참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 1-(Methylsulfonyl)piperidin-4-yl methanesulfonate | HCID 22273065 | — |
| 반응물 | HCID 178418687 | HCID 178418687 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridine | HCID 20086660 | 40.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05587383 |
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| 출처 데이터셋 | uspto-grants-1996_12 |
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| ORD ID | ord-6bf4187ea4814b69931712d96d6048e1 |
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| 출처 메모 | uspto-grants-1996_12 |
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