methyl 5-cyclopropyl-4-(4,4-difluoropiperidin-1-yl)-2-isopropoxybenzoate

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: methyl 5-cyclopropyl-4-(4,4-difluoropiperidin-1-yl)-2-isopropoxybenzoate
• 英文别名: Methyl 5-cyclopropyl-4-(4,4-difluoropiperidin-1-yl)-2-isopropoxybenzoate；methyl 5-cyclopropyl-4-(4,4-difluoropiperidin-1-yl)-2-propan-2-yloxybenzoate
• 化学式: C₁₉H₂₅F₂NO₃
• 分子量: 353.409
• InChiKey: MNJYPOHQSLQCAJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  25
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  38.8
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  methyl 5-bromo-4-(4,4-difluoropiperidin-1-yl)-2-isopropoxybenzoate 、 环丙基硼酸 以the title compound was obtained in the similar manner as in Step D of Example 23的产率得到methyl 5-cyclopropyl-4-(4,4-difluoropiperidin-1-yl)-2-isopropoxybenzoate
  参考文献：
  名称：

  HETEROCYCLIC COMPOUND

  摘要：

  提供的是以下式子（1）所代表的化合物或其盐，具有SSTR5拮抗作用：其中每个符号的定义与说明书中相同。

  公开号：

  US20160060273A1

文献信息

• [EN] SHIP1 MODULATORS AND METHODS RELATED THERETO<br/>[FR] MODULATEURS DE SHIP1 ET MÉTHODES ASSOCIÉES
  申请人：AQUINOX PHARMACEUTICALS INC

  公开号：WO2014143561A1

  公开（公告）日：2014-09-18

  Compounds of formula (I): where R1, R2, R3, R4a, R4b, R5, R6 and R7 are defined herein, or stereoisomers or pharmaceutically acceptable salts thereof, are described herein. Such compounds have activity as SHIP1 modulators, and thus may be used to treat any of a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of formula (I) in combination with a pharmaceutically acceptable carrier or diluent are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

  式（I）的化合物：其中R1、R2、R3、R4a、R4b、R5、R6和R7如本文所定义，或其立体异构体或药学上可接受的盐，在本文中有描述。这些化合物具有SHIP1调节剂的活性，因此可用于治疗任何需要SHIP1调节的各种疾病、疾病或病况。还公开了包含式（I）化合物与药学上可接受的载体或稀释剂组合的组合物，以及通过向需要的动物施用这些化合物来进行SHIP1调节的方法。
• [EN] SPIRO AZETIDINE ISOXAZOLE DERIVATIVES AND THEIR USE AS SSTR5 ANTAGONISTS<br/>[FR] DÉRIVÉS DE SPIRO AZÉTIDINE ISOXAZOLE ET LEUR UTILISATION EN TANT QU'ANTAGONISTES DE SSTR5
  申请人：TAKEDA PHARMACEUTICAL

  公开号：WO2014142363A1

  公开（公告）日：2014-09-18

  Provided is a compound represented by the following formula (1) or a salt thereof, which has an SSTR5 antagonistic action: wherein each symbol has the same definition as in the specification.

  提供一个具有SSTR5拮抗作用的化合物，该化合物由以下公式（1）或其盐表示：其中每个符号的定义与说明书中相同。
• SHIP1 MODULATORS AND METHODS RELATED THERETO
  申请人：Aquinox Pharmaceuticals (Canada) Inc.

  公开号：US20160083387A1

  公开（公告）日：2016-03-24

  Compounds of formula (I): where R 1 , R 2 , R 3 , R 4a , R 4b , R 5 , R 6 and R 7 are defined herein, or stereoisomers or pharmaceutically acceptable salts thereof, are described herein. Such compounds have activity as SHIP1 modulators, and thus may be used to treat any of a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of formula (I) in combination with a pharmaceutically acceptable carrier or diluent are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

  本文描述了式(I)的化合物，其中R1、R2、R3、R4a、R4b、R5、R6和R7的定义如下，或其立体异构体或药学上可接受的盐。这些化合物具有SHIP1调节剂的活性，因此可用于治疗任何需要SHIP1调节的各种疾病、障碍或病况。本文还披露了包含式(I)的化合物与药学上可接受的载体或稀释剂的组合物，以及通过将这些化合物用于需要的动物的给药来进行SHIP1调节的方法。
• SHIP1 modulators and methods related thereto
  申请人：Aquinox Pharmaceuticals (Canada) Inc.

  公开号：US10100056B2

  公开（公告）日：2018-10-16

  Compounds of formula (I): where R1, R2, R3, R4a, R4b, R5, R6 and R7 are defined herein, or stereoisomers or pharmaceutically acceptable salts thereof, are described herein. Such compounds have activity as SHIP1 modulators, and thus may be used to treat any of a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of formula (I) in combination with a pharmaceutically acceptable carrier or diluent are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

  本文描述了式 (I) 的化合物：其中 R1、R2、R3、R4a、R4b、R5、R6 和 R7 在本文中定义，或其立体异构体或药学上可接受的盐。这类化合物具有 SHIP1 调节剂的活性，因此可用于治疗 SHIP1 调节所带来的各种疾病、失调或病症中的任何一种。此外，还公开了由式（I）化合物与药学上可接受的载体或稀释剂组合而成的组合物，以及通过向有需要的动物施用此类化合物来调节 SHIP1 的方法。
• SPIRO AZETIDINE ISOXAZOLE DERIVATIVES AND THEIR USE AS SSTR5 ANTAGONISTS
  申请人：Takeda Pharmaceutical Company Limited

  公开号：EP2970331A1

  公开（公告）日：2016-01-20