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HRID 5478作成日:2026年10月26日

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

https://huagongshe.com/reaction/5478

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium MethoxideHCID 10942334—
反応物1-(Methylsulfonyl)piperidin-4-yl methanesulfonateHCID 22273065—
反応物HCID 178418687HCID 178418687—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
生成物5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridineHCID 2008666040.8%

反応手順

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (1.50 g, 10 mmoles) 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244908
出典データセットuspto-grants-1993_09
ORD IDord-b41679ed788043cfae401763920430fc
出典メモuspto-grants-1993_09