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SYNTHESIS AND DOCKING STUDIES OF 2-AMINOTHIAZOLE-5-AROMATIC CARBOXAMIDE DERIVATIVES

Keywords: 2-amino-thiazole-5-carboxamide derivatives , Piperazine derivatives , Docking and 2GQG , anti-cancer activity

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Abstract:

A novel N-(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-pipear azinyl]-2-methyl-4-pyrimidinyl] amino]-5-thiazolecarboxamide derivatives (6a-6d) and (8a-8b) were synthesized by coupling 2-[(6-chloro-2-methylpyrimidin-4ylamino]-N-(2-chloro-6-methylphenyl) thiazole-5-Carboxamide(3) with Piperazine derivatives(4,7) in butanol and DIPEA (Diisopropylethylamine) at 120oC for 4-5hrs. All the synthesized compounds were characterized physically and elucidated by Infrared spectroscopy, Mass spectroscopy, 1H-NMR spectroscopic techniques. All the synthesized compounds were subjected to Molecular docking studies by using 2GQG as its PDB ID. Among all the compounds, 6a, 6b, 6d, 8c and 8b exhibit anticancer activity.

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