HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoroaniline → 2-bromonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | 6-Bromonicotinic acid | HCID 238932 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-bromonicotinamide | HCID 817161 | — |
Reaction Steps
6-Bromonicotinic acid (5.28 g, 26 mmol) and 4-fluoroaniline (2.90 g, 26 mmol) was dissolved in anhydrous DMF (30 mL). EEDQ was added, and the reaction was allowed to progress overnight at room temperature. The solvent was removed by rotary evaporation, and the crude material was dissolved in hot EtOAc (50 mL). Upon cooling, the product crystallized from the solution. The product was filtered, washed with cold EtOAc to yield 3.29 g (43%) as a white solid. ESI-MS m/z=294.9, 296.8 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981106B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-545ea378a88a45f7be48a088cb7b3f9c |
| Source note | uspto-grants-2015_03 |