HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-7-dimethylamino-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121165 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-7-dimethylamino-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid | HCID 23284822 | 81% |
Reaction Steps
5-Amino-1-(6-amino-3, 5-difluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (100 mg) and an aqueous solution (about 50%; 170 mg) of dimethylamine were added to pyridine (500 mg), and the mixture was stirred at room temperature for 4 days. The reaction mixture was concentrated under reduced pressure, and ethanol (1 ml) was added to the residue. Deposits were collected by filtration and washed with ethanol and diisopropyl ether in that order to obtain the title compound (86 mg) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136823 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-e2ed9ef0e03546638a9f60d060aa2472 |
| Source note | uspto-grants-2000_10 |