Microwave-Assisted and Conventional Synthesis of Benzothieno [3,2-e] [1,3,4] triazolo[4,3-c]pyrimidines: A Comparative Study
Benzothieno[2,3-d]pyrimidines (2,3,4) and benzothieno[3,2-e][1,3,4]triazolo[4,3-c] pyrimidines (5a-c) were synthesized from the precursor 2-amino-7-oxo-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile 1 by employing the conventional method as well as the microwave irradiation technique. The precur...
Gespeichert in:
Veröffentlicht in: | Journal of the Korean Chemical Society 2014, Vol.58 (4), p.388-392 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | kor |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 392 |
---|---|
container_issue | 4 |
container_start_page | 388 |
container_title | Journal of the Korean Chemical Society |
container_volume | 58 |
creator | Gaonkar, Santhosh L Ahn, Chuljin Princia, Princia Shetty, Nitinkumar S |
description | Benzothieno[2,3-d]pyrimidines (2,3,4) and benzothieno[3,2-e][1,3,4]triazolo[4,3-c] pyrimidines (5a-c) were synthesized from the precursor 2-amino-7-oxo-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile 1 by employing the conventional method as well as the microwave irradiation technique. The precursor 2-amino-3-cyanothiophene analogue 1 was synthesized by employing the well-known Gewald reaction. In the present work it has been found that the microwave supported syntheses are more efficient than the conventional classical heating methods. The structures of all the compounds were ascertained by spectral and analytical data. |
format | Article |
fullrecord | <record><control><sourceid>kisti</sourceid><recordid>TN_cdi_kisti_ndsl_JAKO201422354180277</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JAKO201422354180277</sourcerecordid><originalsourceid>FETCH-kisti_ndsl_JAKO2014223541802773</originalsourceid><addsrcrecordid>eNqNjr1qwzAURjW00NDmHe6SzQL9GSXZ3NBSWkqGZDMmqNENucSRgqW6OPTh66EPkOkM5_Dx3bGJFNJyVZr5A5umRF-i1NpasdAT9vtJ-y7-uB55NaqU0YMLHlYx9BgyxeBa2AwhH3G0EA_wjOEa85EwRKh1oTg2UMtCF6aB3JG7xjbWptB831yGjs7kKWBaQjVuni-uc5l6hE3-9sMTuz-4NuH0n49s9vqyXb3x03iEdsGndvdefayVkEYpXRo5F8pafWv3B_GBS-M</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Microwave-Assisted and Conventional Synthesis of Benzothieno [3,2-e] [1,3,4] triazolo[4,3-c]pyrimidines: A Comparative Study</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Gaonkar, Santhosh L ; Ahn, Chuljin ; Princia, Princia ; Shetty, Nitinkumar S</creator><creatorcontrib>Gaonkar, Santhosh L ; Ahn, Chuljin ; Princia, Princia ; Shetty, Nitinkumar S</creatorcontrib><description>Benzothieno[2,3-d]pyrimidines (2,3,4) and benzothieno[3,2-e][1,3,4]triazolo[4,3-c] pyrimidines (5a-c) were synthesized from the precursor 2-amino-7-oxo-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile 1 by employing the conventional method as well as the microwave irradiation technique. The precursor 2-amino-3-cyanothiophene analogue 1 was synthesized by employing the well-known Gewald reaction. In the present work it has been found that the microwave supported syntheses are more efficient than the conventional classical heating methods. The structures of all the compounds were ascertained by spectral and analytical data.</description><identifier>ISSN: 1017-2548</identifier><language>kor</language><ispartof>Journal of the Korean Chemical Society, 2014, Vol.58 (4), p.388-392</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,4025</link.rule.ids></links><search><creatorcontrib>Gaonkar, Santhosh L</creatorcontrib><creatorcontrib>Ahn, Chuljin</creatorcontrib><creatorcontrib>Princia, Princia</creatorcontrib><creatorcontrib>Shetty, Nitinkumar S</creatorcontrib><title>Microwave-Assisted and Conventional Synthesis of Benzothieno [3,2-e] [1,3,4] triazolo[4,3-c]pyrimidines: A Comparative Study</title><title>Journal of the Korean Chemical Society</title><addtitle>Journal of the Korean Chemical Society</addtitle><description>Benzothieno[2,3-d]pyrimidines (2,3,4) and benzothieno[3,2-e][1,3,4]triazolo[4,3-c] pyrimidines (5a-c) were synthesized from the precursor 2-amino-7-oxo-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile 1 by employing the conventional method as well as the microwave irradiation technique. The precursor 2-amino-3-cyanothiophene analogue 1 was synthesized by employing the well-known Gewald reaction. In the present work it has been found that the microwave supported syntheses are more efficient than the conventional classical heating methods. The structures of all the compounds were ascertained by spectral and analytical data.</description><issn>1017-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNqNjr1qwzAURjW00NDmHe6SzQL9GSXZ3NBSWkqGZDMmqNENucSRgqW6OPTh66EPkOkM5_Dx3bGJFNJyVZr5A5umRF-i1NpasdAT9vtJ-y7-uB55NaqU0YMLHlYx9BgyxeBa2AwhH3G0EA_wjOEa85EwRKh1oTg2UMtCF6aB3JG7xjbWptB831yGjs7kKWBaQjVuni-uc5l6hE3-9sMTuz-4NuH0n49s9vqyXb3x03iEdsGndvdefayVkEYpXRo5F8pafWv3B_GBS-M</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Gaonkar, Santhosh L</creator><creator>Ahn, Chuljin</creator><creator>Princia, Princia</creator><creator>Shetty, Nitinkumar S</creator><scope>JDI</scope></search><sort><creationdate>2014</creationdate><title>Microwave-Assisted and Conventional Synthesis of Benzothieno [3,2-e] [1,3,4] triazolo[4,3-c]pyrimidines: A Comparative Study</title><author>Gaonkar, Santhosh L ; Ahn, Chuljin ; Princia, Princia ; Shetty, Nitinkumar S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2014223541802773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gaonkar, Santhosh L</creatorcontrib><creatorcontrib>Ahn, Chuljin</creatorcontrib><creatorcontrib>Princia, Princia</creatorcontrib><creatorcontrib>Shetty, Nitinkumar S</creatorcontrib><collection>KoreaScience</collection><jtitle>Journal of the Korean Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gaonkar, Santhosh L</au><au>Ahn, Chuljin</au><au>Princia, Princia</au><au>Shetty, Nitinkumar S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microwave-Assisted and Conventional Synthesis of Benzothieno [3,2-e] [1,3,4] triazolo[4,3-c]pyrimidines: A Comparative Study</atitle><jtitle>Journal of the Korean Chemical Society</jtitle><addtitle>Journal of the Korean Chemical Society</addtitle><date>2014</date><risdate>2014</risdate><volume>58</volume><issue>4</issue><spage>388</spage><epage>392</epage><pages>388-392</pages><issn>1017-2548</issn><abstract>Benzothieno[2,3-d]pyrimidines (2,3,4) and benzothieno[3,2-e][1,3,4]triazolo[4,3-c] pyrimidines (5a-c) were synthesized from the precursor 2-amino-7-oxo-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile 1 by employing the conventional method as well as the microwave irradiation technique. The precursor 2-amino-3-cyanothiophene analogue 1 was synthesized by employing the well-known Gewald reaction. In the present work it has been found that the microwave supported syntheses are more efficient than the conventional classical heating methods. The structures of all the compounds were ascertained by spectral and analytical data.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1017-2548 |
ispartof | Journal of the Korean Chemical Society, 2014, Vol.58 (4), p.388-392 |
issn | 1017-2548 |
language | kor |
recordid | cdi_kisti_ndsl_JAKO201422354180277 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
title | Microwave-Assisted and Conventional Synthesis of Benzothieno [3,2-e] [1,3,4] triazolo[4,3-c]pyrimidines: A Comparative Study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-15T22%3A02%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kisti&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Microwave-Assisted%20and%20Conventional%20Synthesis%20of%20Benzothieno%20%5B3,2-e%5D%20%5B1,3,4%5D%20triazolo%5B4,3-c%5Dpyrimidines:%20A%20Comparative%20Study&rft.jtitle=Journal%20of%20the%20Korean%20Chemical%20Society&rft.au=Gaonkar,%20Santhosh%20L&rft.date=2014&rft.volume=58&rft.issue=4&rft.spage=388&rft.epage=392&rft.pages=388-392&rft.issn=1017-2548&rft_id=info:doi/&rft_dat=%3Ckisti%3EJAKO201422354180277%3C/kisti%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |