6-Aminoquinoline → HCID 69523688, 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.[CH:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:23]=[CH:22][C:21]([N:24]=[C:25]=[O:26])=[CH:20][CH:19]=2)=[CH:14][CH:13]=1>>[C:18]1([C:15]2[CH:14]=[CH:13][CH:12]=[CH:17][CH:16]=2)[CH:19]=[CH:20][C:21]([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:22][CH:23]=1Participants
3
Procedure
Prepared from 6-aminoquinoline and 4-biphenyl isocyanate. m/z (ES+) 340 (M+H)+.
Sources & evidence
- ORD record
- ord-d4f648db12634134b0f5f6d4ff0a154b
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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