6-Aminoquinoline → HCID 69522933, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][CH:6]=[CH:5]2.[F:12][C:13]([F:25])([F:24])[O:14][C:15]1[CH:20]=[CH:19][C:18]([N:21]=[C:22]=[O:23])=[CH:17][CH:16]=1>>[N:8]1[C:9]2[C:4](=[CH:3][C:2]([NH:1][C:22]([NH:21][C:18]3[CH:19]=[CH:20][C:15]([O:14][C:13]([F:12])([F:24])[F:25])=[CH:16][CH:17]=3)=[O:23])=[CH:11][CH:10]=2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Prepared from 6-aminoquinoline and 4-(trifluoromethoxy)phenyl isocyanate. m/z (ES+) 348 (M+H)+.
Sources & evidence
- ORD record
- ord-c635ed1920fc406393a895461df86605
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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