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HRID 1608624생성일: 2026년 10월 25일

Water → 5-[1-(2-Thienylcarbonyl)-4-piperidyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608624

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물5-Chloroimidazo[1,2-A]pyridineHCID 10953722—
반응물(4-Hydroxypiperidin-1-yl)(thiophen-2-yl)methanoneHCID 23362856—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-[1-(2-Thienylcarbonyl)-4-piperidyloxy]imidazo[1,2-a]pyridineHCID 233629644.6%

반응 단계

To a suspension of 60% sodium hydride in oil (0.40 g, 10 mmoles) in dimethylformamide (30 ml) was added 1-(2-thienylcarbonyl)-4-hydroxypiperidine (2.11 g, 10 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (1.53 g, 10 mmoles) with stirring under ice-cooling, followed by stirring at room temperature for 7 hours. Water was added to the reaction mixture, which was extratced with ethyl acetate and dried. After the solvent was distilled off, the residue was purified with column chromatography [eluent: ethyl acetate/hexane (1:1)→ethyl acetate/hexane (2:1)→ethyl acetate/ethanol (50:1)] to obtain 0.15 g of the desired product (4.6%, pale yellow oily product).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05395839
출처 데이터셋uspto-grants-1995_03
ORD IDord-f920119d838e4b049080b711ad6eda16
출처 메모uspto-grants-1995_03