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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

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
반응물HCID 178438045HCID 178438045—
용매AcetonitrileHCID 6342—
생성물2-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-3-ethyl-4-nitropyrazole-5-carboxamideHCID 60061101—

반응 조건

온도80 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176311B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-e77d4e7f081842e0af2eed0630b013d8
출처 메모uspto-grants-2007_02