HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-Bromo-4-[(2,4-difluorophenyl)methoxy]-1-[(3-fluorophenyl)methyl]-2(1H)-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Bromomethyl)-2,4-difluorobenzene | HCID 90297 | — |
| Reactant | HCID 54724177 | HCID 54724177 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Bromo-4-[(2,4-difluorophenyl)methoxy]-1-[(3-fluorophenyl)methyl]-2(1H)-pyridinone | HCID 10216550 | — |
Reaction Steps
To a solution of 3-bromo-1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one (0.20 g, 0.67) and K2CO3 (0.27 g, 1.34 mmol) in acetone (10 mL) was added 2,4-difluorobenzyl bromide (0.16 g, 0.8 mmol), and the reaction mixture was heated at reflux for 1 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with water and then brine, dried (Na2SO4), filtered and concentrated under reduced pressure. 1H NMR (300 MHz, CDCl3) δ 7.65-7.55 (m, 1H), 7.40-7.25 (m, 2H), 7.15-6.80 (m, 5H), 6.14 (d, J=8 Hz, 1H), 5.22 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 424.0159 (M+H C19H14BrF3NO2 requires 424.0155).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07629363B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-f04d79d86b5d48a681153b214a703a34 |
| Source note | uspto-grants-2009_12 |