Potential Anti-cancer Agents. IV. 3-Substituted 6-Chloropyridazine 1-Oxides
When 3, 6-dichloropyridazine and 3-alkoxy-6-chloropyridazines were oxidized with monoperphthalic acid or hydrogen peroxide-glacial acetic acid, the corresponding Noxides were produced. With the latter reagent, however, 6-substituted-3(2H)-pyridazinones gave rise to byproducts. The N-oxidation of 3-a...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1962/10/25, Vol.10(10), pp.989-992 |
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creator | Itai, Takanobu Sako, Shigeru |
description | When 3, 6-dichloropyridazine and 3-alkoxy-6-chloropyridazines were oxidized with monoperphthalic acid or hydrogen peroxide-glacial acetic acid, the corresponding Noxides were produced. With the latter reagent, however, 6-substituted-3(2H)-pyridazinones gave rise to byproducts. The N-oxidation of 3-alkoxy-6-chloropyridazines was shown to take place at the 1-position of the molecules. By catalytic dehalogenation, several 3-alkoxypyridazine 1-oxides were also prepared. |
doi_str_mv | 10.1248/cpb.10.989 |
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IV. 3-Substituted 6-Chloropyridazine 1-Oxides</title><source>Electronic Journals Library</source><source>MEDLINE</source><source>Free Full-Text Journals in Chemistry</source><source>J-STAGE</source><creator>Itai, Takanobu ; Sako, Shigeru</creator><creatorcontrib>Itai, Takanobu ; Sako, Shigeru</creatorcontrib><description>When 3, 6-dichloropyridazine and 3-alkoxy-6-chloropyridazines were oxidized with monoperphthalic acid or hydrogen peroxide-glacial acetic acid, the corresponding Noxides were produced. With the latter reagent, however, 6-substituted-3(2H)-pyridazinones gave rise to byproducts. The N-oxidation of 3-alkoxy-6-chloropyridazines was shown to take place at the 1-position of the molecules. By catalytic dehalogenation, several 3-alkoxypyridazine 1-oxides were also prepared.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.10.989</identifier><identifier>PMID: 13956972</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Antineoplastic Agents ; Humans ; Oxides ; Pyridazines</subject><ispartof>Chemical and Pharmaceutical Bulletin, 1962/10/25, Vol.10(10), pp.989-992</ispartof><rights>The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 1962</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3929-548e6284992abda67379d803d0e8b7a7b35c08e69e38fe0bdb196d8ae28b84e43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/13956972$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Itai, Takanobu</creatorcontrib><creatorcontrib>Sako, Shigeru</creatorcontrib><title>Potential Anti-cancer Agents. IV. 3-Substituted 6-Chloropyridazine 1-Oxides</title><title>Chemical & pharmaceutical bulletin</title><addtitle>Chem. Pharm. Bull.</addtitle><description>When 3, 6-dichloropyridazine and 3-alkoxy-6-chloropyridazines were oxidized with monoperphthalic acid or hydrogen peroxide-glacial acetic acid, the corresponding Noxides were produced. With the latter reagent, however, 6-substituted-3(2H)-pyridazinones gave rise to byproducts. The N-oxidation of 3-alkoxy-6-chloropyridazines was shown to take place at the 1-position of the molecules. By catalytic dehalogenation, several 3-alkoxypyridazine 1-oxides were also prepared.</description><subject>Antineoplastic Agents</subject><subject>Humans</subject><subject>Oxides</subject><subject>Pyridazines</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1962</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1LwzAUhoMobk5v_AFS8E5IzUfbJJdjTB0OJvhxW5LmbOvY2pq04Pz1Zm46OHAO5zw8B16ErimJKUvkfdGYOMxKqhPUpzwROGWMn6I-IURhxjPeQxferwhhKRH8HPUoV2mmBOuj55e6haot9ToahoYLXRXgouEiLH0cTT7iiOPXzvi2bLsWbJTh0XJdu7rZutLq77KCiOLZV2nBX6KzuV57uDr0AXp_GL-NnvB09jgZDae44IopnCYSMiYTpZg2VmeCC2Ul4ZaANEILw9OCBEQBl3MgxhqqMis1MGlkAgkfoNu9t3H1Zwe-zVd156rwMqdJqrJECJIF6m5PFa723sE8b1y50W6bU5LvcstDbrs55Bbgm4OyMxuwR_QQVADGe2DlW72Af0C7tizWsHNRlcpf918F8fG-1C6Hiv8A2tx-2Q</recordid><startdate>1962</startdate><enddate>1962</enddate><creator>Itai, Takanobu</creator><creator>Sako, Shigeru</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><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>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>1962</creationdate><title>Potential Anti-cancer Agents. IV. 3-Substituted 6-Chloropyridazine 1-Oxides</title><author>Itai, Takanobu ; Sako, Shigeru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3929-548e6284992abda67379d803d0e8b7a7b35c08e69e38fe0bdb196d8ae28b84e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1962</creationdate><topic>Antineoplastic Agents</topic><topic>Humans</topic><topic>Oxides</topic><topic>Pyridazines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Itai, Takanobu</creatorcontrib><creatorcontrib>Sako, Shigeru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Itai, Takanobu</au><au>Sako, Shigeru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential Anti-cancer Agents. IV. 3-Substituted 6-Chloropyridazine 1-Oxides</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1962</date><risdate>1962</risdate><volume>10</volume><issue>10</issue><spage>989</spage><epage>992</epage><pages>989-992</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>When 3, 6-dichloropyridazine and 3-alkoxy-6-chloropyridazines were oxidized with monoperphthalic acid or hydrogen peroxide-glacial acetic acid, the corresponding Noxides were produced. With the latter reagent, however, 6-substituted-3(2H)-pyridazinones gave rise to byproducts. The N-oxidation of 3-alkoxy-6-chloropyridazines was shown to take place at the 1-position of the molecules. By catalytic dehalogenation, several 3-alkoxypyridazine 1-oxides were also prepared.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>13956972</pmid><doi>10.1248/cpb.10.989</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents Humans Oxides Pyridazines |
title | Potential Anti-cancer Agents. IV. 3-Substituted 6-Chloropyridazine 1-Oxides |
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