109481-01-8Relevant academic research and scientific papers
Enamines; Part 46. Synthesis of 5-Dialkylamino-1-aryl-1,2,3-triazoles Functionalized at C-4
Grassivaro, Nicoletta,Rosi, Elisabetta,Stradi, Riccardo
, p. 1010 - 1012 (1986)
Aryl azides undergo a -cycloaddition with 1,1-diaminoethenes having an electron-withdrawing group at C-2 to give unstable 5,5-diamino-4,5-dihydro-1,2,3-triazoles from which one amino group is eliminated to afford 5-amino-1-aryl-1,2,3-triazoles functionalized at C-4.
