Cyclization Reactions of Mono-Thiocarbohydrazones with α-Haloketones: Synthesis and Potential Biological Activities of Substituted 1,3-thiazoles and 1,3,4-thiadiazines

IF 0.4 Q4 CHEMISTRY, MULTIDISCIPLINARY Jordan Journal of Chemistry Pub Date : 2021-08-01 DOI:10.47014/16.2.1
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引用次数: 0

Abstract

A series of new substituted 1,3-thiazole derivatives 10a-h were prepared via the reaction of monothiocarbohydrazones 8a-h with one equivalent of α-bromoketones in ethanol. Similarly, another series of new substituted 1,3,4-thiadiazines 11a-e were prepared from the reaction of monothiocarbohydrazones 8i,j with one equivalent of α-bromoketones in ethanol. The resulting products were obtained as colored crystals in moderate to good yields. All new compounds are fully characterized by 1H-, 13C-NMR, IR and elemental analysis. Pharmacophore modeling study of four of the synthesized compounds revealed that at least two of them have potential biological activities. Some of these activities will be investigated experimentally in the lab.
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单硫代碳腙与α-卤代酮的环化反应:取代1,3-噻唑和1,3,4-噻二嗪的合成及其潜在的生物活性
通过单硫代羧腙8a-h与一当量的α-溴酮在乙醇中的反应,制备了一系列新的取代的1,3-噻唑衍生物10a-h。类似地,由单硫代羧腙8i,j与一当量的α-溴酮在乙醇中的反应制备了另一系列新的取代的1,3,4-噻二嗪11a-e。所得产物以中等至良好的产率获得彩色晶体。所有新化合物均通过1H-、13C-NMR、IR和元素分析进行了表征。对四种合成化合物的药效团建模研究表明,其中至少有两种化合物具有潜在的生物活性。其中一些活动将在实验室进行实验研究。
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来源期刊
Jordan Journal of Chemistry
Jordan Journal of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
0.50
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发文量
7
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