Aluminium lithium hydride → HCID 21904833、化合物
反応式
[F:1][C:2]1[C:14]([O:15][CH3:16])=[CH:13][C:5]2[C:6](=O)[NH:7][CH2:8][C:9](=O)[NH:10][C:4]=2[CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[F:1][C:2]1[C:14]([O:15][CH3:16])=[CH:13][C:5]2[CH2:6][NH:7][CH2:8][CH2:9][NH:10][C:4]=2[CH:3]=1参加物
実験手順
To a solution of 8-fluoro-7-methoxy-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione (5.1 g, 227 mmol) dissolved in THF (39.8 mL) was added lithium aluminum hydride (1M solution in THF, 102.4 mL, 102.4 mmol) dropwise. The reaction mixture was heated to reflux. After 26 hours, an additional equivalent of lithium aluminum hydride in THF (22.7 mmol) was added. At 30 hours, the reaction was quenched with water, 15% NaOH and an additional portion of water. The precipitate was filtered and washed with ethyl acetate. THF was removed from the filtrate, and then ethyl acetate and water were added to the flask. All the contents in the flask were transferred to the separatory funnel and extracted with ethyl acetate (3×). The combined organic layers were then washed with brine (1×), dried with magnesium sulfate, filtered and concentrated to give a brown oil. Further purification (15% ammonia in 2M solution of ethanol/ethyl acetate) yielded the desired product.
後処理
- temperatureThe reaction mixture was heated to reflux
- waitAt 30 hours
- customthe reaction was quenched with water, 15% NaOH
- filtrationThe precipitate was filtered
- washwashed with ethyl acetate
- customTHF was removed from the filtrate
- additionethyl acetate and water were added to the flask
- extractionextracted with ethyl acetate (3×)
- washThe combined organic layers were then washed with brine (1×)
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a brown oil
- customFurther purification (15% ammonia in 2M solution of ethanol/ethyl acetate)
出典と根拠
- ORDレコード
- ord-3957dfda73af40c9b50880138e890ede
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07687620B2
反応ノート
読み込み中…