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Abstract <p>Chelidamic acid was successively converted to 4-chloropyridine-2,6-dicarboxamide and 4-chloro­pyridine-2,6-dicarbonitrile, and reaction of the latter with 2-aminoacetaldehyde diethyl acetal afforded 4-chloro-2,6-bis(1<i>H</i>-imidazol-2-yl)pyridine which is a promising tridentate ligand.</p>

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Synthesis of 4-Chloro-2,6-bis(1H-imidazol-2-yl)pyridine

  • 期刊论文

  • 发表日期：

    2025年3月1日

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  • I. A. Osʼkina,
  • L. G. Lavrenova,
  • A. Ya. Tikhonov

摘要

Abstract

Chelidamic acid was successively converted to 4-chloropyridine-2,6-dicarboxamide and 4-chloro­pyridine-2,6-dicarbonitrile, and reaction of the latter with 2-aminoacetaldehyde diethyl acetal afforded 4-chloro-2,6-bis(1H-imidazol-2-yl)pyridine which is a promising tridentate ligand.