2002-06-11 | Smithkline Beecham Plc | Morpholine derivatives as antagonists of orexin receptors |
| AR033306A1 (es) | 2001-05-05 | 2003-12-10 | Smithkline Beecham Plc | Compuestos |
| EP1435955A2 (fr) | 2001-05-05 | 2004-07-14 | SmithKline Beecham P.L.C. | Derives d'amines cycliques n-aroyl utilises comme antagonistes du recepteur d'orexine |
| MXPA03011706A (es) | 2001-06-28 | 2004-03-19 | Smithkline Beecham Plc | Derivados de n-aroil-amina ciclica como antagonistas del receptor de orexina. |
| GB0115862D0 (en) | 2001-06-28 | 2001-08-22 | Smithkline Beecham Plc | Compounds |
| GB0124463D0 (en) | 2001-10-11 | 2001-12-05 | Smithkline Beecham Plc | Compounds |
| GB0127145D0 (en) | 2001-11-10 | 2002-01-02 | Smithkline Beecham | Compounds |
| GB0130335D0 (en) | 2001-12-19 | 2002-02-06 | Smithkline Beecham Plc | Compounds |
| GB0130393D0 (en) | 2001-12-19 | 2002-02-06 | Smithkline Beecham Plc | Compounds |
| EP1539747B1 (fr) | 2002-09-18 | 2006-11-02 | Glaxo Group Limited | Amines cycliques n-aroyle utilisees comme antagonistes du recepteur d'orexine |
| GB0225944D0 (en) | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| GB0225938D0 (en) | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| GB0225884D0 (en) | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| RU2378257C2 (ru) | 2004-03-01 | 2010-01-10 | Актелион Фармасьютиклз Лтд | Замещенные производные 1,2,3,4-тетрагидроизохинолина |
| UA93903C2 (ru) | 2006-03-15 | 2011-03-25 | Актелион Фармасьютикалз Лтд | Производные тетрагидроизохинолина для повышения функции памяти |
| WO2007135527A2 (fr) * | 2006-05-23 | 2007-11-29 | Pfizer Products Inc. | Composés de benzimidazolyle |
| US7994336B2 (en) | 2006-08-15 | 2011-08-09 | Actelion Pharmaceuticals Ltd. | Azetidine compounds as orexin receptor antagonists |
| ATE481383T1 (de) | 2006-09-29 | 2010-10-15 | Actelion Pharmaceuticals Ltd | 3-aza-bicycloä3.1.0ühexanderivate |
| PE20081229A1 (es) | 2006-12-01 | 2008-08-28 | Merck & Co Inc | Antagonistas de receptor de orexina de diazepam sustituido |
| CL2007003827A1 (es) | 2006-12-28 | 2008-09-26 | Actelion Pharmaceuticals Ltd | Compuestos derivados de n-(2-aza-biciclo(3.1.0)hex-3-ilmetil)amida; y su uso para prevenir o tratar la depresion, neurosis, esquizofrenia, ansiedad, adicciones, epilepsia, dolor, enfermedades cardiacas, entre otras. |
| WO2008087611A2 (fr) | 2007-01-19 | 2008-07-24 | Actelion Pharmaceuticals Ltd | Dérivés de pyrrolidine et de piperidine |
| CL2008000836A1 (es) | 2007-03-26 | 2008-11-07 | Actelion Pharmaceuticals Ltd | Compuestos derivados de tiazolidina, antagonistas del receptor de orexina; composicion farmaceutica que los comprende; y su uso en el tratamiento de neurosis emocional, depresion grave, trastornos psicoticos, alzheimer, parkinson, dolor, entre otras. |
| DE602008002934D1 (de) | 2007-05-14 | 2010-11-18 | Actelion Pharmaceuticals Ltd | 2-cyclopropylthiazolderivate |
| AU2008260647A1 (en) | 2007-05-23 | 2008-12-11 | Merck Sharp & Dohme Corp. | Cyclopropyl pyrrolidine orexin receptor antagonists |
| CL2008001951A1 (es) | 2007-07-03 | 2009-01-09 | Glaxo Group Ltd | Compuestos derivados de imidazo[1,2-a]pirimidin-2-ilmetil sustituidos; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el trastorno del sueno, depresion, ansiedad, trastorno relacionado con el abuso de sustancias, entre otras. |
| AU2008272449A1 (en) | 2007-07-03 | 2009-01-08 | Actelion Pharmaceuticals Ltd | 3-aza-bicyclo[3.3.0]octane compounds |
| GB0712888D0 (en) | 2007-07-03 | 2007-08-15 | Glaxo Group Ltd | Novel compounds |
| WO2009016560A2 (fr) | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | Dérivés de trans-3-aza-bicyclo[3.1.0]hexane |
| AU2008281399A1 (en) | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo[3.3.0]octane derivatives |
| WO2009040730A2 (fr) | 2007-09-24 | 2009-04-02 | Actelion Pharmaceuticals Ltd | Pyrrolidines et pipéridines en tant qu'antagonistes du récepteur de l'orexine |
| PE20091010A1 (es) | 2007-10-10 | 2009-08-08 | Actelion Pharmaceuticals Ltd | Derivados de tetrahidroquinolina |
| ATE555107T1 (de) | 2008-02-21 | 2012-05-15 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo-ä2,2,1-üheptan-derivate |
| GB0806536D0 (en) | 2008-04-10 | 2008-05-14 | Glaxo Group Ltd | Novel compounds |
| CN102083827A (zh) | 2008-07-07 | 2011-06-01 | 埃科特莱茵药品有限公司 | 作为食欲素受体拮抗剂的噻唑烷化合物 |
| WO2010038200A1 (fr) | 2008-10-01 | 2010-04-08 | Actelion Pharmaceuticals Ltd | Composés d'oxazolidine utilisables en tant qu'antagonistes des récepteurs à orexine |
| EP2358712A1 (fr) | 2008-11-26 | 2011-08-24 | Glaxo Group Limited | Dérivés de la pipéridine utiles en tant qu antagonistes du récepteur de l orexine |
| JP2012509910A (ja) | 2008-11-26 | 2012-04-26 | グラクソ グループ リミテッド | 新規の化合物 |
| WO2010060472A1 (fr) | 2008-11-26 | 2010-06-03 | Glaxo Group Limited | Dérivés de l’imidazopyridazine agissant en tant qu’antagonistes de l’orexine |
| WO2010063662A1 (fr) | 2008-12-02 | 2010-06-10 | Glaxo Group Limited | Dérivés de n-{[(1s,4s,6s)-3-(2-pyridinylcarbonyl)-3-azabicyclo[4.1.0]hept-4-yl]methyl}-2-heteroarylamine et leurs utilisations |
| EP2370426A1 (fr) | 2008-12-02 | 2011-10-05 | Glaxo Group Limited | Dérivés de n-{[(1r,4s,6r)-3-(2-pyridinylcarbonyl)-3-azabicyclo[4.1.0]hept-4-yl]methyl}-2-heteroarylamine et leurs utilisations |
| GB0823467D0 (en) | 2008-12-23 | 2009-01-28 | Glaxo Group Ltd | Novel Compounds |
| EA201171293A1 (ru) | 2009-04-24 | 2012-05-30 | Глэксо Груп Лимитед | 3-азабицикло[4.1.0]гептаны, применяемые в качестве антагонистов орексина |
| KR101802726B1 (ko) | 2010-08-24 | 2017-11-29 | 액테리온 파마슈티칼 리미티드 | 오렉신 수용체 안타고니스트로서의 프롤린 술폰아미드 유도체 |
| EP2638008B1 (fr) | 2010-11-10 | 2015-07-01 | Actelion Pharmaceuticals Ltd | Dérivés de lactame utiles en tant qu'antagonistes du récepteur de l'orexine |
| JP5987005B2 (ja) | 2011-02-18 | 2016-09-06 | アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | オレキシン拮抗薬として有用な新規なピラゾール及びイミダゾール誘導体 |
| EA024106B1 (ru) | 2011-11-08 | 2016-08-31 | Актелион Фармасьютиклз Лтд. | Производные 2-(1,2,3-триазол-2-ил)бензамида и 3-(1,2,3-триазол-2-ил)пиколинамида |
| CA2870024C (fr) * | 2012-04-17 | 2020-04-07 | Gilead Sciences, Inc. | Composes et procedes pour un traitement antiviral |
| KR101689093B1 (ko) * | 2012-06-04 | 2016-12-22 | 액테리온 파마슈티칼 리미티드 | 벤즈이미다졸-프롤린 유도체 |
| JP6244365B2 (ja) | 2012-10-10 | 2017-12-06 | アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | [オルトビ−(ヘテロ−)アリール]−[2−(メタビ−(ヘテロ−)アリール)−ピロリジン−1−イル]−メタノン誘導体であるオレキシン受容体アンタゴニスト |
| CN105051040A (zh) | 2013-03-12 | 2015-11-11 | 埃科特莱茵药品有限公司 | 作为食欲素受体拮抗剂的氮杂环丁烷酰胺衍生物 |
| WO2015083070A1 (fr) | 2013-12-03 | 2015-06-11 | Actelion Pharmaceuticals Ltd | Forme cristalline de (s)-(2-(6-chloro-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone et utilisation de celle-ci en tant qu'antagonistes des recepteurs de l'orexine |
| UA119151C2 (uk) * | 2013-12-03 | 2019-05-10 | Ідорсія Фармасьютікалз Лтд | КРИСТАЛІЧНА СОЛЬОВА ФОРМА (S)-(2-(6-ХЛОР-7-МЕТИЛ-1H-БЕНЗО[d]ІМІДАЗОЛ-2-ІЛ)-2-МЕТИЛПІРОЛІДИН-1-ІЛ)(5-МЕТОКСИ-2-(2H-1,2,3-ТРИАЗОЛ-2-ІЛ)ФЕНІЛ)МЕТАНОНУ ЯК АНТАГОНІСТ ОРЕКСИНОВОГО РЕЦЕПТОРА |
| MX366642B (es) | 2013-12-04 | 2019-07-17 | Idorsia Pharmaceuticals Ltd | Uso de derivados de bencimidazol-prolina. |
-
2014
- 2014-02-12 UA UAA201607115A patent/UA119151C2/uk unknown
- 2014-12-02 EA EA201600436A patent/EA030109B1/ru not_active IP Right Cessation
- 2014-12-02 US US15/101,832 patent/US9790208B2/en active Active
- 2014-12-02 KR KR1020167017678A patent/KR101839716B1/ko active Active
- 2014-12-02 CA CA2929720A patent/CA2929720C/fr active Active
- 2014-12-02 MA MA39164A patent/MA39164B1/fr unknown
- 2014-12-02 JP JP2016536106A patent/JP6091716B2/ja active Active
- 2014-12-02 TW TW103141830A patent/TWI636982B/zh active
- 2014-12-02 NZ NZ721493A patent/NZ721493A/en unknown
- 2014-12-02 SI SI201430453T patent/SI3077390T1/sl unknown
- 2014-12-02 WO PCT/IB2014/066509 patent/WO2015083071A1/fr not_active Ceased
- 2014-12-02 AU AU2014358743A patent/AU2014358743B2/en active Active
- 2014-12-02 LT LTEP14824108.6T patent/LT3077390T/lt unknown
- 2014-12-02 SG SG11201604541WA patent/SG11201604541WA/en unknown
- 2014-12-02 EP EP14824108.6A patent/EP3077390B1/fr active Active
- 2014-12-02 PL PL14824108T patent/PL3077390T3/pl unknown
- 2014-12-02 DK DK14824108.6T patent/DK3077390T3/da active
- 2014-12-02 MX MX2016007216A patent/MX362701B/es active IP Right Grant
- 2014-12-02 ES ES14824108.6T patent/ES2651508T3/es active Active
- 2014-12-02 PT PT148241086T patent/PT3077390T/pt unknown
- 2014-12-02 CN CN201480065749.2A patent/CN105793258B/zh active Active
- 2014-12-02 NO NO14824108A patent/NO3077390T3/no unknown
- 2014-12-02 MY MYPI2016701995A patent/MY176244A/en unknown
- 2014-12-02 HR HRP20171772TT patent/HRP20171772T1/hr unknown
- 2014-12-02 HU HUE14824108A patent/HUE034656T2/hu unknown
-
2016
- 2016-05-26 PH PH12016500989A patent/PH12016500989B1/en unknown
- 2016-05-30 IL IL24592216A patent/IL245922B/en active IP Right Grant
- 2016-06-01 SA SA516371248A patent/SA516371248B1/ar unknown
- 2016-06-02 CL CL2016001348A patent/CL2016001348A1/es unknown
- 2016-07-01 ZA ZA2016/04501A patent/ZA201604501B/en unknown
-
2017
- 2017-09-12 US US15/702,281 patent/US10023560B2/en active Active
- 2017-12-12 CY CY20171101302T patent/CY1119687T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA39164B1 (fr) | Forme de sel cristalline de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone comme antagoniste des récepteurs à l'oréxine | |
| MA39163A1 (fr) | Forme cristalline de (s)-(2-(6-chloro-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone et utilisation de celle-ci en tant qu'antagonistes des recepteurs de l'orexine | |
| CY1123365T1 (el) | Ενωσεις που εχουν δραστικοτητα ανταγωνιστη μουσκαρινικου υποδοχεα και αγωνιστη βητα2 αδρενεργικου υποδοχεα | |
| MA39211B1 (fr) | Composés tricycliques comme agents anti-cancers | |
| DOP2010000326A (es) | Compuestos de tiazol y oxazol de bencen-sulfonamida | |
| UA100877C2 (ru) | Замещенные спироциклические производные пиперидина как лиганды рецепторов гистамина-3 (h3) | |
| MX367879B (es) | N-alquil 2-(disustituido)alquiladenosin-5-uronamidas como agonistas a2a. | |
| MA40219A (fr) | Sels cristallins de (s)-6-((1-acétylpipéridin-4-yl)amino)-n-(3-(3,4-dihydroisoquinolin-2(1h)-yl)-2-hydroxypropyl)pyrimidine-4-carboxamide | |
| PH12017501424B1 (en) | Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity | |
| PE20151535A1 (es) | Derivado de dihidropiridazin-3,5-diona | |
| MA35107B1 (fr) | Composition pharmaceutique antihypertensive | |
| EA201692220A1 (ru) | Твердые формы противовирусного соединения | |
| MA32224B1 (fr) | Derives de (pyrazolyl-carbonyl) imidazolidinone pour le traitement de maladies retrovirales | |
| TR201719911A2 (tr) | Raloksi̇fen ve en az bi̇r anti̇psi̇koti̇k ajan i̇çeren kompozi̇syon | |
| MA50899B1 (fr) | Composés utiles pour l'inhibition de cdk7 | |
| UA101367C2 (en) | Normal;heading 1;heading 2;heading 3;HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS | |
| TN2013000429A1 (en) | Compounds having muscarinic receptor antagonist and beta2 adrenergic receptor agonist activity |