Dihydrooxazolones and dihydroimidazolones derived from acylglycines: syntheses, molecular structures and supramolecular assembly

Subbulakshmi, K. N. and Narayana, B. and Yathirajan, H. S. and Akkurt, M. and Celik, O. and Ersanli, C. C. and Glidewell, C. (2015) Dihydrooxazolones and dihydroimidazolones derived from acylglycines: syntheses, molecular structures and supramolecular assembly. ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 71 (8). 742+. ISSN 2053-2296

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Official URL: http://doi.org/10.1107/S2053229615013637

Abstract

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(4H)-one, C17H13NO2, (I), has been identified and the structure of 2-methyl-4-(thiophen-2-yl) methylidene]-1,3-oxazol-5(4H)-one, C9H7NO2S, (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(4H)-one or 2-(4-methylphenyl)-4-(thiophen-2-yl) methylidene]-1,3-oxazol-5(4H)-one yield, respectively, 3-anilino-2-phenyl-5-(thiophen-2-yl) methylidene]-3,5-dihydro-4H-imidazol-4-one, C10H15N3OS, (III), and 3-anilino-2-(4-methylphenyl)-5-(thiophen-2-yl) methylidene]-3,5-dihydro-4H-imidazol-4-one, C21H17N3OS, (IV), which both exhibit orientational disorder in their thienyl groups. The reactions of 2-phenyl-4(thiophen-2-yl) methylidene]-1,3-oxazol-5(4H)-one with hydrazine hydrate or with water yield, respectively, N-3-hydrazinyl-3-oxo-1-(thiophen-2-yl) prop-1en-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-4H-imidazol-4-one, C19H13N3OS2, (V), which exhibits orientational disorder in only one of its thienyl groups, and with methanol to give methyl (2Z)-2-(benzoylamino)-3-(thiophen-2-yl) prop-2-enoate, C15H13NO3S, (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 center dot center dot center dot 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 center dot center dot center dot O hydrogen bonds, while compound (V) forms a centrosymmetric R-2(2)(10) dimer built from C-H center dot center dot center dot O hydrogen bonds. In the structure of compound (VI), a combination of N-H center dot center dot center dot O and C-H center dot center dot center dot pi (arene) hydrogen bonds links the molecules into sheets. Comparisons are made with some similar compounds.

Item Type: Article
Uncontrolled Keywords: oxazolones; imidazolones; orientational disorder; crystal structure; hydrogen bonding; Erlenmeyer azlactones; supramolecular assembly
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: Shrirekha N
Date Deposited: 01 Jun 2019 09:57
Last Modified: 01 Jun 2019 09:57
URI: http://eprints.uni-mysore.ac.in/id/eprint/2055

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