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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72738Generated: October 27, 2026

Water → 8-Acetyl-1-cyclohexylimidazo[1,5-a]quinoxalin-4(5H)-one

https://huagongshe.com/reaction/72738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Cyclohexyl-N,O-dimethyl-4-oxo-4,5-dihydroimidazo[1,5-a]-quinoxaline-8-hydroxamic acidHCID 59198710—
ReactantHCID 178420675HCID 178420675—
SolventTetrahydrofuranHCID 8028—
Product8-Acetyl-1-cyclohexylimidazo[1,5-a]quinoxalin-4(5H)-oneHCID 59198808—

Reaction Steps

To a suspension of 354 mg of 1-cyclohexyl-N,O-dimethyl-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxaline-8-hydroxamic acid as synthesized in above Example 142 in 10 mL of tetrahydrofuran, 1.33 mL of 3M methylmagnesium bromide/tetrahydrofuran solution was added, followed by 3.7 hours' stirring under nitrogen atmosphere and addition of 30 mL of water. The organic layer extracted with ethyl acetate-tetrahydrofuran mixed solvent was washed with water, dried over magnesium sulfate and the solvent therein was distilled off. The crude product was heat-suspended in 10 mL of methanol and purified, to provide 106 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829000B2
Source datasetuspto-grants-2014_09
ORD IDord-0401822033ca4079a7c084434999e5dc
Source noteuspto-grants-2014_09