2-Pyridinecarboxaldehyde → N-(2-{2-[(2-Hydroxy-5-oxo-3-phenyl-cyclopent-1-enyl)-pyridin-2-yl-methyl]-1H-indol-3-yl}-ethyl)-acetamide
Reaction equation
[OH:1][C:2]1[CH:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:5][C:4](=[O:13])[CH:3]=1.[N:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH:20]=O.[NH:22]1[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24]([CH2:31][CH2:32][NH:33][C:34](=[O:36])[CH3:35])=[CH:23]1>>[OH:1][C:2]1[CH:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:5][C:4](=[O:13])[C:3]=1[CH:20]([C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][N:14]=1)[C:23]1[NH:22][C:30]2[C:25]([C:24]=1[CH2:31][CH2:32][NH:33][C:34](=[O:36])[CH3:35])=[CH:26][CH:27]=[CH:28][CH:29]=2Participants
4
Procedure
Using general procedure C, 3-hydroxy-4-phenyl-cyclopent-2-enone (Lit. 17) was reacted with pyridine-2-carbaldehyde and N-[2-(1H-indol-3-yl)-ethyl]-acetamide to give the title compound as a white solid. MS: 466.3 ([M+H]+).
Sources & evidence
- ORD record
- ord-4b2994c1363248d9bc32d341930e5f07
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612099B2
Reaction notes
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