HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229645Generated: October 29, 2026
Triethylamine → 3-(2-pyridyl)-5-phenyl-2(1H)-pyridone
https://huagongshe.com/reaction/229645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 3-(2-Pyridyl)-5-bromo-2-methoxypyridine | HCID 22318954 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2-pyridyl)-5-phenyl-2(1H)-pyridone | HCID 22319253 | 53.4% |
Reaction Steps
A mixture of 1.0 g of 3-(2-pyridyl)-5-bromo-2-methoxypyridine, 0.9 g of phenylboronic acid, 0.3 g of dichlorobistriphenylphosphine palladium and 2 ml of triethylamine was stirred at 120° C. for 1.5 hours in 30 ml of xylene in nitrogen atomosphere. The mixture was returned to room temperature, diluted with ethyl acetate, washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was incorporated with 47% hydrobromic acid and heated at 70° C. for 1 hour. The reaction solution was ice-cooled, diluted with water, and neutralized with potassium carbonate. The resulting precipitates were collected by filtration, washed with water and ether, and then air-dried, to give 0.5 g of the title compound as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07563811B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-f6c1762f7b4f42e6a3f95e62ee3d46b8 |
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| Source note | uspto-grants-2009_07 |
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