Methyl 2-(5-fluoro-2-methyl-1H-indol-1-yl)acetate → HCID 67043933, 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].[CH3:17][N:18]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[S:19]([C:22]1[C:27]([CH:28]=O)=[CH:26][CH:25]=[CH:24][N:23]=1)(=[O:21])=[O:20]>>[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]([CH2:28][C:27]2[C:22]([S:19](=[O:21])(=[O:20])[N:18]([CH3:17])[C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[N:23][CH:24]=[CH:25][CH:26]=2)=[C:6]1[CH3:15]Participants
3
Procedure
The title compound was prepared by the method of Preparation 29a using (5-fluoro-2-methylindol-1-yl)acetic acid methyl ester and 3-formylpyridine-2-sulfonic acid methylphenylamide.
Sources & evidence
- ORD record
- ord-46f0a77143544b1ba338743cb208c759
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08394836B2
Reaction notes
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