首页> 外文期刊>International Scholarly Research Notices >Synthesis and Antimicrobial Screening of Novel 4-Substituted Phenyl-5-[1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-yl]-2H-1,2,4-triazole-3-thiones
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Synthesis and Antimicrobial Screening of Novel 4-Substituted Phenyl-5-[1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-yl]-2H-1,2,4-triazole-3-thiones

机译:新型4-取代的苯基-5- [1-(4-氟苯基)-1,3-二氢异苯并呋喃-5-基] -2H-1,2,4-三唑-3-硫酮的合成及抗菌筛选

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The paper describes a convenient method for the preparation of 4-substituted phenyl-5-[1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-yl]-2H-1,2,4-triazole-3-thiones. The structures of the synthesized compounds are established by the results of LCMS,1H NMR,13C NMR, and IR and elemental analyses. The mercaptotriazoles are indicated to be in thione form by1H NMR spectra. All the synthesized compounds have been screened for antibacterial and antifungal activities. Compounds12dand12hexhibit encouraging results, while the remaining compounds show moderate activities. On the basis of spectral studies, formation of 2-amino-1,3,4-thiadiazoles from the isobenzofuran acyl thiosemicarbazides11(a–h)is ruled out.
机译:该论文描述了一种方便的制备4-取代的苯基-5- [1-(4-氟苯基)-1,3-二氢异苯并呋喃-5-基] -2H-1,2,4-三唑-3-硫酮的方法。通过LCMS,1 H NMR,13 C NMR,IR和元素分析的结果,确定了合成化合物的结构。 1 H NMR谱表明巯基三唑为硫酮形式。已经筛选了所有合成的化合物的抗菌和抗真菌活性。化合物12d和12抑制了令人鼓舞的结果,而其余化合物显示出中等活性。在光谱研究的基础上,排除了由异苯并呋喃酰基硫代氨基脲11(a–h)形成2-氨基-1,3,4-噻二唑的可能性。

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