반응 #2348117

ord-dc337b6f740e46d58b97be5ced8deaf8

반응 방정식

CC=CC(=O)C1C(C)C=CCC1(C)C
1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one
CCN(C(C)C)C(C)C
ethyl diisopropylamine
CCOC(=O)[C@@H](N)CS.Cl
L-Cystein ethyl ester hydrochloride
CCOC(=O)C(CSC(C)CC(=O)C1C(C)C=CCC1(C)C)NC(C)CC(=O)C1C(C)C=CCC1(C)C
title compound
수율 71.0%
CCOC(=O)C(CSC(C)CC(=O)C1C(C)C=CCC1(C)C)NC(C)CC(=O)C1C(C)C=CCC1(C)C
Ethyl 2-(4-oxo-4-(2,6,6-trimethylcyclohex-3-enyl)butan-2-ylamino)-3-(4-oxo-4-(2,6,6-trimethylcyclohex-3-enyl)butan-2-ylthio)propanoate
수율 71.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent is removed in vacuo
  2. 2
    workup.DISSOLUTIONthe residue dissolved in methyl t-butyl ether
  3. 3
    세척The solution is washed with dilute aq. NaCl
  4. 4
    건조dried over MgSO4
  5. 5
    농축concentrated
  6. 6
    기타The residue is purified by chromatography on SiO2

실험 절차

A solution of 1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one (83.0 g, 0.50 mol, 2 equiv.), ethyl diisopropylamine (32.3 g, 0.25 mol, 1 equiv.) and L-Cystein ethyl ester hydrochloride (46.5 g, 0.25 mol, 1 equiv.) in EtOH (600 ml) is heated to 60° C. during 44 h. The solvent is removed in vacuo and the residue dissolved in methyl t-butyl ether. The solution is washed with dilute aq. NaCl, dried over MgSO4 and concentrated. The residue is purified by chromatography on SiO2 to yield 85.5 g (71%) of the title compound as orange oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07846887B2uspto-grants-2010_12