7-amino-6-benzoyl-8,9,10,11-tetrahydrothieno[2,3-c][1,2,4]triazolo[3,4-a]isoquinoline | 1269792-84-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 7-amino-6-benzoyl-8,9,10,11-tetrahydrothieno[2,3-c][1,2,4]triazolo[3,4-a]isoquinoline
• 英文别名: (10-Amino-8-thia-3,4,6-triazatetracyclo[10.4.0.02,6.07,11]hexadeca-1(12),2,4,7(11),9-pentaen-9-yl)-phenylmethanone
• CAS: 1269792-84-8
• 化学式: C₁₉H₁₆N₄OS
• 分子量: 348.428
• InChiKey: KQSGKPJOAYDPGY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.5
• 重原子数：
  25
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  102
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  1-hydrazino-4-cyano-5,6,7,8-tetrahydroisoquinoline-3(2H)-thione 在 sodium ethanolate 、 sodium acetate 作用下， 以 乙醇 为溶剂， 反应 0.92h， 生成 7-amino-6-benzoyl-8,9,10,11-tetrahydrothieno[2,3-c][1,2,4]triazolo[3,4-a]isoquinoline
  参考文献：
  名称：

  Synthesis and biological activity of pyrazolothienotetrahydroisoquinoline and [1,2,4]triazolo[3,4-a]thienotetrahydroisoquinoline derivatives

  摘要：

  1-Hydrazino-3-thioxo-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile (3) was subjected to react with bifunctional compounds namely: acetylacetone, ethyl cyanoacetate, ethyl benzoylactate, diethylmalonate and ethyl acetoacetate to produce pyrazololthienotetrahydroisoquinoline derivatives 6-11. Also, heating of compound (3) with formic acid afforded triazolothienotetrahydroisoquinoline compound 5 which reacted with a-halogenated compounds to afford compounds 13a-e. Compound 13c when heated with triethylorthoformate afforded triazolo derivative 14. Also, compound 6 was used for synthesizing compounds 18-20. Representative compounds of the synthesized triazolo and pyrazolothienotetrahydroisoquinoline products were tested and evaluated as antimicrobial agents. (C) 2010 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2010.11.036