Reaction equation
C(C1C=CC(C2C=CC=C(C(N)=O)C=2)=CC=1)=O.[C:18]([C@@H:22]1[CH2:27][CH2:26][C@H:25]([NH:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([C:36]3[CH:41]=[CH:40][CH:39]=[C:38]([C:42]([NH2:44])=[O:43])[CH:37]=3)=[C:32]([F:45])[CH:31]=2)[CH2:24][CH2:23]1)([CH3:21])([CH3:20])[CH3:19]>>[C:18]([C@H:22]1[CH2:23][CH2:24][C@H:25]([NH:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([C:36]3[CH:41]=[CH:40][CH:39]=[C:38]([C:42]([NH2:44])=[O:43])[CH:37]=3)=[C:32]([F:45])[CH:31]=2)[CH2:26][CH2:27]1)([CH3:21])([CH3:19])[CH3:20]Participants
3
Procedure
The procedure described in Example 56/57 was used to prepare Examples 58 and 59 from 4′-formylbiphenyl-3-carboxylic acid amide (Preparation 1) and the appropriate amine:
Sources & evidence
- ORD record
- ord-6ba77837498140a1901b9aaca5d8ce06
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063247B2
Linked notes
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