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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456689생성일: 2026년 10월 24일

2-Bromo-1-(4-fluorophenyl)ethan-1-one → 8-Chloro-2-(4-fluorophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/456689

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 96749—
반응물Sodium BicarbonateHCID 516892—
반응물2-Amino-3-chloropyridineHCID 693267—
용매EthanolHCID 702—
생성물8-Chloro-2-(4-fluorophenyl)imidazo[1,2-a]pyridineHCID 1797628580.3%

반응 단계

To a solution of 2-amino-3-chloropyridine (6.51 g, 51 mmol) and 2-bromo-4′-fluoroacetophenone (13.0 g, 60 mmol) in ethanol (100 mL) was added sodium bicarbonate (4.91 g, 60 mmol) and the reaction mixture was heated at reflux for 6 hours. The resulting mixture was concentrated to a solid in vacuo. This residue was dissolved in ethyl acetate and the organic phase was washed with water and an aqueous sodium chloride solution. The organic phase was dried (magnesium sulfate), filtered through a silica gel pad and concentrated to give a solid. This solid was recrystallized from acetonitrile, to give 10.1 g (80%) 8-chloro-2-(4-fluorophenyl)imidazo[1,2-α]pyridine as a solid. 1H NMR (CDCl3): δ 8.06 (d, 1H), 7.96 (q, 2H), 7.86 (s, 1H), 7.25 (d, 1H), 7.13 (t, 2H), 6.73 (t, 1H); 19F NMR (CDCl3) δ −114.0; MS m/z 247 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186714B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-33ba5224952445338ce4fa3525dc4b22
출처 메모uspto-grants-2007_03