反应详情

2.4 g (4.728 mmol) of 3(R)-[(4-benzyloxyphenyl)-methyl]-5(S)-[1(S)-(Boc-amino)-2-cyclohexylethyl]dihydrofuran-2-one in 10 ml of dimethoxyethane are hydrolysed, under a protective gas, with 9.45 ml of a 1M lithium hydroxide solution. After 17 h at RT, the reaction mixture is treated with an ice-cold mixture of 324 ml of sat. NH4Cl solution, 27 ml of 10% citric acid solution and 134 ml of methylene chloride. Methanol is added to dissolve the product completely. The aqueous phase is separated off and extracted 2× with methylene chloride. The organic phases are washed with saline, dried with Na2SO4 and evaporated. The crude product is purified by column chromatography (SiO2, eluent C), with the title compound being obtained. TLC Rf (C)=0.35; tRet (II)=17.88 min FAB-MS (M+H+)=526.

1. dissolutionto dissolve the product completely
2. customThe aqueous phase is separated off
3. extractionextracted 2× with methylene chloride
4. washThe organic phases are washed with saline
5. dry with materialdried with Na2SO4
6. customevaporated
7. customThe crude product is purified by column chromatography (SiO2, eluent C), with the title compound
8. custombeing obtained