作者:I. Mieriņa、Z. Tetere、D. Zicāne、I. Rāviņa、M. Turks、M. Jure
DOI:10.1007/s10593-013-1215-3
日期:2013.3
New derivatives of 4-oxo-1,2,3,4-tetrahydroquinazoline, analogs of Quin-C1, have been synthesized by the condensation of aroyl- and heteroaroylhydrazides of anthranilic acid with cinnamic, crotonic, and 4-hydroxy-3-methoxybenzoic aldehydes. The antioxidant activity of the obtained compounds has been determined.
通过邻氨基苯甲酸的芳酰基-和杂芳基酰肼与肉桂酸,巴豆酸和4-羟基-3-甲氧基苯甲酸的缩合反应,合成了4-氧代-1,2,3,4-四氢喹唑啉的新衍生物,即Quin-C1的类似物。醛。已经确定了所获得的化合物的抗氧化活性。