HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218506Generated: October 30, 2026
3-Methoxy-2-pyridone → HCID 59586725, compound
https://huagongshe.com/reaction/218506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxy-2-pyridone | HCID 88731 | — |
| Reactant | 2-(Difluoromethoxy)-1-fluoro-4-nitro-benzene | HCID 20131434 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59586725 | HCID 59586725 | — |
Reaction Steps
302 mg (2.41 mmol) of 3-methoxypyridone are dissolved in 8.2 ml of anhydrous dimethyl sulfoxide and admixed with 325 mg (2.89 mmol) of potassium tert-butoxide. After 30 min, 500 mg (2.41 mmol) of 2-(difluoromethoxy)-1-fluoro-4-nitrobenzene are added and the mixture is heated to 80° C. for 20 h. The reaction solution is diluted with dichloromethane and washed with water and 1N hydrochloric acid. After the organic phase has been dried over sodium sulfate, it is filtered and concentrated to dryness under reduced pressure. The residue is dissolved in dimethyl sulfoxide and purified by preparative HPLC with a water/acetonitrile gradient. The product fractions are combined and concentrated to dryness under reduced pressure. This affords 207 mg (28% of theory) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198267B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-613ac57eb69c41b59e8642ec5330dd1f |
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| Source note | uspto-grants-2012_06 |
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