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Synthesis, characterization, computational study, and screening of novel 1-phenyl-4-(2-phenylacetyl)-thiosemicarbazide derivatives for their antioxidant and antimicrobial activities

机译:新型1-苯基-4-(2-苯基乙酰基)的合成,表征,计算研究和筛选 - 用于其抗氧化剂和抗微生物活性的硫代脲衍生物

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摘要

Condensation reaction of phenyl acetyl isothiocyanate (1) and phenyl hydrazine was performed to obtain 1-phenyl-4-(2-phenylacetyl) thiosemicarbazide (2). Compound (2) was utilized as starting material for synthesis of different fused 1,2,4-triazole compounds. Reaction of (2) with hydrazine hydrate, anthranilic acid and ethyl glycinate under microwave irradiation and traditional thermal conditions afforded 1,2,4-traizol derivatives (4, 5 and 6) respectively. On the other hand, cyclization reaction of compound (2) under microwave irradiation gave 1,2,4-triazole-3-thione derivative (3). The microwave assessed reaction produced higher yield reaction and purity than the traditional thermal reaction. The chemical structures of the synthesized compounds were elucidated using elemental analysis, FTIR, H-1 NMR, and GC/MS spectroscopy. The synthesized compounds (2-7) were evaluated for their antimicrobial and antioxidant potentials. Density functional theory (DFT) was evaluated at B3LYP/3-21G level to study the electronic and geometric characteristics of (4-6) compounds including the optimized structures, relative binding energies, atomic charges, position of HOMO and LUMO of the molecules. (C) 2021 Elsevier B.V. All rights reserved.
机译:苯乙酰异硫氰酸酯(1)与苯肼进行缩合反应,得到1-苯基-4-(2-苯乙酰基)氨基硫脲(2)。以化合物(2)为起始原料合成了不同的稠合1,2,4-三唑化合物。(2)在微波辐射和传统热条件下与水合肼、邻氨基苯甲酸和甘氨酸乙酯反应,分别得到1,2,4-三唑衍生物(4,5和6)。另一方面,化合物(2)在微波辐射下的环化反应得到1,2,4-三唑-3-硫酮衍生物(3)。微波反应比传统的热反应具有更高的产率和纯度。利用元素分析、FTIR、H-1 NMR和GC/MS光谱对合成化合物的化学结构进行了鉴定。对合成的化合物(2-7)的抗菌和抗氧化潜力进行了评估。密度泛函理论(DFT)在B3LYP/3-21G水平上进行了评估,以研究(4-6)化合物的电子和几何特征,包括优化结构、相对结合能、原子电荷、分子的HOMO和LUMO位置。(c)2021爱思唯尔B.V.保留所有权利。

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