4-甲基-2-(2-吡嗪)-1,3-噻唑-5-羰酰氯 | 257876-11-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 中文名称: 4-甲基-2-(2-吡嗪)-1,3-噻唑-5-羰酰氯
• 中文别名: 4-甲基-2-(2-吡嗪基)-1,3-噻唑-5-羰酰氯
• 英文名称: 4-methyl-2-(2-pyrazinyl)-1,3-thiazole-5-carbonyl chloride
• 英文别名: 4-methyl-2-pyrazin-2-yl-1,3-thiazole-5-carbonyl chloride
• CAS: 257876-11-2
• 化学式: C₉H₆ClN₃OS
• mdl: MFCD02681953
• 分子量: 239.685
• InChiKey: AURNSWQWQVJINA-UHFFFAOYSA-N

物化性质

• 熔点：
  101 °C
• 沸点：
  410.8±55.0 °C(Predicted)
• 密度：
  1.439±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.111
• 拓扑面积：
  84
• 氢给体数：
  0
• 氢受体数：
  5

安全信息

• 危险品标志：
  Xi
• 危险类别码：
  R34

反应信息

• 作为反应物：
  描述：

  3-(3-ethoxy-4-methoxy-phenyl)-5,6-dihydro-4H-pyridazin 、 4-甲基-2-(2-吡嗪)-1,3-噻唑-5-羰酰氯 以gives the compound 1-[3-(3-ethoxy-4-methoxyphenyl)-5,6-dihydro-4H-pyridazin-1-yl]-1-(4-methyl-2-pyrazin-2-yl-thiazol-5-yl)methanone (484 mg, HPLC-MS m/e 438)的产率得到1-(3-(3-ethoxy-4-methoxy-phenyl)-5,6-dihydro-4H-pyridazin-1-yl)-1-(4-methyl-2-pyrazin-2-yl-thiazol-5-yl)-methanone
  参考文献：
  名称：

  Thiazole derivatives as phosphodiesterase iv inhibitors

  摘要：

  公式I中的噻唑衍生物，其中R1，R2，R3，V，W，X和B如权利要求1所定义，可作为磷酸二酯酶IV抑制剂，可用于治疗骨质疏松症，肿瘤，消瘦症，动脉粥样硬化，类风湿性关节炎，多发性硬化症，糖尿病，炎症过程，过敏，哮喘，自身免疫疾病，心肌病和艾滋病。

  公开号：

  US20050222160A1

文献信息

• [EN] INDOLE AMIDE DERIVATIVES AND RELATED COMPOUNDS FOR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES<br/>[FR] DÉRIVÉS D'INDOLAMIDE ET COMPOSÉS ASSOCIÉS DESTINÉS À ÊTRE UTILISÉS DANS LE TRAITEMENT DES MALADIES NEURODÉGÉNÉRATIVES
  申请人：UNIV LEUVEN KATH

  公开号：WO2010142801A1

  公开（公告）日：2010-12-16

  This invention provides novel compounds and the novel compounds for use as a medicine, more in particular for the prevention or treatment of neurodegenerative disorders, more specifically certain neurological disorders, such as disorders collectively known as tauopathies, and disorders characterised by cytotoxic α-synuclein amyloidogenesis. The present invention also relates to the use of said novel compounds for the manufacture of medicaments useful for treating such neurodegenerative disorders. The present invention further relates to pharmaceutical compositions including said novel compounds and to methods for the preparation of said novel compounds.

  本发明提供了新型化合物，以及这些新型化合物作为药物的使用，特别是用于预防或治疗神经退行性疾病，更具体地是一些神经系统疾病，例如统称为tauopathies的疾病，以及以细胞毒性α-突触核蛋白淀粉样蛋白生成为特征的疾病。本发明还涉及将所述新型化合物用于制造用于治疗此类神经退行性疾病的药物。本发明还涉及包括所述新型化合物的药物组合物，以及制备所述新型化合物的方法。
• PHENYLPROPIONIC ACID DERIVATIVE AND USE THEREOF
  申请人：MORITA Kohei

  公开号：US20100093819A1

  公开（公告）日：2010-04-15

  A compound represented by the following general formula (1) or a salt thereof, which has superior inhibitory activity against type 4 PLA 2 , and thus has prostaglandin and/or leucotriene production suppressing action [X represents a halogen atom, an alkyl group which may be substituted, or the like, Y represents hydrogen atom or an alkyl group which may be substituted, and Z represents hydrogen atom or an alkyl group which may be substituted].

  由以下一般式（1）表示的化合物或其盐，具有优越的抑制对4型PLA2的活性，因此具有前列腺素和/或白三烯产生抑制作用【X代表卤素原子、可能被取代的烷基或类似物，Y代表氢原子或可能被取代的烷基，Z代表氢原子或可能被取代的烷基】。
• [EN] ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS<br/>[FR] MODULATEURS ALLOSTERIQUES DE RECEPTEURS GLUTAMATE METABOTROPIQUES
  申请人：ADDEX PHARMACEUTICALS SA

  公开号：WO2005044797A1

  公开（公告）日：2005-05-19

  The present invention relates to new compounds of formula (I) wherein A, B, P, Q, W, Rl and R2 are defined in the description; invention compounds are useful in the prevention or treatment of central nervous system disorders as well as other disorders modulated by mGluR5 receptors.

  本发明涉及公式（I）的新化合物，其中A、B、P、Q、W、R1和R2在描述中有定义；发明的化合物可用于预防或治疗中枢神经系统疾病以及其他受mGluR5受体调节的疾病。
• PGD2 receptor antagonists for the treatment of inflammatory diseases
  申请人：Ghosh Shomir

  公开号：US20050256158A1

  公开（公告）日：2005-11-17

  Disclosed herein are compounds represented by Structural Formula (I) and (I-A): Also disclosed is the use of such compounds for inhibiting the G-protein coupled receptor referred to as chemoattractant receptor-homologous molecule expressed on Th2, or simply “CRTH2” for the treatment of inflammatory disorders. The variables in Structural Formula (I) and (I-A) are defined herein.

  本文揭示了由结构式（I）和（I-A）表示的化合物：还披露了利用这些化合物抑制称为Th2表达的G蛋白偶联受体的化学引诱受体同源分子，简称“CRTH2”，用于治疗炎症性疾病。结构式（I）和（I-A）中的变量在此处被定义。
• Thiazole derivatives as phosphodiesterase iv inhibitors
  申请人：Eggenweiler Hans-Michael

  公开号：US20050222160A1

  公开（公告）日：2005-10-06

  Thiazole derivatives of the formula I in which R 1 , R 2 , R 3 , V, W, X and B are as defined in claim 1, act as phosphodiesterase IV inhibitors and can be employed for the treatment of osteoporosis, tumours, cachexia, atherosclerosis, rheumatoid arthritis, multiple sclerosis, diabetes mellitus, inflammatory processes, allergies, asthma, autoimmune diseases, myocardial diseases and AIDS.

  公式I中的噻唑衍生物，其中R1，R2，R3，V，W，X和B如权利要求1所定义，可作为磷酸二酯酶IV抑制剂，可用于治疗骨质疏松症，肿瘤，消瘦症，动脉粥样硬化，类风湿性关节炎，多发性硬化症，糖尿病，炎症过程，过敏，哮喘，自身免疫疾病，心肌病和艾滋病。