反应详情
EQUATION
反应方程式
REACTANTS
反应物
1-Hydroxybenzotriazole
C6H5N3O
Diisopropylethylamine
C8H19N
Methanaminium, N-[(1H-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methyl-, hexafluorophosphate(1-) (1:1)
C11H16F6N5OP
(2S)-2-[[(1,1-Dimethylethoxy)carbonyl]methylamino]butanoic acid
C10H19NO4
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of (S)-2-(tert-butoxycarbonyl-methyl-amino)-butyric acid (53.0 mg, 0.24 mmol) in DMA (2 mL) is added HBTU (125.0 mg, 0.33 mmol), HOBt (44.6 mg, 0.33 mmol) and diisopropylethylamine (192 uL, 1.1 mmol). The mixture is stirred at room temperature for 5 minutes. A solution of compound F in DCM (2 mL) is added to the above mixture at 0° C. The reaction mixture is stirred at room temperature for 1 hour and concentrated under vacuum. The residue is diluted with EtOAc. The organic is washed with brine, citric acid(5%), brine, NaHCO3(Sat.) and brine. The organic layer is then dried and concentrated under vacuum. The crude oil is used directly in the next step without further purification. M+H+=554.
WORKUP
后处理
- stirringThe reaction mixture is stirred at room temperature for 1 hour
- concentrationconcentrated under vacuum
- additionThe residue is diluted with EtOAc
- washThe organic is washed with brine, citric acid(5%), brine, NaHCO3(Sat.) and brine
- customThe organic layer is then dried
- concentrationconcentrated under vacuum
- customThe crude oil is used directly in the next step without further purification