Hydrochloric Acid → 2-amino-N-(3-bromo-2-methylphenyl)-3-methoxybenzamide
반응식
[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].[CH3:10][O:11][C:12]1[C:17]2[NH:18]C(=O)[O:20][C:21](=O)[C:16]=2[CH:15]=[CH:14][CH:13]=1.C[Al](C)C.Cl>C1(C)C=CC=CC=1>[NH2:18][C:17]1[C:12]([O:11][CH3:10])=[CH:13][CH:14]=[CH:15][C:16]=1[C:21]([NH:5][C:4]1[CH:6]=[CH:7][CH:8]=[C:2]([Br:1])[C:3]=1[CH3:9])=[O:20]참가 물질
실험 절차
A mixture of 3-bromo-2-methylaniline (482 mg, 2.59 mmol) and 8-methoxy-1H-benzo[d][1,3]oxazine-2,4-dione (500 mg, 2.59 mmol) in toluene (20 mL) was treated with 2 M trimethylaluminum in toluene (3.24 mL, 6.47 mmol) at 0° C. The mixture was stirred at room temperature for 10 minutes, then was heated at 70° C. overnight. The mixture was cooled to room temperature, treated with 1N aqueous HCl and extracted 3 times with EtOAc. The combined organic phases were washed sequentially with saturated aqueous NaHCO3 and water, dried and concentrated. The residue was subjected to column chromatography on silica gel (40 g), eluting with EtOAc-hexanes (gradient from 0-100%), to provide 2-amino-N-(3-bromo-2-methylphenyl)-3-methoxybenzamide as a white solid (302 mg, 35% yield). Mass spectrum m/z 335, 337 (M+H)+. 1H NMR (400 MHz, chloroform-d) δ 7.72 (d, J=7.3 Hz, 2H), 7.46 (dd, J=8.0, 0.8 Hz, 1H), 7.17-7.10 (m, 2H), 6.90 (dd, J=7.9, 0.9 Hz, 1H), 6.72-6.66 (m, 1H), 5.88 (br. s., 2H), 3.92 (s, 3H), 2.43 (s, 3H).
후처리
- temperaturewas heated at 70° C. overnight
- temperatureThe mixture was cooled to room temperature
- extractionextracted 3 times with EtOAc
- washThe combined organic phases were washed sequentially with saturated aqueous NaHCO3 and water
- customdried
- concentrationconcentrated
- washeluting with EtOAc-hexanes (gradient from 0-100%)
출처 및 근거
- ORD 기록
- ord-c5b7b2f8b5fa4f8fa49c868b34b1cf39
- 출처 데이터셋
- uspto-grants-2016_05
- 특허 번호
- US09334290B2
반응 노트
불러오는 중…