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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107324Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 14052185, compound

https://huagongshe.com/reaction/2107324

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. T he 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 numberUS04933458
Source datasetuspto-grants-1990_06
ORD IDord-20729db147b94c10bced6bfbd02ee089
Source noteuspto-grants-1990_06