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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771852Generated: November 2, 2026

N-bromobutanimide → 2-Amino-5-bromo-3-fluoropyridine

https://huagongshe.com/reaction/1771852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Amino-3-fluoropyridineHCID 2762809—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-Amino-5-bromo-3-fluoropyridineHCID 50851130—

Reaction Steps

To a solution of 2-amino-3-fluoro-pyridine (9.4 g, 83.1 mmol, 1 eq.) in MeCN (470 mL) under argon at 0° C. was added NBS (7.4 g, 41.5 mmol, 0.5 eq.). The reaction mixture was stirred at r.t. for 1 h then cooled to 0° C. before introducing additional NBS (7.39 g, 41.5 mmol, 0.5 eq.). The reaction mixture was stirred at r.t. for 1 h then diluted in EtOAc. The organic layer was washed with a saturated NaHCO3 solution, dried over Na2SO4, filtered and concentrated in vacuo. The residue was diluted in DCM, washed with a 1 N NaOH solution. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo to afford Intermediate Gen-1-a (2-amino-5-bromo-3-fluoropyridine).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249141B2
Source datasetuspto-grants-2016_02
ORD IDord-7179f0dbda3b48288998cb91d7f09781
Source noteuspto-grants-2016_02