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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Di-tert-butyl (chloromethyl) phosphate | HCID 11701630 | — |
| 반응물 | Gsk-5498A | HCID 46945384 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [[(2,6-Difluorophenyl)carbonyl](1-{[2-fluoro-6-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)amino]methyl bis(1,1-dimethylethyl) phosphate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08399436B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-40daeab8295542e8b7ad97be4a230473 |
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| 출처 메모 | uspto-grants-2013_03 |
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