BRPI0709633B8 - derivados de piridina e pirimidina como antagonistas de mglur2, composição farmacêutica e uso dos mesmos - Google Patents
derivados de piridina e pirimidina como antagonistas de mglur2, composição farmacêutica e uso dos mesmosInfo
- Publication number
- BRPI0709633B8 BRPI0709633B8 BRPI0709633A BRPI0709633A BRPI0709633B8 BR PI0709633 B8 BRPI0709633 B8 BR PI0709633B8 BR PI0709633 A BRPI0709633 A BR PI0709633A BR PI0709633 A BRPI0709633 A BR PI0709633A BR PI0709633 B8 BRPI0709633 B8 BR PI0709633B8
- Authority
- BR
- Brazil
- Prior art keywords
- pyridine
- pharmaceutical composition
- pyrimidine derivatives
- mglur2 antagonists
- antagonists
- Prior art date
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- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
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Abstract
derivados de piridina e pirimidina como antagonistas de mgiur2 composição farmacêutica e uso dos mesmos. a presente invenção refere-se a compostos de fórmula (i), um processo para a fabricação destes, seu uso para a preparação de medicamentos para tratar distúrbios do cns e composições farmacêuticas contendo-os: em que a, b, x, y, r^ 1^, r^ 2^, r^ 3^ e r^ 4^ são como definido na descrição e reivindicações.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06111939 | 2006-03-29 | ||
| EP06111939.2 | 2006-03-29 | ||
| PCT/EP2007/052560 WO2007110337A1 (en) | 2006-03-29 | 2007-03-19 | Pyridine and pyrimidine derivatives as mglur2 antagonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| BRPI0709633A2 BRPI0709633A2 (pt) | 2011-07-19 |
| BRPI0709633B1 BRPI0709633B1 (pt) | 2020-03-03 |
| BRPI0709633B8 true BRPI0709633B8 (pt) | 2021-05-25 |
Family
ID=36862654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0709633A BRPI0709633B8 (pt) | 2006-03-29 | 2007-03-19 | derivados de piridina e pirimidina como antagonistas de mglur2, composição farmacêutica e uso dos mesmos |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US7642264B2 (pt) |
| EP (2) | EP2468727A1 (pt) |
| JP (2) | JP5249919B2 (pt) |
| KR (2) | KR101156897B1 (pt) |
| CN (2) | CN102516161A (pt) |
| AR (1) | AR060173A1 (pt) |
| AU (1) | AU2007229552C1 (pt) |
| BR (1) | BRPI0709633B8 (pt) |
| CA (1) | CA2646732C (pt) |
| CY (1) | CY1116027T1 (pt) |
| DK (1) | DK2001849T3 (pt) |
| ES (1) | ES2529457T3 (pt) |
| IL (1) | IL194039A (pt) |
| MX (1) | MX2008012413A (pt) |
| NO (1) | NO344319B1 (pt) |
| PL (1) | PL2001849T3 (pt) |
| PT (1) | PT2001849E (pt) |
| RU (1) | RU2451673C2 (pt) |
| SI (1) | SI2001849T1 (pt) |
| TW (1) | TWI410414B (pt) |
| WO (1) | WO2007110337A1 (pt) |
| ZA (1) | ZA200808191B (pt) |
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| US20130137865A1 (en) * | 2010-08-11 | 2013-05-30 | Taisho Pharmaceutical Co., Ltd. | Heteroaryl-pyrazole derivative |
| JP5809157B2 (ja) | 2010-10-08 | 2015-11-10 | 持田製薬株式会社 | 環状アミド誘導体 |
| KR101802008B1 (ko) * | 2010-12-21 | 2017-11-27 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 피리미딘 화합물을 포함하는 전자 소자 |
| JP2014062047A (ja) * | 2011-01-21 | 2014-04-10 | Taisho Pharmaceutical Co Ltd | ピラゾール誘導体 |
| CN102336720B (zh) * | 2011-03-02 | 2016-01-13 | 华中科技大学 | 2-氨基噻唑衍生物及制备方法和应用 |
| JPWO2012147516A1 (ja) | 2011-04-28 | 2014-07-28 | 持田製薬株式会社 | 環状アミド誘導体 |
| CN102351854B (zh) * | 2011-07-29 | 2014-06-04 | 华中科技大学 | 氨基噻唑衍生物及制备方法和医药用途 |
| EP2666775A1 (en) | 2012-05-21 | 2013-11-27 | Domain Therapeutics | Substituted pyrazoloquinazolinones and pyrroloquinazolinones as allosteric modulators of group II metabotropic glutamate receptors |
| LT6064B (lt) | 2012-10-15 | 2014-08-25 | Vilniaus Universitetas | Fluorinti benzensulfonamidai kaip karboanhidrazės inhibitoriai |
| CN104736140A (zh) * | 2012-10-23 | 2015-06-24 | 霍夫曼-拉罗奇有限公司 | 用于治疗自闭症的mGlu2/3拮抗剂 |
| EP2951157A1 (en) * | 2013-02-04 | 2015-12-09 | Merck Patent GmbH | Positive allosteric modulators of mglur3 |
| TW201609710A (zh) * | 2013-12-10 | 2016-03-16 | 杜邦股份有限公司 | 除草用經取代嘧啶氧基苯化合物 |
| CA2934891C (en) | 2014-01-16 | 2023-02-28 | Nicholas Ryan DEPREZ | Pyrimidinyloxy benzene derivatives as herbicides |
| EP3129025B1 (en) * | 2014-04-09 | 2019-05-15 | Genentech, Inc. | Process for the manufacturing of medicaments |
| JP2017513844A (ja) * | 2014-04-23 | 2017-06-01 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 知的障害の処置のためのmGlu2/3アンタゴニスト |
| BR112016024484A2 (pt) | 2014-04-24 | 2017-08-15 | Novartis Ag | derivados de aminopiridina como inibidores de fosfatidilinositol 3-quinase |
| CA2945212A1 (en) | 2014-04-24 | 2015-10-29 | Novartis Ag | Amino pyrazine derivatives as phosphatidylinositol 3-kinase inhibitors |
| US9862711B2 (en) | 2014-04-24 | 2018-01-09 | Novartis Ag | Pyrazine derivatives as phosphatidylinositol 3-kinase inhibitors |
| WO2015191630A1 (en) | 2014-06-10 | 2015-12-17 | Sanford-Burnham Medical Research Institute | Metabotropic glutamate receptor negative allosteric modulators (nams) and uses thereof |
| EP3000814A1 (en) | 2014-09-26 | 2016-03-30 | Domain Therapeutics | Substituted pyrazoloquinazolinones and pyrroloquinazolinones as allosteric modulators of group II metabotropic glutamate receptors |
| US10538491B2 (en) | 2015-03-16 | 2020-01-21 | Vanderbilt University | 4,5-substituted picolinamide and picolinonitrile metabotropic glutamate receptor 2 negative allosteric modulators |
| TWI713530B (zh) | 2015-06-05 | 2020-12-21 | 美商艾佛艾姆希公司 | 作為除草劑之嘧啶氧基苯衍生物 |
| JP2020100564A (ja) * | 2017-04-03 | 2020-07-02 | 京都薬品工業株式会社 | リードスルー誘導剤およびその医薬用途 |
| CN110785413B (zh) | 2017-05-02 | 2024-08-02 | Fmc公司 | 作为除草剂的嘧啶氧基苯并稠合化合物 |
| CN110951051B (zh) * | 2019-12-16 | 2021-04-20 | 大连理工大学 | 一类侧链含三氟甲基嘧啶的热致延迟荧光共聚物的制法及应用 |
| EP4263916A1 (en) | 2020-12-18 | 2023-10-25 | Basf Se | Composition for tin or tin alloy electroplating comprising leveling agent |
| CN113501772A (zh) * | 2021-07-28 | 2021-10-15 | 上海毕得医药科技股份有限公司 | 一种联苯-3-磺酰氯衍生物的合成方法 |
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