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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1639653생성일: 2026년 10월 25일

N,N-Dimethylaniline → 7-Chloro-2,5-dimethylpyrazolo(1,5-a)pyrimidine

https://huagongshe.com/reaction/1639653

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus oxychlorideHCID 24813—
반응물HCID 178422355HCID 178422355—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물7-Chloro-2,5-dimethylpyrazolo(1,5-a)pyrimidineHCID 1840698759.7%

반응 단계

To a suspension of 2,5-dimethyl-4H-pyrazolo[1,5-a]pyrimidin-7-one (10.0 g, 61.3 mmol) in toluene (150 mL), add N,N-dimethylaniline (9.7 mL, 76.7 mmol). Add phosphorus oxychloride (11.2 mL, 122.6 mmol) dropwise to this white suspension. Reflux for 3 h under an inert atmosphere, cool to room temperature, and concentrate the reaction to a brown oil using reduced pressure. Dissolve the oil in ethyl acetate (250 mL) and basify with 1 N NaOH. Separate and extract the basic aqueous phase with additional ethyl acetate (2×100 mL). Combine the organic phases, dry over anhydrous magnesium sulfate, filter, and concentrate under reduced pressure to yield a brown solid. Purify the material using flash chromatography, eluting with 80% hexane/20% (30% THF/hexane) to 0% hexane/100% (30% THF/hexane) in a step gradient of 20% increments to provide a light green solid (6.65 g, 59%). ES/MS m/z (35Cl) 182.3 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08110580B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-9fc98d642564481ba870ceadaba4a25d
출처 메모uspto-grants-2012_02