反应详情

0.75 g (1.2 mmol) of ethyl (S)-2-(2-benzoylphenylamino)-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propionate (Example 1H) is dissolved in a mixture of 10 ml of tetrahydrofuran, 1 ml of methanol and a few drops of water. 86 mg (2 mmol) of lithium hydroxide are added. The medium is stirred for 6 h and then treated with an aqueous 1N hydrochloric acid solution, extracted with ethyl acetate, dried over magnesium sulfate, and concentrated. The residue obtained is purified by chromatography on a column of silica and eluted with a 1/1 heptane/ethyl acetate mixture. 0.55 g of (S)-2-(2-benzoylphenylamino)-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl)propionic acid is obtained with a 77% yield.

1. extractionextracted with ethyl acetate
2. dry with materialdried over magnesium sulfate
3. concentrationconcentrated
4. customThe residue obtained
5. customis purified by chromatography on a column of silica
6. washeluted with a 1/1 heptane/ethyl acetate mixture