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Synthesis and Antifungal Activity of Some New Fluorine-Substituted 4-Thiazolidinone Bearing 1,2,4-Triazinone

机译:某些新的含1,2,4-三嗪酮的氟代4-噻唑烷酮的合成及抗真菌活性

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摘要

Fluorine substituted 4-thiazolidinone 5 bearing 1,2,4-triazinone obtained from the condensation of 3-Amino-6(2’-aminophenyl)-1,2,4-triazin-5(4H)-one (2) with an aromatic aldehyde followed by cycloaddition with mercaptoacetic acid afforded the thiazolidinone (4), and treatment with ethyl trifluoroacetate. Structure of the products has been deduced from their correct elemental analysis and spectral measurements. The antifungal activity of the new fluorinated target also has been evaluated.
机译:由3-氨基-6(2'-氨基苯基)-1,2,4-三嗪-5(4H)缩合获得的带有1,2,4-三嗪酮的氟取代的4-噻唑烷酮 5 -1( 2 )与芳族醛的混合物,然后与巯基乙酸环加成,得到噻唑烷酮( 4 ),然后用三氟乙酸乙酯处理。产品的结构是根据其正确的元素分析和光谱测量得出的。还评估了新型氟化靶的抗真菌活性。

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