Sodium Methoxide → HCID 86671487, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:14]([N+:15]([O-:17])=[O:16])=[C:13](F)[CH:12]=[C:11]([F:19])[C:10]=2[F:20])=[C:4]([F:21])[CH:3]=1.[CH3:22][O-:23].[Na+]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:14]([N+:15]([O-:17])=[O:16])=[C:13]([O:23][CH3:22])[CH:12]=[C:11]([F:19])[C:10]=2[F:20])=[C:4]([F:21])[CH:3]=1Participants
3
Procedure
Intermediate I-4a was prepared from (4-bromo-2-fluoro-phenyl)-(2,3,5-trifluoro-6-nitro-phenyl)-amine (25 g, 0.069 mol) and sodium methoxide (18.6 g, 0.344 mol) using procedures analogous to Intermediate (I-3a) above to afford the product (81% yield).
Sources & evidence
- ORD record
- ord-fd84938a9de84c82990cdd4acfb7f1e5
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08614239B2
Reaction notes
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