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2-(2,2,2-trifluoroethoxy)pyrimidin-4-amine | 1431654-73-7

中文名称
——
中文别名
——
英文名称
2-(2,2,2-trifluoroethoxy)pyrimidin-4-amine
英文别名
2-(2,2,2-Trifluoroethoxy)pyrimidin-4-amine
2-(2,2,2-trifluoroethoxy)pyrimidin-4-amine化学式
CAS
1431654-73-7
化学式
C6H6F3N3O
mdl
——
分子量
193.128
InChiKey
RTTWPZSZAYCRKF-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    61
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] 2-OXA-5-AZABICYCLO[2.2.1]HEPTAN-3-YL DERIVATIVES<br/>[FR] DÉRIVÉS DU 2-OXA -5-AZABICYCLO [2.2.1] HEPTAN -3-YL
    申请人:HOFFMANN LA ROCHE
    公开号:WO2016016292A1
    公开(公告)日:2016-02-04
    The present invention relates to compounds of formula (I), wherein L is a bond, -C(O)NH-, -NHC(O)-, -CH2NHC(O)-, CH2C(O)NH-, -CH2NH-, -NH- or -NHC(O)NH-; R1 is hydrogen, lower alkyl, halogen, lower alkoxy-alkyl, lower alkoxy substituted by halogen, lower alkyl substituted by halogen or is phenyl or heteroaryl selected from the group consisting of pyridinyl, pyrimidinyl, pyrazinyl or pyrazolyl, and wherein phenyl and heteroaryl are optionally substituted by one, two or three substituents selected from the group consisting of halogen, lower alkyl, lower alkoxy, lower alkyl substituted by halogen, lower alkoxy substituted by halogen, cycloalkyl or O-CH2-cycloalkyl; or to a pharmaceutically suitable acid addition salt thereof, to all racemic mixtures, all their corresponding enantiomers and/or optical isomers, which may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders, schizophrenia, neurological diseases, Parkinson's disease, neurodegenerative disorders, Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse, metabolic disorders, eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及以下化合物的公式(I),其中L是键,-C(O)NH-,-NHC(O)-,- NHC(O)-, C(O)NH-,- NH-,-NH-或-NHC(O)NH-;R1是氢,较低的烷基,卤素,较低的烷氧基烷基,受卤素取代的较低的烷氧基,受卤素取代的较低的烷基或为苯基或杂环芳基,所述苯基和杂环芳基从吡啶基、嘧啶基、吡啉基或吡唑基中选择,其中苯基和杂环芳基可以选择地被来自卤素、较低的烷基、较低的烷氧基、受卤素取代的较低的烷基、受卤素取代的较低的烷氧基、环烷基或O-CH2-环烷基的一个、两个或三个取代基取代;或其药用合适的酸盐,所有的消旋混合物,它们所有对应的对映体和/或光学异构体,可用于治疗抑郁症、焦虑症、躁郁症、注意力缺陷多动障碍(ADHD)、与压力有关的障碍、精神病性障碍、精神分裂症、神经疾病、帕森病、神经退行性疾病、阿尔茨海默病、癫痫、偏头痛、高血压、物质滥用、代谢障碍、进食障碍、糖尿病、糖尿病并发症、肥胖症、血脂异常、能量消耗和吸收障碍、体温稳态障碍、睡眠和昼夜节律障碍、心血管障碍。
  • Aryl, heteroaryl, and heterocyclic compounds for treatment of medical disorders
    申请人:Achillion Pharmaceuticals, Inc.
    公开号:US10011612B2
    公开(公告)日:2018-07-03
    Compounds, methods of use, and processes for making inhibitors of complement Factor D comprising Formula I, or a pharmaceutically acceptable salt or composition thereof wherein R12 or R13 on the A group is an aryl, heteroaryl or heterocycle (R32) are provided. The inhibitors of Factor D described herein reduce the excessive activation of complement.
    提供了包含式 I 或其药学上可接受的盐或组合物的补体因子 D 抑制剂的化合物、使用方法和制造工艺,其中 A 基上的 R12 或 R13 是芳基、杂芳基或杂环 (R32)。本文所述的因子 D 抑制剂可减少补体的过度活化。
  • [EN] SUBSTITUTED BICYCLIC AZA-HETEROCYCLES AND ANALOGUES AS SIRTUIN MODULATORS<br/>[FR] AZAHÉTÉROCYCLES BICYCLIQUES SUBSTITUÉS ET ANALOGUES COMME MODULATEURS DE LA SIRTUINE
    申请人:GLAXOSMITHKLINE LLC
    公开号:WO2013059587A9
    公开(公告)日:2014-10-23
  • SUBSTITUTED BICYCLIC AZA-HETEROCYCLES AND ANALOGUES AS SIRTUIN MODULATORS
    申请人:GlaxoSmithKline LLC
    公开号:EP2768509B1
    公开(公告)日:2017-03-22
  • 2-OXA-5-AZABICYCLO[2.2.1]HEPTAN-3-YL DERIVATIVES
    申请人:F. Hoffmann-La Roche AG
    公开号:EP3174886A1
    公开(公告)日:2017-06-07
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