HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377293Generated: October 29, 2026
HCID 11103220, compound → HCID 502078, compound
https://huagongshe.com/reaction/377293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11103220 | HCID 11103220 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 502078 | HCID 502078 | 71.7% |
Reaction Steps
In 14 ml of acetic acid and 140 mg of 5% palladium-carbon was suspended 140 mg of 7-[2-(benzyl-oxycarbonyl)isoindolin-5-yl]-1-cyclopropyl-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, and the suspension was stirred at room temperature for 2 hours under a hydrogen atomsphere. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Ethanol and diethyl ether were added to the resulting residue and the crystals were collected by filtration. To the crystals collected were added 0.8 ml of ethanol, 0.8 ml of a 1N aqueous sodium hydroxide solution and 0.8 ml of water to dissolve the crystals, after which carbon dioxide was bubbled into the resulting solution and the crystals were collected by filtration to obtain 74 mg of colorless 1-cyclopropyl-7-(isoindolin-5-yl)-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06025370 |
|---|
| Source dataset | uspto-grants-2000_02 |
|---|
| ORD ID | ord-87b2aa7b89df4e44b5566933059c80ca |
|---|
| Source note | uspto-grants-2000_02 |
|---|