(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)acetamide → HCID 22556747, compound

HRID 983981Notes

Reaction equation

HRID 983981 reaction equation
CO[C:3](=[O:21])[C:4]([C:6]1[C:14]2[C:9](=[CH:10][C:11]([C:15]3[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=3)=[CH:12][CH:13]=2)[NH:8][CH:7]=1)=O.[C:22]1([CH2:34][C:35]([NH2:37])=[O:36])[C:32]2=[C:33]3[C:28](=[CH:29][CH:30]=[CH:31]2)[CH2:27][CH2:26][CH2:25][N:24]3[CH:23]=1>>[C:22]1([C:34]2[C:35](=[O:36])[NH:37][C:3](=[O:21])[C:4]=2[C:6]2[C:14]3[C:9](=[CH:10][C:11]([C:15]4[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=4)=[CH:12][CH:13]=3)[NH:8][CH:7]=2)[C:32]2=[C:33]3[C:28](=[CH:29][CH:30]=[CH:31]2)[CH2:27][CH2:26][CH2:25][N:24]3[CH:23]=1

Participants

3

Reactant 2

HCID 16742967(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)acetamideHCID 69744811HCID 69744811, compound

Product 1

HCID 22556747HCID 22556747, compound

Procedure

Beginning with (6-(pyridin-3-yl)indol-3-yl)oxoacetic acid methyl ester and 2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)acetamide, the title compound was prepared essentially as described in Example 1.

Sources & evidence

ORD record
ord-29cc28762c0144e88685c10a00a64250
Source dataset
uspto-grants-2005_03
Patent number
US06867198B2

Reaction notes

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