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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595881Generated: November 1, 2026

N-bromobutanimide → 2-(5-Amino-6-bromopyrazin-2-yl)ethanol

https://huagongshe.com/reaction/595881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(5-Aminopyrazin-2-yl)ethanolHCID 118045507—
SolventAcetonitrileHCID 6342—
Product2-(5-Amino-6-bromopyrazin-2-yl)ethanolHCID 118046118—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(5-aminopyrazin-2-yl)ethanol (30 mg, 0.216 mmol) in CH3CN (719 μL) was added NBS (38.4 mg, 0.216 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 30 min. The reaction mixture was quenched by sat. NaHCO3, then extracted by EtOAc, The combined organic layer was washed with water and brine, dried over anhydrous sodium sulfate. Filtered and concentrated in vacuo yielding crude 2-(5-amino-6-bromopyrazin-2-yl)ethanol which was used in next step reaction without purification. LCMS (m/z): 218.0/220.0 (MH+), 0.33 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-8a4574e641db47e891c13ebf93686b17
Source noteuspto-grants-2016_01