Abstract

The asymmetric unit of the title compound, C16H14N2O, contains three independent molecules differing primarily in the orientations of the benzyl groups. Each independent molecule forms inversion related dimersviaoffset π-stacking interactions. For two of these dimers, stacks are formed approximately along thea-axis direction by a combinations of C—H...N and C—H...π(ring) contacts, in addition to the offset π-stacking interactions. The third set of dimers are also stacked in the same direction but only by pairwise C—H...N hydrogen bonds.

Highlights

  • The asymmetric unit of the title compound, C16H14N2O, contains three independent molecules differing primarily in the orientations of the benzyl groups

  • The third set of dimers are stacked in the same direction but only by pairwise C—HÁ Á ÁN hydrogen bonds

  • Quinoxaline derivatives have a special place in medicinal chemistry and are commonly present in the bioactive molecules used in many therapeutic areas (Kour et al, 2013)

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Summary

Structure description

Quinoxaline derivatives have a special place in medicinal chemistry and are commonly present in the bioactive molecules used in many therapeutic areas (Kour et al, 2013). Compounds containing the quinoxaline moiety show a wide range of biological activities including anti-inflammatory, analgesic, and antidepressant effects. They demonstrate antifungal, antibacterial, antimalarial, antitubercular, anticancer, antidiabetic, anticonvulsant, antianxiety, and metal-binding properties (Rohde et al, 2016; Wang et al, 2007; Berubeet al., 2015; Ramli & Essassi, 2015). The C1—N2— C10—C11, the C17—N4—C26—C27 and the C33—N6—C42—C43 torsion angles are, respectively, 75.76 (13), 76.68 (13) and À82.29 (13). Each independent molecule forms a stack, with each stack oriented approximately along the a-axis direction (Fig. 2). Cg2, Cg3, Cg6, Cg7 and Cg11 are the centroids of the C1–C6, C11–C16, C17– C22, C27–C32 and C43–C48 benzene rings, respectively

DÁ Á ÁA
Data collection Diffractometer Absorption correction
Synthesis and crystallization
Crystal data
Bruker SMART APEX CCD diffractometer
Special details
Full Text
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