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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1946352생성일: 2026년 10월 25일

Potassium Hydroxide → [[(2,6-Difluorophenyl)carbonyl](1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)amino]methyl bis(1,1-dimethylethyl) phosphate

https://huagongshe.com/reaction/1946352

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Di-tert-butyl (chloromethyl) phosphateHCID 11701630—
반응물Gsk-5498AHCID 46945384—
용매DimethylformamideHCID 6228—
생성물[[(2,6-Difluorophenyl)carbonyl](1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)amino]methyl bis(1,1-dimethylethyl) phosphateHCID 59547970—

반응 단계

A solution of 2,6-difluoro-N-(1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)benzamide (for a preparation see Example 29)(61.25 g, 153 mmol), chloromethyl bis(1,1-dimethylethyl) phosphate (for a preparation see Intermediate 60)(47.6 g, 184 mmol) and potassium hydroxide (14.18 g, 215 mmol) in N,N-dimethylformamide (500 ml) was stirred at ambient temperature for 7 days. The reaction mixture was partitioned between ethyl acetate (350 ml) and water/brine (250 ml, 1:1 volume/volume). The organic phase was washed with brine (250 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The sample was loaded in dichloromethane and purified on a silica Redisep cartridge 1500 g using a gradient of 0-75% ethyl acetate-cyclohexane over 8 column volumes. The appropriate fractions were combined and evaporated in vacuo to give the title compound as a colourless gum (which started to crystallise to a white solid (72.44 g); LCMS: (System 8) MH+=622, tRET=3.40 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399436B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-40daeab8295542e8b7ad97be4a230473
출처 메모uspto-grants-2013_03