1-Methyl-4-(2-thienyl)-pyridiniumjodid | 27058-43-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 1-Methyl-4-(2-thienyl)-pyridiniumjodid
• 英文别名: 1-Methyl-4-(2-thienyl)pyridinium iodide；1-methyl-4-thiophen-2-ylpyridin-1-ium;iodide
• CAS: 27058-43-1
• 化学式: C₁₀H₁₀NS*I
• 分子量: 303.167
• InChiKey: XQQWVNSDJQEAKL-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -0.76
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  32.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  对甲苯磺酰叠氮 、 1-Methyl-4-(2-thienyl)-pyridiniumjodid 在 potassium carbonate 作用下， 以 环己酮 为溶剂， 反应 20.0h， 以70%的产率得到4-methyl-N-(1-methyl-4-(thiophen-2-yl)pyridin-2(1H)-ylidene)benzenesulfonamide
  参考文献：
  名称：

  吡啶鎓盐的直接 C-H 磺酰亚胺化

  摘要：

  已经开发了直接吡啶鎓 C-H 磺酰亚胺化，用于高效合成磺酰基亚氨基吡啶衍生物。这种转变的特点是在无金属条件下直接有效地形成具有高官能团耐受性的 C=N 键。光谱特性可能使这些磺酰基亚氨基吡啶化合物成为有用的新型发光材料。

  DOI：

  10.1021/acs.orglett.2c00725
• 作为产物：
  描述：

  4-溴吡啶 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride phenylmalononitrile sodium salt 作用下， 以 乙醚 、 丙酮 为溶剂， 反应 3.0h， 生成 1-Methyl-4-(2-thienyl)-pyridiniumjodid
  参考文献：
  名称：

  Facile, Regioselective Synthesis of Highly Solvatochromic Thiophene-Spaced N-Alkylpyridinium Dicyanomethanides for Second-Harmonic Generation

  摘要：

  The facile and clean synthesis of a navel class of highly solvatochromic chromophores 1 is reported. Compounds 1 are push-pull systems containing a negatively charged dicyanomethanide as a donor group and a positively charged N-alkylpyridinium as an acceptor group. The terminal polar functions are spaced by a thiophene-based moiety containing one or two heterocyclic rings and none, one, or two ethylene bridges. Chromophores 1 have been obtained through a general synthetic scheme involving, as the last step, the 100% regioselective alkylation of the precursor bidentate anions 2, where two competing nucleophilic sites, one neutral at the pyridic nitrogen and one anionic at the carbanionic carbon of the dicyanomethanide group, are present. The unprecedented highly regioselective attack of the alkylating agent onto the neutral pyridic nitrogen rather than the highly charged carbanionic carbon has been also confirmed in the case of the intermolecular competition. Multinuclear (C-13 and N-15) NMR spectroscopy has been used to investigate the structure and the extent of intramolecular charge transfer in 1, which are shown to exist in the ground state as highly charge-separated zwitterionic systems. Experimental results are discussed and compared with semiempirical (PM3) computations. The solvatochromic response of compounds 1, among the highest ever reported in the literature for similar systems, candidates this class of compounds as very attractive active components of nonlinear optical materials.

  DOI：

  10.1021/jo970059x

文献信息

• Preparation of extended di(4-pyridyl)thiophene oligomers
  作者：Willem M. Albers、Gerard W. Canters、Jan Reedijk

  DOI：10.1016/0040-4020(95)00111-k

  日期：1995.3

  Different methods for the coupling of 2-(4-pyridyl)thiophene to a-dibrominated thiophene oligomers and their efficiency to produce a homologous series of extended di(4-pyridyl)thiophene oligomers have been studied. The coupling was found to be most efficient with the organozinc derivative of 2-(4-pyridyl)thiophene, using a Pd(dppf) complex as the catalyst in the coupling reaction. The resulting compounds

  研究了2-（4-吡啶基）噻吩与α-二溴化噻吩低聚物偶联的不同方法，以及它们产生同源系列的扩展二（4-吡啶基）噻吩低聚物的效率。发现在Pd（dppf）络合物作为偶联反应催化剂的情况下，使用2-（4-吡啶基）噻吩的有机锌衍生物偶联最有效。所得化合物有望成为跨膜分子导体的新模型。
• Stille Reaction on Pyridinium Cations
  作者：Juan J. Vaquero、Domingo García-Cuadrado、Ana M. Cuadro、Julio Alvarez-Builla

  DOI：10.1055/s-2002-34903

  日期：——

  A novel unit based on pyridinium cations has been synthesized by the Stille reaction and represents a model for development of molecular electronic devices.

  一种基于吡啶鎓阳离子的新型单元已通过 Stille 反应合成，并代表了分子电子器件开发的模型。
• Facile, Regioselective Synthesis of Highly Solvatochromic Thiophene-Spaced <i>N</i>-Alkylpyridinium Dicyanomethanides for Second-Harmonic Generation
  作者：Alessandro Abbotto、Silvia Bradamante、Antonio Facchetti、Giorgio A. Pagani

  DOI：10.1021/jo970059x

  日期：1997.8.1

  The facile and clean synthesis of a navel class of highly solvatochromic chromophores 1 is reported. Compounds 1 are push-pull systems containing a negatively charged dicyanomethanide as a donor group and a positively charged N-alkylpyridinium as an acceptor group. The terminal polar functions are spaced by a thiophene-based moiety containing one or two heterocyclic rings and none, one, or two ethylene bridges. Chromophores 1 have been obtained through a general synthetic scheme involving, as the last step, the 100% regioselective alkylation of the precursor bidentate anions 2, where two competing nucleophilic sites, one neutral at the pyridic nitrogen and one anionic at the carbanionic carbon of the dicyanomethanide group, are present. The unprecedented highly regioselective attack of the alkylating agent onto the neutral pyridic nitrogen rather than the highly charged carbanionic carbon has been also confirmed in the case of the intermolecular competition. Multinuclear (C-13 and N-15) NMR spectroscopy has been used to investigate the structure and the extent of intramolecular charge transfer in 1, which are shown to exist in the ground state as highly charge-separated zwitterionic systems. Experimental results are discussed and compared with semiempirical (PM3) computations. The solvatochromic response of compounds 1, among the highest ever reported in the literature for similar systems, candidates this class of compounds as very attractive active components of nonlinear optical materials.
• Direct C–H Sulfonylimination of Pyridinium Salts
  作者：Lihua Luo、Juan Tang、Rui Sun、Wenjing Li、Xueli Zheng、Maoling Yuan、Ruixiang Li、Hua Chen、Haiyan Fu

  DOI：10.1021/acs.orglett.2c00725

  日期：2022.4.22

  A direct pyridinium C–H sulfonylimination has been developed for the synthesis of sulfonyl iminopyridine derivatives with high efficiency. This transformation features the direct and efficient formation of a C═N bond with a high functional group tolerance under metal-free conditions. The spectroscopic properties potentially enable these sulfonyl iminopyridine compounds to be useful new emitting materials

  已经开发了直接吡啶鎓 C-H 磺酰亚胺化，用于高效合成磺酰基亚氨基吡啶衍生物。这种转变的特点是在无金属条件下直接有效地形成具有高官能团耐受性的 C=N 键。光谱特性可能使这些磺酰基亚氨基吡啶化合物成为有用的新型发光材料。