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[H-].[Na+].[CH3:3][O:4][C:5]1[CH:6]=[C:7]([CH:13]2[C:18](=[O:19])[N:17]([CH3:20])[C:16]3[CH:21]=[CH:22][CH:23]=[CH:24][C:15]=3[S:14]2)[CH:8]=[CH:9][C:10]=1[O:11][CH3:12].[CH2:25]([O:27][CH:28]([O:32][CH2:33][CH3:34])[CH2:29][CH2:30]Cl)[CH3:26].C(OCC)(=O)C>CN(C)C=O.O>[CH2:25]([O:27][CH:28]([O:32][CH2:33][CH3:34])[CH2:29][CH2:30][C:13]1([C:7]2[CH:8]=[CH:9][C:10]([O:11][CH3:12])=[C:5]([O:4][CH3:3])[CH:6]=2)[C:18](=[O:19])[N:17]([CH3:20])[C:16]2[CH:21]=[CH:22][CH:23]=[CH:24][C:15]=2[S:14]1)[CH3:26]참가 물질
실험 절차
To a stirred suspension of 60% sodium hydride (0.6 g) in dimethylformamide (5 ml), 3,4-dihydro-2-(3,4-dimethoxyphenyl)-4-methyl-3-oxo-2H-1,4-benzothiazine (4.4 g) dissolved in dimethylformamide (15 ml) is added under nitrogen atmosphere and ice-cooling, and the mixture is stirred for 15 minutes at room temperature. β-Chloropropionaldehyde diethyl acetal (2.8 g) is added to the reaction mixture, and the mixture is stirred for 2.5 hours at 60° C. The mixture is poured into a mixture of ethyl acetate and water. The organic layer is washed with 1N sodium hydroxide and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue is purified by silica gel column chromatography to give 4.4 g (71.5 %) of 2-(3,3-diethoxypropyl)-3,4-dihydro-2-(3,4-dimethoxyphenyl)-4-methyl-3-oxo-2H-1,4-benzothiazine as an oily form (compound No. 36, (IR: neat, cm-1) 1660, 1588, 1444, 1325, 1238, 750).
후처리
- additionis added under nitrogen atmosphere
- temperatureice-cooling
- stirringthe mixture is stirred for 2.5 hours at 60° C
- washThe organic layer is washed with 1N sodium hydroxide and saturated aqueous sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue is purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-ad637bf96dca4005bd7f8a8efee8d099
- 출처 데이터셋
- uspto-grants-1988_04
- 특허 번호
- US04739050
연결된 노트
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