HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093915Generated: November 3, 2026
HCID 57998845, compound → HCID 57998831, compound
https://huagongshe.com/reaction/1093915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57998845 | HCID 57998845 | — |
| Reactant | HCID 178476545 | HCID 178476545 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57998831 | HCID 57998831 | 27.1% |
Reaction Steps
A mixture of 3,4-dichlorophenyl lead triacetate (1.63 g), 8-hydroxy-5H-pyrido[2,3-b]pyrazin-6-one (0.254 g) and 4-dimethylaminopyridine (DMAP) (0.549 g) in anhydrous dimethylsulfoxide (10 mL) under a nitrogen atmosphere was heated to 60° C. for four hours. The reaction mixture was then allowed to cool to ambient temperature and stored at ambient temperature for 16 hours. The reaction mixture was diluted with ethyl acetate. The mixture was washed with aqueous hydrochloric acid (1M) and water, and the organic layer concentrated to give 7-(3,4-dichlorophenyl)-8-hydroxy-5H-pyrido[2,3-b]pyrazin-6-one (0.13 g) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133847B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-5673cfd98060475f86e65a3df3657e09 |
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| Source note | uspto-grants-2012_03 |
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