3-氟-6-甲氧基甲酸吡啶 | 1214328-79-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 中文名称: 3-氟-6-甲氧基甲酸吡啶
• 英文名称: 3-fluoro-6-methoxypyridine-2-carboxylic acid
• CAS: 1214328-79-6
• 化学式: C₇H₆FNO₃
• 分子量: 171.128
• InChiKey: AXSBPWGUSHDMMC-UHFFFAOYSA-N

物化性质

• 沸点：
  292.6±35.0 °C(Predicted)
• 密度：
  1.386±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  59.4
• 氢给体数：
  1
• 氢受体数：
  5

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2933399090

反应信息

• 作为反应物：
  描述：

  3-氟-6-甲氧基甲酸吡啶 在 二氧化碳 、 N,N-二异丙基乙胺 、 三氟乙酸 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下， 以 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 20.0~38.0 ℃ 、10.0 MPa 条件下， 生成 3,9-diazabicyclo[4.2.1]non-9-yl(3-fluoro-6-methoxypyridin-2-yl)methanone
  参考文献：
  名称：

  [EN] SUBSTITUTED BRIDGED DIAZEPANE DERIVATIVES AND USE THEREOF
  [FR] DÉRIVÉS DE DIAZÉPANE PONTÉS SUBSTITUÉS ET LEUR UTILISATION

  摘要：

  本申请涉及新型咪唑吡啶基或咪唑嘧啶基取代的、桥联的1,4-二氮杂环庚烷衍生物，以及它们的制备方法，单独或组合用于治疗和/或预防疾病，以及用于制备治疗和/或预防疾病的药物，特别是用于治疗和/或预防呼吸系统疾病，包括与睡眠有关的呼吸系统疾病，如阻塞性睡眠呼吸暂停症、中枢性睡眠呼吸暂停症和打鼾。

  公开号：

  WO2018227427A1

文献信息

• 2-PHENYL-3-(PIPERAZINOMETHYL)IMIDAZO[1,2-A]PYRIDINE DERIVATIVES AS BLOCKERS OF TASK-1 AND TASK-2 CHANNELS, FOR THE TREATMENT OF SLEEP-RELATED BREATHING DISORDERS
  申请人：BAYER PHARMA AKTIENGESELLSCHAFT

  公开号：US20190062326A1

  公开（公告）日：2019-02-28

  The present application relates to novel 2-phenyl-3-(piperazinomethyl)imidazo[1,2-a]pyridine derivatives, to processes for their preparation, to their use alone or in combinations for the treatment and/or prevention of diseases, and to their use for preparing medicaments for the treatment and/or prevention of diseases, in particular for treatment and/or prevention of respiratory disorders including, sleep-related respiratory disorders such as obstructive sleep apnoeas and central sleep apnoeas and snoring.

  本申请涉及新型的2-苯基-3-(哌嗪甲基)咪唑[1,2-a]吡啶衍生物，及其制备过程，以及它们单独或组合用于治疗和/或预防疾病的使用，以及它们用于制备用于治疗和/或预防疾病的药物的使用，特别是用于治疗和/或预防呼吸系统疾病，包括睡眠相关呼吸障碍，如阻塞性睡眠呼吸暂停和中枢性睡眠呼吸暂停以及打鼾。
• [EN] BRIDGED BICYCLIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS<br/>[FR] COMPOSÉS BICYCLIQUES PONTÉS POUR LE TRAITEMENT DES INFECTIONS BACTÉRIENNES
  申请人：KYORIN SEIYAKU KK

  公开号：WO2013003383A1

  公开（公告）日：2013-01-03

  Novel bridged bicyclic compounds are disclosed herein, along with their pharmaceutically acceptable salts, hydrates and prodrugs. Also disclosed are compositions comprising such compounds, methods of preparing such compounds and methods of using such compounds as antibacterial agents. The disclosed compounds, their pharmaceutically acceptable salts, hydrates and prodrugs, as well as compositions comprising such compounds, salts, hydrates and prodrugs, are useful for treating bacterial infections and associated diseases and conditions.

  本文披露了新型桥环双环化合物，以及它们的药用盐、水合物和前药。还披露了包含这些化合物的组合物，制备这些化合物的方法以及将这些化合物用作抗菌剂的方法。所披露的化合物、其药用盐、水合物和前药，以及包含这些化合物、盐、水合物和前药的组合物，可用于治疗细菌感染及相关疾病和症状。
• SUBSTITUTED DIAZAHETERO-BICYCLIC COMPOUNDS AND THEIR USE
  申请人：Bayer Aktiengesellschaft

  公开号：US20210024545A1

  公开（公告）日：2021-01-28

  The present application relates to novel (imidazo[1,2-a]pyridin-3-yl)methyl-substituted diazaheterobicyclic compounds, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of respiratory disorders including sleep-related respiratory disorders such as obstructive sleep apnoea and central sleep apnoea and snoring. The present application further relates to a method of discovering a compound having TASK-1-and/or TASK-3-blocking properties.

  本申请涉及新颖的（咪唑[1,2-a]吡啶-3-基）甲基取代的二氮杂杂双环化合物，其制备方法，单独或组合使用以治疗和/或预防疾病，以及用于生产用于治疗和/或预防疾病的药物的用途，特别是用于治疗和/或预防呼吸系统疾病，包括睡眠相关的呼吸系统疾病，如阻塞性睡眠呼吸暂停症、中枢性睡眠呼吸暂停症和打鼾。本申请还涉及一种发现具有TASK-1和/或TASK-3阻断特性的化合物的方法。
• DIAZABICYCLIC SUBSTITUTED IMIDAZOPYRIMIDINES AND THEIR USE FOR THE TREATMENT OF BREATHING DISORDERS
  申请人：Bayer Aktiengesellschaft

  公开号：US20200109155A1

  公开（公告）日：2020-04-09

  The present invention relates to novel diazabicyclically substituted imidazo[1,2-a]pyrimidine derivatives, to methods for producing the same, to the use thereof either alone or in combinations for the treatment and/or prevention of diseases, as well as to their use for preparing medicaments for the treatment and/or prevention of diseases, especially for treatment and/or prevention of breathing disorders, including sleep-related breathing disorders such as obstructive and central sleep apnoea and snoring.

  本发明涉及新型的二氮杂双环取代咪唑[1,2-a]嘧啶衍生物，以及制备它们的方法。本发明还涉及它们的单独或联合使用用于治疗和/或预防疾病，以及用于制备药物用于治疗和/或预防疾病，特别是用于治疗和/或预防呼吸障碍，包括睡眠相关呼吸障碍，例如阻塞性和中枢性睡眠呼吸暂停和鼾症。
• BRIDGED BICYCLIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS
  申请人：Fukuda Yasumichi

  公开号：US20140243302A1

  公开（公告）日：2014-08-28

  Novel bridged bicyclic compounds are disclosed herein, along with their pharmaceutically acceptable salts, hydrates and prodrugs. Also disclosed are compositions comprising such compounds, methods of preparing such compounds and methods of using such compounds as antibacterial agents. The disclosed compounds, their pharmaceutically acceptable salts, hydrates and prodrugs, as well as compositions comprising such compounds, salts, hydrates and prodrugs, are useful for treating bacterial infections and associated diseases and conditions.

  本文披露了新型桥环双环化合物及其药学上可接受的盐、水合物和前药。还披露了包含这些化合物的组合物、制备这些化合物的方法以及将这些化合物用作抗菌剂的方法。披露的化合物、它们的药学上可接受的盐、水合物和前药，以及包含这些化合物、盐、水合物和前药的组合物，可用于治疗细菌感染及相关疾病和病情。