Trimethylaluminum → 7-bromo-4-[(4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-6-methyl-3,4-dihydro-1,4-benzoxazepin-5(2H)-one
반응식
[Br:1][C:2]1[C:3]([CH3:26])=[C:4]([C:9]([O:12][CH2:13][CH2:14][NH:15][CH2:16][C:17]2[C:18](=[O:25])[NH:19][C:20]([CH3:24])=[CH:21][C:22]=2[CH3:23])=[CH:10][CH:11]=1)[C:5](OC)=[O:6].C[Al](C)C>O1CCOCC1>[Br:1][C:2]1[CH:11]=[CH:10][C:9]2[O:12][CH2:13][CH2:14][N:15]([CH2:16][C:17]3[C:18](=[O:25])[NH:19][C:20]([CH3:24])=[CH:21][C:22]=3[CH3:23])[C:5](=[O:6])[C:4]=2[C:3]=1[CH3:26]참가 물질
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of methyl 3-bromo-6-(2-{[(4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]amino}ethoxy)-2-methylbenzoate (126c, 134 mg, 0.317 mmol) in 1,4-dioxane (1 mL) was added trimethylaluminum (2.0M in heptanes, 32.0 mg, 0.440 mmol). The reaction mixture was stirred at room temperature for 30 minutes, heated at 55° C. for 2 hours, and then 75° C. for 4 hours. The reaction mixture was cooled to room temperature, the solvent removed under vacuum, and the residue was stirred vigorously with EtOAc (25 mL) and 10% aq. solution of Rochell's salts. Once the mixture became homogeneous, the layers were separated and the organic layer was purified directly by column chromatography (silica gel, (7N NH3 in MeOH) in EtOAc) to give 7-bromo-4-[(4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl]-6-methyl-3,4-dihydro-1,4-benzoxazepin-5(2H)-one (126d, 36 mg, 27% yield) as a light tan solid.
후처리
- temperatureheated at 55° C. for 2 hours
- wait75° C. for 4 hours
- temperatureThe reaction mixture was cooled to room temperature
- customthe solvent removed under vacuum
- stirringthe residue was stirred vigorously with EtOAc (25 mL) and 10% aq. solution of Rochell's salts
- customthe layers were separated
- customthe organic layer was purified directly by column chromatography (silica gel, (7N NH3 in MeOH) in EtOAc)
출처 및 근거
- ORD 기록
- ord-c10bea724bbb4b0e9c2bb05e5badc837
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09040515B2
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