4,4'-Diaminobenzophenone → N-(4-(4-Aminobenzoyl)phenyl)-4-morpholinobenzamide
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.[O:17]1[CH2:22][CH2:21][N:20]([C:23]2[CH:31]=[CH:30][C:26]([C:27]([O-])=[O:28])=[CH:25][CH:24]=2)[CH2:19][CH2:18]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:27](=[O:28])[C:26]3[CH:25]=[CH:24][C:23]([N:20]4[CH2:21][CH2:22][O:17][CH2:18][CH2:19]4)=[CH:31][CH:30]=3)=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1Participants
3
Procedure
Compound 485 was prepared according to the procedure described in Scheme IV from 4,4′-diaminobenzophenone and 4-morpholinobenzoate. [M+H]+ calcd for C24H23N3O3: 402.08; found: 402.03.
Sources & evidence
- ORD record
- ord-d783fb0e0f2947469dec64d0aeb10f32
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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