Реакция #1269863

ord-7b82b37af85e4cf198d284c9a811bfe8

Уравнение реакции

CCCCOC(=O)N1CCN(C(=O)[C@H](CO)NC(=O)OC(C)(C)C)CC1
4-((S)-2-tert-butoxycarbonylamino-3-hydroxy-propionyl)-piperazine-1-carboxylic acid butyl ester
Cl
HCl
CCCCOC(=O)N1CCN(C(=O)C(N)CO)CC1.Cl
4-(2-Amino-3-hydroxy-propionyl)-piperazine-1-carboxylic acid butyl ester hydrochloride

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияthe white cake was filtered
  2. 2
    Промывкаwashed with Et2O
  3. 3
    Другоеdried at HV overnight
  4. 4
    ДругоеThe crude (1.19 g) was used without purification

Методика

To a solution of 4-((S)-2-tert-butoxycarbonylamino-3-hydroxy-propionyl)-piperazine-1-carboxylic acid butyl ester (1.79 g, as described in WO2008044217) in CH2Cl2 (22 mL) was added HCl (4M in dioxane, 8.3 mL) and the reaction mixture was stirred for 2 h at RT. The suspension was diluted with Et2O (1000 mL) and the white cake was filtered, washed with Et2O and dried at HV overnight. The crude (1.19 g) was used without purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08664203B2uspto-grants-2014_03