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Synthesis and antibacterial evaluation of some2-[5-(aryloxymethyl)-1, 3, 4-oxadiazol-2-ylsulfanyl] propanoic acids

机译:某些2- [5-(芳氧基甲基)-1,3,4-恶二唑-2-基硫烷基]丙酸的合成及抗菌性能评价

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A series of 2-[5-(aryloxymethyl)-1, 3, 4-oxadiazol-2-ylsulfanyl] propanoic acids were synthesized and studied for their antibacterial activity. These compounds were prepared from aryloxyacetic acid hydrazides. Aryloxyacetic acid hydrazides 1 on refluxing with carbon disulfide and methanolic potassium hydroxide and then on subsequent acidification with hydrochloric acid furnished 5-aryloxymethyl-1, 3, 4-oxadiazole-2-thiones 2. 2-Chloro propanoic acid reacted with 2 in alkaline media and then on subsequent acidification yielded the title compounds 3. These compounds were characterized by modern spectroscopic techniques. All the compounds were evaluated for their in vitro antibacterial activity against two Gram negative strains (Escherichia coli and Pseudomonas aeruginosa) and two Gram positive strains (Bacillus subtilis and Staphylococcus aureus) and their minimum inhibitory concentration (MIC) were determined.
机译:合成了一系列的2- [5-(芳氧基甲基)-1,3,4-恶二唑-2-基硫烷基]丙酸并研究了它们的抗菌活性。这些化合物由芳氧基乙酸酰肼制备。芳氧基乙酸酰肼1与二硫化碳和甲醇氢氧化钾回流,然后与盐酸酸化,得到5-芳氧基甲基-1,3,4-恶二唑-2-硫酮2。2-氯丙酸与2在碱性介质中反应然后酸化得到标题化合物3。这些化合物通过现代光谱技术表征。评价所有化合物对两种革兰氏阴性菌株(大肠杆菌和铜绿假单胞菌)和两种革兰氏阳性菌株(枯草芽孢杆菌和金黄色葡萄球菌)的体外抗菌活性,并测定其最低抑菌浓度(MIC)。

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