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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45855생성일: 2026년 10월 23일

Cesium carbonate → 4-[1-(4-methoxybenzyl)-3-(3-nitrophenyl)-1H-pyrazol-4-yl]pyridine

https://huagongshe.com/ko/reaction/45855

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 2734648—
반응물4-iodo-1-(4-methoxybenzyl)-3-(3-nitrophenyl)-1H-pyrazoleHCID 67184483—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물4-[1-(4-methoxybenzyl)-3-(3-nitrophenyl)-1H-pyrazol-4-yl]pyridineHCID 67184735—

반응 단계

To a solution of 100 mg (0.23 mol) of 4-iodo-1-(4-methoxybenzyl)-3-(3-nitrophenyl)-1H-pyrazole in 16 ml of dioxane and 4 ml of water, 90 mg (0.46 mmol) of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, 52 mg (0.046 mmol) of palladium tetrakis and 150 mg (0.46 mmol) mg of cesium carbonate were added successively. The mixture was submitted to microwave irradiation at 120° C. for 30 minutes in a sealed vial. The reaction was filtered through a celite pad and the solvent evaporated to dryness. The crude was then partitioned between dichloromethane and water, the organic layer dried over sodium sulphate and the solvent removed in vacuo. After purification by flash-chromatography on a silica gel column (CH2Cl2-CH3COCH3) 78 mg (88%) of the title compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541575B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5b86c86302dd4ea9a1ad0c9f3c3e19a2
출처 메모uspto-grants-2013_09