Karthikeyan Mari Sithambaram, Holla Bantwal Shivarama, Kumari Nalilu Suchetha
Department of Chemistry, Mangalore University, Mangalagangothri 574199, India.
Eur J Med Chem. 2008 Feb;43(2):309-14. doi: 10.1016/j.ejmech.2007.03.024. Epub 2007 Apr 7.
Dichlorofluorophenyl containing aminotriazolothiadiazines (6) were synthesized by initial condensation of 2-chloro-N-(substituted phenyl) acetamides (4) with triazole (3) and further cyclization using POCl(3). The structures of newly synthesized compounds were confirmed by IR, NMR, mass and elemental analysis. All the compounds were screened for their antibacterial and antifungal activities. Compounds 5a, 5e, 5n, 5o, 6a, 6n, and 6o showed very good antibacterial and antifungal activities at 6.25 microg/ml concentrations.
通过2-氯-N-(取代苯基)乙酰胺(4)与三唑(3)的初始缩合反应,然后使用POCl₃进一步环化,合成了含二氯氟苯基的氨基三唑并噻二嗪(6)。通过红外光谱、核磁共振、质谱和元素分析确定了新合成化合物的结构。对所有化合物进行了抗菌和抗真菌活性筛选。化合物5a、5e、5n、5o、6a、6n和6o在6.25微克/毫升浓度下表现出非常好的抗菌和抗真菌活性。