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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351324Generated: November 2, 2026

Acetic Acid → Ethyl 4,5-dihydro-5-methyl-4-oxo-imidazo(1,5-a)pyrido(2,3-e)pyrazine-3-carboxylate

https://huagongshe.com/reaction/2351324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethyl chlorophosphateHCID 13139—
ReactantEthyl isocyanoacetateHCID 533707—
Reactant4-Methyl-1,4-dihydropyrido[2,3-b]pyrazine-2,3-dioneHCID 13192942—
SolventDimethylformamideHCID 6228—
ProductEthyl 4,5-dihydro-5-methyl-4-oxo-imidazo(1,5-a)pyrido(2,3-e)pyrazine-3-carboxylateHCID 14460551—

Reaction Steps

To a stirred solution of 1,2,3,4-tetrahydro-4-methyl-2,3-dioxo-pyrido(2,3-b)-pyrazine (5g) in 50 ml of dry dimethyl formamide (DMF) was added potassium-t-butylate (4 g). The mixture was allowed to stir at room temperature for 15 min whereafter it was cooled to -25° C. and charged with diethyl chlorophosphate (5ml). Stirring continued at 0° C. for 15 min, then it was cooled to -20° C. whereafter a preformed -30° C. cold solution of ethyl isocyanoacetate (3.9ml) and pottasium-t-butylate (4 g) in 30ml of dry DMF was added. The resulting solution was allowed to obtain room temperature before acetic acid was added (1,5 ml). The DMF was removed by evaporation in vacuo, whereafter the residue was treated with water to give the crude title compound as pale crystals. Recryst in 96% ETOH M.p. 233°-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873244
Source datasetuspto-grants-1989_10
ORD IDord-6c1095962aec4a8786f3d0036df5a095
Source noteuspto-grants-1989_10