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Synthesis and Biological Evaluation of 1-(6-bromobenzo [d]thiazol-2-yl)-2-(disubstituted methylene) hydrazine derivatives

机译:1-(6-溴苯并[d]噻唑-2-基)-2-(二取代亚甲基)肼衍生物的合成及生物评价

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Synthesis of a series of various 1-(6-bromobenzo[d]thiazol-2-yl)-2-(disubstitutedmethylene)hydrazine derivatives (7a-7e)have been done. Synthesis of a series of intermediates (3 and 5) have been also done, 6-bromo-1,3-benzothiazole-2-amine (3), 2-hydrazino-6-bromo-1, 3-benzothiazole (5) and final product (7a-7e), 1-(6-bromobenzo[d]thiazol-2-yl)-2-(diphenylmethylene) hydrazine (7a), 1-(6-bromobenzo [d]thiazol-2-yl)-2-(propan-2-ylidene) hydrazine (7b), (E)-2-(butan-2-ylidene)-1-(6-bromobenzo[d]thiazol-2-yl)hydrazine (7c), (Z)-1-(6-bromobenzo[d]thiazol-2-yl)-2-(cyclohexylmethylene) hydrazine (7d), 2-(6-bromobenzo[d]thiazol-2-yl)-1-(7,7- dimethylbicyclo [2.2.1] heptan-2-ylidene)hydrazine (7e). Spectral analysis of all intermediates and final products has been done by IR and NMR. After spectral analysis, antibacterial activity has been screened against S. aurius and E. coli bacterias.
机译:已经完成了一系列各种1-(6-溴苯并[d]噻唑-2-基)-2-(二取代亚甲基)肼衍生物(7a-7e)的合成。还完成了一系列中间体(3和5)的合成,6-溴-1,3-苯并噻唑-2-胺(3),2-肼基-6-溴-1、3-苯并噻唑(5)和终产物(7a-7e),1-(6-溴苯并[d]噻唑-2-基)-2-(二苯基亚甲基)肼(7a),1-(6-溴苯并[d]噻唑-2-基)- 2-(丙-2-亚基)肼(7b),(E)-2-(丁亚基)-1-(6-溴苯并[d]噻唑-2-基)肼(7c),(Z )-1-(6-溴苯并[d]噻唑-2-基)-2-(环己基亚甲基)肼(7d),2-(6-溴苯并[d]噻唑-2-基)-1-(7,7 -二甲基双环[2.2.1]庚-2-亚甲基)肼(7e)。所有中间体和最终产物的光谱分析均通过IR和NMR进行。光谱分析后,已筛选出针对金黄色葡萄球菌和大肠杆菌的抗菌活性。

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