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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1081750생성일: 2026년 10월 27일

Sodium Methoxide → 5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081750

반응식

참여 물질

역할이름HCID투입량
반응물Sodium MethoxideHCID 10942334—
반응물1-(Methylsulfonyl)piperidin-4-yl methanesulfonateHCID 22273065—
반응물HCID 178418687HCID 178418687—
용매EthanolHCID 702—
용매MethanolHCID 887—
생성물5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridineHCID 2008666040.8%

반응 단계

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (1.50 g, 10 moles) in ethanol (100 ml) was added a solution of 4.1M sodium methylate (2.44 ml, 10 mmoles) in methanol and the mixture was stirred at room temperature for 10 minutes. To the reaction mixture was added 1-methylsulfonyl-4-methylsulfonyloxypiperidine (2.83 g, 11 mmoles) at room temperature and the mixture was heated under reflux for 14 hours. After the solvent was distilled off, the residue was dissolved in chloroform, which was washed in turn with an aqueous 1N sodium hydroxide solution and water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent:ethyl acetate/ethanol (10:1)] to obtain 1.27 g of the desired product (40.8%, light brown solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05587383
출처 데이터셋uspto-grants-1996_12
ORD IDord-6bf4187ea4814b69931712d96d6048e1
출처 메모uspto-grants-1996_12