Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:16]=[CH:15][CH:14]=[CH:13][C:9]=2[C:10]([OH:12])=O)=[CH:4][CH:3]=1.NC1C=CC([C:22]([N:24]2[C:30]3[CH:31]=[CH:32][CH:33]=[CH:34][C:29]=3[C:28](=[O:35])[CH2:27][CH2:26][CH2:25]2)=[O:23])=CC=1>>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:16]=[C:15]([C:22]([N:24]3[C:30]4[CH:31]=[CH:32][CH:33]=[CH:34][C:29]=4[C:28](=[O:35])[CH2:27][CH2:26][CH2:25]3)=[O:23])[CH:14]=[CH:13][C:9]=2[C:10]([NH:24][C:30]2[CH:31]=[CH:32][CH:33]=[CH:34][CH:29]=2)=[O:12])=[CH:6][CH:7]=1Participants
3
Procedure
Using o-(4-methylphenyl)benzoic acid and 1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one as starting materials, the procedure of Reference Example 3 was repeated to obtain 2-(4-methylphenyl)-4-[(5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)carbonyl]benzanilide.
Sources & evidence
- ORD record
- ord-2c17f8988e57477f8720e9eb3bb18d12
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05856564
Linked notes
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