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
To a stirred mixture of L-allo-threonine (0.150 g, 1.25 mmol) and NaHCO3 (0.158 g, 1.89 mmol) in H2O (3.5 mL), the crude mixture containing 1-(4-phenylphenyl)ethyl-2-pyridyl-carbonate and 5-phenyl-pentyl-2-oxopyridine 1-carboxylate (0.538 g, 1.89 mmol) in THF (3.5 mL) was added. After 15 h at rt, the crude mixture was rotary evaporated to remove the organics and subsequently extracted with Et2O (3×5 mL). The aqueous phase was acidified with 2M HCl solution to pH 2-3 and subsequently extracted with AcOEt (3×10 mL). The organic fraction was dried over Na2SO4, filtered and concentrated to dryness to afford the title compound (0.35 g, 89%) as transparent oil, which was used in the next step without further purification. MS (ESI) m/z: 310 [M−H]+; (ESI) m/z: 308 [M−H]−. 1H NMR (DMSO-d6): δ 1.08 (d, J=6.1 Hz, 3H), 1.28-1.39 (m, 2H), 1.50-1.64 (m, 4H), 2.57 (t, J=7.7 Hz, 2H), 3.83-3.98 (m, 4H), 7.12 (d, J=8.7 Hz, 1H), 7.14-7.21 (m, 3H), 7.23-7.30 (m, 2H) 12.32 (br s, 1H).
WORKUP
后处理
- additionwas added
- customthe crude mixture was rotary evaporated
- customto remove the organics and
- extractionsubsequently extracted with Et2O (3×5 mL)
- extractionsubsequently extracted with AcOEt (3×10 mL)
- dry with materialThe organic fraction was dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated to dryness