WO2007039781A3 - Nouveaux composes - Google Patents
Nouveaux composes Download PDFInfo
- Publication number
- WO2007039781A3 WO2007039781A3 PCT/HU2006/000087 HU2006000087W WO2007039781A3 WO 2007039781 A3 WO2007039781 A3 WO 2007039781A3 HU 2006000087 W HU2006000087 W HU 2006000087W WO 2007039781 A3 WO2007039781 A3 WO 2007039781A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- alkyl
- compounds
- oxadioi
- clutamate
- 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
- 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
- C07D417/14—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 three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'invention concerne de nouveaux composés de formule (I) dans laquelle Y1 et Y2 sont sélectionnés dans le groupe constitué par hydrogène, atome halogène; C1-4 alkyle, C1-4 alkoxy, cyano et un groupe trifluorométhyle, Q représente le groupe -CH- ou N; X1 et X2 sont différents et sont sélectionnés indépendamment dans le groupe N et O; Z désigne le groupe -(CH2)n- ou S; n est égal à 1 ou à 2; R est sélectionné dans le groupe constitué par C1-7 alkyle, C1-4 haloalkyle, C1-4 hydroxyalkyle, C1-4 cyanoalkyle, C1-3 OC1-3 alkyle, C2-7 alcényle, C2-7 alkynyle, C0-2(NR1R2)alkyle éventuellement substitués; par un cycloalkyle éventuellement substitué en C3-7, aryle, hétéroaryle ou hétérocyclyle saturés; R1 et R2 sont sélectionnés indépendamment dans le groupe constitué par hydrogène, C1-7 alkyle ou C1-6 alkanoyle; par des énantiomères et/ou des racémates et/ou des diastéréoisomères et/ou des isomères géométriques et/ou des sels pharmaceutiquement acceptables formés d'acides et de bases; l'invention concerne également des procédés de production desdits composés, des compositions pharmaceutiques renfermant lesdits composés et leur utilisation dans la prévention et/ou le traitement de troubles induits par le récepteur de mGluR5.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HUP0500920 | 2005-10-05 | ||
| HU0500920A HUP0500920A2 (en) | 2005-10-05 | 2005-10-05 | Oxadiazole derivatives, process for their preparation and their use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2007039781A2 WO2007039781A2 (fr) | 2007-04-12 |
| WO2007039781A3 true WO2007039781A3 (fr) | 2010-08-26 |
Family
ID=89986317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/HU2006/000087 Ceased WO2007039781A2 (fr) | 2005-10-05 | 2006-10-05 | Nouveaux composes |
Country Status (2)
| Country | Link |
|---|---|
| HU (1) | HUP0500920A2 (fr) |
| WO (1) | WO2007039781A2 (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2007334436A1 (en) | 2006-12-15 | 2008-06-26 | Abbott Laboratories | Novel oxadiazole compounds |
| US8349852B2 (en) | 2009-01-13 | 2013-01-08 | Novartis Ag | Quinazolinone derivatives useful as vanilloid antagonists |
| EP2421370A4 (fr) * | 2009-04-23 | 2012-12-12 | Merck Sharp & Dohme | Modulateurs du récepteur mglur5 fourrés de 2-alkyl pipéridines |
| WO2011020116A1 (fr) | 2009-08-14 | 2011-02-17 | University Of Virginia Patent Foundation | Imidamides inhibiteurs de sphingosine kinase |
| JP5775094B2 (ja) * | 2009-12-29 | 2015-09-09 | イーライ リリー アンド カンパニー | 統合失調症の処置に有用な選択的mGlu5受容体増強因子としてのテトラヒドロトリアゾロピリジン化合物 |
| WO2011092290A1 (fr) | 2010-02-01 | 2011-08-04 | Novartis Ag | Dérivés de pyrazolo[5,1-b] utilisés en tant qu'antagonistes du récepteur de crf-1 |
| WO2011092293A2 (fr) | 2010-02-01 | 2011-08-04 | Novartis Ag | Dérivés de cyclohexylamide utilisés en tant qu'antagonistes du récepteur du crf |
| ES2527849T3 (es) | 2010-02-02 | 2015-01-30 | Novartis Ag | Derivados de ciclohexilamida como antagonistas del receptor de CRF |
| CN103313977B (zh) * | 2010-10-21 | 2015-06-03 | 拜耳知识产权有限责任公司 | 1-(杂环羰基)哌啶 |
| JP5814491B2 (ja) | 2012-06-04 | 2015-11-17 | 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 | ベンズイミダゾール−プロリン誘導体 |
| WO2014057435A1 (fr) * | 2012-10-10 | 2014-04-17 | Actelion Pharmaceuticals Ltd | Antagonistes des récepteurs de l'orexine, qui sont des dérivés [ortho bi (hetero )aryl]-[2-(meta bi (hetero )aryl)-pyrrolidin-1-yl]-methanone |
| JP2016510810A (ja) | 2013-03-12 | 2016-04-11 | 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 | オレキシン受容体アンタゴニストとしてのアゼチジンアミド誘導体 |
| LT3077391T (lt) | 2013-12-04 | 2018-10-25 | Idorsia Pharmaceuticals Ltd | Benzimidazolo prolino darinių panaudojimas |
| US20220089581A1 (en) * | 2019-01-25 | 2022-03-24 | University Of Virginia Patent Foundation | Inhibitors of spinster homolog 2 (spns2) for use in therapy |
| MX2022003494A (es) * | 2019-10-17 | 2022-04-25 | Givaudan Sa | Azacilos sustituidos como moduladores del miembro 8 de melastatina de potencial receptor transitorio (trmp8). |
| GB202012170D0 (en) * | 2020-08-05 | 2020-09-16 | Givaudan Sa | Organic compounds |
| WO2022056042A1 (fr) * | 2020-09-09 | 2022-03-17 | University Of Virginia Patent Foundation | Inhibiteurs de l'homologue de spinster 2 (spns2) à utiliser en thérapie |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998017652A1 (fr) * | 1996-10-18 | 1998-04-30 | Boehringer Ingelheim Pharma Kg | Oxadiazoles, procedes permettant de les preparer et leur utilisation comme medicaments |
| WO2000039125A1 (fr) * | 1998-12-23 | 2000-07-06 | Pfizer Limited | Piperidines utilises comme modulateurs de ccr5 |
| WO2002092086A1 (fr) * | 2001-03-27 | 2002-11-21 | F. Hoffmann-La Roche Ag | Derives d'imidazo (1,2-a)-pyridine tenant lieu d'antagonistes mglur5 |
| WO2004014902A2 (fr) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Nouveaux composes |
| WO2005044797A1 (fr) * | 2003-11-06 | 2005-05-19 | Addex Pharmaceuticals Sa | Modulateurs allosteriques de recepteurs glutamate metabotropiques |
-
2005
- 2005-10-05 HU HU0500920A patent/HUP0500920A2/hu unknown
-
2006
- 2006-10-05 WO PCT/HU2006/000087 patent/WO2007039781A2/fr not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998017652A1 (fr) * | 1996-10-18 | 1998-04-30 | Boehringer Ingelheim Pharma Kg | Oxadiazoles, procedes permettant de les preparer et leur utilisation comme medicaments |
| WO2000039125A1 (fr) * | 1998-12-23 | 2000-07-06 | Pfizer Limited | Piperidines utilises comme modulateurs de ccr5 |
| WO2002092086A1 (fr) * | 2001-03-27 | 2002-11-21 | F. Hoffmann-La Roche Ag | Derives d'imidazo (1,2-a)-pyridine tenant lieu d'antagonistes mglur5 |
| WO2004014902A2 (fr) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Nouveaux composes |
| WO2005044797A1 (fr) * | 2003-11-06 | 2005-05-19 | Addex Pharmaceuticals Sa | Modulateurs allosteriques de recepteurs glutamate metabotropiques |
Non-Patent Citations (1)
| Title |
|---|
| BING YAN ET AL.: "Quality control on combinatorial chemistry:", JOURNAL OF COMBINATORIAL CHEMISTRY, vol. 5, no. 5, 2003, pages 547 - 559, XP002413033 * |
Also Published As
| Publication number | Publication date |
|---|---|
| HU0500920D0 (en) | 2005-12-28 |
| WO2007039781A2 (fr) | 2007-04-12 |
| HUP0500920A2 (en) | 2007-07-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| NENP | Non-entry into the national phase |
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| 122 | Ep: pct application non-entry in european phase |
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