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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606884생성일: 2026년 10월 25일

3-Bromo-5-methoxypyridine → 3-(4-Fluoro-3-methylphenylethynyl)-5-methoxypyridine

https://huagongshe.com/reaction/606884

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-5-methoxypyridineHCID 817163—
반응물4-Ethynyl-1-fluoro-2-methylbenzeneHCID 16213797—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
용매DiisopropylamineHCID 7912—
생성물3-(4-Fluoro-3-methylphenylethynyl)-5-methoxypyridineHCID 6704745351.1%

반응 조건

온도60 °C

반응 단계

Dissolve 3-bromo-5-methoxypyridine (1.0 g, 5.35 mmol) in diisopropylamine (17 mL) and toluene (10 mL) under nitrogen. Add tetrakis(triphenylphosphine)palladium (0.200 g, 0.16 mmol). Heat at 60° C. and add 4-ethynyl-1-fluoro-2-methylbenzene (717 mg, 5.35 mmol) and copper (I) iodide (20 mg, 0.11 mmol). After 20 h add additional 4-ethynyl-1-fluoro-2-methylbenzene (100 mg, 0.75 mmol) and heat at 60° C. for 5 h. Concentrate and purify using silica gel chromatography, eluting with 30:70 to 40:60 ethyl acetate:hexanes, to give the title compound (660 mg, 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915424B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f3df2be9dc0a47619caf9aebe8412b39
출처 메모uspto-grants-2011_03