Indole-3-acetamide → HCID 22556806, compound

HRID 983955Notes

Reaction equation

HRID 983955 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](=[C:26]([Cl:31])[CH:27]=[CH:28]2)[CH2:24][CH2:23][CH2:22][N:21]3[CH:20]=1)=O>>[Cl:31][C:26]1[CH:27]=[CH:28][C:29]2[C:19]([C:17]3[C:16](=[O:32])[NH:13][C:11](=[O:12])[C:10]=3[C:3]3[C:4]4[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=4)[NH:1][CH:2]=3)=[CH:20][N:21]3[C:30]=2[C:25]=1[CH2:24][CH2:23][CH2:22]3

Participants

3

Reactant 2

HCID 397Indole-3-acetamideHCID 69745081HCID 69745081, compound

Product 1

HCID 22556806HCID 22556806, compound

Procedure

Beginning with indole-3-acetamide and (7-chloro-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-31bc46dd64b44612a80580d1a3b78d36
Source dataset
uspto-grants-2005_03
Patent number
US06867198B2

Reaction notes

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