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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239663생성일: 2026년 10월 24일

Dichloromethane → 2-((4-amino-3-(1H-indazol-6-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-phenyl-4H-chromen-4-one

https://huagongshe.com/ko/reaction/239663

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium CarbonateHCID 10340—
반응물6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazoleHCID 44119250—
반응물2-((4-Amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-phenyl-4H-chromen-4-oneHCID 58269147—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-((4-amino-3-(1H-indazol-6-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-phenyl-4H-chromen-4-oneHCID 582691643%

반응 조건

온도80 °C

반응 단계

To a solution of Example 57a (0.700 g, 1.40 mmoles) in DMF (7 ml), ethanol (3.2 ml) and water (3.2 ml), 6-Indazoleboronic acid pinacol ester (0.687 g, 2.81 mmoles) and sodium carbonate (0.745 g, 7.03 mmoles) were added and the system is degassed for 30 min. Tetrakis triphenylphosphine Palladium (0.320 g, 0.277 mmoles) was added under nitrogen atmosphere and heated to 80° C. After 12 h, the reaction mixture was celite filtered, concentrated and extracted with ethyl acetate. The organic layer was dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol: dichloromethane to afford the title compound as yellow solid (0.020 g, 3% yield). MP: 140-143° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 13.18(s,1H), 8.24(s,1H), 8.13(s,1H), 8.06(dd, J=7.9, 1.6 Hz, 1H), 7.78(m,2H), 7.49-7.30(m, 7H), 6.89(q, J=7.7 Hz,1H),5.53(s, 2H). Mass: 485.76(M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642607B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-67abe6a151d54a04a9de2a9704169a95
출처 메모uspto-grants-2014_02