反应详情

温度

10 °C

Tert-butoxycarbonylamino-(3-hydroxy-adamantan-1-yl)-acetic acid (100 g; 0.307 mole) was added to dichloromethane (500 ml) with stirring. The methanesulfonic acid salt of (1S,3S,5S)-2-azabicyclo[3.1.0]hexane-3-carboxamide (64.8 g; 0.292 mole) was added, and the reaction mixture was stirred for 15 minutes at 25-35° C. In a separate flask, 1-hydroxybenzotriazole monohydrate (11.8 g; 0.077 mole) and triethylamine (34.2 g) were added to dichloromethane (500 ml) and stirred to form a solution. This solution was added to the reaction mixture gradually over 30 minutes at 25-30° C. The reaction mixture was then cooled to 5-15° C., 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC.HCl) (70.6 g) was added, and the mixture was stirred for 15 minutes at 5-15° C. Triethylamine (65.2 g) was added to the reaction mixture and stirred for 30 minutes. Temperature of the reaction mixture was raised to 25-35° C. and stirred continuously for 12 hours. Reaction completion was confirmed by HPLC. Water (500 ml) was added, the mixture was stirred, and the organic layer was separated. The organic layer was washed with dilute hydrochloric acid solution (500 ml, prepared by adding concentrated hydrochloric acid (60 ml) to water (440 ml)), and further washed with sodium bicarbonate solution (3 times), followed by washing with sodium chloride solution. Hydrogen chloride in isopropanol (14.2% w/w, 315.6 g) was added over 60 minutes, and the mixture was stirred for 4 hours. Completion of the reaction was confirmed by HPLC. The mixture was distilled under vacuum to remove dichloromethane. Toluene was added to the residue and distilled under vacuum. Acetonitrile (400 ml) was added to the residue followed by addition of triethylamine (79.2 g) over 15 minutes with stirring. The reaction mixture was cooled to 10-20° C., and trityl chloride (72.7 g) was added gradually, followed by stirring for 2 hours. Completion of the reaction was confirmed by HPLC. The mixture was distilled under vacuum to remove acetonitrile. Toluene was added to the residue and distilled under vacuum. Toluene (500 ml) followed by water (500 ml) were added to the residue, the mixture was heated at 45-55° C. and filtered and dried to obtain the product. (Yield=60.3%; HPLC purity=94%)

1. stirringthe reaction mixture was stirred for 15 minutes at 25-35° C
2. stirringstirred
3. customto form a solution
4. additionThis solution was added to the reaction mixture gradually over 30 minutes at 25-30° C
5. stirringthe mixture was stirred for 15 minutes at 5-15° C
6. stirringstirred for 30 minutes
7. temperatureTemperature of the reaction mixture was raised to 25-35° C.
8. stirringstirred continuously for 12 hours
9. customReaction completion
10. stirringthe mixture was stirred
11. customthe organic layer was separated
12. washThe organic layer was washed with dilute hydrochloric acid solution (500 ml, prepared by adding concentrated hydrochloric acid (60 ml) to water (440 ml))
13. washfurther washed with sodium bicarbonate solution (3 times)
14. washby washing with sodium chloride solution
15. additionHydrogen chloride in isopropanol (14.2% w/w, 315.6 g) was added over 60 minutes
16. stirringthe mixture was stirred for 4 hours
17. distillationThe mixture was distilled under vacuum
18. customto remove dichloromethane
19. additionToluene was added to the residue
20. distillationdistilled under vacuum
21. additionAcetonitrile (400 ml) was added to the residue
22. additionfollowed by addition of triethylamine (79.2 g) over 15 minutes
23. stirringwith stirring
24. temperatureThe reaction mixture was cooled to 10-20° C.
25. additiontrityl chloride (72.7 g) was added gradually
26. stirringby stirring for 2 hours
27. distillationThe mixture was distilled under vacuum
28. customto remove acetonitrile
29. additionToluene was added to the residue
30. distillationdistilled under vacuum
31. additionwere added to the residue
32. temperaturethe mixture was heated at 45-55° C.
33. filtrationfiltered
34. customdried
35. customto obtain the product