HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107324Generated: November 2, 2026
m-Chloroperbenzoic acid → HCID 14052185, compound
https://huagongshe.com/reaction/2107324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 14052172 | HCID 14052172 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14052185 | HCID 14052185 | 28.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933458 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-20729db147b94c10bced6bfbd02ee089 |
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| Source note | uspto-grants-1990_06 |
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