反应详情

温度

0 °C

A mixture of (2S,4S)-1-cyclohexylmethyl-4-[(1-hydroxy-naphthalene-2-carbonyl)-amino]-pyrrolidine-2-carboxylic acid (50 mg, 0.13 mmol) and 2,2,2-trichloro-acetimidic acid tert-butyl ester (70 mg, 0.33 mmol) in THF (1 mL) was stirred at 0° C. for several minutes. Then BF3.OEt2 (20 mg, 0.13 mmol) was added dropwise at 0° C. and the reaction mixture was warmed to room temp. and stirred for 2 h. The reaction mixture was then quenched with brine solution, extracted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate, concentrated and purified by column chromatography (using 5% EtOAc in hexane as eluent) to give (2S,4S)-1-cyclohexylmethyl-4-[(1-hydroxy-naphthalene-2-carbonyl)-amino]-pyrrolidine-2-carboxylic acid tert-butyl ester (20 mg, 35.0% yield) as a bluish sticky liquid. MS calcd. for C27H37N2O4 [(M+H)+] 453.0, obsd. 453.2.

1. temperaturethe reaction mixture was warmed to room temp.
2. stirringstirred for 2 h
3. customThe reaction mixture was then quenched with brine solution
4. extractionextracted with ethyl acetate
5. washwashed with water and brine
6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
7. concentrationconcentrated
8. custompurified by column chromatography (using 5% EtOAc in hexane as eluent)