HRID1371357

反应详情

EQUATION

反应方程式

HRID 1371357 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

97 mg (0.181 mmol) of tert-butyl (3R)-1-{4-[(5S)-5-({[(5-chloro-2-thienyl)carbonyl]amino}methyl)-2-oxo-1,3-oxazolidin-3-yl]phenyl }-2-oxo-3-pyrrolidinylcarbamate are suspended in 4 ml of methylene chloride, 1.5 ml of trifluoroacetic acid are added and the mixture is stirred at room temperature for 1 hour. The mixture is then concentrated under reduced pressure and the residue is purified on an RP-HPLC (acetonitrile/water/0.1% TFA gradient). Evaporation of the appropriate fraction gives 29 mg (37% of theory) of the target compound of melting point 241° C. (decomp.).

WORKUP

后处理

  1. concentrationThe mixture is then concentrated under reduced pressure
  2. customthe residue is purified on an RP-HPLC (acetonitrile/water/0.1% TFA gradient)
  3. customEvaporation of the appropriate fraction
  4. customgives 29 mg (37% of theory) of the target compound of melting point 241° C. (decomp.)