Synthesis of Pyridinecarbothionylaminopyridines and Conversion of Thioamide to Amide
Corresponding Author(s) : D.I. Jung
dijung@dau.ac.kr
Asian Journal of Chemistry,
Vol. 23 No. 11 (2011): Vol 23 Issue 11
Abstract
Pyridinecarbothionylaminopyridines as structural isomers were obtained by the reactions of 2,3-and 2-4-lutidine with aminopyridines and sulfur. Reaction of 2,6-lutidine with active methyl group anilines in the presence of sulfur gave the desired thioamides 5. Reaction of synthesized thioamides 5 with sulfur and SiO2 or SeO2 gave the corresponding amide 6. We now report conversion of thioamide to amide by using oxidizing inorganic reagent.
Keywords
Aminopyridines
Lutidines
Thioamides
Amides
Oxidizing inorganic reagent
Choi, S., Yoon, J., Lee, E., Kim, J., Kim, Y., Jung, D., & Hahn, J. (2011). Synthesis of Pyridinecarbothionylaminopyridines and Conversion of Thioamide to Amide. Asian Journal of Chemistry, 23(11), 4987–4989. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/11026
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