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An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam
An efficient nine-step synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c] -pyrimidine-2-yl) benzenesulfonamide has been developed. The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethyl...
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Published in: | Journal of chemical research 2013-04, Vol.37 (4), p.197-200 |
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container_title | Journal of chemical research |
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creator | Wu, Feifei Gao, Shiguang Chen, Zhiyin Su, Jinyue Zhang, Dayong |
description | An efficient nine-step synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c] -pyrimidine-2-yl) benzenesulfonamide has been developed. The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethylaniline and 2-bromo-4-acetamido-6-trifluoro-methylbenzenesulfonic acid to 2-bromo-6-trilfuoromethylbenzenesulfonic acid. This was then combined with 2-amino-5,8-dimethoxy-1,2,4-triazolo[1.5-c]pyrimidine to give the target molecule. Compared with the reported method, this approach has advantages in its shorter reaction time, milder reaction conditions and easier purifiction. Moreover, the overall yield has been improved to 22.9% which is twice of that of the reported method. |
doi_str_mv | 10.3184/174751913X13619014318618 |
format | article |
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The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethylaniline and 2-bromo-4-acetamido-6-trifluoro-methylbenzenesulfonic acid to 2-bromo-6-trilfuoromethylbenzenesulfonic acid. This was then combined with 2-amino-5,8-dimethoxy-1,2,4-triazolo[1.5-c]pyrimidine to give the target molecule. Compared with the reported method, this approach has advantages in its shorter reaction time, milder reaction conditions and easier purifiction. Moreover, the overall yield has been improved to 22.9% which is twice of that of the reported method.</description><identifier>ISSN: 1747-5198</identifier><identifier>EISSN: 2047-6507</identifier><identifier>DOI: 10.3184/174751913X13619014318618</identifier><language>eng</language><publisher>London: Sage Publications Ltd</publisher><subject>Reaction time ; Synthesis</subject><ispartof>Journal of chemical research, 2013-04, Vol.37 (4), p.197-200</ispartof><rights>Copyright Science Reviews 2000 Ltd Apr 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-de00a404064f6b1cb7f8c84bdc42931f057689aec493538f287ae73e75a417d43</citedby><cites>FETCH-LOGICAL-c370t-de00a404064f6b1cb7f8c84bdc42931f057689aec493538f287ae73e75a417d43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Wu, Feifei</creatorcontrib><creatorcontrib>Gao, Shiguang</creatorcontrib><creatorcontrib>Chen, Zhiyin</creatorcontrib><creatorcontrib>Su, Jinyue</creatorcontrib><creatorcontrib>Zhang, Dayong</creatorcontrib><title>An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam</title><title>Journal of chemical research</title><description>An efficient nine-step synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c] -pyrimidine-2-yl) benzenesulfonamide has been developed. The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethylaniline and 2-bromo-4-acetamido-6-trifluoro-methylbenzenesulfonic acid to 2-bromo-6-trilfuoromethylbenzenesulfonic acid. This was then combined with 2-amino-5,8-dimethoxy-1,2,4-triazolo[1.5-c]pyrimidine to give the target molecule. Compared with the reported method, this approach has advantages in its shorter reaction time, milder reaction conditions and easier purifiction. Moreover, the overall yield has been improved to 22.9% which is twice of that of the reported method.</description><subject>Reaction time</subject><subject>Synthesis</subject><issn>1747-5198</issn><issn>2047-6507</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp10d1qFDEUB_AgCq7Vdwh4s4WJ5iSZJONdLa0KhQoqFIoM2cwJnTKTrJMZ6PRRfFqzbK-EXgX--XE4H4RQ4B8kWPURjDI1NCBvQGpoOKgSa7AvyEZwZZiuuXlJNgfGirOvyZuc7zlXtW5gQ_6eRXoRQu97jDP9scb5DnOfaQpUsK2oBOv6MCxpSjjfpYf1lGk2T0_RWLJ1YDRStq0rW-h4VAwqUakDdI9pSLdQ1cz_3q9TP_ZdH5EJtg6n9DPGR4yYlyGk6MoXfqLfMaaHkrjxLXkV3JDx3dN7Qn5dXvw8_8qurr98Oz-7Yl4aPrMOOXeKK65V0DvwOxOst2rXeSUaCYHXRtvGoVeNrKUNwhqHRqKpnQLTKXlCtse6-yn9WTDP7dhnj8PgIqYlt2C5hbJhfqDv_6P3aZli6a4FXaumrFTIouxR-SnlPGFo92VwN60t8PZwtPa5o8l_vBWI1w</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Wu, Feifei</creator><creator>Gao, Shiguang</creator><creator>Chen, Zhiyin</creator><creator>Su, Jinyue</creator><creator>Zhang, Dayong</creator><general>Sage Publications Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>EHMNL</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20130401</creationdate><title>An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam</title><author>Wu, Feifei ; Gao, Shiguang ; Chen, Zhiyin ; Su, Jinyue ; Zhang, Dayong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-de00a404064f6b1cb7f8c84bdc42931f057689aec493538f287ae73e75a417d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Reaction time</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Feifei</creatorcontrib><creatorcontrib>Gao, Shiguang</creatorcontrib><creatorcontrib>Chen, Zhiyin</creatorcontrib><creatorcontrib>Su, Jinyue</creatorcontrib><creatorcontrib>Zhang, Dayong</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Databases</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>UK & Ireland Database</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Journal of chemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Feifei</au><au>Gao, Shiguang</au><au>Chen, Zhiyin</au><au>Su, Jinyue</au><au>Zhang, Dayong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam</atitle><jtitle>Journal of chemical research</jtitle><date>2013-04-01</date><risdate>2013</risdate><volume>37</volume><issue>4</issue><spage>197</spage><epage>200</epage><pages>197-200</pages><issn>1747-5198</issn><eissn>2047-6507</eissn><abstract>An efficient nine-step synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- N-(5,8-dimethoxy-1,2,4-triazolo[1,5-c] -pyrimidine-2-yl) benzenesulfonamide has been developed. The starting material 4-nitro-2-(trifluoromethyl)aniline starting material was converted via 2-bromo-4-amino-6-trifluoromethylaniline and 2-bromo-4-acetamido-6-trifluoro-methylbenzenesulfonic acid to 2-bromo-6-trilfuoromethylbenzenesulfonic acid. This was then combined with 2-amino-5,8-dimethoxy-1,2,4-triazolo[1.5-c]pyrimidine to give the target molecule. Compared with the reported method, this approach has advantages in its shorter reaction time, milder reaction conditions and easier purifiction. Moreover, the overall yield has been improved to 22.9% which is twice of that of the reported method.</abstract><cop>London</cop><pub>Sage Publications Ltd</pub><doi>10.3184/174751913X13619014318618</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Reaction time Synthesis |
title | An Efficient Synthesis of 2-(2,2-difluoroethoxy)-6-trifluoromethyl- n -(5,8-dimethoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-yl) Benzenesulfonamide: Penoxsulam |
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