Methyl 2-(5-fluoro-2-methyl-1H-indol-1-yl)acetate → HCID 67044289, compound
Reaction equation
[C:1]1([S:7]([C:10]2[C:11]([CH:16]=O)=[N:12][CH:13]=[CH:14][CH:15]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:18][O:19][C:20](=[O:33])[CH2:21][N:22]1[C:30]2[C:25](=[CH:26][C:27]([F:31])=[CH:28][CH:29]=2)[CH:24]=[C:23]1[CH3:32]>>[CH3:18][O:19][C:20](=[O:33])[CH2:21][N:22]1[C:30]2[C:25](=[CH:26][C:27]([F:31])=[CH:28][CH:29]=2)[C:24]([CH2:16][C:11]2[C:10]([S:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)(=[O:8])=[O:9])=[CH:15][CH:14]=[CH:13][N:12]=2)=[C:23]1[CH3:32]Participants
3
Procedure
The title compound was prepared by the method of Preparation 1c using 3-benzenesulfonylpyridine-2-carbaldehyde and (5-fluoro-2-methylindol-1-yl)acetic acid methyl ester.
Sources & evidence
- ORD record
- ord-eae5c3b13a1d4f7999c8785376a25580
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08394836B2
Reaction notes
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