Three-component condensation of aromatic aldehydes with malononitrile and 4-hexylresorcinol in toluene in the presence of a base leads to the formation of 2-amino-4-aryl-6-hexyl-7-hydroxy-4 H -chromene-3-carbonitriles in good yields (79-90%). Structure of the compounds was studied using the methods of two-dimensional NMR spectroscopy. Bioavailability parameters were predicted in silico , and possible protein targets were predicted by protein-ligand docking.