HRID1158535

反应详情

EQUATION

反应方程式

HRID 1158535 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A mixture of (2S)-2-Benzyl-N-((1S)-2,2-dimethyl-1-methylcarbamoyl-propyl)-2,4-dihydroxy-butyramide (52S) (0.337 g, 1.00 mmol), IBX (0.560 g, 2.0 mmol) and 10 mL 1,2-dichloroethane in a reaction vial sealed with a screw cap was heated at 80° C. for 2 h. The resulting suspension was transferred to a 20 mL syringe and filtered through a syringe filter into a solution of hydrazide (9) (0.372 g, 1.00 mmol) in 15 mL DCE in a flame dried 50 mL round-bottom flask equipped with a septum. To this was added acetic acid (0.12 mL 2.0 mmol), mixture was stirred for 10 min and then sodium triacetoxyborohydride (0.636 g, 3.0 mmol) was added. The septum-sealed flask was flushed with nitrogen and the reaction was stirred at room temperature for 24 h. The reaction was quenched by addition of water and volatiles were evaporated. The residue was dissolved in 50% MeCN/water and purified by preparative RP-LC-MS (repeated 1 mL injections) to give 0.191 g of the title compound (28% yield).

WORKUP

后处理

  1. customin a reaction
  2. customvial sealed with a screw
  3. customcap
  4. customThe resulting suspension was transferred to a 20 mL syringe
  5. filtrationfiltered through a syringe
  6. customdried 50 mL round-bottom flask
  7. customequipped with a septum
  8. customThe septum-sealed flask was flushed with nitrogen
  9. stirringthe reaction was stirred at room temperature for 24 h
  10. customThe reaction was quenched by addition of water and volatiles
  11. customwere evaporated
  12. dissolutionThe residue was dissolved in 50% MeCN/water
  13. custompurified by preparative RP-LC-MS (repeated 1 mL injections)