반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:16]3[CH:9]([CH2:10][C:11](=[O:17])[C:12]=3[C:13]=1[O:14][CH3:15])[NH:8][CH2:7][CH2:6]2.C([O-])([O-])=O.[K+].[K+].[Na+].[I-].[C:26]([O:30][C:31](=[O:38])[NH:32][CH2:33][CH2:34][CH2:35][CH2:36]Br)([CH3:29])([CH3:28])[CH3:27]>CN(C=O)C.C(OCC)(=O)C.O>[C:26]([O:30][C:31](=[O:38])[NH:32][CH2:33][CH2:34][CH2:35][CH2:36][N:8]1[CH2:7][CH2:6][C:5]2[C:16]3[CH:9]1[CH2:10][C:11](=[O:17])[C:12]=3[C:13]([O:14][CH3:15])=[C:3]([O:2][CH3:1])[CH:4]=2)([CH3:29])([CH3:28])[CH3:27]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
Over a suspension of 7,8-Dimethoxy-2a,3,4,5-tetrahydro-2H-3-aza-acenaphthylen-1-one (0.950 g, 4.1 mmol), K2CO3 (1.89 g, 13.6 mmol) and NaI (0.061 g, 0.4 mmol) in DMF (20 ml) is slowed added (4-Bromo-butyl)-carbamic acid tert-butyl ester (1.09 g, 4.32 mmol) and the mixture is stirred overnight. Then, water (40 ml) and ethyl acetate (40 ml) are added and the layers are separated. The aqueous phase is extracted with ethyl acetate (2×40 ml). The organic layers are collected and washed with water (3×40 ml). After drying with Na2SO4, filtration and vacuum concentration, a brown oil is obtained, which is purified by silicagel chromatography using a gradient of CH2Cl2/methanol (from 100% to 98% CH2Cl2) to obtain a brown solid (0.730 g, 45% yield)
후처리
- customthe layers are separated
- extractionThe aqueous phase is extracted with ethyl acetate (2×40 ml)
- customThe organic layers are collected
- washwashed with water (3×40 ml)
- dry with materialAfter drying with Na2SO4, filtration and vacuum concentration
- customa brown oil is obtained
- customwhich is purified by silicagel chromatography
출처 및 근거
- ORD 기록
- ord-10329b214e8c4c7994c7ecb739fde7d7
- 출처 데이터셋
- uspto-grants-2009_06
- 특허 번호
- US07553965B2
연결된 노트
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