反应 #1269863

ord-7b82b37af85e4cf198d284c9a811bfe8

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤the white cake was filtered
  2. 2
    洗涤washed with Et2O
  3. 3
    其他dried at HV overnight
  4. 4
    其他The crude (1.19 g) was used without purification

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08664203B2uspto-grants-2014_03