Synthesis of New 5- or 7-Substituted 3-Nitroimidazo[1,2-a]pyridine Derivatives Using SNAr and Palladium-Catalyzed Reactions To Explore Antiparasitic Structure–Activity Relationships

Author:

Primas Nicolas12,Vanelle Patrice12,Paoli-Lombardo Romain1,Bourgeade-Delmas Sandra3,Sournia-Saquet Alix4,Castera-Ducros Caroline12,Jacquet Inès1,Verhaeghe Pierre45,Rathelot Pascal12

Affiliation:

1. Aix Marseille Univ, CNRS, ICR UMR 7273, Laboratoire de Pharmaco-Chimie Radicalaire

2. AP-HM, Service Central de la Qualité et de l’Information Pharmaceutiques

3. UMR 152 PHARMA-DEV, Université de Toulouse, IRD, UPS

4. LCC-CNRS Université de Toulouse, CNRS, UPS

5. Université Grenoble Alpes, CNRS, DPM UMR 5063

Abstract

AbstractTo study the antikinetoplastid structure–activity relationships in a 3-nitroimidazo[1,2-a]pyridine series, we explored the substitution of positions 5 and 7 of the scaffold, developing nucleophilic aromatic substitution reactions and palladium-catalyzed Suzuki–Miyaura, Sonogashira, and Buchwald–Hartwig cross-coupling reactions that had never been reported at these positions in this series. In four steps from 2-amino(bromo)pyridines, 33 original compounds were obtained, allowing a better definition of the antiparasitic pharmacophore.

Funder

Aix-Marseille Université

Centre National de la Recherche Scientifique

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

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