Synthesis and Crystal Structure of (S)-N-(hexahydro-2-oxo-1H-azepin-3-yl)-3-phenyl-2-propenamide

被引:0
作者
Li Xiao-Lin [1 ]
Fang Zheng [1 ]
Zhang Feng [1 ]
Zeng Wen-Bo [2 ]
Guo Kai [2 ]
机构
[1] Nanjing Univ Technol, Sch Pharmaceut Sci, Nanjing 211816, Jiangsu, Peoples R China
[2] Nanjing Univ Technol, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Jiangsu, Peoples R China
关键词
synthesis; propenamide; caprolactam; crystal structure; SPECTRUM CHEMOKINE INHIBITORS; AMINOTHIAZOLE DERIVATIVES; IN-VIVO;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The title compound (S)-N-(hexahydro-2-oxo-1H-azepin-3-yl)-3-phenyl-2-propenamide (C15H18N2O2, M-r= 258.31) was synthesized by the reaction of (S)-alpha-amino-epsilon-caprolactam with 3-phenyl-2- propenoyl chloride. Its chemical structure was determined by H-1 NMR, C-13 NMR, H RMS and X-ray single-crystal diffraction. The crystal belongs to the monoclinic system, space group P2(1)/n with a = 14.957(3), b = 4.884(1), c = 18.630(4) angstrom, beta = 95.91(3)degrees, V = 1353.7(5) angstrom(3), Z = 4, D-c = 1.267 g/cm(3), mu = 0.085 mm(-1), F(000) = 552, R = 0.0671 and wR = 0.1547 for 2473 observed reflections with I> 2 sigma(I).
引用
收藏
页码:851 / 854
页数:4
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