首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >CsF-Celite catalyzed facile N-alkylation of 2(3H)-benzoxazolones and antimicrobial properties of 2-substituted benzoxazole and 3-substituted-2(3H)-benzoxazolone derivatives
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CsF-Celite catalyzed facile N-alkylation of 2(3H)-benzoxazolones and antimicrobial properties of 2-substituted benzoxazole and 3-substituted-2(3H)-benzoxazolone derivatives

机译:CsF-Celite催化2(3H)-苯并恶唑啉酮的简便N-烷基化反应以及2-取代的苯并恶唑和3-取代的2(3H)-苯并恶唑啉酮衍生物的抗菌性能

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摘要

The synthesis and antimicrobial activity studies of a new series of cyclic amine containing benzoxazoles and benzoxazolone-2(3/f)-ones derivatives were described. The alkylation of benzoxazolone was carried out using cesium fluoride-Celite. The newly synthesized compounds with the influence of the induction of the cyclic amine moiety in the benzoxazole scaffold have been evaluated with respect to the antibacterial and antifungal activity. The 2-cyclic amine-1,3-benzoxazoles (5a-l), 5-chloro-3-alkyl substituted-l,3-benzoxazol-2(3H)-ones (8a-f), and 3-[3-(cyclic amine)propyl]-l,3-benzoxazol-2(3H)-ones (9a-f) were synthesized. These derivatives were tested for antibacterial and antifungal activity. Among the compounds tested, 8c and 9f showed moderate to good antibacterial and antifungal activity. Compound 8a showed good antifungal activity.
机译:描述了一系列新的含苯并恶唑和苯并恶唑酮-2(3 / f)-ones衍生物的环胺的合成和抗菌活性。苯并恶唑酮的烷基化是使用氟化铯-Celite进行的。已经评价了在苯并恶唑支架中具有环胺部分的诱导作用的新合成的化合物的抗菌和抗真菌活性。 2-环胺-1,3-苯并恶唑(5a-1),5-氯-3-烷基取代的-1,3-苯并恶唑-2(3H)-ones(8a-f)和3- [3-合成(环胺)丙基] -1,3-苯并恶唑-2(3H)-一(9a-f)。测试了这些衍生物的抗菌和抗真菌活性。在测试的化合物中,8c和9f表现出中等至良好的抗菌和抗真菌活性。化合物8a显示出良好的抗真菌活性。

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