돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42571생성일: 2026년 10월 24일

Water → 4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-2-[3-(tetrahydropyran-2-yloxy)propyl]pyrazolo[3,4-b]pyridine

https://huagongshe.com/ko/reaction/42571

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium HydroxideHCID 14797—
반응물2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
반응물4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridineHCID 11961374—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-2-[3-(tetrahydropyran-2-yloxy)propyl]pyrazolo[3,4-b]pyridineHCID 6844569254%

반응 조건

온도100 °C

반응 단계

A suspension of 4,6-bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine (0.30 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 (10 mL) was heated to 100° C. for 1 h. 2-(3-Bromopropoxy)tetrahydropyran (0.17 g, 0.8 mmol) was added and stirred at 100° C. for 24 h. 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 0.22 g of the desired compound (yield: 54%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536194B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e243f7b805fc4b0a91963963c7482889
출처 메모uspto-grants-2013_09