反应详情
EQUATION
反应方程式
REACTANTS
反应物
Methanesulfonic acid
CH4O3S
1-Hydroxybenzotriazole
C6H5N3O
N-((1,1-Dimethylethoxy)carbonyl)-beta-alanine
C8H15NO4
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
Methyl N-[(benzyloxy)carbonyl]-3-[(tert-butoxycarbonyl)amino]-L-alaninate
C17H24N2O6
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The product (6.0 g) obtained in the above (3) is dissolved in acetonitrile (10 ml), and thereto is added dropwise a solution of methanesulfonic acid (8.181 g) in acetonitrile (15 ml) at a temperature below 20° C., and the mixture is stirred at room temperature for 30 minutes. At a temperature below 20° C., to the mixture are added dropwise DMF (20 ml), triethylamine (8.608 g) successively, and the mixture is stirred for 10 minutes. To the mixture are added N-Boc-β-alanine (3.547 g) and HOBT.H2O (3.13 g), and then further added thereto WSC.HCl (3.928 g) at a temperature of from 5 to 10° C., and the mixture is stirred for 30 minutes. The mixture is further stirred at room temperature for 12 hours, and poured into water, and extracted three time with ethyl acetate. The organic layer is washed successively with 1N HCl (twice), a saturated aqueous sodium hydrogen carbonate solution (twice) and a saturated brine (twice), and dried over anhydrous magnesium sulfate. The desiccant is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is purified by silica gel column chromatography (silica gel; 400 g, solvent; chloroform/acetone=3:1 to 2:1). The fractions containing the title compound are concentrated under reduced pressure to give the title compound (6.974 g).
WORKUP
后处理
- stirringthe mixture is stirred for 10 minutes
- stirringThe mixture is further stirred at room temperature for 12 hours
- extractionextracted three time with ethyl acetate
- washThe organic layer is washed successively with 1N HCl (twice), a saturated aqueous sodium hydrogen carbonate solution (twice) and a saturated brine (twice), and
- dry with materialdried over anhydrous magnesium sulfate
- customThe desiccant is removed by filtration
- concentrationthe filtrate is concentrated under reduced pressure
- customThe residue is purified by silica gel column chromatography (silica gel; 400 g, solvent; chloroform/acetone=3:1 to 2:1)
- additionThe fractions containing the title compound
- concentrationare concentrated under reduced pressure