Synthesis and absolute configuration of optically pure enantiomers of a kappa-opioid receptor selective agonist

FEBS Lett. 1987 Nov 2;223(2):335-9. doi: 10.1016/0014-5793(87)80315-0.

Abstract

The enantiomers of U50,488, ligands highly selective for kappa-opioid receptors, have been prepared by a refined procedure and their optical purity demonstrated. The absolute configuration of (+)-trans-2-pyrrolidinyl-N-methylcyclohexylamine, a chemically versatile intermediate for synthesis of analogs of kappa-opioid receptor ligands with defined chirality, has been determined to be 1S,2S by X-ray crystallographic analysis. This intermediate has been used to synthesize the optically pure U50,488 enantiomers with known absolute configuration.

MeSH terms

  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
  • Ligands
  • Pyrrolidines / chemical synthesis*
  • Receptors, Opioid*
  • Receptors, Opioid, kappa
  • Stereoisomerism
  • X-Ray Diffraction

Substances

  • Ligands
  • Pyrrolidines
  • Receptors, Opioid
  • Receptors, Opioid, kappa
  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer