Abstract
A series of new pyrazole-5-carboxamide derivatives was synthesized containing flexible chain moiety. The synthetic route involved four-step approach starting from ethyl 3-ethyl-1-methyl-1H-pyrazole-5-carboxylate (1). The primarily nematicidal bioassay results have shown that some of them exhibited moderate activity against Meloidogyne incognita at 10 mg/L. In addition, the molecular docking simulation results indicated that compound 5r interacts with succinate dehydrogenase (SDH) through p-cation, p-p, and hydrogen bond interaction, which may provide useful information to further design novel nematicides.. KEYWORDS :Molecular docking, Nematicidal activity, Pyrazole carboxamide, Synthesis.
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