5-Aminoisoquinoline → HCID 44334439, compound
Reaction equation
[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([NH2:11])[C:5]=2[CH:4]=[CH:3][N:2]=1.[F:12][C:13]([F:24])([F:23])[C:14]1[CH:19]=[CH:18][C:17]([N:20]=[C:21]=[O:22])=[CH:16][CH:15]=1>>[CH:1]1[C:10]2[C:5](=[C:6]([NH:11][C:21]([NH:20][C:17]3[CH:16]=[CH:15][C:14]([C:13]([F:12])([F:23])[F:24])=[CH:19][CH:18]=3)=[O:22])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1Participants
3
Procedure
Prepared from isoquinolin-5-amine and 4-(trifluoromethyl)phenyl isocyanate according to Description 61. m/z (ES+) 332 (M+H)+.
Sources & evidence
- ORD record
- ord-1db7cb5a747f4284a1c9a6b0155b148f
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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