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6-甲氧基-2-甲基咪唑并[1,2-b]吡嗪 | 17240-34-5

中文名称
6-甲氧基-2-甲基咪唑并[1,2-b]吡嗪
中文别名
——
英文名称
6-Methoxy-2-methyl-imidazo<1.2-b>pyridazin
英文别名
6-methoxy-2-methyl-imidazo[1,2-b]pyridazine;6-Methoxy-2-methylimidazo[1,2-b]pyridazine
6-甲氧基-2-甲基咪唑并[1,2-b]吡嗪化学式
CAS
17240-34-5
化学式
C8H9N3O
mdl
——
分子量
163.179
InChiKey
FPZJUQYUVJQBLO-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

  • 密度:
    1.26±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    39.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933990090

SDS

SDS:1522a0db4a3bbaabecd4c1e487ac8bd3
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反应信息

  • 作为反应物:
    描述:
    6-甲氧基-2-甲基咪唑并[1,2-b]吡嗪2-重氮丙烷 以39%的产率得到6-methoxy-2,9,9-trimethyl-9H-imidazo<1,2-b>pyrazolo<4,3-d>pyridazine
    参考文献:
    名称:
    Stanovnik, Branko; Furlan, Borut; Kupper, Marko, Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 393 - 398
    摘要:
    DOI:
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文献信息

  • SUBSTITUTED 4-PHENYLPIPERIDINES, THEIR PREPARATION AND USE
    申请人:PETRUKHIN Konstantin
    公开号:US20150315197A1
    公开(公告)日:2015-11-05
    The present invention provides a compound having the structure: wherein R 1 , R 2 , R 3 , R 4 , and R 5 are each independently H, halogen, CF 3 or C 1 -C 4 alkyl, wherein two or more of R 1 , R 2 , R 3 , R 4 , or R 5 are other than H; R 6 is H, OH, or halogen; and B is a substituted or unsubstituted heterobicycle, wherein when R 1 is CF 3 , R 2 is H, R 3 is F, R 4 is H, and R 5 is H, or R 1 is H, R 2 is CF 3 , R 3 is H, R 4 is CF 3 , and R 5 is H, or R 1 is Cl, R 2 is H, R 3 is H, R 4 is F, and R 5 is H, or R 1 is CF 3 , R 2 is H, R 3 is F, R 4 is H, and R 5 is H, or R 1 is CF 3 , R 2 is F, R 3 is H, R 4 is H, and R 5 is H, or R 1 is Cl, R 2 is F, R 3 is H, R 4 is H, and R 5 is H, then B is other than or a pharmaceutically acceptable salt thereof.
    本发明提供了一种具有以下结构的化合物:其中R1、R2、R3、R4和R5各自独立地为H、卤素、CF3或C1-C4烷基,其中R1、R2、R3、R4或R5中的两个或更多个不是H;R6为H、OH或卤素;B为取代或未取代的杂环,其中当R1为CF3、R2为H、R3为F、R4为H和R5为H,或者R1为H、R2为CF3、R3为H、R4为CF3和R5为H,或者R1为Cl、R2为H、R3为H、R4为F和R5为H,或者R1为CF3、R2为H、R3为F、R4为H和R5为H,或者R1为CF3、R2为F、R3为H、R4为H和R5为H,或者R1为Cl、R2为F、R3为H、R4为H和R5为H时,则B不是或其药学上可接受的盐。
  • OCTAHYDROCYCLOPENTAPYRROLES, THEIR PREPARATION AND USE
    申请人:PETRUKHIN Konstantin
    公开号:US20160024007A1
    公开(公告)日:2016-01-28
    The present invention provides Octahydrocyclopentapyrrole compounds having the structure: (structurally represented) wherein psi is absent or present, and when present is a bond; R1, R2, R3, R4, and R5 are each independently H, halogen, CF, or C1-C4 alkyl; R6 is absent or present, and when present is H, OH, or halogen; A is absent or present, and when present is C(O) or C(O)NH; B is substituted or unsubstituted monocycle, bicycle, heteromonocycle, heterobicycle, benzyl, CO2H or (C1-C4 alkyl)-CO2H, wherein when B is CO2H, then A is present and is C(O); and when psi is present, then R6 is absent and when psi is absent, then R6 is present, or a pharmaceutically acceptable salt thereof, for treatment of diseases characterized by excessive lipofuscin accumulation in the retina.
    本发明提供了八氢环戊吡咯化合物,其结构如下:(结构式表示),其中psi不存在或存在,当存在时为键;R1、R2、R3、R4和R5各自独立地为H、卤素、CF或C1-C4烷基;R6不存在或存在,当存在时为H、OH或卤素;A不存在或存在,当存在时为C(O)或C(O)NH;B为取代或未取代的单环、双环、杂单环、杂双环、苄基、CO2H或(C1-C4烷基)-CO2H,其中当B为CO2H时,A存在且为C(O);当psi存在时,R6不存在,当psi不存在时,R6存在,或其药学上可接受的盐,用于治疗以视网膜过多脂褐质沉积为特征的疾病。
  • OCTAHYDROPYRROLOPYRROLES THEIR PREPARATION AND USE
    申请人:PETRUKHIN Konstantin
    公开号:US20160046632A1
    公开(公告)日:2016-02-18
    The present invention provides compounds comprising variously substituted octahydropyrrolopyrroles, their synthesis, methods of making, methods of using, compositions and formulations thereof.
    本发明提供了包含各种取代的八氢吡咯吡咯化合物,它们的合成方法,制备方法,使用方法,以及它们的组成和配方。
  • N-ALKYL-2-PHENOXYETHANAMINES, THEIR PREPARATION AND USE
    申请人:PETRUKHIN Konstantin
    公开号:US20160046649A1
    公开(公告)日:2016-02-18
    The present invention provides a compound having the structure: (structurally represented) wherein R1, R2, R3, R4, and R5 are each independently H, halogen, CF3 or C1-C4 alkyl; R6 is alkyl; A is absent or present, and when present is —C(O)— or —C(O)NH—; B is substituted or unsubstituted monocycle, bicycle, heteromonocycle, heterobicycle, benzyl, CO2H or (C1-C4 alkyl)-CO2H, wherein when B is CO2H, then A is present and is —C(O)—, or a pharmaceutically acceptable salt thereof.
    本发明提供了一种具有以下结构的化合物:(结构表示)其中R1、R2、R3、R4和R5各自独立地为H、卤素、CF3或C1-C4烷基;R6为烷基;A不存在或存在,当存在时为—C(O)—或—C(O)NH—;B为取代或未取代的单环、双环、杂单环、杂双环、苄基、CO2H或(C1-C4烷基)-CO2H,其中当B为CO2H时,A存在且为—C(O)—,或其药学上可接受的盐。
  • STANOVNIK, BRANKO;FURLAN, BORUT;KUPPER, MARKO;MALCZ, LIDIJA;STIMAC, ANTON+, J. HETEROCYCL. CHEM., 25,(1988) N 2, 393-398
    作者:STANOVNIK, BRANKO、FURLAN, BORUT、KUPPER, MARKO、MALCZ, LIDIJA、STIMAC, ANTON+
    DOI:——
    日期:——
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