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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456055Generated: November 3, 2026

1,1'-Carbonyldiimidazole → 2-Methyl-N-[4-(pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]benzamide

https://huagongshe.com/reaction/1456055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
Reactant4,5-Dihydropyrrolo[1,2-a]quinoxalineHCID 11805181—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-N-[4-(pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]benzamideHCID 15340668—

Reaction Steps

A mixture of 0.51 g of, 4-[(2-methylbenzoyl)-amino]benzoyl chloride and 0.36 g of 1,1'-carbonyldiimidazole in 6 ml of tetrahydrofuran is stirred at room temperature for 1 hour. To the reaction mixture is added 0.17 g of 4,5-dihydropyrrolo-[1,2-a]-quinoxaline followed by heating at reflux for 60 hours. The volatiles are concentrated in vacuo to a residue which is dissolved in ethyl acetate. The organic layer is washed with 1N HCl, 1M NaHCO3, brine, dried with Na2SO4 and filtered through hydrous magnesium silicate. The volatiles are concentrated in vacuo to a residue which is chromatographed by elution with 1:2 ethyl acetate-hexanes to give 0.14 g of the desired product as a white solid, m.p. 206°-2070° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843944
Source datasetuspto-grants-1998_12
ORD IDord-aad48d5bd6df4783a580bd7ec94c4f6f
Source noteuspto-grants-1998_12