反应详情

温度

80 °C

To a solution of 2-[5-(4-Bromo-phenyl)-1H-imidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester (1.00 g, 2.5 mmol) and [2-Methyl-1-(2-{5-[6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-naphthalen-2-yl]-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl)-propyl]-carbamic acid methyl ester (1.97 g, 3.6 mmol, 1.5 equiv.) in DME (12.5 mL) was added K3PO4 (aqueous, 2 M, 3.9 mL, 7.8 mmol, 3 equiv.), Pd2 dba3 (0.12 g, 0.13 mmol, 0.05 equiv.), and Xantphos (0.15 g, 0.26 mmol, 0.1 equiv.). The slurry was degassed with argon for 5 minutes and heated to 80° C. for 18 hours. The resulting reaction mixture was diluted with EtOAc/MeOH (10:1) and filtered through CELITE. The solution was washed with water and brine. The aqueous layer was back-extracted with EtOAc and the combined organic layers were dried over Na2SO4 and concentrated. The crude oil was purified by column chromatography (SiO2, 50→100% EtOAc in Hexanes) to provide 2-{5-[4-(6-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-naphthalen-2-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carboxylic acid tert-butyl ester (0.93 g, 49%) as a yellow powder. LCMS-ESI+: calc'd for C42H49N7O5: 731.4 (M+). Found: 732.9 (M+H+).

1. customThe slurry was degassed with argon for 5 minutes
2. customThe resulting reaction mixture
3. filtrationfiltered through CELITE
4. washThe solution was washed with water and brine
5. extractionThe aqueous layer was back-extracted with EtOAc
6. dry with materialthe combined organic layers were dried over Na2SO4
7. concentrationconcentrated
8. customThe crude oil was purified by column chromatography (SiO2, 50→100% EtOAc in Hexanes)