Methanol → Methyl 6-amino-5-bromonicotinate
Reaction equation
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]([OH:10])=[O:9])=[CH:4][C:3]=1[Br:11].[CH3:12]O.[OH-].[Na+]>Cl>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]([O:10][CH3:12])=[O:9])=[CH:4][C:3]=1[Br:11]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
6-Amino-5-bromopyridine-3-carboxylic acid (10 g, 50 mmol) is dissolved in saturated methanolic HCl (100 ml) and refluxed for 24 hours. The solvent, methanol, is re-moved under reduced pressure and the residue is dissolved in ice cold water. The aqueous solution is neutralized with 0.1N NaOH and the solid which separates is filtered; washed well with water and air dried to yield 10 g of product as a solid: mass spectrum 231 (M+) .
Workup
- temperaturerefluxed for 24 hours
- dissolutionthe residue is dissolved in ice cold water
- filtrationthe solid which separates is filtered
- washwashed well with water and air
- customdried
Sources & evidence
- ORD record
- ord-a785f6623c534635b7db369200148464
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719278
Reaction notes
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