2-(Methylsulfonyl)ethyl 4-methylbenzenesulfonate → 1-(2-Methanesulfonyl-ethyl)-1H-indole-3-carboxylic acid thiazol-2-ylamide
Reaction equation
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[NH:6][C:7]([C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:11][CH:10]=1)=[O:8].[CH3:18][S:19]([CH2:22][CH2:23]OS(C1C=CC(C)=CC=1)(=O)=O)(=[O:21])=[O:20]>>[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[NH:6][C:7]([C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]([CH2:23][CH2:22][S:19]([CH3:18])(=[O:21])=[O:20])[CH:10]=1)=[O:8]Participants
3
Procedure
The title compound was prepared using 1H-indole-3-carboxylic acid thiazol-2-ylamide and toluene-4-sulfonic acid 2-methanesulfonyl-ethyl ester as R5X.
Sources & evidence
- ORD record
- ord-1a89225548bb45e787cd5e63405a3d02
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812043B2
Reaction notes
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