1973 年 93 巻 12 号 p. 1581-1584
Reactions of 2, 3-diaminoisocarbostyril with acetyl chloride, acetic anhydride, and benzoyl chloride, in the presence or absence of bases such as pyridine and triethylamine, were examined. In order to see whether acylation took place at the β-position of the enamine (C4 of 3-aminoisocarbostyril) or the other positions, comparison of ultraviolet absorption was found to be a valuable tool.