Benzaldehyde → HCID 57933464, compound
Reaction equation
[OH:1][C:2]1[CH:6]([CH:7]([CH3:9])[CH3:8])[N:5]([CH3:10])[C:4](=[O:11])[CH:3]=1.[CH:12](=O)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[F:20][C:21]1[CH:22]=[C:23]2[C:27](=[CH:28][CH:29]=1)[NH:26][CH:25]=[C:24]2[CH3:30]>>[F:20][C:21]1[CH:22]=[C:23]2[C:27](=[CH:28][CH:29]=1)[NH:26][C:25]([CH:12]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:3]1[C:4](=[O:11])[N:5]([CH3:10])[CH:6]([CH:7]([CH3:9])[CH3:8])[C:2]=1[OH:1])=[C:24]2[CH3:30]Participants
4
Procedure
Using general procedure C, 4-hydroxy-5-isopropyl-1-methyl-1,5-dihydro-pyrrol-2-one (Lit. 12) was reacted with benzaldehyde and 5-fluoro-3-methyl-1H-indole to give the title compound as a yellow solid. MS: 391.3 ([M−H]−).
Sources & evidence
- ORD record
- ord-a7917581a1db4ea99f4c9e5e87a98951
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612099B2
Reaction notes
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