Abstract <p>Previously unknown 2-amino-4,6-di(pyridin-4-yl)benzene-1.3.5-tricarbonitrile has been synthesized by the 2:1 condensation of 2-(pyridin-4-ylmethylidene)malononitrile with malononitrile in the presence of <i>N</i>-methylpiperazine as catalyst. The product structure has been determined by NMR spectroscopy and X-ray analysis, and a probable mechanism of its formation has been proposed.</p>

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Synthesis of a Hexasubstituted Benzene Derivative from Pyridine-4-carbaldehyde and Malononitrile

  • I. G. Mamedov,
  • F. N. Naghiyev,
  • I. A. Yakushev,
  • V. N. Khrustalev

摘要

Abstract

Previously unknown 2-amino-4,6-di(pyridin-4-yl)benzene-1.3.5-tricarbonitrile has been synthesized by the 2:1 condensation of 2-(pyridin-4-ylmethylidene)malononitrile with malononitrile in the presence of N-methylpiperazine as catalyst. The product structure has been determined by NMR spectroscopy and X-ray analysis, and a probable mechanism of its formation has been proposed.