6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one
The titular compound, 6-amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one, was prepared from 7-fluoro-6-nitroquinazolin-4(3H)-one via a nucleophilic aromatic substitution reaction followed by a reduction of the nitro group. Characterization of the target compound via 1H NMR, 13C NMR, and HRMS conf...
Gespeichert in:
Veröffentlicht in: | MolBank 2024-12, Vol.2024 (4), p.M1942 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 4 |
container_start_page | M1942 |
container_title | MolBank |
container_volume | 2024 |
creator | Thapa, Susila Bolliger, Jeanne L. |
description | The titular compound, 6-amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one, was prepared from 7-fluoro-6-nitroquinazolin-4(3H)-one via a nucleophilic aromatic substitution reaction followed by a reduction of the nitro group. Characterization of the target compound via 1H NMR, 13C NMR, and HRMS confirmed its structure. |
doi_str_mv | 10.3390/M1942 |
format | Article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_proquest_journals_3149683132</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_b65954bbedc145308b6055e5dcecaa61</doaj_id><sourcerecordid>3149683132</sourcerecordid><originalsourceid>FETCH-LOGICAL-c209t-9610d574248b247a2c37dc5ff09f38d152bbaa05d4af62c6b697aa00b7c74d103</originalsourceid><addsrcrecordid>eNpNkF1LAkEYhYcoyMxfEYFeTL3zuTuXIpWC0U1dD_O1ObLu6OwK6a9v04iu3g8OzzkchEYEHhhT8PhKFKcXaEA4pbgUSl3-26_RTduuATihDAZISDzdxCbhAo_HHG9Ct0pfBxua46GedKuYJrt9bMwx1bHBfMzmE5yacIuuKlO3YfQ7h-jj-el9NsfLt5fFbLrEjoLqsJIEvCg45aWlvDDUscI7UVWgKlZ6Iqi1xoDw3FSSOmmlKvobbOEK7gmwIVqcuT6Ztd7muDH5oJOJ-vRI-VOb3EVXB22lUIJbG7wjXDAorQQhgvAuOGMk6Vl3Z9Y2p90-tJ1ep31u-viaEa5kyQijver-rHI5tW0O1Z8rAf3Trj61y74BBstoJw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3149683132</pqid></control><display><type>article</type><title>6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Thapa, Susila ; Bolliger, Jeanne L.</creator><creatorcontrib>Thapa, Susila ; Bolliger, Jeanne L.</creatorcontrib><description>The titular compound, 6-amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one, was prepared from 7-fluoro-6-nitroquinazolin-4(3H)-one via a nucleophilic aromatic substitution reaction followed by a reduction of the nitro group. Characterization of the target compound via 1H NMR, 13C NMR, and HRMS confirmed its structure.</description><identifier>ISSN: 1422-8599</identifier><identifier>EISSN: 1422-8599</identifier><identifier>DOI: 10.3390/M1942</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Cancer ; Ethanol ; heterocycles ; Leukemia ; Lymphoma ; Mass spectrometry ; NMR ; Nuclear magnetic resonance ; nucleophilic aromatic substitution ; Pharmaceutical sciences ; quinazolin-4(3H)-one ; quinazoline ; reduction ; Scientific imaging ; Substitution reactions</subject><ispartof>MolBank, 2024-12, Vol.2024 (4), p.M1942</ispartof><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c209t-9610d574248b247a2c37dc5ff09f38d152bbaa05d4af62c6b697aa00b7c74d103</cites><orcidid>0000-0001-6152-5220 ; 0009-0000-5780-6257</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,2096,27901,27902</link.rule.ids></links><search><creatorcontrib>Thapa, Susila</creatorcontrib><creatorcontrib>Bolliger, Jeanne L.</creatorcontrib><title>6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one</title><title>MolBank</title><description>The titular compound, 6-amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one, was prepared from 7-fluoro-6-nitroquinazolin-4(3H)-one via a nucleophilic aromatic substitution reaction followed by a reduction of the nitro group. Characterization of the target compound via 1H NMR, 13C NMR, and HRMS confirmed its structure.</description><subject>Cancer</subject><subject>Ethanol</subject><subject>heterocycles</subject><subject>Leukemia</subject><subject>Lymphoma</subject><subject>Mass spectrometry</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>nucleophilic aromatic substitution</subject><subject>Pharmaceutical sciences</subject><subject>quinazolin-4(3H)-one</subject><subject>quinazoline</subject><subject>reduction</subject><subject>Scientific imaging</subject><subject>Substitution reactions</subject><issn>1422-8599</issn><issn>1422-8599</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNpNkF1LAkEYhYcoyMxfEYFeTL3zuTuXIpWC0U1dD_O1ObLu6OwK6a9v04iu3g8OzzkchEYEHhhT8PhKFKcXaEA4pbgUSl3-26_RTduuATihDAZISDzdxCbhAo_HHG9Ct0pfBxua46GedKuYJrt9bMwx1bHBfMzmE5yacIuuKlO3YfQ7h-jj-el9NsfLt5fFbLrEjoLqsJIEvCg45aWlvDDUscI7UVWgKlZ6Iqi1xoDw3FSSOmmlKvobbOEK7gmwIVqcuT6Ztd7muDH5oJOJ-vRI-VOb3EVXB22lUIJbG7wjXDAorQQhgvAuOGMk6Vl3Z9Y2p90-tJ1ep31u-viaEa5kyQijver-rHI5tW0O1Z8rAf3Trj61y74BBstoJw</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Thapa, Susila</creator><creator>Bolliger, Jeanne L.</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>L7M</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6152-5220</orcidid><orcidid>https://orcid.org/0009-0000-5780-6257</orcidid></search><sort><creationdate>20241201</creationdate><title>6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one</title><author>Thapa, Susila ; Bolliger, Jeanne L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c209t-9610d574248b247a2c37dc5ff09f38d152bbaa05d4af62c6b697aa00b7c74d103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cancer</topic><topic>Ethanol</topic><topic>heterocycles</topic><topic>Leukemia</topic><topic>Lymphoma</topic><topic>Mass spectrometry</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>nucleophilic aromatic substitution</topic><topic>Pharmaceutical sciences</topic><topic>quinazolin-4(3H)-one</topic><topic>quinazoline</topic><topic>reduction</topic><topic>Scientific imaging</topic><topic>Substitution reactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thapa, Susila</creatorcontrib><creatorcontrib>Bolliger, Jeanne L.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>MolBank</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thapa, Susila</au><au>Bolliger, Jeanne L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one</atitle><jtitle>MolBank</jtitle><date>2024-12-01</date><risdate>2024</risdate><volume>2024</volume><issue>4</issue><spage>M1942</spage><pages>M1942-</pages><issn>1422-8599</issn><eissn>1422-8599</eissn><abstract>The titular compound, 6-amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one, was prepared from 7-fluoro-6-nitroquinazolin-4(3H)-one via a nucleophilic aromatic substitution reaction followed by a reduction of the nitro group. Characterization of the target compound via 1H NMR, 13C NMR, and HRMS confirmed its structure.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/M1942</doi><orcidid>https://orcid.org/0000-0001-6152-5220</orcidid><orcidid>https://orcid.org/0009-0000-5780-6257</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-8599 |
ispartof | MolBank, 2024-12, Vol.2024 (4), p.M1942 |
issn | 1422-8599 1422-8599 |
language | eng |
recordid | cdi_proquest_journals_3149683132 |
source | MDPI - Multidisciplinary Digital Publishing Institute; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Cancer Ethanol heterocycles Leukemia Lymphoma Mass spectrometry NMR Nuclear magnetic resonance nucleophilic aromatic substitution Pharmaceutical sciences quinazolin-4(3H)-one quinazoline reduction Scientific imaging Substitution reactions |
title | 6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T20%3A34%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=6-Amino-7-((4-methoxybenzyl)thio)quinazolin-4(3H)-one&rft.jtitle=MolBank&rft.au=Thapa,%20Susila&rft.date=2024-12-01&rft.volume=2024&rft.issue=4&rft.spage=M1942&rft.pages=M1942-&rft.issn=1422-8599&rft.eissn=1422-8599&rft_id=info:doi/10.3390/M1942&rft_dat=%3Cproquest_doaj_%3E3149683132%3C/proquest_doaj_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3149683132&rft_id=info:pmid/&rft_doaj_id=oai_doaj_org_article_b65954bbedc145308b6055e5dcecaa61&rfr_iscdi=true |