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2-甲基-6-[(3-甲氧基苯基)乙炔基]吡啶盐酸盐 | 823198-78-3

中文名称
2-甲基-6-[(3-甲氧基苯基)乙炔基]吡啶盐酸盐
中文别名
2-甲基-6-(苯乙炔基)吡啶,盐酸
英文名称
2-Methyl-6-[(3-methoxyphenyl)ethynyl]pyridine Hydrochloride
英文别名
2-[2-(3-methoxyphenyl)ethynyl]-6-methylpyridine;hydrochloride
2-甲基-6-[(3-甲氧基苯基)乙炔基]吡啶盐酸盐化学式
CAS
823198-78-3
化学式
C15H14ClNO
mdl
——
分子量
259.73
InChiKey
BWGVEMBFNIKUJU-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

  • 熔点:
    170-172°C
  • 溶解度:
    少许溶于甲醇

计算性质

  • 辛醇/水分配系数(LogP):
    3.22
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    22.1
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

文献信息

  • Pyrazolopyrimidines, a process for their preparation and their use as medicine
    申请人:Danysz Wojciech
    公开号:US20080032998A1
    公开(公告)日:2008-02-07
    Substituted pyrazolopyrimidine derivatives of formula (I) wherein R 1 represents chloro or bromo; R 2 , R 3 , R 4 , R 5 , R 6 and R 7 independently represent e.g. hydrogen or C 1-6 -alkyl; R 8 represents a radical R 9 or a radical R 10 , whereby one of the two radicals R 8 represents R 9 and the other radical R 8 represents Ret; R 9 represents e.g. a phenyl or thiophene group, and R 10 represents e.g. hydrogen or methyl; are potent mGluR5 modulators and are useful for the prevention of acute and chronic neurological disorders.
    取代吡唑并嘧啶衍生物的公式(I) 其中 R1代表氯或溴; R2、R3、R4、R5、R6和R7独立代表例如氢或C1-6-烷基; R8代表R9的基团或R10的基团,其中两个R8基团之一代表R9,另一个R8基团代表Ret;R9代表例如苯基或噻吩基团,R10代表例如氢或甲基; 是有效的mGluR5调节剂,可用于预防急性和慢性神经障碍。
  • [EN] METABOTROPIC GLUTAMATE RECEPTOR MODULATORS<br/>[FR] MODULATEURS DES RÉCEPTEURS GLUTAMATERGIQUES MÉTABOTROPES
    申请人:MERZ PHARMA GMBH & CO KGAA
    公开号:WO2012085167A1
    公开(公告)日:2012-06-28
    The invention relates to heterocyclic derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are m GluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorders.
    这项发明涉及杂环衍生物及其药用可接受的盐。该发明还涉及一种制备这类化合物的方法。该发明的化合物是mGluR5调节剂,因此对于控制和预防急性和/或慢性神经系统疾病是有用的。
  • [EN] METABOTROPIC GLUTAMATE RECEPTOR MODULATORS<br/>[FR] MODULATEURS DE RÉCEPTEUR DE GLUTAMATE MÉTABOTROPIQUE
    申请人:MERZ PHARMA GMBH & CO KGAA
    公开号:WO2012152854A1
    公开(公告)日:2012-11-15
    The invention relates to heterocyclic derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are mGluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorders.
    该发明涉及杂环衍生物以及其药用可接受的盐。该发明还涉及制备这类化合物的方法。该发明的化合物是mGluR5调节剂,因此对于控制和预防急性和/或慢性神经系统疾病非常有用。
  • [EN] METABOTROPIC GLUTAMATE RECEPTOR MODULATORS<br/>[FR] MODULATEURS DES RÉCEPTEURS MÉTABOTROPES AU GLUTAMATE
    申请人:MERZ PHARMA GMBH & CO KGAA
    公开号:WO2012052451A1
    公开(公告)日:2012-04-26
    The invention relates to heterocyclic derivatives of formula (I) as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are mGluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorders wherein Y, W, R1, R2 and R3 are as defined in claim 1.
    该发明涉及公式(I)的杂环衍生物及其药学上可接受的盐。该发明还涉及制备这类化合物的方法。该发明的化合物是mGluR5调节剂,因此对于控制和预防急性和/或慢性神经系统疾病是有用的,其中Y、W、R1、R2和R3如权利要求1中所定义。
  • Substituted pyrazolopyrimidines, a process for their preparation and their use as medicine
    申请人:Danysz Wojciech
    公开号:US20080039458A1
    公开(公告)日:2008-02-14
    Substituted pyrazolopyrimidine derivatives of formula (I) wherein Y 1 , Y 2 , Y 3 , Y 4 represent N or C—, whereby at least two of the groups Y 1 to Y 4 represent a carbon atom, R 1 represents chloro or bromo, R 2 to R 7 represent e.g. hydrogen, methyl or ethyl; and R 10 and R 11 independently represent e.g. hydrogen or C 1 -C 6 alkyl, are potent mGluR5 modulators and are useful for the prevention of acute and chronic neurological disorders.
    式(I)中的取代嘧唑嘧啶衍生物,其中Y1、Y2、Y3、Y4代表N或C—,其中至少两个Y1到Y4代表碳原子,R1代表氯或溴,R2到R7代表氢、甲基或乙基等,而R10和R11独立地代表氢或C1-C6烷基。这些衍生物是有效的mGluR5调节剂,并可用于预防急性和慢性神经系统疾病。
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