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HRID 15131생성일: 2026년 10월 26일

Acetonitrile → 1,1-Dimethylethyl [5-fluoro-2-(fluoroacetyl)-6-(methyloxy)-3-pyridinyl]carbamate

https://huagongshe.com/reaction/15131

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Sodium BicarbonateHCID 516892—
반응물SelectfluorHCID 2724933—
반응물1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamateHCID 86614146—
용매WaterHCID 962—
생성물1,1-Dimethylethyl [5-fluoro-2-(fluoroacetyl)-6-(methyloxy)-3-pyridinyl]carbamateHCID 86614147—

반응 단계

A mixture of 1,1-dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate (6.72 g, 21.54 mmol), acetonitrile (70 ml), and saturated aqueous sodium bicarbonate solution (15 ml) was treated portionwise over 5 minutes at 0° C. under argon with [1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor™) (8.9 g, 25.05 mmol). After the addition the mixture was stirred at room temperature for 0.5 hour then treated with saturated aqueous sodium bicarbonate solution (50 ml), stirred for 10 minutes, then diluted with water (100 ml) and extracted with ethyl acetate (3×200 ml). The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed eluting with 0-50% dichloromethane in hexane affording the product as a white solid (3.72 g, 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732460B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-bafbb154d86e4eac85d553a85bf98cb2
출처 메모uspto-grants-2010_06