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Novel Analogues of 2-Pyrazoline:Synthesis,Characterization,and Antimycobacterial Evaluation

机译:2-吡唑啉的新型类似物:合成,表征和抗分枝杆菌评价

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摘要

Fourteen new 1-[(N,N-disubstitutedthiocarbamoylthio)acetyl]-3-(2-thienyl)-5-aryl-2-pyrazoline derivatives were synthesized by reacting 1-(chloroacetyl)-3-(2-thienyl)-5-aryl-2-pyrazolines and appropriate sodium salts of N,N-disubstituted dithiocarbamoic acids in acetone.The structures of the synthesized compounds were confirmed by UV,IR,~1H-NMR,and FAB~+-MS spectral data.The compounds were evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis H37Rv using the BACTEC 460 radiometric system and BACTEC 12B medium.The preliminary results showed that all of the tested compounds were inactive against the test organism.
机译:通过使1-(氯乙酰基)-3-(2-噻吩基)-5反应合成了十四个新的1-[((N,N-二取代硫代氨基甲酰基硫基)乙酰基] -3-(2-噻吩基)-5-芳基-2-吡唑啉衍生物-芳基-2-吡唑啉和N,N-二取代的二硫代氨基甲酸酯在丙酮中的适当的钠盐。合成的化合物的结构通过UV,IR,〜1H-NMR和FAB〜+ -MS光谱数据确认。使用BACTEC 460辐射系统和BACTEC 12B培养基评估了对结核分枝杆菌H37Rv的体外抗分枝杆菌活性。初步结果表明,所有测试化合物均对测试生物无活性。

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