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. 2011 Apr 1;67(Pt 4):o1014.
doi: 10.1107/S1600536811010907. Epub 2011 Mar 31.

N'-[1-(2,4-Dioxo-3,4-dihydro-2H-1-benzopyran-3-yl-idene)eth-yl]thiophene-2-carbo-hydrazide

N'-[1-(2,4-Dioxo-3,4-dihydro-2H-1-benzopyran-3-yl-idene)eth-yl]thiophene-2-carbo-hydrazide

Madeleine Helliwell et al. Acta Crystallogr Sect E Struct Rep Online. .

Abstract

The title compound, C(16)H(12)N(2)O(4)S, was obtained by the condensation of 3-acetyl-4-hy-droxy-coumarin with thien-2-ylcarbonyl hydrazide. The pyran ring adopts a 2,4-dione tautomeric form. The benzopyran ring system is almost coplanar with the thio-phene ring [dihedral angle 0.9 (2)°]. The exocyclic C=C double bond has an E geometry. The mol-ecular conformation is stabilized by an intra-molecular N-H⋯O hydrogen bond. In the crystal, inter-molecular N-H⋯O hydrogen bonds link the mol-ecules into chains along the a axis.

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Figures

Fig. 1.
Fig. 1.
Reaction scheme.
Fig. 2.
Fig. 2.
The molecular structure of the title compound with displacement ellipsoids drawn at the 50% probability level.
Fig. 3.
Fig. 3.
Partial crystal packing of the title compound showing the intra- and intermolecular hydrogen bonds, the latter linking the molecules into one-dimensional chains along the a. H atoms not involved in hydrogen bonding are omitted.

References

    1. Bruker (2001). SMART Bruker AXS Inc., Madison, Wisconsin, USA.
    1. Bruker (2002). SAINT Bruker AXS Inc., Madison, Wisconsin, USA.
    1. Burla, M. C., Caliandro, R., Camalli, M., Carrozzini, B., Cascarano, G. L., De Caro, L., Giacovazzo, C., Polidori, G. & Spagna, R. (2005). J. Appl. Cryst. 38, 381–388.
    1. Kotali, A. (2009). Arkivoc, i, 81–96.
    1. Kotali, A., Kotali, E., Lafazanis, I. S. & Harris, P. A. (2010). Curr. Org. Synth. 7, 62–77.