Synthesis and Biological Properties of 4-Chloro-N1-(5-Chloro-1H-Indol-1-yl)-N2-(2-Chlorophenyl) benzene-1,2-Diamine Derivatives
Background Five-membered heterocycle with one neighbouring nitrogen atoms is present in the indole nucleus. Heterocyclic substances feature two adjacent benzene and pyrrole ring atoms. Indole are heterocyclic compounds with one oxygen ring that have a benzoannelated – pyrrole ring. Indole derivative...
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creator | Andhale, Nikita Shridhar Bhor, Rohit Jaysing Kolhe, Mahesh Hari Pawar, Tanishka Anil Tambe, Pornima Ramdas Ghule, Rupali Mahadev Bhange, Sarthak Anil Thete, Bhakti Sharad Kute, Pruthviraj Vijay Malvade, Pratik Vijay Bhagat, Jyoti Ramkisan Waykar, Poonam Prakash |
description | Background Five-membered heterocycle with one neighbouring nitrogen atoms is present in the indole nucleus. Heterocyclic substances feature two adjacent benzene and pyrrole ring atoms. Indole are heterocyclic compounds with one oxygen ring that have a benzoannelated – pyrrole ring. Indole derivatives are highly valuable chemical synthesis and medicinal intermediates. Recent years have seen a surge in interest in the effective synthesis of indole blocks and associated functionalization’s, particularly the alkylation of indoles. The two following factors will be the main emphasis of this review: i) Recent advancements in the alkylation of indoles, namely those involving the N1-, C2- and C3-positions and the synthesis of indoles, which was facilitated by transition metals. Materials and Methods Benzoic acid and ethanoic acid, propionic acid, hydroxylamine, 2,5 Dichloro aniline are used for the synthesis of indole derivatives were used for the synthesis of indole. Results Compared to indomethacin, the anti-inflammatory results for the substances or their derivatives like N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-indol-1-yl)-4-am inobenzene-1,2-diamine NA5 (Scheme 1B); N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1 H-ind ol-1-yl)-3-aminobenzene-1,2-diamine NA6 (Scheme 1B) and N2-(biphenyl-2-yl)-4-chloro-N1- (5-chloro-1H-indol-1-yl)-2-aminobenzene-1,2-diamine NA7 (Scheme 1B). Conclusion Examined were the anti-inflammatory properties of the substances in the title and their derivatives. The compounds containing indole derivatives with an electron-withdrawing group have a higher activity than those containing an electron-donating group, according to research on the link between structure and activity. Summarising the data from the previously reviewed literature, we can say that indole has a broad spectrum of biological activity. Numerous opportunities exist to investigate indole for new therapeutic uses. Researchers worldwide will benefit from this study’s coverage of the chemistry of indole derivatives in the design and synthesis of new pharmaceuticals that might be utilised to treat a range of diseases. |
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Heterocyclic substances feature two adjacent benzene and pyrrole ring atoms. Indole are heterocyclic compounds with one oxygen ring that have a benzoannelated – pyrrole ring. Indole derivatives are highly valuable chemical synthesis and medicinal intermediates. Recent years have seen a surge in interest in the effective synthesis of indole blocks and associated functionalization’s, particularly the alkylation of indoles. The two following factors will be the main emphasis of this review: i) Recent advancements in the alkylation of indoles, namely those involving the N1-, C2- and C3-positions and the synthesis of indoles, which was facilitated by transition metals. Materials and Methods Benzoic acid and ethanoic acid, propionic acid, hydroxylamine, 2,5 Dichloro aniline are used for the synthesis of indole derivatives were used for the synthesis of indole. Results Compared to indomethacin, the anti-inflammatory results for the substances or their derivatives like N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-indol-1-yl)-4-am inobenzene-1,2-diamine NA5 (Scheme 1B); N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1 H-ind ol-1-yl)-3-aminobenzene-1,2-diamine NA6 (Scheme 1B) and N2-(biphenyl-2-yl)-4-chloro-N1- (5-chloro-1H-indol-1-yl)-2-aminobenzene-1,2-diamine NA7 (Scheme 1B). Conclusion Examined were the anti-inflammatory properties of the substances in the title and their derivatives. The compounds containing indole derivatives with an electron-withdrawing group have a higher activity than those containing an electron-donating group, according to research on the link between structure and activity. Summarising the data from the previously reviewed literature, we can say that indole has a broad spectrum of biological activity. Numerous opportunities exist to investigate indole for new therapeutic uses. Researchers worldwide will benefit from this study’s coverage of the chemistry of indole derivatives in the design and synthesis of new pharmaceuticals that might be utilised to treat a range of diseases.</description><identifier>ISSN: 0975-1483</identifier><identifier>EISSN: 0975-1505</identifier><identifier>DOI: 10.5530/jyp.2024.16.64</identifier><language>eng</language><publisher>Bangalore: InPharm</publisher><subject>Hydrocarbons</subject><ispartof>Journal of young pharmacists, 2024-08, Vol.16 (3), p.498-505</ispartof><rights>Copyright InPharm 2024</rights><lds50>peer_reviewed</lds50><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>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Andhale, Nikita Shridhar</creatorcontrib><creatorcontrib>Bhor, Rohit Jaysing</creatorcontrib><creatorcontrib>Kolhe, Mahesh Hari</creatorcontrib><creatorcontrib>Pawar, Tanishka Anil</creatorcontrib><creatorcontrib>Tambe, Pornima Ramdas</creatorcontrib><creatorcontrib>Ghule, Rupali Mahadev</creatorcontrib><creatorcontrib>Bhange, Sarthak Anil</creatorcontrib><creatorcontrib>Thete, Bhakti Sharad</creatorcontrib><creatorcontrib>Kute, Pruthviraj Vijay</creatorcontrib><creatorcontrib>Malvade, Pratik Vijay</creatorcontrib><creatorcontrib>Bhagat, Jyoti Ramkisan</creatorcontrib><creatorcontrib>Waykar, Poonam Prakash</creatorcontrib><title>Synthesis and Biological Properties of 4-Chloro-N1-(5-Chloro-1H-Indol-1-yl)-N2-(2-Chlorophenyl) benzene-1,2-Diamine Derivatives</title><title>Journal of young pharmacists</title><description>Background Five-membered heterocycle with one neighbouring nitrogen atoms is present in the indole nucleus. Heterocyclic substances feature two adjacent benzene and pyrrole ring atoms. Indole are heterocyclic compounds with one oxygen ring that have a benzoannelated – pyrrole ring. Indole derivatives are highly valuable chemical synthesis and medicinal intermediates. Recent years have seen a surge in interest in the effective synthesis of indole blocks and associated functionalization’s, particularly the alkylation of indoles. The two following factors will be the main emphasis of this review: i) Recent advancements in the alkylation of indoles, namely those involving the N1-, C2- and C3-positions and the synthesis of indoles, which was facilitated by transition metals. Materials and Methods Benzoic acid and ethanoic acid, propionic acid, hydroxylamine, 2,5 Dichloro aniline are used for the synthesis of indole derivatives were used for the synthesis of indole. Results Compared to indomethacin, the anti-inflammatory results for the substances or their derivatives like N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-indol-1-yl)-4-am inobenzene-1,2-diamine NA5 (Scheme 1B); N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1 H-ind ol-1-yl)-3-aminobenzene-1,2-diamine NA6 (Scheme 1B) and N2-(biphenyl-2-yl)-4-chloro-N1- (5-chloro-1H-indol-1-yl)-2-aminobenzene-1,2-diamine NA7 (Scheme 1B). Conclusion Examined were the anti-inflammatory properties of the substances in the title and their derivatives. The compounds containing indole derivatives with an electron-withdrawing group have a higher activity than those containing an electron-donating group, according to research on the link between structure and activity. Summarising the data from the previously reviewed literature, we can say that indole has a broad spectrum of biological activity. Numerous opportunities exist to investigate indole for new therapeutic uses. Researchers worldwide will benefit from this study’s coverage of the chemistry of indole derivatives in the design and synthesis of new pharmaceuticals that might be utilised to treat a range of diseases.</description><subject>Hydrocarbons</subject><issn>0975-1483</issn><issn>0975-1505</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNo1kM9LwzAUx4soOOaungteJpiaNEmbHnVTNxhTUM8hTd9cRpfUpBvUi_-6HZvv8n59-T7eJ4quCU44p_h-0zVJilOWkCzJ2Fk0wEXOEeGYn__XTNDLaBTCBh8ixzktBtHve2fbNQQTYmWr-NG42n0Zrer4zbsGfGsgxG4VMzRZ1847tCRozP8bMkNzW7kaEdTVt2iZonF62jVrsP0sLsH-gAVE7lI0NWprLMRT8GavWrOHcBVdrFQdYHTKw-jz-eljMkOL15f55GGBNME5QxkroP-CrETFlRC40prxLIWCc1wVhNJSKyaUpiWmugRBSCWYzoSqBJSQczqMbo6-jXffOwit3Lidt_1JSQkWOGM8T3tVclRp70LwsJKNN1vlO0mwPHCWPWd54CxJJjNG_wA8O25_</recordid><startdate>20240823</startdate><enddate>20240823</enddate><creator>Andhale, Nikita Shridhar</creator><creator>Bhor, Rohit Jaysing</creator><creator>Kolhe, Mahesh Hari</creator><creator>Pawar, Tanishka Anil</creator><creator>Tambe, Pornima Ramdas</creator><creator>Ghule, Rupali Mahadev</creator><creator>Bhange, Sarthak Anil</creator><creator>Thete, Bhakti Sharad</creator><creator>Kute, Pruthviraj Vijay</creator><creator>Malvade, Pratik Vijay</creator><creator>Bhagat, Jyoti Ramkisan</creator><creator>Waykar, Poonam Prakash</creator><general>InPharm</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>KB0</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>20240823</creationdate><title>Synthesis and Biological Properties of 4-Chloro-N1-(5-Chloro-1H-Indol-1-yl)-N2-(2-Chlorophenyl) benzene-1,2-Diamine Derivatives</title><author>Andhale, Nikita Shridhar ; Bhor, Rohit Jaysing ; Kolhe, Mahesh Hari ; Pawar, Tanishka Anil ; Tambe, Pornima Ramdas ; Ghule, Rupali Mahadev ; Bhange, Sarthak Anil ; Thete, Bhakti Sharad ; Kute, Pruthviraj Vijay ; Malvade, Pratik Vijay ; Bhagat, Jyoti Ramkisan ; Waykar, Poonam Prakash</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1074-649e0971f8d5a880dcc4562e9550d9133bca48ac3b03cbe811d84c68ad8ebe753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Hydrocarbons</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andhale, Nikita Shridhar</creatorcontrib><creatorcontrib>Bhor, Rohit Jaysing</creatorcontrib><creatorcontrib>Kolhe, Mahesh Hari</creatorcontrib><creatorcontrib>Pawar, Tanishka Anil</creatorcontrib><creatorcontrib>Tambe, Pornima Ramdas</creatorcontrib><creatorcontrib>Ghule, Rupali Mahadev</creatorcontrib><creatorcontrib>Bhange, Sarthak Anil</creatorcontrib><creatorcontrib>Thete, Bhakti Sharad</creatorcontrib><creatorcontrib>Kute, Pruthviraj Vijay</creatorcontrib><creatorcontrib>Malvade, Pratik Vijay</creatorcontrib><creatorcontrib>Bhagat, Jyoti Ramkisan</creatorcontrib><creatorcontrib>Waykar, Poonam Prakash</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of young pharmacists</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andhale, Nikita Shridhar</au><au>Bhor, Rohit Jaysing</au><au>Kolhe, Mahesh Hari</au><au>Pawar, Tanishka Anil</au><au>Tambe, Pornima Ramdas</au><au>Ghule, Rupali Mahadev</au><au>Bhange, Sarthak Anil</au><au>Thete, Bhakti Sharad</au><au>Kute, Pruthviraj Vijay</au><au>Malvade, Pratik Vijay</au><au>Bhagat, Jyoti Ramkisan</au><au>Waykar, Poonam Prakash</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Biological Properties of 4-Chloro-N1-(5-Chloro-1H-Indol-1-yl)-N2-(2-Chlorophenyl) benzene-1,2-Diamine Derivatives</atitle><jtitle>Journal of young pharmacists</jtitle><date>2024-08-23</date><risdate>2024</risdate><volume>16</volume><issue>3</issue><spage>498</spage><epage>505</epage><pages>498-505</pages><issn>0975-1483</issn><eissn>0975-1505</eissn><abstract>Background Five-membered heterocycle with one neighbouring nitrogen atoms is present in the indole nucleus. Heterocyclic substances feature two adjacent benzene and pyrrole ring atoms. Indole are heterocyclic compounds with one oxygen ring that have a benzoannelated – pyrrole ring. Indole derivatives are highly valuable chemical synthesis and medicinal intermediates. Recent years have seen a surge in interest in the effective synthesis of indole blocks and associated functionalization’s, particularly the alkylation of indoles. The two following factors will be the main emphasis of this review: i) Recent advancements in the alkylation of indoles, namely those involving the N1-, C2- and C3-positions and the synthesis of indoles, which was facilitated by transition metals. Materials and Methods Benzoic acid and ethanoic acid, propionic acid, hydroxylamine, 2,5 Dichloro aniline are used for the synthesis of indole derivatives were used for the synthesis of indole. Results Compared to indomethacin, the anti-inflammatory results for the substances or their derivatives like N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1H-indol-1-yl)-4-am inobenzene-1,2-diamine NA5 (Scheme 1B); N2-(biphenyl-2-yl)-4-chloro-N1-(5-chloro-1 H-ind ol-1-yl)-3-aminobenzene-1,2-diamine NA6 (Scheme 1B) and N2-(biphenyl-2-yl)-4-chloro-N1- (5-chloro-1H-indol-1-yl)-2-aminobenzene-1,2-diamine NA7 (Scheme 1B). Conclusion Examined were the anti-inflammatory properties of the substances in the title and their derivatives. The compounds containing indole derivatives with an electron-withdrawing group have a higher activity than those containing an electron-donating group, according to research on the link between structure and activity. Summarising the data from the previously reviewed literature, we can say that indole has a broad spectrum of biological activity. Numerous opportunities exist to investigate indole for new therapeutic uses. Researchers worldwide will benefit from this study’s coverage of the chemistry of indole derivatives in the design and synthesis of new pharmaceuticals that might be utilised to treat a range of diseases.</abstract><cop>Bangalore</cop><pub>InPharm</pub><doi>10.5530/jyp.2024.16.64</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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title | Synthesis and Biological Properties of 4-Chloro-N1-(5-Chloro-1H-Indol-1-yl)-N2-(2-Chlorophenyl) benzene-1,2-Diamine Derivatives |
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