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].[CH3:17][O:18][C:19](OC)(OC)[CH:20]([CH3:22])[CH3:21]>>[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:19]([O:18][CH3:17])[CH:20]([CH3:22])[CH3:21])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and 1.1.1-trimethoxy-2-methylpropane
Sources & evidence
- ORD record
- ord-25426a5ea9734ae8b074e177beb43064
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176231B2
Linked notes
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