New derivatives of 1,3,4-thiadiazole based on hydrazide of 3-methoxyphenoxyacetic acid
2-Substituted 1,3,4-thiadiazole-5-thiol has been synthesized basing on hydrazide of 3-methoxy-phenoxyacetic acid. Methods of SH-alkylation, aminomethylation, and cyanoethylation of the product have been elaborated. Reactions of the starting hydrazide leading to 4-amino-3,5-substituted 4 Н -1,2,4-tri...
Gespeichert in:
Veröffentlicht in: | Russian journal of general chemistry 2016-08, Vol.86 (8), p.1845-1849 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1849 |
---|---|
container_issue | 8 |
container_start_page | 1845 |
container_title | Russian journal of general chemistry |
container_volume | 86 |
creator | Hovsepyan, T. R. Hakobyan, M. R. Minasyan, N. S. Melik-Ohanjanyan, R. G. |
description | 2-Substituted 1,3,4-thiadiazole-5-thiol has been synthesized basing on hydrazide of 3-methoxy-phenoxyacetic acid. Methods of SH-alkylation, aminomethylation, and cyanoethylation of the product have been elaborated. Reactions of the starting hydrazide leading to 4-amino-3,5-substituted 4
Н
-1,2,4-triazoles and acyl hydrazides of dicarboxylic acids containing pharmacophore groups in the molecule have been studied. |
doi_str_mv | 10.1134/S1070363216080119 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1880861811</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1880861811</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-c690da0a8c737e2a1e31d23bc2e35e4ca5c5ddc0267568b59a80c66dab2386733</originalsourceid><addsrcrecordid>eNp1UMtKw0AUHUTBWv0AdwG3jd47t5lMl1J8QdGFj22YzNzaKW1SZ9Jq-_Um1IUgrs6B84IjxDnCJSINr54RciBFEhVoQBwdiF5HU6IMDlveymmnH4uTGOcACKBkT7w98mfiOPiNafyGY1JPExzQYJg2M2-cN7t6wUlpIrukrpLZ1gWz8447H6VLbmb113Y146oFY7nxNjHWu1NxNDWLyGc_2Bevtzcv4_t08nT3ML6epJZQNalVI3AGjLY55SwNMqGTVFrJlPHQmsxmzlmQKs-ULrOR0WCVcqaUpFVO1BcX-95VqD_WHJtiXq9D1U4WqDVohbq9py9w77KhjjHwtFgFvzRhWyAU3X3Fn_vajNxnYuut3jn8av439A2uqHBa</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1880861811</pqid></control><display><type>article</type><title>New derivatives of 1,3,4-thiadiazole based on hydrazide of 3-methoxyphenoxyacetic acid</title><source>SpringerLink Journals</source><creator>Hovsepyan, T. R. ; Hakobyan, M. R. ; Minasyan, N. S. ; Melik-Ohanjanyan, R. G.</creator><creatorcontrib>Hovsepyan, T. R. ; Hakobyan, M. R. ; Minasyan, N. S. ; Melik-Ohanjanyan, R. G.</creatorcontrib><description>2-Substituted 1,3,4-thiadiazole-5-thiol has been synthesized basing on hydrazide of 3-methoxy-phenoxyacetic acid. Methods of SH-alkylation, aminomethylation, and cyanoethylation of the product have been elaborated. Reactions of the starting hydrazide leading to 4-amino-3,5-substituted 4
Н
-1,2,4-triazoles and acyl hydrazides of dicarboxylic acids containing pharmacophore groups in the molecule have been studied.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363216080119</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Alkylation ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Cyanoethylation ; Dicarboxylic acids ; Hydrazides ; Substitutes ; Thiadiazoles</subject><ispartof>Russian journal of general chemistry, 2016-08, Vol.86 (8), p.1845-1849</ispartof><rights>Pleiades Publishing, Ltd. 2016</rights><rights>Copyright Springer Science & Business Media 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-c690da0a8c737e2a1e31d23bc2e35e4ca5c5ddc0267568b59a80c66dab2386733</citedby><cites>FETCH-LOGICAL-c316t-c690da0a8c737e2a1e31d23bc2e35e4ca5c5ddc0267568b59a80c66dab2386733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363216080119$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363216080119$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Hovsepyan, T. R.</creatorcontrib><creatorcontrib>Hakobyan, M. R.</creatorcontrib><creatorcontrib>Minasyan, N. S.</creatorcontrib><creatorcontrib>Melik-Ohanjanyan, R. G.</creatorcontrib><title>New derivatives of 1,3,4-thiadiazole based on hydrazide of 3-methoxyphenoxyacetic acid</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>2-Substituted 1,3,4-thiadiazole-5-thiol has been synthesized basing on hydrazide of 3-methoxy-phenoxyacetic acid. Methods of SH-alkylation, aminomethylation, and cyanoethylation of the product have been elaborated. Reactions of the starting hydrazide leading to 4-amino-3,5-substituted 4
Н
-1,2,4-triazoles and acyl hydrazides of dicarboxylic acids containing pharmacophore groups in the molecule have been studied.</description><subject>Alkylation</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Cyanoethylation</subject><subject>Dicarboxylic acids</subject><subject>Hydrazides</subject><subject>Substitutes</subject><subject>Thiadiazoles</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1UMtKw0AUHUTBWv0AdwG3jd47t5lMl1J8QdGFj22YzNzaKW1SZ9Jq-_Um1IUgrs6B84IjxDnCJSINr54RciBFEhVoQBwdiF5HU6IMDlveymmnH4uTGOcACKBkT7w98mfiOPiNafyGY1JPExzQYJg2M2-cN7t6wUlpIrukrpLZ1gWz8447H6VLbmb113Y146oFY7nxNjHWu1NxNDWLyGc_2Bevtzcv4_t08nT3ML6epJZQNalVI3AGjLY55SwNMqGTVFrJlPHQmsxmzlmQKs-ULrOR0WCVcqaUpFVO1BcX-95VqD_WHJtiXq9D1U4WqDVohbq9py9w77KhjjHwtFgFvzRhWyAU3X3Fn_vajNxnYuut3jn8av439A2uqHBa</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Hovsepyan, T. R.</creator><creator>Hakobyan, M. R.</creator><creator>Minasyan, N. S.</creator><creator>Melik-Ohanjanyan, R. G.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20160801</creationdate><title>New derivatives of 1,3,4-thiadiazole based on hydrazide of 3-methoxyphenoxyacetic acid</title><author>Hovsepyan, T. R. ; Hakobyan, M. R. ; Minasyan, N. S. ; Melik-Ohanjanyan, R. G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-c690da0a8c737e2a1e31d23bc2e35e4ca5c5ddc0267568b59a80c66dab2386733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Alkylation</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Cyanoethylation</topic><topic>Dicarboxylic acids</topic><topic>Hydrazides</topic><topic>Substitutes</topic><topic>Thiadiazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hovsepyan, T. R.</creatorcontrib><creatorcontrib>Hakobyan, M. R.</creatorcontrib><creatorcontrib>Minasyan, N. S.</creatorcontrib><creatorcontrib>Melik-Ohanjanyan, R. G.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hovsepyan, T. R.</au><au>Hakobyan, M. R.</au><au>Minasyan, N. S.</au><au>Melik-Ohanjanyan, R. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New derivatives of 1,3,4-thiadiazole based on hydrazide of 3-methoxyphenoxyacetic acid</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2016-08-01</date><risdate>2016</risdate><volume>86</volume><issue>8</issue><spage>1845</spage><epage>1849</epage><pages>1845-1849</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>2-Substituted 1,3,4-thiadiazole-5-thiol has been synthesized basing on hydrazide of 3-methoxy-phenoxyacetic acid. Methods of SH-alkylation, aminomethylation, and cyanoethylation of the product have been elaborated. Reactions of the starting hydrazide leading to 4-amino-3,5-substituted 4
Н
-1,2,4-triazoles and acyl hydrazides of dicarboxylic acids containing pharmacophore groups in the molecule have been studied.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363216080119</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1070-3632 |
ispartof | Russian journal of general chemistry, 2016-08, Vol.86 (8), p.1845-1849 |
issn | 1070-3632 1608-3350 |
language | eng |
recordid | cdi_proquest_journals_1880861811 |
source | SpringerLink Journals |
subjects | Alkylation Chemistry Chemistry and Materials Science Chemistry/Food Science Cyanoethylation Dicarboxylic acids Hydrazides Substitutes Thiadiazoles |
title | New derivatives of 1,3,4-thiadiazole based on hydrazide of 3-methoxyphenoxyacetic acid |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T02%3A03%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=New%20derivatives%20of%201,3,4-thiadiazole%20based%20on%20hydrazide%20of%203-methoxyphenoxyacetic%20acid&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Hovsepyan,%20T.%20R.&rft.date=2016-08-01&rft.volume=86&rft.issue=8&rft.spage=1845&rft.epage=1849&rft.pages=1845-1849&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363216080119&rft_dat=%3Cproquest_cross%3E1880861811%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1880861811&rft_id=info:pmid/&rfr_iscdi=true |