2,4,6- 三取代 1,3,5- 三嗪衍生物的合成、表征和生物评估

V. P. Gilava, P. K. Patel
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引用次数: 0

摘要

在三乙胺催化下,以 2,4,6-三氯-1,3,5-三嗪(氰尿酰氯)和 4-(4-氨基苯基)吗啉-3-酮为原料,通过与取代的芳基胺进行区域选择性反应和回流,合成了一系列新的 2,4,6-三取代的 1,3,5-三嗪衍生物。所有合成化合物均通过红外光谱、1HNMR、质量和元素分析进行了表征。此外,还对新合成的化合物进行了体外抗菌活性筛选,发现其中一些化合物具有显著的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SYNTHESIS, CHARACTERIZATION AND BILOGICAL EVALUATION OF 2,4,6- TRISUBSTITUTED 1,3,5-TRIAZINE DERIVATIVES
A new series of 2,4,6-trisubstituted 1,3,5-triazine derivatives were synthesized from 2,4,6-trichloro-1,3,5-triazine(Cyanuric Chloride) and 4-(4-aminophenyl)morpholin-3-one via regioselective reaction followed by reflux with substituted aryl amine in the presence of catalytic amount of triethyl amine. All the synthesized compounds were characterized by IR, 1HNMR, Mass and Elemental Analysis. The newly synthesized compounds were also screened for their in vitro antimicrobial activity against standard drugs and some of them found to be remarkably active.
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