(4-fluoro-1-methyl-1H-indol-3-yl)-oxo-acetyl chloride → 3-(4-Fluoro-1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-pyrrole-2,5-dione
Reaction equation
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4]([C:12](=O)[C:13](Cl)=[O:14])=[CH:5][N:6]2[CH3:11].Cl.C([O:21][C:22](=[NH:37])[CH2:23][C:24]1[C:32]2[C:27](=[CH:28][C:29]([N+:33]([O-:35])=[O:34])=[CH:30][CH:31]=2)[N:26]([CH3:36])[CH:25]=1)(C)C>>[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4]([C:12]1[C:13](=[O:14])[NH:37][C:22](=[O:21])[C:23]=1[C:24]1[C:32]3[C:27](=[CH:28][C:29]([N+:33]([O-:35])=[O:34])=[CH:30][CH:31]=3)[N:26]([CH3:36])[CH:25]=1)=[CH:5][N:6]2[CH3:11]Participants
3
Procedure
3-(4-Fluoro-1-methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-pyrrole-2,5-dione was prepared from (4-fluoro-1-methyl-1H-indol-3-yl)-oxo-acetyl chloride and 2-(1-methyl-6-nitro-1H-indol-3-yl)-acetimidic acid isopropyl ester hydrochloride.
Sources & evidence
- ORD record
- ord-62aad09d4eaa488ba59d37f3d720d4e3
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06228877B1
Reaction notes
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