HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Bromosuccinamide → 3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Reactant | 3-(benzyloxy)-1-(biphenyl-3-yl)pyridin-4(1H)-one | HCID 67418143 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-one | HCID 67420197 | — |
Reaction Steps
To a solution of 3-(benzyloxy)-1-(biphenyl-3-yl)pyridin-4(1H)-one (2.41 g, 6.8 mmol) in AcOH (68 mL) was added N-bromosuccinamide (2.67 g, 15 mmol) and the reaction mixture was stirred at room temperature. After 1 h, the mixture was concentrated under reduced pressure and purified by flash chromatography (80 g SiO2, 0-100% ethyl acetate/hexanes) to provide 3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-one. LC/MS (M+H)+ 432/434.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09024032B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-fb7072b6dfc2433f8f16a82eba73b744 |
| Source note | uspto-grants-2015_05 |