Scalable (Enantioselective) Syntheses of Novel 3-Methylated Analogs of Pazinaclone, (S)-PD172938 and Related Biologically Relevant Isoindolinones

Molecules. 2022 Sep 1;27(17):5647. doi: 10.3390/molecules27175647.

Abstract

Herein, we report the application of an efficient and practical K2CO3 promoted cascade reaction of 2-acetylbenzonitrile in the synthesis of novel 3-methylated analogs of Pazinaclone and PD172938, belonging to isoindolinones heterocyclic class bearing a tetrasubstituted stereocenter. Organocatalytic asymmetric synthesis of the key intermediate and its transformation into highly enantioenriched 3-methylated analog of (S)-PD172938 was also developed. These achievements can be of particular interest also for medicinal chemistry, since the methyl group is a very useful structural modification in the rational design of new and more effective bioactive compounds.

Keywords: asymmetric synthesis; heterocycles; isoindolinones.

MeSH terms

  • Isoindoles* / chemistry
  • Naphthyridines
  • Phthalimides*
  • Spiro Compounds
  • Stereoisomerism

Substances

  • Isoindoles
  • Naphthyridines
  • Phthalimides
  • Spiro Compounds
  • phthalimidine
  • pazinaclone

Grants and funding

This research received no external funding.