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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13333생성일: 2026년 10월 24일

p-Toluenesulfonic acid → HCID 23145188, 화합물

https://huagongshe.com/ko/reaction/13333

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Potassium CarbonateHCID 11430—
반응물Stannous chloride dihydrateHCID 61436—
반응물2,6-DifluorophenolHCID 94392—
반응물N-(2,3-difluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-6-nitro-phenyl)pyrazinecarboxamideHCID 23145537—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물HCID 23145188HCID 23145188—

반응 조건

온도90 °C

반응 단계

8 mg of 2,6-difluorophenol and 8 mg of potassium carbonate were added to an N-methylpyrrolidinone (0.5 ml) solution of 8.6 mg of N-(2,3-difluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-6-nitro-phenyl)pyrazinecarboxamide, and the reaction liquid was stirred at 90° C. for 15 minutes. 75 mg of tin(II) chloride dihydrate was added to it, and the reaction liquid was stirred overnight at 90° C. Further, 3 mg of p-toluenesulfonic acid was added to it, and the reaction liquid was stirred at 90° C. for 2 hours. The deposit was taken out through filtration, and purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid]. The solvent of the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c87dc0f010dc41a69867e6328807e9df
출처 메모uspto-grants-2010_06