Issue 95, 2015

Novel synthesis and cytotoxic activity of 1,4-disubstituted 3-methylidene-3,4-dihydroquinolin-2(1H)-ones

Abstract

A novel, efficient synthesis of 1,4-disubstituted 3-methylidene-3,4-dihydrodihydroquinolin-2(1H)-ones was accomplished via a three step reaction sequence comprising N-alkylation of 3-diethoxyphosphorylquinolin-2(1H)-one, Michael addition of various Grignard reagents to N-alkylated 3-diethoxyphosphorylquinolin-2(1H)-ones and a Horner–Wadsworth–Emmons reaction of the obtained adducts with formaldehyde. Effective synthesis of the starting 3-diethoxyphosphorylquinolin-2(1H)-one was also developed. Furthermore, the obtained 3-methylidene-3,4-dihydroquinolin-2(1H)-ones were evaluated for their cytotoxic activity.

Graphical abstract: Novel synthesis and cytotoxic activity of 1,4-disubstituted 3-methylidene-3,4-dihydroquinolin-2(1H)-ones

Supplementary files

Article information

Article type
Paper
Submitted
18 Aug 2015
Accepted
09 Sep 2015
First published
10 Sep 2015

RSC Adv., 2015,5, 78324-78335

Novel synthesis and cytotoxic activity of 1,4-disubstituted 3-methylidene-3,4-dihydroquinolin-2(1H)-ones

M. Pięta, J. Kędzia, A. Janecka, D. K. Pomorska, M. Różalski, U. Krajewska and T. Janecki, RSC Adv., 2015, 5, 78324 DOI: 10.1039/C5RA16673J

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