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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030802Generated: November 2, 2026

Sodium Chloride → 2-[2-(Methylamino)benzylsulfinyl]imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1030802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[2-(Methylamino)benzylthio]imidazo[4,5-b]pyridineHCID 14839441—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product2-[2-(Methylamino)benzylsulfinyl]imidazo[4,5-b]pyridineHCID 14839442—

Reaction Steps

In a mixture of 1 ml of methanol and 30 ml of chloroform was dissolved 1.5 g of 2-[2-(methylamino)benzylthio]imidazo[4,5-b]pyridine. To the resulting solution was portionwise added under chilling with ice and aqueous sodium chloride solution to -5° C. 1.08 g of m-chloroperbenzoic acid (purity: 80%) over a period of 20 min., maintaining the temperature of the solution at -5° C.±3° C. The reaction mixture was stirred for additional 15 min. at the same temperature, and to the mixture was added a saturated NaHCO3 solution. The resulting mixture was then stirred. The organic phase was separated and extracted with two portions of 14 ml of 0.1N NaOH. The alkaline extracts were combined and neutralized by NH4Cl, and the deposited oil was extracted with chloroform. The chloroform extract was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and placed under reduced pressure to distill of the solvent. The residue was crystallized by addition of acetonitrile to give 2-[2-(methylamino)benzylsulfinyl]imidazo[4,5-b]-pyridine. m.p.: 120° C. (decompn.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106976
Source datasetuspto-grants-1992_04
ORD IDord-3f74dd9369964a90bb92101b9569c571
Source noteuspto-grants-1992_04