Green Approach for the Synthesis of Chalcogenyl‐ 2,3‐dihydrobenzofuran Derivatives Through Allyl‐phenols/ Naphthols and Their Potential as MAO‐B Inhibitors

Author:

Azevedo Amanda R.1,Cordeiro Pâmella1,Strelow Dianer N.2,de Andrade Karine N.3,Neto Marcos R. S.4,Goetze Fiorot Rodolfo3,Brüning César A.2,Braga Antonio L.4,Lião Luciano M.5,Bortolatto Cristiani F.2,Neto José S. S.5,Nascimento Vanessa1ORCID

Affiliation:

1. SupraSelen Laboratory Department of Organic Chemistry Universidade Federal Fluminense Niterói Institute of Chemistry, Campus do Valonguinho 24020-141 RJ Brazil

2. Molecular Biochemistry and Neuropharmacology Laboratory (LABIONEM), Chemical Pharmaceutical and Food Sciences Center (CCQFA) Federal University of Pelotas Pelotas 96010-900 RS Brazil

3. Department of Organic Chemistry Institute of Chemistry Universidade Federal Fluminense Niterói, Outeiro São João Batista, s/n 24020-141 RJ Brazil

4. LabSelen Department of Chemistry Federal University of Santa Catarina Santa Catarina 88040-900 SC Brazil

5. LabRMN Chemistry Institute Federal University of Goiás Goiânia 74690-900 GO Brazil

Abstract

AbstractThis work presents the design, synthesis, and MAO‐B inhibitor activity of a series of chalcogenyl‐2,3‐dihydrobenzofurans derivatives. Using solvent‐ and metal‐free methodology, a series of chalcogen‐containing dihydrobenzofurans 79 was obtained with yields ranging from 40% to 99%, using an I2/DMSO catalytic system. All compounds were fully structurally characterized using 1H and 13C NMR analysis, and the unprecedented compounds were additionally analyzed using high‐resolution mass spectrometry (HRMS). In addition, the mechanistic proposal that iodide is the most likely species to act in the transfer of protons along the reaction path was studied through theoretical calculations. Finally, the compounds 7be, 8ae, and 9a showed great promise as inhibitors against MAO‐B activity.

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

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