HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-acetyl-3-(dimethylamino)acrylate → Ethyl-2-(4-fluorophenyl)-4-methylpyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-acetyl-3-(dimethylamino)acrylate | HCID 3806790 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-Fluorobenzamidine Hydrochloride | HCID 12456160 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl-2-(4-fluorophenyl)-4-methylpyrimidine-5-carboxylate | HCID 69279303 | 88.5% |
Reaction Steps
4-Fluorobenzamidine hydrochloride (1.25 g, 7.16 mmol) is added to a solution of sodium metal (0.17 g, 7.39 mmol) in dry ethanol (25 mL) and stirred at room temperature for 20 min. Ethyl-2-acetyl-3-(dimethylamino)acrylate (1.35 g, 7.16 mmol) is added. The mixture is heated to reflux for 3 hours. The solvent is removed in vacuo. The residue is dissolved in EtOAc, washed with water and brine, dried (MgSO4), filtered and concentrated in vacuo to afford ethyl-2-(4-fluorophenyl)-4-methyl-pyrimidine-5-carboxylate (1.65 g, 87%) as a solid. MS: 261 (M+H) 261.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202863B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-49464ad095e64e3e876387f003083b10 |
| Source note | uspto-grants-2012_06 |