首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Synthesis of pyrazole imines and azetidinone compounds using conventional and microwave technique and studies of their antibacterial activity
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Synthesis of pyrazole imines and azetidinone compounds using conventional and microwave technique and studies of their antibacterial activity

机译:常规和微波技术合成吡唑亚胺和氮杂环丁酮化合物及其抗菌活性的研究

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摘要

A series of compounds 4-[spiro-{1'-(4"-methylphenyl)-3'-methyl)-pyrazole]-3-chloro-l-(substitutedbenzothiazole)-2-azetidinone 4a-j have been prepared by the reaction of l-(4'-methylphenyl)-3-methyl-5-(2"-iminosubstitutedbenzo-thiazole)pyrazoles 3a-j with chloroacety! chloride in the presence of triethylamine.The pyrazole derivatives 3a-j have been prepared by the condensation of substituted 2-aminobenzothiazole 1 with l-(4'-methylphenyl)-3-methyl-5-pyrazolone 2.Both the reactions have been carried out by conventional and microwave methods.The synthesized compounds are screened for their antibacterial activity against Staphylococcus aureus,Bacillus subtilis,Escherichia coli and Salmonella typhi.
机译:通过以下方法制备了一系列化合物4- [螺​​-{1'-(4”-甲基苯基)-3'-甲基)-吡唑] -3-氯-1-(取代的苯并噻唑)-2-氮杂环丁酮4a-j。 -(4'-甲基苯基)-3-甲基-5-(2“-亚氨基取代的苯并噻唑)吡唑3a-j与氯乙炔基的反应!吡唑衍生物3a-j是通过取代的2-氨基苯并噻唑1与1-(4'-甲基苯基)-3-甲基-5-吡唑啉酮2的缩合反应制得的。通过常规方法和微波方法筛选合成的化合物。它们对金黄色葡萄球菌,枯草芽孢杆菌,大肠杆菌和鼠伤寒沙门氏菌具有抗菌活性。

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