Dimethyl Sulfide → 3-Amino-4-(3-fluorophenyl)-6-methoxyquinoline-2-(1H)-one
반응식
[NH2:1][C:2]1[C:3](=[O:32])[N:4](CC2C=CC(OC)=CC=2OC)[C:5]2[C:10]([C:11]=1[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)=[CH:9][C:8]([O:19][CH3:20])=[CH:7][CH:6]=2.CSC>FC(F)(F)C(O)=O>[NH2:1][C:2]1[C:3](=[O:32])[NH:4][C:5]2[C:10]([C:11]=1[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)=[CH:9][C:8]([O:19][CH3:20])=[CH:7][CH:6]=2참가 물질
4
실험 절차
To a solution of 3-amino-1-(2,4-dimethoxybenzyl)-4-(3-fluorophenyl)-6-methoxyquinolin-2-(1H)-one (62 mg, 0.143 mmol) in 3 mL of trifluoroacetic acid was added dimethyl sulfide (0.30 mL). After stirring for 2 days, the reaction was heated to reflux for 3 hours, then concentrated in vacuo. The crude residue was purified by flash chromatography through SiO2 (1-3% MeOH/CH2Cl2) to provide the titled product as a yellow solid. Proton NMR for the product was consistent with the titled compound. HRMS (ES) exact mass calculated for C16H13FN2O2 (M+H+): 285.1034. Found 285.1029.
후처리
- temperaturethe reaction was heated
- temperatureto reflux for 3 hours
- concentrationconcentrated in vacuo
- customThe crude residue was purified by flash chromatography through SiO2 (1-3% MeOH/CH2Cl2)
출처 및 근거
- ORD 기록
- ord-3fd066e5e62a442880bfaee480f939f1
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07825131B2
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