反应详情

Piperidine (0.14 g, 1.22 mmol) was dissolved in 50 ml of dry dimethylformamide under a nitrogen atmosphere and sodium hydride (60% in oil) (47 mg, 1.16 mmol) was added. The mixture was stirred for 1/2 hour. 5-Benzyloxy-2-(4-benzyloxyphenyl)-3-((4-chlorobutoxy)methyl)-1-ethylpyrrolo[2,1,5-cd ]indolizine (0.337 g, 0.583 mmol) was added and the mixture was stirred at 55-64° for 7 days. Ethanol (10 ml) was added dropwise, and the reaction mixture was diluted with 250 ml of water. The organic material was extracted into ethyl acetate (3×100 ml), and the combined organic layers were washed with brine and dried over sodium sulfate. The solvent was evaporated and the crude product was purified by column chromatography over silica gel 60, using 5% of methanol in dichloromethane as the eluent. Fractions contaiing the product wre collected to afford 165 mg (52%) of 5-benzyloxy-2-(4-benzyloxyphenyl)-3-((but-3-enyloxy)methyl)-1-ethylpyrrolo[2,1,5-cd ]indolizine as an oil. MS(SP): m/z 541 (M+). 1H-NMR (DMSO-d6, 300 MHz) δ: 1.33 (t, 3H); 2.18 (m, 2H); 3.05 (q, 2H); 3.43 (t, 2H); 4.71 (s, 2H); 4.93-5.07 (m, 2H); 5.19 (s, 2H); 5.58 (s, 2H); 5.72 (m, 1H); 7.18 (d, 2H); 7.30-7.62 (m, 14H); 7.98 (d, 1H).

1. stirringthe mixture was stirred at 55-64° for 7 days
2. extractionThe organic material was extracted into ethyl acetate (3×100 ml)
3. washthe combined organic layers were washed with brine
4. dry with materialdried over sodium sulfate
5. customThe solvent was evaporated
6. customthe crude product was purified by column chromatography over silica gel 60
7. customcollected