4-(Trifluoromethyl)benzoic acid → HCID 178465958, compound
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].[F:17][C:18]([F:29])([F:28])[C:19]1[CH:27]=[CH:26][C:22]([C:23](O)=[O:24])=[CH:21][CH:20]=1>>[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:23]([C:22]2[CH:21]=[CH:20][C:19]([C:18]([F:17])([F:28])[F:29])=[CH:27][CH:26]=2)[OH:24])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and 4-trifluoromethyl-benzoic acid
Sources & evidence
- ORD record
- ord-2bace1ad79c847458434ad9ea73fafd0
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07262206B2
Reaction notes
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