6-Trifluoroacetylamino-quinoline → N-(1,2,3,4-tetrahydro-6-quinolyl)trifluoroacetamide
Reaction equation
[F:1][C:2]([F:17])([F:16])[C:3]([NH:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[N:12]=[CH:11][CH:10]=[CH:9]2)=[O:4]>C(O)(=O)C.[Pt]=O>[F:17][C:2]([F:1])([F:16])[C:3]([NH:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[NH:12][CH2:11][CH2:10][CH2:9]2)=[O:4]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
2,4 g (0.01 mol) of 6-trifluoroacetylamino-quinoline are dissolved in 20 ml glacial acetic acid and hydrogenated for I hour with 0.6 g platinum oxide at 3 bar. Then the catalyst is suction filtered and the solution is concentrated by evaporation. The residue is washed with a little sodium hydrogen carbonate solution and dried.
Workup
- filtrationfiltered
- concentrationthe solution is concentrated by evaporation
- washThe residue is washed with a little sodium hydrogen carbonate solution
- customdried
Sources & evidence
- ORD record
- ord-6bb49db1d3da4364b87f89882f92cf6a
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300342B1
Reaction notes
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