Sodium hydride → 6-Bromo-1-(4-dimethylsulfamoyl-benzyl)-2-oxo-1,2-dihydro-indole-3,3-dicarboxylic acid di-tert-butyl ester
反応式
[C:1]([O:5][C:6]([C:8]1([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[C:16]2[C:11](=[CH:12][C:13]([Br:17])=[CH:14][CH:15]=2)[NH:10][C:9]1=[O:18])=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].Br[CH2:29][C:30]1[CH:35]=[CH:34][C:33]([S:36]([N:39]([CH3:41])[CH3:40])(=[O:38])=[O:37])=[CH:32][CH:31]=1>CN(C)C=O>[C:1]([O:5][C:6]([C:8]1([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[C:16]2[C:11](=[CH:12][C:13]([Br:17])=[CH:14][CH:15]=2)[N:10]([CH2:29][C:30]2[CH:31]=[CH:32][C:33]([S:36](=[O:38])(=[O:37])[N:39]([CH3:40])[CH3:41])=[CH:34][CH:35]=2)[C:9]1=[O:18])=[O:7])([CH3:4])([CH3:3])[CH3:2]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
6-Bromo-2-oxo-1,2-dihydro-indole-3,3-dicarboxylic acid di-tert-butyl ester (5.10 g, 12.4 mmol) was dissolved in 40 ml of anhydrous N,N-dimethylformamide (DMF) under an atmosphere of dry N2. The solution was cooled to 0° C. after which time 60% sodium hydride in oil (500 mg, 12.4 mmol) was added and the solution was then stirred for 15 minutes at this temperature. The reaction mixture was the warmed to ambient temperature and stirred for 15 minutes after which time 4-bromomethyl-N,N-dimethyl-benzenesulfonamide (3.44 g, 12.4 mmol) was added. The mixture was stirred overnight after which time it was concentrated under vacuum and partitioned between DCM and water. The DCM layer was washed 3 more times with water, once with brine, dried over MgSO4, filtered and concentrated under vacuum to give 8.63 g of the titled compound as a yellow solid
後処理
- additionwas added
- additionwas added
- stirringThe mixture was stirred overnight after which time it
- concentrationwas concentrated under vacuum
- custompartitioned between DCM and water
- washThe DCM layer was washed 3 more times with water
- dry with materialonce with brine, dried over MgSO4
- filtrationfiltered
- concentrationconcentrated under vacuum
出典と根拠
- ORDレコード
- ord-1e2bd8fd3cdd4f49bff0f5aae27a6315
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06586447B1
反応ノート
読み込み中…