Synthesis and Molecular Docking Study of Novel Heterocyclic Compounds from Cyanoacetohydrazide

Abstract

The present study reports the synthesis of some novel heterocyclic derivatives by reacting cyanoacetohydrazide in a basic medium with different electrophilic reagents. Initially, its reaction with H 2 O 2 afforded 1,2,3-triazine-4,6(1H,5H)-dione, which upon addition to benzylidenemalononitrile under Michael's condition yielded 7-amino-4-oxo-5-phenyl-1,5-dihydro-4Hpyrano [2,3-d][1,2,3]triazine-6-carbonitrile. Azidolysis of cyanoacetohydrazide resulted in the formation of 5,8dihydrotetrazolo[1,5-c][1,2,3]triazin-7-ol. On the other hand, heterocyclization of cyanoacetohydrazide with ethyl cyanoacetate and/or chloroacetyl chloride produced 2,5-dioxo-2,4,5,6-tetrahydro-1H-pyrazolo[1,5-b]pyrazole-3-carbonitrile and 3,5-dihydroxy-1,2-dihydropyridazine-4-carbonitrile, respectively. The later undergoes [2+3] intermolecular cycloaddition to the heteroallene system produced 4-(1,2,4-thiadiazol-3-yl)-1,2-dihydropyridazine-3,5-diol. Furthermore, Knoevenagel condensation and intramolecular heterocyclization of cyanoacetohydrazide with benzaldehyde and acetylacetone afforded 3hydroxy-5-phenyl-4H-pyrazole-4-carbonitrile and 5,6a-dimethyl-3-oxo-1,2,3,6a-tetrahydro-3aH-furo[3,2-c]pyrazole-3acarbonitrile, respectively. Intermolecular heterocyclization of cyanoacetohydrazide with diethyl oxalate and carbon disulphide gave 5-Hydroxy-2,3a-dihydropyrrolo[2,3-c]pyrazole-3,4-dione and 4-hydroxy-1,3a-dihydro-3H-pyrazolo[3,4- c]isothiazole-3-thione, respectively. All reactions proceeded in good to excellent yields and the synthesized compounds were identified by different spectroscopic techniques. All the obtained compounds are virtually screened by molecular docking on the target protein 1KZN by the MOE for potency as antibacterial agent. Also, pharmacophore and ADME studies were applied. Efficient binding to the target protein was found for some of the synthesized compounds.