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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Resumo

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.

Sobre autores

P. Filippova

St. Petersburg State Chemical Pharmaceutical University

Email: nikita.chernov@pharminnotech.com
Rússia, St. Petersburg, 197376

N. Chernov

St. Petersburg State Chemical Pharmaceutical University

Autor responsável pela correspondência
Email: nikita.chernov@pharminnotech.com
Rússia, St. Petersburg, 197376

R. Shutov

St. Petersburg State Chemical Pharmaceutical University

Email: nikita.chernov@pharminnotech.com
Rússia, St. Petersburg, 197376

I. Yakovlev

St. Petersburg State Chemical Pharmaceutical University

Email: nikita.chernov@pharminnotech.com
Rússia, St. Petersburg, 197376


Declaração de direitos autorais © Pleiades Publishing, Ltd., 2019

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