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Reaction of 1-substituted 3-(2-hydroxyethylamino)quinoline-2,4(1H,3H)-diones with isothiocyanic acid

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dc.title Reaction of 1-substituted 3-(2-hydroxyethylamino)quinoline-2,4(1H,3H)-diones with isothiocyanic acid en
dc.contributor.author Klásek, Antonín
dc.contributor.author Lyčka, Antonín
dc.contributor.author Rouchal, Michal
dc.contributor.author Bartošík, Radek
dc.relation.ispartof Chemistry of Heterocyclic Compounds
dc.identifier.issn 0009-3122 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2020
utb.relation.volume 56
utb.relation.issue 5
dc.citation.spage 566
dc.citation.epage 571
dc.type article
dc.language.iso en
dc.publisher Springer
dc.identifier.doi 10.1007/s10593-020-02701-9
dc.relation.uri https://link.springer.com/content/pdf/10.1007/s10593-020-02701-9.pdf
dc.subject isocyanic acid en
dc.subject isothiocyanic acid en
dc.subject 2-thioxo-1H-imidazo[4 en
dc.subject 5-c]quinolin-4(2H)-ones en
dc.subject 2-thioxo-1H-imidazo[4 en
dc.subject 5-c]quinolin-4(5H)-ones en
dc.subject quinoline-2 en
dc.subject 4-diones en
dc.subject nuclear magnetic resonance en
dc.subject rearrangement en
dc.description.abstract 3-Chloroquinoline-2,4-diones react with ethanolamine to form 3-(3-hydroxyethylamino)quinoline-2,4-diones. These compounds afford, depending on substituents in positions 1 and 3, four different products from their reaction with isothiocyanic acid: 3-(2-hydroxyethyl)-2-thioxo-3,3a-dihydro-1H-imidazo[4,5-c]quinolin-4(5H)-ones, 9b-hydroxy-3-(2-hydroxyethyl)-2-thioxo-3,3a,5,9b-tetrahydro-1Himidazo[4,5-c]quinolin-4(2H)-ones, 3-(2-hydroxyethyl)-2-thioxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-4(5H)-ones, or 1 '-methyl-7a-phenyl-5-thioxo-3,5,6,7a-tetrahydro-2H-spiro[imidazo[5,1-b]oxazole-7,3 '-indolin]-2 '-one. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1009715
utb.identifier.obdid 43881597
utb.identifier.scopus 2-s2.0-85085591845
utb.identifier.wok 000536434500001
utb.identifier.coden CHCCA
utb.source j-scopus
dc.date.accessioned 2020-06-24T08:32:12Z
dc.date.available 2020-06-24T08:32:12Z
dc.description.sponsorship TBU in Zlin [IGA/FT/2019/010]
utb.contributor.internalauthor Klásek, Antonín
utb.contributor.internalauthor Rouchal, Michal
utb.contributor.internalauthor Bartošík, Radek
utb.fulltext.affiliation Antonín Klásek 1*, Antonín Lyčka 2, Michal Rouchal 1, Radek Bartošík 1 1 Department of Chemistry, Faculty of Technology, Tomas Bata University, CZ-76272 Zlín, Czech Republic; e-mail: klasek@utb.cz 2 Research Institute for Organic Syntheses (VUOS), CZ-533 54 Pardubice, Czech Republic; e-mail: Antonin.Lycka@vuos.com
utb.fulltext.dates Submitted November 7, 2019 Accepted after revision January 30, 2020
utb.fulltext.sponsorship A. K. and M. R. thank for financial support from the internal grant of TBU in Zlín (No. IGA/FT/2019/010), funded from the resources of specific university research. The authors thank Mrs. H. Geržová (Faculty of Technology, Tomas Bata University in Zlín) for technical help.
utb.wos.affiliation [Klasek, Antonin; Rouchal, Michal; Bartosik, Radek] Tomas Bata Univ, Fac Technol, Dept Chem, CZ-76272 Zlin, Czech Republic; [Lyecka, Antonin] Res Inst Organ Syntheses VUOS, CZ-53354 Pardubice, Czech Republic
utb.scopus.affiliation Department of Chemistry, Faculty of Technology, Tomas Bata University, Zlín, CZ-76272, Czech Republic; Research Institute for Organic Syntheses (VUOS), Pardubice, CZ-533 54, Czech Republic
utb.fulltext.projects IGA/FT/2019/010
utb.fulltext.faculty Faculty of Technology
utb.fulltext.faculty Faculty of Technology
utb.fulltext.faculty Faculty of Technology
utb.fulltext.ou Department of Chemistry
utb.fulltext.ou Department of Chemistry
utb.fulltext.ou Department of Chemistry
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