Oxindole → HCID 72506438, compound

HRID 2101643Notes

Reaction equation

HRID 2101643 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[CH3:11][N:12]([CH3:27])[CH2:13][CH2:14][NH:15][C:16]([C:18]1[C:22]([CH3:23])=[C:21]([CH:24]=O)[NH:20][C:19]=1[CH3:26])=[O:17]>>[CH3:11][N:12]([CH3:27])[CH2:13][CH2:14][NH:15][C:16]([C:18]1[C:22]([CH3:23])=[C:21]([CH:24]=[C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[NH:1][C:2]2=[O:10])[NH:20][C:19]=1[CH3:26])=[O:17]

Participants

3

Reactant 2

HCID 321710OxindoleHCID 54380946HCID 54380946, compound

Product 1

HCID 72506438HCID 72506438, compound

Procedure

1,3-Dihydro-indol-2-one was condensed with 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-dimethylaminoethyl)amide to give the title compound.

Sources & evidence

ORD record
ord-908bad8f81184d1c968ec49b32a5ba4d
Source dataset
uspto-grants-2009_08
Patent number
US07572924B2

Reaction notes

Loading…