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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081743Generated: October 26, 2026

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

https://huagongshe.com/reaction/1081743

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 numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-33bfcac35ff749b49b4b727683e36d3a
Source noteuspto-grants-1996_12