Benzaldehyde → N-{2-[(2-Hydroxy-3-methyl-4-oxo-3-p-tolyl-cyclobut-1-enyl)-phenyl-methyl]-6-methyl-1H-indol-3-ylmethyl}-acetamide
Reaction equation
[CH3:1][C:2]1([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[C:5](=[O:6])[CH2:4][C:3]1=[O:7].[CH:15](=O)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[CH3:23][C:24]1[CH:32]=[C:31]2[C:27]([C:28]([CH2:33][NH:34][C:35](=[O:37])[CH3:36])=[CH:29][NH:30]2)=[CH:26][CH:25]=1>>[OH:7][C:3]1[C:2]([CH3:1])([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[C:5](=[O:6])[C:4]=1[CH:15]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:29]1[NH:30][C:31]2[C:27]([C:28]=1[CH2:33][NH:34][C:35](=[O:37])[CH3:36])=[CH:26][CH:25]=[C:24]([CH3:23])[CH:32]=2Participants
4
Procedure
Using general procedure C, 2-methyl-2-p-tolyl-cyclobutane-1,3-dione (from Example 4.1) was reacted with benzaldehyde and N-(6-methyl-1H-indol-3-ylmethyl)-acetamide (from Example 10.3) to give the title compound as a pale red solid. MS: 477.3 ([M−H]−).
Sources & evidence
- ORD record
- ord-43df1c27ffe145709e8daed30dfeedf9
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07705034B2
Reaction notes
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