HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 8-Acetyl-1-cyclohexylimidazo[1,5-a]quinoxalin-4(5H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Cyclohexyl-N,O-dimethyl-4-oxo-4,5-dihydroimidazo[1,5-a]-quinoxaline-8-hydroxamic acid | HCID 59198710 | — |
| Reactant | HCID 178420675 | HCID 178420675 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Acetyl-1-cyclohexylimidazo[1,5-a]quinoxalin-4(5H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829000B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-0401822033ca4079a7c084434999e5dc |
| Source note | uspto-grants-2014_09 |