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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2260534생성일: 2026년 10월 27일

Acetyl chloride → 3-(1-Acetyl-l,2-dihydro-2-methylpyridin-4-yl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2260534

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물Sodium BicarbonateHCID 516892—
반응물2-(4-Fluorophenyl)-3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidineHCID 19957280—
반응물HCID 178418573HCID 178418573—
용매TetrahydrofuranHCID 8028—
생성물3-(1-Acetyl-l,2-dihydro-2-methylpyridin-4-yl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidineHCID 19957261—

반응 단계

To a solution of 2-(4-fluorophenyl)-3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidine (480 mg) in dry tetrahydrofuran (15 ml) was added acetyl chloride (0.89 ml) dropwise under ice cooling. The mixture was stirred at ambient temperature for 1 hour and to the mixture was added a solution of methyl magnesium bromide in tetrahydrofuran (1 mole solution, 12.42 ml) under ice cooling. The mixture was stirred at ambient temperature for 2 hours and to the mixture was added an aqueous saturated sodium bicarbonate solution. The separated oil was extracted with dichloromethane and the solution was washed with brine, dried and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give 3-(1-acetyl-l,2-dihydro-2-methylpyridin-4-yl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine (327 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05478827
출처 데이터셋uspto-grants-1995_12
ORD IDord-ba5291ff62ad44d885faf03c5746fc87
출처 메모uspto-grants-1995_12