JP2009541415A5 - - Google Patents
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- Publication number
- JP2009541415A5 JP2009541415A5 JP2009517107A JP2009517107A JP2009541415A5 JP 2009541415 A5 JP2009541415 A5 JP 2009541415A5 JP 2009517107 A JP2009517107 A JP 2009517107A JP 2009517107 A JP2009517107 A JP 2009517107A JP 2009541415 A5 JP2009541415 A5 JP 2009541415A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- tetrazol
- hetero
- halo
- 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.)
- Granted
Links
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81729806P | 2006-06-29 | 2006-06-29 | |
| US60/817,298 | 2006-06-29 | ||
| PCT/EP2007/055997 WO2008000645A1 (en) | 2006-06-29 | 2007-06-18 | Tetrazole-substituted arylamides |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012134357A Division JP5456846B2 (ja) | 2006-06-29 | 2012-06-14 | テトラゾール置換アリールアミド |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009541415A JP2009541415A (ja) | 2009-11-26 |
| JP2009541415A5 true JP2009541415A5 (enExample) | 2012-06-07 |
| JP5021734B2 JP5021734B2 (ja) | 2012-09-12 |
Family
ID=38462418
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009517107A Active JP5021734B2 (ja) | 2006-06-29 | 2007-06-18 | テトラゾール置換アリールアミド |
| JP2012134357A Active JP5456846B2 (ja) | 2006-06-29 | 2012-06-14 | テトラゾール置換アリールアミド |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012134357A Active JP5456846B2 (ja) | 2006-06-29 | 2012-06-14 | テトラゾール置換アリールアミド |
Country Status (15)
| Country | Link |
|---|---|
| US (5) | US7595405B2 (enExample) |
| EP (2) | EP2038264B1 (enExample) |
| JP (2) | JP5021734B2 (enExample) |
| KR (1) | KR101103143B1 (enExample) |
| CN (2) | CN103159692B (enExample) |
| AR (1) | AR061667A1 (enExample) |
| AU (1) | AU2007263809B2 (enExample) |
| BR (2) | BR122019017036B8 (enExample) |
| CA (1) | CA2654915C (enExample) |
| CL (1) | CL2007001887A1 (enExample) |
| ES (2) | ES2604542T3 (enExample) |
| IL (2) | IL195786A (enExample) |
| MX (1) | MX2008016423A (enExample) |
| TW (1) | TWI334414B (enExample) |
| WO (1) | WO2008000645A1 (enExample) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8501933B2 (en) | 2006-11-09 | 2013-08-06 | Roche Palo Alto Llc | Thiazole and oxazole-substituted arylamides as P2X3 and P2X2/3 antagonists |
| CN101528717B (zh) * | 2006-11-09 | 2013-04-24 | 弗·哈夫曼-拉罗切有限公司 | 噻唑和*唑-取代的芳基酰胺类化合物 |
| KR101186704B1 (ko) | 2007-10-04 | 2012-09-27 | 에프. 호프만-라 로슈 아게 | 테트라졸-치환된 아릴 아마이드 유도체 및 이의 용도 |
| WO2009058299A1 (en) * | 2007-10-31 | 2009-05-07 | Merck & Co., Inc. | P2x3 receptor antagonists for treatment of pain |
| EP2215049B1 (en) * | 2007-10-31 | 2019-06-12 | Merck Sharp & Dohme Corp. | P2x3, receptor antagonists for treatment of pain |
| ES2517602T3 (es) * | 2007-12-17 | 2014-11-03 | F. Hoffmann-La Roche Ag | Derivados arilamida sustituidos con tetrazol y su utilización como antagonistas de receptores purinérgicos P2X3 y/o P2X2/3 |
| AU2013273626B2 (en) * | 2007-12-17 | 2016-04-28 | F.Hoffmann-La Roche Ag | Triazole-substituted arylamide derivatives and their use as P2X3 and /or P2X2/3 purinergic receptor antagonists |
| EP2234981B1 (en) * | 2007-12-17 | 2016-03-30 | F. Hoffmann-La Roche AG | Novel imidazole-substituted arylamides |
| SI2234976T1 (sl) * | 2007-12-17 | 2013-07-31 | F. Hoffmann-La Roche Ag | Novi s pirazolom substituirani arilamidi |
| KR101405746B1 (ko) | 2007-12-17 | 2014-06-10 | 에프. 호프만-라 로슈 아게 | 트리아졸 치환된 아릴아미드 유도체 및 p2x3 및/또는 p2x2/3 퓨린성 수용체 길항제로서의 용도 |
| JP5539235B2 (ja) | 2008-02-29 | 2014-07-02 | エボテック・アーゲー | アミド化合物、組成物およびそれらの使用 |
| WO2010033168A2 (en) * | 2008-09-18 | 2010-03-25 | Renovis, Inc. | Amide compounds, compositions and uses thereof |
| US8598209B2 (en) * | 2008-10-31 | 2013-12-03 | Merck Sharp & Dohme Corp. | P2X3, receptor antagonists for treatment of pain |
| BRPI0922645A2 (pt) * | 2008-12-16 | 2019-09-24 | Hoffmann La Roche | "arilamidas tiadiazol substituídas". |
| US9238647B2 (en) | 2009-03-23 | 2016-01-19 | Merck Sharp & Dohme Corp. | P2X3 receptor antagonists for treatment of pain |
| EP2410858B1 (en) | 2009-03-23 | 2016-09-07 | Merck Sharp & Dohme Corp. | P2x3 receptor antagonists for treatment of pain |
| EP2411001B1 (en) | 2009-03-23 | 2018-01-17 | Merck Sharp & Dohme Corp. | P2x3, receptor antagonists for treatment of pain |
| EP2246259B1 (en) | 2009-04-29 | 2012-12-12 | Eurocopter Deutschland GmbH | Rotor wing with integrated tension-torque-transmission element and method for its production |
| JP5685203B2 (ja) * | 2009-05-29 | 2015-03-18 | ラクオリア創薬株式会社 | カルシウムチャネル遮断薬またはナトリウムチャネル遮断薬としてのアリール置換カルボキサミド誘導体 |
| AR077033A1 (es) * | 2009-06-11 | 2011-07-27 | Hoffmann La Roche | Compuestos inhibidores de las quinasas de janus y su uso en el tratamiento de enfermedades inmunologicas |
| EP2445868B1 (en) | 2009-06-22 | 2013-12-18 | F.Hoffmann-La Roche Ag | Biphenyl amides useful as p2x3 and/or p2x2/3 receptors modulators |
| SG177301A1 (en) | 2009-06-22 | 2012-02-28 | Hoffmann La Roche | Novel indole, indazole and benzimidazole arylamides as p2x3 and/or p2x2/3 antagonists |
| WO2010149541A1 (en) * | 2009-06-22 | 2010-12-29 | F. Hoffmann-La Roche Ag | Novel oxazolone and pyrrolidinone-substituted arylamides |
| CA2801074A1 (en) * | 2010-06-04 | 2011-12-08 | Albany Molecular Research, Inc. | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
| PT3381917T (pt) * | 2013-01-31 | 2021-10-27 | Bellus Health Cough Inc | Compostos imidazopiridina e suas utilizações |
| HUE055290T2 (hu) | 2014-12-09 | 2021-11-29 | Bayer Ag | 1,3-Tiazol-2-il-csoporttal szubsztituált benzamid-származékok |
| US10183937B2 (en) | 2014-12-09 | 2019-01-22 | Bayer Aktiengesellschaft | 1,3-thiazol-2-yl substituted benzamides |
| CN107207449B (zh) * | 2015-04-23 | 2020-11-10 | 豪夫迈·罗氏有限公司 | 用于治疗精神障碍的四唑衍生物 |
| JP6877359B2 (ja) * | 2015-06-04 | 2021-05-26 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | イミダゾール誘導体 |
| JP6831376B2 (ja) * | 2015-10-06 | 2021-02-17 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | トリアゾール誘導体 |
| CN108473462B (zh) | 2016-02-02 | 2021-06-22 | 豪夫迈·罗氏有限公司 | 作为eaat3抑制剂的吡唑-吡啶衍生物 |
| TWI696615B (zh) * | 2016-05-05 | 2020-06-21 | 瑞士商伊蘭科動物健康公司 | 雜芳基-1,2,4-三唑及雜芳基-三唑化合物 |
| EP3464246B1 (en) | 2016-05-27 | 2020-07-08 | H. Hoffnabb-La Roche Ag | Pyrazol compounds as eaat3 inhibitors |
| CN109563049B (zh) | 2016-10-14 | 2022-11-29 | 豪夫迈·罗氏有限公司 | 作为eaat3抑制剂的咪唑化合物 |
| TWI741040B (zh) * | 2016-10-20 | 2021-10-01 | 德商拜耳作物科學公司 | 製備3-烷基硫基-2-氯-n-(1-烷基-1h-四唑-5-基)-4-三氟甲基苯甲醯胺之方法 |
| RU2650780C1 (ru) | 2016-12-06 | 2018-04-17 | Общество с ограниченной ответственностью "Анальгетики будущего" | Пептидный модулятор пуринергических рецепторов |
| KR20220016074A (ko) | 2019-05-31 | 2022-02-08 | 키에시 파르마슈티시 엣스. 피. 에이. | P2x3 억제제로서 피리도피리미딘 유도체 |
| BR112021022099A2 (pt) | 2019-05-31 | 2021-12-28 | Chiesi Farm Spa | Derivados de amino quinazolina como inibidores de p2x3 |
| CA3196335A1 (en) | 2020-11-27 | 2022-06-02 | Chiesi Farmaceutici S.P.A. | Phthalazine derivatives as p2x3 inhibitors |
| AU2021386684A1 (en) | 2020-11-27 | 2023-05-25 | Chiesi Farmaceutici S.P.A. | (aza)quinoline 4-amines derivatives as p2x3 inhibitors |
| CN116601149A (zh) | 2020-11-27 | 2023-08-15 | 奇斯药制品公司 | 作为p2x3抑制剂的氨基喹唑啉衍生物 |
| AR131715A1 (es) * | 2023-01-30 | 2025-04-23 | Eurofarma Laboratorios S A | AMIDAS BLOQUEADORAS DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, COMPOSICIONES, USOS, MÉTODOS DE TRATAMIENTO DE LOS MISMOS Y KITS |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL109570A0 (en) * | 1993-05-17 | 1994-08-26 | Fujisawa Pharmaceutical Co | Guanidine derivatives, pharmaceutical compositions containing the same and processes for the preparation thereof |
| JPH10501122A (ja) * | 1994-05-27 | 1998-02-03 | グラクソ、グループ、リミテッド | P▲下2x▼レセプター(プリノセプターファミリー) |
| US6133434A (en) * | 1997-04-28 | 2000-10-17 | Glaxo Group Limited | Purinergic receptor |
| JP2000281664A (ja) * | 1999-03-30 | 2000-10-10 | Otsuka Pharmaceut Co Ltd | チアゾール誘導体 |
| AU773892B2 (en) | 1999-06-30 | 2004-06-10 | H. Lundbeck A/S | Selective NPY (Y5) antagonists |
| US6599926B2 (en) | 2000-06-23 | 2003-07-29 | Bristol-Myers Squibb Company | Heteroaryl-phenyl substituted factor Xa inhibitors |
| DE10055713A1 (de) | 2000-11-10 | 2002-05-23 | Dingwei Tim Yu | Neue Klasse von Antifungimitteln |
| PA8557501A1 (es) * | 2001-11-12 | 2003-06-30 | Pfizer Prod Inc | Benzamida, heteroarilamida y amidas inversas |
| TW200304374A (en) * | 2001-11-30 | 2003-10-01 | Smithkline Beecham Plc | Novel compounds |
| US20030236439A1 (en) | 2002-01-30 | 2003-12-25 | Gregory Agoston | Non-steroidal analogs of 2-methoxyestradiol |
| CA2480856A1 (en) * | 2002-04-05 | 2003-10-23 | Merck & Co., Inc. | Substituted aryl amides |
| WO2004009816A1 (en) | 2002-07-18 | 2004-01-29 | Ceretek Llc | Methods of treating conditions associated with an edg-1 receptor |
| US7078423B2 (en) * | 2002-07-18 | 2006-07-18 | Inotek Pharmaceuticals Corporation | 5-Aryltetrazole compounds, compositions thereof, and uses therefor |
| DE10312963A1 (de) * | 2003-03-24 | 2004-10-07 | Aventis Pharma Deutschland Gmbh | Substituierte 4-Phenyltetrahydroisochinoline, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament, sowie sie enthaltendes Medikament |
| JP2006523701A (ja) | 2003-04-18 | 2006-10-19 | メルク エンド カムパニー インコーポレーテッド | ナトリウムチャネルブロッカーとしてのビアリール置換チアゾール、オキサゾール、およびイミダゾール |
| NZ551974A (en) * | 2004-07-02 | 2010-01-29 | Inst Medical W & E Hall | Alpha-helical minetics |
| EP1917262B1 (en) * | 2005-08-15 | 2011-12-14 | F. Hoffmann-La Roche AG | Piperidine and piperazine derivatives as p2x3 antagonists |
-
2007
- 2007-06-18 KR KR1020087031545A patent/KR101103143B1/ko active Active
- 2007-06-18 WO PCT/EP2007/055997 patent/WO2008000645A1/en not_active Ceased
- 2007-06-18 ES ES07730213.1T patent/ES2604542T3/es active Active
- 2007-06-18 JP JP2009517107A patent/JP5021734B2/ja active Active
- 2007-06-18 AU AU2007263809A patent/AU2007263809B2/en not_active Ceased
- 2007-06-18 EP EP07730213.1A patent/EP2038264B1/en active Active
- 2007-06-18 ES ES12194476.3T patent/ES2596706T3/es active Active
- 2007-06-18 BR BR122019017036A patent/BR122019017036B8/pt active IP Right Grant
- 2007-06-18 EP EP12194476.3A patent/EP2592070B1/en active Active
- 2007-06-18 CN CN201310005567.3A patent/CN103159692B/zh active Active
- 2007-06-18 CA CA2654915A patent/CA2654915C/en active Active
- 2007-06-18 CN CN2007800241415A patent/CN101479250B/zh active Active
- 2007-06-18 MX MX2008016423A patent/MX2008016423A/es active IP Right Grant
- 2007-06-18 BR BRPI0714315A patent/BRPI0714315B8/pt active IP Right Grant
- 2007-06-26 TW TW096122982A patent/TWI334414B/zh not_active IP Right Cessation
- 2007-06-27 CL CL200701887A patent/CL2007001887A1/es unknown
- 2007-06-27 AR ARP070102859A patent/AR061667A1/es not_active Application Discontinuation
- 2007-06-28 US US11/823,808 patent/US7595405B2/en active Active
-
2008
- 2008-12-08 IL IL195786A patent/IL195786A/en not_active IP Right Cessation
-
2009
- 2009-08-18 US US12/583,325 patent/US8193368B2/en active Active
-
2012
- 2012-05-02 US US13/462,115 patent/US8846945B2/en active Active
- 2012-06-14 JP JP2012134357A patent/JP5456846B2/ja active Active
-
2014
- 2014-01-09 US US14/151,680 patent/US9593128B2/en active Active
- 2014-12-28 IL IL236492A patent/IL236492A0/en unknown
-
2017
- 2017-02-01 US US15/422,121 patent/US10201525B2/en active Active
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