1,2-Benzenediamine, N,N-dimethyl- → HCID 23104899, compound
Reaction equation
[CH3:1][N:2]([CH3:10])[C:3]1[C:4]([NH2:9])=[CH:5][CH:6]=[CH:7][CH:8]=1.[N+:11]([C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][CH2:22][CH2:23][C:24](O)=[O:25])=[CH:16][CH:15]=1)([O-:13])=[O:12]>>[CH3:1][N:2]([CH3:10])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[NH:9][C:24](=[O:25])[CH2:23][CH2:22][CH2:21][CH2:20][C:17]1[CH:18]=[CH:19][C:14]([N+:11]([O-:13])=[O:12])=[CH:15][CH:16]=1Participants
3
Procedure
The experimental protocol used is the same as that described for intermediate 5.1), N,N-dimethyl-1,2-benzenediamine replacing 4-(N-methylpiperazinyl)aniline and 5-(4-nitropheny)pentanoic acid replacing 4-(4-nitrophenyl)butanoic acid.
Sources & evidence
- ORD record
- ord-7abfc3f19d9d4b5db9016f7ecacc156f
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196084B2
Reaction notes
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