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首页> 外文期刊>Journal of Molecular Structure >Novel substituted benzothiazole and Imidazo[2,1b][1,3,4]Thiadiazole derivatives: Synthesis, characterization, molecular docking study, and investigation of their in vitro antileishmanial and antibacterial activities
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Novel substituted benzothiazole and Imidazo[2,1b][1,3,4]Thiadiazole derivatives: Synthesis, characterization, molecular docking study, and investigation of their in vitro antileishmanial and antibacterial activities

机译:新型取代的苯并噻唑和咪唑[2,1b] [1,3,4]噻二唑衍生物:合成,表征,分子对接研究和对体外抗菌和抗菌活性的研究

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摘要

In this study, we synthesized new imidazo[2,1-b][1,3,4]thiadiazole derivatives containing benzothiazole group. To this end, we firstly obtained the benzo[d]thiazol-2-ylthio/oxy acetonitrile compounds (3a,b), the starting materials, in high yields (82% and 87%, respectively). Then, we synthesized the 2-amino-1,3,4-thiadiazole derivatives (4a,b) from the reaction of these nitrile derivatives (3a,b) with thio-semicarbazide in trifluoroacetic acid (TFA) (in yields of 83% and 84%). Finally, we synthesized the imidazo [2,1-b][1,3,4]thiadiazole derivatives (5-24) containing benzothiazole group, which are the target compounds, from reactions of 2-amino-1,3,4-thiadiazole derivatives (4a,b) with phenacyl bromide derivatives (in yields of 53%-73%).
机译:在这项研究中,我们合成了含有苯并噻唑基团的新咪唑[2,1-B] [1,3,4]噻二唑衍生物。 为此,我们首先得到了高产率(分别为82%和87%)的苯并[d]噻唑-2-基硫基/氧乙腈化合物(3a,b),原料。 然后,我们将2-氨基-1,3,4-噻二唑衍生物(4a,b)与三氟乙酸(TFA)中的硫代氨基脲(TFA)的反应合成(3a,b)(以83%的产率为83%) 和84%)。 最后,我们合成了含有苯并噻唑基团的咪唑(2,1-B] [1,3,4]噻二唑衍生物(5-24),其是目标化合物,来自2-氨基-1,3,4-的反应 噻二唑衍生物(4A,B)具有苯酰基溴衍生物(产率为53%-73%)。

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