4.5 Article

NH4OAc-Promoted Cascade Approach towards Aberrant Synthesis of Chromene-Fused Quinolinones

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2019, Issue 4, Pages 705-714

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201801292

Keywords

Nitrogen heterocycles; Domino reactions; Coumarin; Quinolinones; Cyclization

Funding

  1. Science and Engineering Research Board (SERB), New Delhi [EMR/2017/000598]
  2. UGC, New Delhi

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A concise cascade strategy for the synthesis of 6H-chromeno[4,3-b]quinolin-6-ones was developed from 4-hydroxycoumarins and arylhydrazine hydrochlorides in DMSO. The synthetic strategy relies on dual role of ammonium acetate in generating 4-aminophenyl coumarin from arylhydrazine via aryl radical formation, and Csp(2)-H formylation of coumarin using DMSO as a methine source. The strategy is scalable, and an array of arylhydrazine hydrochlorides delivered chromene-fused quinolinones in good to excellent yields.

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