Methanol → 4-Chloro-2-methoxy-6-methylpyrimidine
반응식
[Na].Cl[C:3]1[N:8]=[C:7]([Cl:9])[CH:6]=[C:5]([CH3:10])[N:4]=1.[OH2:11].[CH3:12]O>>[Cl:9][C:7]1[CH:6]=[C:5]([CH3:10])[N:4]=[C:3]([O:11][CH3:12])[N:8]=1참가 물질
5
실험 절차
To anhydrous methanol (10 ml) was added sodium (230 mg, 10 mmol) and the mixture was stirred under an argon atmosphere until a clear solution had formed. This solution was added dropwise over two hours with stirring to a solution of 2,4-dichloro-6-methylpyrimidine (1.79 g, 11 mmol) in anhydrous methanol (10 ml) under cooling so that the temperature remained below 10° C. Stirring was continued for 30 minutes, then water was added (2 ml), the mixture was filtered and the filtrate was evaporated to dryness under reduced pressure. The residue was purified by column chromatography (pre-packed silica column, gradient of heptane/ethyl acetate). 750 mg was obtained (4.75 mmol, 47%). MS (APCI) m/z=159.2 [M+H]+.
후처리
- customhad formed
- additionThis solution was added dropwise over two hours
- temperatureunder cooling so that the temperature
- customremained below 10° C
- stirringStirring
- filtrationthe mixture was filtered
- customthe filtrate was evaporated to dryness under reduced pressure
- customThe residue was purified by column chromatography (pre-packed silica column, gradient of heptane/ethyl acetate)
- custom750 mg was obtained (4.75 mmol, 47%)
출처 및 근거
- ORD 기록
- ord-ff1bbdd973f8423086e675f8be01fd11
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08877934B2
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