Abstract
A series of new N-benzoyl-N'-triazine thiourea derivatives have been synthesized via the reaction of 4-amino-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one with benzoyl chloride derivatives and ammonium thiocyanate in acetone under reflux conditions. 4-Amino-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one was prepared from the reaction of two equivalents of hydrazine hydrate with carbon disulfide and sodium pyruvate. The chemical structure of thioureas was confirmed using FT-IR, 1H NMR, 13C NMR, and high-resolution mass spectrometry, and elemental analysis. The synthesized thioureas were assayed for their antibacterial activity against both gram-positive (Micrococcusluteus and Bacilluscereus) and gram-negative (Pseudomonasaeruginosa and Escherichiacoli) bacteria using the agar well diffusion method.
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Corresponding author: e-mail: Kshams49@gmail.com (Kh. Pourshamsian); abolfazl.shiroudi@iauet.ac.ir (A. Shiroudi).
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Marzi, M., Pourshamsian, K., Hatamjafari, F. et al. Synthesis of New N-Benzoyl-N'-Triazine Thiourea Derivatives and Their Antibacterial Activity. Russ J Bioorg Chem 45, 391–397 (2019). https://doi.org/10.1134/S106816201905008X
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DOI: https://doi.org/10.1134/S106816201905008X