4-Dimethylaminobenzoate → HCID 178490975, compound
Reaction equation
[CH3:1][N:2]([CH3:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([O-:9])=O)=[CH:5][CH:4]=1.[NH2:13][C:14]1[CH:31]=[CH:30][C:17]2[N:18]=[C:19]([NH:21][C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([O:28][CH3:29])[CH:23]=3)[NH:20][C:16]=2[CH:15]=1>>[CH3:12][N:2]([CH3:1])[C:3]1[CH:4]=[CH:5][C:6]([C:7]([NH:13][C:14]2[CH:31]=[CH:30][C:17]3[NH:18][C:19]([NH:21][C:22]4[CH:27]=[CH:26][CH:25]=[C:24]([O:28][CH3:29])[CH:23]=4)=[N:20][C:16]=3[CH:15]=2)=[O:9])=[CH:10][CH:11]=1Participants
3
Procedure
Compound 429 was prepared from 4-dimethylaminobenzoate and 5-amino-2-(3-methoxyphenylamino)benzimidazole by standard conditions. [M+H]+ calcd for C23H23N5O2: 402.19; found: 401.96.
Sources & evidence
- ORD record
- ord-643bf467eae5443c8545f542f1b161de
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
Loading…