HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576753Generated: October 30, 2026
Sodium Carbonate → HCID 86723867, compound
https://huagongshe.com/reaction/576753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Reactant | 2-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine | HCID 12067061 | — |
| Reactant | HCID 90197008 | HCID 90197008 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 86723867 | HCID 86723867 | 20.9% |
Reaction Steps
5-Iodo-3-isopropyl-6-methyl-1-(3-trifluoromethylphenyl)pyrimidin-2,4(1H,3H)-dione (prepared in Reference Example 85) (600 mg) and 2-bromo-3-pyridine boronic acid pinacol ester (878 mg) were dissolved in 1,2-dimethoxyethane (30 ml). Thereto were added under nitrogen atmosphere water (6 ml), sodium carbonate (290 mg), 2-(dicyclohexylphosphino)biphenyl (57.6 mg) and tetrakis(triphenylphosphine)palladium (316 mg) and the resulting mixture was stirred with heating under reflux for four and a half hours. The reaction solution was concentrated under reduced pressure and to the residue was added water, and the resulting mixture was extracted with ethyl acetate (50 ml). The organic layer was washed with saturated saline (50 ml), dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford 5-(2-bromopyridin-3-yl)-3-isopropyl-6-methyl-1-(3-(trifluoromethyl)phenyl)pyrimidin-2,4(1H,3H)-dione (134 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040516B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-a3ef9d94cb2e4c5a89fb053494a3ad3e |
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| Source note | uspto-grants-2015_05 |
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