HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14096377, compound → 5-Amino-1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14096377 | HCID 14096377 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | N,N-dimethylformamide ethanol | HCID 19794673 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | 5-Amino-1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 10566894 | 62.3% |
Reaction Steps
To a solution of 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-5-nitro-4-oxo-3-quinolinecarboxylic acid (322 mg) in ethanol-DMF (4:1) was added 10% palladium-carbon (25 mg) and the mixture was stirred in hydrogen gas atomosphere for 6 hours at room temperature. The catalyst was filtered off and washed with a solution of chloroform-methanol-concentrated aqueous ammonia (10:10:3). The filtrate and washings were combined and concentrated. The residue was recrystallized from a solution of chloroform-methanol-concentrated aqueous ammonia (20:6:1) to give the title compound (183 mg) as yellow prisms, mp 291°-291.5° C. (decompd.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980470 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-a316201c238e42468acfdcc363c0b13b |
| Source note | uspto-grants-1990_12 |