Sodium Hydroxide → (2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid
Reaction equation
[NH2:1][C:2]1[N:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[C:10]([O:12]CC2C=CC=CC=2)=[O:11])=[CH:4][CH:3]=1.[OH-].[Na+]>CO>[NH2:1][C:2]1[N:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of benzyl (E)-3-(6-aminopyridin-3-yl)acrylate (1.3 g, 5.1 mmole) and 1.0 N NaOH (10 mL, 10 mmole) in MeOH was heated at reflux overnight. The solution was concentrated in vacuo, and the residue was dissolved in H2O. The pH was adjusted to 6 with dilute HCl, and the solid precipitate was collected by suction filtration and dried to give the title compound (0.6 g, 72%) as a white solid: MS (ES) m/e 165 (M+H)+.
Workup
- temperatureat reflux overnight
- concentrationThe solution was concentrated in vacuo
- dissolutionthe residue was dissolved in H2O
- filtrationthe solid precipitate was collected by suction filtration
- customdried
Sources & evidence
- ORD record
- ord-22dff599117b4496afa28250ead3d7ed
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741339B2
Reaction notes
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