HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-(2-Cyanophenyl)-5-(alpha-hydroxy-2-picolyl)-1-phenyl-1,2-dihydropyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(2-Cyanophenyl)-5-(2-pyridinecarbonyl)-1-phenyl-1,2-dihydropyridin-2-one | HCID 22319092 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 3-(2-Cyanophenyl)-5-(alpha-hydroxy-2-picolyl)-1-phenyl-1,2-dihydropyridin-2-one | HCID 86591046 | — |
Reaction Steps
To a solution of 25 mg of 3-(2-cyanophenyl)-5-(2-pyridinecarbonyl)-1-phenyl-1,2-dihydropyridin-2-one in 5 ml of methanol was added 2 mg of sodium borohydride under ice-cooling. After 30 minutes, the mixture was diluted with a saturated aqueous solution of sodium hydrogen carbonate, followed by extracting with ethyl acetate. The ethyl acetate layer 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), to give 15 mg of the title compound as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939549B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-82a33880e1b74a19850f735a7ce6f719 |
| Source note | uspto-grants-2011_05 |