Revista Colombiana de Química (Jan 2018)

Transamidation and transamidation-reduction of N-benzyltyramine with DMF

  • Christian Díaz Oviedo,
  • Ariel Rodolfo Quevedo Pastor

DOI
https://doi.org/10.15446/rev.colomb.quim.v47n1.63976
Journal volume & issue
Vol. 47, no. 1
pp. 5 – 9

Abstract

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Tyramine and N-benzyltyramine react with formaldehyde to form azacyclophanes by means of aromatic Mannich reactions and react with non-enolizable aldehydes to form the respective Schiff bases. In this paper we present the unexpected synthesis of N-formyl-N-benzyltyramine and N-methyl-N-benzyltyramine by means of transamidation and transamidation-reduction of N-benzyltyramine with N,N-dimethylformamide. A reaction mechanism involving formylation of N-benzyltiramine followed by a Leuckart-Wallach reduction is proposed for rationalising such transformation.

Keywords