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

HRID 178513Notes

Reaction equation

HRID 178513 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:51]([O-:52])(=[O:53])[CH3:54].[C:56]([O-:57])(=[O:58])[CH3:59].[CH3:1][NH:2][S:3](=[O:4])(=[O:5])[CH:6]=[CH2:7].[CH3:40][CH2:41][N:42]([CH2:43][CH3:44])[CH2:45][CH3:46].[CH:47]([OH:48])([CH3:49])[CH3:50].[Pd+2:55].[c:18]1([CH3:19])[cH:20][cH:21][cH:22][cH:23][c:24]1[P:25]([c:26]1[cH:27][cH:28][cH:29][cH:30][c:31]1[CH3:32])[c:33]1[cH:34][cH:35][cH:36][cH:37][c:38]1[CH3:39]>>[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

8

Reactant 7

HCID 175Acetate2×HCID 3776IsopropanolHCID 8471TriethylamineHCID 249055-BromoindoleHCID 80271Tri-o-tolylphosphineHCID 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-ce06cea6c5f0407da2853fb6a46c7f8c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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