5-(1H-imidazol-1-ylmethyl)indole-2-carboxylic acid methyl ester | 102870-05-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 5-(1H-imidazol-1-ylmethyl)indole-2-carboxylic acid methyl ester
• 英文别名: methyl 5-(imidazol-1-ylmethyl)-1H-indole-2-carboxylate
• CAS: 102870-05-3
• 化学式: C₁₄H₁₃N₃O₂
• 分子量: 255.276
• InChiKey: YYASWFJJUQHHHA-UHFFFAOYSA-N

物化性质

• 熔点：
  195-196.5 °C
• 沸点：
  507.1±35.0 °C(Predicted)
• 密度：
  1.30±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  19.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  59.91
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  5-(1H-imidazol-1-ylmethyl)indole-2-carboxylic acid methyl ester 在 氢氧化钾 作用下， 以 甲醇 、 水 为溶剂， 反应 2.0h， 以72%的产率得到5-Imidazol-1-ylmethyl-1H-indole-2-carboxylic acid
  参考文献：
  名称：

  Selective thromboxane synthetase inhibitors. 3. 1H-Imidazol-1-yl-substituted benzo[b]furan-, benzo[b]thiophene- and indole-2- and 3-carboxylic acids

  摘要：

  The preparation of a series of 1H-imidazol-1-yl-substituted benzo[b]furan-, benzo[b]thiophene-, and indolecarboxylic acids is described. Most of the compounds were potent inhibitors of TxA2 synthetase in vitro, and the distance between the imidazole and carboxylic acid groups was found to be important for optimal potency. The most potent compound in vivo was 6-(1H-imidazol-1-ylmethyl)-3-methylbenzo[b]thiophene-2-carboxylic acid (71), which, in conscious dogs, showed a similar profile of activity to that of dazoxiben (1).

  DOI：

  10.1021/jm00159a012
• 作为产物：
  描述：

  1-乙酰基-5-甲基吲哚-2-甲酸甲酯 在 N-溴代丁二酰亚胺(NBS) 、 偶氮二异丁腈 、 乙醇 、 氨 作用下， 以 四氯化碳 为溶剂， 反应 7.5h， 生成 5-(1H-imidazol-1-ylmethyl)indole-2-carboxylic acid methyl ester
  参考文献：
  名称：

  Selective thromboxane synthetase inhibitors. 3. 1H-Imidazol-1-yl-substituted benzo[b]furan-, benzo[b]thiophene- and indole-2- and 3-carboxylic acids

  摘要：

  The preparation of a series of 1H-imidazol-1-yl-substituted benzo[b]furan-, benzo[b]thiophene-, and indolecarboxylic acids is described. Most of the compounds were potent inhibitors of TxA2 synthetase in vitro, and the distance between the imidazole and carboxylic acid groups was found to be important for optimal potency. The most potent compound in vivo was 6-(1H-imidazol-1-ylmethyl)-3-methylbenzo[b]thiophene-2-carboxylic acid (71), which, in conscious dogs, showed a similar profile of activity to that of dazoxiben (1).

  DOI：

  10.1021/jm00159a012

文献信息

• CROSS P. E.; DICKINSON R. P.; PARRY M. J.; RANDALL M. J., J. MED. CHEM., 1986, 29, N 9, 1637-1643
  作者：CROSS P. E.、 DICKINSON R. P.、 PARRY M. J.、 RANDALL M. J.

  DOI：——

  日期：——