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dimethyl(3-(pyridin-3-yloxy)propyl)amine | 310880-30-9

中文名称
——
中文别名
——
英文名称
dimethyl(3-(pyridin-3-yloxy)propyl)amine
英文别名
dimethyl(3-(3-pyridyloxy)propyl)amine;N,N-dimethyl-3-pyridin-3-yloxypropan-1-amine
dimethyl(3-(pyridin-3-yloxy)propyl)amine化学式
CAS
310880-30-9
化学式
C10H16N2O
mdl
——
分子量
180.25
InChiKey
FLWDJFMSFAQNEJ-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):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    25.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    dimethyl(3-(pyridin-3-yloxy)propyl)amine碘甲烷 生成 Trimethyl-[3-(pyridin-3-yloxy)-propyl]-ammonium; iodide
    参考文献:
    名称:
    Quaternary ammonium 3-(aminoethoxy)pyridines as antinociceptive agents
    摘要:
    Quaternization via N-methylation of the terminal amines of a series of 3-(dialkylaminoethoxy)pyridines resulted in analogues that displayed up to 50-60-fold enhanced affinity for nicotinic acetylcholinergic (nACh) receptors. Several of these compounds displayed antinociceptive properties in mice using the tail-flick assay and serve as possible leads for the development of novel analgesic agents. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00585-7
  • 作为产物:
    描述:
    3-chloro-1-(pyridin-3-yloxy)propane二甲胺 、 sodium chloride 作用下, 以 甲醇 为溶剂, 以1.95 g (92.9%)的产率得到dimethyl(3-(pyridin-3-yloxy)propyl)amine
    参考文献:
    名称:
    Pharmaceutical compositions and methods for use
    摘要:
    对于容易受到或患有中枢神经系统疾病等疾病和疾病的患者,可以通过给予需要的患者芳基氧烷胺来进行治疗,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-(甲基氨基)-丙氧基)苯基)胺,甲基(3-三环[7.3.1.0<5,13>]十三烷-2-氧基丙基)胺,(3-苯并[3,4-d]1,3-二噁烷-5-氧基丙基)甲基胺,3-(4-哌啶氧基)吡啶和3-((3S)-3-吡咯烷氧基)吡啶。
    公开号:
    US06441006B2
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文献信息

  • 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-(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--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-(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-丙氧基)-3-硝基苯,(3-(3-基苯氧基)丙基)甲基胺,二甲基(3-(3-(甲基)-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
  • Substituted Fused Heteroaromatic Tricyclic Compounds as Kinase Inhibitors and The Use Thereof
    申请人:IMPACT THERAPEUTICS, INC.
    公开号:US20210128535A1
    公开(公告)日:2021-05-06
    The disclosure relates to substituted fused heteroaromatic tricyclic compounds and the use thereof. Specifically, the disclosure provides compounds of the following Formula I: or a pharmaceutically acceptable salt or prodrug thereof, wherein A 1 -A 3 , B 1 -B 3 , D 1 -D 4 and R 1 -R 2 are defined herein. Compounds having Formula I are ATM kinase inhibitors. Therefore, compounds of the disclosure may be used to treat clinical conditions caused by DDR functional defects, such as cancer.
    本公开涉及替代的融合杂环三环化合物及其用途。具体而言,本公开提供以下式I的化合物:或其药学上可接受的盐或前药,其中A1-A3,B1-B3,D1-D4和R1-R2在此定义。具有式I的化合物为ATM激酶抑制剂。因此,本公开的化合物可用于治疗由DDR功能缺陷引起的临床病症,如癌症。
  • PYRIDO[3,4-d]PYRIMIDINE DERIVATIVE AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
    申请人:Teijin Pharma Limited
    公开号:EP3305785A1
    公开(公告)日:2018-04-11
    The purpose of the present invention is to provide a compound having an excellent CDK4/6 inhibiting activity. The present invention is a compound represented by general formula (I) or a pharmaceutically acceptable salt thereof.
    本发明的目的是提供一种具有优异 CDK4/6 抑制活性的化合物。本发明是通式(I)代表的化合物或其药学上可接受的盐。
  • 薬学的組成物およびその使用
    申请人:ターガセプト,インコーポレイテッド
    公开号:JP2003500393A
    公开(公告)日:2003-01-07
    \n (57)【要約】\n中枢神経系障害などの病態および障害に感受性であるかそれを罹患している患者を、ピリジルオキシルアルキルアミン、フェノキシアルキルアミン、ピリジルチオールアルキルアミン、およびフェニルチオアルキルアミンを含むアリールオキシアルキルアミンおよびアリールチオアルキルアミンの必要時の患者への投与によって治療する。\n
    和芳基代烷基胺的治疗方法是在必要时给病人用药。\n
  • ARYL SUBSTITUTED ALKYLAMINES CAPABLE OF ACTIVATING NICOTINIC CHOLINERGIC RECEPTORS
    申请人:Targacept, Inc.
    公开号:EP1185513A2
    公开(公告)日:2002-03-13
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