1H AND 13C NMR SPECTRAL ASSIGNMENTS AND X-RAY CRYSTALLOGRAPHY OF N-(3-(1H-IMIDAZOL-1-YL)PROPYL)-2-PHENYLQUINAZOLIN-4-AMINE

被引:0
|
作者
Perez-Fehrmann, Marcia [1 ]
Kesternich, Victor [1 ]
Verdugo, Felipe [1 ]
Marcourt, Laurence [2 ]
Christen, Philippe [2 ]
Brito, Ivan [3 ]
机构
[1] Univ Catolica Norte, Dept Quim, Antofagasta, Chile
[2] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, CH-1211 Geneva 4, Switzerland
[3] Univ Antofagasta, Dept Quim, Antofagasta, Chile
来源
JOURNAL OF THE CHILEAN CHEMICAL SOCIETY | 2013年 / 58卷 / 02期
关键词
ANTIINFLAMMATORY ACTIVITY; MULTIPLE-MYELOMA; INHIBITORS; DERIVATIVES; ANTAGONISTS; DISCOVERY; POTENT;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
N-(3-(1H-Imidazol-1-yl)propyl)-2-phenylquinazolin-4-amine (2) was obtained by nucleophilic substitution of 1-(3-aminopropyl)-imidazole over 4-chloro-2-phenylquinazoline (1) with DMF/TEA at room temperature. The precursor and product were characterized by NMR spectroscopy. The structure of the title compound was confirmed by X-ray diffraction methods. The quinazoline fragment (2) is essentially planar and makes a dihedral angle of 66.35 degrees with the imidazole plane. In the crystal packing the molecules are associated by two strong intermolecular NH center dot center dot center dot N hydrogen bonds with graph-set motif R-2(2)(16). These pairs are linked by two pi-pi interactions.
引用
收藏
页码:1771 / 1774
页数:4
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