5-Benzyloxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester | 937240-87-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并吡啶类
• 英文名称: 5-Benzyloxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester
• 英文别名: methyl 5-phenylmethoxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
• CAS: 937240-87-4
• 化学式: C₁₆H₁₄N₂O₃
• 分子量: 282.299
• InChiKey: HLYORDYFLAPNHW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  64.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  5-benzyloxy-pyrrolo[2,3-b]pyridine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 在 甲醇 、 硫酸 作用下， 反应 4.5h， 以78%的产率得到5-Benzyloxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester
  参考文献：
  名称：

  WO2007/57329

  摘要：

  公开号：

文献信息

• Tricyclic amide derivatives
  申请人：Nettekoven Matthias

  公开号：US20070135416A1

  公开（公告）日：2007-06-14

  The present invention relates to compounds of formula I wherein A, G, r and R 1 to R 5 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are associated with the modulation of H3 receptors.

  本发明涉及式I的化合物 其中A、G、r和R 1 至R 5 如描述和索赔中所定义，并且其药学上可接受的盐。这些化合物可用于治疗和/或预防与H3受体调节相关的疾病。
• Azaindole-2-Carboxamide Derivatives
  申请人：Nettekoven Matthias

  公开号：US20090005379A1

  公开（公告）日：2009-01-01

  The present invention relates to compounds of formula (I) wherein R 1 to R 5 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are associated with the modulation of H3 receptors.

  本发明涉及式(I)的化合物，其中R1至R5如描述和权利要求中所定义，并且其药学上可接受的盐。该化合物对于与H3受体调节相关的疾病的治疗和/或预防是有用的。
• Azaindole-2-carboxamide derivatives
  申请人：Hoffman-La Roche Inc.

  公开号：US07622466B2

  公开（公告）日：2009-11-24

  The present invention relates to compounds of formula (I) wherein R1 to R5 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are associated with the modulation of 113 receptors.

  本发明涉及式(I)化合物，其中R1至R5如描述和权利要求中定义，并且其药学上可接受的盐。这些化合物可用于治疗和/或预防与调节113受体有关的疾病。
• Tricyclic amide derivatives as modulators of H3 receptors
  申请人：Hoffmann-La Roche Inc.

  公开号：US07786109B2

  公开（公告）日：2010-08-31

  The present invention relates to compounds of formula I wherein A, G, r and R1 to R5 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are associated with the modulation of H3 receptors such as, for example, diabetes mellitus.

  本发明涉及式I的化合物，其中A、G、r和R1到R5在说明书和权利要求中定义，并且其药学上可接受的盐。这些化合物可用于治疗和/或预防与调节H3受体相关的疾病，例如糖尿病。
• Tricyclic Amide Derivatives
  申请人：Nettekoven Matthias

  公开号：US20090156583A1

  公开（公告）日：2009-06-18

  The present invention relates to compounds of formula I wherein A, G, r and R 1 to R 5 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are associated with the modulation of H3 receptors.

  本发明涉及式I的化合物，其中A，G，r和R1至R5如描述和要求中所定义，并且其药学上可接受的盐。这些化合物可用于治疗和/或预防与H3受体调节有关的疾病。