6-bromo-3-chloro-2-(trifluoromethyl)pyridine | 1211536-90-1

• 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
• 英文名称: 6-bromo-3-chloro-2-(trifluoromethyl)pyridine
• 英文别名: 6-Bromo-3-chloro-2-(trifluoromethyl)pyridine
• CAS: 1211536-90-1
• 化学式: C₆H₂BrClF₃N
• 分子量: 260.441
• InChiKey: XLIIXISXSYYYSZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  12.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  6-bromo-3-chloro-2-(trifluoromethyl)pyridine 在 titanium(IV) tetraethanolate 、 正丁基锂 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 3.0h， 生成 (R,E)-N-((5-chloro-6-(trifluoromethyl)pyridin-2-yl)(3-(trifluoromethyl)cyclobutyl)methylene)-2-methylpropane-2-sulfinamide
  参考文献：
  名称：

  [EN] CYCLOALKYL 3-OXOPIPERAZINE CARBOXAMIDES AND CYCLOHETEROALKYL 3-OXOPIPERAZINE CARBOXAMIDES AS NAV1.8 INHIBITORS
  [FR] CYCLOALKYL 3-OXOPIPÉRAZINE CARBOXAMIDES ET CYCLOHÉTÉROALKYLE 3-OXOPIPÉRAZINE CARBOXAMIDES EN TANT QU'INHIBITEURS DE NAV1.8

  摘要：

  Novel compounds of structural formula (I), and the pharmaceutically acceptable salts thereof, are inhibitors of Nav1.8 channel activity and may be useful in the treatment, prevention, management, amelioration, control and suppression of diseases mediated by Nav1.8 channel activity. The compounds of Formula I may be useful in the treatment, prevention or management of pain disorders, cough disorders, acute itch disorders, and chronic itch disorders.

  公开号：

  WO2022235859A1
• 作为产物：
  描述：

  5-氯-6-三氟甲基吡啶-2-胺 在 亚硝酸特丁酯 、 copper(ll) bromide 作用下， 以 乙腈 为溶剂， 生成 6-bromo-3-chloro-2-(trifluoromethyl)pyridine
  参考文献：
  名称：

  [EN] CYCLOALKYL 3-OXOPIPERAZINE CARBOXAMIDES AND CYCLOHETEROALKYL 3-OXOPIPERAZINE CARBOXAMIDES AS NAV1.8 INHIBITORS
  [FR] CYCLOALKYL 3-OXOPIPÉRAZINE CARBOXAMIDES ET CYCLOHÉTÉROALKYLE 3-OXOPIPÉRAZINE CARBOXAMIDES EN TANT QU'INHIBITEURS DE NAV1.8

  摘要：

  Novel compounds of structural formula (I), and the pharmaceutically acceptable salts thereof, are inhibitors of Nav1.8 channel activity and may be useful in the treatment, prevention, management, amelioration, control and suppression of diseases mediated by Nav1.8 channel activity. The compounds of Formula I may be useful in the treatment, prevention or management of pain disorders, cough disorders, acute itch disorders, and chronic itch disorders.

  公开号：

  WO2022235859A1

文献信息

• NEW PHENYLAZETIDINECARBOXYLATE OR -CARBOXAMIDE COMPOUNDS
  申请人：INVENTIVA

  公开号：US20170066717A1

  公开（公告）日：2017-03-09

  The invention relates to compounds of formula (I). where R, R 1 , R 2 , n, A and Cy have the meanings indicated in the description. The compounds of formula (I) are Nurr-1 modulators.

  这项发明涉及式(I)的化合物。 其中R、R1、R2、n、A和Cy的含义如描述中所示。 式(I)的化合物是Nurr-1调节剂。
• [EN] PYRIMIDINONE COMPOUNDS FOR USE IN THE TREATMENT OF DISEASES OR CONDITIONS MEDIATED BY LP - PLA2<br/>[FR] COMPOSÉS DE PYRIMIDINONE UTILES DANS LE TRAITEMENT DE MALADIES OU D'ÉTATS PATHOLOGIQUES INDUITS PAR LA LP-PLA2
  申请人：GLAXO GROUP LTD

  公开号：WO2012076435A1

  公开（公告）日：2012-06-14

  The present invention relates to novel compounds that inhibit Lp-PLA2 activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA2, for example atherosclerosis, Alzheimer's disease, and/or diabetic macular edema (I).

  本发明涉及抑制Lp-PLA2活性的新化合物，其制备方法，含有这些化合物的组合物以及它们在治疗与Lp-PLA2活性相关的疾病中的应用，例如动脉粥样硬化、阿尔茨海默病和/或糖尿病黄斑水肿。
• COMPOUNDS
  申请人：JIN Yun

  公开号：US20120142717A1

  公开（公告）日：2012-06-07

  The present invention relates to novel compounds that inhibit Lp-PLA 2 activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA 2 , for example atherosclerosis, Alzheimer's disease, and/or diabetic macular edema.

  本发明涉及一种新型化合物，其抑制Lp-PLA2活性，制备这些化合物的方法，含有它们的组合物以及它们在治疗与Lp-PLA2活性相关的疾病中的应用，例如动脉粥样硬化，阿尔茨海默病和/或糖尿病黄斑水肿。
• PYRIMIDINONE COMPOUNDS FOR USE IN THE TREATMENT OF DISEASE OR CONDITIONS MEDIATED BY LP-PLA2
  申请人：Jin Yun

  公开号：US20130252963A1

  公开（公告）日：2013-09-26

  The present invention relates to novel compounds that inhibit Lp-PLA 2 activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA 2 , or example atherosclerosis, Alzheimer's disease, and/or diabetic macular edema.

  本发明涉及一种新的化合物，其抑制Lp-PLA2活性，其制备过程，包含它们的组合物以及它们在治疗与Lp-PLA2活性相关的疾病中的应用，例如动脉粥样硬化，阿尔茨海默病和/或糖尿病黄斑水肿。
• Pyrimidinone compounds for use in the treatment of diseases or conditions mediated by Lp-PLA2
  申请人：Jin Yun

  公开号：US08637536B2

  公开（公告）日：2014-01-28

  The present invention relates to novel compounds that inhibit Lp-PLA2 activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA2, for example atherosclerosis, Alzheimer's disease, and/or diabetic macular edema.

  本发明涉及一种新型化合物，可抑制Lp-PLA2活性，其制备过程，包含它们的组合物以及它们在与Lp-PLA2活性相关的疾病治疗中的应用，例如动脉粥样硬化、阿尔茨海默病和/或糖尿病黄斑水肿。