2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide

The title compound, 2-methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl) ethenyl-3, 4-dihydroquinazolin-3-yl] benzene-1-sulfonamide <strong>2</strong> has been synthesized by the reaction of 3-(4-methoxyphenyl)-2-styryl-4(3<em&gt...

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Main Authors: Sumi Hudiyono, Hayun, Arry Yanuar, Muhammad Hanafi
Format: Article
Language:English
Published: MDPI AG 2012-07-01
Series:Molbank
Subjects:
Online Access:http://www.mdpi.com/1422-8599/2012/3/M765
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spelling doaj-11f56f471009462082b704d0ad467b832020-11-24T21:51:06ZengMDPI AGMolbank1422-85992012-07-0120123M76510.3390/M7652-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamideSumi HudiyonoHayunArry YanuarMuhammad HanafiThe title compound, 2-methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl) ethenyl-3, 4-dihydroquinazolin-3-yl] benzene-1-sulfonamide <strong>2</strong> has been synthesized by the reaction of 3-(4-methoxyphenyl)-2-styryl-4(3<em>H</em>)-quinazolinone <strong>1</strong> with an excess of chlorosulfonic acid, followed by amidation of the sulfonyl chloride product with ammonia gas. The structure of the synthesized compound was confirmed on the basis of IR, <sup>1</sup>H-NMR, <sup>13</sup>C-NMR and mass spectral data.http://www.mdpi.com/1422-8599/2012/3/M7654(3<em>H</em>)-quinazolinone2-styryl-4(3<em>H</em>)-quinazolinonebenzenesulfonamidechlorosulfonation-amidation
collection DOAJ
language English
format Article
sources DOAJ
author Sumi Hudiyono
Hayun
Arry Yanuar
Muhammad Hanafi
spellingShingle Sumi Hudiyono
Hayun
Arry Yanuar
Muhammad Hanafi
2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
Molbank
4(3<em>H</em>)-quinazolinone
2-styryl-4(3<em>H</em>)-quinazolinone
benzenesulfonamide
chlorosulfonation-amidation
author_facet Sumi Hudiyono
Hayun
Arry Yanuar
Muhammad Hanafi
author_sort Sumi Hudiyono
title 2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
title_short 2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
title_full 2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
title_fullStr 2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
title_full_unstemmed 2-Methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
title_sort 2-methoxy-5-{4-oxo-2-[(<em>e</em>)-2-(4-sulfamoylphenyl)ethenyl-3,4-dihydroquinazolin-3-yl]benzene-1-sulfonamide
publisher MDPI AG
series Molbank
issn 1422-8599
publishDate 2012-07-01
description The title compound, 2-methoxy-5-{4-oxo-2-[(<em>E</em>)-2-(4-sulfamoylphenyl) ethenyl-3, 4-dihydroquinazolin-3-yl] benzene-1-sulfonamide <strong>2</strong> has been synthesized by the reaction of 3-(4-methoxyphenyl)-2-styryl-4(3<em>H</em>)-quinazolinone <strong>1</strong> with an excess of chlorosulfonic acid, followed by amidation of the sulfonyl chloride product with ammonia gas. The structure of the synthesized compound was confirmed on the basis of IR, <sup>1</sup>H-NMR, <sup>13</sup>C-NMR and mass spectral data.
topic 4(3<em>H</em>)-quinazolinone
2-styryl-4(3<em>H</em>)-quinazolinone
benzenesulfonamide
chlorosulfonation-amidation
url http://www.mdpi.com/1422-8599/2012/3/M765
work_keys_str_mv AT sumihudiyono 2methoxy54oxo2ltemgteltemgt24sulfamoylphenylethenyl34dihydroquinazolin3ylbenzene1sulfonamide
AT hayun 2methoxy54oxo2ltemgteltemgt24sulfamoylphenylethenyl34dihydroquinazolin3ylbenzene1sulfonamide
AT arryyanuar 2methoxy54oxo2ltemgteltemgt24sulfamoylphenylethenyl34dihydroquinazolin3ylbenzene1sulfonamide
AT muhammadhanafi 2methoxy54oxo2ltemgteltemgt24sulfamoylphenylethenyl34dihydroquinazolin3ylbenzene1sulfonamide
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