Different Synthetic Methods for the Preparation of Triazolopyrimidines and their Biological Profile

Author:

Hibot Achraf12,Oumessaoud Asmaa12,Hafid Abderrafia1,Khouili Mostafa1,Pujol Maria Dolors2ORCID

Affiliation:

1. Laboratory of Molecular Chemistry, Materials and Catalysis Faculty of Sciences and Technics Sultan Moulay Slimane University BP 523 23000 Beni-Mellal Morocco

2. Laboratori de Química Farmacèutica Facultat de Farmàcia i Ciències de l'Alimentació Universitat de Barcelona Av. Joan XXIII, 27–31 08028 Barcelona Spain

Abstract

AbstractOne or more nitrogen‐containing molecules constitute an important class of heterocyclic compounds in organic synthesis, due to their reactivity and their presence in many molecules of natural, human or plant origin. These nitrogenous heterocycles play an essential role in various scientific domains, whether they are chemical, biological or pharmacological. N‐heterocycles are the privileged source of many research topics developed by several groups of researchers. Thus, different methods have been developed to access these heterocyclic compounds with nitrogenous rings, such as triazolopyrimidines. In this review, a bibliographic study summarizing the pharmacological importance of the triazolo[1,5‐a]pyrimidine ring, the different synthesis routes of these derivatives as well as their reactivity was reported.

Funder

Université Sultan Moulay Slimane

Universitat de Barcelona

Publisher

Wiley

Subject

General Chemistry

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