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Updated: Jun 24, 2026

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
New imidazo[1,2-a]quinoxaline derivatives: synthesis and in vitro activity against human melanoma
Carine Deleuze-Masquefa1, Georges Moarbess, Sonia Khier
1EA 4215, Laboratoire de Chimie des Biomolécules et de l'Environnement, Pharmacochimie et Biomolécules, Université Montpellier I, Faculté de Pharmacie, 15 av. Charles Flahault, BP 14491, 34 093 Montpellier Cedex 5, France. carine.masquefa@univ-montp1.fr
Abstract:
New imidazo[1,2-a]quinoxaline analogues have been synthesized in good yields via a bimolecular condensation of 2-imidazole carboxylic acid, followed by a coupling with ortho-fluoroaniline and subsequent substitution on the imidazole ring by Suzuki Cross-coupling reaction using microwave assistance. Antitumor activities of these derivatives were evaluated by growth inhibition of A375 cells in vitro. All compounds exhibited high activities compared to imiquimod and fotemustine used as references.
