Indole-3-acetamide → HCID 22556866, compound

HRID 983958Notes

Reaction equation

HRID 983958 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:32])[C:17]([C:19]1[C:29]2=[C:30]3[C:25](=[CH:26][CH:27]=[CH:28]2)[CH2:24][CH:23]([CH3:31])[CH2:22][N:21]3[CH:20]=1)=O>>[CH3:31][CH:23]1[CH2:24][C:25]2[C:30]3=[C:29]([C:19]([C:17]4[C:16](=[O:32])[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]=2

Participants

3

Reactant 2

HCID 397Indole-3-acetamideHCID 69743772HCID 69743772, compound

Product 1

HCID 22556866HCID 22556866, compound

Procedure

Beginning with indole-3-acetamide and (5-methyl-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-506d88e84b7a42088671ab62a4014d6b
Source dataset
uspto-grants-2005_03
Patent number
US06867198B2

Reaction notes

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