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dc.contributor.authorKalogirou, Andreas S.en
dc.contributor.authorKoutentis, Panayiotis A.en
dc.creatorKalogirou, Andreas S.en
dc.creatorKoutentis, Panayiotis A.en
dc.date.accessioned2021-01-25T09:44:47Z
dc.date.available2021-01-25T09:44:47Z
dc.date.issued2019
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/63031
dc.description.abstract4,6-Dichloro-2-(methylthio)pyrimidine (7) was converted to 4-chloro-6-methoxy-2-(methylthio)pyrimidine (15) and 4,6-dimethoxy-2-(methylthio)pyrimidine (14). Chlorination of the latter with N-chlorosuccinimide (NCS) affords 5-chloro-4,6-dimethoxy-2-(methylthio)pyrimidine (16) in 56% yield. Both methylthiopyrimidines 15 and 14 were converted in two steps to 4-chloro-6-methoxypyrimidine-2-carbonitrile (13) and 4,6-dimethoxypyrimidine-2-carbonitrile (12), respectively, after oxidation to sulfones and displacement of the sulfinate group with KCN. 4,6-Dimethoxypyrimidine-2-carbonitrile (12) was chlorinated with NCS to give 5-chloro-4,6-dimethoxypyrimidine-2-carbonitrile (10) in 53% yield. All new compounds were fully characterized.en
dc.language.isoenen
dc.sourceMolbanken
dc.source.urihttps://www.mdpi.com/1422-8599/2019/4/M1086
dc.titleSynthesis of 2-Cyanopyrimidinesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/M1086
dc.description.volume2019
dc.description.issue4
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.contributor.orcidKalogirou, Andreas S. [0000-0002-5476-5805]
dc.contributor.orcidKoutentis, Panayiotis A. [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-5476-5805
dc.gnosis.orcid0000-0002-4652-7567


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