First Organocatalytic Asymmetric Synthesis of 1-Benzamido-1,4-Dihydropyridine Derivatives

Molecules. 2018 Oct 19;23(10):2692. doi: 10.3390/molecules23102692.

Abstract

Preliminary results concerning the first asymmetric synthesis of highly functionalized 1-benzamido-1,4-dihydropyridine derivatives via the reaction of hydrazones with alkylidenemalononitriles in the presence of β-isocupreidine catalyst are reported. The moderate, but promising, enantioselectivity observed (40⁻54% ee), opens the door to a new area of research for the asymmetric construction of new chiral 1,4-dihydropyridine derivatives, whose enantioselective catalytic preparation are still very limited. Moreover, the use of hydrazones for the enantioselective construction of chiral 1,4-dihydropyridines has been overlooked in the literature so far. Therefore, our research represents a pivotal example in this field which remains still unexplored.

Keywords: 1,4-dihydropyridine; chiral base; enantioselective; hydrazone; organocatalysis.

MeSH terms

  • Calcium Channel Blockers / chemical synthesis*
  • Calcium Channel Blockers / chemistry
  • Catalysis*
  • Dihydropyridines / chemical synthesis*
  • Dihydropyridines / chemistry
  • Dihydropyridines / therapeutic use
  • Heterocyclic Compounds / chemical synthesis*
  • Heterocyclic Compounds / chemistry
  • Hydrazones / chemistry
  • Hydroxyquinolines / chemistry
  • Molecular Structure
  • Quinuclidines / chemistry
  • Stereoisomerism

Substances

  • Calcium Channel Blockers
  • Dihydropyridines
  • Heterocyclic Compounds
  • Hydrazones
  • Hydroxyquinolines
  • Quinuclidines
  • beta-isocupreidine
  • 1,4-dihydropyridine