反应详情

温度

60 °C

A solution of 1-tert-butyl 2-methyl (2S,4R)-4-hydroxypyrrolidine-1,2-dicarboxylate (10.1 g, 41.4 mmol) in DMF (90 mL) under nitrogen was cooled to 0° C. Solid 1,1′-carbonyldiimidazole (6.70 g, 41.4 mmol) was added to the reaction. The contents of the reaction flask were warmed to room temperature and after 2 h a solution of 4-vinylisoindoline (6.00 g, 41.4 mmol) in DMF (10 mL) was added. The reaction was heated in a 60° C. oil bath for 2 h then cooled and poured into water and 5% potassium bisulfate. The resulting mixture was extracted with ethyl acetate (4×250 mL). Combined organics were washed with brine, dried with anhydrous sodium sulfate, filtered and evaporated. Flash column chromatography eluting with hexane/ethyl acetate 70/30 gave the title compound as a white foam, 13.9 g (33.4 mmol, 81% yield). LRMS (ESI) m/z 417 [(M+H)+; calcd for C22H29N2O6: 417].

1. additionwas added
2. temperaturethen cooled
3. extractionThe resulting mixture was extracted with ethyl acetate (4×250 mL)
4. washCombined organics were washed with brine
5. dry with materialdried with anhydrous sodium sulfate
6. filtrationfiltered
7. customevaporated
8. washFlash column chromatography eluting with hexane/ethyl acetate 70/30