2-Chlorobenzoic Acid → HCID 178465957, 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].[Cl:17][C:18]1[CH:26]=[CH:25][CH:24]=[CH:23][C:19]=1[C:20](O)=[O: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:20]([C:19]2[CH:23]=[CH:24][CH:25]=[CH:26][C:18]=2[Cl:17])[OH:21])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and 2-chlorobenzoic acid
Sources & evidence
- ORD record
- ord-cb576e38821c469188d473bf1d10c1e3
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07262206B2
Reaction notes
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