3-(2H-1,5-dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)-2-naphthalenecarboxylic acid | 860030-22-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 3-(2H-1,5-dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)-2-naphthalenecarboxylic acid
• CAS: 860030-22-4
• 化学式: C₂₂H₁₃N₃O₄
• 分子量: 383.363
• InChiKey: FOUNTWSDRSUKCU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.13
• 重原子数：
  29.0
• 可旋转键数：
  2.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  100.76
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  乙酸酐 、 3-(2H-1,5-dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)-2-naphthalenecarboxylic acid 反应 2.0h， 以86%的产率得到14H-isoquino[2',3':3,4]imidazo[2,1-b]benzo[g]quinazoline-8,14,16-trione
  参考文献：
  名称：

  SYNTHESIS OF 15H-ISOQUINO[2′,3′:3,4]IMIDAZO[2,1-B]QUINAZOLINE-7,13,15-TRIONES AND 14H-ISOQUINO[2′,3′:3,4]IMIDAZO[2,1-B]BENZO[G]QUINAZOLINE-8,14,16-TRIONE AS NEW POLYCYCLIC FUSED-RING SYSTEMS

  摘要：

  3-Thioxo-2H-imidazo[1,5-b]isoquinoline-1,5-dione (3) and 2-substituted-3-thioxo-2H-imidazo[1,5-b]isoquinoline-1,5-diones(4a-l) were prepared from the reaction of 2-thioliydantoin. (2) and 3-substituted 2-thiohydantoin (5a-l) with 2-formyl benzoic acid (1). Alkylation of 3 under an anhydrous basic conditions afforded 4a-i. The alkylation of 3 in. aqueous basic solution, afforded 3-(alkyl-mercapto)imidazo[1,5-b]isoquinoline-1,5-diones (7a,b). Reactions of the aromatic amino acids 9a,b and 12 with 7a afforded 2-(2H-1,5dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)benzoic acids (10a,b) and 3-(2H-1,5-dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)-2-naphthalenecarboxylic acid (13), which were then cyclyzed by heating in acetic anhydride to afford 15H-isoquino[2',3':3,4]-imidazo[2,1-b]quinazoline-7,13,15-triones (11a,b) and 14H-isoquino[2',3':3,4]imidazo[2,1-b]benzo[g]quinazoline-8,14,16-trione (14). Some of the new compounds were tested for their antitumor activities.

  DOI：

  10.1080/104265090507533
• 作为产物：
  描述：

  邻羧基苯甲醛 在 sodium hydroxide 、 sodium acetate 、 溶剂黄146 作用下， 以 甲醇 、 乙醇 为溶剂， 反应 40.0h， 生成 3-(2H-1,5-dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)-2-naphthalenecarboxylic acid
  参考文献：
  名称：

  SYNTHESIS OF 15H-ISOQUINO[2′,3′:3,4]IMIDAZO[2,1-B]QUINAZOLINE-7,13,15-TRIONES AND 14H-ISOQUINO[2′,3′:3,4]IMIDAZO[2,1-B]BENZO[G]QUINAZOLINE-8,14,16-TRIONE AS NEW POLYCYCLIC FUSED-RING SYSTEMS

  摘要：

  3-Thioxo-2H-imidazo[1,5-b]isoquinoline-1,5-dione (3) and 2-substituted-3-thioxo-2H-imidazo[1,5-b]isoquinoline-1,5-diones(4a-l) were prepared from the reaction of 2-thioliydantoin. (2) and 3-substituted 2-thiohydantoin (5a-l) with 2-formyl benzoic acid (1). Alkylation of 3 under an anhydrous basic conditions afforded 4a-i. The alkylation of 3 in. aqueous basic solution, afforded 3-(alkyl-mercapto)imidazo[1,5-b]isoquinoline-1,5-diones (7a,b). Reactions of the aromatic amino acids 9a,b and 12 with 7a afforded 2-(2H-1,5dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)benzoic acids (10a,b) and 3-(2H-1,5-dioxoimidazo[1,5-b]isoquinazolin-3-ylideneamino)-2-naphthalenecarboxylic acid (13), which were then cyclyzed by heating in acetic anhydride to afford 15H-isoquino[2',3':3,4]-imidazo[2,1-b]quinazoline-7,13,15-triones (11a,b) and 14H-isoquino[2',3':3,4]imidazo[2,1-b]benzo[g]quinazoline-8,14,16-trione (14). Some of the new compounds were tested for their antitumor activities.

  DOI：

  10.1080/104265090507533