Reacción #1178486

ord-d5c7517da7614fc0acfb8db975970eae

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction liquor was concentrated under reduced pressure
  2. 2
    Extracciónthe obtained residue was extracted with methylene chloride
  3. 3
    LavadoThe extract was washed with saturated brine
  4. 4
    Secadodried over anhydrous sodium sulfate
  5. 5
    ConcentraciónThe solvent was concentrated under reduced pressure
  6. 6
    Otrothe obtained residue was purified by thin layer chromatography (ethyl acetate

Procedimiento

To an aqueous solution (1 mL) of methyl N-benzyloxycarbonyl-2,5-dideoxy-3-O-ethyl-2,5-imino-D-lyxofuranoside, trifluoroacetic acid (1 mL) was added, and the mixture was stirred for three hours. The reaction liquor was concentrated under reduced pressure, and the obtained residue was extracted with methylene chloride. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure, and the obtained residue was purified by thin layer chromatography (ethyl acetate:n-hexane=1:1, v/v), to obtain the title compound (92 mg, 77%) as an oily matter.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08129366B2uspto-grants-2012_03