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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57806생성일: 2026년 10월 25일

N,N'-Dimethylethylenediamine → 6-Chloro-1-(6-fluoropyridin-2-yl)-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/57806

반응식

참여 물질

역할이름HCID투입량
반응물N,N'-DimethylethylenediamineHCID 8070—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-6-fluoropyridineHCID 639438—
반응물6-Chloro-1H-pyrazolo(4,3-c)pyridineHCID 56932109—
촉매Copper iodideHCID 83717—
용매1,4-DioxaneHCID 31275—
생성물6-Chloro-1-(6-fluoropyridin-2-yl)-1H-pyrazolo[4,3-c]pyridineHCID 8628024355.5%

반응 조건

온도100 °C

반응 단계

A mixture of 6-chloro-1H-pyrazolo[4,3-c]pyridine (13.778 mmol, 2115.9 mg), 2-bromo-6-fluoro-pyridine (15.156 mmol, 2667.3 mg), N,N′-Dimethylethylenediamine (13.778 mmol; 1.215 g; 1.37 mL), Copper iodide (13.778 mmol; 2650.5 mg), and potassium carbonate (15.156 mmol; 2.12 g) in 1,4-Dioxane (10 mL) was purged with Argon, then sealed and stirred at 100° C. for 20 hours. The mixture was cooled to room temperature, and then filtered through Celite. The filtrate was concentrated; the residue was purified on silica and eluted with 0 to 100% Ethyl acetate in Heptane to give 6-Chloro-1-(6-fluoro-2-pyridyl)pyrazolo[4,3-c]pyridine as an off-white solid (1.90 g, 55%) MS (ESI) m/z: 249 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434725B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-0ae3849eb90847e88320600dde5b5d9f
출처 메모uspto-grants-2016_09