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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539891생성일: 2026년 10월 26일

Acetonitrile → ethyl 1-(2-chloro-5-fluoropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/539891

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 4-methyl-1h-pyrrole-3-carboxylateHCID 235044—
반응물2,4-Dichloro-5-fluoropyrimidineHCID 250705—
용매Ethyl AcetateHCID 8857—
생성물ethyl 1-(2-chloro-5-fluoropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylateHCID 8665925385%

반응 조건

온도80 °C

반응 단계

To a solution of ethyl 3-methyl-1H-pyrrole-4-carboxylate (3.15 g, 20.5 mmol) in acetonitrile (MeCN) were added potassium carbonate (5.7 g, 41 mmol) and 2,4-dichloro-5-fluoropyrimidine (3.4 g, 20.5 mmol) at room temperature. The resulting slurry was heated at 80° C. for 3 hours with monitoring a reaction with LC-MS or thin layer chromatography (TLC). It was diluted with ethyl acetate and washed with brine. The collected organic layer was dried over anhydrous sodium sulfate and then partially concentrated in vacuo. To this, n-hexanes were added to form pale yellow precipitates. The resulting solids were collected by filtration and rinsed with n-hexanes and then dried under high vacuum to give 4.9 g (85%) of the target intermediate 3; MS (ESI) m/z 285 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871778B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-2857bc4ecf8a41a8893758f890bd6447
출처 메모uspto-grants-2014_10