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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (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 |
|---|---|---|---|
| HU0500920A HUP0500920A2 (en) | 2005-10-05 | 2005-10-05 | Oxadiazole derivatives, process for their preparation and their use |
| HUP0500920 | 2005-10-05 |
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 (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0720043A2 (pt) | 2006-12-15 | 2014-01-07 | Abbott Lab | Composto oxadiazol |
| US8349852B2 (en) | 2009-01-13 | 2013-01-08 | Novartis Ag | Quinazolinone derivatives useful as vanilloid antagonists |
| US20120040998A1 (en) * | 2009-04-23 | 2012-02-16 | Mercer Swati P | 2-alkyl piperidine mglur5 receptor modulators |
| US9421177B2 (en) | 2009-08-14 | 2016-08-23 | University Of Virginia Patent Foundation | Imidamide sphingosine kinase inhibitors |
| WO2011082010A1 (fr) * | 2009-12-29 | 2011-07-07 | Eli Lilly And Company | Composés de tétrahydrotriazolopyridine en tant que potentialisateurs sélectifs de récepteur mglu5 utiles pour le traitement de la schizophrénie |
| AR080055A1 (es) | 2010-02-01 | 2012-03-07 | Novartis Ag | Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de los receptores 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 |
| WO2011095450A1 (fr) | 2010-02-02 | 2011-08-11 | Novartis Ag | Dérivés de cyclohexylamide à titre d'antagonistes du récepteur crf |
| US9545105B2 (en) | 2010-10-21 | 2017-01-17 | Bayer Intellectual Property Gmbh | 1-(heterocyclic carbonyl) piperidines |
| PT2855453T (pt) | 2012-06-04 | 2017-03-09 | Actelion Pharmaceuticals Ltd | Derivados de benzimidazol-prolina |
| AU2013328301A1 (en) * | 2012-10-10 | 2015-05-28 | Actelion Pharmaceuticals Ltd | Orexin receptor antagonists which are [ortho bi (hetero-)aryl]-[2-(meta bi (hetero-)aryl)-pyrrolidin-1-yl]-methanone derivatives |
| 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 |
| MX366642B (es) | 2013-12-04 | 2019-07-17 | Idorsia Pharmaceuticals Ltd | Uso de derivados de bencimidazol-prolina. |
| WO2020154431A1 (fr) * | 2019-01-25 | 2020-07-30 | Lynch Kevin R | Inhibiteurs de l'homologue 2 de spinster (spns2) destinés à être utilisés en thérapie |
| KR20220085798A (ko) * | 2019-10-17 | 2022-06-22 | 지보당 에스아 | Trmp8 조절제로서의 치환된 아자사이클 |
| GB202012170D0 (en) * | 2020-08-05 | 2020-09-16 | Givaudan Sa | Organic compounds |
| US20230373937A1 (en) * | 2020-09-09 | 2023-11-23 | University Of Virginia Patent Foundation | Inhibitors of spinster homolog 2 (spns2) for use in therapy |
| CN119317620A (zh) | 2022-06-13 | 2025-01-14 | 亚力维克希斯股份有限公司 | 氮杂环烷基羰基环状胺化合物 |
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 |
|---|---|
| WO2007039781A2 (fr) | 2007-04-12 |
| HU0500920D0 (en) | 2005-12-28 |
| 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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