4,4'-Diaminobenzophenone → HCID 67112548, compound
Reaction equation
[NH2:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[NH:17]1[C:25]2[C:20](=[CH:21][C:22]([C:26]([O-])=[O:27])=[CH:23][CH:24]=2)[CH:19]=[CH:18]1>>[NH2:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([NH:14][C:26]([C:22]3[CH:21]=[C:20]4[C:25](=[CH:24][CH:23]=3)[NH:17][CH:18]=[CH:19]4)=[O:27])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1Participants
3
Procedure
Compound 346 was prepared according to the procedure described in Scheme IV from 4,4′-diaminobenzophenone and 1H-indole-5-carboxylate. [M+H]+ calcd for C22H17N3O2: 356.14; found: 355.90.
Sources & evidence
- ORD record
- ord-b0d7c4281e6144e88b26a1b4f108f9f8
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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