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3-(哌啶-4-氧基)吡啶 | 310881-48-2

中文名称
3-(哌啶-4-氧基)吡啶
中文别名
——
英文名称
3-(Piperidin-4-yloxy)pyridine
英文别名
3-piperidin-4-yloxypyridine
3-(哌啶-4-氧基)吡啶化学式
CAS
310881-48-2
化学式
C10H14N2O
mdl
MFCD08689439
分子量
178.23
InChiKey
URPWHVAXGCXZOR-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

物化性质

  • 沸点:
    301.8±32.0 °C(Predicted)
  • 密度:
    1.078±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    34.2
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2933990090

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    盐酸3-(哌啶-4-氧基)吡啶乙醇异丙醇 作用下, 以to afford 233 mg (63.7%) of an off-white solid, mp 152-155° C的产率得到3-(4-哌啶基氧基)哌啶二盐酸盐
    参考文献:
    名称:
    PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USE
    摘要:
    患有或易感染中枢神经系统疾病等疾病和疾病的患者,通过向需要此类治疗的患者施用芳氧基烷基胺和芳硫基烷基胺进行治疗,包括吡啶氧基烷基胺,苯氧基烷基胺,吡啶硫基烷基胺和苯硫基烷基胺。示例化合物包括(2-(5-溴(3-吡啶硫基))乙基)甲基胺,(2-(5-溴(3-吡啶硫基))异丙基)甲基胺,(2-(5-溴(3-吡啶硫基))丙基)甲基胺,(3-(5-溴(3-吡啶硫基))丙基)甲基胺,3-((3S)-3-吡咯烷氧基)吡啶,3-(4-哌啶氧基)吡啶,3-(1-甲基-4-哌啶氧基)吡啶,(3-苯并[3,4-d]1,3-二氧杂环戊基)甲基胺和甲基(3-三环七[7.3.1.0<5,13>]十三烷基氧基)丙基胺。
    公开号:
    US20010031771A1
  • 作为产物:
    描述:
    1,1-dimethylethyl 4-(3'-pyridinyloxy)-1-piperidinecarboxylate三氟乙酸氯仿potassium carbonate 、 crude product 、 silica gel 、 chloroform+acetone 作用下, 以 苯甲醚 为溶剂, 反应 0.5h, 以to give 260 mg (81.2%) of an off-white, viscous liquid的产率得到3-(哌啶-4-氧基)吡啶
    参考文献:
    名称:
    Pharmaceutical compositions and methods for use
    摘要:
    患有或易感染中枢神经系统疾病等疾病和疾病的患者,通过向需要此类治疗的患者施用芳氧基烷胺和芳硫基烷胺来治疗。这些化合物包括吡啶氧基烷胺、苯氧基烷胺、吡啶硫基烷胺和苯硫基烷胺。示例化合物包括(2-(5-溴(3-吡啶硫基))-乙基)甲基胺,(2-(5-溴(3-吡啶硫基))异丙基)甲基胺,(2-(5-溴(3-吡啶硫基))丙基)甲基胺,(3-(5-溴(3-吡啶硫基))-丙基)甲基胺,3-((3S)-3-吡咯烷氧基)吡啶,3-(4-哌啶氧基)吡啶,3-(1-甲基-4-哌啶氧基)吡啶,(3-苯并[3,4-d]1,3-二氧杂环戊基)甲基胺和甲基(3-三环[7.3.1.0<5,13>]十三烷-2-氧基丙基)胺。
    公开号:
    US06627648B1
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文献信息

  • SUBSTITUTED SULFONAMIDE COMPOUNDS
    申请人:OBERBOERSCH Stefan
    公开号:US20080153843A1
    公开(公告)日:2008-06-26
    Substituted sulfonamide derivatives, a process for their preparation, pharmaceutical compositions containing these compounds, and to the use of substituted sulfonamide derivatives in the treatment or inhibition of pain and/or various disorders or disease states.
    磺胺取代物,其制备方法,含有这些化合物的药物组合物,以及磺胺取代物在治疗或抑制疼痛和/或各种疾病或疾病状态中的用途。
  • [EN] LINEAR GLYCOSIDASE INHIBITORS<br/>[FR] INHIBITEURS LINÉAIRES DE LA GLYCOSIDASE
    申请人:ASCENEURON S A
    公开号:WO2019037860A1
    公开(公告)日:2019-02-28
    Compounds of formula (I) wherein A, R, W, Q, L, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.
    式(I)中A、R、W、Q、L、n和m的含义如权利要求所述,可用于治疗tau病和阿尔茨海默病。
  • [EN] BENZODIOXANES FOR INHIBITING LEUKOTRIENE PRODUCTION<br/>[FR] BENZODIOXANNES POUR INHIBER LA PRODUCTION DE LEUCOTRIÈNES
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2013134226A1
    公开(公告)日:2013-09-12
    The present invention relates to compounds of formula (I) wherein R1 to R3, A, X and n are as defined herein. The compounds of formula (I) are useful as inhibitors of leukotriene A4 hydrolase (LTA4H) and treating LTA4H related disorder. The present invention also relates to pharmaceutical compositions comprising the compounds of formula (I), methods of using these compounds in the treatment of various diseases and disorders, and processes for preparing these compounds.
    本发明涉及式(I)的化合物,其中R1至R3,A,X和n如本文所定义。式(I)的化合物可用作白三烯A4水解酶(LTA4H)的抑制剂,并用于治疗与LTA4H相关的疾病。本发明还涉及包含式(I)化合物的药物组合物,使用这些化合物治疗各种疾病和疾病的方法,以及制备这些化合物的方法。
  • BENZODIOXANE INHIBITORS OF LEUKOTRIENE PRODUCTION FOR COMBINATION THERAPY
    申请人:BYLOCK Lars Anders
    公开号:US20130236468A1
    公开(公告)日:2013-09-12
    The present invention relates to a combination comprising compounds of formula (I): wherein R 1 to R 3 , A, X and n are as defined herein, and an additional active agent. The present invention also relates to pharmaceutical compositions comprising these combinations, and methods of using these combinations to treat various diseases and disorders.
    本发明涉及一种组合物,包括式(I)的化合物: 其中R1至R3,A,X和n如本文所定义,并且另外包括一种活性剂。本发明还涉及包括这些组合物的药物组合物,以及使用这些组合物治疗各种疾病和疾病的方法。
  • PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USE
    申请人:——
    公开号:US20010014691A1
    公开(公告)日:2001-08-16
    Patients susceptible to or suffering from conditions and disorders, such as central nervous system disorders, are treated by administering to a patient in need thereof aryloxyalkylamines, including pyridyloxylalkylamines and phenoxyalkylamines. Exemplary compounds include dimethyl(2-(3-pyridyloxy)ethylamine, dimethyl(4-(3-pyridyloxy)butyl)amine, 2-(3-pyridyloxy)ethylamine, 4-(3-pyridyloxy)butylamine, methyl(3-(5-methoxy-3-pyridyloxy)propyl)amine, ethyl(3-(3-pyridyloxy)propyl)amine, methyl(2-(3-pyridyloxy)ethyl)amine, methyl(3-(6-methyl(3-pyridyloxy))propyl)amine, (3-(3-methoxyphenoxy)propyl)methylamine, (3-(5-chloro(3-pyridyloxy))-1-methylpropyl)methylamine, dimethyl(3-(3-pyridyloxy)propyl)amine, 3-(3-pyridyloxy)propylamine, methyl(4-(3-pyridyloxy)butyl)amine, 3-(5-chloro-3-pyridyloxy)propyl amine, methyl(3-(5-isopropoxy-3-pyridyloxy)propyl)amine, (3-(5-chloro(3-pyridyloxy))propyl) methylamine, methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine, methyl(3-(2-methyl(3-pyridyloxy))propyl)amine, (methylethyl)(3-(3-pyridyloxy)propyl)amine, benzyl(3-(3-pyridyloxy)propyl)amine, cyclopropyl(3-(3-pyridyloxy)-propyl)amine, methyl(1-methyl-3-(3-pyridyloxy)propyl)amine, methyl(3-(3-nitrophenoxy)propyl)amine, 1-(3-chloropropoxy)-3-nitrobenzene, (3-(3-aminophenoxy)propyl)methylamine,dimethyl (3-(3-(methylamino)-propoxy)phenyl)amine, methyl(3-tricyclo[7.3.1.0<5,13>]tridec-2-yloxypropyl)amine, (3-benzo[3,4-d]1,3-dioxolan-5-yloxypropyl)methylamine, 3-(4-piperidinyloxy)pyridine and 3-((3S)-3-pyrrolidinyloxy)pyridine.
    患有或易受中枢神经系统疾病等病症和紊乱的患者,通过向需要的患者施用芳基氧烷胺类化合物进行治疗,包括吡啶氧烷胺和苯氧烷胺。示例化合物包括二甲基(2-(3-吡啶氧基)乙基)胺,二甲基(4-(3-吡啶氧基)丁基)胺,2-(3-吡啶氧基)乙基胺,4-(3-吡啶氧基)丁基胺,甲基(3-(5-甲氧基-3-吡啶氧基)丙基)胺,乙基(3-(3-吡啶氧基)丙基)胺,甲基(2-(3-吡啶氧基)乙基)胺,甲基(3-(6-甲基(3-吡啶氧基))丙基)胺,(3-(3-甲氧基苯氧基)丙基)甲基胺,(3-(5-氯(3-吡啶氧基))-1-甲基丙基)甲基胺,二甲基(3-(3-吡啶氧基)丙基)胺,3-(3-吡啶氧基)丙基胺,甲基(4-(3-吡啶氧基)丁基)胺,3-(5-氯-3-吡啶氧基)丙基胺,甲基(3-(5-异丙氧基-3-吡啶氧基)丙基)胺,(3-(5-氯(3-吡啶氧基))丙基)甲基胺,甲基(3-(5-(苯甲氧基)(3-吡啶氧基))丙基)胺,甲基(3-(2-甲基(3-吡啶氧基))丙基)胺,(甲基乙基)(3-(3-吡啶氧基)丙基)胺,苄基(3-(3-吡啶氧基)丙基)胺,环丙基(3-(3-吡啶氧基)-丙基)胺,甲基(1-甲基-3-(3-吡啶氧基)丙基)胺,甲基(3-(3-硝基苯氧基)丙基)胺,1-(3-氯丙氧基)-3-硝基苯,(3-(3-氨基苯氧基)丙基)甲基胺,二甲基(3-(3-(甲氨基)-丙氧基)苯基)胺,甲基(3-三环七叁.壹.零<5,13>三十二氧基丙基)胺,(3-苯并三.四-壹,三-二氧杂环戊氧基丙基)甲基胺,3-(4-哌啶氧基)吡啶和3-((3S)-3-吡咯啶氧基)吡啶。
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