7-amino-5,8-dihydroxy-2-methoxy-1,4-naphthoquinone | 909721-28-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 7-amino-5,8-dihydroxy-2-methoxy-1,4-naphthoquinone
• 英文别名: 7-Amino-5,8-dihydroxy-2-methoxynaphthalene-1,4-dione；7-amino-5,8-dihydroxy-2-methoxynaphthalene-1,4-dione
• CAS: 909721-28-4
• 化学式: C₁₁H₉NO₅
• 分子量: 235.196
• InChiKey: MWSNOYQDBDOWMB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  110
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  5,8-二羟基-2-甲氧基-1,4-萘醌 在 盐酸 、 sodium azide 作用下， 以 甲醇 为溶剂， 反应 20.0h， 生成 7-amino-5,8-dihydroxy-2-methoxy-1,4-naphthoquinone 、 6-amino-5,8-dihydroxy-2-methoxy-1,4-naphthoquinone
  参考文献：
  名称：

  Synthesis of Echinamines A and B, the First Aminated Hydroxynaphthazarins Produced by the Sea Urchin Scaphechinus mirabilis and Its Analogues

  摘要：

  The first total synthesis of two marine aminated hydroxynaphthazarins, echinamines A (3-amino-7-ethyl- 2,5,6,8-tetrahydroxy-1,4- naphthoquinone) and B (2-amino-7-ethyl- 3,5,6,8-tetrahydroxy-1,4- naphthoquinone), produced by the sea urchin Scaphechinus mirabilis is described. This was achieved from 1,2,4-triacetoxybenzene (13) through a sequence involving double Fries rearrangement of 13, reduction of 3,5-diacetyl-1,2,4-trihydroxybenzene (14), methylation of 3,5-diethyl-1,2,4- trihydroxybenzene (15), simultaneous double acylation of 3,5-diethyl-1,2,4- trimethoxybenzene ( 16) with a dichloromaleic anhydride-ethyl radical elimination process, methylation of 6,7-dichloro-3-ethyl-2-hydroxynaphthazarin (17), nucleophilic substitution of a chlorine atom by the methoxy group in 6,7-dichloro-3-ethyl-2-methoxynaphthazarin (18), introduction of an amino group via direct substitution of a chlorine atom in 7-chloro-3-ethyl-2,6- dimethoxy- (11) and 7-chloro-2-ethyl-3,6-dimethoxynaphthazarins (12) by an azido group, and functional group deprotection. The synthesis of amino analogues of spinazarin and spinochrome D is also described.

  DOI：

  10.1021/np0502185

文献信息

• Synthesis of Echinamines A and B, the First Aminated Hydroxynaphthazarins Produced by the Sea Urchin <i>Scaphechinus </i><i>m</i><i>irabilis</i> and Its Analogues
  作者：Nataly D. Pokhilo、Maria I. Shuvalova、Maxim V. Lebedko、Galina I. Sopelnyak、Alla Ya. Yakubovskaya、Natalia P. Mischenko、Sergey A. Fedoreyev、Victor Ph. Anufriev

  DOI：10.1021/np0502185

  日期：2006.8.1

  The first total synthesis of two marine aminated hydroxynaphthazarins, echinamines A (3-amino-7-ethyl- 2,5,6,8-tetrahydroxy-1,4- naphthoquinone) and B (2-amino-7-ethyl- 3,5,6,8-tetrahydroxy-1,4- naphthoquinone), produced by the sea urchin Scaphechinus mirabilis is described. This was achieved from 1,2,4-triacetoxybenzene (13) through a sequence involving double Fries rearrangement of 13, reduction of 3,5-diacetyl-1,2,4-trihydroxybenzene (14), methylation of 3,5-diethyl-1,2,4- trihydroxybenzene (15), simultaneous double acylation of 3,5-diethyl-1,2,4- trimethoxybenzene ( 16) with a dichloromaleic anhydride-ethyl radical elimination process, methylation of 6,7-dichloro-3-ethyl-2-hydroxynaphthazarin (17), nucleophilic substitution of a chlorine atom by the methoxy group in 6,7-dichloro-3-ethyl-2-methoxynaphthazarin (18), introduction of an amino group via direct substitution of a chlorine atom in 7-chloro-3-ethyl-2,6- dimethoxy- (11) and 7-chloro-2-ethyl-3,6-dimethoxynaphthazarins (12) by an azido group, and functional group deprotection. The synthesis of amino analogues of spinazarin and spinochrome D is also described.