Molecules (Jan 2011)

A Route to Dicyanomethylene Pyridines and Substituted Benzonitriles Utilizing Malononitrile Dimer as a Precursor

  • Noha M. Helmy,
  • Monirah A. Al-Alshaikh,
  • Fatma E. M. El-Baih,
  • Moustafa S. Moustafa

DOI
https://doi.org/10.3390/molecules16010298
Journal volume & issue
Vol. 16, no. 1
pp. 298 – 306

Abstract

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The conditions of the reaction of malononitrile dimer with enaminones and arylidenemalononitrile could be adapted to yield either pyridines or benzene derivatives. A new synthesis of pyrido[1,2-a]pyrimidines from the reaction of malononitrile dimer 1 and 2-phenyl-3-piperidin-1-yl-acrylonitrile (11) is described. Compound 1 condensed with DMFDMA to yield an enaminonitrile that reacted with hydrazine hydrate to yield N',4,6-triamino-2H-pyrazolo[3,4-b]pyridine-5-carboxamidine (17).

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