HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229705Generated: October 28, 2026
Dimethylformamide → 3-(2-Cyanophenyl)-5-(2-pyridinecarbonyl)-1-phenyl-1,2-dihydropyridin-2-one
https://huagongshe.com/reaction/229705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-(2-Pyridinecarbonyl)-1-phenyl-3-bromo-1,2-dihydropyridin-2-one | HCID 22318928 | — |
| Reactant | 2-(2-Cyanophenyl)-1,3,2-dioxaborinate | HCID 86590373 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2-Cyanophenyl)-5-(2-pyridinecarbonyl)-1-phenyl-1,2-dihydropyridin-2-one | HCID 22319092 | 21.2% |
Reaction Steps
To a mixed liquid of 200 mg of 5-(2-pyridinecarbonyl)-1-phenyl-3-bromo-1,2-dihydropyridin-2-one, 130 mg of 2-(2-cyanophenyl)-1,3,2-dioxaborinate, 400 mg of cesium carbonate and 6 ml of dimethylformamide was added 60 mg of tetrakistriphenylphosphine palladium, followed by stirring at 130° C. for 5 hours in nitrogen atmosphere. After cooling to room temperature, ethyl acetate was added thereto. The extract was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (ethyl acetate/hexane), to give 45 mg 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-0a0db510fbdb44368fa08234588982bf |
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| Source note | uspto-grants-2009_07 |
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