RX 811010 | 84141-84-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并二恶烷
• 英文名称: RX 811010
• 英文别名: 2-(3-phenyl-2H-1,4-benzodioxin-3-yl)-4,5-dihydro-1H-imidazole
• CAS: 84141-84-4
• 化学式: C₁₇H₁₆N₂O₂
• 分子量: 280.326
• InChiKey: IYDBIPFBXGYQOK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  42.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2,3-dihydro-2-hydroxy-2-phenyl-1,4-benzodioxin 在 盐酸 、 sodium methylate 、 四氯化锡 作用下， 以 二氯甲烷 为溶剂， 反应 94.5h， 生成 RX 811010
  参考文献：
  名称：

  .alpha.-Adrenoreceptor reagents. 3. Synthesis of some 2-substituted 1,4-benzodioxans as selective presynaptic .alpha.2-adrenoreceptor antagonists

  摘要：

  The synthesis and pharmacological activity of a series of 2-substituted derivatives of the selective alpha 2-adrenoreceptor antagonist idazoxan (RX 781094) is described. Substitution in this position by alkyl, alkenyl, cycloalkenyl, and alkoxy groups in many cases gives compounds whose potencies and selectivities are significantly greater than those of the parent compound.

  DOI：

  10.1021/jm00146a013

文献信息

• Imidazoline derivatives, process for the preparation thereof, pharmaceutical compositions containing them and their use
  申请人：RECKITT AND COLMAN PRODUCTS LIMITED

  公开号：EP0058006A1

  公开（公告）日：1982-08-18

  Imidazoline derivatives of the formula wherein R1 is alkyl C1-7, alkenyl C2-4, cycloalkenyl C4-7, cycloalkyl C4-7 or phenyl; and their non-toxic salts. Processes for the preparation and pharmaceutical compositions thereof. The compounds exhibit presynaptic az- adrenoreceptor antagonism.

  式中的咪唑啉衍生物 其中 R1 为 C1-7 烷基、C2-4 烯基、C4-7 环烯基、C4-7 环烷基或苯基；以及它们的无毒盐。 制备方法及其药物组合物。这些化合物具有突触前az-肾上腺素受体拮抗作用。
• US4397860A
  申请人：——

  公开号：US4397860A

  公开（公告）日：1983-08-09
• .alpha.-Adrenoreceptor reagents. 3. Synthesis of some 2-substituted 1,4-benzodioxans as selective presynaptic .alpha.2-adrenoreceptor antagonists
  作者：Michael R. Stillings、Christopher B. Chapleo、Richard C. M. Butler、J. Alfred Davis、C. David England、Malcolm Myers、Peter L. Myers、Neil Tweddle、Anthony P. Welbourn

  DOI：10.1021/jm00146a013

  日期：1985.8

  The synthesis and pharmacological activity of a series of 2-substituted derivatives of the selective alpha 2-adrenoreceptor antagonist idazoxan (RX 781094) is described. Substitution in this position by alkyl, alkenyl, cycloalkenyl, and alkoxy groups in many cases gives compounds whose potencies and selectivities are significantly greater than those of the parent compound.