Title:Synthesis of New Thiazolidinones and Thiazoles in Indole Series
Volume: 20
Issue: 1
Author(s): Sofiane Khanoussi, Abdelmadjid Benmohammed*, Omar Khoumeri, Mokhtaria Kadiri, Ayada Djafri, Thierry Terme and Patrice Vanelle*
Affiliation:
- Laboratoire de Synthèse Organique Appliquée (LSOA), Département de Chimie, Faculté des Sciences Exactes et Appliquées, Université Oran1 Ahmed Ben Bella, BP 1524 El M’Naouer, Oran 31000, Algeria
- Department of Chemistry, Faculty of Exact Sciences, University of Mascara, Mascara 29000, Algeria.
- Laboratoire de Pharmaco Chimie Radicalaire,
Aix Marseille Université, CNRS, ICR Institut de Chimie Radicalaire, UMR 7273, Faculté de Pharmacie, 27 Boulevard
Jean Moulin-CS 30064, 13385 Marseille Cedex 05, France
Keywords:
Thiosemicarbazone, thiazolidinone, thiazole, indole, condensation, cyclization.
Abstract: Recent findings confirm that thiosemicarbazones and thiazoles offer a wide range of biological
properties. We report here the synthesis of two series of highly functionalized thiazole-derived
compounds from the reactions of various indole-derived thiosemicarbazones with diethyl acetylenedicarboxylate
and 4-bromophenacyl bromide. As a result, a series of new derivatives of thiosemicarbazone,
thiazolidinone, and thiazole bearing an indole moiety was synthesized and developed in good
yields.