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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414859Generated: November 1, 2026

Acetic Acid → 5-Methyl-4-oxo-4lambda~5~-pyrazine-2-carboxamide

https://huagongshe.com/reaction/1414859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant5-methylpyrazine-2-carboxamideHCID 2760054—
SolventHydrogen PeroxideHCID 784—
Product5-Methyl-4-oxo-4lambda~5~-pyrazine-2-carboxamideHCID 12571044—

Reaction Conditions

Temperature70 °C

Reaction Steps

2-Carboxy-5-methylpyrazine (9.7 g) in dry dioxan (114 ml) and tributylamine (17.7 ml) was treated with ethyl chloroformate (7.5 ml), keeping the temperature at 0°-5° C. After ten minutes, dioxan (190 ml) saturated with ammonia was added. The mixture was stirred for 3 hours at room temperature, then dioxan was distilled off, and the residue was taken up in saturated aqueous sodium bicarbonate (20 ml). The mixture was filtered and the product washed with water to give 2-carbamoyl-5-methylpyrazine (9.2 g), m.p. 204°- 206° C. This amide (7 g) in glacial acetic acid (30 ml) and 35% hydrogen peroxide (20 ml.) was heated with stirring at 70° C for 7 hours. The reaction mixture was cooled, the product which separated was filtered and washed with water to give 2-carbamoyl-5-methylpyrazine 4-oxide (5.5 g), m.p. 206°- 208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04002750
Source datasetuspto-grants-1977_01
ORD IDord-c9610651d45d4b0e9a3184ef052ec71a
Source noteuspto-grants-1977_01