HRID1777283

反应详情

EQUATION

反应方程式

HRID 1777283 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

5

PROCEDURE

实验过程

34.7 mL of BSTFA are added to a suspension of 6.3 g of azacytosine in 126 mL of acetonitrile. The mixture is brought to 50° C. and it is stirred for 90 minutes. 11.35 mL of trimethylsilyltriflate and then a suspension of 29.0 g of 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose in 50 mL of acetonitrile are added to the limpid solution, in about ten minutes. Stirring is maintained for 75 minutes, it is cooled to ambient temperature and it is slowly poured onto a mixture constituted by 500 ml of dichloromethane and 330 ml of water into which 9.5 g of sodium bicarbonate had been previously dissolved. Stirring is carried out for 15 minutes and the pH is adjusted to pH=4.5 using acetic acid. The mixture is left to settle and phases are separated. The aqueous phase is washed twice using 125 ml of dichloromethane for each washing. The organic phases which are anhydrified by treating them with anhydrous calcium chloride are combined. Concentration is carried out at low pressure until a viscous residue is obtained. The residue is recovered with 250 mL of methanol, it is concentrated once again at low pressure until a viscous residue is obtained. 250 mL of methanol are added, it is heated to 50° C. and 15 mL of a 10% solution of sodium methylate in methanol are added. It is stirred for 1 hour, it is cooled to ambient temperature, it is stirred to complete precipitation and the solid is filtered by washing it on the filter with methanol. 5.4 g of azacitidine with HPLC purity (UV 254 nm) of 94.1% are obtained after drying at low pressure.

WORKUP

后处理

  1. customis brought to 50° C.
  2. additionare added to the limpid solution, in about ten minutes
  3. stirringStirring
  4. temperatureis maintained for 75 minutes
  5. additionit is slowly poured onto a mixture
  6. dissolutionhad been previously dissolved
  7. stirringStirring
  8. waitis carried out for 15 minutes
  9. waitThe mixture is left
  10. customphases are separated
  11. washThe aqueous phase is washed twice
  12. additionby treating them with anhydrous calcium chloride
  13. concentrationConcentration
  14. customis obtained
  15. customThe residue is recovered with 250 mL of methanol, it
  16. concentrationis concentrated once again at low pressure until a viscous residue
  17. customis obtained
  18. temperatureit is heated to 50° C.
  19. stirringIt is stirred for 1 hour
  20. temperatureit is cooled to ambient temperature
  21. stirringit is stirred to complete precipitation
  22. filtrationthe solid is filtered
  23. washby washing it on the
  24. filtrationfilter with methanol