Publication:
Synthesis and crystal structure of 3-amino-1-(5-Chloro-2-Hydroxyphenyl) Imidazolidine-2,4-dione

dc.contributor.authorAydin A., Önkol T., Akkurt M., Büyükgüngör O., Şahin M.F.
dc.contributor.authorAydin, A, Onkol, T, Akkurt, M, Buyukgungor, O, Sahin, MF
dc.date.accessioned2023-05-09T18:23:37Z
dc.date.available2023-05-09T18:23:37Z
dc.date.issued2013-01-01
dc.date.issued2013.01.01
dc.description.abstractThe present study describes the synthesis, spectral data, and single crystal X-ray structural analysis of 3-amino-1-(5-chloro-2-hydroxyphenyl) imidazolidine-2,4-dione. X-Ray analysis revealed that the title compound did not have the anticipated structure, but had that of a different substance. This unexpected conformation generated the interest in studying the synthesis of this compound. The inspected compound, 3-amino-1-(5-chloro-2-hydroxyphenyl) imidazolidine-2,4-dione, is a pharmaceutical intermediate and is nonplanar. Its benzene and five-membered rings have a dihedral angle of 53.95(7)°. The conformation is stabilized by intermolecular OH. O, OH. N, and NH. O interactions and a weak CH. π interaction. © 2013 Copyright Taylor and Francis Group, LLC.
dc.identifier.doi10.1080/15421406.2012.707593
dc.identifier.endpage127
dc.identifier.issn1542-1406
dc.identifier.scopus2-s2.0-84873353098
dc.identifier.startpage119
dc.identifier.urihttps://hdl.handle.net/20.500.12597/13249
dc.identifier.volume570
dc.identifier.wosWOS:000316060900014
dc.relation.ispartofMolecular Crystals and Liquid Crystals
dc.relation.ispartofMOLECULAR CRYSTALS AND LIQUID CRYSTALS
dc.rightsfalse
dc.subject3-amino | 4-dione | structure | synthesis | X-ray
dc.titleSynthesis and crystal structure of 3-amino-1-(5-Chloro-2-Hydroxyphenyl) Imidazolidine-2,4-dione
dc.titleSynthesis and Crystal Structure of 3-Amino-1-(5-Chloro-2-Hydroxyphenyl)Imidazolidine-2,4-Dione
dc.typeArticle
dspace.entity.typePublication
oaire.citation.issue1
oaire.citation.volume570
relation.isScopusOfPublicationb1c99a56-234c-4984-8a9f-d3266c093e6f
relation.isScopusOfPublication.latestForDiscoveryb1c99a56-234c-4984-8a9f-d3266c093e6f
relation.isWosOfPublicatione162a495-7cd5-49a1-b048-29fafe6580ca
relation.isWosOfPublication.latestForDiscoverye162a495-7cd5-49a1-b048-29fafe6580ca

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