2-Pyrazinecarboxylic acid → HCID 178465971, 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].[N:17]1[CH:22]=[CH:21][N:20]=[CH:19][C:18]=1[C:23](O)=[O:24]>>[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:18]2[CH:19]=[N:20][CH:21]=[CH:22][N:17]=2)[OH:24])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and pyrazine-2-carboxylic acid
Sources & evidence
- ORD record
- ord-f1b14561e61245b39e9592d396deaf57
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07262206B2
Reaction notes
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