Reacción #3771

ord-2a578e8b392e4d4384fa2f1bad0efe35

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter 4 hours
  2. 2
    Otropartition the reaction mixture between ethyl acetate and 5% sodium bicarbonate solution
  3. 3
    SecadoDry the organic layer over Na2SO4
  4. 4
    Filtraciónfilter
  5. 5
    Otroevaporate in vacuo
  6. 6
    Otroto give a residue

Procedimiento

Add a solution of (S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine (1.1 g, 3.1 mmol) in dichloromethane (2 mL) to trifluoromethanesulfonic acid (1.2 mL). After 2.5 hours, add trifluoromethanesulfonic acid (1.2 mL). After 4 hours, partition the reaction mixture between ethyl acetate and 5% sodium bicarbonate solution. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 10% ethyl acetate/hexane and then 25% ethyl acetate/hexane to give the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05734049uspto-grants-1998_03