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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40843생성일: 2026년 10월 24일

Pentafluorophenol → 2-(perfluorophenoxy)-4-(1-tosyl-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrile

https://huagongshe.com/ko/reaction/40843

반응식

참여 물질

역할이름HCID투입량
반응물PentafluorophenolHCID 13041—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물2-(Methylthio)-4-(1-tosyl-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrileHCID 59414537—
용매DichloromethaneHCID 6344—
생성물2-(perfluorophenoxy)-4-(1-tosyl-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrileHCID 5941437831%

반응 단계

2-(Methylthio)-4-(1-tosyl-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrile (150 mg, 0.31 mmol) was dissolved in dichloromethane at room temperature. Meta-chloroperbenzoic acid (110 mg, 0.64 mmol) was added in one portion and the reaction was stirred for 5 minutes. Pentafluorophenol (285 mg, 1.55 mmol) was added and the solution was stirred at room temperature for 3 hours. The crude mixture was washed with a diluted solution of sodium bicarbonate and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as a solid (60 mg, 31% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530489B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-998258ca017c4116b9667045a1ff24a8
출처 메모uspto-grants-2013_09