The Synthesis, spectral, molecular docking and antimicrobial studies of some substituted 4-([1,1’-biphenyl]-4-yl) pyrimidine-2(1H)-thiones
DOI:
https://doi.org/10.56042/ijc.v64i5.9338Keywords:
Pyrimidinethiones, 4-acetylbiphenyl, thiourea, NMR spectra, Molecular docking, anti-bacterial activitiesAbstract
Some substituted 4-([1,1’-biphenyl]-4-yl)pyrimidine-2(1H)-thione derivatives were synthesized by one-pot three component synthesis reaction of 4-acetyl biphenyl, various substituted aryl aldehydes and thiourea in the presence of sodium hydroxide. In this reaction the obtained yield was more than 85%. The synthesized pyrimidine thiones were characterized by their physical constants, micro-analysis and spectroscopic data. The molecular docking study of these pyrimidinethiones were investigated with protein interaction-affinity measurements. Using the Bauer-Kirby technique, the antimicrobial abilities of synthesized pyrimidinethiones were evaluated.