Abstract
Quinoxaline during the reaction with 3-methyl-1-phenylpyrazol-5-one in the presence of triethylamine at room temperature in dimethylsulfoxide eliminates o-phenylenediamine and gives 4,4’-methylene-bis(3-methyl-1-phenylpyrazol-5-one) and 1,1,2,2-tetrakis(5-methyl-2-oxo-2-phenyl-1,2-dihydro-3H-pyrazol-4-yl)ethane. The latter was proved to be the intermediate to form the above dipyrazolylmethane derivative.
References
1.
Rusinov G.L., Slepukhin P.A., Charushin V.N., Dyachenko O.A., Kazheva O.N., Chekhlov A.N., Verbitsky E.V., Kodess M.I., Chupakhin O.N.
Mendeleev Communications,
2006
2.
M. G. Ponizovskii, O.N. Chupakhin, V.N. Charushin and G. G. Aleksandrov, Khim. Geterotsikl. Soedin., 1982, 1410.[Chem. Heterocycl. Compd. (Engl. Transl.), 1982, 18, 1098].
3.
Azev Y.A., Neunhoeffer H., Foro S., Lindner H.J., Shorshnev S.V.
Mendeleev Communications,
1995
4.
Azev Y.A., Shorshnev S.V., Golomolzin B.V.
Tetrahedron Letters,
2009
5.
Sheldrick G.M.
Acta Crystallographica Section A Foundations of Crystallography,
2007