Isopropyl isocyanate → HCID 68629262, compound
Reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-])=O)[CH:8]=2)[N:3]=1.[CH3:15][O:16][C:17]1[CH:24]=[C:23]([O:25][CH3:26])[CH:22]=[CH:21][C:18]=1[CH2:19][NH2:20].[CH:27]([N:30]=[C:31]=[O:32])([CH3:29])[CH3:28]>>[CH3:15][O:16][C:17]1[CH:24]=[C:23]([O:25][CH3:26])[CH:22]=[CH:21][C:18]=1[CH2:19][NH:20][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:12][C:31]([NH:30][CH:27]([CH3:29])[CH3:28])=[O:32])[CH:8]=2)[N:3]=1Participants
4
Procedure
The title compound, MS: m/e=395.4 (M+H+), was prepared in accordance with the general method of example 14 from 2-chloro-6-nitro-quinoline, 2,4-dimethoxy-benzylamine and isopropyl isocyanate.
Sources & evidence
- ORD record
- ord-b3774061f889408ab8c789b1ade6ea39
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08350028B2
Reaction notes
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