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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398388Generated: October 30, 2026

Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate → 3-(2-Ethylpyrid-3-ylamino)-6-methyl-1-(ethoxycarbonylmethyl)pyrazinone

https://huagongshe.com/reaction/398388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetateHCID 1514288—
Reactant2-Ethylpyridin-3-amineHCID 21881800—
SolventNitrobenzeneHCID 7416—
Product3-(2-Ethylpyrid-3-ylamino)-6-methyl-1-(ethoxycarbonylmethyl)pyrazinoneHCID 23000164—

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 2-ethyl-3-aminopyridine (0.35 g, 2.8 mMol, 2 eq) from step 2 above and 3-bromo-6-methyl-1-(ethoxycarbonylmethyl)pyrazinone (0.39 g, 1.4 mMol) in 1 mL of nitrobenzene was heated at 200 ° C. for 2 h. The reaction was concentrated in vacuo and the residue purified by flash silica gel chromatography using 1% methanol in methylene chloride as an eluent to afford the title compound as a yellow oil that crystallizes upon sitting. (0.058 g; HPLC RT=4.45 min, method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610692B1
Source datasetuspto-grants-2003_08
ORD IDord-23a1c050591b4dd991041f4cac13ed91
Source noteuspto-grants-2003_08