Synthesis, Characterization and biological activity of some novel heterocyclic β-lactam/thiazol compounds derived from 4-phenyl-4,5-dihydrothiazol-2-yl-imino
Ram Prakash, R.B. Singh, R.K. Vishnoi, K. Srivastava
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引用次数: 0
Abstract
An efficient and convenient synthesis of β-lactam/ thiazol derivatives has been achieved by the reaction of acetophenone, substituted aromatic aldehyde and thiourea yield substituted schiff’s bases which further undergo the cyclization in the presence of chloroacetyl chloride, triethyl amine/ZnCl2, thioglycoolic acid. All the synthesized novel derivatives have been established by % of C, N, S elements, FT-IR, 1H NMR and Mass spectral studies. Further in-vitro antimicrobial activity of novel derivatives was carried out against some Gram-positive and Gram-negative bacteria by serial dilution method. The activity of IIIc, IIId, IIc, IId, IIf derivatives showed significant response against the tested microbes.
以苯乙酮、取代芳醛和硫脲为原料,在氯乙酰氯、三乙胺/ZnCl2、巯基乙酸的存在下,生成取代席夫碱,并进行环化反应,合成了一种高效、方便的β-内酰胺/噻唑衍生物。所有合成的新衍生物均通过C, N, S元素的%,FT-IR, 1H NMR和质谱研究得到证实。采用连续稀释法进一步测定了新型衍生物对革兰氏阳性菌和革兰氏阴性菌的体外抑菌活性。IIIc、IIId、IIc、IId、IIf衍生物对被试微生物的活性有显著的响应。