HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043174Generated: October 26, 2026
N-bromobutanimide → Methyl 2-(6-amino-5-bromopyridin-3-yloxy)-4-fluorobenzoate
https://huagongshe.com/reaction/1043174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-(6-aminopyridin-3-yloxy)-4-fluorobenzoate | HCID 67226188 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(6-amino-5-bromopyridin-3-yloxy)-4-fluorobenzoate | HCID 67226738 | — |
Reaction Steps
A mixture of EXAMPLE 318B (1.6 g) in N,N-dimethylformamide (50 mL) was cooled to 0° C., followed by the addition of N-bromosuccinimide (1.195 g) in N,N-dimethylformamide (10 mL) solution. The reaction mixture was stirred at 0° C. for 1 hour, and quenched with ice-cold saturated NaHCO3 aqueous solution. The reaction mixture was extracted with ethyl acetate. The combined organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude material was purified using flash column purification with 30-40% ethyl acetate/hexane to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08557983B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-b8e07de85a7f46c0a93517d3e87ed05b |
|---|
| Source note | uspto-grants-2013_10 |
|---|