2-(Bromomethyl)pyridine hydrobromide → 2,6-Difluoro-4-(pyridin-2-ylmethoxy)-benzoic Acid Methyl Ester
Reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]1[C:9]([F:10])=[CH:8][C:7]([OH:11])=[CH:6][C:5]=1[F:12].Br.Br[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=1>>[CH3:1][O:2][C:3](=[O:13])[C:4]1[C:5]([F:12])=[CH:6][C:7]([O:11][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=2)=[CH:8][C:9]=1[F:10]Participants
3
Procedure
The title compound is prepared in a manner substantially analogous to Procedure E from 2,6-Difluoro-4-hydroxy-benzoic acid methyl ester and 2-(bromomethyl)pyridine hydrobromide. MS (ES+) 280
Sources & evidence
- ORD record
- ord-0ac095cd3c9544a683063b8750173a50
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696234B2
Reaction notes
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