Synthesis and antimicrobial activities of 1-(3-benzyl-4-oxo-3H-quinazolin-2-yl)-4-(substituted)thiosemicarbazide derivatives
A series of 1-(3-benzyl-4-oxo-3H-quinazolin-2-yl)-4-(substituted) thiosemicarbazides (AS1-AS10) were obtained by the reaction of 2-hydrazino- 3-benzyl quinazolin-4(3H)-one (6) with different dithiocarbamic acid methyl ester derivatives. The key intermediate 3-benzyl-2-thioxo-2,3-dihydro-...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Serbian Chemical Society
2015-01-01
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Series: | Journal of the Serbian Chemical Society |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0352-5139/2015/0352-51391500053A.pdf |
Summary: | A series of 1-(3-benzyl-4-oxo-3H-quinazolin-2-yl)-4-(substituted)
thiosemicarbazides (AS1-AS10) were obtained by the reaction of 2-hydrazino-
3-benzyl quinazolin-4(3H)-one (6) with different dithiocarbamic acid methyl
ester derivatives. The key intermediate
3-benzyl-2-thioxo-2,3-dihydro-1Hquinazolin-4-one (4) was obtained by reacting
benzyl amine (1) with carbon disulphide and sodium hydroxide in dimethyl
sulphoxide to give sodium dithiocarbamate, which was methylated with dimethyl
sulfate to yield the dithiocarbamic acid methyl ester (2) and condensed with
methyl anthranilate (3) in ethanol yielded the desired compound (4) via the
thiourea intermediate. The SH group of compound (4) was methylated for the
favorable nucleophilic displacement reaction with hydrazine hydrate, which
afford 2-hydrazino-3- benzyl-3H-quinazolin-4-one (6). The IR, 1H, and 13C NMR
spectrum of these compounds showed the presence of peaks due to
thiosemicarbazides, carbonyl (C=O), NH and aryl groups. The quinazolin-4-one
moiety molecular ion peaks (m/z 144) were observed all the mass spectrum of
compounds (AS1-AS10). Elemental (C, H, N) analysis satisfactorily confirmed
purity of the synthesized compounds and elemental composition. All
synthesized compounds were also screened for their antimicrobial activity
against selective gram positive and gram negative by agar dilution method. In
the present study compounds AS8 and AS9 were emerged as the most active
compounds of the series. |
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ISSN: | 0352-5139 1820-7421 |