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首页> 外文期刊>Structural Chemistry >Synthesis, characterization, crystal and molecular structure analysis of a novel 1-benzhydryl piperazine derivative: 1-benzhydryl-4-(2-nitro-benzenesulfonyl)-piperazine
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Synthesis, characterization, crystal and molecular structure analysis of a novel 1-benzhydryl piperazine derivative: 1-benzhydryl-4-(2-nitro-benzenesulfonyl)-piperazine

机译:新型1-苯甲酰基哌嗪衍生物1-苯甲酰基-4-(2-硝基苯磺酰基)-哌嗪的合成,表征,晶体和分子结构分析

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摘要

A novel 1-benzhydryl piperazine derivative 1-benzhydryl-4-(2-nitro-benzenesulfonyl)-piperazine was synthesized by the nucleophilic substitution of 1-benzhydryl piperazine with 2-nitro-benzenesulfonyl chloride. The product obtained was characterized spectroscopically and finally confirmed by X-ray diffraction study. The title compound, C23H23N3O4S crystallizes in the monoclinic space group C2/c with cell parameters a = 13.1120(9) ?, b = 21.4990(9) ?, c = 16.655(1) ?, β = 111.352(2)°, Z = 8, and V = 4372.7(4) ?. The structure reveals that the piperazine ring is in a chair conformation. The geometry around the S atom is distorted tetrahedral. There is a large discrepancy in the bond angles around the piperazine N atoms. The structure is stablized by C–H···O type intermolecular hydrogen bonding interactions.
机译:通过用2-硝基-苯磺酰氯进行1-苯甲基哌嗪的亲核取代,合成了一种新型的1-苯甲基哌嗪衍生物1-苯甲基-4-(2-硝基-苯磺酰基)-哌嗪。光谱分析得到的产物,最后通过X射线衍射研究证实。标题化合物C23 H23 N3 O4 S在单斜空间群C2 / c中结晶,单元参数a = 13.1120(9)?,b = 21.4990(9) ),c = 16.655(1),β= 111.352(2)°,Z = 8,V = 4372.7(4)。该结构表明,哌嗪环处于椅子构型。 S原子周围的几何形状是扭曲的四面体。哌嗪N原子周围的键角存在很大差异。该结构通过C–H···O型分子间氢键相互作用而稳定。

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