8-Nitroquinoline-2-carboxylic acid → 5-Nitro-3-isoquinolinecarboxylic acid
Reaction equation
C(C1N=CC2C(C=1)=CC=CC=2)(O)=O.[C:14]([C:17]1[CH:26]=[CH:25][C:24]2[C:19](=[C:20]([N+:27]([O-:29])=[O:28])[CH:21]=[CH:22][CH:23]=2)[N:18]=1)([OH:16])=[O:15]>>[C:14]([C:17]1[N:18]=[CH:19][C:24]2[C:25]([CH:26]=1)=[C:20]([N+:27]([O-:29])=[O:28])[CH:21]=[CH:22][CH:23]=2)([OH:16])=[O:15]Participants
3
Procedure
3-Carboxy-5-nitroisoquinoline was prepared from 3-carboxyisoquinoline using a method similar to that used for the preparation of 2-carboxy-8-nitroquinoline in example 10 (Yield: 93%).
Sources & evidence
- ORD record
- ord-22eb5018b77440a1be5427abb54b9713
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441949
Reaction notes
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