Derivatives of benzo-1,4-thiazine-3-carboxylic acid and the corresponding amino acid conjugates

Beilstein J Org Chem. 2022 Sep 9:18:1195-1202. doi: 10.3762/bjoc.18.124. eCollection 2022.

Abstract

Herein, we present the synthesis and utilization of derivatives of 4H-benzo[b][1,4]thiazine-3-carboxylic acid. These benzothiazine compounds were assembled via the coupling of aminothiols and bromopyruvates. Oxidative dimerization of these starting materials was also observed and the corresponding benzothiazine dimers were isolated. Moreover, the coupling of benzothiazines with amino acids was realized. In doing so, an enantioselective synthesis of the nonproteinogenic amino acid 2-amino-3-propylhexanoic acid was accomplished.

Keywords: amino acid; benzothiazine; oxidative dimerization; peptide coupling; stereoselective hydrogenation.

Grants and funding

This work was supported by the Slovak Research and Development Agency under the Contract no. PP-COVID-20-0010. This study was supported by the Operation Program of Integrated Infrastructure for the project Advancing University Capacity and Competence in Research, Development and Innovation, ITMS2014+: 313021X329, co-financed by the European Regional Development Fund.