Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596123Generated: October 28, 2026

N-bromobutanimide → Ethyl 5-amino-6-bromopyrazine-2-carboxylate

https://huagongshe.com/reaction/596123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 5-Aminopyrazine-2-carboxylateHCID 22271413—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-amino-6-bromopyrazine-2-carboxylateHCID 11804526978%

Reaction Steps

To a solution of ethyl 5-aminopyrazine-2-carboxylate (880 mg, 5.26 mmol) in acetonitrile (20 mL) at RT was added NBS (984 mg, 5.53 mmol), the resultant solution was stirred at RT for 1 hour. The reaction mixture was diluted with EtOAc, washed with sat NaHCO3, brine and water, dried, filtered, and concentrated to afford the crude product, which was purified by ISCO 24 g silica gel column, 0 to 50% EtOAc in Heptane, 30 min). 1.01 g, 78% yield. LC-MS (m/z): 247.9 (MH+), 0.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-4d15e50efdc24c098cb0aeb7d6f0b9fa
Source noteuspto-grants-2016_01