تفاعل #1269863

ord-7b82b37af85e4cf198d284c9a811bfe8

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe white cake was filtered
  2. 2
    غسيلwashed with Et2O
  3. 3
    أخرىdried at HV overnight
  4. 4
    أخرىThe crude (1.19 g) was used without purification

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08664203B2uspto-grants-2014_03