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Paper | Regular issue | Vol 45, No. 3, 1997, pp.537-554
Published online, 1st January, 1970
DOI: 10.3987/COM-96-7712
Synthesis of New Arylethanolamine and Aryloxypropanolamine Derivatives Including 1,4-Benzodioxine Moiety

Sophie Boyé, Gérald Guillaumet, and Marie-Claude Viaud*

*Institute de Chimie Organique et Analytique, associe au CNRS, Université d'Orléans, B.P. 6759, Rue de Chartres, 45067 Orleans Cedex 2, France


The synthesis of new arylethanolamines and aryloxypropanolamines variously substituted on the nitrogen atom are described. Access to these compounds, which are potential β3-adrenergic ligands, involves, as key step, a reductive amination reaction between 2-amino alcohols and 1,4-benzodioxine aldehyde derivatives.