3-chloro-4-fluoroaniline was taken in dioxane, solution of p-toluenesulfonyl chloride in dioxane was added dropwise with stirring. Then the mixture was refluxed to get 3-chloro-4-fluorosulphanilamide. Solution of sulphanilamide in DMSO was refluxed with various primary and secondary amines to get 3-amino substituted fluorosulphanilamides.
Copy the following to cite this article:
N. T. Havannavar; S. U; L. Nargund, "SYNTHESIS AND EVALUATION OF FLUORO-ULPHANILAMIDES AS POSSIBLE ANTI-MICROBIAL AGENTS", Journal of Ultra Chemistry, Volume 3, Issue 2, Page Number 145-148, 2018Copy the following to cite this URL:
N. T. Havannavar; S. U; L. Nargund, "SYNTHESIS AND EVALUATION OF FLUORO-ULPHANILAMIDES AS POSSIBLE ANTI-MICROBIAL AGENTS", Journal of Ultra Chemistry, Volume 3, Issue 2, Page Number 145-148, 2018Available from: http://www.journalofchemistry.org/paper/653/