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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030790Generated: November 3, 2026

m-Chloroperbenzoic acid → HCID 14052185, compound

https://huagongshe.com/reaction/1030790

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 14052172HCID 14052172—
SolventChloroformHCID 6212—
ProductHCID 14052185HCID 1405218528.3%

Reaction Steps

In 14 ml of chloroform was dissolved 1.4 g of 2-methyl-3-(2-pyridylmethylthio)pyrido[2,3-b]pyrazine. To the solution under chilling with ice was added portionwise 1.1 g of m-chloroperbenzoic acid (purity: 80%). The reaction mixture was then left to have room temperature, and poured into saturated aqueous NaHCO3 solution. The aqueous mixture was extracted with chloroform. The chloroform layer was washed with water and saturated aqueous sodium chloride solution, and dried over sodium sulfate. The sodium sulfate was then removed by filtration, and the solvent was evaporated under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography (chloroform/methanol), to give 420 mg of 2-methyl-3-(2-pyridylmethylsulfinyl)-pyrido[2,3-b]pyrazine as a brown crystalline powder, m.p. 120°-125° C. (decompn.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106976
Source datasetuspto-grants-1992_04
ORD IDord-2d2578c345dd41939901b3bf28e4bda9
Source noteuspto-grants-1992_04