Methyl 2-(5-fluoro-2-methyl-1H-indol-1-yl)acetate → HCID 67044088, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:16])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([F:14])=[CH:11][CH:12]=2)[CH:7]=[C:6]1[CH3:15].[F:17][C:18]1[CH:19]=[C:20]([CH:23]=[CH:24][C:25]=1[S:26]([C:29]1[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=1)(=[O:28])=[O:27])[CH:21]=O>>[CH3:1][O:2][C:3](=[O:16])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([F:14])=[CH:11][CH:12]=2)[C:7]([CH2:21][C:20]2[CH:23]=[CH:24][C:25]([S:26]([C:29]3[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=3)(=[O:28])=[O:27])=[C:18]([F:17])[CH:19]=2)=[C:6]1[CH3:15]Participants
3
Procedure
The title compound was prepared by the method of Preparation 1c using (5-fluoro-2-methylindol-1-yl)acetic acid methyl ester and 3-fluoro-4-(4-fluorobenzenesulfonyl)benzaldehyde.
Sources & evidence
- ORD record
- ord-fe27ba91346c41ab9423b7e2d8a83037
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08394836B2
Reaction notes
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