Molecular and crystal structure characteristics of 2-phenylaminotetrahydro-1,3-thiazepine hydrochloride and 2-phenyliminohexahydro-1,3-thiazepine

Mukhriddin Umirov, A. Eshimbetov, J. Ashurov, K. Turgunov, Khamid Khodjaniyazov
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Abstract

The current research includes the synthesis and crystallographic characterization of 2-phenylaminotetrahydro-1,3-thiazepine hydrochloride (HPAT) and 2-phenyliminohexa- hydro-1,3-thiazepine (PIT) compounds. 2-Phenylaminotetrahydro-1,3-thiazepine hydro-chloride was synthesized by cyclization of 1-(4-hydroxybutyl)-3-phenylthiourea in an acidic condition. The second compound, 2-phenyliminohexahydro-1,3-thiazepine, was obtained by neutralizing 2-phenylaminotetrahydro-1,3-thiazepine hydrochloride with sodium hydrocarbonate. Both compounds were characterized by the single-crystal X-ray diffraction method. Crystal data for C11H17N2OClS (HPAT): orthorhombic, space group P212121 (no. 19), a = 4.97183(14) Å, b = 15.1169(4) Å, c = 17.7376(5) Å, V = 1333.14(6) Å3, Z = 4, μ(CuKα) = 3.859 mm-1, Dcalc = 1.299 g/cm3, 9243 reflections measured (7.684° ≤ 2Θ ≤ 152.042°), 2749 unique (Rint = 0.0314, Rsigma = 0.0255) which were used in all calculations. The final R1 was 0.0351 (I > 2σ(I)) and wR2 was 0.0911 (all data). Crystal data for C11H14N2S (PIT): monoclinic, space group P21/n (no. 14), a = 9.6303(9) Å, b = 9.8938(6) Å, c = 11.5627(9) Å, β = 103.419(8)°, V = 1071.62(14) Å3, Z = 4, μ(CuKα) = 2.357 mm-1, Dcalc = 1.279 g/cm3, 3938 reflections measured (10.798° ≤ 2Θ ≤ 152.328°), 2172 unique (Rint = 0.0288, Rsigma = 0.0330) that were used in all calculations. The final R1 was 0.0431 (I > 2σ(I)) and wR2 was 0.1219 (all data). The asymmetric unit of HPAT contains one protonated amine, one chlorine anion, and one water molecule. Chlorine anion and water molecules play the role of the bridge in chain formation along the a- and b-axis through H-bonds with N-H hydrogen atoms. Furthermore, the Hirshfeld surface analyses are performed to determine the nature of the intermolecular contacts stabilizing the crystal structures of 2-phenylaminotetrahydro-1,3-thiazepine hydrochloride and 2-phenyliminohexahydro-1,3-thiazepine.
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2-苯基氨基四氢-1,3-噻嗪平盐酸盐和2-苯基亚氨基六氢-1,3-硫嗪平的分子和晶体结构特征
目前的研究包括2-苯基氨基四氢-1,3-噻嗪平盐酸盐(HPAT)和2-苯基亚氨基六氢-1,-3-噻嗪平(PIT)化合物的合成和晶体表征。以1-(4-羟基丁基)-3-苯基硫脲为原料,在酸性条件下进行环化反应,合成了2-苯基氨基四氢-1,3-硫氮杂平盐酸盐。第二种化合物,2-苯基亚氨基六氢-1,3-硫氮杂平,是通过用碳酸氢钠中和2-苯基氨基四氢-1,3-噻氮杂平盐酸盐而获得的。用单晶X射线衍射法对两种化合物进行了表征。C11H17N2OClS(HPAT)的晶体数据:斜方晶系,空间群P212121(编号19),a=4.97183(14)Å,b=15.1169(4)Å、c=17.7376(5)Å和V=1133.14(6)Å3,Z=4,μ(CuKα)=3.859 mm-1,Dcalc=1.299 g/cm3,测量到9243次反射(7.684°≤2θ≤152.042°),2749次独特反射(Rint=0.0314,Rsigma=0.00255),这些反射用于所有计算。最终R1为0.0351(I>2σ(I)),wR2为0.0911(所有数据)。C11H14N2S(PIT)的晶体数据:单斜晶系,空间群P21/n(编号14),a=9.6303(9)Å,b=9.8938(6)Å、c=11.5627(9)å,β=103.419(8)°,V=107.162(14)Å3,Z=4,μ(CuKα)=2.357 mm-1,Dcalc=1.279 g/cm3,测量到3938个反射(10.798°≤2θ≤152.328°),2172个独特反射(Rint=0.0288,Rsigma=0.030),这些反射用于所有计算。最终R1为0.0431(I>2σ(I)),wR2为0.1219(所有数据)。HPAT的不对称单元包含一个质子化的胺、一个氯阴离子和一个水分子。氯阴离子和水分子通过与N-H氢原子的氢键在沿着a轴和b轴的链形成中发挥桥梁作用。此外,进行Hirshfeld表面分析以确定稳定2-苯基氨基四氢-1,3-噻嗪平盐酸盐和2-苯基亚氨基六氢-1,-3-噻嗪平晶体结构的分子间接触的性质。
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