反応 #1269863

ord-7b82b37af85e4cf198d284c9a811bfe8

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過the white cake was filtered
  2. 2
    洗浄washed with Et2O
  3. 3
    その他dried at HV overnight
  4. 4
    その他The crude (1.19 g) was used without purification

実験手順

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.

出典

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