4-(2-Fluorophenyl)phenol → HCID 11191447, compound
Reaction equation
[C:1]([N:4]1[CH2:8][CH2:7][CH:6]([F:9])[CH:5]1[C:10]1[C:15](F)=[CH:14][C:13]([NH:17][C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=2)=O)=[C:12]([N+:26]([O-])=O)[CH:11]=1)(=[O:3])[CH3:2].[F:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=1[C:36]1[CH:41]=[CH:40][C:39]([OH:42])=[CH:38][CH:37]=1>>[C:1]([N:4]1[CH2:8][CH2:7][CH:6]([F:9])[CH:5]1[C:10]1[C:15]([O:42][C:39]2[CH:38]=[CH:37][C:36]([C:31]3[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=3[F:29])=[CH:41][CH:40]=2)=[CH:14][C:13]2[N:17]=[C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=3)[NH:26][C:12]=2[CH:11]=1)(=[O:3])[CH3:2]Participants
3
Procedure
The entitled compound was obtained in the same method as in Example 338 (step 5) or in accordance with the method or by combining it with an ordinary method but using N-(4-(1-acetyl-3-fluoropyrrolidin-2-yl)-5-fluoro-2-nitrophenyl)pyridin-2-carboxamide enantiomer A and 2′-fluorobiphenyl-4-ol.
Workup
- customThe entitled compound was obtained in the same method as in Example 338 (step 5) or in accordance with the method
Sources & evidence
- ORD record
- ord-acdc3df757bc47a89ef49b81fdb00d19
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07728025B2
Reaction notes
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