Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1506537생성일: 2026년 10월 26일
Diisopropylethylamine → ethyl 1-(5-fluoropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate
https://huagongshe.com/reaction/1506537
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Ethyl ethoxymethylene-3-oxo-4,4,4-trifluorobutyrate | HCID 6185754 | — |
| 반응물 | 5-Fluoro-2-hydrazinylpyridine hydrofluoride | HCID 71721388 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | ethyl 1-(5-fluoropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate | HCID 67171373 | 29.7% |
반응 단계
To (E)-ethyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoate (0.441 g, 1.835 mmol) in ethanol (2 mL) was added diisopropylethylamine (0.427 mL, 2.447 mmol) followed by 5-fluoro-2-hydrazinylpyridine, hydrofluoride (0.3 g, 2.039 mmol) dissolved in 1 mL of ethanol (slightly exothermic). The reaction mixture was heated at 80° C. for 1 h. The reaction mixture was concentrated under reduced pressure, dissolved in dichloromethane (2 mL) and subjected to column chromatography using an ISCO setup (40 g, RediSep® silica gel column). The desired fractions were collected and concentrated to yield ethyl 1-(5-fluoropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate (0.165 g, 27%) as a white solid. LC/MS M+1=304.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09216972B2 |
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| 출처 데이터셋 | uspto-grants-2015_12 |
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| ORD ID | ord-a4f8b5e232224f2db07a166844118c3d |
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| 출처 메모 | uspto-grants-2015_12 |
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