发明名称 UN PROCEDIMIENTO PARA LA OBTENCION DE DERIVADOS DE BI- Y TRICICLICOS DE PIRIDONA
摘要 <p>The novel compounds of the general formula <IMAGE> in which Q<1>, together with the nitrogen atom, denotes a group of the formula <2bL>N-CH2CH2- (a) <2bL>N-CH2CH2CH2- (b), <2bL>N-CH=CH- (c), <2bL>N-CH2-CH=CH- (d), <2bL>N-CH2-S(O)p- (e), <2bL>N-CH2CH2-S(O)p- (f) or <2bL>N-CH=CH-S(O)p- (g), p denotes the number 0, 1 or 2, Ra denotes a phenyl, pyridyl or thienyl group which is optionally substituted by halogen, trifluoromethyl, nitro, lower alkyl or lower alkoxy, Rb and Rc, together with the carbon atom marked alpha , denote a group of the formula <2bL>C alpha -S-CH=CH- (h) <2bL>C alpha -CH=CH-S- (i) or <2bL>C alpha CH=CH-CH=CH- (j) which is optionally substituted by halogen, trifluoromethyl, lower alkyl, lower alkoxy, nitro, amino or mono- or di(lower alkyl) amino, and the dashed line denotes an additional bond, are intermediates for the preparation of novel therapeutic active compounds having muscle-relaxing, sedative/hypnotic, anxiolytic and/or anticonvulsive properties.</p>
申请公布号 ES554428(D0) 申请公布日期 1987.12.01
申请号 ES19280005544 申请日期 1986.04.28
申请人 F. HOFFMANN-LA ROCHE & CO. AKTIENGESELLSCHAFT 发明人
分类号 A61K;A61K31/435;A61K31/54;A61K31/55;A61P21/02;A61P25/20;C07D;C07D205/04;C07D333/38;C07D455/02;C07D455/06;C07D471/04;C07D495/04;C07D495/14;C07D501/14;C07D513/04;C07D513/14;C07D513/18;C07D513/22;C07D519/00;(IPC1-7):C07D455/00 主分类号 A61K
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