作者:M. A. Eshonov、V. I. Vinogradova、Kh. A. Rasulova、K. K. Turgunov、B. Tashkhodzhaev
DOI:10.1007/s10600-021-03398-8
日期:2021.5
Oxidation of the alkaloid skimmianine produced a formyl derivative that reacted with homoveratrylamine to give the product of nucleophilic ipso-substitution 3-formyl-4-(3,4-dimethoxyphenylethylamino)-7,8- dimethoxyquinolin-2-one. The presence of the formyl group in the latter stimulated its further ipso-substitution at the H atom in acidic solution to form 4-(3,4-dimethoxyphenylethylamino)-7,8-dimethoxyquinolin-2-one, the structure of which was confirmed by an X-ray crystal structure analysis.
生物碱 skimmianine 氧化产生了甲酰基衍生物,该衍生物与高藜芦碱反应生成了亲核同素异形反应产物 3-甲酰基-4-(3,4-二甲氧基苯乙基氨基)-7,8-二甲氧基喹啉-2-酮。后者中甲酰基团的存在促使其在酸性溶液中进一步在 H 原子上发生同素异形反应,生成 4-(3,4-二甲氧基苯乙基氨基)-7,8-二甲氧基喹啉-2-酮,其结构已通过 X 射线晶体结构分析得到证实。