Реакция #48419

ord-05b88843e0924f9dafdd0709a0e60adf

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеthe solution was concentrated
  2. 2
    workup.ADDITIONSaturated aqueous sodium bicarbonate solution was added
  3. 3
    Экстракцияthe mixture was extracted with dichloromethane (3×)
  4. 4
    ПромывкаThe combined organic extracts were washed with saturated brine
  5. 5
    Сушкаdried over magnesium sulfate
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеconcentrated

Методика

Trifluoroacetic acid (1 mL) was added to a solution of tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-1-[2-(methylsulfonyl)ethyl]-2-oxoazepan-3-ylcarbamate (23.7 mg, 0.053 mmol) in dichloromethane (2 mL). After 4 h, the solution was concentrated. Saturated aqueous sodium bicarbonate solution was added and the mixture was extracted with dichloromethane (3×). The combined organic extracts were washed with saturated brine, dried over magnesium sulfate, filtered and concentrated to give the title compound. MS 347 (M+1).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745427B2uspto-grants-2010_06