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Asymmetric Synthesis of CIDD-0072424 via an Enantioselective Nitro-Mannich Reaction: A Central Nervous System Penetrant, Selective Small Molecule Inhibitor of Protein Kinase C Epsilon.

Harmannus De KrakerHua-Yu Leo WangHadi D ArmanRachel N RenteriaCaleb N FleischerRobert O MessingStanton F McHardy
Published in: The Journal of organic chemistry (2024)
CIDD-0072424 is a novel small molecule developed in silico with remarkable activity for the inhibition of protein kinase C (PKC)-epsilon to treat alcohol use disorder. We developed a concise synthesis of ( S )- 2 that is highly enantioselective, scalable, and amenable for 3-point structure-activity relationship (SAR) studies for compound optimization. The highly enantioselective nitro-Mannich reaction was achieved through a dual-reagent catalysis system. The overall utility and the efficiency of the enantioselective route provided a scalable synthesis of both PKCε inhibitors 1 and 2 .
Keyphrases
  • small molecule
  • protein kinase
  • alcohol use disorder
  • structure activity relationship
  • protein protein
  • molecular docking
  • case control
  • solid state