反应详情

356 mg (1 mM) of 1,4-dihydro-2,6-dimethyl-5-methoxycarbonyl-4-(2,3-dichlorophenyl)pyridine-3-carboxylic acid together with 215 mg (1 mM) of (E)-3-[4-(1-imidazolylmethyl)phenyl]-2-propen-1-ol, 248 mg (1.2 mM) of dicyclohexyl-carbodiimide and 134 mg (1.1 mM) of 4-N,N-dimethylamino-pyridine were dissolved in 5 ml of toluene, while heating, and refluxed for six hours. The solution was cooled to room temperature, and the crystals produced were filtered off. The filtrate was washed with water and dried over anhydrous sodium sulfate. After the solvent was distilled away, the residue was purified by chromatography on a silica gel column, whereby the captioned compound was obtained. The yield was 481 mg (87%).

1. temperaturewhile heating
2. temperaturerefluxed for six hours
3. customthe crystals produced
4. filtrationwere filtered off
5. washThe filtrate was washed with water
6. dry with materialdried over anhydrous sodium sulfate
7. distillationAfter the solvent was distilled away
8. customthe residue was purified by chromatography on a silica gel column, whereby the captioned compound
9. customwas obtained