N-(2-oxoindolin-5-yl)acetamide → HCID 68526677, compound

HRID 1220125Notes

Reaction equation

HRID 1220125 reaction equation
[CH3:1][c:2]1[c:3]([CH:20]=[O:21])[nH:4][c:5]2[c:6]1[C:7](=[O:19])[N:8]([CH2:12][CH2:13][N:14]1[CH2:15][CH2:16][CH2:17][CH2:18]1)[CH2:9][CH2:10][CH2:11]2.[O:22]=[C:23]1[NH:24][c:25]2[cH:26][cH:27][c:28]([NH:32][C:33]([CH3:34])=[O:35])[cH:29][c:30]2[CH2:31]1>>[CH3:1][c:2]1[c:3]([CH:20]=[C:31]2[C:23](=[O:22])[NH:24][c:25]3[cH:26][cH:27][c:28]([NH:32][C:33]([CH3:34])=[O:35])[cH:29][c:30]32)[nH:4][c:5]2[c:6]1[C:7](=[O:19])[N:8]([CH2:12][CH2:13][N:14]1[CH2:15][CH2:16][CH2:17][CH2:18]1)[CH2:9][CH2:10][CH2:11]2

Participants

3

Reactant 2

HCID 11206280N-(2-oxoindolin-5-yl)acetamideHCID 592500963-Methyl-4-oxo-5-(2-pyrrolidin-1-yl-ethyl)-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-c]azepine-2-carbaldehyde

Product 1

HCID 68526677HCID 68526677, compound

Sources & evidence

ORD record
ord-0bf4e23d63b54f67b5910e27f39b1884
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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