4.4 Article

An efficient synthesis of diimidazo[1,2-a:1′,2′-c]quinazolines via a copper-catalyzed double Ullmann cross-coupling reaction

Journal

TETRAHEDRON
Volume 81, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2020.131918

Keywords

Diimidazoquinazoline; Ullmann reaction; Cross-coupling; Copper-catalyzed; 2-Bromo-1H-imidazole

Funding

  1. NSFC of China [21702078, 21772070]
  2. Natural Science Foundation of Jiangsu Higher Education Institution [17KJA150003]
  3. TAPP

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2,3-Bisaryldiimidazo [1,2-a:1',2'-c]quinazolines were successfully synthesized via a copper-catalyzed reaction, with good yields. This reaction employed a double Ullmann cross-coupling to build two new Csp(2)-N bonds in one-pot procedure, resulting in the formation of a tetracyclic heterocycle bearing four nitrogen atoms.
2,3-Bisaryldiimidazo [1,2-a:1',2'-c]quinazolines were obtained via a copper-catalyzed reaction between 2-(2-bromophenyl)-4,5-diphenyl-1H-imidazole and 2-bromo-1H- imidazole in good yields. This double Ullmann cross-coupling built two new Csp(2)-N bonds and fused tetracyclic heterocycle bearing four nitrogen atoms in one-pot procedure. (C) 2021 Elsevier Ltd. All rights reserved.

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