A facile one-pot synthesis of novel substituted 1,2,3,4-tetrahydropyrimidine, part 2: Synthesis of 1-(aralkyl/aryl)-3-(alkyl/aralkyl/aryl)-5-aroyl-1,2,3,4-tetrahydropyrimidines
1‐(Aralkyl/aryl)‐3‐(alkyyaralkyl)‐5‐aroyl‐1,2,3,4‐tetrahydropyrimidines (2a‐c) have been synthesized by dethiomethylation of 5‐aroyl‐6‐methylthio‐1,2,3,4‐tetrahydropyrimidines (1a‐c). An alternative one‐pot synthetic strategy has been developed for the title compounds 2a‐t by the reaction of enamino...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2004-07, Vol.41 (4), p.627-631 |
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container_title | Journal of heterocyclic chemistry |
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creator | Chanda, Kaushik Dutta, Milan Ch Karim, Enamul Vishwakarma, Jai N. |
description | 1‐(Aralkyl/aryl)‐3‐(alkyyaralkyl)‐5‐aroyl‐1,2,3,4‐tetrahydropyrimidines (2a‐c) have been synthesized by dethiomethylation of 5‐aroyl‐6‐methylthio‐1,2,3,4‐tetrahydropyrimidines (1a‐c). An alternative one‐pot synthetic strategy has been developed for the title compounds 2a‐t by the reaction of enaminones 3 with pri mary amine and formaldehyde in refluxing methanol in good yields. |
doi_str_mv | 10.1002/jhet.5570410425 |
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An alternative one‐pot synthetic strategy has been developed for the title compounds 2a‐t by the reaction of enaminones 3 with pri mary amine and formaldehyde in refluxing methanol in good yields.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.5570410425</identifier><language>eng</language><publisher>Hoboken: Wiley-Blackwell</publisher><ispartof>Journal of heterocyclic chemistry, 2004-07, Vol.41 (4), p.627-631</ispartof><rights>Copyright © 2004 Journal of Heterocyclic Chemistry</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3295-92fa86e992d0b2f5d57ade434a709d85bf5c2eb7808c8d88d1f871d72d13acbd3</citedby><cites>FETCH-LOGICAL-c3295-92fa86e992d0b2f5d57ade434a709d85bf5c2eb7808c8d88d1f871d72d13acbd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjhet.5570410425$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhet.5570410425$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Chanda, Kaushik</creatorcontrib><creatorcontrib>Dutta, Milan Ch</creatorcontrib><creatorcontrib>Karim, Enamul</creatorcontrib><creatorcontrib>Vishwakarma, Jai N.</creatorcontrib><title>A facile one-pot synthesis of novel substituted 1,2,3,4-tetrahydropyrimidine, part 2: Synthesis of 1-(aralkyl/aryl)-3-(alkyl/aralkyl/aryl)-5-aroyl-1,2,3,4-tetrahydropyrimidines</title><title>Journal of heterocyclic chemistry</title><description>1‐(Aralkyl/aryl)‐3‐(alkyyaralkyl)‐5‐aroyl‐1,2,3,4‐tetrahydropyrimidines (2a‐c) have been synthesized by dethiomethylation of 5‐aroyl‐6‐methylthio‐1,2,3,4‐tetrahydropyrimidines (1a‐c). An alternative one‐pot synthetic strategy has been developed for the title compounds 2a‐t by the reaction of enaminones 3 with pri mary amine and formaldehyde in refluxing methanol in good yields.</description><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAQhC0EEqVw5uojSHXrR1wncEKlNKAKkCiPm-XEjpo2NJHtAvlX_ERStYJygdNqVvPNrgaAY4K7BGPam02N73IucEBwQPkOaJEoYIiTiO2CVuOgiHD6sg8OnJs1kjAhWuDzAmYqzQsDy4VBVemhqxd-alzuYJnBRflmCuiWifO5X3qjIenQDusEyBtv1bTWtqxqm7_mOl-YDqyU9ZCewYftEIJOlFXFvC56ytbFKWLNYiO31xwpW9YF-uuEOwR7mSqcOdrMNni8Gk4GMRrfja4HF2OUMhpxFNFMhX0TRVTjhGZcc6G0CVigBI50yJOMp9QkIsRhGuow1CQLBdGCasJUmmjWBr11bmpL56zJZNX80DwqCZarwuWqcPlTeEOcr4n3ps76P7u8iYeTXzRa07nz5uObVnYu-4IJLp9vR3IUc8ov759kzL4Ah06Wrg</recordid><startdate>200407</startdate><enddate>200407</enddate><creator>Chanda, Kaushik</creator><creator>Dutta, Milan Ch</creator><creator>Karim, Enamul</creator><creator>Vishwakarma, Jai N.</creator><general>Wiley-Blackwell</general><general>Wiley‐Blackwell</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200407</creationdate><title>A facile one-pot synthesis of novel substituted 1,2,3,4-tetrahydropyrimidine, part 2: Synthesis of 1-(aralkyl/aryl)-3-(alkyl/aralkyl/aryl)-5-aroyl-1,2,3,4-tetrahydropyrimidines</title><author>Chanda, Kaushik ; Dutta, Milan Ch ; Karim, Enamul ; Vishwakarma, Jai N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3295-92fa86e992d0b2f5d57ade434a709d85bf5c2eb7808c8d88d1f871d72d13acbd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chanda, Kaushik</creatorcontrib><creatorcontrib>Dutta, Milan Ch</creatorcontrib><creatorcontrib>Karim, Enamul</creatorcontrib><creatorcontrib>Vishwakarma, Jai N.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chanda, Kaushik</au><au>Dutta, Milan Ch</au><au>Karim, Enamul</au><au>Vishwakarma, Jai N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A facile one-pot synthesis of novel substituted 1,2,3,4-tetrahydropyrimidine, part 2: Synthesis of 1-(aralkyl/aryl)-3-(alkyl/aralkyl/aryl)-5-aroyl-1,2,3,4-tetrahydropyrimidines</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2004-07</date><risdate>2004</risdate><volume>41</volume><issue>4</issue><spage>627</spage><epage>631</epage><pages>627-631</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>1‐(Aralkyl/aryl)‐3‐(alkyyaralkyl)‐5‐aroyl‐1,2,3,4‐tetrahydropyrimidines (2a‐c) have been synthesized by dethiomethylation of 5‐aroyl‐6‐methylthio‐1,2,3,4‐tetrahydropyrimidines (1a‐c). An alternative one‐pot synthetic strategy has been developed for the title compounds 2a‐t by the reaction of enaminones 3 with pri mary amine and formaldehyde in refluxing methanol in good yields.</abstract><cop>Hoboken</cop><pub>Wiley-Blackwell</pub><doi>10.1002/jhet.5570410425</doi><tpages>5</tpages></addata></record> |
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title | A facile one-pot synthesis of novel substituted 1,2,3,4-tetrahydropyrimidine, part 2: Synthesis of 1-(aralkyl/aryl)-3-(alkyl/aralkyl/aryl)-5-aroyl-1,2,3,4-tetrahydropyrimidines |
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