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Synthesis of some new urea and thiourea derivatives and evaluation of their antimicrobial activities

机译:一些新的尿素和硫脲衍生物的合成及其抗菌活性的评价

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摘要

In the present stndy, 18 new compounds were synthesized, 9 of which were urea (9a-e, 10a-d) while the others were thiourea (11a-e. 12a-d) derivatives. These derivatives were prepared by the reaction of 6-amino-5-nonsubstituted/chloro-3-methyl-2(3H)-benzoxazolones used as key intermediates with the appropriate isocyanates and isothiocyanates. The chemical structures of new compounds were confirmed by H-NMR, mass, and elemental analysis. The synthesized compounds were screened for their antibacterial and antifungal activities against some pathogenic strains. Compounds 9a. 9b. 9e, 10a. and 10c, urea derivatives, and compounds 12a and 12d, thiourea derivatives, exhibited a relatively good inhibitory profile against E. c.oli. with a MIC value of 32 μg/μL when compared with the other target compounds.
机译:在目前的研究中,合成了18种新化合物,其中9种是脲(9a-e,10a-d),而其他则是硫脲(11a-e。12a-d)衍生物。这些衍生物是通过将用作关键中间体的6-氨基-5-非取代/氯-3-甲基-2(3H)-苯并恶唑酮与适当的异氰酸酯和异硫氰酸酯反应制得的。通过1 H-NMR,质量和元素分析证实了新化合物的化学结构。筛选合成的化合物对某些病原菌株的抗菌和抗真菌活性。化合物9a。 9b。 9e,10a。 10c是脲衍生物,而化合物12a和12d是硫脲衍生物,表现出对大肠杆菌的相对良好的抑制特性。与其他目标化合物相比,MIC值为32μg/μL。

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