RU2015131137A - Производное амида коричной кислоты - Google Patents

Производное амида коричной кислоты Download PDF

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RU2015131137A
RU2015131137A RU2015131137A RU2015131137A RU2015131137A RU 2015131137 A RU2015131137 A RU 2015131137A RU 2015131137 A RU2015131137 A RU 2015131137A RU 2015131137 A RU2015131137 A RU 2015131137A RU 2015131137 A RU2015131137 A RU 2015131137A
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substituted
carbon atoms
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propenamide
fluorophenyl
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Томохиро ООКУБО
Ко НАКАМУРА
Йоситака НАКАДЗАВА
Хиройоси НАНБА
Хироюки ЙОСИДА
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Ниппон Дзоки Фармасьютикал Ко., Лтд.
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Claims (56)

1. Соединение или его фармацевтически приемлемая соль или гидрат, где соединение представлено следующей общей формулой (I):
Figure 00000001
,
где n означает целое число от 0 до 4;
X1 и X2, являющиеся одинаковыми или различными, означают водород, фтор, трифторметил или карбокси, и один из X1 и X2 означает заместитель, иной чем водород;
R1 означает:
имидазолил, замещенный алкилом с 1-6 атомами углерода или фенилом;
пирролил, который может быть замещен алкилом с 1-4 атомами углерода;
фенил, замещенный амино, изоксазолилом или морфолино;
фенил, замещенный тиоморфолино, который может быть замещен оксо;
пиперазино, замещенный алкилом с 1-4 атомами углерода или циклогексилом;
тиоморфолино, который может быть замещен одним или двумя оксо; или
любой из заместителей, выбираемых из гуанидино, индазолила и циклогексиламино; и
R2 означает водород, циано или алкил с 1-4 атомами углерода, при условии, что в случае n=0, R1 означает заместитель, иной чем фенил, замещенный морфолино.
2. Соединение или его фармацевтически приемлемая соль или гидрат по п. 1, где R2 означает водород и где один из X1 и X2 означает водород, а другой означает фтор.
3. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает имидазолил, замещенный алкилом с 1-6 атомами углерода или фенилом.
4. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает пирролил, который может быть замещен алкилом с 1-4 атомами углерода.
5. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает фенил, замещенный амино, изоксазолилом или морфолино.
6. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает фенил, замещенный тиоморфолино, который может быть замещен оксо.
7. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает пиперазино, замещенный алкилом с 1-4 атомами углерода или циклогексилом.
8. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает тиоморфолино, который может быть замещен одним или двумя оксо.
9. Соединение или его фармацевтически приемлемая соль или гидрат по п. 2, где R1 означает любой из заместителей, выбираемых из гуанидино, индазолила и циклогексиламино.
10. Соединение или его фармацевтически приемлемая соль или гидрат по п. 1, которые выбирают из группы, состоящей из (E)-N-[2-(4-циклогексилпиперазин-1-ил)этил]-3-(2-фторфенил)-2-пропенамида, (E)-N-[3-(4-циклогексилпиперазин-1-ил)пропил]-3-(2-фторфенил)-2-пропенамида, (E)-3-(2-фторфенил)-N-[3-(4-метилпиперазин-1-ил)пропил]-2-пропенамида, (E)-3-(2-фторфенил)-N-[3-(изоксазол-5-ил)фенил]-2-пропенамида, (E)-3-(4-фторфенил)-N-(3-тиоморфолинопропил)-2-пропенамида, (E)-3-(2-фторфенил)-N-(3-тиоморфолинопропил)-2-пропенамида, (E)-N-[3-(1,1-диоксо-1,4-тиазинан-4-ил)пропил]-3-(2-фторфенил)-2-пропенамида, (E)-N-[3-(1,1-диоксо-1,4-тиазинан-4-ил)пропил]-3-(4-фторфенил)-2-пропенамида, (E)-3-(4-фторфенил)-N-[3-(1-оксо-1,4-тиазинан-4-ил)пропил]-2-пропенамида и (E)-3-(2-фторфенил)-N-[3-(1-оксо-1,4-тиазинан-4-ил)пропил]-2-пропенамида.
11. Соединение или его фармацевтически приемлемая соль или гидрат по п. 1, которые выбирают из группы, состоящей из (E)-3-(4-фторфенил)-N-(3-тиоморфолинопропил)-2-пропенамида, (E)-3-(2-фторфенил)-N-(3-тиоморфолинопропил)-2-пропенамида, (E)-3-(4-фторфенил)-N-[3-(1-оксо-1,4-тиазинан-4-ил)пропил]-2-пропенамида и (E)-3-(2-фторфенил)-N-[3-(1-оксо-1,4-тиазинан-4-ил)пропил]-2-пропенамида.
12. Фармацевтическое средство, включающее в качестве активного ингредиента, по меньшей мере одно соединение или его фармацевтически приемлимую соль или гидрат, где соединение представлено следующей общей формулой (I):
Figure 00000002
,
где n означает целое число от 0 до 4;
X1 и X2, являющиеся одинаковыми или различными, означают водород, фтор, трифторметил или карбокси, и один из X1 и X2 означает заместитель, иной чем водород;
R1 означает:
имидазолил, который может быть замещен алкилом с 1-6 атомами углерода или фенилом;
пирролил, который может быть замещен алкилом с 1-4 атомами углерода;
фенил, замещенный амино, алкокси с 1-4 атомами углерода, пиразолилом, изоксазолилом или морфолино;
фенил, замещенный тиоморфолино, который может быть замещен оксо;
пиперазино, который может быть замещен алкилом с 1-4 атомами углерода или циклогексилом;
тиоморфолино, который может быть замещен одним или двумя оксо; или
любой из заместителей, выбираемых из амино, карбокси, гуанидино, индолила, бензоимидазолила, индазолила, пиразолила, триазолила, пиридила, пирролидинила, пиперидино, гексаметиленимино, морфолино и циклогексиламино; и
R2 означает водород, циано или алкил с 1-4 атомами углерода.
13. Фармацевтическое средство по п. 12, которое представляет собой аналгетик.
14. Фармацевтическое средство по п. 13, где аналгетик представляет собой терапевтическое средство для лечения хронических болей.
15. Фармацевтическое средство по п. 14, где терапевтическое средство для лечения хронических болей представляет собой терапевтическое средство для лечения люмбаго, артралгии или невропатических болей.
16. Фармацевтическое средство по п. 13, где аналгетик представляет собой терапевтическое средство для лечения невропатических болей.
17. Фармацевтическое средство по любому из пп. 12-16, которое представляет собой пероральный препарат.
18. Фармацевтическое средство по любому из пп. 12-16, которое представляет собой инъекционный препарат.
19. Применение соединения или его фармацевтически приемлемой соли или гидрата в качестве фармацевтического средства, где соединение представлено следующей общей формулой (I):
Figure 00000003
,
где n означает целое число от 0 до 4;
X1 и X2, являющиеся одинаковыми или различными, означают водород, фтор, трифторметил или карбокси, и один из X1 и X2 означает заместитель, иной чем водород;
R1 означает:
имидазолил, который может быть замещен алкилом с 1-6 атомами углерода или фенилом;
пирролил, который может быть замещен алкилом с 1-4 атомами углерода;
фенил, замещенный амино, алкокси с 1-4 атомами углерода, пиразолилом, изоксазолилом или морфолино;
фенил, замещенный тиоморфолино, который может быть замещен оксо;
пиперазино, который может быть замещен алкилом с 1-4 атомами углерода или циклогексилом;
тиоморфолино, который может быть замещен одним или двумя оксо; или
любой из заместителей, выбираемых из амино, карбокси, гуанидино, индолила, бензоимидазолила, индазолила, пиразолила, триазолила, пиридила, пирролидинила, пиперидино, гексаметиленимино, морфолино и циклогексиламино; и
R2 означает водород, циано или алкил с 1-4 атомами углерода.
20. Применение по п. 19, где фармацевтическое средство представляет собой аналгетик.
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Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5726266B2 (ru) * 1973-07-17 1982-06-03
US4568687A (en) * 1983-02-28 1986-02-04 American Cyanamid Company N-[2-4-(1H-Imidazol-1-yl)alkyl]-arylamides and pharmaceutical compositions
EP0117462A3 (en) * 1983-02-28 1986-08-20 American Cyanamid Company N-(2-4-(1h-imidazol-1-yl)alkyl)arylamides
GB9318637D0 (en) * 1993-09-08 1993-10-27 Ferring Res Ltd Enzyme inhibitors
JPH08248567A (ja) * 1995-03-14 1996-09-27 Konica Corp ハロゲン化銀写真感光材料
US5650386A (en) * 1995-03-31 1997-07-22 Emisphere Technologies, Inc. Compositions for oral delivery of active agents
EP1264820A4 (en) * 2000-03-14 2004-09-15 Fujisawa Pharmaceutical Co amide compounds
CA2468544A1 (en) 2001-12-10 2003-06-19 Amgen Inc. Vanilloid receptor ligands
EP1764358A3 (en) * 2001-12-10 2007-03-28 Amgen, Inc Cyclic amides as vanilloid receptor ligands and their use in treatments of inflammatory and neuropathic pain
EP1581516A4 (en) * 2002-11-22 2007-10-17 Bristol Myers Squibb Co BENZYLAMIDE 3-HETEROCYCLIC DERIVATIVES AS POTASIC CHANNEL OPENING AGENTS
AU2003294441A1 (en) * 2002-11-22 2004-06-18 Bristol-Myers Squibb Company 1-aryl-2-hydroxyethyl amides as potassium channel openers
DE102004039373A1 (de) * 2004-08-12 2006-02-23 Grünenthal GmbH Para-Alkyl-substituierte N-(4-Hydroxy-3-methoxy-benzyl)-zimtsäureamide und deren Verwendung zur Herstellung von Arzneimitteln
AU2006225496A1 (en) * 2005-03-19 2006-09-28 Amorepacific Corporation Novel compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same
WO2006102645A1 (en) * 2005-03-24 2006-09-28 Janssen Pharmaceutica, N.V. Biaryl derived amide modulators of vanilloid vr1 receptor
US20070032475A1 (en) * 2005-04-15 2007-02-08 Ye Xiaocong M Novel compounds useful for bradykinin B1 receptor antagonism
AU2007208819B2 (en) * 2006-01-24 2012-06-07 Nippon Zoki Pharmaceutical Co., Ltd. Novel histidine derivative
JP2007210974A (ja) * 2006-02-13 2007-08-23 Sankyo Co Ltd 置換されたウレア化合物を含有する医薬
WO2008005954A2 (en) 2006-06-30 2008-01-10 The Board Of Regents Of The University Of Texas System Tryphostin-analogs for the treatment of cell proliferative diseases
CA2658925C (en) * 2006-07-27 2015-07-14 Amorepacific Corporation Novel sulfonylamino acrylamide derivatives, isomer thereof,or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same
WO2008144933A1 (en) * 2007-05-29 2008-12-04 Université de Montréal Cinnamoyl inhibitors of transglutaminase
EP2003118A1 (de) 2007-06-13 2008-12-17 Bayer Schering Pharma Aktiengesellschaft Zimtsäurederivate als Modulatoren des EP2-Rezeptors
CN101730467A (zh) * 2007-07-06 2010-06-09 努恩治疗学股份有限公司 神经病性疼痛的治疗
WO2009096701A2 (en) * 2008-01-28 2009-08-06 Amorepacific Corporation Novel compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same
JP2012510512A (ja) * 2008-12-03 2012-05-10 マサチューセッツ インスティテュート オブ テクノロジー 記憶を推進するためのhdac2の阻害
HUE047515T2 (hu) * 2009-09-09 2020-04-28 Novaremed Ltd N-Szubsztituált benzolpropánamidok fájdalom és gyulladás kezelésében történõ alkalmazásra
US9518044B2 (en) * 2011-06-20 2016-12-13 Emory University Prostaglandin receptor EP2 antagonists, derivatives, compositions, and uses related thereto

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