Reaction equation
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:16])(=[O:3])[CH3:2].[C:17](O)(=[O:23])[CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[C:6](=[C:17]([OH:23])[CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and hexanoic acid
Sources & evidence
- ORD record
- ord-e1b8fe2311c44211830659526da46f0d
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07262206B2
Linked notes
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