Loading…
Synthesis, spectral characterization, and biological evaluation of imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazole‐2‐amine
A series of new imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazol‐2‐amine 3–12 were synthesized by treating various amines 1(a–d) with alkyl/aryl isothiocyanate 2(a‐c) at 60–90°C in isopropyl alcohol without using any catalyst with high yields. The structures of all the newly syn...
Saved in:
Published in: | Journal of the Chinese Chemical Society (Taipei) 2019-12, Vol.66 (12), p.1700-1707 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3 |
---|---|
cites | cdi_FETCH-LOGICAL-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3 |
container_end_page | 1707 |
container_issue | 12 |
container_start_page | 1700 |
container_title | Journal of the Chinese Chemical Society (Taipei) |
container_volume | 66 |
creator | Mahaboob Basha, Shaik Varalakshmi, Mavallur Thaslim Basha, Shaik Venkataramaiah, Chintha Syed Shafi, Suban Naga Raju, Chamarthi Rajendra, Wudayagiri |
description | A series of new imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazol‐2‐amine 3–12 were synthesized by treating various amines 1(a–d) with alkyl/aryl isothiocyanate 2(a‐c) at 60–90°C in isopropyl alcohol without using any catalyst with high yields. The structures of all the newly synthesized compounds were characterized using IR, NMR (1H, 13C), mass, and elemental analyses. All the newly synthesized compounds were screened for their in vitro antioxidant and antimicrobial activities to understand their biological potency. All the title compounds exhibited good antioxidant and antimicrobial activities in vitro when compared to the standard drugs.
A series of new imidazole substituted pyridine‐2‐amine and benzo substituted imidazole‐2‐amine has been synthesized by treating various diamines with alkyl/aryl isothiocyanate in isopropylalcohol without using any catalyst with high yields. These compounds were screened for their antimicrobial and antioxidant activities. |
doi_str_mv | 10.1002/jccs.201800461 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2323121524</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2323121524</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3</originalsourceid><addsrcrecordid>eNqFkU1OwzAQhS0EEqWwZR2JbVP8m8RLVPGrSiyAteU4DnWVxsF2QOmKI3ABLsdJSAkqiA2L0Yxmvvdm8QA4RnCKIMSnS6X8FEOUQUgTtANGGHEcJ4zyXTCCEPKYMpLsgwPvlz1CMOMj8H7X1WGhvfGTyDdaBSerSC2kkypoZ9YyGFtPIlkXUW5sZR-N6gH9LKv26xTZMjIrU8i1rfTH65tvcx9MaIMuoqZzpjD1Zo37kqt-Hpx0vbZ_4N8mW_oQ7JWy8vrou4_Bw8X5_ewqnt9eXs_O5rEijKIYZVzzJM9TnsKCEFLmMiEkUziBLFVcpjhlTKeQ0TSnkPIMpowWGCGMk4yWiozByeDbOPvUah_E0rau7l8KTDBBGDFMe2o6UMpZ750uRePMSrpOICg2EYhNBGIbQS_gg-DFVLr7hxY3s9ndj_YTPCSTNw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2323121524</pqid></control><display><type>article</type><title>Synthesis, spectral characterization, and biological evaluation of imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazole‐2‐amine</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Mahaboob Basha, Shaik ; Varalakshmi, Mavallur ; Thaslim Basha, Shaik ; Venkataramaiah, Chintha ; Syed Shafi, Suban ; Naga Raju, Chamarthi ; Rajendra, Wudayagiri</creator><creatorcontrib>Mahaboob Basha, Shaik ; Varalakshmi, Mavallur ; Thaslim Basha, Shaik ; Venkataramaiah, Chintha ; Syed Shafi, Suban ; Naga Raju, Chamarthi ; Rajendra, Wudayagiri</creatorcontrib><description>A series of new imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazol‐2‐amine 3–12 were synthesized by treating various amines 1(a–d) with alkyl/aryl isothiocyanate 2(a‐c) at 60–90°C in isopropyl alcohol without using any catalyst with high yields. The structures of all the newly synthesized compounds were characterized using IR, NMR (1H, 13C), mass, and elemental analyses. All the newly synthesized compounds were screened for their in vitro antioxidant and antimicrobial activities to understand their biological potency. All the title compounds exhibited good antioxidant and antimicrobial activities in vitro when compared to the standard drugs.
A series of new imidazole substituted pyridine‐2‐amine and benzo substituted imidazole‐2‐amine has been synthesized by treating various diamines with alkyl/aryl isothiocyanate in isopropylalcohol without using any catalyst with high yields. These compounds were screened for their antimicrobial and antioxidant activities.</description><identifier>ISSN: 0009-4536</identifier><identifier>EISSN: 2192-6549</identifier><identifier>DOI: 10.1002/jccs.201800461</identifier><language>eng</language><publisher>Weinheim: Wiley‐VCH Verlag GmbH & Co. KGaA</publisher><subject>Amines ; Antiinfectives and antibacterials ; antioxidant and antimicrobial activities ; Antioxidants ; Aromatic compounds ; aryl/alkyl isocyanates ; Imidazole ; Isopropanol ; NMR ; Nuclear magnetic resonance ; Substitutes</subject><ispartof>Journal of the Chinese Chemical Society (Taipei), 2019-12, Vol.66 (12), p.1700-1707</ispartof><rights>2019 The Chemical Society Located in Taipei & Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3</citedby><cites>FETCH-LOGICAL-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Mahaboob Basha, Shaik</creatorcontrib><creatorcontrib>Varalakshmi, Mavallur</creatorcontrib><creatorcontrib>Thaslim Basha, Shaik</creatorcontrib><creatorcontrib>Venkataramaiah, Chintha</creatorcontrib><creatorcontrib>Syed Shafi, Suban</creatorcontrib><creatorcontrib>Naga Raju, Chamarthi</creatorcontrib><creatorcontrib>Rajendra, Wudayagiri</creatorcontrib><title>Synthesis, spectral characterization, and biological evaluation of imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazole‐2‐amine</title><title>Journal of the Chinese Chemical Society (Taipei)</title><description>A series of new imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazol‐2‐amine 3–12 were synthesized by treating various amines 1(a–d) with alkyl/aryl isothiocyanate 2(a‐c) at 60–90°C in isopropyl alcohol without using any catalyst with high yields. The structures of all the newly synthesized compounds were characterized using IR, NMR (1H, 13C), mass, and elemental analyses. All the newly synthesized compounds were screened for their in vitro antioxidant and antimicrobial activities to understand their biological potency. All the title compounds exhibited good antioxidant and antimicrobial activities in vitro when compared to the standard drugs.
A series of new imidazole substituted pyridine‐2‐amine and benzo substituted imidazole‐2‐amine has been synthesized by treating various diamines with alkyl/aryl isothiocyanate in isopropylalcohol without using any catalyst with high yields. These compounds were screened for their antimicrobial and antioxidant activities.</description><subject>Amines</subject><subject>Antiinfectives and antibacterials</subject><subject>antioxidant and antimicrobial activities</subject><subject>Antioxidants</subject><subject>Aromatic compounds</subject><subject>aryl/alkyl isocyanates</subject><subject>Imidazole</subject><subject>Isopropanol</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Substitutes</subject><issn>0009-4536</issn><issn>2192-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkU1OwzAQhS0EEqWwZR2JbVP8m8RLVPGrSiyAteU4DnWVxsF2QOmKI3ABLsdJSAkqiA2L0Yxmvvdm8QA4RnCKIMSnS6X8FEOUQUgTtANGGHEcJ4zyXTCCEPKYMpLsgwPvlz1CMOMj8H7X1WGhvfGTyDdaBSerSC2kkypoZ9YyGFtPIlkXUW5sZR-N6gH9LKv26xTZMjIrU8i1rfTH65tvcx9MaIMuoqZzpjD1Zo37kqt-Hpx0vbZ_4N8mW_oQ7JWy8vrou4_Bw8X5_ewqnt9eXs_O5rEijKIYZVzzJM9TnsKCEFLmMiEkUziBLFVcpjhlTKeQ0TSnkPIMpowWGCGMk4yWiozByeDbOPvUah_E0rau7l8KTDBBGDFMe2o6UMpZ750uRePMSrpOICg2EYhNBGIbQS_gg-DFVLr7hxY3s9ndj_YTPCSTNw</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Mahaboob Basha, Shaik</creator><creator>Varalakshmi, Mavallur</creator><creator>Thaslim Basha, Shaik</creator><creator>Venkataramaiah, Chintha</creator><creator>Syed Shafi, Suban</creator><creator>Naga Raju, Chamarthi</creator><creator>Rajendra, Wudayagiri</creator><general>Wiley‐VCH Verlag GmbH & Co. KGaA</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201912</creationdate><title>Synthesis, spectral characterization, and biological evaluation of imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazole‐2‐amine</title><author>Mahaboob Basha, Shaik ; Varalakshmi, Mavallur ; Thaslim Basha, Shaik ; Venkataramaiah, Chintha ; Syed Shafi, Suban ; Naga Raju, Chamarthi ; Rajendra, Wudayagiri</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amines</topic><topic>Antiinfectives and antibacterials</topic><topic>antioxidant and antimicrobial activities</topic><topic>Antioxidants</topic><topic>Aromatic compounds</topic><topic>aryl/alkyl isocyanates</topic><topic>Imidazole</topic><topic>Isopropanol</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Substitutes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahaboob Basha, Shaik</creatorcontrib><creatorcontrib>Varalakshmi, Mavallur</creatorcontrib><creatorcontrib>Thaslim Basha, Shaik</creatorcontrib><creatorcontrib>Venkataramaiah, Chintha</creatorcontrib><creatorcontrib>Syed Shafi, Suban</creatorcontrib><creatorcontrib>Naga Raju, Chamarthi</creatorcontrib><creatorcontrib>Rajendra, Wudayagiri</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahaboob Basha, Shaik</au><au>Varalakshmi, Mavallur</au><au>Thaslim Basha, Shaik</au><au>Venkataramaiah, Chintha</au><au>Syed Shafi, Suban</au><au>Naga Raju, Chamarthi</au><au>Rajendra, Wudayagiri</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, spectral characterization, and biological evaluation of imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazole‐2‐amine</atitle><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle><date>2019-12</date><risdate>2019</risdate><volume>66</volume><issue>12</issue><spage>1700</spage><epage>1707</epage><pages>1700-1707</pages><issn>0009-4536</issn><eissn>2192-6549</eissn><abstract>A series of new imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazol‐2‐amine 3–12 were synthesized by treating various amines 1(a–d) with alkyl/aryl isothiocyanate 2(a‐c) at 60–90°C in isopropyl alcohol without using any catalyst with high yields. The structures of all the newly synthesized compounds were characterized using IR, NMR (1H, 13C), mass, and elemental analyses. All the newly synthesized compounds were screened for their in vitro antioxidant and antimicrobial activities to understand their biological potency. All the title compounds exhibited good antioxidant and antimicrobial activities in vitro when compared to the standard drugs.
A series of new imidazole substituted pyridine‐2‐amine and benzo substituted imidazole‐2‐amine has been synthesized by treating various diamines with alkyl/aryl isothiocyanate in isopropylalcohol without using any catalyst with high yields. These compounds were screened for their antimicrobial and antioxidant activities.</abstract><cop>Weinheim</cop><pub>Wiley‐VCH Verlag GmbH & Co. KGaA</pub><doi>10.1002/jccs.201800461</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-4536 |
ispartof | Journal of the Chinese Chemical Society (Taipei), 2019-12, Vol.66 (12), p.1700-1707 |
issn | 0009-4536 2192-6549 |
language | eng |
recordid | cdi_proquest_journals_2323121524 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Amines Antiinfectives and antibacterials antioxidant and antimicrobial activities Antioxidants Aromatic compounds aryl/alkyl isocyanates Imidazole Isopropanol NMR Nuclear magnetic resonance Substitutes |
title | Synthesis, spectral characterization, and biological evaluation of imidazole‐substituted pyridine‐2‐amine and benzo‐substituted imidazole‐2‐amine |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T11%3A35%3A58IST&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=Synthesis,%20spectral%20characterization,%20and%20biological%20evaluation%20of%20imidazole%E2%80%90substituted%20pyridine%E2%80%902%E2%80%90amine%20and%20benzo%E2%80%90substituted%20imidazole%E2%80%902%E2%80%90amine&rft.jtitle=Journal%20of%20the%20Chinese%20Chemical%20Society%20(Taipei)&rft.au=Mahaboob%20Basha,%20Shaik&rft.date=2019-12&rft.volume=66&rft.issue=12&rft.spage=1700&rft.epage=1707&rft.pages=1700-1707&rft.issn=0009-4536&rft.eissn=2192-6549&rft_id=info:doi/10.1002/jccs.201800461&rft_dat=%3Cproquest_cross%3E2323121524%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3541-189e96bb7970d333fba6338c26057c9a72755e70547b404980754d21122684fc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2323121524&rft_id=info:pmid/&rfr_iscdi=true |