Methylamine → 7,8-Dimethoxy-3-[3-(methylamino)propyl]-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one
반응식
[CH3:1][O:2][C:3]1[C:18]([O:19][CH3:20])=[CH:17][C:6]2[CH2:7][C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH:14]=O)[CH2:10][CH2:11][C:5]=2[CH:4]=1.[CH3:21][NH2:22].[BH4-].[Na+]>CO>[CH3:1][O:2][C:3]1[C:18]([O:19][CH3:20])=[CH:17][C:6]2[CH2:7][C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH2:14][NH:22][CH3:21])[CH2:10][CH2:11][C:5]=2[CH:4]=1참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
Dissolve 50 g (0.18 mol) of 3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)propanal in 625 ml of methanol. Cool the resulting solution to 0° C. and then add 62.5 ml (0.81 mol; 4.5 equivalents) of an aqueous 40% methylamine solution. Stir for one hour at 0° C. and then add 7.5 g (0.2 mol; 1.1 equivalent) of NaBH4. Stir for 30 minutes at 0° C. and then stir for 12 hours at ambient temperature. Evaporate off the methanol. The residue is taken up in aqueous hydrochloric acid solution (1N), and washed with ethyl acetate. The aqueous phase is then adjusted to pH=8 by adding 20% sodium hydroxide solution and extracted with dichloromethane. The organic phase is washed with water, dried over MgSO4, filtered and then evaporated to dryness to obtain 52 g of an oil, which is purified by flash chromatography on 1.5 kg of silica (eluant=dichloromethane/−ethanol/NH4OH:80/20/2). 42 g of the expected product are obtained in the form of a white solid.
후처리
- stirringStir for 30 minutes at 0° C.
- stirringstir for 12 hours at ambient temperature
- customEvaporate off the methanol
- washwashed with ethyl acetate
- additionby adding 20% sodium hydroxide solution
- extractionextracted with dichloromethane
- washThe organic phase is washed with water
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated to dryness
출처 및 근거
- ORD 기록
- ord-3bc61f152e194724a8376a50b10b9cec
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08097720B2
반응 노트
불러오는 중…