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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030801Generated: October 30, 2026

HCID 14839440, compound → 2-[2-(Methylamino)benzylthio]imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1030801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14839440HCID 14839440—
ReactantHCID 178527819HCID 178527819—
SolventEthanolHCID 702—
Product2-[2-(Methylamino)benzylthio]imidazo[4,5-b]pyridineHCID 1483944168.1%

Reaction Steps

To a dispersion of 1.51 g of 2-mercaptoimidazo[4,5-b]pyridine in 25 ml of ethanol was added at once 1.92 g of 2-(methylamino)benzyl chloride hydrochloride at room temperature under stirring. The resulting mixture was further stirred for 3.5 hours. The precipitated crystals were collected by filtration and washed with ethanol. The obtained crystals were added portionwise to a mixture of 100 ml of chloroform and 100 ml of 1N NaOH solution for neutralization. The aqueous NaOH phase was separated, and to this phase were successively added 200 ml of chloroform and a saturated ammonium chloride solution until the aqueous phase showed no turbidity upon addition of the solution. The chloroform phase was separated, washed with a saturated aqueous sodium chloride solution, and dried over sodium sulfate. The solvent was then distilled off under reduced pressure and the residue was crystallized by addition of diethyl ether. The crystalline product was collected by filtration and dried to give 1.84 g (yield: 68.1%) of 2-[2-(methylamino)benzylthio]imidazo[4,5-b]pyridine as a white crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106976
Source datasetuspto-grants-1992_04
ORD IDord-91c92b58b24942088563f8854507a3f7
Source noteuspto-grants-1992_04