HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-2-methyl-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 1-(Bromomethyl)-2,4-difluorobenzene | HCID 90297 | — |
| Reactant | 3-(4-hydroxy-2-methyl-6-oxo-6H-pyrimidin-1-yl)-4-methyl-benzoic acid methyl ester | HCID 136387805 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-2-methyl-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoate | HCID 21089018 | 36% |
Reaction Steps
To a solution of Intermediate 2 (500 mg, 1.82 mmol) in N,N-dimethylformamide (2 mL) was added 2,4-difluorobenzyl bromide (0.23 mL, 1.82 mmol), potassium carbonate (376 mg, 2.73 mmol) and 18-crown-6 (40 mg). The slurry was stirred at ambient temperature for one hour. The reaction was partitioned between ethyl acetate and water. The organic layer was washed with water and brine and dried over magnesium sulfate. The slurry was filtered and concentrated in vacuo. The crude material was purified using normal phase chromatography (ethyl acetate/heptane) to provide the alkylated product as a white semi-solid (260 mg, 36% yield). MS (M+H): 401
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056110B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-293d797cccb14002b479f1e58fb0c840 |
| Source note | uspto-grants-2015_06 |