2-(4-Dimethylaminophenyl)benzimidazole-5-caboxylate → HCID 178490974, compound
Reaction equation
[CH3:1][N:2]([CH3:21])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[NH:10][C:11]3[CH:17]=[C:16]([C:18]([O-:20])=O)[CH:15]=[CH:14][C:12]=3[N:13]=2)=[CH:5][CH:4]=1.[NH2:22][C:23]1[CH:40]=[CH:39][C:26]2[N:27]=[C:28]([NH:30][C:31]3[CH:36]=[CH:35][CH:34]=[C:33]([O:37][CH3:38])[CH:32]=3)[NH:29][C:25]=2[CH:24]=1>>[CH3:38][O:37][C:33]1[CH:32]=[C:31]([NH:30][C:28]2[NH:27][C:26]3[CH:39]=[CH:40][C:23]([NH:22][C:18]([C:16]4[CH:15]=[CH:14][C:12]5[NH:13][C:9]([C:6]6[CH:5]=[CH:4][C:3]([N:2]([CH3:21])[CH3:1])=[CH:8][CH:7]=6)=[N:10][C:11]=5[CH:17]=4)=[O:20])=[CH:24][C:25]=3[N:29]=2)[CH:36]=[CH:35][CH:34]=1Participants
3
Procedure
Compound 439 was prepared from 2-(4-dimethylaminophenyl)benzimidazole-5-carboxylate and 5-amino-2-(3-methoxyphenyl)aminobenzimidazole by standard conditions. [M+H]+ calcd for C30H27N7O2: 518.22; found: 518.03.
Sources & evidence
- ORD record
- ord-94587593f9dd4d9c955334a8e3a2edff
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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