9-Ethynyl-6,7,9,11-tetrahydroxy-5-imino-7,8,9,10-tetrahydronaphthacen-12-one | 138569-38-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 蒽
• 英文名称: 9-Ethynyl-6,7,9,11-tetrahydroxy-5-imino-7,8,9,10-tetrahydronaphthacen-12-one
• 英文别名: 8-ethynyl-6,8,10,11-tetrahydroxy-12-imino-9,10-dihydro-7H-tetracen-5-one
• CAS: 138569-38-7
• 化学式: C₂₀H₁₅NO₅
• 分子量: 349.343
• InChiKey: NUTIAIMSDCCOJQ-UHFFFAOYSA-N

物化性质

• 沸点：
  588.2±50.0 °C(Predicted)
• 密度：
  1.53±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  26
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  122
• 氢给体数：
  5
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  9-Ethynyl-6,7,9,11-tetrahydroxy-5-imino-7,8,9,10-tetrahydronaphthacen-12-one 在 硫酸 、 mercury(II) oxide 作用下， 以 丙酮 为溶剂， 生成 (+/-)-4-Demethoxy-5-iminodaunomycinone
  参考文献：
  名称：

  Total synthesis of (±)-5-iminodaunomycinone and (±)-4-demethoxy-5-iminodaunomycinone

  摘要：

  The total synthesis of (+/-)-5-iminodaunomycinone (4a) and (+/-)-4-demethoxy-5-iminodaunomycinone (4b) has been achieved from the readily available 5-methoxy-1,4-dihydroxy-9,10-anthraquinone (5a) and 1,4-dihydroxy-9,10-anthraquinone (5b), respectively. A short and convenient synthesis of (+/-)-daunomycinone (4c) has also been achieved by acid hydrolysis of 4a.

  DOI：

  10.1016/s0040-4039(00)74501-1
• 作为产物：
  描述：

  N,N,O-Tris(2,2,2-trichloroethoxycarbonyl)-5-amino-12-hydroxy-7-<(trimethylsilyl)oxy>-6a,7,8,9,10,10a-hexahydronaphthacene-6,9,11-trione 在 potassium dihydrogenphosphate 、 溶剂黄146 、 锌 作用下， 以 四氢呋喃 为溶剂， 生成 9-Ethynyl-6,7,9,11-tetrahydroxy-5-imino-7,8,9,10-tetrahydronaphthacen-12-one
  参考文献：
  名称：

  Total synthesis of (±)-5-iminodaunomycinone and (±)-4-demethoxy-5-iminodaunomycinone

  摘要：

  The total synthesis of (+/-)-5-iminodaunomycinone (4a) and (+/-)-4-demethoxy-5-iminodaunomycinone (4b) has been achieved from the readily available 5-methoxy-1,4-dihydroxy-9,10-anthraquinone (5a) and 1,4-dihydroxy-9,10-anthraquinone (5b), respectively. A short and convenient synthesis of (+/-)-daunomycinone (4c) has also been achieved by acid hydrolysis of 4a.

  DOI：

  10.1016/s0040-4039(00)74501-1

文献信息

• Total synthesis of (±)-5-iminodaunomycinone and (±)-4-demethoxy-5-iminodaunomycinone
  作者：Francisco Fariña、Pedro Noheda、M.Carmen Paredes

  DOI：10.1016/s0040-4039(00)74501-1

  日期：1991.2

  The total synthesis of (+/-)-5-iminodaunomycinone (4a) and (+/-)-4-demethoxy-5-iminodaunomycinone (4b) has been achieved from the readily available 5-methoxy-1,4-dihydroxy-9,10-anthraquinone (5a) and 1,4-dihydroxy-9,10-anthraquinone (5b), respectively. A short and convenient synthesis of (+/-)-daunomycinone (4c) has also been achieved by acid hydrolysis of 4a.
• Polycyclic hydroxy quinones. 28. Synthesis and Diels-Alder reactions of N,N,O-triacyl derivatives of 10-amino-9-hydroxy-1,4-anthraquinones. An efficient, regiospecific synthesis of (.+-.)-5-iminodaunomycinone, (.+-.)-4-demethoxy-5-iminodaunomycinone, and (.+-.)-daunomycinone
  作者：Francisco Farina、Pedro Noheda、M. Carmen Paredes

  DOI：10.1021/jo00078a019

  日期：1993.12

  The development of a general strategy for the construction of anthracyclinones based on a Diels-Alder reaction of substituted derivatives of 10-amino-9-hydroxy-1,4-anthraquinone is described. The key stages are (i) formation of N,O,O-triacyl derivatives of 1,4-dihydroxy-9,10-anthraquinone monoimines in a tautomer specific fashion, (ii) transacylation into N,N,O-triacyl derivatives of the corresponding 10-amino-9-hydroxy-1,4-anthraquinone, and (iii) Diels-Alder reaction with an appropriately substituted 1,3-diene regiocontrolled by steric factors. This strategy has been applied to the total synthesis of (+/-)-5-iminodaunomycinone (4) and (+/-)-4-demethoxy-5-iminodaunomycinone (3) and to a novel and short synthesis of (+/-)-daunomycinone (5).