3-Bromopropionitrile → 1-(2-Cyano-ethyl)-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].Br[CH2:19][CH2:20][C:21]#[N:22]>>[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]([CH2:19][CH2:20][C:21]#[N:22])[CH:10]=1)=[O:8]Participants
3
Procedure
The title compound was prepared using 1H-indole-3-carboxylic acid thiazol-2-ylamide and 3-bromo propionitrile as R5X.
Sources & evidence
- ORD record
- ord-33fa0a5ff0c045968067f03e23579780
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812043B2
Reaction notes
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