Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 570129생성일: 2026년 10월 25일
Potassium Carbonate → 6-(4-Fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole
https://huagongshe.com/reaction/570129
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,3-Butanediol, dimethanesulfonate | HCID 99909 | — |
| 반응물 | 3-(4-fluorophenyl)-1H-pyrazol-5-ol | HCID 178515624 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-(4-Fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole | HCID 89488312 | 71.8% |
반응 단계
To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (3 g, 16.8 mmol) in DMF (15 mL) was added K2CO3 (9.3 g, 67.4 mmol) and butane-2,3-diyl dimethanesulfonate (4.8 g, 18.5 mmol) (prepared as described in US2010/41748) at room temperature and then stirred for 16 h at 60° C. Thereafter, the reaction mixture was diluted with cold water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether) yielded 6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole (2.8 g, 71%) as yellow oil and a mixture of diastereoisomers.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09023844B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-5fdc646e557142ff9c0d88ee8192ca33 |
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| 출처 메모 | uspto-grants-2015_05 |
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