5-[(2-chlorophenyl)(1-methyl-2-phenyl-1H-indol-3-yl)methyl]-6-hydroxy-2-thioxo-2,3-dihydropyrimidin-4(1H)-one | 1609076-41-6

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二芳基庚烷
• 英文名称: 5-[(2-chlorophenyl)(1-methyl-2-phenyl-1H-indol-3-yl)methyl]-6-hydroxy-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
• CAS: 1609076-41-6
• 化学式: C₂₆H₂₀ClN₃O₂S
• 分子量: 473.983
• InChiKey: VKGFPETYXLOETE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.13
• 重原子数：
  33.0
• 可旋转键数：
  4.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  73.81
• 氢给体数：
  3.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  4,6-二羟基-2-巯基嘧啶 、 1-甲基-2-苯基吲哚 、 2-氯苯甲醛 在 L-脯氨酸 作用下， 以 乙醇 为溶剂， 反应 4.0h， 以96%的产率得到5-[(2-chlorophenyl)(1-methyl-2-phenyl-1H-indol-3-yl)methyl]-6-hydroxy-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
  参考文献：
  名称：

  芳香醛与两种不同亲核试剂的三组分反应及其离解能力的下游转化率决定

  摘要：

  AbstractMany three‐component reactions of aromatic aldehydes with activated methylene derivatives and an associated nucleophile have been developed by using L‐proline as the catalyst. Nucleophiles, such as indoles, thiophenols, mercaptans, 2‐methylfuran and benzenesulfinic acid, could be successfully used in the reactions while the activated methylene derivatives can be 1,3‐cyclohexanedione, dimedone, 1,3‐cyclopentanedione, 1‐phenyl‐3‐methyl‐5‐pyrazolone, 4‐hydroxycoumarin, 4,6‐dihydroxy‐2‐mercaptopyrimidine, 4‐hydroxy‐1‐methyl‐2quinolone, 4‐hydroxy‐6‐methyl‐2‐pyrone and 2‐hydroxy‐1,4‐naphthoquinone. Investigation of the downstream utilization of the products from the above multicomponent reactions (MCRs) revealed that selective cleavages of carbon‐carbon and carbon‐heteroatom bonds in these molecules are indeed possible, which opens an avenue to access some new SN1‐type reactions. Particularly, when the MCR product of an aromatic aldehyde, dimedone and thiophenol was treated with an acid catalyst in the presence of an appropriate nucleophile, cleavage of the carbon‐sulfur bond occurred preferentially, thus providing many complex molecules that cannot be attained by other known methods.magnified image

  DOI：

  10.1002/adsc.201300790