5-Nitroindole-2-carboxylic acid → HCID 58747091, compound
Reaction equation
[F:1][C:2]1[C:7]([O:8][C:9]([C:11]2[NH:12][C:13]3[C:18]([CH:19]=2)=[CH:17][C:16]([N+]([O-])=O)=[CH:15][CH:14]=3)=[O:10])=[C:6]([F:23])[C:5]([F:24])=[C:4]([F:25])[C:3]=1[F:26].[N+:27](C1C=C2C(=CC=1)NC(C(O)=O)=C2)([O-:29])=[O:28]>>[F:1][C:2]1[C:7]([O:8][C:9]([C:11]2[NH:12][C:13]3[C:18]([CH:19]=2)=[CH:17][CH:16]=[C:15]([N+:27]([O-:29])=[O:28])[CH:14]=3)=[O:10])=[C:6]([F:23])[C:5]([F:24])=[C:4]([F:25])[C:3]=1[F:26]Participants
3
Procedure
Compound 192 was synthesized as described for Compound 105 in Example 93, except instead of 104, 191 was used. It was used without isolation.
Sources & evidence
- ORD record
- ord-61ca1e3f94404732a4758149bb824b53
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07141680B2
Reaction notes
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