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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42567생성일: 2026년 10월 24일

Pyrazol-3-ylamine → 4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/ko/reaction/42567

반응식

참여 물질

역할이름HCID투입량
반응물Pyrazol-3-ylamineHCID 74561—
반응물1-(4-Fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoateHCID 68445862—
촉매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridineHCID 1196137423%

반응 단계

To a solution of 3-amino-2H-pyrazole (60 mg, 71.8 mmol) in EtOH (2 mL) and 1 drop of 37% HCl, 1-(4-fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoate (0.22 g, 65.0 mmol, obtained in reference example 4) was added under argon atmosphere. This was heated to reflux for 3 days. The mixture was diluted with CHCl3 and MeOH. It was washed with saturated NaHCO3. The aqueous phase was extracted with CHCl3 (×2). The organic phase was dried over Na2SO4 and concentrated to dryness. The crude product obtained was purified by chromatography on silica gel using hexane-EtOAc mixtures of increasing polarity as eluent, to afford 58 mg of the desired product in a solid white form (yield: 23%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536194B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4cbd8a706b52416aa85386b5b15613c0
출처 메모uspto-grants-2013_09