Indole-3-acetamide → 3-(5,5-dimethyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(1H-indol-3-yl)pyrrole-2,5-dione
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11]([NH2:13])=[O:12])=[CH:2]1.CO[C:16](=[O:33])[C:17]([C:19]1[C:29]2=[C:30]3[C:25](=[CH:26][CH:27]=[CH:28]2)[CH2:24][C:23]([CH3:32])([CH3:31])[CH2:22][N:21]3[CH:20]=1)=O>>[CH3:32][C:23]1([CH3:31])[CH2:24][C:25]2[C:30]3=[C:29]([C:19]([C:17]4[C:16](=[O:33])[NH:13][C:11](=[O:12])[C:10]=4[C:3]4[C:4]5[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=5)[NH:1][CH:2]=4)=[CH:20][N:21]3[CH2:22]1)[CH:28]=[CH:27][CH:26]=2Participants
3
Procedure
Beginning with (indol-3-yl)acetamide and (5,5-dimethyl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)oxo-acetic acid methyl ester, the title compound was prepared essentially as described in Example 1.
Sources & evidence
- ORD record
- ord-31aa92201ad34e4bbfa73775cae5b80b
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06867198B2
Reaction notes
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