6-Aminoquinoline → N-[3,5-bis(trifluoromethyl)phenyl]-N'-[quinolin-6-yl]urea
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:28])([F:27])[C:14]1[CH:15]=[C:16]([N:24]=[C:25]=[O:26])[CH:17]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:19]=1>>[F:12][C:13]([F:27])([F:28])[C:14]1[CH:15]=[C:16]([NH:24][C:25]([NH:1][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[N:8]=[CH:7][CH:6]=[CH:5]3)=[O:26])[CH:17]=[C:18]([C:20]([F:23])([F:21])[F:22])[CH:19]=1Participants
3
Procedure
Prepared from 6-aminoquinoline and 3,5-bis(trifluoromethyl)phenyl isocyanate. m/z (ES+) 400 (M+H)+.
Sources & evidence
- ORD record
- ord-ef326adb973845d3a07fdedb8db42cfc
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
Loading…