تفاعل #48671

ord-aac62cd8718c4cf7ae0a7d5cf0f125f9

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلWash with water and saturated aqueous sodium chloride
  2. 2
    تجفيفdry (magnesium sulfate)
  3. 3
    ترشيحfilter
  4. 4
    تركيزconcentrate
  5. 5
    أخرىPurify on silica gel
  6. 6
    غسيلeluting with 20

الإجراء التجريبي

Add triethylamine (0.030 g, 0.30 mmol) and acetic anhydride (0.024 g, 0.23 mmol) to (R)-5-[(1S,2S)-2-amino-3-(3,5-difluorophenyl)-1-hydroxypropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl ester (0.095 g, 0.228 mmol) in tetrahydrofuran (4 mL) at room temperature. Stir 4 hours and dilute with ethyl acetate. Wash with water and saturated aqueous sodium chloride, dry (magnesium sulfate), filter and concentrate. Purify on silica gel, eluting with 20:80 to 100% ethyl acetate:hexanes to give the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745438B2uspto-grants-2010_06