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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Ethyl 4-methyl-1h-pyrrole-3-carboxylate | HCID 235044 | — |
| 반응물 | 2,4-Dichloro-5-fluoropyrimidine | HCID 250705 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | ethyl 1-(2-chloro-5-fluoropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylate | HCID 86659253 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08871778B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-2857bc4ecf8a41a8893758f890bd6447 |
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| 출처 메모 | uspto-grants-2014_10 |
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