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Syntheses of 2-(6’-Fluorobenzothiazol-2’-ylamino)-4, 6-(disubstituted thiouriedo)-1,3-pyrimidine Derivatives as Antimicrobial Agents

机译:合成2-(6'-氟苯噻唑-2'- ylamino)-4,6-(二取代的硫替二替二替二替替替替替替替替替替替替司)-1,3-嘧啶衍生物作为抗微生物剂

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摘要

A new series of 1,3-pyrimidine derivatives (3a-f) have been synthesized by reacting 2,4,6-Trichloropyrimidine with nucleophilic reagents 2-amino-6-fluorobenzothiazole (1) in the presence of acetone. The (4,6- dichloro-pyrimidin-2-yl)-amine (2) so produced was then reacted to two moles of phenylthiourea derivatives to yield title compounds (3a-f). The structural assessment of the compounds (3a-f) was made on the basis of spectral data. The synthesized compounds were screened for their in vitro growth inhibiting activity against different strains of bacteria viz., B. subtilis, E. coli, P. aeruginosa and S. aureus using agar diffusion technique. Compounds 3c and 3f exhibited highest antibacterial activity.
机译:通过在丙酮存在下反应2,4,6-三氯吡啶胺2-氨基-6-氟苯噻唑(1),通过将2,4,6-三氯嘧啶与丙酮反应合成了一种新的1,3-嘧啶衍生物(3A-F)。然后制备的(4,6-二氯嘧啶-2-基)-amine(2)反应到两摩尔的苯硫脲衍生物,得到标题化合物(3A-F)。化合物(3A-F)的结构评估是在光谱数据的基础上进行的。筛选合成的化合物,用于对不同菌株的体外生长抑制活性,免受不同菌株的抑制活性。,B.枯草芽孢杆菌,大肠杆菌,使用琼脂扩散技术的金黄色葡萄球菌。化合物3C和3F表现出最高的抗菌活性。

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