Hydrochloric Acid → HCID 70285340, compound
Reaction equation
[F:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[N:8]1[C:17]2[C:12](=[CH:13][C:14]([F:27])=[C:15]([N:18]3[CH2:22][CH2:21][CH:20]([NH:23]C(=O)C)[CH2:19]3)[CH:16]=2)[C:11](=[O:28])[C:10]([C:29]([OH:31])=[O:30])=[CH:9]1.C(O)C.[ClH:35]>O>[ClH:35].[F:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[N:8]1[C:17]2[C:12](=[CH:13][C:14]([F:27])=[C:15]([N:18]3[CH2:22][CH2:21][CH:20]([NH2:23])[CH2:19]3)[CH:16]=2)[C:11](=[O:28])[C:10]([C:29]([OH:31])=[O:30])=[CH:9]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
0.5 g of 1-(3-fluoro-4-pyridyl)-6-fluoro-7-(3-acetamido-1-pyrrolidyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid is added to 15 ml of ethanol, 10 ml of water and 5 ml of conc. hydrochloric acid. The reaction mixture is refluxed for 18 hours, cooled and concentrated under a reduced pressure to remove the solvent completely.
Workup
- temperatureThe reaction mixture is refluxed for 18 hours
- temperaturecooled
- concentrationconcentrated under a reduced pressure
- customto remove the solvent completely
Sources & evidence
- ORD record
- ord-2bf61209620b4f199d961388e48e93b2
- Source dataset
- uspto-grants-1996_03
- Patent number
- US05496947
Reaction notes
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