Aboul-Enein H Y, Schauberger C W, Hansen A R, Fischer L J
J Med Chem. 1975 Jul;18(7):736-41. doi: 10.1021/jm00241a019.
Two synthetic pathways are described for the preparation of 4-hydroxy-2-ethyl-2-phenylglutarimide (2), an active hydroxylated metabolite of glutethimide (1). Fourteen other glutethimide analogs were also synthesized and tested for biological activity. Most of the analogs exhibited sedative-hypnotic properties and compound 2 possessed the greatest activity compared to the parent drug. 4-Amino-2-ethyl-2-phenylglutarimide and 4-hydroxy-2-ethyl-2-phenylglutaconimide (13) exhibited the greatest potential as anticonvulsant agents. The structure-activity relationships of the series are discussed.
描述了两种合成途径用于制备4-羟基-2-乙基-2-苯基戊二酰亚胺(2),它是格鲁米特(1)的一种活性羟基化代谢产物。还合成了其他十四种类格鲁米特类似物并测试了其生物活性。大多数类似物表现出镇静催眠特性,与母体药物相比,化合物2具有最大的活性。4-氨基-2-乙基-2-苯基戊二酰亚胺和4-羟基-2-乙基-2-苯基戊烯二酰亚胺(13)表现出作为抗惊厥剂的最大潜力。讨论了该系列的构效关系。