苯并咪唑新衍生物的设计、合成及其镇痛抗癌作用

Helmy M. Sakr, R. Ayyad, Kazem Mahmoud, A. Mansour, A. G. Ahmed
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引用次数: 2

摘要

这项工作包含了苯并咪唑衍生物中的一些新化合物,它是由邻苯二胺和二硫化碳缩合而成的2-巯基苯并咪唑,经醇氢氧化钾处理后形成2-巯基苯并咪唑钾盐,与不同物质(氯乙酸烷基酯、氯乙酸氯烷基酯、卤代烷基酯)反应,乙氧基羰基甲基硫代苯并咪唑与不同的胺。除了由邻苯二胺和氯乙酸反应产生的氯甲基苯并咪唑外,氯乙酸还与不同的胺反应。合成的化合物作为镇痛剂和抗癌活性测试,新的衍生物显示出中等、强烈和非常强烈的镇痛剂和中等和强烈的抗癌活性。
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Design, Synthesis of Analgesics and Anticancer of Some New Derivatives of Benzimidazole
This work, contains some new compounds from benzimidazole derivatives, which are synthesized by condensation of Orthophenylene diamine and Carbon disulfide resulting in 2-Mercapto-benzimidazole which is treated by alcoholic potassium hydroxide forming potassium salt of 2-mercaptobenzimidazole which reacts with different substances (alkyl chloroacetates, chloroacetic chloride, alkyl halides) also the ethoxy carbonyl methyl thiobenzimidazole reacts with different amines. In addition to chloromethyl benzimidazole which resulted from the reaction between orthophenylene diamine and chloroacetic acid, which reacted with different amines. The synthesized compound tested as analgesics and anticancer activity the new derivatives revealed moderate, strong and very strong analgesics and moderate and strong anticancer activity.
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