Reaction equation
F[C:2]1[C:3]([O:12][C:13]2[CH:14]=[N:15][C:16]([S:19]([CH3:22])(=[O:21])=[O:20])=[CH:17][CH:18]=2)=[CH:4][C:5]([N+:9]([O-])=O)=[C:6]([NH2:8])[CH:7]=1.[Cl:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[OH:30]>>[Cl:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[O:30][C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[CH:4][C:3]=1[O:12][C:13]1[CH:14]=[N:15][C:16]([S:19]([CH3:22])(=[O:21])=[O:20])=[CH:17][CH:18]=1Participants
3
Procedure
The entitled compound was obtained in the same method as in Example 196 (step 4) to (step 5) or in accordance with the method or by combining it with an ordinary method but using 5-fluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-2-nitro-phenylamine obtained in Example 196 (step 3) and 2-chlorophenol.
Workup
- customThe entitled compound was obtained in the same method as in Example 196 (step 4) to (step 5) or in accordance with the method
Sources & evidence
- ORD record
- ord-e471d69060334adabfb28ef08a560b4d
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07728025B2
Linked notes
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