反应详情

A mixture of 1,4-benzodioxan-2-ylmethyl toluene-4-sulphonate (1.68 g, prepared in a similar manner to that described in Example 1), 1-[1-(2-chlorophenyl)piperid-4-yl]methylamine (1.8 g) and potassium carbonate (10 g) in acetonitrile (150 ml) was heated under reflux with stirring for 24 hours. Potassium iodide (0.2 g) was added to the reaction mixture and heating under reflux continued for a further 24 hours. The cooled mixture was filtered and the solvent removed from the filtrate in vacuo. The residue was passed through a silica column using a 1:1 mixture of petroleum ether (b.p. 40°-60° C.) and ethyl acetate as eluant. The solvent was removed from the eluate in vacuo and the clear oily residue dissolved in ether. An excess of an etheral solution of hydrogen chloride was added, and the solvent removed in vacuo to give N-(1,4-benzodioxan-2-ylmethyl)-1-[1-(2-chlorophenyl)piperid-4-yl]methylamine hydrochloride (0.37 g), m.p. 275°-278° C. (dec).

1. customprepared in a similar manner to that
2. temperaturewas heated
3. temperatureunder reflux
4. temperatureheating
5. temperatureunder reflux
6. waitcontinued for a further 24 hours
7. filtrationThe cooled mixture was filtered
8. customthe solvent removed from the filtrate in vacuo
9. additiona 1:1 mixture of petroleum ether (b.p. 40°-60° C.) and ethyl acetate as eluant
10. customThe solvent was removed from the eluate in vacuo
11. dissolutionthe clear oily residue dissolved in ether
12. additionAn excess of an etheral solution of hydrogen chloride was added
13. customthe solvent removed in vacuo