ABSTRACT
The aim of this study is the direct synthesis of new (4,6-dimethylpyrimidin-2-yl)thio-N-acetamides derivatives aspossible anticonvulsants. The interaction of thiourea with acetylacetone in sodium ethoxide resulted in the scaffoldof 4,6-dimethyl-2-thiopyrimidine. Thioacetamide derivatives were synthesized by alkylation of 4,6-dimethyl-2-thiopyrimidine with comparable α-chloroacetamides in the Dimethylformamide (DMF) environment and in the presenceof К2СО3. The methods of 1H and 13C Nuclear magnetic resonance (NMR) spectroscopy, Liquid chromatography–mass spectrometry (LS/MS), and elemental analysis established the structure of the synthesized compounds. Theaffinity of the studied compounds with anticonvulsant biotargets— Type-A γ-aminobutyric acid receptor (GABAAR)and the gamma-aminobutyric acid-aminotransferase enzyme—was carried out using the molecular-docking method.The highest affinity was predicted for the compound having 4-bromophenyl substituent: −7.0 (GABAA) and −8.0(GABAАТ) kcal/mol. Nevertheless, all the studied compounds conceded to the reference ligands—phenobarbital(−7.6 kcal/mol) and vigabatrin (−9.0 kcal/mol). The model of pentylenetetrazole-induced seizures in rats has shownthat the studied compounds have moderate anticonvulsant activity. 4-Bromophenyl acetamide has also shown the mostpronounced activity: the substance statistically significantly extended the latency period and reduced the duration ofseizures by 3.4 and 2.2 times, respectively; moreover, it reduced lethality of the laboratory animals by 80% and by2.5 times severity of seizures. Correspondence between the docking results and in vivo studies, using PTZ-inducedseizures, as well as some parameters of “structure-anticonvulsant activity” correlation, was determined.