Reaction equation
[Cl:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=O)[C:5]([OH:11])=[CH:4][CH:3]=1.[NH2:12][C:13]1[CH:14]=[C:15]([C:28]([F:31])([F:30])[F:29])[CH:16]=[CH:17][C:18]=1[O:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][CH:21]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([CH:10]=1)[C:7]([NH:12][C:13]1[CH:14]=[C:15]([C:28]([F:31])([F:30])[F:29])[CH:16]=[CH:17][C:18]=1[O:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][CH:21]=1)=[O:9]Participants
3
Procedure
Using 5-chlorosalicylic acid and 3-amino-4-(4-methoxyphenoxy)-benzotrifluoride as the raw materials, the same operation as the Example 1(1) gave the title compound.
Sources & evidence
- ORD record
- ord-61f64c96bb6b434080b015eb1fc08e71
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07626042B2
Linked notes
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