반응 #86032

ord-c7d2588b8770488eb71154d498eea4ee

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the mixture was extracted with ethyl acetate
  2. 2
    세척The extract was washed with saturated brine
  3. 3
    건조dried over anhydrous magnesium sulfate
  4. 4
    기타The solvent was evaporated under reduced pressure
  5. 5
    세척the residue was subjected to silica gel column chromatography, in which elution
  6. 6
    기타was performed with n-hexane/ethyl acetate (1:1) for purification
  7. 7
    기타recrystallized from ethyl acetate/n-hexane

실험 절차

(R)-1-Benzyl ethyl 3-t-butyloxycarbonylamino-3-carbamoylsuccinate (550 mg) obtained in Example 20 was dissolved in acetone (11 mL) and water (6 mL), the solution was added with potassium carbonate (231 mg), the mixture was stirred for 5 hours, and poured with 1 mol/L hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography, in which elution was performed with n-hexane/ethyl acetate (1:1) for purification, and then recrystallized from ethyl acetate/n-hexane to obtain the title compound (358 mg, yield: 90%) as colorless crystals. Optical rotation [α]D25 was −29.5° (c 0.50, ethanol).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09434737B2uspto-grants-2016_09