HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214409Generated: October 30, 2026
Potassium Carbonate → HCID 21933544, compound
https://huagongshe.com/reaction/2214409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene | HCID 12115509 | — |
| Reactant | HCID 21933570 | HCID 21933570 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21933544 | HCID 21933544 | 85.4% |
Reaction Steps
To a mixture of 0.26 g of 3-hydroxy-2-(methoxycarbonyl)methylthiopyridine, 0.38 g of 2,5-difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene, and 2 ml of N,N-dimethylformamide was added 0.17 g of potassium carbonate, and the mixture was stirred at 70° C. for 2 hours. The reaction mixture was cooled to room temperature and then poured into ice water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.49 g of 3-{4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]-2-nitrophenoxy}-2-(methoxycarbonyl)methylthiopyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109148B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-1232ec3cc93b4941ad5b1c3c5dd21e6e |
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| Source note | uspto-grants-2006_09 |
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