WO2007039781A3 - 1,2,4-oxadioi.e derivatives with activity at the metabotropic clutamate receptors - Google Patents
1,2,4-oxadioi.e derivatives with activity at the metabotropic clutamate receptors 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
The present invention relates to new compounds of formula (I) wherein Y1 and Y2 selected from the group consisting of hydrogen, halogen atom; C1-4 alkyl, C1-4 alkoxy, cyano and trifluoromethyl group, Q is -CH- group or N; X1 and X2 are different and are independently selected from N and O; Z is -(CH2)n- group or S; n is 1 or 2; R is selected from the group consisting of optionally substituted C1-7 alkyl, C1-4 haloalkyl, C1-4 hydroxyalkyl, C1-4 cyanoalkyl, C1-3 OC1-3 alkyl, C2-7 alkenyl, C2-7 alkynyl, C0-2(NR1R2)alkyl; an optionally substituted C3-7 cycloalkyl, aryl, heteroaryl or saturated heterocyclyl; R1 and R2 are independently selected from hydrogen, C1-7 alkyl or C1-6 alkanoyl group - and/or enentiomers and/or racemates and/or diastereomers and/or geometric isomers and/or pharmaceutically acceptable salts thereof formed with acids and bases, to the processes for producing said compounds, to pharmaceutical compositions containing said compounds and to their use in the prevention and/or treatment of mGluR5 receptor-mediated disorders.
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 (en) | 2007-04-12 |
| WO2007039781A3 true WO2007039781A3 (en) | 2010-08-26 |
Family
ID=89986317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/HU2006/000087 Ceased WO2007039781A2 (en) | 2005-10-05 | 2006-10-05 | New compounds |
Country Status (2)
| Country | Link |
|---|---|
| HU (1) | HUP0500920A2 (en) |
| WO (1) | WO2007039781A2 (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2672616A1 (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 |
| CA2758731A1 (en) * | 2009-04-23 | 2010-10-28 | Merck Sharp & Dohme Corp. | 2-alkyl piperidine mglur5 receptor modulators |
| CA2808582A1 (en) | 2009-08-14 | 2011-02-17 | University Of Virginia Patent Foundation | Imidamide sphingosine kinase inhibitors |
| WO2011082010A1 (en) * | 2009-12-29 | 2011-07-07 | Eli Lilly And Company | Tetrahydrotriazolopyridine compounds as selective mglu5 receptor potentiators useful for the treatment of schizophrenia |
| JP2013518085A (en) | 2010-02-01 | 2013-05-20 | ノバルティス アーゲー | Pyrazolo [5,1b] oxazole derivatives as CRF-1 receptor antagonists |
| WO2011092293A2 (en) | 2010-02-01 | 2011-08-04 | Novartis Ag | Cyclohexyl amide derivatives as crf receptor antagonists |
| CN102753527B (en) | 2010-02-02 | 2014-12-24 | 诺华股份有限公司 | Cyclohexyl amide derivatives as crf receptor antagonists |
| CN103313977B (en) * | 2010-10-21 | 2015-06-03 | 拜耳知识产权有限责任公司 | 1-(Heterocyclic carbonyl)piperidine |
| AR091257A1 (en) | 2012-06-04 | 2015-01-21 | Actelion Pharmaceuticals Ltd | BENCIMIDAZOL-PROLINA DERIVATIVES |
| EA201500399A1 (en) | 2012-10-10 | 2015-09-30 | Актелион Фармасьютиклз Лтд. | OREXIN RECEPTOR ANTAGONISTS, WHICH ARE REPRESENTING DERIVATIVES OF [ORTO-BI- (HETERO) ARYL] - [2- (META-BI- (HETERO) ARYL) PYRROLIDIN-1-IL] METHANON |
| EP2970241A1 (en) | 2013-03-12 | 2016-01-20 | Actelion Pharmaceuticals Ltd. | Azetidine amide derivatives as orexin receptor antagonists |
| DK3077391T3 (en) | 2013-12-04 | 2018-10-22 | Idorsia Pharmaceuticals Ltd | USE OF BENZIMIDAZOLE PROLINE DERIVATIVES |
| EP3914592A1 (en) * | 2019-01-25 | 2021-12-01 | University of Virginia Patent Foundation | Inhibitors of spinster homolog 2 (spns2) for use in therapy |
| KR20220085798A (en) * | 2019-10-17 | 2022-06-22 | 지보당 에스아 | Substituted azacycles as TRMP8 modulators |
| GB202012170D0 (en) * | 2020-08-05 | 2020-09-16 | Givaudan Sa | Organic compounds |
| EP4210824A1 (en) * | 2020-09-09 | 2023-07-19 | University of Virginia Patent Foundation | Inhibitors of spinster homolog 2 (spns2) for use in therapy |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998017652A1 (en) * | 1996-10-18 | 1998-04-30 | Boehringer Ingelheim Pharma Kg | Oxadiazoles, processes for their preparation and their use as medicaments |
| WO2000039125A1 (en) * | 1998-12-23 | 2000-07-06 | Pfizer Limited | Piperidines as ccr5 modulators |
| WO2002092086A1 (en) * | 2001-03-27 | 2002-11-21 | F. Hoffmann-La Roche Ag | Imidazo (1,2-a)-pyridine derivatives as mglur5 antagonists |
| WO2004014902A2 (en) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors |
| WO2005044797A1 (en) * | 2003-11-06 | 2005-05-19 | Addex Pharmaceuticals Sa | Allosteric modulators of metabotropic glutamate receptors |
-
2005
- 2005-10-05 HU HU0500920A patent/HUP0500920A2/en unknown
-
2006
- 2006-10-05 WO PCT/HU2006/000087 patent/WO2007039781A2/en not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998017652A1 (en) * | 1996-10-18 | 1998-04-30 | Boehringer Ingelheim Pharma Kg | Oxadiazoles, processes for their preparation and their use as medicaments |
| WO2000039125A1 (en) * | 1998-12-23 | 2000-07-06 | Pfizer Limited | Piperidines as ccr5 modulators |
| WO2002092086A1 (en) * | 2001-03-27 | 2002-11-21 | F. Hoffmann-La Roche Ag | Imidazo (1,2-a)-pyridine derivatives as mglur5 antagonists |
| WO2004014902A2 (en) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors |
| WO2005044797A1 (en) * | 2003-11-06 | 2005-05-19 | Addex Pharmaceuticals Sa | Allosteric modulators of metabotropic glutamate receptors |
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 (en) | 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 |
Ref country code: DE |
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| 122 | Ep: pct application non-entry in european phase |
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