某些1-((苯并[d]噻唑-2-基)甲基)-4,5-二氢-3-甲基- n -苯基- 1h -吡唑-5-亚胺和2-((5-芳基- 1h -1,2,4-三唑-3-基)甲基)苯并[d]噻唑的合成、表征和生物活性研究

P. Uma, K. Rajanna, Firasath Unnisa, P. Saiprakash
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引用次数: 2

摘要

摘要本文以2-((苯并[d]噻唑-2-1-(苯并[d]噻唑-2-基)甲基)-3-甲基-1H-吡唑-5(4H)-酮(2)与不同芳香胺的缩合反应为原料,成功合成了1-(苯并[d]噻唑2-基)甲基-4,5-二氢-3-甲基-N-苯基-1H-吡嗪-5-亚胺(3a-h)。另一方面,在另一方案中,2-(苯并[d]噻唑-2-基)乙酰酰肼(4)与不同的芳族醛的环化得到2-((5-芳基-1H-1,2,4-三唑-3-基)甲基)苯并[d]噻唑(5a-h)。仔细阅读生物活性研究表明,以氯为取代基的衍生物对所有六种细菌的毒性都更大。在氯代化合物中,含甲氧基的化合物毒性较大。
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Synthesis, characterization and biological activity studies of certain 1-((benzo[d]thiazol-2-yl) methyl)-4,5-dihydro-3-methyl-N-phenyl-1H-pyrazol-5-imine and 2-((5-aryl-1H-1,2,4-triazol-3-yl) methyl)benzo[d]thiazoles
Abstract In this work, 1-((benzo[d]thiazol-2-yl)methyl)-4,5-dihydro-3-methyl-N-phenyl-1H-pyrazol-5-imine (3a-h) have been successfully synthesized from the condensation of 2-((Benzo[d]thiazol-2-1-((benzo[d]thiazol-2-yl)methyl)-3-methyl-1H-pyrazol-5(4H)-one (2) with different aromatic amines. On the other hand, in another protocol, cyclization of 2-(benzo[d]thiazol-2-yl) acetohydrazide (4) with different aromatic aldehydes afforded 2-((5-aryl-1H-1,2,4-triazol-3-yl)methyl)benzo[d]thiazoles (5a-h). A perusal of the biological activity studies revealed that the derivatives having chlorine as substituent are more toxic to all six bacteria. Among the chloro group compounds, the compound which has methoxy group is more toxic.
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Cogent Chemistry
Cogent Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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