Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions
Herein, we report on the discovery and development of novel cascade N−N bond forming reactions for the synthesis of rare indazole acetic acid scaffolds. This approach allows for convenient synthesis of three distinct indazole acetic acid derivatives (unsubstituted, hydroxy, and alkoxy) by heating 3‐...
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Veröffentlicht in: | European journal of organic chemistry 2023-08, Vol.26 (29), p.n/a |
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container_title | European journal of organic chemistry |
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creator | Odell, Luke R. Skillinghaug, Bobo Matt, Christof Wu, Peng Koolmeister, Tobias Desroses, Matthieu Llona‐Minguez, Sabin Wallner, Olov Helleday, Thomas Scobie, Martin |
description | Herein, we report on the discovery and development of novel cascade N−N bond forming reactions for the synthesis of rare indazole acetic acid scaffolds. This approach allows for convenient synthesis of three distinct indazole acetic acid derivatives (unsubstituted, hydroxy, and alkoxy) by heating 3‐amino‐3‐(2‐nitroaryl)propanoic acids with an appropriate nucleophile/solvent under basic conditions. The reaction tolerates a range of functional groups and electronic effects and, in total, 23 novel indazole acetic acids were synthesized and characterized. This work offers a valuable strategy for the synthesis of useful scaffolds for drug discovery programs.
Herein, the discovery of a novel solvent directed cascade synthesis of biologically relevant indazole acetic acid derivatives is described. Notably, the method is simple, transition‐metal free and provides access to new heterocyclic building‐ blocks in moderate to excellent yields. |
doi_str_mv | 10.1002/ejoc.202300291 |
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Herein, the discovery of a novel solvent directed cascade synthesis of biologically relevant indazole acetic acid derivatives is described. Notably, the method is simple, transition‐metal free and provides access to new heterocyclic building‐ blocks in moderate to excellent yields.</description><identifier>ISSN: 1434-193X</identifier><identifier>ISSN: 1099-0690</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.202300291</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Acetic acid ; annulation ; Chemical synthesis ; cyclization ; Functional groups ; Michael addition ; nitrogen heterocycles ; Nucleophiles ; Propionic acid ; Scaffolds ; synthetic methods</subject><ispartof>European journal of organic chemistry, 2023-08, Vol.26 (29), p.n/a</ispartof><rights>2023 The Authors. European Journal of Organic Chemistry published by Wiley-VCH GmbH</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3871-4d42b68c05207d4160edbc37b33d5608151b71beb939ef0d4fc6714fc269278b3</cites><orcidid>0000-0003-4152-3855 ; 0000-0002-8014-5757 ; 0000-0002-7073-8495 ; 0000-0002-6481-237X ; 0000-0001-7658-5103 ; 0000-0002-7384-092X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fejoc.202300291$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejoc.202300291$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-519647$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:152626107$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Odell, Luke R.</creatorcontrib><creatorcontrib>Skillinghaug, Bobo</creatorcontrib><creatorcontrib>Matt, Christof</creatorcontrib><creatorcontrib>Wu, Peng</creatorcontrib><creatorcontrib>Koolmeister, Tobias</creatorcontrib><creatorcontrib>Desroses, Matthieu</creatorcontrib><creatorcontrib>Llona‐Minguez, Sabin</creatorcontrib><creatorcontrib>Wallner, Olov</creatorcontrib><creatorcontrib>Helleday, Thomas</creatorcontrib><creatorcontrib>Scobie, Martin</creatorcontrib><title>Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions</title><title>European journal of organic chemistry</title><description>Herein, we report on the discovery and development of novel cascade N−N bond forming reactions for the synthesis of rare indazole acetic acid scaffolds. This approach allows for convenient synthesis of three distinct indazole acetic acid derivatives (unsubstituted, hydroxy, and alkoxy) by heating 3‐amino‐3‐(2‐nitroaryl)propanoic acids with an appropriate nucleophile/solvent under basic conditions. The reaction tolerates a range of functional groups and electronic effects and, in total, 23 novel indazole acetic acids were synthesized and characterized. This work offers a valuable strategy for the synthesis of useful scaffolds for drug discovery programs.
Herein, the discovery of a novel solvent directed cascade synthesis of biologically relevant indazole acetic acid derivatives is described. Notably, the method is simple, transition‐metal free and provides access to new heterocyclic building‐ blocks in moderate to excellent yields.</description><subject>Acetic acid</subject><subject>annulation</subject><subject>Chemical synthesis</subject><subject>cyclization</subject><subject>Functional groups</subject><subject>Michael addition</subject><subject>nitrogen heterocycles</subject><subject>Nucleophiles</subject><subject>Propionic acid</subject><subject>Scaffolds</subject><subject>synthetic methods</subject><issn>1434-193X</issn><issn>1099-0690</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>D8T</sourceid><recordid>eNqFkU1PwjAYxxejiYhePTfx6rBdu249IoJiCCSixluzvgyLsOK6heAn8OxH9JNYMoIn4-V5y-__JM_zD4JzBDsIwuhKz63sRDDCvmHoIGghyFgIKYOHviaYhIjhl-PgxLk5hJBRilrBeLopqlftjAM2B9NauMpUdaUVGBYq-7ALDbpSV0b6ZJQDYgPG359fY3BtCwUGtlyaYgYedCYrYwt3Ghzl2cLps11uB0-D_mPvLhxNboe97iiUOE1QSBSJBE0ljCOYKIIo1EpInAiMVUxhimIkEiS0YJjpHCqSS5ogHyPKoiQVuB2EzV631qta8FVpllm54TYzfDd685XmNMUEJ56__JO_Mc9dbssZr2seI0bJFr9o8FVp32vtKj63dVn4i3iUEuJ_TNIt1WkoWVrnSp3v1yLIt5bwrSV8b4kXsEawNgu9-Yfm_ftJ71f7A25xkDU</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Odell, Luke R.</creator><creator>Skillinghaug, Bobo</creator><creator>Matt, Christof</creator><creator>Wu, Peng</creator><creator>Koolmeister, Tobias</creator><creator>Desroses, Matthieu</creator><creator>Llona‐Minguez, Sabin</creator><creator>Wallner, Olov</creator><creator>Helleday, Thomas</creator><creator>Scobie, Martin</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0003-4152-3855</orcidid><orcidid>https://orcid.org/0000-0002-8014-5757</orcidid><orcidid>https://orcid.org/0000-0002-7073-8495</orcidid><orcidid>https://orcid.org/0000-0002-6481-237X</orcidid><orcidid>https://orcid.org/0000-0001-7658-5103</orcidid><orcidid>https://orcid.org/0000-0002-7384-092X</orcidid></search><sort><creationdate>20230801</creationdate><title>Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions</title><author>Odell, Luke R. ; Skillinghaug, Bobo ; Matt, Christof ; Wu, Peng ; Koolmeister, Tobias ; Desroses, Matthieu ; Llona‐Minguez, Sabin ; Wallner, Olov ; Helleday, Thomas ; Scobie, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3871-4d42b68c05207d4160edbc37b33d5608151b71beb939ef0d4fc6714fc269278b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetic acid</topic><topic>annulation</topic><topic>Chemical synthesis</topic><topic>cyclization</topic><topic>Functional groups</topic><topic>Michael addition</topic><topic>nitrogen heterocycles</topic><topic>Nucleophiles</topic><topic>Propionic acid</topic><topic>Scaffolds</topic><topic>synthetic methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Odell, Luke R.</creatorcontrib><creatorcontrib>Skillinghaug, Bobo</creatorcontrib><creatorcontrib>Matt, Christof</creatorcontrib><creatorcontrib>Wu, Peng</creatorcontrib><creatorcontrib>Koolmeister, Tobias</creatorcontrib><creatorcontrib>Desroses, Matthieu</creatorcontrib><creatorcontrib>Llona‐Minguez, Sabin</creatorcontrib><creatorcontrib>Wallner, Olov</creatorcontrib><creatorcontrib>Helleday, Thomas</creatorcontrib><creatorcontrib>Scobie, Martin</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>CrossRef</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Odell, Luke R.</au><au>Skillinghaug, Bobo</au><au>Matt, Christof</au><au>Wu, Peng</au><au>Koolmeister, Tobias</au><au>Desroses, Matthieu</au><au>Llona‐Minguez, Sabin</au><au>Wallner, Olov</au><au>Helleday, Thomas</au><au>Scobie, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions</atitle><jtitle>European journal of organic chemistry</jtitle><date>2023-08-01</date><risdate>2023</risdate><volume>26</volume><issue>29</issue><epage>n/a</epage><issn>1434-193X</issn><issn>1099-0690</issn><eissn>1099-0690</eissn><abstract>Herein, we report on the discovery and development of novel cascade N−N bond forming reactions for the synthesis of rare indazole acetic acid scaffolds. This approach allows for convenient synthesis of three distinct indazole acetic acid derivatives (unsubstituted, hydroxy, and alkoxy) by heating 3‐amino‐3‐(2‐nitroaryl)propanoic acids with an appropriate nucleophile/solvent under basic conditions. The reaction tolerates a range of functional groups and electronic effects and, in total, 23 novel indazole acetic acids were synthesized and characterized. This work offers a valuable strategy for the synthesis of useful scaffolds for drug discovery programs.
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subjects | Acetic acid annulation Chemical synthesis cyclization Functional groups Michael addition nitrogen heterocycles Nucleophiles Propionic acid Scaffolds synthetic methods |
title | Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions |
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