Abstract

In the tricyclic title compound, C11H12N2OS, the 2,3,4,5-tetra-hydro-pyridine ring adopts a half-chair conformation. This ring makes dihedral angles of 27.72 (7) and 45.17 (7)°, respectively, with the isoxazole and the cyclo-hexa-1,3-diene rings while the isoxazole ring is oriented at an acute angle of 63.46 (7)° with respect to the cyclo-hexa-1,3-diene ring. In the crystal, mol-ecules associate via C-H⋯N hydrogen bonds and C-H⋯π inter-actions, forming a three-dimensional network.

Highlights

  • In the tricyclic title compound, C11H12N2OS, the 2,3,4,5-tetrahydropyridine ring adopts a half-chair conformation. This ring makes dihedral angles of 27.72 (7) and 45.17 (7), respectively, with the isoxazole and the cyclohexa-1,3-diene rings while the isoxazole ring is oriented at an acute angle of 63.46 (7) with respect to the cyclohexa-1,3-diene ring

  • Molecules associate via C—HÁ Á ÁN hydrogen bonds and C—HÁ Á Á interactions, forming a three-dimensional network

  • Diazadihydroacenaphthylene derivatives contain an isoxazoline scaffold and constitute an important class of heterocyclic compounds whose chemical properties have been investigated over the years (Jager & Buss, 1980; Jager et al, 1980)

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Summary

Structure description

Diazadihydroacenaphthylene derivatives contain an isoxazoline scaffold and constitute an important class of heterocyclic compounds whose chemical properties have been investigated over the years (Jager & Buss, 1980; Jager et al, 1980). This scaffold is used in the synthesis of several complex natural products (Saha & Bhattacharjya, 1997; Copp et al.,1992) and is a pharmacophore of numerous medicinal chemistry compounds (Brandi et al, 2003; King et al, 1982; Bacher et al, 1997; You et al, 1995). Cg is the centroid of the cyclohexa-1,3-diene ring

DÁ Á ÁA
Synthesis and crystallization
No of parameters
Crystal data
Bruker CCD area detector diffractometer
Special details
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