The arylhydrizocyanacetamides (1) was prepared from the reaction of diazonium salts of substituted aniline with active methylene compounds such as cyanoacetamide. The compounds were reacted with substituted phenyl isothiocyanates in dry pyridine to give corresponding 2,4-N-aryl-as-1,2,4-triazine 3-thiones. Some of the compounds show promising anti-inflammatory activity.
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R. Antony; Shantharam.u; S. L. ; L. Nargund, "Synthesis and antiinflammatory activity of 2,4,N-aryl-as-triazines", Journal of Ultra Chemistry, Volume 3, Issue 2, Page Number 141-144, 2018Copy the following to cite this URL:
R. Antony; Shantharam.u; S. L. ; L. Nargund, "Synthesis and antiinflammatory activity of 2,4,N-aryl-as-triazines", Journal of Ultra Chemistry, Volume 3, Issue 2, Page Number 141-144, 2018Available from: http://www.journalofchemistry.org/paper/652/