Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 348413생성일: 2026년 10월 24일
Cesium carbonate → 2-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-3-ethyl-4-nitropyrazole-5-carboxamide
https://huagongshe.com/ko/reaction/348413
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | (2-Bromoethoxy)-tert-butyldimethylsilane | HCID 3608067 | — |
| 반응물 | HCID 178438045 | HCID 178438045 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-3-ethyl-4-nitropyrazole-5-carboxamide | HCID 60061101 | — |
반응 단계
A mixture of 3-ethyl-4-nitro-1H-pyrazole-5-carboxamide (WO, 9849166), (4.9 g, 26.6 mmol), cesium carbonate (21.0 g, 64.5 mmol) and (2-bromoethoxy)-tert-butyldimethylsilane (7.0 g, 29.0 mmol) in acetonitrile (400 ml) was stirred at 80° C. for 20 hours. The cooled mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate (200 ml) and water (100 ml). The layers were separated, the organic phase washed with water (3×50 ml), dried (Na2SO4) and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel, using ethyl acetate as eluant, and repeated using an elution gradient of pentane:ethyl acetate (50:50 to 0:100), to give some of the desired compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07176311B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-e77d4e7f081842e0af2eed0630b013d8 |
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| 출처 메모 | uspto-grants-2007_02 |
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