5-Ethyl-1,3-dihydro-2H-indol-2-one → HCID 54554150, compound

HRID 24385Notes

Reaction equation

HRID 24385 reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:14]([CH3:16])[CH3:15])[C:11]=1[O:12][CH3:13])[CH:7]=O)([CH3:3])[CH3:2].[CH2:17]([C:19]1[CH:20]=[C:21]2[C:25](=[CH:26][CH:27]=1)[NH:24][C:23](=[O:28])[CH2:22]2)[CH3:18]>>[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:14]([CH3:16])[CH3:15])[C:11]=1[O:12][CH3:13])[CH:7]=[C:22]1[C:21]2[C:25](=[CH:26][CH:27]=[C:19]([CH2:17][CH3:18])[CH:20]=2)[NH:24][C:23]1=[O:28])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 101541895-Ethyl-1,3-dihydro-2H-indol-2-oneHCID 105850253,5-Diisopropyl-4-methoxybenzaldehyde

Product 1

HCID 54554150HCID 54554150, compound

Procedure

3,5-Diisopropyl-4-methoxybenzaldehyde was condensed with 5-ethyl-2-oxindole to give 0.3 g of 3-(3,5-diisopropyl-4-methoxybenzylidene)-5-ethyl-1,3-dihydroindol-2-one as a yellow-orange solid.

Sources & evidence

ORD record
ord-d5beca2a27654c929780beeca0ae4a8b
Source dataset
uspto-grants-2005_02
Patent number
US06855730B2

Reaction notes

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