Reacción #67956

ord-e15549b6a8e941b89f1e8161579091a5

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.STIRRINGstirred at the same temperature for 30 minutes
  3. 3
    OtroThe organic layer was separated
  4. 4
    Extracciónthe aqueous layer was extracted with chloroform
  5. 5
    Lavadothe resultant solution was washed sequentially with water
  6. 6
    Secadoan aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate
  7. 7
    Otrothe solvent was removed under reduced pressure
  8. 8
    OtroThe residue thus obtained
  9. 9
    Otrowas purified by silica gel column chromatography [eluent; chloroform:methanol=10:1]

Procedimiento

To 5 mL of a dichloromethane solution containing 0.30 g of tert-butyl 4-amino-4-((methylamino)carbonyl)piperidine-1-carboxylate, 0.16 g of 2,3-dihydro-1,4-benzodioxin-6-carbaldehyde and 57 μL of acetic acid were added, the mixture was stirred at room temperature for 2 hours. The reaction mixture was added with 0.32 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes. Thereto were added chloroform and an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=10:1] to obtain 0.31 g of a pale yellow oily substance, tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-((methylamino)carbonyl)piperidine-1-carboxylate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524738B2uspto-grants-2013_09