Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 23284805 | HCID 23284805 | — |
| Product | HCID 23284665 | HCID 23284665 | — |
Reaction Steps
5-Amino-1-(5-amino-2,4-difluorophenyl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (100 mg) and a methylamine solution (82 mg) were added to pyridine (1 ml), and the mixture was heated and stirred at 30° C. for 4 days. After the reaction mixture was allowed to cool, it was concentrated under reduced pressure. Ethanol was added to the residue, and solids were collected by filtration and washed with diethyl ether to obtain the title compound (63 mg) as a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06136823 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-5a5bd4864aac42f687b98d38db1ca459 |
|---|
| Source note | uspto-grants-2000_10 |
|---|