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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608625Generated: October 25, 2026

Water → 5-[2-(N-benzylmethylsulfonylamino)ethyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1608625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloroimidazo[1,2-A]pyridineHCID 10953722—
Reactant2-(N-benzylmethylsulfonylamino)-1-ethanolHCID 14947395—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-[2-(N-benzylmethylsulfonylamino)ethyloxy]imidazo[1,2-a]pyridineHCID 2336295139.4%

Reaction Steps

To a suspension of 60% sodium hydride in oil (0.20 g, 5 mmoles) in dimethylformamide (20 ml) was added 2-(N-benzylmethylsulfonylamino)-1-ethanol (1.14 g, 5 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (0.763 g, 5 mmoles) with stirring under ice-cooling, followed by stirring at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, which was extratced with ethyl acetate and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethyl acetate/hexane (1:1)→ethyl acetate/hexane (2:1)] to obtain 0.68 g of the desired product (39.4%, pale yellow oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-2d6cc3daaf54412ead075b27adceee08
Source noteuspto-grants-1995_03