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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 |