反应详情

The crude methyl N-[(2R)-2-(2,3-dihydro-1H-inden-2-yl)-2-({[(phenylmethyl)oxy]carbonyl}amino)acetyl]-N-[1-(2,6-dimethyl-3-pyridinyl)-2-oxo-2-({2-[(phenylmethyl)oxy]phenyl}amino)ethyl]-D-alloisoleucinate (intermediate 1) (7.46 g) was dissolved in ethanol (150 mL) and acetic acid (10 mL) and the mixture was hydrogenated at 1 atmosphere of H2 over 10% palladium on carbon (Degussa type) (1.8 g wetted with water 1:1 w:w) for 18 h. The reaction mixture was evaporated under reduced pressure and the residue was partitioned between ethyl acetate and water with saturated aqueous sodium hydrogen carbonate added until the aqueous phase was basic (pH 8). The aqueous phase was extracted with ethyl acetate and the combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate:water 3:1 (100 mL) then with saturated brine before being dried over anhydrous magnesium sulphate and evaporated under reduced pressure. The crude product was purified on a Redisep silica column (120 g) eluted with 0-10% methanol in ethyl acetate to give the title compound as a pair of diastereomers (2.94 g).

1. customThe reaction mixture was evaporated under reduced pressure
2. customthe residue was partitioned between ethyl acetate and water with saturated aqueous sodium hydrogen carbonate
3. additionadded until the aqueous phase
4. extractionThe aqueous phase was extracted with ethyl acetate
5. washthe combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate:water 3:1 (100 mL)
6. dry with materialwith saturated brine before being dried over anhydrous magnesium sulphate
7. customevaporated under reduced pressure
8. customThe crude product was purified on a Redisep silica column (120 g)
9. washeluted with 0-10% methanol in ethyl acetate