Modified Coumarins. 11. Synthesis and Biological Activity of Mannich Bases of Substituted 1,3-Dihydrocyclopenta[c]chromen-4-ones
作者:Ya. L. Garazd、T. N. Panteleimonova、M. M. Garazd、V. P. Khilya
DOI:10.1023/b:conc.0000003410.74701.dc
日期:2003.7
Mannich bases containing the dialkylaminomethyl group in the 6- and 8-positions of 2,3-di-hydrocyclopenta[c]chromen-4-ones were prepared by condensation of 7- and 9-hydroxy-2,3-dihydrocyclopenta[c]chromen-4-ones with substituted 1,1-diaminomethanes. The effects of 8-chloro-7-hydroxy-6-(1-pyrrolidinylmethyl)-2,3-dihydrocyclopenta[c]chromen-4-one and 8-chloro-7-hydroxy-6-(morpholinomethyl)-2,3-dihyd
曼尼希碱在 2,3-di-hydrocyclopenta[c]chromen-4-ones 的 6-和 8-位含有二烷基氨基甲基,是通过 7-和 9-羟基-2,3-dihydrocyclopenta[c] 缩合制备的chromen-4-ones 与取代的 1,1-二氨基甲烷。8-chloro-7-hydroxy-6-(1-pyrrolidinylmethyl)-2,3-dihydrocyclopenta[c]chromen-4-one 和 8-chloro-7-hydroxy-6-(morpholinomethyl)-2,3 的作用-dihydrocyclopenta[c]chromen-4-one 对中枢和外周神经系统进行了定义,并能够预测镇静和精神安定特性的存在。