(Diethylamino)sulfur trifluoride → 4-Chloro-6-(fluoromethyl)-5-methylpyrimidine
반응식
CCN(S(F)(F)[F:7])CC.[Cl:10][C:11]1[N:16]=[CH:15][N:14]=[C:13]([CH2:17]O)[C:12]=1[CH3:19]>ClCCl>[Cl:10][C:11]1[C:12]([CH3:19])=[C:13]([CH2:17][F:7])[N:14]=[CH:15][N:16]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
DAST (1.5 mL, 11.35 mmol) was added to dichloromethane (DCM) (64 mL), cooled to −78° C. and treated dropwise with a solution of (6-chloro-5-methyl-4-pyrimidinyl)methanol (Intermediate 50, 1.70 g, 10.72 mmol) in DCM (24 mL) under argon. The resulting mixture was allowed to warm to room temperature and stirred for 3 hours. The reaction was quenched by adding water (45 ml) and extracted with DCM (×2). The DCM layers were separated, combined, dried under magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (SP4, 40+M) eluting with a gradient of 0-50% ethyl acetate and iso-hexane. Product containing fractions were combined and evaporated under reduced pressure to give the title compound as a yellow oil (1.29 g) m/z (ES+) 161 (M+1), title compound is 42% pure by LCMS. Also contains 4-bromo-6-(fluoromethyl)-5-methylpyrimidine, m/z (ES+) 205, 207 (M+1) (44% by LCMS)
후처리
- temperatureto warm to room temperature
- customThe reaction was quenched
- additionby adding water (45 ml)
- extractionextracted with DCM (×2)
- customThe DCM layers were separated
- customdried under magnesium sulfate
- customevaporated under reduced pressure
- customThe residue was purified by column chromatography (SP4, 40+M)
- washeluting with a gradient of 0-50% ethyl acetate and iso-hexane
- additionProduct containing fractions
- customevaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-0ac1a5344e2f4ebe9549d288aed52367
- 출처 데이터셋
- uspto-grants-2014_08
- 특허 번호
- US08796283B2
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