反应详情

To a solution of 1-(4-ethylpiperazin-1-yl)-3-(4-hydroxyphenyl)isoquinoline (0.30 g) obtained in Example 7 in tetrahydrofuran (15 ml) was added 60% sodium hydride (36 mg) at room temperature. After the evolution of hydrogen was ceased, bromopropionitrile (0.14 g) was added thereto, and the resulting mixture was reacted at room temperature for 12 hr. Ethyl acetate and an aqueous solution of ammonium chloride were added to the reaction solution, and the resulting organic layer was then separated, washed with water, dried and concentrated. To the resulting residue were added ethanol and a 2N aqueous solution of hydrochloric acid, and the resulting mixture was reacted at 50° C. for 30 min, followed by the evaporation. The resulting residue was partitioned between ethyl acetate and water. The resulting organic layer was washed with water and brine, and dried. The solvent was removed, and the resulting residue was purified by NH-silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a pale yellow oil. The oil was converted into a hydrochloride in a conventional manner, to give 0.12 g of the title compound as a yellow powder.

1. customthe resulting mixture was reacted at room temperature for 12 hr
2. customthe resulting organic layer was then separated
3. washwashed with water
4. customdried
5. concentrationconcentrated
6. additionTo the resulting residue were added ethanol
7. customa 2N aqueous solution of hydrochloric acid, and the resulting mixture was reacted at 50° C. for 30 min
8. customfollowed by the evaporation
9. customThe resulting residue was partitioned between ethyl acetate and water
10. washThe resulting organic layer was washed with water and brine
11. customdried
12. customThe solvent was removed
13. customthe resulting residue was purified by NH-silica gel column chromatography (ethyl acetate/hexane system)