N-[2-(Bromomethyl)phenyl]-4-(tetradecyloxy) benzeneacetamide | 139907-03-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-[2-(Bromomethyl)phenyl]-4-(tetradecyloxy) benzeneacetamide
• 英文别名: N-[2-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide；N-[2-(bromomethyl)phenyl]-4-(tetradecyloxy)benzeneacetamide；N-[2-(bromomethyl)phenyl]-2-(4-tetradecoxyphenyl)acetamide
• CAS: 139907-03-2
• 化学式: C₂₉H₄₂BrNO₂
• 分子量: 516.562
• InChiKey: VNWIWQLBBYOXSW-UHFFFAOYSA-N

物化性质

• 沸点：
  632.6±50.0 °C(Predicted)
• 密度：
  1.144±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  9.9
• 重原子数：
  33
• 可旋转键数：
  18
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  38.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5-甲基噻唑 、 N-[2-(Bromomethyl)phenyl]-4-(tetradecyloxy) benzeneacetamide 以 甲苯 为溶剂， 生成 5-Methyl-3-[[2-[[[-4-(tetradecyloxy) phenyl]acetyl]amino]phenyl]methyl]thiazolium bromide
  参考文献：
  名称：

  Method of preparing bis-aryl amide and urea antagonists of platelet

  摘要：

  制备一般式为：##STR1##的双芳基酰胺和尿素化合物的方法，其中x是双价酰胺或尿素取代基，Y是含氮杂环，这些化合物是血小板活化因子的抑制剂。

  公开号：

  US05077409A1
• 作为产物：
  描述：

  4-羟基苯乙酸甲酯 在 吡啶 、 氢氧化钾 、 草酰氯 、 potassium carbonate 、 三乙胺 、 N,N-二甲基甲酰胺 、 lithium bromide 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 丙酮 为溶剂， 反应 108.0h， 生成 N-[2-(Bromomethyl)phenyl]-4-(tetradecyloxy) benzeneacetamide
  参考文献：
  名称：

  Analogs of platelet activating factor. 7. Bis-aryl amide and bis-aryl urea receptor antagonists of PAF

  摘要：

  A series of bis-aryl amide (13-57 and 66-81) and bis-aryl urea (58 and 85) antagonists of platelet-activating factor (PAF) was prepared that contain, separating the two aromatic rings, linear amide linkages of the form -(CH2)nCONH- (n = 0-2), -OCH2CONH-, and -(CH2)nNHCO- (n = 0-1), branched amide linkages of the form -(CH2)nN(COR)- (n = 1-3, R = CH3 or n-C3H7), and -N(COCH3)CH2-, and urea linkages of the form -NHCONH- and -CH2N(CONHCH3)-. These compounds were examined for their ability to inhibit PAF-induced platelet aggregation of rabbit platelets. These in vitro data were compared to similar data obtained for a number of known PAF antagonists. The compounds were evaluated in vivo, in the mouse, for their ability to prevent death induced by a lethal challenge of PAF. The relationships between the biological activity and the nature, lipophilicity, and position of substituents of the aromatic rings were studied. Best activity was observed for compounds having linkages of the type -CH2CONH-, -CH2N(COR)-, and -CH2NHCO-. Many of these compounds inhibit PAF-induced platelet aggregation with IC50's under 1 muM.

  DOI：

  10.1021/jm00104a002

文献信息

• Bis-aryl amide and urea antagonists of platelet activating factor
  申请人：American Cyanamid Company

  公开号：US05128351A1

  公开（公告）日：1992-07-07

  Bis-aryl amide and urea compounds of the general formula: ##STR1## wherein X is a divalent amide or urea substituent and Y is a nitrogen containing heterocycle, which compounds are inhibitors of platelet activating factor. Pharmaceutical compositions containing the compounds and methods of treating platelet activating factor associated conditions are also included.

  一般公式为：其中 X 是双价酰胺或尿素取代基，Y 是含氮杂环的双芳基酰胺和尿素化合物，这些化合物是血小板活化因子的抑制剂。还包括含有这些化合物的药物组合物和治疗血小板活化因子相关疾病的方法。
• Method of making certain aryl containing amides
  申请人：American Cyanamid Company

  公开号：US05231182A1

  公开（公告）日：1993-07-27

  Methods of preparing bis-aryl amide and urea compounds of the general formula: ##STR1## wherein x is a divalent amide or urea substituent and Y is a nitrogen containing heterocycle, which compounds are inhibitors of platelet activating factor.

  制备一般式为##STR1##的双芳基酰胺和脲化合物的方法：其中x是二价酰胺或脲取代基，Y是含氮杂环，这些化合物是血小板活化因子抑制剂。
• Bis-aryl amide antagonists of platelet activating factor
  申请人：——

  公开号：US05350759A1

  公开（公告）日：1994-09-27

  Bis-aryl amide and urea compounds of the general formula: ##STR1## wherein X is a divalent amide or urea substituent and Y is a nitrogen containing heterocycle, which compounds are inhibitors of platelet activating factor. Pharmaceutical compositions containing the compounds and methods of treating platelet activating factor associated conditions are also included.

  通式为：##STR1## 的二芳基酰胺和脲类化合物，其中X是二价的酰胺或脲基团，Y是含氮杂环，这些化合物是血小板活化因子的抑制剂。还包括含有这些化合物的药物组合物和治疗血小板活化因子相关疾病的方法。
• US5077409A
  申请人：——

  公开号：US5077409A

  公开（公告）日：1991-12-31
• US5128351A
  申请人：——

  公开号：US5128351A

  公开（公告）日：1992-07-07