HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Amino-3-bromo-5-fluoropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Amino-5-fluoropyridine | HCID 2737701 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Amino-3-bromo-5-fluoropyridine | HCID 16126434 | 48.4% |
Reaction Steps
NBS (10 g, 56.2 mmol) was added slowly to a solution of 5-fluoro-pyridin-2-ylamine (55) (12.4 g, 56.2 mmol) in MeCN (200 mL). The reaction mixture was stirred at RT overnight. After completion, the solution was filtered and the filtrate was concentrated to obtain a residue, which was purified by silica gel chromatography (10% to 20% EtOAc in petroleum ether) to give 3-bromo-5-fluoro-pyridin-2-ylamine (56) (5.2 g, 27.2 mmol, 31% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957073B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-807b54899cbe43579f903a4d5acd56b3 |
| Source note | uspto-grants-2015_02 |