Sulfuric Acid → (2S,4R)-4-methanesulfonyloxy-1(4-nitrobenzyloxycarbonyl)-2-(2-oxoimidazolidin-1-yl)carbonylpyrrolidine

温度

5 °C

To a mixture of N,N-dimethylformamide (0.6 ml) and tetrahydrofuran (1.2 ml) was added dropwise phosphorus oxychloride (0.58 ml) at -5° C. and the mixture was stirred at 5° C. for 5 minutes. To the mixture was added a solution of (2S,4R)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)proline (2.0 g) in tetrahydrofuran (20 ml) under ice-cooling. The solution was stirred at the same temperature for 30 minutes. To a solution were added ethylene urea (2.22 g) and concentrated sulfuric acid (0.035 ml), and the mixture was stirred at 45°-50° C. for 3 hours. Ethyl acetate (100 ml) and water (40 ml) was poured into the reaction mixture. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and evaporated in vacuo to give a residue. The residue was chromatographed on silica gel (100 g) eluting with a mixture of chloroform and methanol (9:1, V/V). The fractions containing the desired compound were collected and evaporated in vacuo to give (2S,4R)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)-2-(2-oxoimidazolidin-1-yl)carbonylpyrrolidine (1.98 g).

1. temperaturecooling
2. stirringThe solution was stirred at the same temperature for 30 minutes
3. stirringthe mixture was stirred at 45°-50° C. for 3 hours
4. washThe organic layer was washed with saturated aqueous sodium chloride
5. dry with materialdried over anhydrous magnesium sulfate
6. customevaporated in vacuo
7. customto give a residue
8. customThe residue was chromatographed on silica gel (100 g)
9. washeluting with a mixture of chloroform and methanol (9:1, V/V)
10. additionThe fractions containing the desired compound
11. customwere collected
12. customevaporated in vacuo

ORDレコード

ord-5d7910c57b4d493f81a3cea44747f497

出典データセット

uspto-grants-1990_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04925838