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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468934생성일: 2026년 10월 25일

Water → 7-(5-Fluoro-4-methylpyridin-3-yl)isoquinolin-3-amine

https://huagongshe.com/reaction/468934

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물7-Bromoisoquinolin-3-amineHCID 52987757—
반응물3-Fluoro-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 67976400—
촉매Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
용매Ethyl AcetateHCID 8857—
생성물7-(5-Fluoro-4-methylpyridin-3-yl)isoquinolin-3-amineHCID 6797484483.2%

반응 조건

온도120 °C

반응 단계

A mixture of 3-fluoro-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (261 mg; 0.7706 mmol), 7-bromoisoquinolin-3-amine (233.1 mg; 1.045 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (52.8 mg; 0.0746 mmol), potassium carbonate (338 mg; 2.44566 mmol), acetonitrile (3.0 mL; 57 mmol) and water (0.30 mL; 17 mmol) was heated at 120° C. for 40 minutes. The reaction mixture was diluted with ethyl acetate, washed with water and brine, dried over magnesium sulfate, filtered, and evaporated in vacuo. The crude product was purified via flash chromatography on silica gel (25 g silica, solvent gradient: 0-5% methanol in dichloromethane) to yield 162.4 mg (83%) of the title compound. LCMS (ESI): M+H=254.2; 1H NMR (400 MHz, DMSO) δ 8.88 (s, 1H), 8.50 (s, 1H), 8.37 (s, 1H), 7.86 (s, 1H), 7.63 (d, J=8.6 Hz, 1H), 7.51 (dd, J=8.6, 1.6 Hz, 1H), 6.67 (s, 1H), 6.04 (s, 2H), 2.25 (d, J=2.0 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623889B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-6eeb8ecb78ed45bc8159d582b0f8525a
출처 메모uspto-grants-2014_01