참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | HCID 178468630 | HCID 178468630 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 6-(4-Fluorophenyl)-3-methylpyrazolo[5,1-b][1,3]oxazole | HCID 89488364 | 46.3% |
반응 단계
To a stirred solution of 1-{[3-(4-fluorophenyl)-1H-pyrazol-5-yl]oxy}acetone (0.25 g, 1.0 mmol) in toluene, equipped with dean stark apparatus, acetic acid (2 ml) and p-TsOH (25 mg, cat.) was charged at RT and the reaction mass was refluxed at 130° C. for 16 h. After completion, the reaction was diluted with EtOAc (50 ml) and washed with brine. The organic layer dried over sodium sulphate and concentrated under reduced pressure to get the crude which was then purified by column chromatography 100-200 mesh) eluted with 5-10% ethyl acetate in hexane as eluent to get compound 6-(4-fluorophenyl)-3-methylpyrazolo[5,1-b][1,3]oxazole (0.1 g, yield 43%).
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-3c0b78a0836c4cfebba1d3ef6e030625 |
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| 출처 메모 | uspto-grants-2015_05 |
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