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Facile Synthesis of 2-Amino-4-alkoxypyrimidines via Consecutive Nucleophilic Aromatic Substitution (SNAr) Reactions

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dc.contributor.authorKim, Juhyeon-
dc.contributor.authorCho, Yong Seo-
dc.contributor.authorMin, Sun-Joon-
dc.date.accessioned2021-06-22T15:44:08Z-
dc.date.available2021-06-22T15:44:08Z-
dc.date.issued2016-12-
dc.identifier.issn0253-2964-
dc.identifier.issn1229-5949-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/12171-
dc.description.abstractA transition-metal-free and regioselective synthesis of a series of 2-amino-4-alkoxypyrimidines is described. The SNAr alkoxylation of 2,4-dichloropyrimidines regioselectively provided 2-chloro-4-alkoxypyrimidines, which were subsequently subject to the second SNAr amination with cyclic amines in the presence of triethylamine at high temperature to afford 2-amino-4-alkoxypyrimidines in good overall yield.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisher대한화학회-
dc.titleFacile Synthesis of 2-Amino-4-alkoxypyrimidines via Consecutive Nucleophilic Aromatic Substitution (SNAr) Reactions-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1002/bkcs.11014-
dc.identifier.scopusid2-s2.0-85003703938-
dc.identifier.wosid000390270200018-
dc.identifier.bibliographicCitationBulletin of the Korean Chemical Society, v.37, no.12, pp 1998 - 2008-
dc.citation.titleBulletin of the Korean Chemical Society-
dc.citation.volume37-
dc.citation.number12-
dc.citation.startPage1998-
dc.citation.endPage2008-
dc.type.docTypeArticle-
dc.identifier.kciidART002172604-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCROSS-COUPLING REACTIONS-
dc.subject.keywordPlusREGIOSELECTIVE 4-AMINO-DE-CHLORINATION-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusPYRIMIDINES-
dc.subject.keywordPlusINHIBITOR-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordAuthor2-Amino-4-alkoxypyrimidines-
dc.subject.keywordAuthorNucleophilic aromatic substitution-
dc.subject.keywordAuthorRegioselectivity-
dc.subject.keywordAuthorAlkoxylation-
dc.subject.keywordAuthorAmination-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/bkcs.11014-
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