HCID 27187797, compound → HCID 86674589, compound
Reaction equation
Br[CH2:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:13])([CH3:12])[C:10]#[N:11])[CH:6]=[CH:7][CH:8]=1.[CH3:14][C:15]1[NH:16][C:17]2[C:22]([C:23]=1[CH3:24])=[CH:21][C:20]([C:25]([O:27][CH2:28][CH:29]=[CH2:30])=[O:26])=[CH:19][CH:18]=2>>[C:10]([C:9]([C:5]1[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=1)[CH2:2][N:16]1[C:17]2[C:22](=[CH:21][C:20]([C:25]([O:27][CH2:28][CH:29]=[CH2:30])=[O:26])=[CH:19][CH:18]=2)[C:23]([CH3:24])=[C:15]1[CH3:14])([CH3:13])[CH3:12])#[N:11]Participants
3
Procedure
The title compound was prepared following the same general protocol as described in Step 2, Example 1, using 2-(3-(bromomethyl)phenyl)-2-methylpropanenitrile and allyl 2,3-dimethyl-1H-indole-5-carboxylate. ESI-MS (m/z): 387 [M+H]+.
Sources & evidence
- ORD record
- ord-1c285e35cd71488caf926db770f77c74
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051265B2
Reaction notes
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