Methyl 2-bromopropionate → Methyl 2-(5-cyano-4-(trifluoromethyl)-1H-indol-1-yl)propanoate
Reaction equation
[F:1][C:2]([F:15])([F:14])[C:3]1[C:11]([C:12]#[N:13])=[CH:10][CH:9]=[C:8]2[C:4]=1[CH:5]=[CH:6][NH:7]2.Br[CH:17]([CH3:22])[C:18]([O:20][CH3:21])=[O:19]>>[C:12]([C:11]1[C:3]([C:2]([F:14])([F:1])[F:15])=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH:17]([CH3:22])[C:18]([O:20][CH3:21])=[O:19])[CH:6]=[CH:5]2)#[N:13]Participants
3
Procedure
Synthesized as described in Example 4 from 4-(trifluoromethyl)-1H-indole-5-carbonitrile and methyl 2-bromopropanoate: MS (APCl) m/z 297 (M+1).
Workup
- customSynthesized
Sources & evidence
- ORD record
- ord-b6a28161896f47fda4a4ae6c65cdc9ce
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07572820B2
Reaction notes
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