Ynthesis of 6-piperazinyl-3,4-dihydroquinazolin-2(1H)-ones

N. Ullah*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

A series of new 6-piperazinyl-3,4-dihydroquinazolin-2(1H)-ones have been synthesized. The described compounds are structurally related to adoprazine, a potential atypical antipsychotics bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties. Buchwald- Hartwig coupling of suitably modified aryl bromides with tert-butyl piperazine-1-carboxylate afforded the advanced intermediate piperazinyl-3,4-dihydroquinazolin-2(1H)-one. The reductive amination of the latter with appropriately designed biarylaldehydes accomplished the synthesis of 6-piperazinyl-3,4-dihydroquinazolin-2(1H)-ones.

Original languageEnglish
Pages (from-to)2031-2036
Number of pages6
JournalAsian Journal of Chemistry
Volume26
Issue number7
DOIs
StatePublished - 2014

Keywords

  • 4-dihydroquinazolin-2(1h)-ones
  • 5-ht1a receptor
  • 6-piperazinyl-3
  • Buchwald-hartwig coupling
  • Schizophrenia

ASJC Scopus subject areas

  • General Chemistry

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