6-(2,4-dimethoxyphenyl)-4-methylthio-2-oxo-2H-pyran-3-carbonitrile | 905577-85-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 6-(2,4-dimethoxyphenyl)-4-methylthio-2-oxo-2H-pyran-3-carbonitrile
• 英文别名: 6-(2,4-Dimethoxy-phenyl)-4-methylsulfanyl-2-oxo-2H-pyran-3-carbonitrile；6-(2,4-dimethoxyphenyl)-4-methylsulfanyl-2-oxopyran-3-carbonitrile
• CAS: 905577-85-7
• 化学式: C₁₅H₁₃NO₄S
• 分子量: 303.339
• InChiKey: NACPZIBAGIAZLV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  93.8
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  6-(2,4-dimethoxyphenyl)-4-methylthio-2-oxo-2H-pyran-3-carbonitrile 、 丙二腈 在 sodium hydroxide 作用下， 以 二甲基亚砜 为溶剂， 以85%的产率得到3-amino-2',4'-dimethoxy-5-methylsulfanyl-biphenyl-2,4-dicarbonitrile
  参考文献：
  名称：

  Reaction of 6‐aryl‐ or styryl‐4‐methylsulfanyl‐2‐oxo‐2H‐pyrans with active methylene compounds and fluorescence properties of the products

  摘要：

  Abstractmagnified imageNew 2‐pyrone derivatives, dialkyl 3‐cyano‐6‐phenyl‐2‐oxo‐2H‐pyran‐4‐ylmalonates and alkyl 3‐cyano‐6‐phenyl‐2‐oxo‐2H‐pyran‐4‐ylacetates, which were easily prepared by the reaction of 6‐aryl‐4‐methyl‐sulfanyl‐2‐oxo‐2H‐pyran‐3‐carbonitriles with active methylene compounds in the presence of potassium carbonate, show fluorescence emission radiation. The light‐emitting region of dimethyl 3‐cyano‐6‐(4‐N,N‐dimethylamino)styryl‐2‐oxo‐2H‐pyran‐4‐ylmalonate (7h) was 620 nm in dichloromethane, making this compound a typical red fluorescent compound. Methyl 8‐hydroxy‐6‐methyl‐1‐oxo‐3‐phenyl‐1H‐pyrano‐[3,4‐c]pyridine‐5‐carboxylate deriv‐atives also showed fluorescence in the solid state. This is the first example of fluorescence in fused 2‐pyrone derivatives.

  DOI：

  10.1002/jhet.5570450133
• 作为产物：
  描述：

  2-氰-3,3-二(甲硫基)丙烯酸甲酯 、 2,4-二甲氧基苯乙酮 在 sodium hydroxide 作用下， 以 二甲基亚砜 为溶剂， 反应 3.0h， 以33%的产率得到6-(2,4-dimethoxyphenyl)-4-methylthio-2-oxo-2H-pyran-3-carbonitrile
  参考文献：
  名称：

  用于有机发光二极管（OLED）的2 h-吡喃酮衍生物的合成和荧光

  摘要：

  2 H-吡喃酮衍生物是通过芳基乙酰基化合物与乙烯酮二硫缩醛在氢氧化钠的存在下反应合成的，它们在固态时显示出非常强的荧光。在固态下，这两个H-吡喃酮的发光区域为447-630 nm。

  DOI：

  10.1002/jhet.5570440120

文献信息

• Synthesis and fluorescence of 2<i>h</i>-pyrone derivatives for organic light-emitting diodes (OLED)
  作者：Naoko Mizuyama、Yuka Murakami、Shinya Kohra、Kazuo Ueda、Kyoko Hiraoka、Yoshinori Tominaga、Junko Nagaoka、Kojiro Takahashi、Yasuhiro Shigemitsu

  DOI：10.1002/jhet.5570440120

  日期：2007.1

  2H-Pyrone derivatives were synthesized through the reaction of aryl acetyl compounds with ketene dithioacetals in the presence of sodium hydroxide, and they showed very strong fluorescence in the solid state. The light-emitting region of these 2H-pyrones is 447-630 nm in the solid states.

  2 H-吡喃酮衍生物是通过芳基乙酰基化合物与乙烯酮二硫缩醛在氢氧化钠的存在下反应合成的，它们在固态时显示出非常强的荧光。在固态下，这两个H-吡喃酮的发光区域为447-630 nm。
• Reaction of 6‐aryl‐ or styryl‐4‐methylsulfanyl‐2‐oxo‐2<i>H</i>‐pyrans with active methylene compounds and fluorescence properties of the products
  作者：Naoko Mizuyama、Yuka Murakami、Takatoshi Nakatani、Keiko Kuronita、Shinya Kohra、Kazuo Ueda、Kyoko Hiraoka、Yoshinori Tominaga

  DOI：10.1002/jhet.5570450133

  日期：2008.1

  Abstractmagnified imageNew 2‐pyrone derivatives, dialkyl 3‐cyano‐6‐phenyl‐2‐oxo‐2H‐pyran‐4‐ylmalonates and alkyl 3‐cyano‐6‐phenyl‐2‐oxo‐2H‐pyran‐4‐ylacetates, which were easily prepared by the reaction of 6‐aryl‐4‐methyl‐sulfanyl‐2‐oxo‐2H‐pyran‐3‐carbonitriles with active methylene compounds in the presence of potassium carbonate, show fluorescence emission radiation. The light‐emitting region of dimethyl 3‐cyano‐6‐(4‐N,N‐dimethylamino)styryl‐2‐oxo‐2H‐pyran‐4‐ylmalonate (7h) was 620 nm in dichloromethane, making this compound a typical red fluorescent compound. Methyl 8‐hydroxy‐6‐methyl‐1‐oxo‐3‐phenyl‐1H‐pyrano‐[3,4‐c]pyridine‐5‐carboxylate deriv‐atives also showed fluorescence in the solid state. This is the first example of fluorescence in fused 2‐pyrone derivatives.