Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives

New 1,2,4-triazole-3-thiols were synthesized by reactions of the corresponding carboxylic acid hydrazides with isothiocyanates and subsequent cyclization of intermediate 1,4-substituted thiosemicarbazides. Alkylation of 1,2,4-triazole-3-thiols with benzyl chlorides and bromacetophenones gave only S-...

Full description

Saved in:
Bibliographic Details
Published in:Russian journal of organic chemistry 2010-04, Vol.46 (4), p.551-555
Main Authors: Kochikyan, T. V, Samvelyan, M. A, Arutyunyan, V. S, Avetisyan, A. A, Tamazyan, R. A, Aivazyan, A. G
Format: Article
Language:English
Subjects:
Chemistry
Chemistry and Materials Science
Organic Chemistry
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813
cites cdi_FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813
container_end_page 555
container_issue 4
container_start_page 551
container_title Russian journal of organic chemistry
container_volume 46
creator Kochikyan, T. V
Samvelyan, M. A
Arutyunyan, V. S
Avetisyan, A. A
Tamazyan, R. A
Aivazyan, A. G
description New 1,2,4-triazole-3-thiols were synthesized by reactions of the corresponding carboxylic acid hydrazides with isothiocyanates and subsequent cyclization of intermediate 1,4-substituted thiosemicarbazides. Alkylation of 1,2,4-triazole-3-thiols with benzyl chlorides and bromacetophenones gave only S-substituted derivatives.
doi_str_mv 10.1134/S1070428010040184
format article
fullrecord <record><control><sourceid>fao_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1134_S1070428010040184</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>US201301842096</sourcerecordid><originalsourceid>FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813</originalsourceid><addsrcrecordid>eNp9kM1KAzEUhYMoWH8ewJXzAI3em5vpTJZS1AoFF2PXIZ1J2pQ6I0laqE9vSt0Jrs6Bc77L5TB2h_CASPKxQahAihoQQALW8oyNcAI1J1J0nn2O-TG_ZFcxbiC3UNKIzZpDn9Y2-lgMrsCxGEuegjffw9Zy4mnth20sTN8VueVD0fC4W8bk0y7Zruhs8HuT_N7GG3bhzDba21-9ZouX54_pjM_fX9-mT3PeEorErcVatGVlHJlSOokd1batHNSqE1ZVxlTLsqWsrXJGCZKlIsAKrRRG1EjXDE932zDEGKzTX8F_mnDQCPo4hf4zRWbEiYm5269s0JthF_r85r_Q_QlyZtBmFXzUi0YA0jEVoCb0AzQOaFc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives</title><source>Springer Nature</source><creator>Kochikyan, T. V ; Samvelyan, M. A ; Arutyunyan, V. S ; Avetisyan, A. A ; Tamazyan, R. A ; Aivazyan, A. G</creator><creatorcontrib>Kochikyan, T. V ; Samvelyan, M. A ; Arutyunyan, V. S ; Avetisyan, A. A ; Tamazyan, R. A ; Aivazyan, A. G</creatorcontrib><description>New 1,2,4-triazole-3-thiols were synthesized by reactions of the corresponding carboxylic acid hydrazides with isothiocyanates and subsequent cyclization of intermediate 1,4-substituted thiosemicarbazides. Alkylation of 1,2,4-triazole-3-thiols with benzyl chlorides and bromacetophenones gave only S-substituted derivatives.</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S1070428010040184</identifier><language>eng</language><publisher>Dordrecht: Dordrecht : SP MAIK Nauka/Interperiodica</publisher><subject>Chemistry ; Chemistry and Materials Science ; Organic Chemistry</subject><ispartof>Russian journal of organic chemistry, 2010-04, Vol.46 (4), p.551-555</ispartof><rights>Pleiades Publishing, Ltd. 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813</citedby><cites>FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kochikyan, T. V</creatorcontrib><creatorcontrib>Samvelyan, M. A</creatorcontrib><creatorcontrib>Arutyunyan, V. S</creatorcontrib><creatorcontrib>Avetisyan, A. A</creatorcontrib><creatorcontrib>Tamazyan, R. A</creatorcontrib><creatorcontrib>Aivazyan, A. G</creatorcontrib><title>Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives</title><title>Russian journal of organic chemistry</title><addtitle>Russ J Org Chem</addtitle><description>New 1,2,4-triazole-3-thiols were synthesized by reactions of the corresponding carboxylic acid hydrazides with isothiocyanates and subsequent cyclization of intermediate 1,4-substituted thiosemicarbazides. Alkylation of 1,2,4-triazole-3-thiols with benzyl chlorides and bromacetophenones gave only S-substituted derivatives.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Organic Chemistry</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KAzEUhYMoWH8ewJXzAI3em5vpTJZS1AoFF2PXIZ1J2pQ6I0laqE9vSt0Jrs6Bc77L5TB2h_CASPKxQahAihoQQALW8oyNcAI1J1J0nn2O-TG_ZFcxbiC3UNKIzZpDn9Y2-lgMrsCxGEuegjffw9Zy4mnth20sTN8VueVD0fC4W8bk0y7Zruhs8HuT_N7GG3bhzDba21-9ZouX54_pjM_fX9-mT3PeEorErcVatGVlHJlSOokd1batHNSqE1ZVxlTLsqWsrXJGCZKlIsAKrRRG1EjXDE932zDEGKzTX8F_mnDQCPo4hf4zRWbEiYm5269s0JthF_r85r_Q_QlyZtBmFXzUi0YA0jEVoCb0AzQOaFc</recordid><startdate>20100401</startdate><enddate>20100401</enddate><creator>Kochikyan, T. V</creator><creator>Samvelyan, M. A</creator><creator>Arutyunyan, V. S</creator><creator>Avetisyan, A. A</creator><creator>Tamazyan, R. A</creator><creator>Aivazyan, A. G</creator><general>Dordrecht : SP MAIK Nauka/Interperiodica</general><general>SP MAIK Nauka/Interperiodica</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20100401</creationdate><title>Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives</title><author>Kochikyan, T. V ; Samvelyan, M. A ; Arutyunyan, V. S ; Avetisyan, A. A ; Tamazyan, R. A ; Aivazyan, A. G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Organic Chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kochikyan, T. V</creatorcontrib><creatorcontrib>Samvelyan, M. A</creatorcontrib><creatorcontrib>Arutyunyan, V. S</creatorcontrib><creatorcontrib>Avetisyan, A. A</creatorcontrib><creatorcontrib>Tamazyan, R. A</creatorcontrib><creatorcontrib>Aivazyan, A. G</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><jtitle>Russian journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kochikyan, T. V</au><au>Samvelyan, M. A</au><au>Arutyunyan, V. S</au><au>Avetisyan, A. A</au><au>Tamazyan, R. A</au><au>Aivazyan, A. G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives</atitle><jtitle>Russian journal of organic chemistry</jtitle><stitle>Russ J Org Chem</stitle><date>2010-04-01</date><risdate>2010</risdate><volume>46</volume><issue>4</issue><spage>551</spage><epage>555</epage><pages>551-555</pages><issn>1070-4280</issn><eissn>1608-3393</eissn><abstract>New 1,2,4-triazole-3-thiols were synthesized by reactions of the corresponding carboxylic acid hydrazides with isothiocyanates and subsequent cyclization of intermediate 1,4-substituted thiosemicarbazides. Alkylation of 1,2,4-triazole-3-thiols with benzyl chlorides and bromacetophenones gave only S-substituted derivatives.</abstract><cop>Dordrecht</cop><pub>Dordrecht : SP MAIK Nauka/Interperiodica</pub><doi>10.1134/S1070428010040184</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1070-4280
ispartof Russian journal of organic chemistry, 2010-04, Vol.46 (4), p.551-555
issn 1070-4280
1608-3393
language eng
recordid cdi_crossref_primary_10_1134_S1070428010040184
source Springer Nature
subjects Chemistry
Chemistry and Materials Science
Organic Chemistry
title Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T02%3A28%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-fao_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%201,2,4-triazole-3-thiols%20and%20their%20S-substituted%20derivatives&rft.jtitle=Russian%20journal%20of%20organic%20chemistry&rft.au=Kochikyan,%20T.%20V&rft.date=2010-04-01&rft.volume=46&rft.issue=4&rft.spage=551&rft.epage=555&rft.pages=551-555&rft.issn=1070-4280&rft.eissn=1608-3393&rft_id=info:doi/10.1134/S1070428010040184&rft_dat=%3Cfao_cross%3EUS201301842096%3C/fao_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c312t-ee182c57af3a54f41d38ec7f089d2e97aa7b5c37aac9fa92345930171e42a2813%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true