HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-bromo-N-ethyl-N-methylpyrimidine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | 5-Bromopyrimidine-2-carbonyl chloride | HCID 59674657 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-bromo-N-ethyl-N-methylpyrimidine-2-carboxamide | HCID 59483315 | — |
Reaction Steps
5-Bromo-pyrimidine-2-carbonyl chloride (1600 mg, 7.225 mmol) was dissolved in dichloromethane (25 ml) and triethylamine (4.03 ml, 28.9 mmol) was added followed by ethyl-methyl-amine (0.68 mL, 7.92 mmol). The reaction was stirred at room temperature under nitrogen for 16 ours, after which time, LCMS indicated completion. The mixture was diluted with dichloromethane (50 ml) and washed with water (50 ml) followed by 10% citric acid (50 ml) and brine (50 ml). The organic layer was separated and dried over MgSO4, the residue was filtered and the solvent was removed in vacuo to afford the title compound 5-bromo-N-ethyl-N-methylpyrimidine-2-carboxamide (SM-3): (1.4 g, 79.4%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735396B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-0c14297aed774874a82f544e3ae66413 |
| Source note | uspto-grants-2014_05 |