74687-16-4Relevant articles and documents
v-Triazolines. Part XIV. 1-Aryl-5-dialkylaminomethyl-4,5-dihydro-v-triazoles
Pocar, Donato,Rossi, Luisa Maria,Trimarco, Paqualina
, p. 267 - 270 (2007/10/02)
The cycloaddition of arylazides to 1-methyl- and 1-benzyl-2,5-dihydropyrrole affords pyrrolo-v-triazole derivatives which react with methyl iodide, yielding the corresponding quaternary ammonium salts.On base-catalyzed elimination 1-aryl-5-dialkyl-aminomethyl-4-methylene-4,5-dihydro-v-triazoles are formed.Their structure and behaviour toward methoxide and secondary amines are discussed.