Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-butyl 4-[(4-oxo-2-phenyl-4,5-dihydro-2H-pyrazolo[3,4-c]quinolin-1-yl)acetyl]piperazine-1-carboxylate | HCID 57446245 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66781746 | HCID 66781746 | — |
Reaction Steps
A mixture of tert-butyl 4-[(4-oxo-2-phenyl-4,5-dihydro-2H-pyrazolo[3,4-c]quinolin-1-yl)acetyl]piperazine-1-carboxylate, 4 mL of 6 N aqueous hydrochloric acid, and 12 mL of ethanol was heated at 60° C. for 5 hours. The mixture was allowed to cool to ambient temperature and was concentrated under reduced pressure. The residue was triturated with acetonitrile, isolated by filtration, and dried to afford 1.60 g of 1-(2-oxo-2-piperazin-1-ylethyl)-2-phenyl-2,5-dihydro-4H-pyrazolo[3,4-c]quinolin-4-one; hydrochloride as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08138173B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-12d006ab18454fa7b50d2ef833293080 |
|---|
| Source note | uspto-grants-2012_03 |
|---|