3-Allylsulfanyl-1-thiophen-2-yl-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 3-Allylsulfanyl-1-thiophen-2-yl-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile
• 英文别名: 3-prop-2-enylsulfanyl-1-thiophen-2-yl-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile
• 化学式: C₁₇H₁₆N₂S₂
• 分子量: 312.459
• InChiKey: QUUJYLZPZVVMKX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  90.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2-(2-thenoyl)-1-cyclohexanone 在 氢氧化钾 、 三乙胺 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 1.0h， 生成 3-Allylsulfanyl-1-thiophen-2-yl-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile
  参考文献：
  名称：

  摘要：

  By condensation of 2-(2-thenoyl)-1-cyclohexanone with cyanothioacetamide a new compound of a series of chalcogen-containing isoquinolines with a thiophene fragment in its structure was prepared. It was demonstrated that alkylation of the compound with haloalkanes and their derivatives, in particular with those having electron-withdrawing substituents furnished 3-alkylthio-4-cyano-5,6,7,8-tetrahydroisoquinolines. Some of the latter underwent cyclization into 3-amino-2-R-5-(2-thienyl)-6,7,8,9-tetrahydrothieno[2,3-c]-isoquinoline.

  DOI：

  10.1023/a:1022522420258

文献信息

• ——
  作者：M. O. Lozinskii、A. N. Chernega、V. V. Shelyakin

  DOI：10.1023/a:1022522420258

  日期：——

  By condensation of 2-(2-thenoyl)-1-cyclohexanone with cyanothioacetamide a new compound of a series of chalcogen-containing isoquinolines with a thiophene fragment in its structure was prepared. It was demonstrated that alkylation of the compound with haloalkanes and their derivatives, in particular with those having electron-withdrawing substituents furnished 3-alkylthio-4-cyano-5,6,7,8-tetrahydroisoquinolines. Some of the latter underwent cyclization into 3-amino-2-R-5-(2-thienyl)-6,7,8,9-tetrahydrothieno[2,3-c]-isoquinoline.