Date Published: June 01, 2012
Publisher: International Union of Crystallography
Author(s): Hong-Xia Wei, Jing Zhu, Ming Li, Jian-qiang Wang, Cheng Guo.
http://doi.org/10.1107/S1600536812020909
Abstract
In the title compound, C22H14ClN3, prepared by a one-pot reaction under microwave irradiation, the dihedral angles between the central pyridine ring and the pendant naphthyl and chlorobenzene ring systems are 49.2 (2) and 58.2 (3)°, respectively. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate R22(8) loops. The pyridine N atom is the acceptor.
Partial Text
For the use of 2-amino-3-cyanopyridines as intermediates in the preparation of heterocyclic compounds, see: Shishoo et al. (1983 ▶). For the synthesis, see: Mantri et al. (2008 ▶). For related structures, see: Mkhalid et al. (2006 ▶).
Source:
http://doi.org/10.1107/S1600536812020909