A simple general synthesis of 1-aryl-6-azaisocytosine-5-carbonitriles is described. This method is based on coupling diazonium salts with cyanoacetylcyanamide and then cyclization of the formed 2-arylhydrazono-2-cyanoacetylcyanamides . The 6-azaisocytosines were studied with respect to tautomeric equilibrium and the transformation of functional groups, and used in the synthesis of the condensed heterocyclic compounds: Purine isosteric imidazo[2,1-]-[1,2,4]triazine and the 1,2,4-triazino[2,3-]quinazolines -.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804241 | PMC |
http://dx.doi.org/10.3390/molecules24193558 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!