1-phenyl-1H-benzo[d]imidazole-5-carboxylic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: 1-phenyl-1H-benzo[d]imidazole-5-carboxylic acid
• 英文别名: 1-Phenylbenzimidazole-5-carboxylic acid；1-Phenyl-1H-benzoimidazole-5-carboxylic acid
• 化学式: C₁₄H₁₀N₂O₂
• mdl: MFCD11007740
• 分子量: 238.246
• InChiKey: QTVKJLNIUBHSTK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  55.1
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  甲醇 、 1-phenyl-1H-benzo[d]imidazole-5-carboxylic acid 在 [Ir(dF(CF₃)ppy)₂(dtbbpy)](PF₆) 、 三氟乙酸 、 过氧化苯甲酰 作用下， 反应 8.0h， 以68%的产率得到2-(hydroxymethyl)-1-phenyl-1H-benzo[d]imidazole-5-carboxylic acid
  参考文献：
  名称：

  光氧化还原催化杂芳族碱的羟甲基化

  摘要：

  我们报告了杂芳烃室温C–H羟甲基化方法的发展。这项工作取得了关键的进展，这是通过实施可见光光氧化还原催化来实现的，该催化被证明适用于多种类别的杂芳烃，并能耐受类药物分子中发现的各种官能团。

  DOI：

  10.1021/acs.joc.6b00811
• 作为产物：
  描述：

  4-氯-3-硝基苯甲酸 在 palladium on activated charcoal N-甲基吗啉 、 氢气 、 铜 作用下， 以 甲醇 、 异戊醇 、 乙二醇甲醚 为溶剂， 反应 24.0h， 生成 1-phenyl-1H-benzo[d]imidazole-5-carboxylic acid
  参考文献：
  名称：

  Structure−Activity Relationships for 1-Phenylbenzimidazoles as Selective ATP Site Inhibitors of the Platelet-Derived Growth Factor Receptor

  摘要：

  1-Phenylbenzimidazoles are shown to be a new class of ATP-site inhibitors of the platelet-derived growth factor receptor (PDGFR). Structure-activity relationships (SARs) are narrow, with closely related heterocycles being inactive. A systematic study of substituted 1-phenyl-benzimidazoles showed clear SARs. Substituents at the 4'- and 3'-positions of the phenyl ring are tolerated but do not significantly improve activity, while substituents at the 2'-position abolish it. Substituents in the 2-, 4-, and 7-positions of the benzimidazole ring (with the exception of 4-OH) also abolish activity. Most substituents at the 5- and B-positions maintain or increase activity, with the 5-OH, 5-OMe, 5-COMe, and 5-CO2Me analogues being >10-fold more potent than the parent 1-phenylbenzimidazole. The 5-OMe analogue was both the most potent inhibitor, and showed the highest selectivity (50-fold) between PDGFR and FGFR isolated enzymes, and also a moderately effective inhibitor (IC50 = 1.9 mu M) of PDGF-stimulated PDGFR autophosphorylation in rat aorta smooth muscle cells.

  DOI：

  10.1021/jm9804681

文献信息

• PIPERIDIN-4-YL-AZETIDINE DIAMIDES AS MONOACYLGLYCEROL LIPASE INHIBITORS
  申请人：Connolly Peter J.

  公开号：US20130102584A1

  公开（公告）日：2013-04-25

  Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds, and enantiomers, diastereomers, and pharmaceutically acceptable salts thereof, are represented by Formula (I) as follows: wherein Y, Z, and R are defined herein.

  揭示了用于治疗各种疾病、综合症、症状和障碍的化合物、组合物和方法，包括疼痛。这些化合物及其对映体、二对映体和其药用可接受盐如下所示： 其中Y、Z和R在此处定义。
• DI-AZETIDINYL DIAMIDE AS MONOACYLGLYCEROL LIPASE INHIBITORS
  申请人：Connolly Peter J.

  公开号：US20120058986A1

  公开（公告）日：2012-03-08

  Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula (I) as follows: wherein Q and Z are defined herein.

  揭示了用于治疗各种疾病、综合症、症状和障碍的化合物、组合物和方法，包括疼痛。这些化合物由以下式（I）表示： 其中Q和Z在此处定义。
• [EN] AZETIDINYL DIAMIDES AS MONOACYLGLYCEROL LIPASE INHIBITORS<br/>[FR] AZÉTIDINYL DIAMIDES EN TANT QU'INHIBITEURS DE LA MONOACYLGLYCÉROL LIPASE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2010124082A1

  公开（公告）日：2010-10-28

  Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula (I), wherein Y, Z, R1, and s are defined herein.

  公开了用于治疗各种疾病、综合症、状况和障碍，包括疼痛的化合物、组合物和方法。这些化合物由式（I）表示，其中Y、Z、R1和s在此定义。
• AZETIDINYL DIAMIDES AS MONOACYLGLYCEROL LIPASE INHIBITORS
  申请人：Janssen Pharmaceutica NV

  公开号：US20130102585A1

  公开（公告）日：2013-04-25

  Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula (I) as follows: wherein Y, Z, R 1 , and s are defined herein.

  本发明涉及化合物、组合物和治疗各种疾病、综合症、病况和障碍的方法，包括疼痛。这些化合物由以下式子（I）所表示：其中，Y、Z、R1和s在此被定义。
• DI-AZETIDINYL DIAMIDE AS MONOACYLGLCEROL LIPASE INHIBITORS
  申请人：Janssen Pharmaceutica, NV

  公开号：US20130196969A1

  公开（公告）日：2013-08-01

  Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula (I) as follows: wherein Q and Z are defined herein.

  本发明涉及一种治疗各种疾病、综合征、病况和障碍，包括疼痛的化合物、组合物和方法。这些化合物由以下式子（I）表示：其中Q和Z在此定义。