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Acetyidinyl diamides as monoacrylic glycerol lipase inhibitors
专利权人:
JANSSEN PHARMACEUTICA N.V.
发明人:
BIAN, HAIYAN,CHEVALIER, KRISTEN M.,CONNOLLY, PETER J.,FLORES, CHRISTOPHER M.,LIN, SHU-CHEN,LIU, LI,MABUS, JOHN,MACIELAG, MARK J.,MCDONNELL, MARK E.,PITIS, PHILIP M.,ZHANG, SUI-PO,ZHANG, YUE-MEI,ZHU, B
申请号:
ES10715457
公开号:
ES2538326T3
申请日:
2010.04.22
申请国别(地区):
ES
年份:
2015
代理人:
摘要:
A compound of formula (I) Formula ** in which Y and Z are independently selected from a) or b), so that one of Y and Z is selected from group a) and the other is selected from group b); Group a) is i) substituted C6-10 axyl, ii) C3-8 cycloalkyl, iii) trifluoromethyl; or iv) heteroaryl selected from the group consisting of thienyl, furanyl, thiazolyl, isothiazolyl, oxazolyl, pyrrolyl, pyridinyl, isoxazolyl, imidazolyl, furazan-3-yl, benzothienyl, thieno [3,2-b] thiophene-2-yl, pyrazolyl , triazolyl, tetrazolyl and [1,2,3] thiadiazolyl; wherein C6-10 aryl is replaced by; and the heteroaryl is optionally substituted by; from one to two substituents independently selected from the group consisting of fluorine, chlorine, bromine, C 1-4 alkyl, cyano and trifluoromethyl; Group b) is i) C6-10 aryl; ii) heteroaryl selected from the group consisting of thiazolyl, pyridinyl, indolyl, indazolyl, pyrrolyl, benzoxazolyl, benzothiazolyl, benzothienyl, benzofuranyl, imidazo [1, 2-a] pyridin-2-yl, furo [2,3-b] pyridinyl, furazan-3-yl, pyrrolo [2,3-b] pyridinyl, pyrrolo [3,2-b] pyridinyl, thieno [2,3-b] pyridinyl, quinolinyl, quinazolinyl, thienyl and benzimidazolyl; iii) benzofused heterocyclyl attached through a carbon atom, and when the heterocyclyl part contains a nitrogen atom, this nitrogen atom is optionally substituted by a substituent selected from the group consisting of C3-7 cycloalkylcarbonyl; C3-7 cycloalkylsulfonyl; phenyl; phenylcarbonyl; thienylcarbonyl; pyrrolyl carbonyl; phenylsulfonyl; phenyl (C1-4) alkyl; (C1-4 alkyl) aminocarbonyl; C1-6 alkylcarbonyl; C1-6 alkylcarbonyl-C1-4 alkyl; C1-6 alkylsulfonyl; pyrimidinyl; pyridinyl; and 4-4-4alkoxycarbonyl; wherein C3-7 cycloalkylcarbonyl, phenyl, phenylcarbonyl, phenyl (C1-4) alkyl and phenylsulfonyl are optionally substituted by trifluoromethyl or one to two fluorine substituents; and wherein the benzofused heterocyclyl is optionally substituted by an oxo carbon atom and optionally substituted independently by one to t
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