関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 1-(Methylsulfonyl)piperidin-4-yl methanesulfonate | HCID 22273065 | — |
| 反応物 | HCID 178418687 | HCID 178418687 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridine | HCID 20086660 | 40.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05244908 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-b41679ed788043cfae401763920430fc |
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| 出典メモ | uspto-grants-1993_09 |
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