Indole-5-carboxaldehyde → 3-(1H-Indol-5-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid methylamide

HRID 49102

Reaction equation

HRID 49102 reaction equation
[CH3:1][NH:2][S:3]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[NH:11][C:10](=[O:15])[CH2:9]2)(=[O:5])=[O:4].[NH:16]1[C:24]2[C:19](=[CH:20][C:21]([CH:25]=O)=[CH:22][CH:23]=2)[CH:18]=[CH:17]1>>[CH3:1][NH:2][S:3]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[NH:11][C:10](=[O:15])[C:9]2=[CH:25][C:21]1[CH:20]=[C:19]2[C:24](=[CH:23][CH:22]=1)[NH:16][CH:17]=[CH:18]2)(=[O:5])=[O:4]

Participants

3

Reactant 2

HCID 589040Indole-5-carboxaldehydeHCID 10176909N-methyl-2-oxoindoline-5-sulfonamide

Product 1

HCID 693442543-(1H-Indol-5-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid methylamide

Procedure

5-Methylaminosulfonyl-2-oxindole was condensed with indole-5-carbaldehyde to give the title compound.

Sources & evidence

ORD record
ord-77467b4aa411466ab70973ddf0660724
Source dataset
uspto-grants-2004_03
Patent number
US06706709B2

Linked notes

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