The Journal of organic chemistry

Synthesis of C-carbamoyl-1, 2, 3-triazoles by microwave-induced 1, 3-dipolar cycloaddition of organic azides to acetylenic amides

AR Katritzky, SK Singh

Index: Katritzky, Alan R.; Singh, Sandeep K. Journal of Organic Chemistry, 2002 , vol. 67, # 25 p. 9077 - 9079

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Citation Number: 125

Abstract

1, 3-Dipolar cycloaddition of organic azides 1, 2, or 3 to acetylenic amides 4 or 5 under solvent-free microwave irradiation produced the corresponding N-substituted C-carbamoyl- 1, 2, 3-triazoles 7a-12a in good to excellent yields. Under similar reaction conditions, 1, 3- dipolar cycloaddition of diazide 6 and acetylenic amide 4 gave the azido-triazole 13a.