反应详情
EQUATION
反应方程式
REACTANTS
反应物
Sodium Hydroxide
HNaO
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
3-(4-Bromophenyl)propionic acid
C9H9BrO2
1H-Benzotriazol-1-ol--water (1/1)
C6H7N3O2
(1R)-2-Amino-1-(pyridin-3-yl)ethan-1-ol--hydrogen chloride (1/2)
C7H12Cl2N2O
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a suspension of (1R)-2-amino-1-(3-pyridyl)ethanol dihydrochloride (2.90 g), 3-(4-bromophenyl)propionic acid (3.30 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.77 g) and 1-hydroxybenzotriazole hydrate (2.92 g) in N,N-dimethylformamide (30 ml) was added triethylamine (4.02 ml) at 4° C. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was poured into water (145 ml) and the pH was adjusted to 10 with 24% aqueous sodium hydroxide solution at 4° C. The mixture was stirred at room temperature for 30 minutes. The precipitate was collected by filtration, washed with water and dried at 50° C. to give 3-(4-bromophenyl)-N-[(2R)-2-hydroxy-2-(3-pyridyl)ethyl]propanamide (4.32 g) as a white solid. The filtrate was extracted with ethyl acetate, washed with water and brine and dried over magnesium sulfate. Filtration followed by evaporation under reduced pressure gave 3-(4-bromophenyl)-N-[(2R)-2-hydroxy-2-(3-pyridyl)ethyl]propanamide (0.43 g) as a white solid.
WORKUP
后处理
- stirringThe mixture was stirred at room temperature for 30 minutes
- filtrationThe precipitate was collected by filtration
- washwashed with water
- customdried at 50° C.