Loading…
Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles
Ethyl naphtho[2,1-b]furan-2-carboxylate (2) on reaction with hydrazine hydrate in presence of acid catalyst in ethanol medium affords naphtho[2,1-b]furan-2-carbohydrazide (3). The reaction of substituted acetophenones (4a-c) with aromatic aldehydes (5a-e) produces chalcones (6a-o) via the Claisen co...
Saved in:
Published in: | Indian journal of pharmaceutical sciences 2008-11, Vol.70 (6), p.715-720 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | 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-c459t-b12ee9c89b7350027956fa52d56af623a325c21764a8751ee9f2f9c93b370c9f3 |
---|---|
cites | |
container_end_page | 720 |
container_issue | 6 |
container_start_page | 715 |
container_title | Indian journal of pharmaceutical sciences |
container_volume | 70 |
creator | Kumaraswamy, M N Chandrashekhar, C Shivakumar, H Prathima Mathias, D A Mahadevan, K M Vaidya, V P |
description | Ethyl naphtho[2,1-b]furan-2-carboxylate (2) on reaction with hydrazine hydrate in presence of acid catalyst in ethanol medium affords naphtho[2,1-b]furan-2-carbohydrazide (3). The reaction of substituted acetophenones (4a-c) with aromatic aldehydes (5a-e) produces chalcones (6a-o) via the Claisen condensation. The reaction of naphtho[2,1-b]furan-2-carbohydrazide (3) with chalcones (6a-6o) in presence of acetic acid as catalyst in dioxane produces 1-(naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles (7a-o). The structures of newly synthesized compounds have been established by elemental analysis and spectral studies. The compounds 7a-o have been evaluated for their antimicrobial activity and some selected compounds evaluated for antiinflammatory, analgesic, anthelmintic, diuretic and antipyretic activities. |
doi_str_mv | 10.4103/0250-474X.49090 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3040863</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A197387223</galeid><sourcerecordid>A197387223</sourcerecordid><originalsourceid>FETCH-LOGICAL-c459t-b12ee9c89b7350027956fa52d56af623a325c21764a8751ee9f2f9c93b370c9f3</originalsourceid><addsrcrecordid>eNptkt1rFDEUxYModtv67JsM-KCFzTYfk8nkRVhKtULBBysIIiGTSTqR2WSbZFamf70z3bpYkPtw4d7fOSScC8BrjFYlRvQcEYZgycvvq1IggZ6BBRaihpSX9DlYHLZH4DilXwhRQSh_CY4IppUoKVqA319HnzuTXCqUb4u1zm7n8lhc7lQ_qOyCL4ItCHyPoVfbLnfhB1li2Py0Q1QeEjj2UKvYBD_2Z5AuGWxdGpqUXR6yaSFZ0mnSjW0MEF_B7RjVfehNOgUvrOqTefXYT8C3j5c3F1fw-sunzxfra6hLJjJsMDFG6Fo0nDKECBessoqRllXKVoQqSpgmmFelqjnDE2uJFVrQhnKkhaUn4MPedzs0G9Nq43NUvdxGt1FxlEE5-XTjXSdvw05SVKK6opPBu0eDGO4Gk7LcuKRN3ytvwpBkzRhBgmM-kW_35K3qjXTehslQz7RcY8FpzQmZ_Vb_oaZqzcbp4I110_yJ4Hwv0DGkFI09PB4jOR-BnGOWc8zy4QgmxZt__3zg_6ZO_wB8yqsX</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>855209717</pqid></control><display><type>article</type><title>Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles</title><source>PubMed Central</source><creator>Kumaraswamy, M N ; Chandrashekhar, C ; Shivakumar, H ; Prathima Mathias, D A ; Mahadevan, K M ; Vaidya, V P</creator><creatorcontrib>Kumaraswamy, M N ; Chandrashekhar, C ; Shivakumar, H ; Prathima Mathias, D A ; Mahadevan, K M ; Vaidya, V P</creatorcontrib><description>Ethyl naphtho[2,1-b]furan-2-carboxylate (2) on reaction with hydrazine hydrate in presence of acid catalyst in ethanol medium affords naphtho[2,1-b]furan-2-carbohydrazide (3). The reaction of substituted acetophenones (4a-c) with aromatic aldehydes (5a-e) produces chalcones (6a-o) via the Claisen condensation. The reaction of naphtho[2,1-b]furan-2-carbohydrazide (3) with chalcones (6a-6o) in presence of acetic acid as catalyst in dioxane produces 1-(naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles (7a-o). The structures of newly synthesized compounds have been established by elemental analysis and spectral studies. The compounds 7a-o have been evaluated for their antimicrobial activity and some selected compounds evaluated for antiinflammatory, analgesic, anthelmintic, diuretic and antipyretic activities.</description><identifier>ISSN: 0250-474X</identifier><identifier>EISSN: 1998-3743</identifier><identifier>DOI: 10.4103/0250-474X.49090</identifier><identifier>PMID: 21369430</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. Ltd</publisher><subject>Research Paper</subject><ispartof>Indian journal of pharmaceutical sciences, 2008-11, Vol.70 (6), p.715-720</ispartof><rights>COPYRIGHT 2008 Medknow Publications and Media Pvt. Ltd.</rights><rights>Indian Journal of Pharmaceutical Sciences 2008</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-b12ee9c89b7350027956fa52d56af623a325c21764a8751ee9f2f9c93b370c9f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040863/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040863/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21369430$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumaraswamy, M N</creatorcontrib><creatorcontrib>Chandrashekhar, C</creatorcontrib><creatorcontrib>Shivakumar, H</creatorcontrib><creatorcontrib>Prathima Mathias, D A</creatorcontrib><creatorcontrib>Mahadevan, K M</creatorcontrib><creatorcontrib>Vaidya, V P</creatorcontrib><title>Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles</title><title>Indian journal of pharmaceutical sciences</title><addtitle>Indian J Pharm Sci</addtitle><description>Ethyl naphtho[2,1-b]furan-2-carboxylate (2) on reaction with hydrazine hydrate in presence of acid catalyst in ethanol medium affords naphtho[2,1-b]furan-2-carbohydrazide (3). The reaction of substituted acetophenones (4a-c) with aromatic aldehydes (5a-e) produces chalcones (6a-o) via the Claisen condensation. The reaction of naphtho[2,1-b]furan-2-carbohydrazide (3) with chalcones (6a-6o) in presence of acetic acid as catalyst in dioxane produces 1-(naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles (7a-o). The structures of newly synthesized compounds have been established by elemental analysis and spectral studies. The compounds 7a-o have been evaluated for their antimicrobial activity and some selected compounds evaluated for antiinflammatory, analgesic, anthelmintic, diuretic and antipyretic activities.</description><subject>Research Paper</subject><issn>0250-474X</issn><issn>1998-3743</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNptkt1rFDEUxYModtv67JsM-KCFzTYfk8nkRVhKtULBBysIIiGTSTqR2WSbZFamf70z3bpYkPtw4d7fOSScC8BrjFYlRvQcEYZgycvvq1IggZ6BBRaihpSX9DlYHLZH4DilXwhRQSh_CY4IppUoKVqA319HnzuTXCqUb4u1zm7n8lhc7lQ_qOyCL4ItCHyPoVfbLnfhB1li2Py0Q1QeEjj2UKvYBD_2Z5AuGWxdGpqUXR6yaSFZ0mnSjW0MEF_B7RjVfehNOgUvrOqTefXYT8C3j5c3F1fw-sunzxfra6hLJjJsMDFG6Fo0nDKECBessoqRllXKVoQqSpgmmFelqjnDE2uJFVrQhnKkhaUn4MPedzs0G9Nq43NUvdxGt1FxlEE5-XTjXSdvw05SVKK6opPBu0eDGO4Gk7LcuKRN3ytvwpBkzRhBgmM-kW_35K3qjXTehslQz7RcY8FpzQmZ_Vb_oaZqzcbp4I110_yJ4Hwv0DGkFI09PB4jOR-BnGOWc8zy4QgmxZt__3zg_6ZO_wB8yqsX</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Kumaraswamy, M N</creator><creator>Chandrashekhar, C</creator><creator>Shivakumar, H</creator><creator>Prathima Mathias, D A</creator><creator>Mahadevan, K M</creator><creator>Vaidya, V P</creator><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081101</creationdate><title>Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles</title><author>Kumaraswamy, M N ; Chandrashekhar, C ; Shivakumar, H ; Prathima Mathias, D A ; Mahadevan, K M ; Vaidya, V P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-b12ee9c89b7350027956fa52d56af623a325c21764a8751ee9f2f9c93b370c9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Research Paper</topic><toplevel>online_resources</toplevel><creatorcontrib>Kumaraswamy, M N</creatorcontrib><creatorcontrib>Chandrashekhar, C</creatorcontrib><creatorcontrib>Shivakumar, H</creatorcontrib><creatorcontrib>Prathima Mathias, D A</creatorcontrib><creatorcontrib>Mahadevan, K M</creatorcontrib><creatorcontrib>Vaidya, V P</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Indian journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumaraswamy, M N</au><au>Chandrashekhar, C</au><au>Shivakumar, H</au><au>Prathima Mathias, D A</au><au>Mahadevan, K M</au><au>Vaidya, V P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles</atitle><jtitle>Indian journal of pharmaceutical sciences</jtitle><addtitle>Indian J Pharm Sci</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>70</volume><issue>6</issue><spage>715</spage><epage>720</epage><pages>715-720</pages><issn>0250-474X</issn><eissn>1998-3743</eissn><abstract>Ethyl naphtho[2,1-b]furan-2-carboxylate (2) on reaction with hydrazine hydrate in presence of acid catalyst in ethanol medium affords naphtho[2,1-b]furan-2-carbohydrazide (3). The reaction of substituted acetophenones (4a-c) with aromatic aldehydes (5a-e) produces chalcones (6a-o) via the Claisen condensation. The reaction of naphtho[2,1-b]furan-2-carbohydrazide (3) with chalcones (6a-6o) in presence of acetic acid as catalyst in dioxane produces 1-(naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles (7a-o). The structures of newly synthesized compounds have been established by elemental analysis and spectral studies. The compounds 7a-o have been evaluated for their antimicrobial activity and some selected compounds evaluated for antiinflammatory, analgesic, anthelmintic, diuretic and antipyretic activities.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>21369430</pmid><doi>10.4103/0250-474X.49090</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0250-474X |
ispartof | Indian journal of pharmaceutical sciences, 2008-11, Vol.70 (6), p.715-720 |
issn | 0250-474X 1998-3743 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3040863 |
source | PubMed Central |
subjects | Research Paper |
title | Synthesis and Activity Evaluation of 2-(1-naphtho[2,1-b]furan-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T22%3A33%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20Activity%20Evaluation%20of%202-(1-naphtho%5B2,1-b%5Dfuran-2-yl-carbonyl)-3,5-disubstituted-2,3-dihydro-1H-pyrazoles&rft.jtitle=Indian%20journal%20of%20pharmaceutical%20sciences&rft.au=Kumaraswamy,%20M%20N&rft.date=2008-11-01&rft.volume=70&rft.issue=6&rft.spage=715&rft.epage=720&rft.pages=715-720&rft.issn=0250-474X&rft.eissn=1998-3743&rft_id=info:doi/10.4103/0250-474X.49090&rft_dat=%3Cgale_pubme%3EA197387223%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c459t-b12ee9c89b7350027956fa52d56af623a325c21764a8751ee9f2f9c93b370c9f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=855209717&rft_id=info:pmid/21369430&rft_galeid=A197387223&rfr_iscdi=true |