HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13146122, compound → HCID 13146123, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13146122 | HCID 13146122 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13146123 | HCID 13146123 | — |
Reaction Steps
A mixture of 1-ethyl-6,8-difluoro-1,4-dihydro-7-[4-(p-nitrobenzyl)-1-piperazinyl]-4-oxoquinoline-3-carboxylic acid (6.0 g), acetic acid (150 ml), and 5% palladium on charcoal (1.0 g) was hydrogenated. The slurry was filtered and the filtrate concentrated to dryness. The residue was treated with water, neutralized with aqueous sodium hydroxide solution and extracted with dichloromethane. The organic layer was dried and evaporated. The residue was chromatographed on silica gel. Elution with a mixture of chloroform and ethanol (20:1) and recrystallization from a mixture of chloroform and ethanol gave 7-[4-(p-aminobenzyl)-1-piperazinyl]-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04429127 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-b854a8968e544a2f9bc1316fe77be1e6 |
| Source note | uspto-grants-1984_01 |