HCID 7667367, compound → HCID 69344476, compound

HRID 2322393Notes

Reaction equation

HRID 2322393 reaction equation
[N:1]1([S:11](=[O:12])(=[O:13])[c:14]2[cH:15][c:16]3[c:20]([cH:21][cH:22]2)[NH:19][C:18](=[O:23])[CH2:17]3)[CH2:2][CH2:3][CH2:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]21.[N:24]1([CH2:29][CH2:30][O:31][c:32]2[cH:33][c:34]3[cH:35][c:36]([CH:41]=[O:42])[nH:37][c:38]3[cH:39][cH:40]2)[CH2:25][CH2:26][CH2:27][CH2:28]1>>[N:1]1([S:11](=[O:12])(=[O:13])[c:14]2[cH:15][c:16]3[c:20]([cH:21][cH:22]2)[NH:19][C:18](=[O:23])[C:17]3=[CH:41][c:36]2[cH:35][c:34]3[cH:33][c:32]([O:31][CH2:30][CH2:29][N:24]4[CH2:25][CH2:26][CH2:27][CH2:28]4)[cH:40][cH:39][c:38]3[nH:37]2)[CH2:2][CH2:3][CH2:4][c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]21

Participants

3

Reactant 2

HCID 7667367HCID 7667367, compoundHCID 220420925-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde

Product 1

HCID 69344476HCID 69344476, compound

Sources & evidence

ORD record
ord-2cacd09242e74f81a0c59810eb7a23f1
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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