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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040372Generated: October 30, 2026

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

https://huagongshe.com/reaction/1040372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 5-aminopyrazine-2-carboxylateHCID 14536427—
SolventAcetonitrileHCID 6342—
SolventWater ethylacetateHCID 22728543—
ProductMethyl 5-amino-6-bromopyrazine-2-carboxylateHCID 2998331578.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

Add 1.79 g (10.05 mmol) of N-bromosuccinimide to a solution of 1.4 g (9.14 mmol) of methyl 5-aminopyrazine-2-carboxylate in 10 mL of acetonitrile. Stir the reaction mixture for 2 h at 20° C. then distribute in 100 mL of EtOAc/water 1:1 mixture. Wash the organic phase with 2×50 mL of water, dry over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a cyclohexane/EtOAc gradient from 0 to 50% of EtOAc. After concentration under reduced pressure, we obtain 1.66 g of methyl 5-amino-6-bromopyrazine-2-carboxylate in the form of yellow wax.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552201B2
Source datasetuspto-grants-2013_10
ORD IDord-c650f43a3d7c4499b5767d2488d3d667
Source noteuspto-grants-2013_10