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Synthesis, characterization and biological activity of benzothiazoles derivatives

机译:苯并噻唑衍生物的合成,表征和生物活性

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In the present investigation 2-(hydrazinylmethyl)-1,3-benzothiazole was reacted with aryl aldehyde to give 2-{[2Z)-2-arylhydrazinyl]methyl}-1,3-benzothiazole (3a-f), which in absolute ethanol treated with thioglycolic acid (0.001 mol) and anhydrous zinc chloride under reflux for 8 hr to get 3-[1,3-benzothiazol-2-ylmethyl) amino]-5-(aryl)-1,3-thiazolidin-2-ones (4a-f). On the other hand [Benzothiozole N-aryl thiozolemethanamines] (5a-f) were obtained, when the compounds (3a-f), are treated with diazomethane.
机译:在本发明的研究中,将2-(肼基甲基)-1,3-苯并噻唑与芳基醛反应,得到2 - {[2z)-2-芳基肼基]甲基} -1,3-苯并噻唑(3A-F),这是绝对的 在回流下用巯基乙酸(0.001mol)和无水氯化锌处理的乙醇,得到8小时,得到3- [1,3-苯并噻唑-2-基甲基)氨基] -5-(芳基)-1,3-噻唑烷-2- 那些(4A-F)。 另一方面,当化合物(3A-F)处理用重氮甲烷处理时,得到苯并噻唑N-芳基甲基甲酰胺](5A-F)。

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