4-(2,2-二甲氧基乙基)苯胺 | 392630-73-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 4-(2,2-二甲氧基乙基)苯胺
• 英文名称: 4-(2,2-dimethoxyethyl)aniline
• CAS: 392630-73-8
• 化学式: C₁₀H₁₅NO₂
• mdl: MFCD09878881
• 分子量: 181.235
• InChiKey: VMTBZWCYAQYHBL-UHFFFAOYSA-N

物化性质

• 沸点：
  260.2±25.0 °C(Predicted)
• 密度：
  1.062±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  44.5
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2922199090

反应信息

• 作为反应物：
  描述：

  4-(2,2-二甲氧基乙基)苯胺 在 palladium on activated charcoal 三乙酰氧基硼氢化钠 、 溶剂黄146 、 sodium sulfate 、 环己烯 作用下， 以 乙醇 为溶剂， 生成 N-[4-(2,2-dimethoxyethyl)phenyl]-4-piperidinamine
  参考文献：
  名称：

  4-Aminopiperidine ureas as potent selective agonists of the human β3-Adrenergic receptor

  摘要：

  The preparation and structure-activity relationships (SARs) of potent agonists of the human beta (3)-adrenergic receptor (AR) derived from a 4-aminopiperidine scaffold are described. Examples combine human beta (3)-AR potency with selectivity over human beta (1)-AR and/or human beta (2)-AR agonism. Compound 29s was identified as a potent (EC50= 1 nM) and selective (greater than 400-fold over beta (1)- with no beta (2)-AR agonism) full beta (3)-AR agonist with in vivo activity in a transgenic mouse model of thermogenesis. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(01)00645-x
• 作为产物：
  描述：

  1-(2,2-二甲氧基乙基)-4-硝基苯 在 钯 ammonium formate 作用下， 以 乙醇 为溶剂， 生成 4-(2,2-二甲氧基乙基)苯胺
  参考文献：
  名称：

  Heterocyclic beta-3 adrenergic receptor agonists

  摘要：

  这项发明提供了具有结构式I的化合物 1 其中U、V、W、X和Y如前文所定义， 或其药学上可接受的盐，用于治疗或抑制与胰岛素抵抗或高血糖相关的代谢紊乱（通常与肥胖或葡萄糖不耐受有关）、动脉粥样硬化、胃肠道疾病、神经炎症、青光眼、眼压增高和频繁排尿；特别适用于治疗或抑制2型糖尿病。

  公开号：

  US20020028832A1

文献信息

• Heterocyclic beta-3 adrenergic receptor agonists
  申请人：American Home Products Corporation

  公开号：US20020028832A1

  公开（公告）日：2002-03-07

  This invention provides compounds of Formula I having the structure 1 U, V, W, X, and Y are as defined hereinbefore, or a pharmaceutically acceptable salt thereof, which are useful in treating or inhibiting metabolic disorders related to insulin resistance or hyperglycemia (typically associated with obesity or glucose intolerance), atherosclerosis, gastrointestinal disorders, neurogenetic inflammation, glaucoma, ocular hypertension and frequent urination; and are particularly useful in the treatment or inhibition of type II diabetes.

  这项发明提供了具有结构式I的化合物 1 其中U、V、W、X和Y如前文所定义， 或其药学上可接受的盐，用于治疗或抑制与胰岛素抵抗或高血糖相关的代谢紊乱（通常与肥胖或葡萄糖不耐受有关）、动脉粥样硬化、胃肠道疾病、神经炎症、青光眼、眼压增高和频繁排尿；特别适用于治疗或抑制2型糖尿病。
• US6451814B1
  申请人：——

  公开号：US6451814B1

  公开（公告）日：2002-09-17
• US6605618B2
  申请人：——

  公开号：US6605618B2

  公开（公告）日：2003-08-12
• [EN] HETEROCYCLIC BETA-3 ADRENERGIC RECEPTOR AGONISTS<br/>[FR] AGONISTES DES BETA-3 RECEPTEURS ADRENERGIQUES HETEROCYCLIQUES
  申请人：AMERICAN HOME PROD

  公开号：WO2002006229A2

  公开（公告）日：2002-01-24

  This invetion provides compounds of Formula (1) having the structure (A), wherein U, V, W, X, and Y are as defined herinbefore, or a pharmaceutically acceptable salt thereof, which are useful in treating or inhibiting metabolic disorders related to insulin resistance or hyperglycemia (typically associated with obesity or glucose intolerance), atherosclerosis, gastrointestinal disorders, neurogenetic inflammation, glaucoma, ocular hypertension and frequent urination; and are particularly useful in the treatment or inhibition of type II diabetes.
• 4-Aminopiperidine ureas as potent selective agonists of the human β3-Adrenergic receptor
  作者：Mark A Ashwell、William R Solvibile、Stella Han、Elwood Largis、Ruth Mulvey、Jeffrey Tillet

  DOI：10.1016/s0960-894x(01)00645-x

  日期：2001.12

  The preparation and structure-activity relationships (SARs) of potent agonists of the human beta (3)-adrenergic receptor (AR) derived from a 4-aminopiperidine scaffold are described. Examples combine human beta (3)-AR potency with selectivity over human beta (1)-AR and/or human beta (2)-AR agonism. Compound 29s was identified as a potent (EC50= 1 nM) and selective (greater than 400-fold over beta (1)- with no beta (2)-AR agonism) full beta (3)-AR agonist with in vivo activity in a transgenic mouse model of thermogenesis. (C) 2001 Elsevier Science Ltd. All rights reserved.