Sodium Hydroxide → 6-[(Propan-2-yl)oxy]pyridine-3-carboxylic acid
Reaction equation
[CH:1]([O:4][C:5]1[CH:16]=[CH:15][C:8]([C:9]([O:11]C(C)C)=[O:10])=[CH:7][N:6]=1)([CH3:3])[CH3:2].[OH-].[Na+]>>[CH:1]([O:4][C:5]1[CH:16]=[CH:15][C:8]([C:9]([OH:11])=[O:10])=[CH:7][N:6]=1)([CH3:3])[CH3:2]Participants
3
Procedure
In a similar manner to that described in Example 2, a reaction was carried out using isopropyl 6-isopropoxynicotinate (130 mg), which is the product of Reference example 18(a) and aqueous sodium hydroxide solution (1N, 0.87 ml) and the reaction mixture was treated to afford the title compound (106 mg) as crystals.
Workup
- additionthe reaction mixture was treated
Sources & evidence
- ORD record
- ord-831b9ce2d6f041a8830776380c06becd
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
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