Indole-3-acetamide → HCID 22556672, compound
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.C[O:15][C:16](=O)[C:17]([C:19]1[C:29]2=[C:30]3[C:25](=[CH:26][C:27]([O:31][CH3:32])=[CH:28]2)[CH2:24][CH2:23][CH2:22][N:21]3[CH:20]=1)=O>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]2[C:11](=[O:12])[NH:13][C:16](=[O:15])[C:17]=2[C:19]2[C:29]3=[C:30]4[C:25](=[CH:26][C:27]([O:31][CH3:32])=[CH:28]3)[CH2:24][CH2:23][CH2:22][N:21]4[CH:20]=2)=[CH:2]1Participants
3
Procedure
Beginning with indole-3-acetamide and (8-methoxy-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)oxoacetic acid methyl ester, the title compound was prepared essentially as described in Example 1.
Sources & evidence
- ORD record
- ord-5a58f6eab8fa4f2b881dda7467509fd8
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06867198B2
Reaction notes
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