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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040371Generated: November 1, 2026

Boron trifluoride etherate → Methyl 5-aminopyrazine-2-carboxylate

https://huagongshe.com/reaction/1040371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Aminopyrazine-2-carbonitrileHCID 13925294—
SolventMethanolHCID 887—
ProductMethyl 5-aminopyrazine-2-carboxylateHCID 1453642749%

Reaction Steps

Reflux a solution of 2.24 g (18.65 mmol) of 5-aminopyrazine-2-carbonitrile and 9.45 mL (74.40 mmol) of boron trifluoride etherate in 50 mL of methanol for 2 h. Concentrate the reaction mixture under reduced pressure and take up the residue obtained in 200 mL of EtOAc and 10 mL of a saturated aqueous solution of NaHCO3. Dry the organic phase over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a cyclohexane/EtOAc 1:1 mixture. After concentration under reduced pressure, we obtain 1.4 g of methyl 5-aminopyrazine-2-carboxylate in the form of oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552201B2
Source datasetuspto-grants-2013_10
ORD IDord-ac94c59b721c4e578cdf1797aa3cb712
Source noteuspto-grants-2013_10