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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1852843생성일: 2026년 10월 26일

Water → HCID 178460611, 화합물

https://huagongshe.com/reaction/1852843

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물tert-Butyl(dimethyl){[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-yl]oxy}silaneHCID 16069431—
반응물HCID 178461197HCID 178461197—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매1,4-DioxaneHCID 31275—
생성물HCID 178460611HCID 178460611—

반응 조건

온도100 °C

반응 단계

To a stirred solution of 2-bromo-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile (Preparative Example 3.1; 3.0 g, 6.93 mmol) in 1,4-dioxane (60 mL), tert-butyldimethyl((2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl)oxy)silane (3.09 g 10.39 mmol), potassium phosphate (2.94 g, 13.86 mmol), and water (6 mL) were added, and the mixture was degassed with argon for 15 minutes. PdCl2(dppf) (0.85 g, 1.04 mmol), was added, and the mixture was degassed with argon again for 5 minutes. The reaction was then heated at 100° C. for 16 h. The reaction mixture was cooled to room temperature, quenched with water (20 mL), and extracted with ethyl acetate (100 mL). The organic layer was separated, washed with brine (50 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography using 15% ethyl acetate/petroleum ether as eluent to yield 2-(3-{[tert-butyl(dimethyl)silyl]oxy}prop-1-en-2-yl)-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ES/APCI calcd. for C29H38ClN5OSi [M+H]+ 536. found 536.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962611B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-5a1d5477b1164c1b9699aaf4681877b0
출처 메모uspto-grants-2015_02