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].C([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]Br)(=O)C>>[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]([CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][OH:21])[CH:10]=1)=[O:8]Participants
3
Procedure
The title compound was prepared using 1H-indole-3-carboxylic acid thiazol-2-ylamide and 5-bromopentyl acetate as R5X.
Sources & evidence
- ORD record
- ord-26c5554202ae43df8b1a8ee56009d122
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812043B2
Linked notes
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