HRID2104930

反应详情

EQUATION

反应方程式

HRID 2104930 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

70 mg of N-methyl-N-(2,3,4,5,6-pentahydroxyhexyl)-6-{4-[3-[3-(tert-butyldimethylsilanyloxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxoazetidin-2-yl]phenyl}hex-5-enamide are dissolved in 6 ml of methanol. 0.1 N HCl(aq) is then added, and the mixture is stirred at room temperature overnight. The mixture is then neutralized with 1 N aqueous sodium hydroxide solution and concentrated using a rotary evaporator. The residue is stirred with dichloromethane and filtered and the mother liquor is concentrated using a rotary evaporator. The product is obtained following purification by preparative HPLC: C31H44F2N2O8 (682) MS (ESI): M+-18

WORKUP

后处理

  1. concentrationconcentrated
  2. customa rotary evaporator
  3. stirringThe residue is stirred with dichloromethane
  4. filtrationfiltered
  5. concentrationthe mother liquor is concentrated
  6. customa rotary evaporator
  7. customThe product is obtained
  8. custompurification by preparative HPLC