6-(Alkylamino)-9-benzyl-9H-purines. A new class of anticonvulsant agents
作者:James L. Kelley、Mark P. Krochmal、James A. Linn、Ed W. McLean、Francis E. Soroko
DOI:10.1021/jm00398a019
日期:1988.3
electroshock-induced seizures (MES) in rats. Most compounds were prepared in three steps from 5-amino-4,6-dichloropyrimidine or in two steps via alkylation of 6-chloropurine. Potent anticonvulsant activity against MES resided in compounds that contain a benzyl substituent at the 9-position of 6-(methylamino)- or 6-(dimethyl-amino)purine. Among commonly used agents for control of seizures, this type of structure represents
合成了几种9-烷基-6-取代的嘌呤,并测试了其对大鼠最大电击诱发的癫痫发作(MES)的抗惊厥活性。大多数化合物是从3-氨基-4,6-二氯嘧啶分三步制备的,也可以通过6-氯嘌呤的烷基化分两步制备的。针对MES的有效的抗惊厥活性存在于在6-(甲基氨基)-或6-(二甲基-氨基)嘌呤的9位上含有苄基取代基的化合物中。在控制癫痫发作的常用药物中,这种类型的结构代表了一类新型的强效惊厥药物。