Synthesis and Investigation of the Pharmacological Activity of Oreoselone Nitrogen-Containing Derivatives

被引:0
作者
Lipeeva, A. V. [1 ]
Shults, E. E. [1 ]
Morozova, E. A. [1 ]
Tolstikova, T. G. [1 ]
Tolstikov, G. A. [1 ]
机构
[1] Russian Acad Sci, Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Prospekt Akademika Lavrentyeva 9, Novosibirsk 630090, Russia
来源
CHEMISTRY FOR SUSTAINABLE DEVELOPMENT | 2010年 / 18卷 / 04期
关键词
furocoumarins; bromoreoselone; 2-(1,3-dibromopropane-2-ylidene)-2I-furo-[3,2-g][1]benzopyran3,7-dione; motion activity; chloral hydrate sleep;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The bromination of peucedanine using different reagents resulted in the formation of 2-bromoreoselone. Via the reaction with the derivatives of pi peridine and piperazine we synthesized 2-piperazino and 2-pi peridino derivatives of oreoselone. Conditions were determined for the formation of 2-(1,3-dibromopropane-2-ylidene)-2H-furo-[3,2-g][1]-benzopyran-3,7-dione. The interaction of the latter with tyramine resulted in obtaining bis(diaminophenethyl) derivative of furocoumarin. The amination of the mentioned dibromide with the help of spermine resulted in the formation of a macrocyclic compound containing both furocoumarin and polyamine fragments. The effect of novel oreoselone derivatives on the central nervous system was investigated.
引用
收藏
页码:381 / 388
页数:8
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