Réaction #531892

ord-64d3637cf11f405ebc08fa57c9171a4e

Équation de réaction

O=C(NC1CCC(C(=O)O)CC1)OCc1ccccc1
4-benzyloxycarbonylamino-cyclohexanecarboxylic acid
CC(C)(C)O
t-butanol
CC(C)N=C=NC(C)C
DIPC
CC(C)(C)OC(=O)C1CCC(NC(=O)OCc2ccccc2)CC1
4-benzyloxycarbonylamino-cyclohexanecarboxylic acid tert-butyl ester
Rendement 54.2%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe resulting mixtures stirs 18 h
  2. 2
    Autrepurified by flash chromatography (gradient elution: 0-60% EtOAc/Hep) which

Mode opératoire

To a solution of 4-benzyloxycarbonylamino-cyclohexanecarboxylic acid (8.0 g, 28.78 mmol) in DCM (35 mL) and DMF (35 mL) is added t-butanol (10 mL, 105.4 mmol) and DMAP (1.4 g, 11.50 mmol). DIPC (10 mL) is added portionwise over 1 h. The resulting mixtures stirs 18 h. The mixture is mounted onto SiO2 and purified by flash chromatography (gradient elution: 0-60% EtOAc/Hep) which affords 5.2 g of 4-benzyloxycarbonylamino-cyclohexanecarboxylic acid tert-butyl ester. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.14 (m, 2 H) 1.30 (m, 2 H) 1.38 (m, 9 H) 1.82 (m, 4 H) 2.07 (m, 1 H) 3.20 (m, 1 H) 3.47 (m, 3 H) 4.99 (m, 2 H) 7.27 (m, 5 H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08476224B2uspto-grants-2013_07