2-Aminopyridine → 2-Amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromide
Reaction equation
[Br:1][CH:2]([CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:3](=[O:9])[C:4]([O:6][CH2:7][CH3:8])=[O:5].[NH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=1>C1COCC1>[Br-:1].[NH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N+:20]=1[CH:2]([CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:3](=[O:9])[C:4]([O:6][CH2:7][CH3:8])=[O:5]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of ethyl 3-bromo-2-oxo-5-phenylpentanoate (1.9 g) in THF (10 ml) was added 2-aminopyridine (600 mg) at room temperature, and the reaction mixture was heated under reflux for 15 hr. The precipitated crystals were collected by filtration, washed with THF to give 2-amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromide (1.36 g). 2-Amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromide (1.36 g) was dissolved in ethanol (10 ml), and the mixture was refluxed under heating for 3 hr. The reaction mixture was concentrated, and dissolved in dichloromethane. The solution was washed successively with aqueous sodium bicarbonate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate-diethyl ether to give the object product (950 mg).
Workup
- temperaturethe reaction mixture was heated
- temperatureunder reflux for 15 hr
- filtrationThe precipitated crystals were collected by filtration
- washwashed with THF
Sources & evidence
- ORD record
- ord-2d49868b92164fe7a3e7cbccf989430c
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221836B2
Reaction notes
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