Acetate → Ethenesulfonamide, 2-(1H-indol-5-yl)-N-methyl-

HRID 2160679Notes

Reaction equation

[Br:8][c:9]1[cH:10][c:11]2[cH:12][cH:13][nH:14][c:15]2[cH:16][cH:17]1.[C:29]([O-:30])(=[O:31])[CH3:32].[C:34]([O-:35])(=[O:36])[CH3:37].[CH3:18][CH2:19][N:20]([CH2:21][CH3:22])[CH2:23][CH3:24].[CH3:1][NH:2][S:3](=[O:4])(=[O:5])[CH:6]=[CH2:7].[CH:25]([OH:26])([CH3:27])[CH3:28].[Pd+2:33]>>[CH3:1][NH:2][S:3](=[O:4])(=[O:5])[CH:6]=[CH:7][c:9]1[cH:10][c:11]2[cH:12][cH:13][nH:14][c:15]2[cH:16][cH:17]1

Participants

Reactant 6

HCID 175Acetate2×

HCID 3776Isopropanol

HCID 8471Triethylamine

HCID 249055-Bromoindole

HCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)

HCID 21895383N-Methylethenesulfonamide

Product 1

HCID 54193929Ethenesulfonamide, 2-(1H-indol-5-yl)-N-methyl-

Sources & evidence

ORD record: ord-f51d26aec7bd43ce83aa26c2cf8cc2d4
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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