3-Furoic acid → HCID 178465969, 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].[O:17]1[CH:21]=[CH:20][C:19]([C:22](O)=[O:23])=[CH:18]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:22]([C:19]2[CH:20]=[CH:21][O:17][CH:18]=2)[OH:23])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and furan-3-carboxylic acid
Sources & evidence
- ORD record
- ord-dfaa54f551d84085b8a20e551c876dfe
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176231B2
Reaction notes
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