申请人:Hoechst Aktiengesellschaft
公开号:US04766241A1
公开(公告)日:1988-08-23
The invention relates to 2-aminomethylphenols of the formula I ##STR1## in which R.sup.1 and R.sup.2 represent hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl or benzyl which is optionally substituted by alkyl, alkoxy or halogen, R.sup.3 and R.sup.5 denote hydrogen, halogen, alkyl or alkoxy, R.sup.4 denotes halogen, alkyl or cycloalkyl and R.sup.6 and R.sup.7 represent hydrogen or alkyl, it being possible for the radicals R.sup.1 and R.sup.2, R.sup.6 R.sup.7 and/or two of the radicals R.sup.3, R.sup.4 and R.sup.5 to form an alkylene chain which is optionally substituted by methyl groups and which, in the case of the radicals R.sup.1, R.sup.2, R.sup.6 and R.sup.7, can also be interrupted by oxygen atoms, sulfur atoms and/or imino groups, and to physiologically acceptable salts thereof, a process for their preparation, and their use and to pharmaceutical formulations based on these compounds.
本发明涉及式I的2-
氨甲基酚化合物:##
STR1## 其中,R1和R2代表
氢、烷基、
烯基、炔基、
环烷基或
苄基,该
苄基可选地被烷基、烷
氧基或卤素取代,R3和R5代表
氢、卤素、烷基或烷
氧基,R4代表卤素、烷基或
环烷基,R6和R7代表
氢或烷基,其中基团R1和R2、R6和R7和/或基团R3、R4和R5中的两个可以形成一个可选地被
甲基基团取代的烷基链,对于基团R1、R2、R6和R7,该烷基链也可以被
氧原子、
硫原子和/或
亚胺基所中断,以及其生理上可接受的盐,其制备方法及其用途和基于这些化合物的制药配方。