5-phenyl-2-(3-pyridyl)thiazole | 106950-01-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 5-phenyl-2-(3-pyridyl)thiazole
• 英文别名: 5-phenyl-2-(pyridin-3-yl)thiazole；3-<5-phenyl-thiazolyl-(2)>-pyridin；3-(5-phenyl-thiazol-2-yl)-pyridine；3-(5-Phenyl-thiazol-2-yl)-pyridin；5-Phenyl-2-pyridin-3-yl-1,3-thiazole；5-phenyl-2-pyridin-3-yl-1,3-thiazole
• CAS: 106950-01-0
• 化学式: C₁₄H₁₀N₂S
• 分子量: 238.313
• InChiKey: OHNNBCXJZPPPQF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  烟酰氯 在 4-二甲氨基吡啶 、 bis(1,5-cyclooctadiene)nickel (0) 、 potassium phosphate 、 三乙胺 、 1,2-双(二环己基磷基)-乙烷 作用下， 以 四氢呋喃 、 1,4-二氧六环 为溶剂， 反应 25.0h， 生成 5-phenyl-2-(3-pyridyl)thiazole
  参考文献：
  名称：

  Decarbonylative C–H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to the Synthesis of Muscoride A

  摘要：

  A nickel-catalyzed decarbonylative C-H biaryl coupling of azoles and aryl esters is described. The newly developed catalytic system does not require the use of expensive metal catalysts or silver- or copper-based stoichiometric oxidants. We have successfully applied this new C-H arylation reaction to a convergent formal synthesis of muscoride A.

  DOI：

  10.1021/ja306062c

文献信息

• Straightforward microwave-assisted synthesis of 2-thiazolines using Lawesson's reagent under solvent-free conditions
  作者：Julio A. Seijas、M. Pilar Vázquez-Tato、José Crecente-Campo

  DOI：10.1016/j.tet.2008.07.027

  日期：2008.9

  2-Thiazolines are synthesized from carboxylic acids and 1,2-aminoalcohols in the presence of Lawesson's reagent under solventless conditions. The developed method is valid for either substituted or unsubstituted aminoalcohols and a wide variety of aromatic, heteroaromatic and aliphatic carboxylic acids; thus it constitutes a general synthetic method for these kinds of compounds. The role of Lawesson's

  2-噻唑啉是在Lawesson试剂存在下于无溶剂条件下由羧酸和1,2-氨基醇合成的。所开发的方法适用于取代或未取代的氨基醇以及多种芳香族，杂芳香族和脂肪族羧酸；因此，它构成了这类化合物的通用合成方法。Lawesson试剂的作用是双重的：将1，2-氨基醇转化为1，2-氨基硫醇并激活其与羧酸的反应，从而形成噻唑啉环，所有反应都在一个罐中进行。
• Liquid Scintillators. VIII. The Effect of the Dialkylamino Group¹
  作者：V. N. KERR、F. N. HAYES、D. G. OTT、R. LIER、E. HANSBURY

  DOI：10.1021/jo01094a007

  日期：1959.12
• Decarbonylative C–H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to the Synthesis of Muscoride A
  作者：Kazuma Amaike、Kei Muto、Junichiro Yamaguchi、Kenichiro Itami

  DOI：10.1021/ja306062c

  日期：2012.8.22

  A nickel-catalyzed decarbonylative C-H biaryl coupling of azoles and aryl esters is described. The newly developed catalytic system does not require the use of expensive metal catalysts or silver- or copper-based stoichiometric oxidants. We have successfully applied this new C-H arylation reaction to a convergent formal synthesis of muscoride A.