Indole-2-carboxaldehyde → HCID 69343725, compound

HRID 49103Notes

Reaction equation

HRID 49103 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][CH:21]=[CH:22][CH:23]=2)[CH:18]=[C:17]1[CH:25]=O>>[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:17]1[NH:16][C:24]2[C:19]([CH:18]=1)=[CH:20][CH:21]=[CH:22][CH:23]=2)(=[O:5])=[O:4]

Participants

3

Reactant 2

HCID 96389Indole-2-carboxaldehydeHCID 10176909N-methyl-2-oxoindoline-5-sulfonamide

Product 1

HCID 69343725HCID 69343725, compound

Procedure

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

Sources & evidence

ORD record
ord-80edee5d56c146ceb67a3adf763beff6
Source dataset
uspto-grants-2004_03
Patent number
US06706709B2

Reaction notes

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