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Synthesis of 4-alkyl- and 4-(.beta.-alkylvinyl) derivatives of primaquine as potential antimalarials
4(beta-Alkylvinyl)-6-methoxy-8-nitroquinolines (6) were prepared from 6-methoxy-8-nitroquinoline-4-carboxaldehyde (5) via a Wittig reaction. Stannous chloride reduction of 6 gave 4-(beta-alkylvinyl)-8-amino-6-methoxyquinolines (8), whereas catalytic reduction of 6 using Raney nickel catalyst gave 4-...
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Published in: | Journal of medicinal chemistry 1979-11, Vol.22 (11), p.1363-1367 |
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container_title | Journal of medicinal chemistry |
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creator | Carroll, F. Ivy Berrang, Bertold D Linn, C. Preston |
description | 4(beta-Alkylvinyl)-6-methoxy-8-nitroquinolines (6) were prepared from 6-methoxy-8-nitroquinoline-4-carboxaldehyde (5) via a Wittig reaction. Stannous chloride reduction of 6 gave 4-(beta-alkylvinyl)-8-amino-6-methoxyquinolines (8), whereas catalytic reduction of 6 using Raney nickel catalyst gave 4-alkyl-8-amino-6-methoxyquinolines (7). Alkylation of 7 and 8 with 4-iodo-1-phthalimidopentane, followed by removal of the phthaloyl-protecting group with hydrazine, gave 4-alkyl and 4-(beta-alkylvinyl) derivatives of primiquine, respectively. These compounds were evaluated for antimalarial activity against P. berghei and P. berghei yoelii in mice and against P. cynomolgi in rhesus monkeys. Several of the compounds were active in the P. bergheii yoelii screen. None of the compounds showed significant activity in the other two screens. |
doi_str_mv | 10.1021/jm00197a016 |
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Ivy ; Berrang, Bertold D ; Linn, C. Preston</creator><creatorcontrib>Carroll, F. Ivy ; Berrang, Bertold D ; Linn, C. Preston</creatorcontrib><description>4(beta-Alkylvinyl)-6-methoxy-8-nitroquinolines (6) were prepared from 6-methoxy-8-nitroquinoline-4-carboxaldehyde (5) via a Wittig reaction. Stannous chloride reduction of 6 gave 4-(beta-alkylvinyl)-8-amino-6-methoxyquinolines (8), whereas catalytic reduction of 6 using Raney nickel catalyst gave 4-alkyl-8-amino-6-methoxyquinolines (7). Alkylation of 7 and 8 with 4-iodo-1-phthalimidopentane, followed by removal of the phthaloyl-protecting group with hydrazine, gave 4-alkyl and 4-(beta-alkylvinyl) derivatives of primiquine, respectively. These compounds were evaluated for antimalarial activity against P. berghei and P. berghei yoelii in mice and against P. cynomolgi in rhesus monkeys. Several of the compounds were active in the P. bergheii yoelii screen. None of the compounds showed significant activity in the other two screens.</description><identifier>ISSN: 0022-2623</identifier><identifier>EISSN: 1520-4804</identifier><identifier>DOI: 10.1021/jm00197a016</identifier><identifier>PMID: 118257</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Haplorhini ; Macaca mulatta ; Malaria - prevention & control ; Mice ; Plasmodium ; Plasmodium berghei ; Primaquine - analogs & derivatives ; Primaquine - chemical synthesis</subject><ispartof>Journal of medicinal chemistry, 1979-11, Vol.22 (11), p.1363-1367</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a268t-601efb878b7b7505ee1b562f806246a679676440b8d01d478d55cac3f237d7e43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jm00197a016$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jm00197a016$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27064,27924,27925,56766,56816</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/118257$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carroll, F. Ivy</creatorcontrib><creatorcontrib>Berrang, Bertold D</creatorcontrib><creatorcontrib>Linn, C. Preston</creatorcontrib><title>Synthesis of 4-alkyl- and 4-(.beta.-alkylvinyl) derivatives of primaquine as potential antimalarials</title><title>Journal of medicinal chemistry</title><addtitle>J. Med. Chem</addtitle><description>4(beta-Alkylvinyl)-6-methoxy-8-nitroquinolines (6) were prepared from 6-methoxy-8-nitroquinoline-4-carboxaldehyde (5) via a Wittig reaction. Stannous chloride reduction of 6 gave 4-(beta-alkylvinyl)-8-amino-6-methoxyquinolines (8), whereas catalytic reduction of 6 using Raney nickel catalyst gave 4-alkyl-8-amino-6-methoxyquinolines (7). Alkylation of 7 and 8 with 4-iodo-1-phthalimidopentane, followed by removal of the phthaloyl-protecting group with hydrazine, gave 4-alkyl and 4-(beta-alkylvinyl) derivatives of primiquine, respectively. These compounds were evaluated for antimalarial activity against P. berghei and P. berghei yoelii in mice and against P. cynomolgi in rhesus monkeys. Several of the compounds were active in the P. bergheii yoelii screen. None of the compounds showed significant activity in the other two screens.</description><subject>Animals</subject><subject>Haplorhini</subject><subject>Macaca mulatta</subject><subject>Malaria - prevention & control</subject><subject>Mice</subject><subject>Plasmodium</subject><subject>Plasmodium berghei</subject><subject>Primaquine - analogs & derivatives</subject><subject>Primaquine - chemical synthesis</subject><issn>0022-2623</issn><issn>1520-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><recordid>eNptkM1P3DAQxS1EKVvoqVcOOUFRle34I7Y5wooC0qqtBL1wsZxkonrJJovtrNj_vmaDCgdOo5n3mzeaR8gXClMKjH5fLAHombJA5Q6Z0IJBLjSIXTIBYCxnkvF98imEBQBwyvhHskepZoWakPp208W_GFzI-iYTuW0fNm2e2a5OzddpidFOx-HadZv2NKvRu7WNbo3bjZV3S_s4uA4zG7JVH7GLzrbJICahtT414ZB8aFLBzy_1gPz5cXk3u87nv65uZufz3DKpYy6BYlNqpUtVqgIKRFoWkjUaJBPSSnUmlRQCSl0DrYXSdVFUtuIN46pWKPgBOR59V75_HDBEs3Shwra1HfZDMEpoKbjkCfw2gpXvQ_DYmO0ffmMomOdIzZtIE330YjuUS6xf2W2GSc5H2YWIT_9V6x-MVFwV5u73rbmfq3s-ExfmZ-JPRt5WwSz6wXcpk3cP_wNQdIvf</recordid><startdate>197911</startdate><enddate>197911</enddate><creator>Carroll, F. Ivy</creator><creator>Berrang, Bertold D</creator><creator>Linn, C. Preston</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>197911</creationdate><title>Synthesis of 4-alkyl- and 4-(.beta.-alkylvinyl) derivatives of primaquine as potential antimalarials</title><author>Carroll, F. Ivy ; Berrang, Bertold D ; Linn, C. Preston</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a268t-601efb878b7b7505ee1b562f806246a679676440b8d01d478d55cac3f237d7e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>Animals</topic><topic>Haplorhini</topic><topic>Macaca mulatta</topic><topic>Malaria - prevention & control</topic><topic>Mice</topic><topic>Plasmodium</topic><topic>Plasmodium berghei</topic><topic>Primaquine - analogs & derivatives</topic><topic>Primaquine - chemical synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carroll, F. Ivy</creatorcontrib><creatorcontrib>Berrang, Bertold D</creatorcontrib><creatorcontrib>Linn, C. Preston</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carroll, F. Ivy</au><au>Berrang, Bertold D</au><au>Linn, C. Preston</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 4-alkyl- and 4-(.beta.-alkylvinyl) derivatives of primaquine as potential antimalarials</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. Med. Chem</addtitle><date>1979-11</date><risdate>1979</risdate><volume>22</volume><issue>11</issue><spage>1363</spage><epage>1367</epage><pages>1363-1367</pages><issn>0022-2623</issn><eissn>1520-4804</eissn><abstract>4(beta-Alkylvinyl)-6-methoxy-8-nitroquinolines (6) were prepared from 6-methoxy-8-nitroquinoline-4-carboxaldehyde (5) via a Wittig reaction. Stannous chloride reduction of 6 gave 4-(beta-alkylvinyl)-8-amino-6-methoxyquinolines (8), whereas catalytic reduction of 6 using Raney nickel catalyst gave 4-alkyl-8-amino-6-methoxyquinolines (7). Alkylation of 7 and 8 with 4-iodo-1-phthalimidopentane, followed by removal of the phthaloyl-protecting group with hydrazine, gave 4-alkyl and 4-(beta-alkylvinyl) derivatives of primiquine, respectively. These compounds were evaluated for antimalarial activity against P. berghei and P. berghei yoelii in mice and against P. cynomolgi in rhesus monkeys. Several of the compounds were active in the P. bergheii yoelii screen. None of the compounds showed significant activity in the other two screens.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>118257</pmid><doi>10.1021/jm00197a016</doi><tpages>5</tpages></addata></record> |
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language | eng |
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source | ACS CRKN Legacy Archives |
subjects | Animals Haplorhini Macaca mulatta Malaria - prevention & control Mice Plasmodium Plasmodium berghei Primaquine - analogs & derivatives Primaquine - chemical synthesis |
title | Synthesis of 4-alkyl- and 4-(.beta.-alkylvinyl) derivatives of primaquine as potential antimalarials |
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