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Dihydrooxazolones and dihydroimidazolones derived from acylglycines: syntheses, molecular structures and supramolecular assembly
Author(s) -
Subbulakshmi Karanth N.,
Narayana Badiadka,
Yathirajan Hemmige S.,
Akkurt Mehmet,
Çelik Ömer,
Ersanlı Cem Cüneyt,
Glidewell Christopher
Publication year - 2015
Publication title -
acta crystallographica section c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.304
H-Index - 17
ISSN - 2053-2296
DOI - 10.1107/s2053229615013637
Subject(s) - triclinic crystal system , chemistry , hydrate , hydrazine (antidepressant) , supramolecular chemistry , crystal structure , yield (engineering) , molecule , phenylhydrazine , medicinal chemistry , thiophene , stereochemistry , crystallography , materials science , organic chemistry , chromatography , metallurgy
Syntheses and structures are described for some alkylidene‐substituted dihydrooxazolones and dihydroimidazoles derived from simple acylglycines. A second, triclinic, polymorph of 4‐benzylidene‐2‐(4‐methylphenyl)‐1,3‐oxazol‐5(4 H )‐one, C 17 H 13 NO 2 , (I), has been identified and the structure of 2‐methyl‐4‐[(thiophen‐2‐yl)methylidene]‐1,3‐oxazol‐5(4 H )‐one, C 9 H 7 NO 2 S, (II), has been rerefined taking into account the orientational disorder of the thienyl group in each of the two independent molecules. The reactions of phenylhydrazine with 2‐phenyl‐4‐[(thiophen‐2‐yl)methylidene]‐1,3‐oxazol‐5(4 H )‐one or 2‐(4‐methylphenyl)‐4‐[(thiophen‐2‐yl)methylidene]‐1,3‐oxazol‐5(4 H )‐one yield, respectively, 3‐anilino‐2‐phenyl‐5‐[(thiophen‐2‐yl)methylidene]‐3,5‐dihydro‐4 H ‐imidazol‐4‐one, C 10 H 15 N 3 OS, (III), and 3‐anilino‐2‐(4‐methylphenyl)‐5‐[(thiophen‐2‐yl)methylidene]‐3,5‐dihydro‐4 H ‐imidazol‐4‐one, C 21 H 17 N 3 OS, (IV), which both exhibit orientational disorder in their thienyl groups. The reactions of 2‐phenyl‐4‐[(thiophen‐2‐yl)methylidene]‐1,3‐oxazol‐5(4 H )‐one with hydrazine hydrate or with water yield, respectively, N ‐[3‐hydrazinyl‐3‐oxo‐1‐(thiophen‐2‐yl)prop‐1‐en‐2‐yl]benzamide and 2‐(benzoylamino)‐3‐(thiophen‐2‐yl)prop‐2‐enoic acid, which in turn react, respectively, with thiophene‐2‐carbaldehyde to form 2‐phenyl‐5‐[(thiophen‐2‐yl)methylidene]‐3‐{[( E )‐(thiophen‐2‐yl)methylidene]amino}‐3,5‐dihydro‐4 H ‐imidazol‐4‐one, C 19 H 13 N 3 OS 2 , (V), which exhibits orientational disorder in only one of its thienyl groups, and with methanol to give methyl (2 Z )‐2‐(benzoylamino)‐3‐(thiophen‐2‐yl)prop‐2‐enoate, C 15 H 13 NO 3 S, (VI). There are no direction‐specific intermolecular interactions in the crystal structure of the triclinic polymorph of (I), but the molecules of (II) are linked by two independent C—H...O hydrogen bonds to form C 2 2 (14) chains. Compounds (III) and (IV) both form centrosymmetric R 2 2 (10) dimers built from N—H...O hydrogen bonds, while compound (V) forms a centrosymmetric R 2 2 (10) dimer built from C—H...O hydrogen bonds. In the structure of compound (VI), a combination of N—H...O and C—H...π(arene) hydrogen bonds links the molecules into sheets. Comparisons are made with some similar compounds.