Synthesis and Anticholinesterase Activity of 3-{[4-Methyl-3-(4-methylpiperazin-1-yl)]pent-1-en-1-yl}-4H-chromen-4-ones


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详细

A procedure has been developed and optimized for the synthesis of 3-{[4-methyl-3-(4-methylpiperazin-1-yl)]pent-1-en-1-yl}-4H-chromen-4-ones (as dihydrochlorides) by an unusual version of the Morita–Baylis–Hillman reaction. A number of the title compounds with various substituents in the chromene fragment and their deamination products have been synthesized, and their inhibitory activity against butyrylcholinesterase has been studied.

作者简介

P. Filippova

St. Petersburg State Chemical Pharmaceutical University

Email: nikita.chernov@pharminnotech.com
俄罗斯联邦, St. Petersburg, 197376

N. Chernov

St. Petersburg State Chemical Pharmaceutical University

编辑信件的主要联系方式.
Email: nikita.chernov@pharminnotech.com
俄罗斯联邦, St. Petersburg, 197376

R. Shutov

St. Petersburg State Chemical Pharmaceutical University

Email: nikita.chernov@pharminnotech.com
俄罗斯联邦, St. Petersburg, 197376

I. Yakovlev

St. Petersburg State Chemical Pharmaceutical University

Email: nikita.chernov@pharminnotech.com
俄罗斯联邦, St. Petersburg, 197376


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