Synthesis of Highly Substituted Imidazole Uracil Containing Molecules via Ugi-4CR and Passerini-3CR

ACS Comb Sci. 2018 Apr 9;20(4):192-196. doi: 10.1021/acscombsci.7b00145. Epub 2018 Feb 26.

Abstract

The synthesis of uracil/thymine containing tetra/trisubstituted imidazole derivatives was demonstrated using Ugi/Passerini-reaction followed by a postcyclization reaction sequence. The approach enables the one-pot facile construction of diverse compounds in moderate to excellent yields (47-82%). The 5-fluorouracil and 5-methyluracil moieties afford potentially bioactive molecules with drug-like properties. These scaffolds are currently being utilized in the screening deck of the European Lead Factory.

Keywords: Passerini-3CR; Ugi-4CR; imidazole; one-pot; uracil/thymine.

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Humans
  • Hydrogen Bonding
  • Imidazoles / chemical synthesis*
  • Magnetic Resonance Spectroscopy / methods
  • Models, Molecular
  • Molecular Structure
  • Small Molecule Libraries
  • Thymine / analogs & derivatives
  • Thymine / chemical synthesis
  • Uracil / analogs & derivatives*
  • Uracil / chemical synthesis*

Substances

  • Imidazoles
  • Small Molecule Libraries
  • Uracil
  • Thymine