Design and Synthesis of New Pyrazole-Based Heterotricycles and their Derivatization by Automated Library Synthesis

ChemMedChem. 2020 Sep 3;15(17):1634-1638. doi: 10.1002/cmdc.202000187. Epub 2020 Jun 8.

Abstract

Small-molecule heterocycles bearing orthogonal functionality have the potential to deliver diverse structural motifs that aid the drug-discovery effort. This work highlights how a readily assembled N-hydroxyethyl pyrazole trifluoroborate offers rapid access to architecturally distinct 5-6-6- and 5-7-6-fused tricyclic compounds. This chemistry is not only amenable to single compound synthesis, but also to high-throughput experimentation. It gives easy access to diverse compound arrays with various physicochemical and ADME profiles by fully automated library synthesis. The combination of the high-throughput experimentation with rapid testing of the compounds in an integrated physicochemical and ADME profiling workflow allows accelerated design of novel lead compounds in drug-discovery projects.

Keywords: ADME; boron; compound libraries; physicochemical properties; pyrazoles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Automation*
  • Drug Design*
  • Heterocyclic Compounds / chemical synthesis
  • Heterocyclic Compounds / chemistry*
  • Molecular Structure
  • Pyrazoles / chemical synthesis
  • Pyrazoles / chemistry*
  • Small Molecule Libraries / chemical synthesis
  • Small Molecule Libraries / chemistry*

Substances

  • Heterocyclic Compounds
  • Pyrazoles
  • Small Molecule Libraries
  • pyrazole