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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1431453생성일: 2026년 10월 27일

Potassium Phosphate, Tribasic → N-(5-(3,6-dihydro-2H-pyran-4-yl)-3-pyridinyl)-5,7-difluoro-3-methyl-2-(2-pyridinyl)-4-quinolinamine

https://huagongshe.com/reaction/1431453

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참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물3,6-Dihydro-2H-pyran-4-boronic acid pinacol esterHCID 11218053—
반응물N-(5-bromo-3-pyridinyl)-5,7-difluoro-3-methyl-2-(2-pyridinyl)-4-quinolinamineHCID 59631407—
반응물2-Dicyclohexylphosphino-2,6-dimethoxybiphenylHCID 66545337—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(5-(3,6-dihydro-2H-pyran-4-yl)-3-pyridinyl)-5,7-difluoro-3-methyl-2-(2-pyridinyl)-4-quinolinamineHCID 59631281—

반응 조건

온도90 °C

반응 단계

A mixture of N-(5-bromo-3-pyridinyl)-5,7-difluoro-3-methyl-2-(2-pyridinyl)-4-quinolinamine (38.0 mg, 0.089 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyran (29.1 mg, 0.139 mmol), 2-dicyclohexylphosphino-2,6-dimethoxybiphenyl (S-Phos) (7.7 mg, 0.019 mmol), palladium(II) acetate (6.9 mg, 10.24 μmol), and potassium phosphate tribasic (60.4 mg, 0.29 mmol) in DMF (1 mL) and water (0.05 mL) was degassed by nitrogen. The mixture was heated to 90° C. After 21.5 h, the reaction was cooled to rt, then treated with water. After extracting twice with EtOAc, the organic layers were combined and dried over anhydrous magnesium sulfate. After filtration and concentration the residue was purified on basic alumina (0-35% EtOAc in hexanes) to afford an impure yellow residue. The light yellow film was further purified by HPLC (10-60% of 0.1% TFA acetonitrile solution in 0.1% TFA water solution.) The desired fractions were concentrated then diluted with EtOAc. After washing twice with satd aq. sodium bicarbonate solution and once with brine, the solvent was removed under reduced pressure to yield a white solid as N-(5-(3,6-dihydro-2H-pyran-4-yl)-3-pyridinyl)-5,7-difluoro-3-methyl-2-(2-pyridinyl)-4-quinolinamine. 1H NMR (400 MHz, CDCl3) δ ppm 8.76 (1H, m), 8.31 (1H, d, J=1.8 Hz), 8.18 (1H, d, J=2.5 Hz), 7.94 (2H, m), 7.69 (1H, m), 7.38 (1H, dddd, J=7.4, 4.9, 1.3, 0.7 Hz), 7.12 (3H, m), 6.25 (1H, m), 4.33 (2H, q, J=2.7 Hz), 3.94 (2H, t, J=5.5 Hz), 2.51 (2H, td, J=5.0, 2.2 Hz), 2.17 (3H, s). Mass Spectrum (pos.) m/e: 431.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08940724B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-b61a76cb78e94f16877c34cae1570b75
출처 메모uspto-grants-2015_01