2-Cyano-N′-[(1,3-diphenyl-1H-pyrazol-4-yl)methylidene]acetohydrazide in the Synthesis of Nitrogen Heterocycles

Some interesting nitrogen heterocycles, as well as other products, were synthesized by reactions of 2-cyano- N′ -[(1,3-diphenyl-1 H -pyrazol-4-yl)methylidene]acetohydrazide with phenyl isothiocyanate/elemental sulfur, 3,4,5-trimethoxybenzaldehyde, 4-hydroxy-1,1′-biphenyl-3-carbaldehyde, 2-oxoquinoli...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Russian journal of organic chemistry 2019-12, Vol.55 (12), p.1940-1945
Hauptverfasser:	Ramadan, S. K., El-Helw, E. A. E., Azab, M. E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Chemical synthesis Chemistry Chemistry and Materials Science Nitrogen Organic Chemistry
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

container_end_page	1945
container_issue	12
container_start_page	1940
container_title	Russian journal of organic chemistry
container_volume	55
creator	Ramadan, S. K. El-Helw, E. A. E. Azab, M. E.
description	Some interesting nitrogen heterocycles, as well as other products, were synthesized by reactions of 2-cyano- N′ -[(1,3-diphenyl-1 H -pyrazol-4-yl)methylidene]acetohydrazide with phenyl isothiocyanate/elemental sulfur, 3,4,5-trimethoxybenzaldehyde, 4-hydroxy-1,1′-biphenyl-3-carbaldehyde, 2-oxoquinoline-3-caraldehyde, triethyl orthoformate, ethyl cyanoacetate, and thiosemicarbazide. The structures of all isolated compounds were established from their analytical and spectral data.
doi_str_mv	10.1134/S1070428019120224
format	Article
fullrecord	<record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2347665315</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2347665315</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-9d310fd06a543ecedff1f0f018849fa729fc122fc100e104d98f4be7cd928ad93</originalsourceid><addsrcrecordid>eNp1UM1Kw0AQDqJgrT6At4AXBVdndrdpcpSiVih6qJ5EQszONilpNu6mh_XkM_lIPolbKngQL_MN8_0MfFF0jHCBKOTlHGEMkqeAGXLgXO5EA0wgZUJkYjfsgWYbfj86cG4JABKlGEQdZxNftIbdf318sudTPBdM1V1FrW8YTlnnbfFuGiaZb85W1Fe-qRW19FKU1JvKq0CHQ1y3cV9RPPdtAFe72Oj4vu6tWVAbT6kna0pfNuQOoz1dNI6OfnAYPd1cP06mbPZweze5mrFSYNKzTAkErSApRlJQSUpr1KAB01RmuhjzTJfIeRgAhCBVlmr5SuNSZTwtVCaG0ck2t7PmbU2uz5dmbdvwMudCjpNkJHAUVLhVldY4Z0nnna1XhfU5Qr4pNv9TbPDwrccFbbsg-5v8v-kbAd57JQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2347665315</pqid></control><display><type>article</type><title>2-Cyano-N′-[(1,3-diphenyl-1H-pyrazol-4-yl)methylidene]acetohydrazide in the Synthesis of Nitrogen Heterocycles</title><source>SpringerLink Journals - AutoHoldings</source><creator>Ramadan, S. K. ; El-Helw, E. A. E. ; Azab, M. E.</creator><creatorcontrib>Ramadan, S. K. ; El-Helw, E. A. E. ; Azab, M. E.</creatorcontrib><description>Some interesting nitrogen heterocycles, as well as other products, were synthesized by reactions of 2-cyano- N′ -[(1,3-diphenyl-1 H -pyrazol-4-yl)methylidene]acetohydrazide with phenyl isothiocyanate/elemental sulfur, 3,4,5-trimethoxybenzaldehyde, 4-hydroxy-1,1′-biphenyl-3-carbaldehyde, 2-oxoquinoline-3-caraldehyde, triethyl orthoformate, ethyl cyanoacetate, and thiosemicarbazide. The structures of all isolated compounds were established from their analytical and spectral data.</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S1070428019120224</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Nitrogen ; Organic Chemistry</subject><ispartof>Russian journal of organic chemistry, 2019-12, Vol.55 (12), p.1940-1945</ispartof><rights>Pleiades Publishing, Ltd. 2019</rights><rights>2019© Pleiades Publishing, Ltd. 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-9d310fd06a543ecedff1f0f018849fa729fc122fc100e104d98f4be7cd928ad93</citedby><cites>FETCH-LOGICAL-c316t-9d310fd06a543ecedff1f0f018849fa729fc122fc100e104d98f4be7cd928ad93</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/S1070428019120224$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070428019120224$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Ramadan, S. K.</creatorcontrib><creatorcontrib>El-Helw, E. A. E.</creatorcontrib><creatorcontrib>Azab, M. E.</creatorcontrib><title>2-Cyano-N′-[(1,3-diphenyl-1H-pyrazol-4-yl)methylidene]acetohydrazide in the Synthesis of Nitrogen Heterocycles</title><title>Russian journal of organic chemistry</title><addtitle>Russ J Org Chem</addtitle><description>Some interesting nitrogen heterocycles, as well as other products, were synthesized by reactions of 2-cyano- N′ -[(1,3-diphenyl-1 H -pyrazol-4-yl)methylidene]acetohydrazide with phenyl isothiocyanate/elemental sulfur, 3,4,5-trimethoxybenzaldehyde, 4-hydroxy-1,1′-biphenyl-3-carbaldehyde, 2-oxoquinoline-3-caraldehyde, triethyl orthoformate, ethyl cyanoacetate, and thiosemicarbazide. The structures of all isolated compounds were established from their analytical and spectral data.</description><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Nitrogen</subject><subject>Organic Chemistry</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1UM1Kw0AQDqJgrT6At4AXBVdndrdpcpSiVih6qJ5EQszONilpNu6mh_XkM_lIPolbKngQL_MN8_0MfFF0jHCBKOTlHGEMkqeAGXLgXO5EA0wgZUJkYjfsgWYbfj86cG4JABKlGEQdZxNftIbdf318sudTPBdM1V1FrW8YTlnnbfFuGiaZb85W1Fe-qRW19FKU1JvKq0CHQ1y3cV9RPPdtAFe72Oj4vu6tWVAbT6kna0pfNuQOoz1dNI6OfnAYPd1cP06mbPZweze5mrFSYNKzTAkErSApRlJQSUpr1KAB01RmuhjzTJfIeRgAhCBVlmr5SuNSZTwtVCaG0ck2t7PmbU2uz5dmbdvwMudCjpNkJHAUVLhVldY4Z0nnna1XhfU5Qr4pNv9TbPDwrccFbbsg-5v8v-kbAd57JQ</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Ramadan, S. K.</creator><creator>El-Helw, E. A. E.</creator><creator>Azab, M. E.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20191201</creationdate><title>2-Cyano-N′-[(1,3-diphenyl-1H-pyrazol-4-yl)methylidene]acetohydrazide in the Synthesis of Nitrogen Heterocycles</title><author>Ramadan, S. K. ; El-Helw, E. A. E. ; Azab, M. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-9d310fd06a543ecedff1f0f018849fa729fc122fc100e104d98f4be7cd928ad93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Nitrogen</topic><topic>Organic Chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramadan, S. K.</creatorcontrib><creatorcontrib>El-Helw, E. A. E.</creatorcontrib><creatorcontrib>Azab, M. E.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramadan, S. K.</au><au>El-Helw, E. A. E.</au><au>Azab, M. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2-Cyano-N′-[(1,3-diphenyl-1H-pyrazol-4-yl)methylidene]acetohydrazide in the Synthesis of Nitrogen Heterocycles</atitle><jtitle>Russian journal of organic chemistry</jtitle><stitle>Russ J Org Chem</stitle><date>2019-12-01</date><risdate>2019</risdate><volume>55</volume><issue>12</issue><spage>1940</spage><epage>1945</epage><pages>1940-1945</pages><issn>1070-4280</issn><eissn>1608-3393</eissn><abstract>Some interesting nitrogen heterocycles, as well as other products, were synthesized by reactions of 2-cyano- N′ -[(1,3-diphenyl-1 H -pyrazol-4-yl)methylidene]acetohydrazide with phenyl isothiocyanate/elemental sulfur, 3,4,5-trimethoxybenzaldehyde, 4-hydroxy-1,1′-biphenyl-3-carbaldehyde, 2-oxoquinoline-3-caraldehyde, triethyl orthoformate, ethyl cyanoacetate, and thiosemicarbazide. The structures of all isolated compounds were established from their analytical and spectral data.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070428019120224</doi><tpages>6</tpages></addata></record>
fulltext	fulltext
identifier	ISSN: 1070-4280
ispartof	Russian journal of organic chemistry, 2019-12, Vol.55 (12), p.1940-1945
issn	1070-4280 1608-3393
language	eng
recordid	cdi_proquest_journals_2347665315
source	SpringerLink Journals - AutoHoldings
subjects	Chemical synthesis Chemistry Chemistry and Materials Science Nitrogen Organic Chemistry
title	2-Cyano-N′-[(1,3-diphenyl-1H-pyrazol-4-yl)methylidene]acetohydrazide in the Synthesis of Nitrogen Heterocycles
url	https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T21%3A24%3A53IST&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=2-Cyano-N%E2%80%B2-%5B(1,3-diphenyl-1H-pyrazol-4-yl)methylidene%5Dacetohydrazide%20in%20the%20Synthesis%20of%20Nitrogen%20Heterocycles&rft.jtitle=Russian%20journal%20of%20organic%20chemistry&rft.au=Ramadan,%20S.%20K.&rft.date=2019-12-01&rft.volume=55&rft.issue=12&rft.spage=1940&rft.epage=1945&rft.pages=1940-1945&rft.issn=1070-4280&rft.eissn=1608-3393&rft_id=info:doi/10.1134/S1070428019120224&rft_dat=%3Cproquest_cross%3E2347665315%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=2347665315&rft_id=info:pmid/&rfr_iscdi=true