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2-(4-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-propanoic acid ethyl ester | 118695-91-3

中文名称
——
中文别名
——
英文名称
2-(4-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-propanoic acid ethyl ester
英文别名
Ethyl 3-[2-(4-chlorophenyl)imidazo[4,5-b]pyridin-3-yl]propanoate
2-(4-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-propanoic acid ethyl ester化学式
CAS
118695-91-3
化学式
C17H16ClN3O2
mdl
——
分子量
329.786
InChiKey
AFVVTZIPTGQGSC-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):
    3.1
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    57
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    beta-丙氨酸乙酯盐酸盐 在 palladium on activated charcoal 氢气三乙胺 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 2.88h, 生成 2-(4-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-propanoic acid ethyl ester
    参考文献:
    名称:
    2-Phenyl-3H-imidazo[4,5-b]pyridine-3-acetamides as nonbenzodiazepine anticonvulsants and anxiolytics
    摘要:
    A series of 2-phenyl-3H-imidazo[4,5-b]pyridine-3-acetamides were designed and synthesized as non-benzodiazepine anxiolytics based on a molecular disconnection of a typical 1,4-benzodiazepine (BZD). A number of these compounds showed submicromolar potency in a [H-3]benzodiazepine binding assay in vitro and good potency in protecting rodents against pentylenetetrazole-induced seizures. Compound 84 appears to be a selective anticonvulsant (pentylenetetrazole) agent when tested against a profile of chemically and electrically induced seizures in mice. In addition, compound 148 appears to be a selective anxiolytic/hypnotic agent on the basis of biochemical and pharmacological characterization. It appears to be a full BZD agonist as assessed by GABA shift ratio and to be effective in punishment and nonpunishment animal models of anxiety. In addition, it shows a lower side-effect profile than diazepam as assessed by rotorod neurotoxicity and potentiation of ethanol-induced sleep time in mice. The chemistry and structure-activity relationships of this series is discussed.
    DOI:
    10.1021/jm00114a007
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文献信息

  • Fused imidazoheterocyclic compounds and pharmaceutical compositions
    申请人:A. H. Robins Company, Inc.
    公开号:US04772600A1
    公开(公告)日:1988-09-20
    Imidazoheterocyclic compounds having the formula: ##STR1## wherein the A ring is pyridine in any of its four positions; B is carbonyl, thioxomethyl or hydroxymethylene; Z is hydrogen, halogen, loweralkyl, hydroxy, loweralkoxy, diloweralkylamino or nitro; Ar is phenyl, pyrido, thienyl or furanyl; and W forms a wide combination of groups with B, including acids, esters, alcohols, amides and ketones. The compounds have CNS activity in a method for treating a living animal body as muscle relaxants, anticonvulsants and antianxiety agents.
    咪唑杂环化合物化学式为:##STR1## 其中A环是吡啶的四个位置中的任意一个;B是羰基、代甲基或羟甲基;Z是氢、卤素、较低烷基、羟基、较低烷氧基、二较低烷基基或硝基;Ar是苯基、吡啶基、噻吩基或呋喃基;W与B形成多种组合,包括酸、酯、醇、酰胺和酮。这些化合物在治疗活体动物身体的方法中具有中枢神经系统活性,可用作肌肉松弛剂、抗惊厥剂和抗焦虑剂。
  • Fused imidazoheterocyclic compounds
    申请人:A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation)
    公开号:EP0255217A1
    公开(公告)日:1988-02-03
    Imidazoheterocyclic compounds having the formula: wherein A is a pyridine ring in any of its four positions; B is carbonyl, thioxomethyl or hydroxymethylene; Z is hydrogen, halogen, loweralkyl, hydroxy, loweralkoxy, diloweralkylamino or nitro; Ar is phenyl, pyrido, thienyl or furanyl; and W forms a wide combination of groups with B, including acids, esters, alcohols, amides and ketones. The compounds have CNS activity and find use as muscle relaxants, anticonvulsants and antianxiety agents.
    具有以下式子的咪唑杂环化合物:其中 A 是处于四个位置中任何一个位置的吡啶环;B 是羰基、氧甲基或羟甲基;Z 是氢、卤素、低级烷基、羟基、低级烷氧基、稀低级烷基基或硝基;Ar 是苯基、吡啶基、噻吩基或呋喃基;W 与 B 形成多种基团组合,包括酸、酯、醇、酰胺和酮。 这些化合物具有中枢神经系统活性,可用作肌肉松弛剂、抗惊厥剂和抗焦虑剂。
  • TOMCZUK, BRUCE E.;SUTHERLAND, DEBORAH S.
    作者:TOMCZUK, BRUCE E.、SUTHERLAND, DEBORAH S.
    DOI:——
    日期:——
  • US4772600A
    申请人:——
    公开号:US4772600A
    公开(公告)日:1988-09-20
  • US4824951A
    申请人:——
    公开号:US4824951A
    公开(公告)日:1989-04-25
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