Tetrahydrofuran → (2R,5S)-1-benzyl-2,5-dimethylpiperazine
반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].C1COCC1.[CH2:12]([N:19]1[C@H:24]([CH3:25])[C:23](=O)[NH:22][C@@H:21]([CH3:27])[C:20]1=O)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[OH-].[Na+]>O>[CH2:12]([N:19]1[CH2:20][C@H:21]([CH3:27])[NH:22][CH2:23][C@H:24]1[CH3:25])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
In an atmosphere of argon, 0.57 g of lithium aluminum hydride was added at 0° C. to 30 ml of THF solution containing 1.0 g of (3S,6R)-1-benzyl-3,6-dimethylpiperazine-2,5-dione, and the mixture was stirred overnight with heating under reflux. The reaction mixture was cooled to 0° C., 1.0 ml of water was added dropwise thereto and 1.0 ml of 10% aqueous sodium hydroxide was added dropwise thereto, and then the mixture was further mixed with 1.0 ml of water and stirred for 30 minutes. The precipitate was separated by filtration and washed with ethyl acetate, and the filtrate was washed with 10% aqueous potassium carbonate and saturated brine, dried over anhydrous magnesium sulfate, filtered and then concentrated. The residue was subjected to a silica gel column chromatography and eluted with chloroform-methanol-28% aqueous ammonia (25:1:0.1, v/v/v) to obtain 0.75 g of the title compound as a yellow oily substance.
후처리
- temperaturewith heating
- temperatureunder reflux
- stirringstirred for 30 minutes
- customThe precipitate was separated by filtration
- washwashed with ethyl acetate
- washthe filtrate was washed with 10% aqueous potassium carbonate and saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- washeluted with chloroform-methanol-28% aqueous ammonia (25:1:0.1, v/v/v)
출처 및 근거
- ORD 기록
- ord-82e08a76750a4893b775c813a58a4ed4
- 출처 데이터셋
- uspto-grants-2004_01
- 특허 번호
- US06673799B1
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