Potassium Hydroxide → Fluoroquinolonic acid
Reaction equation
[H-].[Na+].Cl[C:4]1[CH:22]=[C:21]([Cl:23])[C:20]([F:24])=[CH:19][C:5]=1[C:6]([C:8](=[CH:14][NH:15][CH:16]1[CH2:18][CH2:17]1)[C:9]([O:11]CC)=[O:10])=[O:7].[OH-].[K+]>O1CCOCC1.O>[Cl:23][C:21]1[CH:22]=[C:4]2[C:5]([C:6](=[O:7])[C:8]([C:9]([OH:11])=[O:10])=[CH:14][N:15]2[CH:16]2[CH2:18][CH2:17]2)=[CH:19][C:20]=1[F:24]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
3.44 g of 80 percent sodium hydride were added in portions to a solution of 31.9 g of ethyl 2-(2,4-dichloro-5-fluoro-benzoyl)-3-cyclopropylamino-acrylate (R1 =C2H5) in 100 ml of anhydrous dioxane while cooling with ice and stirring. The mixture was then stirred at room temperature for 30 minutes and under reflux for 2 hours, and the dioxane was stripped off in vacuo. The residue (40.3 g) was suspended in 150 ml of water, 6.65 g of caustic potash were added, and the mixture was refluxed for 1.5 hours. The warm solution was filtered and the residue was rinsed with H2O. The filtrate was then acidified to pH=1 to 2 with semiconcentrated hydrochloric acid, while cooling with ice, and the precipitate was filtered off under suction, washed with water and dried in vacuo at 100° C. 27.7 g of 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid (R1 =H) of melting point 234° to 237° C. were obtained in this manner.
Workup
- temperaturewhile cooling with ice
- stirringThe mixture was then stirred at room temperature for 30 minutes
- temperatureunder reflux for 2 hours
- temperaturethe mixture was refluxed for 1.5 hours
- filtrationThe warm solution was filtered
- washthe residue was rinsed with H2O
- temperaturewhile cooling with ice
- filtrationthe precipitate was filtered off under suction
- washwashed with water
- customdried in vacuo at 100° C
Sources & evidence
- ORD record
- ord-c382d00f054146a1b9e6322841f9359e
- Source dataset
- uspto-grants-1986_10
- Patent number
- US04620007
Reaction notes
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