HRID549438

反应详情

EQUATION

反应方程式

HRID 549438 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of NaOH (6.5 g, 153.6 mmol; assay=94.52%), water (157 ml), ethanol (157 ml, technical grade, contains ˜5% 2-propanol) and Trandolapril (31.5 g, 72.94 mmol; assay=99.7%) was stirred at an internal temperature ranging from about 20° C. to about 25° C. for 15 hours. After an in-process control showed an almost complete saponification (by HPLC), the clear solution was concentrated in vacuo to an amount of 167.05 g, and n-butanol (160 ml) was added to the concentrated product. This mixture was heated to an internal temperature ranging from about 60° C. to about 70° C., and 2N aqueous hydrochloric acid was added (150.4 mmol), whereupon the pH dropped down from 12.09 to 3.66. The organic layer was separated at an internal temperature of 66° C., and the aqueous layer was extracted again with n-butanol (80 ml) at an internal temperature of 65° C. The combined organic layers were washed twice with water (each 40 ml) at an internal temperature ranging from about 63° C. to about 65° C. The organic layer then obtained (total amount 306.4 g) was concentrated in vacuo at a temperature ranging from about 50° C. to about 60° C., whereupon after concentration to an amount of 190 g a white solid precipitated. This suspension was further concentrated in vacuo to an amount of 75.1 g, and 80 ml MTBE was added to complete the precipitation. The suspension was stirred at an internal temperature ranging from about 20° C. to about 25° C. for 3.5 hours. After filtration, the wet product was washed twice with MTBE (each 80 ml) and dried in vacuo for 15 hours at 40° C. to give Trandolaprilat as disolvate with n-butanol (yield: 36.51 g, 66.67 mmol, 91.4%; assay (0.1N HClO4)=73.5%; HPLC purity=100%).

WORKUP

后处理

  1. concentrationthe clear solution was concentrated in vacuo to an amount of 167.05 g, and n-butanol (160 ml)
  2. additionwas added to the concentrated product
  3. temperatureThis mixture was heated to an internal temperature
  4. customranging from about 60° C. to about 70° C.
  5. addition2N aqueous hydrochloric acid was added (150.4 mmol)
  6. additionwhereupon the pH dropped down from 12.09 to 3.66
  7. customThe organic layer was separated at an internal temperature of 66° C.
  8. extractionthe aqueous layer was extracted again with n-butanol (80 ml) at an internal temperature of 65° C
  9. washThe combined organic layers were washed twice with water (each 40 ml) at an internal temperature
  10. customranging from about 63° C. to about 65° C
  11. customThe organic layer then obtained (total amount 306.4 g)
  12. concentrationwas concentrated in vacuo at a temperature
  13. customranging from about 50° C. to about 60° C.
  14. concentrationwhereupon after concentration to an amount of 190 g a white solid
  15. customprecipitated
  16. concentrationThis suspension was further concentrated in vacuo to an amount of 75.1 g, and 80 ml MTBE
  17. additionwas added
  18. customthe precipitation
  19. waitranging from about 20° C. to about 25° C. for 3.5 hours
  20. filtrationAfter filtration
  21. washthe wet product was washed twice with MTBE (each 80 ml) and
  22. customdried in vacuo for 15 hours at 40° C.