Reaction equation
[C:1]([C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH2:11]2)(=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[C:18](OC(=O)C)(=[O:20])[CH3:19]>>[C:18]([N:13]1[C:14]2[C:10](=[CH:9][C:8]([C:1](=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[CH:16][CH:15]=2)[CH2:11][C:12]1=[O:17])(=[O:20])[CH3:19]Participants
3
Procedure
Prepared from 5-hexanoyl-2-indolinone and acetic anhydride
Sources & evidence
- ORD record
- ord-6db36c75aa3a45db823f5f846523106a
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176231B2
Linked notes
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