Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([NH2:7])=[O:6].[F:11][C:12]([F:19])([F:18])[C:13]([F:17])([F:16])[CH:14]=O.[NH:20]1[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[N:22]=[N:21]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[N:20]1([CH:14]([NH:7][C:5](=[O:6])[C:4]2[CH:8]=[CH:9][CH:10]=[C:2]([Cl:1])[CH:3]=2)[C:13]([F:17])([F:16])[C:12]([F:19])([F:18])[F:11])[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[N:22]=[N:21]1Participants
5
Procedure
3-Chlorobenzamide, pentafluoropropanal, benzotriazole, and p-toluenesulfonic acid were processed as described in Example 53A to provide the desired product.
Sources & evidence
- ORD record
- ord-e31ca9abff8e488d9e4753447502a2c9
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645968B2
Linked notes
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