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F. A. Abu-Shanab, S. A. S. Mousa, et al., “Dimethylformamide Dimethyl acetal as a Building Block in Heterocyclic Synthesis,” Journal of Heterocyclic Chemistry, Vol. 46, No. 5, 2009, pp. 801-827. doi:10.1002/jhet.69

has been cited by the following article:

• TITLE: Dimethylformamide Dimethyl Acetal (DMFDMA) in Heterocyclic Synthesis: Synthesis of Polysubstituted Pyridines, Pyrimidines, Pyridazine and Their Fused Derivatives

  AUTHORS: Fathi A. Abu-Shanab, Sayed A. S. Mousa, E. A. Eshak, Ahmed Z. Sayed, Ahmed Al-Harrasi

  KEYWORDS: DMFDMA, Malononitrile Dimer, Pyridazine-3, 5-carbonitrile, Pyridine-4-alkoxide

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.1 No.4, December 27, 2011

  ABSTRACT: Reaction of N,N’-dimethylformamide dimethyl acetal (DMFDMA) with malononitrile dimer 8 (1:1) mole afforded 9 while, this reaction when carried out in (2:1) mole to give amidine 11 which can be used for the preparation of pyrimidine 13, amidine 14 and pyridine 19 when reacted with 4-nitroaniline, 4-methylaniline and alkoxide respectively. Malononitrile dimer reacted with diazonium chloride to give pyridazine 21, which can be reacted with DMFDMA, AcOH/HCl and cyanoacetamide to give pyridazine 22, 23 and pyrido[4,3-c] pyridazine 24 respectively. The latter reacted with DMFDMA to afford tricyclic compound 25.