反应详情

温度

50 °C

To a mixture of (R)-1-(3-amino-4-chlorobenzyl)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]pyrrolidine (44.9 mg), methanol (0.95 mL), aceticacid (0.05 mL), and 37% aqueous HCHO solution (0.15 mL) was added NaBH3CN (38 mg). The reaction mixture was stirred at 50° C. overnight. The mixture was cooled to room temperature and evaporated. To the residue was added 2 N aqueous NaOH solution and ethyl acetate, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried and concentrated, and the residue was loaded onto Varian™ SCX column and washed with CH3OH. Product was eluted off using 2 N NH3 in CH3OH and concentrated. The residue was dissolved in 50% conc. HCl/dioxane and the solution was stirred at room temperature for 1 h. The reaction mixture was adjusted to pH 10 with 5 N aqueous NaOH solution and extracted with ethyl acetate (2 times). The combined extracts were dried over Na2SO4, filtered, and evaporated. Preparative TLC (SiO2, 20% MeOH/AcOEt) gave (R)3-[{N-(2-amino-5-trifluoromethylbenzoyl)glycyl}amino]-1-{4-chloro-3-(dimethylamino)benzyl)pyrrolidine (Compound No. 2133). (10.9 mg, 28%): The purity was determined by RPLC/MS (95%); ESI/MS m/e 498.3 (M++H, C23H25ClF3N5O2).

1. temperatureThe mixture was cooled to room temperature
2. customevaporated
3. additionTo the residue was added 2 N aqueous NaOH solution and ethyl acetate
4. customthe organic layer was separated
5. extractionthe aqueous layer was extracted with ethyl acetate
6. customThe combined organic layers were dried
7. concentrationconcentrated
8. washwashed with CH3OH
9. washProduct was eluted off
10. concentrationconcentrated
11. dissolutionThe residue was dissolved in 50% conc. HCl/dioxane
12. stirringthe solution was stirred at room temperature for 1 h
13. extractionextracted with ethyl acetate (2 times)
14. dry with materialThe combined extracts were dried over Na2SO4
15. filtrationfiltered
16. customevaporated