Dimethylamine → HCID 18439838, compound
Reaction equation
Cl[C:2]1[CH:3]=[C:4]([C:8]2[CH:17]=[C:16]([N:18]([CH3:20])[CH3:19])[C:15]3[C:10](=[CH:11][CH:12]=[C:13]([N+:21]([O-])=O)[CH:14]=3)[N:9]=2)[CH:5]=[CH:6][CH:7]=1.[CH3:24][NH:25][CH3:26]>>[CH3:24][N:25]([CH3:26])[C:2]1[CH:3]=[C:4]([C:8]2[CH:17]=[C:16]([N:18]([CH3:20])[CH3:19])[C:15]3[C:10](=[CH:11][CH:12]=[C:13]([NH2:21])[CH:14]=3)[N:9]=2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared from N-[2-(3-chlorophenyl)-6-nitro-4-quinolinyl]-N,N-dimethylamine by the procedure of step D2 of Method D using dimethylamine.
Sources & evidence
- ORD record
- ord-a692b2668036414aa839b9b4727bebb4
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07348340B2
Reaction notes
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