HCID 57855910, compound → HCID 57855900, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:12]([N+:13]([O-])=O)=[C:11]([C:16]([OH:18])=[O:17])[CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][C:7]([C:19]([F:22])([F:21])[F:20])=[N:8]2>C(O)C.[Ni]>[NH2:13][C:12]1[C:3]([O:2][CH3:1])=[C:4]2[C:9](=[CH:10][C:11]=1[C:16]([OH:18])=[O:17])[N:8]=[C:7]([C:19]([F:20])([F:21])[F:22])[CH:6]=[CH:5]2Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A sample of 5-Methoxy-6-nitro-2-trifluoromethyl-quinoline-7-carboxylic acid is hydrogenated in ethanol in the presence of Raney-Ni analogously to the procedure described for example H-18, step g). This gives the title product as yellow crystals.
Sources & evidence
- ORD record
- ord-183f3605603340248f422792f16c53d8
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580785B2
Reaction notes
Loading…