반응식
[CH3:1][CH:2]1[CH:7]=[CH:6][CH2:5][C:4]([CH3:9])([CH3:8])[CH:3]1[C:10](=[O:14])[CH:11]=[CH:12][CH3:13].C(N([CH:21]([CH3:23])[CH3:22])C(C)C)C.Cl.[CH3:25][O:26][C:27](=[O:32])[C@H:28]([CH2:30][SH:31])[NH2:29]>CO>[O:14]=[C:10]([CH:3]1[C:4]([CH3:8])([CH3:9])[CH2:5][CH:6]=[CH:7][CH:2]1[CH3:1])[CH2:11][CH:12]([NH:29][CH:28]([CH2:30][S:31][CH:12]([CH2:11][C:10](=[O:14])[CH:3]1[C:4]([CH3:8])([CH3:9])[CH2:5][CH:6]=[CH:23][CH:21]1[CH3:22])[CH3:13])[C:27]([O:26][CH3:25])=[O:32])[CH3:13]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one (19.28 g, 100 mmol, 2 equiv.), ethyl diisopropylamine (6.45 g, 50 mmol, 1 equiv.) and L-Cystein methyl ester hydrochloride (8.60 g, 50 mmol, 1 equiv.) in MeOH (120 ml) is heated to reflux during 28 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 21.3 g (82%) of the title compound as yellowish, viscous oil.
후처리
- temperatureto reflux during 28 h
- customThe solvent is removed in vacuo
- dissolutionthe residue dissolved in methyl t-butyl ether
- washThe solution is washed with dilute aq. NaCl
- dry with materialdried over MgSO4
- concentrationconcentrated
- customThe residue is purified by chromatography on SiO2
출처 및 근거
- ORD 기록
- ord-c9b7ced433ec4f2986752cd133d4161c
- 출처 데이터셋
- uspto-grants-2010_12
- 특허 번호
- US07846887B2
연결된 노트
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