N-(2-Oxoindolin-6-yl)acetamide → HCID 69706924, compound
Reaction equation
[O:1]=[C:2]1[CH2:10][C:9]2[C:4](=[CH:5][C:6]([NH:11][C:12](=[O:14])[CH3:13])=[CH:7][CH:8]=2)[NH:3]1.[O:15]=[C:16]1[C:21]2=[CH:22][NH:23][C:24]([CH:25]=O)=[C:20]2[CH2:19][CH2:18][O:17]1>>[O:1]=[C:2]1[C:10](=[CH:25][C:24]2[NH:23][CH:22]=[C:21]3[C:16](=[O:15])[O:17][CH2:18][CH2:19][C:20]=23)[C:9]2[C:4](=[CH:5][C:6]([NH:11][C:12](=[O:14])[CH3:13])=[CH:7][CH:8]=2)[NH:3]1Participants
3
Procedure
N-(2-Oxo-2,3-dihydro-1H-indol-6-yl)-acetamide was condensed with 4-oxo-2,4,6,7-tetrahydro-pyrano[3,4-c]pyrrole-1-carbaldehyde to give the title compound.
Sources & evidence
- ORD record
- ord-4f63962a0a164ac8bc50e026d0e36542
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06465507B2
Reaction notes
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