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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 510985생성일: 2026년 10월 27일

Potassium Carbonate → Tert-butyl {1-[5-chloro-3-(5-fluoropyridin-3-yl)-2-methoxy-4-methylphenyl]propyl}carbamate

https://huagongshe.com/reaction/510985

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Fluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 16414268—
반응물Tert-butyl[1-(3-bromo-5-chloro-2-methoxy-4-methylphenyl)propyl]carbamateHCID 88540645—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물Tert-butyl {1-[5-chloro-3-(5-fluoropyridin-3-yl)-2-methoxy-4-methylphenyl]propyl}carbamateHCID 8666690077%

반응 조건

온도90 °C

반응 단계

The tert-butyl [1-(3-bromo-5-chloro-2-methoxy-4-methylphenyl)propyl]carbamate peak 2 (0.075 g, 0.19 mmol) was combined with 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.081 g, 0.29 mmol, Frontier Scientific, catalog #F2018) in 1,4-dioxane (4.6 mL) and potassium carbonate (0.053 g, 0.38 mmol) in water (1.5 mL) in a tube. This was degassed with nitrogen and the tetrakis(triphenylphosphine)palladium(0) (0.02 g, 0.02 mmol) was added. The reaction was degassed with nitrogen, sealed and heated to 90° C. in an oil bath. The reaction was complete after 18 h, and the reaction mixture was allowed to cool and partitioned between EtOAc and water. The organic layer was washed with brine, dried over magnesium sulfate and concentrated to give the crude product as an oil. The product was purified by chromatography on silica gel eluting with a hexane:EtOAc gradient to give tert-butyl {1-[5-chloro-3-(5-fluoropyridin-3-yl)-2-methoxy-4-methylphenyl]propyl}carbamate as a viscous oil (0.05 g, 77%). LCMS calculated for C21H27ClFN2O3 (M+H)+: m/z=409.1. found: 409.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096600B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-38429a9892754a228cf01455b0010639
출처 메모uspto-grants-2015_08