Synthesis of Novel Pyrazolyl-1,3,4-Thiadiazole Analogues
In the present study, we have designed a novel series of pyrazolyl-1,3,4-thiadiazole analogues by accommodating 1,3,4-thiadiazole ring at C – 4 of pyrazole ring with and without an amide linkage; 5-methyl-1,3-diphenyl-N-(5-phenyl-1,3,4-thiadiazol-2-yl)-1H-pyrazole-4-carboxamide and 2-(5-methyl-1,3-d...
Gespeichert in:
| Hauptverfasser: | , , , |
|---|---|
| Format: | Dataset |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext bestellen |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | |
|---|---|
| container_issue | |
| container_start_page | |
| container_title | |
| container_volume | |
| creator | Ningaiah, Srikantamurthy Bhadraiah, Umesha K. Sobha, Anjali Shridevi, Doddamani |
| description | In the present study, we have designed a novel series of pyrazolyl-1,3,4-thiadiazole analogues by accommodating 1,3,4-thiadiazole ring at C – 4 of pyrazole ring with and without an amide linkage; 5-methyl-1,3-diphenyl-N-(5-phenyl-1,3,4-thiadiazol-2-yl)-1H-pyrazole-4-carboxamide and 2-(5-methyl-1,3-diphenyl-1H-pyrazol-4-yl)-5-phenyl-1,3,4-thiadiazole respectively. We have designed this class of heterocycles by keeping a wide audience in mind, which augment their scientific knowledge. Newly synthesized compounds were characterized by 1H NMR, 13C NMR, mass, IR spectral studies. Single crystal X-ray analysis of some compounds also gave insight into the structural information. |
| doi_str_mv | 10.6084/m9.figshare.12389225 |
| format | Dataset |
| fullrecord | <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_12389225</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_12389225</sourcerecordid><originalsourceid>FETCH-LOGICAL-d915-408272d8406406f97ca013898b5cbec6ae98ab2bc642180945b46d77fc23cae73</originalsourceid><addsrcrecordid>eNo1j8lqwzAYhHXJoaR9gx78AJGrzVqOIXSD0Bbqu_i1xQI7DpZbcJ--CW1gYGAO3_AhdE9JLYkWD4OpUz6UDqZYU8a1Yay5QfpzOc5dLLlUY6rexu_YVx_LBD9jv_SYbvhG4LbLEPJlitX2CP14-IrlFq0S9CXe_fcatU-P7e4F79-fX3fbPQ6GNlgQzRQLWhB5TjLKA6Hnb-0a76KXEI0Gx5yXglFNjGickEGp5Bn3EBVfI_GHDTCDz3O0pykPMC2WEnvxsoOxVy979eK_3nNIVw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>dataset</recordtype></control><display><type>dataset</type><title>Synthesis of Novel Pyrazolyl-1,3,4-Thiadiazole Analogues</title><source>DataCite</source><creator>Ningaiah, Srikantamurthy ; Bhadraiah, Umesha K. ; Sobha, Anjali ; Shridevi, Doddamani</creator><creatorcontrib>Ningaiah, Srikantamurthy ; Bhadraiah, Umesha K. ; Sobha, Anjali ; Shridevi, Doddamani</creatorcontrib><description>In the present study, we have designed a novel series of pyrazolyl-1,3,4-thiadiazole analogues by accommodating 1,3,4-thiadiazole ring at C – 4 of pyrazole ring with and without an amide linkage; 5-methyl-1,3-diphenyl-N-(5-phenyl-1,3,4-thiadiazol-2-yl)-1H-pyrazole-4-carboxamide and 2-(5-methyl-1,3-diphenyl-1H-pyrazol-4-yl)-5-phenyl-1,3,4-thiadiazole respectively. We have designed this class of heterocycles by keeping a wide audience in mind, which augment their scientific knowledge. Newly synthesized compounds were characterized by 1H NMR, 13C NMR, mass, IR spectral studies. Single crystal X-ray analysis of some compounds also gave insight into the structural information.</description><identifier>DOI: 10.6084/m9.figshare.12389225</identifier><language>eng</language><publisher>Taylor & Francis</publisher><subject>Biochemistry ; Biophysics ; Biotechnology ; Chemical Sciences not elsewhere classified ; FOS: Chemical sciences ; FOS: Physical sciences ; FOS: Sociology ; Physical Sciences not elsewhere classified ; Sociology</subject><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1892</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.12389225$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Ningaiah, Srikantamurthy</creatorcontrib><creatorcontrib>Bhadraiah, Umesha K.</creatorcontrib><creatorcontrib>Sobha, Anjali</creatorcontrib><creatorcontrib>Shridevi, Doddamani</creatorcontrib><title>Synthesis of Novel Pyrazolyl-1,3,4-Thiadiazole Analogues</title><description>In the present study, we have designed a novel series of pyrazolyl-1,3,4-thiadiazole analogues by accommodating 1,3,4-thiadiazole ring at C – 4 of pyrazole ring with and without an amide linkage; 5-methyl-1,3-diphenyl-N-(5-phenyl-1,3,4-thiadiazol-2-yl)-1H-pyrazole-4-carboxamide and 2-(5-methyl-1,3-diphenyl-1H-pyrazol-4-yl)-5-phenyl-1,3,4-thiadiazole respectively. We have designed this class of heterocycles by keeping a wide audience in mind, which augment their scientific knowledge. Newly synthesized compounds were characterized by 1H NMR, 13C NMR, mass, IR spectral studies. Single crystal X-ray analysis of some compounds also gave insight into the structural information.</description><subject>Biochemistry</subject><subject>Biophysics</subject><subject>Biotechnology</subject><subject>Chemical Sciences not elsewhere classified</subject><subject>FOS: Chemical sciences</subject><subject>FOS: Physical sciences</subject><subject>FOS: Sociology</subject><subject>Physical Sciences not elsewhere classified</subject><subject>Sociology</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2020</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNo1j8lqwzAYhHXJoaR9gx78AJGrzVqOIXSD0Bbqu_i1xQI7DpZbcJ--CW1gYGAO3_AhdE9JLYkWD4OpUz6UDqZYU8a1Yay5QfpzOc5dLLlUY6rexu_YVx_LBD9jv_SYbvhG4LbLEPJlitX2CP14-IrlFq0S9CXe_fcatU-P7e4F79-fX3fbPQ6GNlgQzRQLWhB5TjLKA6Hnb-0a76KXEI0Gx5yXglFNjGickEGp5Bn3EBVfI_GHDTCDz3O0pykPMC2WEnvxsoOxVy979eK_3nNIVw</recordid><startdate>20200529</startdate><enddate>20200529</enddate><creator>Ningaiah, Srikantamurthy</creator><creator>Bhadraiah, Umesha K.</creator><creator>Sobha, Anjali</creator><creator>Shridevi, Doddamani</creator><general>Taylor & Francis</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20200529</creationdate><title>Synthesis of Novel Pyrazolyl-1,3,4-Thiadiazole Analogues</title><author>Ningaiah, Srikantamurthy ; Bhadraiah, Umesha K. ; Sobha, Anjali ; Shridevi, Doddamani</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d915-408272d8406406f97ca013898b5cbec6ae98ab2bc642180945b46d77fc23cae73</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Biochemistry</topic><topic>Biophysics</topic><topic>Biotechnology</topic><topic>Chemical Sciences not elsewhere classified</topic><topic>FOS: Chemical sciences</topic><topic>FOS: Physical sciences</topic><topic>FOS: Sociology</topic><topic>Physical Sciences not elsewhere classified</topic><topic>Sociology</topic><toplevel>online_resources</toplevel><creatorcontrib>Ningaiah, Srikantamurthy</creatorcontrib><creatorcontrib>Bhadraiah, Umesha K.</creatorcontrib><creatorcontrib>Sobha, Anjali</creatorcontrib><creatorcontrib>Shridevi, Doddamani</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Ningaiah, Srikantamurthy</au><au>Bhadraiah, Umesha K.</au><au>Sobha, Anjali</au><au>Shridevi, Doddamani</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Synthesis of Novel Pyrazolyl-1,3,4-Thiadiazole Analogues</title><date>2020-05-29</date><risdate>2020</risdate><abstract>In the present study, we have designed a novel series of pyrazolyl-1,3,4-thiadiazole analogues by accommodating 1,3,4-thiadiazole ring at C – 4 of pyrazole ring with and without an amide linkage; 5-methyl-1,3-diphenyl-N-(5-phenyl-1,3,4-thiadiazol-2-yl)-1H-pyrazole-4-carboxamide and 2-(5-methyl-1,3-diphenyl-1H-pyrazol-4-yl)-5-phenyl-1,3,4-thiadiazole respectively. We have designed this class of heterocycles by keeping a wide audience in mind, which augment their scientific knowledge. Newly synthesized compounds were characterized by 1H NMR, 13C NMR, mass, IR spectral studies. Single crystal X-ray analysis of some compounds also gave insight into the structural information.</abstract><pub>Taylor & Francis</pub><doi>10.6084/m9.figshare.12389225</doi><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext_linktorsrc |
| identifier | DOI: 10.6084/m9.figshare.12389225 |
| ispartof | |
| issn | |
| language | eng |
| recordid | cdi_datacite_primary_10_6084_m9_figshare_12389225 |
| source | DataCite |
| subjects | Biochemistry Biophysics Biotechnology Chemical Sciences not elsewhere classified FOS: Chemical sciences FOS: Physical sciences FOS: Sociology Physical Sciences not elsewhere classified Sociology |
| title | Synthesis of Novel Pyrazolyl-1,3,4-Thiadiazole Analogues |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T00%3A31%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Ningaiah,%20Srikantamurthy&rft.date=2020-05-29&rft_id=info:doi/10.6084/m9.figshare.12389225&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_12389225%3C/datacite_PQ8%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 |