4,4'-Diaminobenzophenone → HCID 67113410, 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.[OH:17][CH2:18][CH2:19][N:20]([C:22]1[CH:30]=[CH:29][C:25]([C:26]([O-])=[O:27])=[CH:24][CH:23]=1)[CH3:21]>>[C:6]([C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:26](=[O:27])[C:25]2[CH:29]=[CH:30][C:22]([N:20]([CH2:19][CH2:18][OH:17])[CH3:21])=[CH:23][CH:24]=2)=[CH:10][CH:9]=1)([C:5]1[CH:15]=[CH:16][C:2]([NH:1][C:26](=[O:27])[C:25]2[CH:24]=[CH:23][C:22]([N:20]([CH2:19][CH2:18][OH:17])[CH3:21])=[CH:30][CH:29]=2)=[CH:3][CH:4]=1)=[O:7]Participants
3
Procedure
Compound 330 was prepared according to the procedure described in Scheme IV from 4,4′-diaminobenzophenone and 4-(N-2-hydroxylethyl-N-methylamino)benzoate. [M+H]+ calcd for C33H35N4O5: 567.26; found: 567.04.
Sources & evidence
- ORD record
- ord-9832287dd2ea4e518bc75ef00c7ac547
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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