4-(4-Dimethylaminobenzamido)aniline → HCID 178482818, compound
Reaction equation
[CH3:1][N:2]([CH3:19])[C:3]1[CH:18]=[CH:17][C:6]([C:7]([NH:9][C:10]2[CH:16]=[CH:15][C:13]([NH2:14])=[CH:12][CH:11]=2)=[O:8])=[CH:5][CH:4]=1.[CH3:20][N:21]([CH3:40])[C:22]1[CH:27]=[CH:26][C:25]([C:28]2[NH:29][C:30]3[CH:36]=[C:35]([C:37]([O-])=[O:38])[CH:34]=[CH:33][C:31]=3[N:32]=2)=[CH:24][CH:23]=1>>[CH3:1][N:2]([CH3:19])[C:3]1[CH:4]=[CH:5][C:6]([C:7]([NH:9][C:10]2[CH:16]=[CH:15][C:13]([NH:14][C:37]([C:35]3[CH:34]=[CH:33][C:31]4[NH:32][C:28]([C:25]5[CH:24]=[CH:23][C:22]([N:21]([CH3:40])[CH3:20])=[CH:27][CH:26]=5)=[N:29][C:30]=4[CH:36]=3)=[O:38])=[CH:12][CH:11]=2)=[O:8])=[CH:17][CH:18]=1Participants
3
Procedure
Compound 443 was prepared from 4-(4-dimethylaminobenzamido)aniline and 2-(4-dimethylaminophenyl)benzimidazole-5-carboxylate by standard conditions. [M+H]+ calcd for C31H30N6O2: 519.24; found: 519.04.
Sources & evidence
- ORD record
- ord-985c556bdbf14af8b0da1b341b89f9d2
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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