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芳基氯化肼与2-氯喹啉-3-甲醛之间的反应:一种腙、一种4,9-二氢-1H-吡唑并[3,4-b]喹啉和两种1H-吡唑并[3,4-b]喹啉的分子和超分子结构

Reactions between arylhydrazinium chlorides and 2-chloroquinoline-3-carbaldehydes: molecular and supramolecular structures of a hydrazone, a 4,9-dihydro-1H-pyrazolo[3,4-b]quinoline and two 1H-pyrazolo[3,4-b]quinolines.

作者信息

Kumara Tholappanavara H Suresha, Nagendrappa Gopalpur, Chandrika Nanjappa, Sowmya Haliwana B V, Kaur Manpreet, Jasinski Jerry P, Glidewell Christopher

机构信息

Department of Chemistry, Jain University, 52 Bellary Road, Hebbal, Bangalore 560 024, India.

Department of Chemistry, Keene State College, 229 Main Street, Keene, NH 03435-2001, USA.

出版信息

Acta Crystallogr C Struct Chem. 2016 Sep 1;72(Pt 9):670-8. doi: 10.1107/S205322961601278X. Epub 2016 Aug 23.

Abstract

Hydrazone derivatives exhibit a wide range of biological activities, while pyrazolo[3,4-b]quinoline derivatives, on the other hand, exhibit both antimicrobial and antiviral activity, so that all new derivatives in these chemical classes are potentially of value. Dry grinding of a mixture of 2-chloroquinoline-3-carbaldehyde and 4-methylphenylhydrazinium chloride gives (E)-1-[(2-chloroquinolin-3-yl)methylidene]-2-(4-methylphenyl)hydrazine, C17H14ClN3, (I), while the same regents in methanol in the presence of sodium cyanoborohydride give 1-(4-methylphenyl)-4,9-dihydro-1H-pyrazolo[3,4-b]quinoline, C17H15N3, (II). The reactions between phenylhydrazinium chloride and either 2-chloroquinoline-3-carbaldehyde or 2-chloro-6-methylquinoline-3-carbaldehyde give, respectively, 1-phenyl-1H-pyrazolo[3,4-b]quinoline, C16H11N3, (III), which crystallizes in the space group Pbcn as a nonmerohedral twin having Z' = 3, or 6-methyl-1-phenyl-1H-pyrazolo[3,4-b]quinoline, C17H13N3, (IV), which crystallizes in the space group R\overline{3}. The molecules of compound (I) are linked into sheets by a combination of N-H...N and C-H...π(arene) hydrogen bonds, and the molecules of compound (II) are linked by a combination of N-H...N and C-H...π(arene) hydrogen bonds to form a chain of rings. In the structure of compound (III), one of the three independent molecules forms chains generated by C-H...π(arene) hydrogen bonds, with a second type of molecule linked to the chains by a second C-H...π(arene) hydrogen bond and the third type of molecule linked to the chain by multiple π-π stacking interactions. A single C-H...π(arene) hydrogen bond links the molecules of compound (IV) into cyclic centrosymmetric hexamers having \overline{3} (S6) symmetry, which are themselves linked into a three-dimensional array by π-π stacking interactions.

摘要

腙衍生物具有广泛的生物活性,而另一方面,吡唑并[3,4 - b]喹啉衍生物具有抗菌和抗病毒活性,因此这些化学类别中的所有新衍生物都可能具有价值。将2 - 氯喹啉 - 3 - 甲醛与4 - 甲基苯肼盐酸盐的混合物进行干磨,得到(E)-1 - [(2 - 氯喹啉 - 3 - 基)亚甲基]-2 - (4 - 甲基苯基)肼,C17H14ClN3,(I),而相同的试剂在甲醇中于氰基硼氢化钠存在下反应得到1 - (4 - 甲基苯基)-4,9 - 二氢 - 1H - 吡唑并[3,4 - b]喹啉,C17H15N3,(II)。苯肼盐酸盐与2 - 氯喹啉 - 3 - 甲醛或2 - 氯 - 6 - 甲基喹啉 - 3 - 甲醛之间的反应分别得到1 - 苯基 - 1H - 吡唑并[3,4 - b]喹啉,C16H11N3,(III),其在空间群Pbcn中结晶为具有Z' = 3的非merohedral孪晶,或6 - 甲基 - 1 - 苯基 - 1H - 吡唑并[3,4 - b]喹啉,C17H13N3,(IV),其在空间群R\overline{3}中结晶。化合物(I)的分子通过N - H...N和C - H...π(芳烃)氢键的组合连接成片,化合物(II)的分子通过N - H...N和C - H...π(芳烃)氢键的组合连接形成环链。在化合物(III)的结构中,三个独立分子中的一个通过C - H...π(芳烃)氢键形成链,第二种类型的分子通过第二个C - H...π(芳烃)氢键连接到链上,第三种类型的分子通过多个π - π堆积相互作用连接到链上。一个单一的C - H...π(芳烃)氢键将化合物(IV)的分子连接成具有\overline{3} (S6)对称性的环状中心对称六聚体,这些六聚体本身通过π - π堆积相互作用连接成三维阵列。

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