Ding C Z, Silverman R B
Department of Chemistry, Northwestern University, Evanston, Illinois 60208-3113.
J Enzyme Inhib. 1992;6(3):223-31. doi: 10.3109/14756369209020172.
Both 4-(aminomethyl)-1-phenyl-2-pyrrolidinone (4a) and 4-(aminomethyl)-1- (methoxyphenyl)-2-pyrrolidinone (4b) hydrochlorides were synthesized via a six-step sequence, which represents a general approach to 1,4-disubstituted 2-pyrrolidinones. Both of these compounds inactivated monoamine oxidase B and represent the first in a new class of monomamine oxidase inactivators.
4-(氨甲基)-1-苯基-2-吡咯烷酮(4a)盐酸盐和4-(氨甲基)-1-(甲氧基苯基)-2-吡咯烷酮(4b)盐酸盐均通过六步反应合成,这是一种合成1,4-二取代2-吡咯烷酮的通用方法。这两种化合物均可使单胺氧化酶B失活,是新型单胺氧化酶失活剂中的首例。