作者:E. Campaigne、Richard Yodice
DOI:10.1002/jhet.5570170408
日期:1980.6
The syntheses of two compounds, which are fused-ring succinimides, prepared as potential anticon-vulsants, are described. The compounds are 3,4,5,6-tetrahydro-7-methyl-6-oxoindeno[7,1-bc]thiepin-4a,5-(2H)dicarboximide and 6,7,8,9-tetrahydro-2-oxo-1H-benz[cd]azulene-1,9a-(2H)dicarboximide. The spirodioxolane of the latter compound was also prepared by ketalization.
描述了两种化合物的合成,它们是作为潜在的抗惊厥药制备的稠合环的琥珀酰亚胺。化合物是3,4,5,6-四氢-7-甲基-6-氧代茚并[ 7,1- bc ]噻吩-4a,5-(2 H)二甲酰亚胺和6,7,8,9-四氢-2 -oxo-1 H-苯并[ cd ] azulene-1,9a-(2 H)二苯甲酰亚胺。后一种化合物的螺二氧戊环也通过缩酮化制备。