5-Nitroindole-2-carboxylic acid → HCID 21880795, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([C:12]([NH:14][C:15]3[CH:16]=[C:17]4[C:21](=[CH:22][CH:23]=3)[NH:20][C:19]([C:24]([OH:26])=[O:25])=[CH:18]4)=[O:13])=[CH:9][C:8]=2[CH:27]=1)([O-])=O.[N+](C1C=C2C(=CC=1)NC(C(O)=O)=C2)([O-])=O>>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([C:12]([NH:14][C:15]3[CH:16]=[C:17]4[C:21](=[CH:22][CH:23]=3)[NH:20][C:19]([C:24]([OH:26])=[O:25])=[CH:18]4)=[O:13])=[CH:9][C:8]=2[CH:27]=1Participants
3
Procedure
Compound 129 was reduced as described for Compound 126 in Example 115, to give 130 which was used immediately as described in Example 118.
Sources & evidence
- ORD record
- ord-0ae6a16e3a55455397d7ce95a1c33f1b
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07141680B2
Reaction notes
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