1-Bromo-5-fluoro-2-methyl-3-nitrobenzene → 4-Bromo-6-fluoro-1H-indole
Reaction equation
CN(C)S([C:6]1[CH:14]=[C:13]2[C:9]([CH:10]=[CH:11][NH:12]2)=[C:8]([Br:15])[CH:7]=1)(=O)=O.BrC1C=C([F:24])C=C([N+]([O-])=O)C=1C>>[Br:15][C:8]1[CH:7]=[C:6]([F:24])[CH:14]=[C:13]2[C:9]=1[CH:10]=[CH:11][NH:12]2Participants
3
Procedure
Prepared according to the method used in the preparation of 4-bromo-1H-indole-6-sulfonic acid dimethylamide using 1-bromo-5-fluoro-2-methyl-3-nitro-benzene in place of 3-bromo-4-N,N-trimethyl-5-nitro-benzenesulfonamide. The title compound was obtained as a white solid (6.06 g, 33%).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-fc678e33e145496ba290d55824f81a21
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08293735B2
Reaction notes
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