Potassium Hydroxide → Brequinar
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=O.[CH3:13][CH2:14][C:15]([C:17]1[CH:22]=[CH:21][C:20]([C:23]2[C:28]([F:29])=[CH:27][CH:26]=[CH:25][CH:24]=2)=[CH:19][CH:18]=1)=O.[OH-:30].[K+]>C(O)C.O>[F:29][C:28]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:20]1[CH:21]=[CH:22][C:17]([C:15]2[C:14]([CH3:13])=[C:5]([C:6]([OH:11])=[O:30])[C:4]3[C:8](=[CH:9][CH:10]=[C:2]([F:1])[CH:3]=3)[N:7]=2)=[CH:18][CH:19]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
5-Fluoroisatin (72.6 g, 0.44 mole) and 4-(2-fluorophenyl)propiophenone (100 g, 0.44 mole) were suspended in 720 ml of ethanol and stirred mechanically as a solution of KOH (147.8 g, 2.64 mole) in 300 ml of water was added dropwise over 15 minutes. The reaction mixture was heated at reflux for 12 hours, cooled and the ethanol evaporated under reduced pressure. The resulting solid was dissolved in water and washed with ethyl ether. The aqueous layer was cooled to 5° and acidified with glacial acetic acid. The resulting precipitate was filtered, washed 2 times with 300 ml of ethyl ether and dried. Recrystallization from dimethylformamide and water gave 84 g of a white 2-(2'-Fluoro-1,1'-biphenyl-4-yl)-6-fluoro-3-methyl-4-quinolinecarboxylic acid, m.p. 315°-317°.
Workup
- additionwas added dropwise over 15 minutes
- temperatureThe reaction mixture was heated
- temperatureat reflux for 12 hours
- temperaturecooled
- customthe ethanol evaporated under reduced pressure
- dissolutionThe resulting solid was dissolved in water
- washwashed with ethyl ether
- temperatureThe aqueous layer was cooled to 5°
- filtrationThe resulting precipitate was filtered
- washwashed 2 times with 300 ml of ethyl ether
- customdried
- customRecrystallization from dimethylformamide and water
Sources & evidence
- ORD record
- ord-cef2614ef3ad49798825c253130c48bb
- Source dataset
- uspto-grants-1987_07
- Patent number
- US04680299
Reaction notes
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