6-Phenyl-1,3-dihydro-indol-2-one → 3-(3,5-Diisopropyl-4-methoxybenzylidene)-6-phenyl-1,3-dihydroindol-2-one

HRID 1860865Notes

Reaction equation

HRID 1860865 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].[C:17]1([C:23]2[CH:31]=[C:30]3[C:26]([CH2:27][C:28](=[O:32])[NH:29]3)=[CH:25][CH:24]=2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[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:27]1[C:26]2[C:30](=[CH:31][C:23]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:24][CH:25]=2)[NH:29][C:28]1=[O:32])([CH3:3])[CH3:2]

Participants

3

Procedure

3,5-Diisopropyl-4-methoxybenzaldehyde was condensed with 6-phenyl-2-oxindole to give 0.4 g of 3-(3,5-diisopropyl-4-methoxybenzylidene)-6-phenyl-1,3-dihydroindol-2-one as a yellow-orange solid.

Sources & evidence

ORD record
ord-bdb22917a7d24ce0910d2d9b80f65777
Source dataset
uspto-grants-2003_03
Patent number
US06531502B1

Reaction notes

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