Abstract:
An expedient access to novel 4-phosphonomethyl-containing 2,6-disubstituted 4,5-dihydropyridazin-3(2H)-ones involves the reaction of β-phosphono γ'-keto ester intermediates with hydrazines. The construction of the pyridazinone ring allows the installation of various substituents at the positions 2 and 6 as well as a valuable 4-positioned phosphonomethyl fragment.
Keywords:
pyridazin-3(2H)-ones, phosphonates, nitroalkanes, γ-keto ester, Michael addition, Nef reaction.
Citation:
O. Bejaoui, A. Abdelli, H. M'rabet, X. Moreau, M. L. Efrit, D. Prim, “A convenient synthesis of new phosphonomethyl-containing 4,5-dihydropyridazin-3(2H)-ones”, Mendeleev Commun., 33:5 (2023), 640–641