CL2008001951A1 - 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. - Google Patents
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.Info
- Publication number
- CL2008001951A1 CL2008001951A1 CL2008001951A CL2008001951A CL2008001951A1 CL 2008001951 A1 CL2008001951 A1 CL 2008001951A1 CL 2008001951 A CL2008001951 A CL 2008001951A CL 2008001951 A CL2008001951 A CL 2008001951A CL 2008001951 A1 CL2008001951 A1 CL 2008001951A1
- Authority
- CL
- Chile
- Prior art keywords
- compound
- pyrimidin
- ylmethyl
- anxiety
- depression
- Prior art date
Links
Classifications
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61P25/20—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
- A61P25/24—Antidepressants
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
Abstract
Compuestos derivados de imidazo[1,2-a]pirimidin-2-ilmetil sustituidos; composición farmacéutica que comprende a dicho compuesto; y uso del compuesto para el trastorno del sueno, depresión, ansiedad, trastorno relacionado con el abuso de sustancias, entre otras.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0712887A GB0712887D0 (en) | 2007-07-03 | 2007-07-03 | Novel compounds |
GB0804317A GB0804317D0 (en) | 2008-03-07 | 2008-03-07 | Novel compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2008001951A1 true CL2008001951A1 (es) | 2009-01-09 |
Family
ID=39789338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2008001951A CL2008001951A1 (es) | 2007-07-03 | 2008-07-01 | 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. |
Country Status (18)
Country | Link |
---|---|
US (2) | US20120095034A1 (es) |
EP (1) | EP2176258A1 (es) |
JP (1) | JP2010531848A (es) |
KR (1) | KR20100030635A (es) |
CN (1) | CN101796053A (es) |
AR (1) | AR067396A1 (es) |
AU (1) | AU2008270294A1 (es) |
BR (1) | BRPI0812981A2 (es) |
CA (1) | CA2691638A1 (es) |
CL (1) | CL2008001951A1 (es) |
CO (1) | CO6270320A2 (es) |
DO (1) | DOP2009000293A (es) |
EA (1) | EA201070091A1 (es) |
IL (1) | IL202665A0 (es) |
MA (1) | MA31470B1 (es) |
PE (1) | PE20090441A1 (es) |
TW (1) | TW200911242A (es) |
WO (1) | WO2009003993A1 (es) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009016564A2 (en) * | 2007-07-27 | 2009-02-05 | Actelion Pharmaceuticals Ltd | 2-aza-bicyclo[3.3.0]octane derivatives |
EP2207778A2 (en) * | 2007-09-24 | 2010-07-21 | Actelion Pharmaceuticals Ltd. | Pyrrolidines and piperidines as orexin receptor antagonists |
JP2011512400A (ja) * | 2008-02-21 | 2011-04-21 | アクテリオン ファーマシューティカルズ リミテッド | 2−アザ−ビシクロ[2.2.1]ヘプタン誘導体 |
WO2009133522A1 (en) * | 2008-04-30 | 2009-11-05 | Actelion Pharmaceuticals Ltd | Piperidine and pyrrolidine compounds |
US8129384B2 (en) * | 2008-10-09 | 2012-03-06 | Glaxo Group Limited | Imidazo[1,2-a]pyrazines as orexin receptor antagonists |
US8093255B2 (en) | 2008-10-09 | 2012-01-10 | Glaxo Group Limited | Imidazo[1,2-A]pyrimidines as orexin receptor antagonists |
JP2012509912A (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 |
JP2012509911A (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 |
EP2358711A1 (en) * | 2008-11-26 | 2011-08-24 | Glaxo Group Limited | Piperidine derivatives useful as orexin receptor antagonists |
TW201031407A (en) | 2008-12-02 | 2010-09-01 | Glaxo Group Ltd | Novel compounds |
GB0823467D0 (en) * | 2008-12-23 | 2009-01-28 | Glaxo Group Ltd | Novel Compounds |
EP2421850A1 (en) | 2009-04-24 | 2012-02-29 | Glaxo Group Limited | 3 -azabicyclo [4.1.0]heptanes used as orexin antagonists |
EP2491038B1 (en) | 2009-10-23 | 2016-04-06 | Janssen Pharmaceutica N.V. | Disubstituted octahy - dropyrrolo [3,4-c]pyrroles as orexin receptor modulators |
WO2011076744A1 (en) * | 2009-12-21 | 2011-06-30 | Novartis Ag | Disubstituted heteroaryl-fused pyridines |
WO2011138266A1 (en) * | 2010-05-03 | 2011-11-10 | Evotec Ag | Indolizine and imidazopyridine derivatives as orexin receptor antagonists |
CN103201261A (zh) * | 2010-11-10 | 2013-07-10 | 埃科特莱茵药品有限公司 | 用作为食欲素受体拮抗剂的内酰胺衍生物 |
WO2012089607A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Novel compounds with a 3a-azabicyclo [4.1.0] heptane core acting on orexin receptors |
WO2012089606A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Azabicyclo [4.1.0] hept - 4 - yl derivatives as human orexin receptor antagonists |
GB201101678D0 (en) | 2011-02-01 | 2011-03-16 | Rolls Royce Plc | A cooling arrangement for a magnetic gearbox |
MY169986A (en) | 2012-06-04 | 2019-06-19 | Idorsia Pharmaceuticals Ltd | Benzimidazole-proline derivatives |
CA2885180C (en) | 2012-10-10 | 2021-03-02 | Actelion Pharmaceuticals Ltd | Orexin receptor antagonists which are [ortho bi-(hetero-)aryl]-[2-(meta bi-(hetero-)aryl)-pyrrolidin-1-yl]-methanone derivatives |
EP2970241A1 (en) | 2013-03-12 | 2016-01-20 | Actelion Pharmaceuticals Ltd. | Azetidine amide derivatives as orexin receptor antagonists |
GB201318222D0 (en) * | 2013-10-15 | 2013-11-27 | Takeda Pharmaceutical | Novel compounds |
DK3077389T3 (da) | 2013-12-03 | 2017-11-13 | Idorsia Pharmaceuticals Ltd | Krystallinsk form af (s)-(2-(6-chlor-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1-yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanon og dens anvendelse som orexinreceptorantagonister |
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 |
US9914721B2 (en) | 2013-12-04 | 2018-03-13 | Idorsia Pharmaceuticals Ltd | Use of benzimidazole-proline derivatives |
TW201613864A (en) * | 2014-02-20 | 2016-04-16 | Takeda Pharmaceutical | Novel compounds |
US10370380B2 (en) | 2015-11-23 | 2019-08-06 | Sunshine Lake Pharma Co., Ltd. | Octahydropyrrolo[3,4-c]pyrrole derivatives and uses thereof |
SI3426251T1 (sl) | 2016-03-10 | 2022-07-29 | Janssen Pharmaceutica Nv | Postopki za zdravljenje depresije z antagonisti receptorja oreksina-2 |
US20190151304A1 (en) | 2016-05-10 | 2019-05-23 | Inserm (Institut National De La Santé Et De La Rechercjae Médicale | Methods and pharmaceutical compositions for the treatment of autoimmune inflammatory |
WO2020007964A1 (en) | 2018-07-05 | 2020-01-09 | Idorsia Pharmaceuticals Ltd | 2-(2-azabicyclo[3.1.0]hexan-1-yl)-1h-benzimidazole derivatives |
WO2020099511A1 (en) | 2018-11-14 | 2020-05-22 | Idorsia Pharmaceuticals Ltd | Benzimidazole-2-methyl-morpholine derivatives |
WO2023218023A1 (en) | 2022-05-13 | 2023-11-16 | Idorsia Pharmaceuticals Ltd | Thiazoloaryl-methyl substituted cyclic hydrazine-n-carboxamide derivatives |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20040029326A (ko) * | 2001-06-28 | 2004-04-06 | 스미스클라인비이참피이엘시이 | 오렉신 수용체 길항제로서의 n-아로일 시클릭 아민 유도체 |
-
2008
- 2008-07-01 TW TW097124654A patent/TW200911242A/zh unknown
- 2008-07-01 AU AU2008270294A patent/AU2008270294A1/en not_active Abandoned
- 2008-07-01 EP EP08785891A patent/EP2176258A1/en not_active Withdrawn
- 2008-07-01 US US12/664,945 patent/US20120095034A1/en not_active Abandoned
- 2008-07-01 US US12/165,894 patent/US20090022670A1/en not_active Abandoned
- 2008-07-01 JP JP2010513961A patent/JP2010531848A/ja active Pending
- 2008-07-01 CA CA002691638A patent/CA2691638A1/en not_active Abandoned
- 2008-07-01 AR ARP080102851A patent/AR067396A1/es not_active Application Discontinuation
- 2008-07-01 CL CL2008001951A patent/CL2008001951A1/es unknown
- 2008-07-01 KR KR1020097027582A patent/KR20100030635A/ko not_active Application Discontinuation
- 2008-07-01 BR BRPI0812981-9A2A patent/BRPI0812981A2/pt not_active IP Right Cessation
- 2008-07-01 PE PE2008001119A patent/PE20090441A1/es not_active Application Discontinuation
- 2008-07-01 WO PCT/EP2008/058423 patent/WO2009003993A1/en active Application Filing
- 2008-07-01 EA EA201070091A patent/EA201070091A1/ru unknown
- 2008-07-01 CN CN200880105361A patent/CN101796053A/zh active Pending
-
2009
- 2009-12-10 IL IL202665A patent/IL202665A0/en unknown
- 2009-12-29 DO DO2009000293A patent/DOP2009000293A/es unknown
- 2009-12-30 CO CO09149373A patent/CO6270320A2/es not_active Application Discontinuation
- 2009-12-30 MA MA32459A patent/MA31470B1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
CN101796053A (zh) | 2010-08-04 |
DOP2009000293A (es) | 2010-03-31 |
BRPI0812981A2 (pt) | 2014-12-16 |
WO2009003993A1 (en) | 2009-01-08 |
AR067396A1 (es) | 2009-10-07 |
JP2010531848A (ja) | 2010-09-30 |
TW200911242A (en) | 2009-03-16 |
PE20090441A1 (es) | 2009-05-08 |
IL202665A0 (en) | 2010-06-30 |
AU2008270294A1 (en) | 2009-01-08 |
MA31470B1 (fr) | 2010-06-01 |
KR20100030635A (ko) | 2010-03-18 |
CO6270320A2 (es) | 2011-04-20 |
EP2176258A1 (en) | 2010-04-21 |
EA201070091A1 (ru) | 2010-06-30 |
US20090022670A1 (en) | 2009-01-22 |
US20120095034A1 (en) | 2012-04-19 |
CA2691638A1 (en) | 2009-01-08 |
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