Reacción #1269863

ord-7b82b37af85e4cf198d284c9a811bfe8

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe white cake was filtered
  2. 2
    Lavadowashed with Et2O
  3. 3
    Otrodried at HV overnight
  4. 4
    OtroThe crude (1.19 g) was used without purification

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08664203B2uspto-grants-2014_03