反应详情

A solution of 1.58 g (3.47 mmol) of 5(S)-[1(S)-(Boc-amino)-2-phenylethyl]-3(R)-[(2,4-dimethoxyphenyl)methyl]dihydrofuran-2-(3H)-one in 56 ml of ethylene glycol dimethyl ether and 28.2 ml of water is treated, at RT, with 13.87 ml of a 1M solution of LiOH in water, and this mixture is stirred for 1.75 h. After that, the reaction mixture is diluted with ethyl acetate and a little THF and the whole is washed firstly with a mixture consisting of 170.6 ml of sat. ammonium chloride solution and 14.25 ml of 10% citric acid solution (both being cold) and then with saline. The combined aqueous phases are reextracted with ethyl acetate. The combined organic phases are dried over Na2SO4 and evaporated on a RE at about 30° C. The residue, which is the title compound, is triturated with hexane and filtered off with suction. M.p.: 144-145 C.-TLC Rf (D)=at the start.-FAB-MS (M+H)+ =474.-HPLC tRet =14.34 min (gradient II).-IR(KBr) =u.a. 3420, 3350, 2818, 1686, 1518 and 1508 cm-1.-1H-NMR(CD3OD)=inter alia 7.30-7.09/m (5H); 6.94/d (1H); 6.47/d (1H); 6.37/dxd (1H); 3,78 and 3.75/each s (each 3H); 1.33/s (9H).

1. washa little THF and the whole is washed firstly with a mixture
2. dry with materialThe combined organic phases are dried over Na2SO4
3. customevaporated on a RE at about 30° C
4. customis triturated with hexane
5. filtrationfiltered off with suction
6. customat the start.-FAB-MS (M+H)+ =474.-HPLC tRet =14.34 min (gradient II)