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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15130생성일: 2026년 10월 27일

Cesium fluoride → 1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate

https://huagongshe.com/reaction/15130

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물Potassium FluorideHCID 522689—
반응물Stannane, tributyl(1-ethoxyethenyl)-HCID 619414—
반응물tert-Butyl (2-chloro-5-fluoro-6-methoxypyridin-3-yl)carbamateHCID 71463986—
촉매Bis(tri-tert-butylphosphine)palladium(0)HCID 2734558—
용매1,4-DioxaneHCID 31275—
생성물1,1-Dimethylethyl [2-[1-(ethyloxy)ethenyl]-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamateHCID 86614146—

반응 조건

온도100 °C

반응 단계

A degassed solution of 1,1-dimethylethyl [2-chloro-5-fluoro-6-(methyloxy)-3-pyridinyl]carbamate (20 g, 72.2 mmol) in 1,4-dioxane (200 ml) was treated with bis(tri-tert-butylphosphine) palladium(0) (1.05 g), caesium fluoride (21.93 g) and tributyl[1-(ethyloxy)ethenyl]stannane (26.9 ml) then heated to 100° C. overnight. The cooled mixture was treated with 10% aqueous potassium fluoride solution. After 0.5 hour stirring, the mixture was filtered through Kieselguhr, washing with 1,4-dioxane. Ethyl acetate and water were added to the filtrate. The phases were separated and the aqueous phase extracted twice with ethyl acetate. The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was rapidly chromatographed eluting with 25-50% dichloromethane in hexane affording the product as a light brown oil (22.2 g, 99%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732460B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7f2d49d4ac4a426ea06dc7242d782435
출처 메모uspto-grants-2010_06