1,3 -噻嗪衍生物的合成、表征及抗结核活性

Hemant Kumar Bansal, K. Daniel, N. Jain
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引用次数: 0

摘要

杂环化合物由于其强大的生物活性,在药理学研究中得到了广泛的应用。杂环分子噻嗪引起了研究人员的兴趣,它有四个碳原子,一个氮原子和一个硫原子。它有有趣的药理特性。本文以取代查尔酮衍生物为原料,合成了一系列新的噻嗪衍生物。起始原料为苯乙酮衍生物。这些化合物的结构经红外光谱、核磁共振、质谱和元素分析证实。对合成的化合物(IVa-IVe)进行了抗结核活性筛选,结果表明部分衍生物具有较好的抗结核活性。
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SYNTHESIS, CHARACTERIZATION AND ANTI-TUBERCULAR ACTIVITY OF 1, 3- THIAZINE DERIVATIVES
Due to their potent biological activity, heterocyclic compounds have been used extensively in pharmacological research.Researchers' interest has been drawn to the heterocyclic molecule thiazine, which has four carbon atoms, one nitrogenatom, and one sulphur atom. It has interesting pharmacological properties. In the present work, a series of new thiazinederivatives were synthesized from substituted chalcone derivatives. Starting material was acetophenone derivatives. Thestructures of these compounds were confirmed by IR, NMR, Mass and elemental analysis. The synthesized compounds(IVa-IVe) were screened for anti-tuberculosis activity against Mycobacterium tuberculosis and the results show that some ofthese derivatives possess good activity against Mycobacterium tuberculosis.
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