Indole-3-acetamide → HCID 22556833, compound

HRID 983977Notes

Reaction equation

HRID 983977 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:35])[C:17]([C:19]1[C:29]2=[C:30]3[C:25](=[CH:26][CH:27]=[C:28]2[CH3:31])[CH:24]([CH3:32])[CH2:23][C:22]([CH3:34])([CH3:33])[N:21]3[CH:20]=1)=O>>[CH3:34][C:22]1([CH3:33])[CH2:23][CH:24]([CH3:32])[C:25]2[C:30]3=[C:29]([C:19]([C:17]4[C:16](=[O:35])[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]13)[C:28]([CH3:31])=[CH:27][CH:26]=2

Participants

3

Reactant 2

HCID 397Indole-3-acetamideHCID 69743981HCID 69743981, compound

Product 1

HCID 22556833HCID 22556833, compound

Procedure

Beginning with (indol-3-yl)acetamide and (4,4,6,9-tetramethyl-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-8a8f0564ed434e4183a612709a0bbee6
Source dataset
uspto-grants-2005_03
Patent number
US06867198B2

Reaction notes

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