HRID1837965

反应详情

EQUATION

反应方程式

HRID 1837965 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-20 °C

PROCEDURE

实验过程

To a −30° C. solution of 2-(N-methyl-3-phenylprop-2-ynoylamino)acetic acid (100.0 g, 0.460 mol, 1.1 equiv) and Et3N (117 mL, 0.836 mol, 2 equiv) in THF (1100 mL) was added a solution of PivCl (57 mL, 0.460 mol, 1.1 equiv) in THF (100 mL) at such a rate that the temperature was maintained below −20° C. The resulting white slurry was stirred at −20° C. Meanwhile, a −78° C. solution of (S)-(−)-4-benzyl-2-oxazolidinone (74.1 g, 0.418 mol) in THF (900 mL) was treated with a solution of n-BuLi (2.5M in hexane, 185 mL, 0.460 mol, 1.1 equiv) at such a rate that the temperature was maintained below −68° C. The reaction was stirred at −78° C. for 15 min. To this mixture was added via cannula a −78° C. solution of the mixed anhydride prepared above. The reaction was allowed to warm to −10° C. over 30 min and treated with a saturated NH4Cl solution (500 mL). The resulting mixture was concentrated under reduced pressure and the residue was partitioned between water (200 mL) and EtOAc (500 mL). The organic layer was washed with water (3×300 mL), a saturated NaHCO3 solution (2×300 mL) and a saturated NaCl solution (2×300 mL), dried (Na2SO4) and concentrated under reduced pressure. The crude product was purified by flash chromatography (gradient from 25% to 65% EtOAc/hex) to give N-{2-[(4S)-2-oxo-4-benzyl(1,3-oxazolidin-3-yl)]-2-oxoethyl}-N-methyl-3-phenylprop-2-ynamide (119.6 g, 74%) as a white foam. Analytical data of this product was identical to Intermediate R obtained by Method 1.

WORKUP

后处理

  1. temperaturewas maintained below −20° C
  2. temperaturewas maintained below −68° C
  3. stirringThe reaction was stirred at −78° C. for 15 min
  4. customprepared above
  5. temperatureto warm to −10° C. over 30 min
  6. concentrationThe resulting mixture was concentrated under reduced pressure
  7. customthe residue was partitioned between water (200 mL) and EtOAc (500 mL)
  8. washThe organic layer was washed with water (3×300 mL)
  9. dry with materiala saturated NaHCO3 solution (2×300 mL) and a saturated NaCl solution (2×300 mL), dried (Na2SO4)
  10. concentrationconcentrated under reduced pressure
  11. customThe crude product was purified by flash chromatography (gradient from 25% to 65% EtOAc/hex)