5-Phenylaminosulfonyl-2-oxindole → HCID 69344981, compound

HRID 310263Notes

Reaction equation

HRID 310263 reaction equation
[N:21]1([CH2:26][CH2:27][O:28][c:29]2[cH:30][c:31]3[cH:32][c:33]([CH:38]=[O:39])[nH:34][c:35]3[cH:36][cH:37]2)[CH2:22][CH2:23][CH2:24][CH2:25]1.[c:1]1([NH:7][S:8](=[O:9])(=[O:10])[c:11]2[cH:12][c:13]3[c:17]([cH:18][cH:19]2)[NH:16][C:15](=[O:20])[CH2:14]3)[cH:2][cH:3][cH:4][cH:5][cH:6]1>>[c:1]1([NH:7][S:8](=[O:9])(=[O:10])[c:11]2[cH:12][c:13]3[c:17]([cH:18][cH:19]2)[NH:16][C:15](=[O:20])[C:14]3=[CH:38][c:33]2[cH:32][c:31]3[cH:30][c:29]([O:28][CH2:27][CH2:26][N:21]4[CH2:22][CH2:23][CH2:24][CH2:25]4)[cH:37][cH:36][c:35]3[nH:34]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1

Participants

3

Reactant 2

HCID 163836185-Phenylaminosulfonyl-2-oxindoleHCID 220420925-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde

Product 1

HCID 69344981HCID 69344981, compound

Sources & evidence

ORD record
ord-09c7e83a03a24681b8fb2c6696254903
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

Loading…