40995-50-4Relevant articles and documents
1,3-Dipolar cycloaddition of diazomethane to differently substituted 2-methylpyridazin-3(2H)-ones
Farina, Francisco,Martin, M.Victoria,Romanach, Magali,Sanchez, Felix
, p. 1431 - 1436 (2007/10/02)
Cycloaddition of diazomethane to 4- or 5-substituted 2-methylpyridazin-3 (2H)-ones 1,2 occurs in a practically regiospecific manner to give the expected adducts, which are not stable enough to be isolated and under the reaction conditions are transformed into N, N′-dimethylpyrazolopyridazinones and/or 2,4 (or 2,5)-dimethylpyridazin-3(2H)-ones, depending on the nature and position of the substituents. The regiochemistry of the cycloaddition and the reactivity of pyridazin-3 (2H)-ones 1,2 have been accounted for theoretically by the FMO approach.