4.4 Article

One-pot, two-step synthesis of 3,4-dihydroquinazoline-2(1H)-thiones from o-azidobenzenealdehydes, aryl amines and carbon disulfide

Journal

TETRAHEDRON LETTERS
Volume 81, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2021.153361

Keywords

3,4-Dihydroquinazoline-2(1H)-thione; Reductive amination; Staudinger-aza-Wittig reaction; o-Azidobenzaldehyde; One-pot synthesis

Funding

  1. Program for Science and Technology Development of Henan [212102310883]
  2. Key Natural Science Research Program of Henan Education Department [20B150014, 21B150013]
  3. Key Scientific Research Projects of Jiyuan Vocational and Technical College [JZXY-2020-]

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This method involves the reductive amination of o-azidobenzaldehydes and aryl amines followed by the Staudinger-aza-Wittig reaction with CS2 to synthesize 3-aryl-3,4-dihydroquinazoline-2(1H)-thiones in one pot and two steps.
A one-pot, two-step method was developed for the synthesis of 3-aryl-3,4-dihydroquinazoline-2(1H)-thiones involving the reductive amination of o-azidobenzaldehydes and aryl amines followed by the Staudinger-aza-Wittig reaction with CS2. (C) 2021 Elsevier Ltd. All rights reserved.

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