反应详情

温度

70 °C

A N,N-dimethylformamide (20 mL) solution of (4R,5R)-4,5-bis(nitrooxy)hexyl 1-chloroethyl carbonate (1.15 g, 3.48 mmol) was added to a stirred N,N-dimethylformamide (20 mL) suspension of 2-butyl-4-chloro-1-{[2′-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylic acid (2.54 g, 3.74 mmol) and cesium carbonate (1.25 g, 3.84 mmol). The solution was stirred at 70° C. for 2 hours. Water (100 mL) was added, and the solution was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with 20-60% ethyl acetate/hexanes to give the title compound as a white solid. 1H NMR (500 MHz, CDCl3) δ 7.90 (d, J=7.4 Hz, 1H), 7.49 (dt, J=1.4, 7.6 Hz, 1H), 7.45 (dt, J=1.1, 7.5 Hz, 1H), 7.31-7.36 (m, 4H), 7.26 (t, J=7.8 Hz, 6H), 7.10 (d, J=8.0 Hz, 6H), 6.93 (d, J=7.8 Hz, 2H), 6.86 (q, J=5.5 Hz, 1H), 6.79 (d, J=8.0 Hz, 2H), 5.54 (d, J=15.4 Hz, 1H), 5.32 (d, J=16.2 Hz, 1H), 5.14-5.24 (m, 2H), 4.10-4.20 (m, 2H), 2.50 (t, J=7.8 Hz, 2H), 1.7-1.9 (m, 4H), 1.62 (quintet, J=7.7 Hz, 2H), 1.54 (d, J=5.5 Hz, 3H), 1.37 (d, J=6.1 Hz, 3H), 1.27 (sextet, J=7.4 Hz, 2H), 0.85 (t, J=7.3 Hz, 3H).

1. extractionthe solution was extracted with ethyl acetate (3×100 mL)
2. dry with materialThe combined organic layers were dried (magnesium sulfate)
3. filtrationfiltered
4. concentrationconcentrated in vacuo
5. customThe residue was purified by column chromatography on silica gel
6. washeluting with 20-60% ethyl acetate/hexanes