HCID 178469125, compound → 4-Hydroxy-2-(trifluoromethyl)quinoline-3-carboxylic acid
Reaction equation
[F:1][C:2]([F:20])([F:19])[C:3]1[C:12]([C:13]([O:15]CC)=[O:14])=[C:11]([OH:18])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1>CCOCC>[F:20][C:2]([F:1])([F:19])[C:3]1[C:12]([C:13]([OH:15])=[O:14])=[C:11]([OH:18])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Using the procedure of Step E of Example 8, 30 g of the product of Step D were reacted to obtain without ether purification 26.3 g of 2-trifluoromethyl-4-hydroxy-3-quinoline-carboxylic acid melting at 262° C.
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-26d1f82ff02340d5bfcadec49ef05996
- Source dataset
- uspto-grants-1981_11
- Patent number
- US04299831
Reaction notes
Loading…