Methyl 3-(bromomethyl)benzoate → Methyl 3-[(2-amino-5-chloro-3-pyridinyl)oxy]methylbenzoate
Reaction equation
[NH2:1][C:2]1[C:7]([OH:8])=[CH:6][C:5]([Cl:9])=[CH:4][N:3]=1.Br[CH2:11][C:12]1[CH:13]=[C:14]([CH:19]=[CH:20][CH:21]=1)[C:15]([O:17][CH3:18])=[O:16]>>[NH2:1][C:2]1[C:7]([O:8][CH2:11][C:12]2[CH:13]=[C:14]([CH:19]=[CH:20][CH:21]=2)[C:15]([O:17][CH3:18])=[O:16])=[CH:6][C:5]([Cl:9])=[CH:4][N:3]=1Participants
3
Procedure
The title compound was prepared using the method of Preparation 22 from 2-amino-5-chloro-3-pyridinol and methyl 3-(bromomethyl)benzoate to give a tan solid:
Workup
- customto give a tan solid
Sources & evidence
- ORD record
- ord-b9afb52e7ae046cf81a1ee8c9cfc6952
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583162B1
Reaction notes
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