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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42569생성일: 2026년 10월 23일

Water → 2-Ethyl-4,6-bis(4-fluorophenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine

https://huagongshe.com/ko/reaction/42569

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물IodoethaneHCID 6340—
반응물Potassium HydroxideHCID 14797—
반응물4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridineHCID 11961374—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물1-Ethyl-4,6-bis(4-fluorophenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridineHCID 100702619%
생성물2-Ethyl-4,6-bis(4-fluorophenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridineHCID 6844477661%

반응 조건

온도100 °C

반응 단계

A suspension of 4,6-bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine (0.39 g, 0.8 mmol, obtained in example 1), KOH (0.05 g, 0.8 mmol) and crown ether 18-C-6 (0.01 g, 0.03 mmol) in toluene (3 mL) was heated to 100° C. for 2 h. A solution of iodoethane (0.18 g, 1.2 mmol) in toluene (1 mL) was added and stirred at 100° C. for 2 days. It was allowed to cool, water and EtOAc were added and the phases were separated. The aqueous phase was extracted with EtOAc. 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 0.20 g of 2-ethyl-4,6-bis(4-fluorophenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine (yield: 61%) and 28 mg of 1-ethyl-4,6-bis(4-fluorophenyl)-5-(4-pyridyl)pyrazolo[3,4-b]pyridine (yield: 9%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536194B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-70f938120ee34765b5e2ca34d2ea6fad
출처 메모uspto-grants-2013_09