Reacción #67951

ord-ea7f4eea487243e5bfaa01ff26bd8467

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.STIRRINGstirred at the same temperature for 30 minutes
  4. 4
    OtroThe solvent was removed under reduced pressure
  5. 5
    workup.ADDITIONwater and ethyl acetate were added
  6. 6
    OtroThe aqueous layer was separated
  7. 7
    Lavadowashed with ethyl acetate
  8. 8
    workup.ADDITIONethyl acetate was added
  9. 9
    OtroThe organic layer was separated
  10. 10
    Extracciónthe aqueous layer was extracted with ethyl acetate
  11. 11
    Lavadothe resultant solution was washed with an aqueous saturated sodium chloride solution
  12. 12
    Secadodried over anhydrous magnesium sulfate
  13. 13
    Otrothe solvent was removed under reduced pressure

Procedimiento

To 20 mL of a dichloromethane suspension containing 1.0 g of 1-(trifluoroacetyl)piperidine-4-amine hydrochloride, 0.71 g of 2,3-dihydro-1,4-benzodioxin-6-carbaldehyde and 0.25 mL of acetic acid were added, the mixture was stirred at room temperature for 2 hours. The reaction mixture was added with 1.37 g of sodium triacetoxyborohydride was added and stirred at the same temperature for 30 minutes. The solvent was removed under reduced pressure, then water and ethyl acetate were added thereto, and the reaction mixture was adjusted to pH 1.5 with 1 mol/L hydrochloric acid. The aqueous layer was separated and washed with ethyl acetate, then ethyl acetate was added thereto, and the resultant solution was adjusted to pH 7.8 with an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, and the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 1.4 g of a colorless oily substance, N-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-1-(trifluoroacetyl)piperidine-4-amine.

Fuente

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