HRID465196

反应详情

EQUATION

反应方程式

HRID 465196 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of 0.228 g of DMF in 5 ml of methylene chloride is added at -10° C. 0.137 ml of diphosgene. The mixture is then stirred for 30 minutes at room temperature, to which is added at a temperature of -70° C. 15 ml of methylene chloride solution containing 0.80 g of 2-(2-chloroacetamidothiazol-4-yl)-2-methoxyiminoacetic acid and 0.316 g of triethylamine. The mixture is stirred for two hours at -25° C., then cooled to -70° C., followed by addition of 0.632 g of triethyl amine, 0.69 g of tosyl salt of (3R,4S)-3-amino-4-methylthio-2-oxoazetidine and 2 ml of propylene oxide. The temperature of the mixture is raised up to 0° C. in the course of one hour, while stirring. The mixture is stirred for further two hours at the same temperature, then concentrated, followed by addition of THF and removal of the resulting insolubles by filtration. The filtrate is concentrated and the residue is purified on a silica-gel column (AcOEt:CHCl3 :CH3OH =3:3:1) to yield 0.461 g of (3R,4S)-3-[2-(2-chloroacetamidothiazol-4-yl)-2-methoxyiminoacetamido]-4-methylthio-2-oxoazetidine.

WORKUP

后处理

  1. additionis added at a temperature of -70° C
  2. stirringThe mixture is stirred for two hours at -25° C.
  3. temperaturecooled to -70° C.
  4. temperatureThe temperature of the mixture is raised up to 0° C. in the course of one hour
  5. stirringwhile stirring
  6. stirringThe mixture is stirred for further two hours at the same temperature
  7. concentrationconcentrated
  8. additionfollowed by addition of THF and removal of the resulting insolubles by filtration
  9. concentrationThe filtrate is concentrated
  10. customthe residue is purified on a silica-gel column (AcOEt:CHCl3 :CH3OH =3:3:1)