HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 5-Bromo-N,N-dimethylpyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Bromonicotinoyl chloride | HCID 2781223 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Bromo-N,N-dimethylpyridine-3-carboxamide | HCID 23437049 | 89% |
Reaction Steps
Into a 100 mL round bottomed flask were added 5-bromonicotinoyl chloride (0.531 g, 2.41 mmol) and anhydrous pyridine (5 mL). A 2M solution of dimethylamine in THF (5 mL, 10.0 mmol) was added dropwise, and the reaction mixture was stirred at rt under N2 for 6 h after which it was concentrated under vacuum. The crude residue was partitioned between EtOAc and water. The layers were separated, and the organic phase was washed 3× with water, then treated with brine, dried (Na2SO4), filtered and concentrated to afford 5-Bromo-N,N-dimethyl-nicotinamide as a brown oil (0.4951 g, 89%). MS: m/z 229/231 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709645B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-cf7c964f65424371ab1c309676986125 |
| Source note | uspto-grants-2010_05 |