3-[3-(Trifluoromethoxy)phenyl]-1-oxa-8-azaspiro[4.5]decane | 1227566-37-1

• 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: 3-[3-(Trifluoromethoxy)phenyl]-1-oxa-8-azaspiro[4.5]decane
• CAS: 1227566-37-1
• 化学式: C₁₅H₁₈F₃NO₂
• 分子量: 301.309
• InChiKey: XIVMKBQCZWRSHV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  30.5
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  phenyl (3,4-dimethylisoxazol-5-yl)carbamate 、 3-[3-(Trifluoromethoxy)phenyl]-1-oxa-8-azaspiro[4.5]decane 在 N,N-二异丙基乙胺 作用下， 以 乙腈 为溶剂， 生成 (3RS)-N-(3,4-dimethylisoxazol-5-yl)-3-[3-(trifluoromethoxy)phenyl]-1-oxa-8-azaspiro[4.5]decane-8-carboxamide
  参考文献：
  名称：

  Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 2. Discovery of 7-azaspiro[3.5]nonane urea PF-04862853, an orally efficacious inhibitor of fatty acid amide hydrolase (FAAH) for pain

  摘要：

  Fatty acid amide hydrolase (FAAH) is an integral membrane serine hydrolase responsible for the degradation of fatty acid amide signaling molecules such as endocannabinoid anandamide (AEA), which has been shown to possess cannabinoid-like analgesic properties. Herein we report the optimization of spirocyclic 7-azaspiro[3.5]nonane and 1-oxa-8-azaspiro[4.5]decane urea covalent inhibitors of FAAH. Using an iterative design and optimization strategy, lead compounds were identified with a remarkable reduction in molecular weight and favorable CNS drug like properties. 3,4-Dimethylisoxazole and 1-methyltetrazole were identified as superior urea moieties for this inhibitor class. A dual purpose in vivo efficacy and pharmacokinetic screen was designed to be the key decision enabling experiment affording the ability to move quickly from compound synthesis to selection of preclinical candidates. On the basis of the remarkable potency, selectivity, pharmacokinetic properties and in vivo efficacy, PF-04862853 (15p) was advanced as a clinical candidate. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.08.048
• 作为产物：
  描述：

  3-溴-1-噁-8-氮杂螺[4.5]癸烷-8-羧酸叔丁酯 在 nickel(II) iodide 、 盐酸 、 lithium hexamethyldisilazane 作用下， 以 1,4-二氧六环 、 二氯甲烷 、 异丙醇 为溶剂， 生成 3-[3-(Trifluoromethoxy)phenyl]-1-oxa-8-azaspiro[4.5]decane
  参考文献：
  名称：

  Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 2. Discovery of 7-azaspiro[3.5]nonane urea PF-04862853, an orally efficacious inhibitor of fatty acid amide hydrolase (FAAH) for pain

  摘要：

  Fatty acid amide hydrolase (FAAH) is an integral membrane serine hydrolase responsible for the degradation of fatty acid amide signaling molecules such as endocannabinoid anandamide (AEA), which has been shown to possess cannabinoid-like analgesic properties. Herein we report the optimization of spirocyclic 7-azaspiro[3.5]nonane and 1-oxa-8-azaspiro[4.5]decane urea covalent inhibitors of FAAH. Using an iterative design and optimization strategy, lead compounds were identified with a remarkable reduction in molecular weight and favorable CNS drug like properties. 3,4-Dimethylisoxazole and 1-methyltetrazole were identified as superior urea moieties for this inhibitor class. A dual purpose in vivo efficacy and pharmacokinetic screen was designed to be the key decision enabling experiment affording the ability to move quickly from compound synthesis to selection of preclinical candidates. On the basis of the remarkable potency, selectivity, pharmacokinetic properties and in vivo efficacy, PF-04862853 (15p) was advanced as a clinical candidate. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.08.048

文献信息

• [EN] 1,1,1-TRIFLUORO-3-HYDROXYPROPAN-2-YL CARBAMATE DERIVATIVES AND 1,1,1-TRIFLUORO-4-HYDROXYBUTAN-2-YL CARBAMATE DERIVATIVES AS MAGL INHIBITORS<br/>[FR] DÉRIVÉS DE CARBAMATE DE 1,1,1-TRIFLUORO-3-HYDROXYPROPAN-2-YLE ET DÉRIVÉS DE CARBAMATE DE 1,1,1-TRIFLUORO-4-HYDROXYBUTAN-2-YLE COMME INHIBITEURS DE MAGL
  申请人：PFIZER

  公开号：WO2017021805A1

  公开（公告）日：2017-02-09

  The present invention provides, in part, compounds of Formula I and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, traumatic brain injury, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.

  本发明部分提供了Formula I的化合物及其药用盐；制备这些化合物的方法；制备中使用的中间体；含有这些化合物或盐的组合物，以及它们用于治疗MAGL介导的疾病和紊乱的用途，包括但不限于疼痛、炎症性紊乱、创伤性脑损伤、抑郁症、焦虑症、阿尔茨海默病、代谢紊乱、中风或癌症。
• HETEROCYCLIC SPIRO COMPOUNDS AS MAGL INHIBITORS
  申请人：PFIZER INC.

  公开号：US20180208608A1

  公开（公告）日：2018-07-26

  The present invention provides, in part, heterocyclic spiro compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.

  本发明部分提供具有下式I的杂环螺化合物： 以及它们的药用盐；其制备过程；用于其制备的中间体；以及包含这些化合物或盐的药物组合物，以及它们用于治疗MAGL介导的疾病和障碍，例如疼痛、炎症性障碍、抑郁症、焦虑症、阿尔茨海默病、代谢障碍、中风或癌症的使用。
• 1,1,1-TRIFLUORO-3-HYDROXYPROPAN-2-YL CARBAMATE DERIVATIVES AND 1,1,1-TRIFLUORO-4-HYDROXYBUTAN-2-YL CARBAMATE DERIVATIVES AS MAGL INHIBITORS
  申请人：PFIZER INC.

  公开号：US20170029390A1

  公开（公告）日：2017-02-02

  The present invention provides, in part, compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, traumatic brain injury, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.

  本发明提供了部分I式化合物及其药学上可接受的盐；制备所用的中间体；以及含有这种化合物或盐的组合物，以及它们用于治疗MAGL介导的疾病和障碍，包括但不限于疼痛，炎症性疾病，创伤性脑损伤，抑郁症，焦虑症，阿尔茨海默病，代谢紊乱，中风或癌症。
• 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives and 1,1,1-trifluoro-4-hydroxybutan-2-yl carbamate derivatives as MAGL inhibitors
  申请人：PFIZER INC.

  公开号：US10428034B2

  公开（公告）日：2019-10-01

  The present invention provides, in part, compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, traumatic brain injury, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.

  本发明部分提供了式 I 的化合物： 及其药学上可接受的盐；制备过程；制备过程中使用的中间体；以及含有此类化合物或盐的组合物，以及它们在治疗 MAGL 介导的疾病和失调方面的用途，这些疾病和失调包括疼痛、炎症性失调、创伤性脑损伤、抑郁、焦虑、阿尔茨海默病、代谢性失调、中风或癌症等。
• Heterocyclic spiro compounds as MAGL inhibitors
  申请人：Pfizer Inc.

  公开号：US10858373B2

  公开（公告）日：2020-12-08

  The present invention provides, in part, heterocyclic spiro compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating MAGL-mediated diseases and disorders including, e.g., pain, an inflammatory disorder, depression, anxiety, Alzheimer's disease, a metabolic disorder, stroke, or cancer.

  本发明部分提供了式 I 的杂环螺化合物： 及其药学上可接受的盐；制备过程；制备过程中使用的中间体；含有此类化合物或盐的组合物，以及它们在治疗 MAGL 介导的疾病和失调（包括疼痛、炎症性失调、抑郁、焦虑、阿尔茨海默病、代谢性失调、中风或癌症等）方面的用途。