Methyl iodide → HCID 118021625, 화합물
반응식
[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([CH3:9])[C:5](=[O:8])[NH:6][CH:7]=1.[H-].[Na+].[CH3:13]I.[NH4+].[Cl-]>C1COCC1>[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([CH3:9])[C:5](=[O:8])[N:6]([CH3:13])[CH:7]=1참가 물질
6
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- 온도
- 0 °C
실험 절차
To a solution of 5-bromo-3,4-dimethyl-1H-pyridin-2-one (402.0 mg, 2.0 mmol) in anhydrous THF (20 mL) was added NaH (96.0 mg, 2.4 mmol). The resulting mixture was stirred at 0° C. for 30 min. Methyl iodide (568.0 mg, 4.0 mmol) was added and the reaction was stirred at 32° C. for 3 h. Then, saturated aqueous NH4Cl (100 mL) was added and the mixture extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography on silica gel (PE:EA=10:1 to 2:1) to give the title compound (350.0 mg, 80%) as a white solid. 1H NMR (CDCl3, 400 MHz) δ 7.38 (s, 1H), 3.52 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H). LCMS (M+H)+ 216.
후처리
- stirringthe reaction was stirred at 32° C. for 3 h
- extractionthe mixture extracted with ethyl acetate (100 mL×3)
- washThe combined organic layers were washed with brine (100 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified by column chromatography on silica gel (PE:EA=10:1 to 2:1)
출처 및 근거
- ORD 기록
- ord-e93a66c876564b4083eb395b26aa0694
- 출처 데이터셋
- uspto-grants-2015_08
- 특허 번호
- US09115114B2
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