Реакция #66552

ord-1ac27f39dc7c470f9810920706515d93

Уравнение реакции

O=C(O)C(F)(F)F
TFA
CCOC(=O)CNCc1ccccc1
ethyl JV-benzylglycinate
C(=NC1CCCCC1)=NC1CCCCC1
DCC
CCC(N)C(=O)O
aminobutyric acid
CC[C@@H]1NC(=O)CN(Cc2ccccc2)C1=O
title compound
CC[C@@H]1NC(=O)CN(Cc2ccccc2)C1=O
(3S)-3-Ethyl-1-(phenylmethyl)-2,5-piperazinedione

Реагенты

Нет

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияfiltered
  2. 2
    Концентрированиеthe concentrated
  3. 3
    Другоеto give an oil
  4. 4
    КонцентрированиеThe solution was concentrated under reduced pressure
  5. 5
    workup.STIRRINGThe residue was stirred in saturated aq NaHCO3 (125 ml)
  6. 6
    workup.WAITEtOAc (125 ml) for 6 h
  7. 7
    ДругоеThe organics were separated
  8. 8
    Сушкаdried (Na2SO4)
  9. 9
    Концентрированиеconcentrated

Методика

To a solution of DCC (5.07 g) in DCM (140 mL) at 0° C. was added N—BOC-L-□-aminobutyric acid (5 g) followed by ethyl JV-benzylglycinate (4.6 mL) dropwise. The resulting solution was stirred at 0° C. for 2 h and RT 1 h, filtered and the concentrated to give an oil. This was dissolved in DCM (100 mL) and TFA (100 ml) and stirred for 1 h. The solution was concentrated under reduced pressure. The residue was stirred in saturated aq NaHCO3 (125 ml) and EtOAc (125 ml) for 6 h. The organics were separated, dried (Na2SO4), and concentrated to give the sub title compound as a white solid. (5.68 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524715B2uspto-grants-2013_09