Реакция #89752

ord-11bc39fb4e5d41da9dd49d4b36931e4f

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter quenched with aq. sodium bicaronate
  2. 2
    Экстракцияthe reaction was extracted with ethyl acetate
  3. 3
    ПромывкаThe combined organic layers were washed with brine
  4. 4
    Другоеdried
  5. 5
    Концентрированиеconcentrated
  6. 6
    Другоеto dry

Методика

To a mixture of methyl(2S,3S,5S)-5-methoxy-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-3-carboxylate (0.0233 g, 0.0000645 mol) and 4-dimethylaminopyridine (0.0118 g, 0.0000967 mol) in methylene chloride (1.00 mL, 0.0156 mol) was added methyl chloroformate (0.00648 mL, 0.0000838 mol). The reaction was stirred at rt overnight. After quenched with aq. sodium bicaronate, the reaction was extracted with ethyl acetate. The combined organic layers were washed with brine, dried, concentrated to dry. The resulting residue was used directly in next step. MS (ESI): (M+H)+=420.2.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09440958B2uspto-grants-2016_09