6-Aminoquinoline → HCID 69523661, 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.[C:12]1([CH:18]([N:20]=[C:21]=[O:22])[CH3:19])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[C:12]1([CH:18]([NH:20][C:21]([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:22])[CH3:19])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
3
Procedure
Prepared from 6-aminoquinoline and (+/−)-1-phenylethyl isocyanate. m/z (ES+) 292 (M+H)+.
Sources & evidence
- ORD record
- ord-1c0b2d8f5fdc410d96d227690586ad27
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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