反应详情
EQUATION
反应方程式
REACTANTS
反应物
1-Hydroxybenzotriazole
C6H5N3O
Diisopropylethylamine
C8H19N
Morpholin-4-yl-acetic acid
C6H11NO3
Sodium Bicarbonate
CHNaO3
Methanaminium, N-[(1H-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methyl-, hexafluorophosphate(1-) (1:1)
C11H16F6N5OP
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)-benzyl 2-((S)-2-aminopropanamido)-3-(4-methoxyphenyl)propanoate (HCl salt, 21.0 g, 53.5 mmol) in DMF (200 mL) at 0° C. was added HBTU (30.4 g, 80.3 mmol) and HOBt (10.8 g, 80.3 mmol). The mixture was stirred for 5 min then 2-morpholinoacetic acid (8.15 g, 56.2 mmol) and DIEA (46.5 mL, 214 mmol) were added. The reaction mixture was stirred at ambient temperature for 30 min. Saturated aqueous NaHCO3 (200 mL) was then added and the resulting mixture was extracted with EtOAc (300 mL×2). The combined extracts were washed with brine (400 mL), dried over anhydrous sodium sulfate, and concentrated. Purification of the residue by flash column chromatography on silica gel (heptane to EtOAc/heptane=3:2) afforded (S)-benzyl 3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoate (23.0 g, 89% yield) as a colorless solid.
WORKUP
后处理
- stirringThe reaction mixture was stirred at ambient temperature for 30 min
- extractionthe resulting mixture was extracted with EtOAc (300 mL×2)
- washThe combined extracts were washed with brine (400 mL)
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated
- customPurification of the residue by flash column chromatography on silica gel (heptane to EtOAc/heptane=3:2)