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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608633Generated: October 26, 2026

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

https://huagongshe.com/reaction/1608633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant1-(Methylsulfonyl)piperidin-4-yl methanesulfonateHCID 22273065—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product5-[1-(Methylsulfonyl)-4-piperidylthio]imidazo[1,2-a]pyridineHCID 2008666040.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-aafba9e9bba34e7697423ff017d1e70c
Source noteuspto-grants-1995_03