Réaction #716038

ord-ef7a5bbe6d95489da2e150cc4a0822db

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter aqueous work-up with EtOAc and column purification
  2. 2
    Lavageeluting with EtOAc/hexane

Mode opératoire

Ethyl piperidine-4-carboxylate (100 mg) was treated with 2-chloro-6-methoxyquinoline (Intermediate 1) (90 mg) in MeCN (0.8 mL) and TEA (100 mg) in a sealed tube at 180° C. for 6 h in a microwave reactor. After aqueous work-up with EtOAc and column purification, eluting with EtOAc/hexane, ethyl 4-(6-methoxyquinolin-2-yl)cyclohexanecarboxylate (90 mg) was afforded as a solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09315462B2uspto-grants-2016_04