Cyanoacetic acid hydrazide: An efficient access for the synthesis of multi‐functional azine and azole derivatives

Abstract

Herein, the synthesis of nitrogen-containing heterocyclic scaffolds from heterocyclization of cyanoacetic acid hydrazide derivatives is described. Thiosemicarbazide derivative 1a undergoes base-mediated cyclization producing pyrazole derivative of type 2. The triazolopyridine 5 was obtained by double cyclization of 1a and benzylidene malononitrile. Compound 1b condensed with ethyl chloroformate to furnish pyrazolooxazine 8. Compound 1b was added to benzoyl isothiocyanate under thermal condition to form oxadiazine derivative 10 while, keeping the above reactant under room temperature to form acyclic derivative 11. Using CS 2 as a cyclizing agent for compound 1b yielded pyrazole derivative 13. Treatment of 1b with I 2 resulted in oxidative cyclization producing pyridazine derivative 14. Compound 1c cyclized with benzoyl isothiocyanate forming triazolothiazine derivative 18. While using cinnamoyl isothiocyanate, the acyclic product 22 was obtained. Compound 1c was condensed with formaldehyde leading to oxadiazole derivative 25.

Imidazo[1,2,4]triazolone and fused imidazo[1,2,4]triazolone derivatives: Synthesis, in vitro anticancer screening, CDK2 inhibitory activity, and molecular modeling studies

“…Cyanoacetohydrazide and thiocarbohydrazide are versatile intermediates for the synthesis of a wide range of heterocyclic compounds [41][42][43][44]. In this approach, we utilized those reagents for the synthesis of the tricyclic derivatives 13 and 14 via their cyclocondensation reaction with derivative 9.…”

Tandem Ring‐Opening/Double Ring‐Closing Synthesis of 1,2,4‐Triazolo[1,5‐a]pyridines from Chromone‐Containing Acrylonitriles

“…On the other hand, available 1,3-amphiphiles are acid hydrazidesversatile building blocks for a construction of heterocycles. [10] Moreover, they often act as 1,3amphiphilic reagents in the synthesis of pyrazole, 1,2,4-triazole and 1,3,4-thiadiazole rings.…”