1H-Indole-5-Carboxylic Acid → HCID 67113235, compound
Reaction equation
[NH2:1][C:2]1[CH:17]=[CH:16][C:5]2[N:6]([C:9]3[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][CH:10]=3)[CH:7]=[N:8][C:4]=2[CH:3]=1.[NH:18]1[C:26]2[C:21](=[CH:22][C:23]([C:27]([OH:29])=O)=[CH:24][CH:25]=2)[CH:20]=[CH:19]1>>[NH:18]1[C:26]2[C:21](=[CH:22][C:23]([C:27]([NH:1][C:2]3[CH:17]=[CH:16][C:5]4[N:6]([C:9]5[CH:10]=[CH:11][C:12]([NH:15][C:27]([C:23]6[CH:22]=[C:21]7[C:26](=[CH:25][CH:24]=6)[NH:18][CH:19]=[CH:20]7)=[O:29])=[CH:13][CH:14]=5)[CH:7]=[N:8][C:4]=4[CH:3]=3)=[O:29])=[CH:24][CH:25]=2)[CH:20]=[CH:19]1Participants
3
Procedure
Compound 564 was prepared according to the procedure described in Scheme IV from 5-amino-1-(4-aminophenyl)benzimidazole and indole-5-carboxylic acid. [M+H]+ calcd for C31H22N6O2: 511.19; found: 511.07.
Sources & evidence
- ORD record
- ord-33fc2b96ef274af08d3b837155f226c9
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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