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SUBSTITUTED PYRIMIDINES AS ANTAGONISTS OF PROSTAGLANDINE RECEPTORS D2
专利权人:
АВЕНТИС ФАРМАСЬЮТИКАЛЗ ИНК. (US)
发明人:
ХАРРИС Кит Дж. (US),АГИАР Жуаси К. (US),ШУМ Патрик Ваи-Квок (US),ЧЖАО Чжичэн (US),ПОЛИ Грегори Б. (US),СТОКЛОЗА Грегори (US),ЧОИ-СЛЕДЕСКИ Йонг-Ми (US),РАЙЛИНГ Штефан (US),СТЕФАНИ Дэвид (US),ГАРДНЕР Ча
申请号:
RU2012143897/04
公开号:
RU2012143897A
申请日:
2011.03.15
申请国别(地区):
RU
年份:
2014
代理人:
摘要:
1. The compound of formula (I) where m and n are independently selected from integers 0, 1, 2 or 3; X and Y are independently selected from CRR, NR or O, where X and Y cannot simultaneously be O ; or X and Y, taken together with the bond between them, form a phenyl group optionally substituted with one to four R groups; each Z independently represents CRR; R, R and R are independently selected from the group containing H, halogen , aryl, amino, optionally substituted alkyl, optionally substituted alkoxy, as well as carboxy; where optionally substituted th alkyl may be substituted by one to three identical or different groups selected from halogen, carboxy, cyano, hydroxy, amino or aryl; where optionally substituted alkoxy may be substituted by one to three identical or different groups selected from halogen, carboxy, cyano, amino or aryl; where each aryl moiety independently of each other may optionally be substituted with hydroxy, amino, alkyl, alkoxy, carboxy or alkoxycarbonyl; provided that the halogen cannot be bound to N; and provided that the compound is not (1- {2-methoxy-6- [2- (4-trifluoromethoxyphenyl) ethylamino] pyrimidin-4-yl} piperidin-3-yl) acetic acid; or its enantiomer or its prodrug or pharmaceutically acceptable salt. 2. The compound according to claim 1, selected from the group consisting of: 4- {2-methoxy-6- [2- (4-trifluoromethoxyphenyl) ethylamino] pyrimidin-4-yl} morpholine-2-carboxylic acid, (4- {2- methoxy-6- [2- (4-trifluoromethoxyphenyl) ethylamino] pyrimidin-4-yl} piperazin-1-yl) acetic acid, 1- {2-methoxy-6- [2- (4-trifluoromethoxyphenyl) ethylamino] pyrimidine- 4-yl} piperidin-2-carboxylic acid, (1- {2-methoxy-6- [2- (4-trifluoromethoxyphenyl) ethyl1. Соединение формулы (I)где m и n независимо друг от друга выбраны из целых чисел 0, 1, 2 или 3;X и Y независимо друг от друга выбраны из CRR, NRили O, где X и Y одновременно не могут быть O;или X и Y, взятые вместе со связью между ними, образуют фенильную группу, необязательно замещенную о
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