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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1866899생성일: 2026년 10월 26일

Potassium Carbonate → 3-bromo-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

https://huagongshe.com/reaction/1866899

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물alpha,alpha'-Dichloro-p-xyleneHCID 12171—
반응물3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-oneHCID 22050832—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물3-bromo-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-oneHCID 2205002743.1%

반응 조건

온도110 °C

반응 단계

To a solution of 3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (0.60 g, 2.5 mmol) in DMF (40 mL) was added K2CO3 (0.70 g, 5.1 mmol) and α,α′-dichloro-p-xylene (0.53 g, 3.0 mmol), and the reaction mixture was stirred at 110° C. for 2 h. The reaction mixture was cooled to room temperature, diluted with brine, and extracted with CHCl3 (4×100 mL). The combined organics were washed water and then brine, dried (Na2SO4), filtered, and concentrated under reduced pressure to afford 3-bromo-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as an off-white solid (0.49 g, 43%): 1H NMR (300 MHz, CDCl3) δ 7.54 (app q, J=8 Hz, 1H), 7.38-7.28 (m, 5H), 6.94 (td, J=8, 2 Hz, 1H), 6.85 (td, J=8, 2 Hz, 1H), 6.10 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.16 (s, 2H), 4.56 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07629363B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-01b20223ab4f4040a6329045fb962d4f
출처 메모uspto-grants-2009_12