ISSN: 1813-0410

Author : Hadi, Ali

Synthesis of Novel [1,2,4]Triazolo[1,5-a]Pyridines via concerted reactions between 2‾-cinnamoyl-2-cyanoacetohydrazide and α-cyanocinamonitriles

Ali Hadi

journal of kerbala university, 2010, Volume 6, Issue 4, Pages 55-75

A novel one step synthesis of derivatives [1,2,4]triazolo[1,5-a]pyridines (6) from 2′-cinnamoyl-2-cyanoacetohydrazide (3) and α-cyanocinnamonitriles (2) is described. The reaction takes place by 6-exo-dig cyclization followed by an 5-exo-trig process to afford salts 6. Compound 7 were solated from the reaction mixture as the corresponding piperidinium salts due to the high stability of the heterocyclic anion. Acidification with dilute hydrochloric acid yielded the neutral [1,2,4]triazolo [1,5-a]pyridines. Now, an alternative 7-endo trig cyclization can take place and, in addition to the [1,2,4]triazolo[1,5-a] pyridines 6, the novel heterocyclic compound of seven membered ring are obtained