HRID85407
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
tert-Butyl 2-((2-aminoethyl)(methyl)amino)ethylcarbamate (500 mg, 2.3 mmol) was taken up in CH3CN (10 mL) along with salicylic acid (310 mg, 2.3 mmol) and EDCI (485 mg, 2.53 mmol). The resulting reaction mixture was stirred at room temperature for 18 h and then diluted with EtOAc. The organic layer was washed with saturated aqueous NaHCO3, brine, dried over Na2SO4 and concentrated under reduced pressure. The resulting residue was purified by chromatography (MeOH—CH2Cl2, 5%) to afford tert-butyl 2-((2-(2-hydroxybenzamido)ethyl)(methyl)amino)ethylcarbamate (380 mg, 49%). Mass calculated for C17H27N3O4: 337.2; found: [M+H]+=338.
WORKUP
后处理
- customThe resulting reaction mixture
- washThe organic layer was washed with saturated aqueous NaHCO3, brine
- dry with materialdried over Na2SO4
- concentrationconcentrated under reduced pressure
- customThe resulting residue was purified by chromatography (MeOH—CH2Cl2, 5%)