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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7639생성일: 2026년 10월 23일

Methanol → 2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one

https://huagongshe.com/ko/reaction/7639

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Potassium peroxymonosulphateHCID 10313463—
반응물2-(4-fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 12991404—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Sodium BicarbonateHCID 516892—
생성물2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 12991405—

반응 단계

To a solution of 2-(4-fluorophenyl)-3-(2-methylsulfanyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one, 4, (1.3 g, 3.8 mmol) in THF:methanol (56 mL of a 1:1 mixture) is added dropwise a solution of Oxone® (potassium peroxymonosulfate) (9.34 g, 15.2 mmol) in water (42 mL). The reaction is stirred 1 hour at room temperature, diluted with aqueous NaHCO3 and extract three times with ethyl acetate. The organic layers are combined, dried, and concentrated in vacuo too afford the crude desired product which is used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087615B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-245f887f4b944d7aa69c92de847409da
출처 메모uspto-grants-2006_08