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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599419Generated: November 4, 2026

1-(4,5-Dichloro-1-imidazolyl)methyl-2-ethoxycarbonyl-7-trifluoromethylimidazo[1,2-a]quinoxalin-4(5H)-one → 2-Carboxy-1-(4,5-dichloro-1-imidazolyl)methyl-7-trifluoromethylimidazo[1,2-a]quinoxalin-4(5H)-one

https://huagongshe.com/reaction/1599419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4,5-Dichloro-1-imidazolyl)methyl-2-ethoxycarbonyl-7-trifluoromethylimidazo[1,2-a]quinoxalin-4(5H)-oneHCID 18928126—
SolventHydrogen BromideHCID 260—
Product2-Carboxy-1-(4,5-dichloro-1-imidazolyl)methyl-7-trifluoromethylimidazo[1,2-a]quinoxalin-4(5H)-oneHCID 18928131—

Reaction Steps

A suspendion of 1-(4,5-dichloro-1-imidazolyl)methyl-2-ethoxycarbonyl-7trifluoromethylimidazo[1,2-a]quinoxalin-4(5H)-one (Example 9) (120 mg, 0.25 mmol) in hydrobromic acid (48% in water) (10 ml) was stirred at 80° C. for 6 h. The mixture was concentrated in vacuo and the residue added acetone. The title compound was isolated by filtration to yield 80 mg (61%) as a hydrobromic salt. M.p. 213°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05741785
Source datasetuspto-grants-1998_04
ORD IDord-91f0e3032ff3418b814d935c055775d4
Source noteuspto-grants-1998_04