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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192914Generated: November 1, 2026

Water → Methyl 5-(((allyloxy)carbonyl)amino)pyrazine-2-carboxylate

https://huagongshe.com/reaction/2192914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantAllyl chloroformateHCID 18052—
ReactantMethyl 5-aminopyrazine-2-carboxylateHCID 14536427—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(((allyloxy)carbonyl)amino)pyrazine-2-carboxylateHCID 59570895—

Reaction Steps

To a solution of methyl 5-aminopyrazine-2-carboxylate (2 g) in dichloromethane (20 mL) were added pyridine (36.4 mL) and allyl chloroformate (25.2 mL) in 4 divided portions respectively, under ice-cooling, followed by stirring at room temperature overnight. To the reaction mixture was added water under ice-cooling, followed by extraction with ethyl acetate. The organic layer was sequentially washed with 1 M hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated brine. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The obtained solid was collected by filtration while washing with a solvent (hexane:ethyl acetate=3:1) to obtain methyl 5-{[(allyloxy)carbonyl]amino}pyrazine-2-carboxylate (481 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329707B2
Source datasetuspto-grants-2012_12
ORD IDord-5f0e2b42efed48c28445b77afe091370
Source noteuspto-grants-2012_12