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Asymmetric Synthesis of Nortropanes via Rh-Catalyzed Allylic Arylation.

Yan ZhangF Wieland GoetzkeKirsten E ChristensenStephen P Fletcher
Published in: ACS catalysis (2022)
Tropane derivatives are extensively used in medicine, but catalytic asymmetric methods for their synthesis are underexplored. Here, we report Rh-catalyzed asymmetric Suzuki-Miyaura-type cross-coupling reactions between a racemic N -Boc-nortropane-derived allylic chloride and (hetero)aryl boronic esters. The reaction proceeds via an unexpected kinetic resolution, and the resolved enantiopure allyl chloride can undergo highly enantiospecific reactions with N-, O-, and S-containing nucleophiles. The method was applied in a highly stereoselective formal synthesis of YZJ-1139(1), a potential insomnia treatment that recently completed Phase II clinical trials. Our report represents an asymmetric catalytic method for the synthesis of YZJ-1139(1) and related compounds.
Keyphrases
  • clinical trial
  • phase ii
  • open label
  • randomized controlled trial
  • room temperature
  • multidrug resistant
  • depressive symptoms
  • single molecule
  • crystal structure
  • double blind
  • ionic liquid
  • combination therapy
  • drug induced