HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081750Generated: October 26, 2026
Sodium Methoxide → 5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridine
https://huagongshe.com/reaction/1081750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-(Methylsulfonyl)piperidin-4-yl methanesulfonate | HCID 22273065 | — |
| Reactant | HCID 178418687 | HCID 178418687 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridine | HCID 20086660 | 40.8% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587383 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-6bf4187ea4814b69931712d96d6048e1 |
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| Source note | uspto-grants-1996_12 |
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