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Rapid synthesis and biological evaluation of 1,4-dihydropyridine derivatives containing a benzothiazolyl moiety

机译:含苯并噻唑基部分的1,4-二氢吡啶衍生物的快速合成和生物学评估

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摘要

A series of N-(6-methylbenzothiazolyl)-2,3,5,6-tetrasubstituted-4-(aryl)-1,4-dihydropyridines were synthesized by reaction of 2-amino- 6-methylbenzothiazole, aromatic aldehyde and active methylene compound in methanol by conventional, as well as, microwave irradiation (solvent free and solid support) methods. The microwave irradiation technique gives better yield and shorter reaction time. Among solid supported microwave irradiation better yields are obtained in acidic alumina as compared to silica, neutral alumina, and basic alumina. All compounds were tested for antibacterial and antifungal activities and results have been compared with standard drugs. Entomological activities were also tested. The results showed that a change in the substitution pattern in 1,4-dihydropyridine derivatives may cause a marked effect on their antimicrobial activity.
机译:通过2-氨基-6-甲基苯并噻唑,芳香醛与活性亚甲基的反应合成了一系列的N-(6-甲基苯并噻唑基)-2,3,5,6-四取代-4-(芳基)-1,4-二氢吡啶通过常规方法以及微波辐射(无溶剂和固体支持物)方法将化合物溶于甲醇中。微波辐照技术可提高收率,缩短反应时间。与二氧化硅,中性氧化铝和碱性氧化铝相比,在固体负载的微波辐射中,酸性氧化铝可获得更好的产率。测试所有化合物的抗菌和抗真菌活性,并将结果与​​标准药物进行比较。还测试了昆虫活动。结果表明,1,4-二氢吡啶衍生物中取代模式的改变可能对其抗菌活性产生显着影响。

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