反应详情

145 mg of 3-[4,5-diphenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-2-yl]-propionic acid were dissolved in THF (0.13 mL)/DCM (0.5 mL). 0.160 mL of DIPEA, 50 mg of HOBt and 71 mg of EDC were added sequentially at rt. The reaction mixture was stirred for 5 min then 80 mg of rac-(1R*,2R*,4R*)-2-(2-methylamino-ethyl)-5-phenyl-bicyclo[2.2.2]oct-5-en-2-ol were added at rt. The reaction mixture was stirred on at rt then diluted with DCM and washed with sat.-NaHCO3 and brine. The organic phase was dried over anh. Na2SO4, filtered and concentrated in vacuo. The resulting crude material was purified by CC using EtOAc/MeOH/NEt3 as eluant from 100/0/1 to 95/5/1 to yield 189 mg of rac-3-[4,5-diphenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-2-yl]-N-[2-((1R*,2R*,4R*)-2-hydroxy-5-phenyl-bicyclo[2.2.2]oct-5-en-2-yl)-ethyl]-N-methyl-propionamide as a yellow oil.

1. stirringThe reaction mixture was stirred on at rt
2. washwashed with sat.-NaHCO3 and brine
3. dry with materialThe organic phase was dried over anh. Na2SO4
4. filtrationfiltered
5. concentrationconcentrated in vacuo
6. customThe resulting crude material was purified by CC