N-(1,5-Dimethyl-3-oxo-2-phenyl-2,3dihydro-1H-pyrazol-4-yl)acetamide-naphthalene-2,3-diol (1/1)

Tan, Kong Wai and Ng, S.W. and Asiri, A.M. and Khan, S.A. (2010) N-(1,5-Dimethyl-3-oxo-2-phenyl-2,3dihydro-1H-pyrazol-4-yl)acetamide-naphthalene-2,3-diol (1/1). Acta Crystallographica Section E: Structure Reports Online, 66 (7). O1850-U963. ISSN 1600-5368, DOI https://doi.org/10.1107/s1600536810024438.

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Abstract

In the reaction of naphthalene-2,3-diol and 4-aminoantipyrine in the presence of acetic acid, the amine function is acetylated and the resulting acetamide co-crystallizes with the diol in the title compound, C(13)H(15)N(3)O(2)center dot C(10)H(8)O(2), with 1:1 molar stoichiometry. The two components are linked by two O-H center dot center dot center dot O=C hydrogen bonds. One of the hydroxy groups interacts with the pyrazolone carbonyl O atom and the other hydroxy group interacts with the amide O atom of another component, generating a chain motif. Adjacent chains are linked into a layer motif via N-H center dot center dot center dot O interactions involving only the heterocyclic acetamide component.

Item Type:	Article
Funders:	UNSPECIFIED
Additional Information:	Department of Chemistry, Faculty of Science Building, University of Malaya, 50603 Kuala Lumpur, MALAYSIA
Uncontrolled Keywords:	Acetic acid; Amine function; Acetylated; Acetamide co-crystallizes; Molar stoichiometry; Hydrogen bonds; Hydroxy groups; Pyrazolone carbonyl; Amide; Chain motif; Heterocyclic acetamide component
Subjects:	Q Science > QD Chemistry
Divisions:	Faculty of Science > Department of Chemistry
Depositing User:	Miss Malisa Diana
Date Deposited:	05 Jul 2013 08:45
Last Modified:	30 Jan 2019 08:48
URI:	http://eprints.um.edu.my/id/eprint/8018

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