3-amino-10-morpholin-4-yl-6,7,8,9-tetrahydrofuro[2'',3'':4',5']pyrido[2',3':4,5]thieno[2,3-c]isoquinolin-9-carbohydrazide | 1338471-57-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并嘧啶酮衍生物
• 英文名称: 3-amino-10-morpholin-4-yl-6,7,8,9-tetrahydrofuro[2'',3'':4',5']pyrido[2',3':4,5]thieno[2,3-c]isoquinolin-9-carbohydrazide
• 英文别名: 3-amino-10-morpholin-4-yl-6,7,8,9-tetrahydrofuro[2",3":4',5']pyrido[2',3':4,5]thieno[2,3-c]isoquinolin-9-carbohydrazide
• CAS: 1338471-57-0
• 化学式: C₂₁H₂₂N₆O₃S
• 分子量: 438.51
• InChiKey: OFKCMTBLUJLRPI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.49
• 重原子数：
  31.0
• 可旋转键数：
  2.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  132.53
• 氢给体数：
  3.0
• 氢受体数：
  9.0

反应信息

• 作为产物：
  描述：

  ethyl 1-amino-5-morpholin-4-yl-6,7,8,9-tetrahydrothieno[2,3-c]isoquinolin-2-carboxylate 在 sodium ethanolate 、 potassium carbonate 、 一水合肼 、 potassium hydroxide 作用下， 以 乙醇 、 溶剂黄146 、 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 生成 3-amino-10-morpholin-4-yl-6,7,8,9-tetrahydrofuro[2'',3'':4',5']pyrido[2',3':4,5]thieno[2,3-c]isoquinolin-9-carbohydrazide
  参考文献：
  名称：

  Synthesis and Reactions of 1-Amino-5-morpholin-4-yl-6,7,8,9-tetrahydrothieno[2,3-c]isoquinoline

  摘要：

  AbstractThe pyrazolone derivative 4 was synthesized by reaction of carbohydrazide 2 with ethyl benzoylacetate in ethanol and p‐toluene sulphonic acid followed by cyclization upon heating in acetic acid. Chloroacylation of amino ester and amino benzoyl compounds 1, 19 gave the chloro acetylamino derivatives 5 and 20 respectively which both of them react with different amines to afford compounds 6, 23a‐d. Hydrolysis and decarboxlation of compound 1 yielded the aminothienotetrahydroisoquinoline 8 which was used as versatile material for synthesizing other heterocyclic compounds 9‐18. Compound 20 react with hexamethylenetetramine and malononitrile yielded thediazepino and pyrrolo derivatives 21, 22 respectively.

  DOI：

  10.1002/jccs.201190019