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3-Chloro-5-(1,3-thiazol-2-ylethynyl)pyridine | 329202-23-5

中文名称
——
中文别名
——
英文名称
3-Chloro-5-(1,3-thiazol-2-ylethynyl)pyridine
英文别名
2-[2-(5-chloropyridin-3-yl)ethynyl]-1,3-thiazole
3-Chloro-5-(1,3-thiazol-2-ylethynyl)pyridine化学式
CAS
329202-23-5
化学式
C10H5ClN2S
mdl
——
分子量
220.682
InChiKey
GSLNKTDEEIHHTN-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):
    2.6
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-溴噻唑3-氯-5-乙炔基吡啶 在 PdCl2(PPh3)2 CuI 、 三乙胺 作用下, 以 乙二醇二甲醚乙酸乙酯 为溶剂, 以23%的产率得到3-Chloro-5-(1,3-thiazol-2-ylethynyl)pyridine
    参考文献:
    名称:
    Pyridazine, pyrimidine and pyrazine ethyne compounds
    摘要:
    根据本发明,提供了一类新颖的杂环化合物。该发明的化合物包含一个取代或未取代的六元杂环环,其中至少包含两个氮原子。该环另外包含四个碳原子。杂环环至少有一个取代基位于邻近环氮原子的环位置。该环的强制性取代基包括一个通过碳-碳三键与杂环环相连的基团(B)。强制性取代基位于环氮原子的邻近位置。发明的化合物能够具有各种用途。例如,杂环化合物可以通过作为神经系统受体的激动剂和拮抗剂来调节生理过程。发明的化合物也可以作为杀虫剂和杀菌剂。含有发明化合物的药物组合物也具有广泛的用途。
    公开号:
    US20050245542A1
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文献信息

  • Imidazolyl and pyrazolyl ethyne compounds
    申请人:Cosford D. Nicholas
    公开号:US20050085523A1
    公开(公告)日:2005-04-21
    In accordance with the present invention, there is provided a novel class of heterocyclic compounds. Compounds of the invention contain a substituted, unsaturated five, six or seven membered heterocyclic ring that includes at least one nitrogen atom and at least one carbon atom. The ring additionally includes three, four or five atoms independently selected from carbon, nitrogen, sulfur and oxygen atoms. The heterocyclic ring has at least one substituent located at a ring position adjacent to a ring nitrogen atom. This mandatory substituent of the ring includes a moiety (B), linked to the heterocyclic ring via a carbon-carbon double bond, a carbon-carbon triple bond or an azo group. The mandatory substituent is positioned adjacent to the ring nitrogen atom. Invention compounds are capable of a wide variety of uses. For example heterocyclic compounds can act to modulate physiological processes by functioning as agonists and antagonists of receptors in the nervous system. Invention compounds may also act as insecticides, and as fungicides. Pharmaceutical compositions containing invention compounds also have wide utility.
    根据本发明,提供了一类新型的杂环化合物。该发明的化合物包含一个取代的、不饱和的五、六或七元杂环环,其中至少包含一个氮原子和至少一个碳原子。该环另外包括三、四或五个独立选择的碳、氮、硫和氧原子。杂环环在至少一个邻近环氮原子的环位置上具有至少一个取代基。该环的强制性取代基包括一个通过碳-碳双键、碳-碳三键或偶氮基与杂环环相连的基团(B)。强制性取代基位于环氮原子的邻近位置。本发明的化合物能够具有各种用途。例如,杂环化合物可以通过作为神经系统受体的激动剂和拮抗剂来调节生理过程。本发明的化合物也可以作为杀虫剂和杀菌剂。含有本发明化合物的药物组合物也具有广泛的用途。
  • Thiazolyl(pyridyl)ethyne compounds
    申请人:Merck & Co., Inc.
    公开号:US06774138B2
    公开(公告)日:2004-08-10
    In accordance with the present invention, there is provided a novel class of heterocyclic compounds. Compounds of the invention contain a substituted, unsaturated five, six or seven membered heterocyclic ring that includes at least one nitrogen atom and at least one carbon atom. The ring additionally includes three, four or five atoms independently selected from carbon, nitrogen, sulfur and oxygen atoms. The heterocyclic ring has at least one substituent located at a ring position adjacent to a ring nitrogen atom. This mandatory substituent of the ring includes a moiety (B), linked to the heterocyclic ring via a carbon-carbon double bond, a carbon-carbon triple bond or an azo group. The mandatory substituent is positioned adjacent to the ring nitrogen atom. Invention compounds are capable of a wide variety of uses. For example heterocyclic compounds can act to modulate physiological processes by functioning as agonists and antagonists of receptors in the nervous system. Invention compounds may also act as insecticides, and as fungicides. Pharmaceutical compositions containing invention compounds also have wide utility.
    根据本发明,提供了一类新型的杂环化合物。该发明的化合物包含一个取代的、不饱和的五、六或七元杂环环,其中至少包含一个氮原子和至少一个碳原子。该环另外包括三、四或五个独立选择的碳、氮、硫和氧原子。杂环环至少有一个取代基位于邻近环氮原子的环位置。该环的强制性取代基包括一个通过碳-碳双键、碳-碳三键或偶氮基与杂环环连接的基团(B)。强制性取代基位于环氮原子的邻近位置。发明的化合物能够具有各种用途。例如,杂环化合物可以通过作为神经系统受体的激动剂和拮抗剂来调节生理过程。发明的化合物也可以作为杀虫剂和杀菌剂。含有发明化合物的药物组合物也具有广泛的用途。
  • [EN] HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF<br/>[FR] COMPOSES HETEROCYCLIQUES ET PROCEDES D'UTILISATION DE CEUX-CI
    申请人:MERCK & CO INC
    公开号:WO2001016121A1
    公开(公告)日:2001-03-08
    In accordance with the present invention, there are provided novel class of heterocyclic compounds and methods of use thereof. Compounds of the invention contain a substituted, unsaturated five, six or seven membered heterocyclic ring that includes at least one nitrogen atom and at least one carbon atom. At a ring position adjacent to a ring nitrogen atom, the heterocyclic ring has at least one substituent which includes a moiety, linked to the heterocyclic ring via an alkylene moiety, an alkynylene moiety or an azo group. Invention compounds are capable of a wide variety of uses including modulating physiological processes by functioning as agonists and antagonists of receptors in the nervous system, as insecticides, and as fungicides. The invention further provides methods of modulating the activity of excitatory amino acid receptors using a specifically defined class of heterocyclic compounds including the novel compounds referred to above. In one embodiment, there are provided methods of modulating metabotropic glutamate receptors. The present invention also discloses methods of treating disease using heterocyclic compounds. The invention further discloses methods of preventing disease conditions related to diseases of the pulmonary system, diseases of the nervous system, diseases of the cardiovascular system, diseases of the gastrointestinal system, diseases of the endocrine system, diseases of the exocrine system, diseases of the skin, cancer and diseases of the ophthalmic system. The invention also discloses pharmaceutically acceptable salt forms of the above-described heterocyclic compounds.
    根据本发明,提供了一类新型的杂环化合物及其使用方法。该发明的化合物包含一个取代的、不饱和的五、六或七元杂环环,其中至少包含一个氮原子和至少一个碳原子。在靠近环氮原子的环位置上,杂环环有至少一个取代基,包括一个官能团,通过烷基官能团、炔基官能团或偶氮基团连接到杂环环上。发明的化合物能够广泛应用,包括通过作为神经系统受体的激动剂和拮抗剂来调节生理过程,作为杀虫剂和杀菌剂。本发明还提供了使用特定定义的杂环化合物类来调节兴奋性氨基酸受体活性的方法,包括上述新型化合物。在一种实施例中,提供了调节代谢性谷氨酸受体的方法。本发明还揭示了使用杂环化合物治疗疾病的方法。本发明还揭示了预防与肺系统疾病、神经系统疾病、心血管系统疾病、胃肠系统疾病、内分泌系统疾病、外分泌系统疾病、皮肤疾病、癌症和眼科系统疾病相关的疾病状态的方法。本发明还揭示了上述杂环化合物的药物可接受的盐形式。
  • HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF
    申请人:Merck & Co., Inc.
    公开号:EP1214303A1
    公开(公告)日:2002-06-19
  • US6774138B2
    申请人:——
    公开号:US6774138B2
    公开(公告)日:2004-08-10
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