Issue 22, 2015

Synthesis of 4(3H)quinazolinimines by reaction of (E)-N-(aryl)-acetimidoyl or -benzimidoyl chloride with amines

Abstract

An efficient one-step method to access 4(3H)quinazolinimines by reaction of phenylchloroimines with 2-aminobenzonitrile is described. The reaction of (E)-N-(2-cyanophenyl)benzimidoyl chloride with substituted anilines that yields a number of their corresponding C2, N3-substituted quinazoliniminium chlorides or neutral products is also reported. These methods provide direct and flexible access to diverse substituted iminoquinazolines substituted at the C2, N3-positions. All the new compounds were fully characterized and six examples are given with their single-crystal X-ray structure.

Graphical abstract: Synthesis of 4(3H)quinazolinimines by reaction of (E)-N-(aryl)-acetimidoyl or -benzimidoyl chloride with amines

Supplementary files

Article information

Article type
Paper
Submitted
05 Mar 2015
Accepted
23 Apr 2015
First published
23 Apr 2015

Org. Biomol. Chem., 2015,13, 6183-6193

Author version available

Synthesis of 4(3H)quinazolinimines by reaction of (E)-N-(aryl)-acetimidoyl or -benzimidoyl chloride with amines

C. Quintero, M. Valderrama, A. Becerra, C. G. Daniliuc and R. S. Rojas, Org. Biomol. Chem., 2015, 13, 6183 DOI: 10.1039/C5OB00444F

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