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首页> 外文期刊>Phosphorus, Sulfur, and Silicon and the Related Elements >Reaction of hydrazonoyl halides 52: Synthesis and antimicrobial activity of some new pyrazolines and 1,3,4-thiadiazolines
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Reaction of hydrazonoyl halides 52: Synthesis and antimicrobial activity of some new pyrazolines and 1,3,4-thiadiazolines

机译:hydr酰卤的反应52:一些新型吡唑啉和1,3,4-噻二唑啉的合成和抑菌活性

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摘要

[5-Substituted 2-(3-phenyl-5-substituted 2-pyrazolinyl)(1,3-thiazol-4-yl)] phenyldiazene and 2,3-dihydro-1,3,4-thiadiazoles were synthesized via reactions of hydrazonoyl halides with 5-substituted-3-phenyl-4,5-dihydropyrazole-1-carboximidothionic acid and {[2-2-{aza-2-((methylthioxomethyl)-amino]-vinyl} phenyl)1-azavinyl] amino} methylthiomethane-1-thione, respectively. All structures of the newly synthesized compounds were elucidated by elemental analysis, spectral data, X-ray single crystal, and alternative synthesis methods whenever possible. Some of the new compounds were tested towards bacteria. In general, all tested compounds were capable of a high inhibiting the growth of gram positive and gram negative.
机译:[5-取代的2-(3-苯基-5-取代的2-吡唑啉基)(1,3-噻唑-4-基)]苯基二氮烯和2,3-二氢-1,3,4-噻二唑是通过以下反应合成的卤代酰基卤化物与5-取代的-3-苯基-4,5-二氢吡唑-1-羧酰亚胺二羧酸和{[[2-2- {aza-2-((methylthioxomethyl)-amino] -vinyl}苯基}苯基)1-azavinyl]氨基}分别为甲硫基甲烷-1-硫酮。尽可能通过元素分析,光谱数据,X射线单晶和替代合成方法阐明了新合成化合物的所有结构。一些新化合物已针对细菌进行了测试。通常,所有测试的化合物都能够高度抑制革兰氏阳性和革兰氏阴性的生长。

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