2-methyl>amino-1-<(phenyl)methyl>-1H-benzimidazole | 144858-14-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 2-methyl>amino-1-<(phenyl)methyl>-1H-benzimidazole
• 英文别名: 4-[[(1-Benzylbenzimidazol-2-yl)amino]methyl]-2-methoxy-6-(morpholinomethyl)phenol；4-[[(1-benzylbenzimidazol-2-yl)amino]methyl]-2-methoxy-6-(morpholin-4-ylmethyl)phenol
• CAS: 144858-14-0
• 化学式: C₂₇H₃₀N₄O₃
• 分子量: 458.56
• InChiKey: OYNMCGBPANWDLQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  34
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  71.8
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  2-氨基-1-苄基苯并咪唑 在 sodium tetrahydroborate 作用下， 以 甲醇 、 乙醇 、 水 、 甲苯 为溶剂， 反应 27.0h， 生成 2-methyl>amino-1-<(phenyl)methyl>-1H-benzimidazole
  参考文献：
  名称：

  1-substituted 2-benzylaminobenzimidazole derivatives: compounds with H1-antihistaminic activity

  摘要：

  The preparation of 1-substituted 2-benzylaminobenzimidazole derivatives 13-24 is described. Although these compounds have a different structure from the general structure I of antihistamines, they showed some antihistaminic activity (pA2:5-7) when tested in vitro on guinea pig ileum. The introduction of an additional basic centre as in the Mannich bases 25-27 did not cause any improvement of activity. All the compounds tested proved to be inactive in in vivo induced passive cutaneous anaphylaxis (PCA) and cutaneous vasopermeability in rats.

  DOI：

  10.1016/0223-5234(92)90153-r

文献信息

• 1-substituted 2-benzylaminobenzimidazole derivatives: compounds with H1-antihistaminic activity
  作者：A Da Settimo、G Primofiore、F Da Settimo、L Calzolari、P Cazzulani、A Passoni、O Tofanetti

  DOI：10.1016/0223-5234(92)90153-r

  日期：1992.6

  The preparation of 1-substituted 2-benzylaminobenzimidazole derivatives 13-24 is described. Although these compounds have a different structure from the general structure I of antihistamines, they showed some antihistaminic activity (pA2:5-7) when tested in vitro on guinea pig ileum. The introduction of an additional basic centre as in the Mannich bases 25-27 did not cause any improvement of activity. All the compounds tested proved to be inactive in in vivo induced passive cutaneous anaphylaxis (PCA) and cutaneous vasopermeability in rats.