摘要
本文报导以对茴香胺为原料,通过硝化、酰化、环化、缩合和还原合成标题化合物。该化合物是一种新型吲哚醌衍生物,可用作合成二氢吲哚酮的酰胺衍生物的前体,其合成方法尚未见报导。
This paper describes the synthesis of new indole derivatives(Ⅵ ) dy the several steps reactions of nitration, acylation, cyciization, condensation, and reduction from 4-amidoanjsle, The title compound have not been nitherto reported in literature. It is important intermediate of preparation of 3-amide-2-one indole.
出处
《河北大学学报(自然科学版)》
CAS
1989年第3期65-70,共6页
Journal of Hebei University(Natural Science Edition)
关键词
吲哚醌
茴香胺
环化
还原
合成
P-amidoanisole
isatin
Cycl Ration
reduction.