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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antimicrobial activity of thiosemicarbazides, s-triazoles and their Mannich bases bearing 3-chlorophenyl moiety.
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Synthesis and antimicrobial activity of thiosemicarbazides, s-triazoles and their Mannich bases bearing 3-chlorophenyl moiety.

机译:硫代氨基脲,s-三唑及其带有3-氯苯基部分的曼尼希碱的合成及其抗菌活性。

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摘要

A fast and efficient synthesis of some 1,4-disubstituted thiosemicarbazide derivatives is described. The reaction of 3-chlorobenzoic acid hydrazide with various aryl isothiocyanates gave thiosemicarbazide derivatives (1-11) in good yield. The cyclization of compounds (1-11) in the presence of 2% NaOH resulted in the formation of compounds (12-22) containing the 1,2,4-triazole ring. A series of new Mannich bases (23-33) related to the structure of 1,2,4-triazole has been also synthesized. All of these compounds were tested for their in vitro antibacterial activity against the reference strains of aerobic bacteria - 6 Gram-positive and 3 Gram-negative ones; 12 Staphylococcus aureus clinical isolates were also examined. An attempt was made to clarify the influence of the nature/position of substituents on antibacterial activity of compounds described.
机译:描述了一些1,4-二取代的硫代氨基脲衍生物的快速有效的合成。 3-氯苯甲酸酰肼与各种异硫氰酸芳基酯的反应以高收率得到了硫代氨基脲衍生物(1-11)。在2%NaOH的存在下化合物(1-11)的环化导致形成包含1,2,4-三唑环的化合物(12-22)。还合成了与1,2,4-三唑结构有关的一系列新的曼尼希碱(23-33)。测试了所有这些化合物对有氧细菌参考菌株的体外抗菌活性-6革兰氏阳性和3革兰氏阴性;还检查了12株金黄色葡萄球菌临床分离株。试图阐明取代基的性质/位置对所述化合物的抗菌活性的影响。

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