Stereoselective Catalytic Synthesis of Active Pharmaceutical Ingredients in Homemade 3D-Printed Mesoreactors

Angew Chem Int Ed Engl. 2017 Apr 3;56(15):4290-4294. doi: 10.1002/anie.201612192. Epub 2017 Mar 27.

Abstract

3D-printed flow reactors were designed, fabricated from different materials (PLA, HIPS, nylon), and used for a catalytic stereoselective Henry reaction. The use of readily prepared and tunable 3D-printed reactors enabled the rapid screening of devices with different sizes, shapes, and channel dimensions, aimed at the identification of the best-performing reactor setup. The optimized process afforded the products in high yields, moderate diastereoselectivity, and up to 90 % ee. The method was applied to the continuous-flow synthesis of biologically active chiral 1,2-amino alcohols (norephedrine, metaraminol, and methoxamine) through a two-step sequence combining the nitroaldol reaction with a hydrogenation. To highlight potential industrial applications of this method, a multistep continuous synthesis of norephedrine has been realized. The product was isolated without any intermediate purifications or solvent switches.

Keywords: 3D printing; amino alcohols; flow reactors; nitroaldol reactions; stereoselective catalysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Equipment Design
  • Heterocyclic Compounds, 3-Ring / chemistry
  • Hydrogenation
  • Metaraminol / chemical synthesis*
  • Metaraminol / chemistry
  • Methoxamine / chemical synthesis*
  • Methoxamine / chemistry
  • Molecular Structure
  • Nitro Compounds / chemistry
  • Phenylpropanolamine / chemical synthesis*
  • Phenylpropanolamine / chemistry
  • Printing, Three-Dimensional*
  • Stereoisomerism

Substances

  • Heterocyclic Compounds, 3-Ring
  • Nitro Compounds
  • nitroaldol
  • Phenylpropanolamine
  • Metaraminol
  • Methoxamine