HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524028Generated: October 27, 2026
Potassium peroxymonosulphate → 6-(3,5-Dimethoxyphenyl)-8-methyl-2-(methylsulfonyl)pyrido[2,3-d]pyrimidin-7(8H)-one
https://huagongshe.com/reaction/524028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 6-(3,5-dimethoxyphenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one | HCID 86713559 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Water methylene chloride | HCID 21908982 | — |
| Product | 6-(3,5-Dimethoxyphenyl)-8-methyl-2-(methylsulfonyl)pyrido[2,3-d]pyrimidin-7(8H)-one | HCID 86713560 | 78% |
Reaction Steps
To a solution of 6-(3,5-dimethoxyphenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one (1.05 g, 3.1 mmol) in methanol/dichloromethane (MeOH/DCM) (20 mL/20 mL) was added a solution of Oxone® (potassium peroxymonosulfate) (11.3 g, 18.4 mmol) in H2O (20 mL) at room temperature, and the reaction mixture was stirred at 40° C. for 18 hours. The reaction was monitored by LCMS. The reaction mixture was diluted with H2O/DCM (150 mL/100 mL), and the aqueous phase was extracted with DCM (100 mL). The combined organic layers were washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered, and concentrated. The crude product was recrystallizated with EtOAc to afford 6-(3,5-dimethoxyphenyl)-8-methyl-2-(methylsulfonyl)pyrido[2,3-d]pyrimidin-7(8H)-one (8) (910 mg, yield 78%) as yellow solid. MS (ES+) C17H17N3O5S, requires: 375. found: 376 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340514B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-4ebee1bf44724b07bc8eeaa7909821bd |
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| Source note | uspto-grants-2016_05 |
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