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2-氯-4-(3-甲氧基苯基)噻唑 | 46295-54-9

中文名称
2-氯-4-(3-甲氧基苯基)噻唑
中文别名
——
英文名称
2-chloro-4-(3-methoxyphenyl)thiazole
英文别名
2-chloro-4-(3-methoxyphenyl)-1,3-thiazole
2-氯-4-(3-甲氧基苯基)噻唑化学式
CAS
46295-54-9
化学式
C10H8ClNOS
mdl
——
分子量
225.699
InChiKey
GRDIFMSQPNLPRN-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):
    3.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    50.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-氯-4-(3-甲氧基苯基)噻唑正丁基锂盐酸肼N,N-二异丙基乙胺 作用下, 以 四氢呋喃N-甲基吡咯烷酮正己烷 为溶剂, 反应 2.83h, 生成 2-hydrazinyl-5-(isopropylthio)-4-(3-methoxyphenyl)thiazole
    参考文献:
    名称:
    [EN] SUBSTITUTED PYRAZOLE AND PYRROLE COMPOUNDS AND METHODS FOR USING THEM FOR INHIBITION OF INITIATION OF TRANSLATION AND TREATMENT OF DISEASES AND DISORDERS RELATING THERETO
    [FR] COMPOSÉS PYRAZOLE ET PYRROLE SUBSTITUÉS ET PROCÉDÉS D'UTILISATION DE CES DERNIERS POUR L'INHIBITION DE L'INITIATION DE LA TRADUCTION ET LE TRAITEMENT DE MALADIES ET DE TROUBLES ASSOCIÉS À CETTE DERNIÈRE
    摘要:
    揭示了吡唑化合物,以及其药物组合物和使用方法。其中一种实施例是具有结构(I)及其药用可接受的盐和/或氧化物,其中X1、X2、Z1、Z2、由“a”表示的环系统、R1、A1A、L1B、A1B、L1A、L2、Q、L3、R3、A4A、L4B、A4B、L4A、R4、L5和R5如本文所述。在某些实施例中,本文所披露的化合物破坏elF4E/eiF4G相互作用,并可用于治疗过度增殖性疾病、神经系统疾病或障碍,或自闭症。
    公开号:
    WO2016196644A1
  • 作为产物:
    描述:
    1-(3-methoxyphenyl)-2-thiocyanatoethan-1-one 在 盐酸 作用下, 以 1,4-二氧六环 为溶剂, 反应 20.0h, 以99%的产率得到2-氯-4-(3-甲氧基苯基)噻唑
    参考文献:
    名称:
    [EN] SUBSTITUTED PYRAZOLE AND PYRROLE COMPOUNDS AND METHODS FOR USING THEM FOR INHIBITION OF INITIATION OF TRANSLATION AND TREATMENT OF DISEASES AND DISORDERS RELATING THERETO
    [FR] COMPOSÉS PYRAZOLE ET PYRROLE SUBSTITUÉS ET PROCÉDÉS D'UTILISATION DE CES DERNIERS POUR L'INHIBITION DE L'INITIATION DE LA TRADUCTION ET LE TRAITEMENT DE MALADIES ET DE TROUBLES ASSOCIÉS À CETTE DERNIÈRE
    摘要:
    揭示了吡唑化合物,以及其药物组合物和使用方法。其中一种实施例是具有结构(I)及其药用可接受的盐和/或氧化物,其中X1、X2、Z1、Z2、由“a”表示的环系统、R1、A1A、L1B、A1B、L1A、L2、Q、L3、R3、A4A、L4B、A4B、L4A、R4、L5和R5如本文所述。在某些实施例中,本文所披露的化合物破坏elF4E/eiF4G相互作用,并可用于治疗过度增殖性疾病、神经系统疾病或障碍,或自闭症。
    公开号:
    WO2016196644A1
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文献信息

  • [EN] SUBSTITUTED PYRAZOLE AND PYRROLE COMPOUNDS AND METHODS FOR USING THEM FOR INHIBITION OF INITIATION OF TRANSLATION AND TREATMENT OF DISEASES AND DISORDERS RELATING THERETO<br/>[FR] COMPOSÉS PYRAZOLE ET PYRROLE SUBSTITUÉS ET PROCÉDÉS D'UTILISATION DE CES DERNIERS POUR L'INHIBITION DE L'INITIATION DE LA TRADUCTION ET LE TRAITEMENT DE MALADIES ET DE TROUBLES ASSOCIÉS À CETTE DERNIÈRE
    申请人:BANTAM PHARMACEUTICAL LLC
    公开号:WO2016196644A1
    公开(公告)日:2016-12-08
    Disclosed are pyrazole compounds, as well as pharmaceutical compositions and methods of use thereof. One embodiment is a compound having the structure (I) and pharmaceutically acceptable salts and /V-oxides thereof, wherein X1, X2, Z1, Z2, the ring system denoted by "a", R1, A1A, L1B, A1B, L1A, L2, Q, L3, R3, A4A, L4B, A4B, L4A, R4, L5, and R5 are as described herein. In certain embodiments, compounds disclosed herein disrupt the elF4E/eiF4G interaction, and can be used to treat hyperproliferative disorder, a neurological disease or disorder, or autism.
    揭示了吡唑化合物,以及其药物组合物和使用方法。其中一种实施例是具有结构(I)及其药用可接受的盐和/或氧化物,其中X1、X2、Z1、Z2、由“a”表示的环系统、R1、A1A、L1B、A1B、L1A、L2、Q、L3、R3、A4A、L4B、A4B、L4A、R4、L5和R5如本文所述。在某些实施例中,本文所披露的化合物破坏elF4E/eiF4G相互作用,并可用于治疗过度增殖性疾病、神经系统疾病或障碍,或自闭症。
  • SUBSTITUTED PYRAZOLE AND PYRROLE COMPOUNDS AND METHODS FOR USING THEM FOR INHIBITION OF INITIATION OF TRANSLATION AND TREATMENT OF DISEASES AND DISORDERS RELATING THERETO
    申请人:Bantam Pharmaceutical, LLC
    公开号:EP3303332A1
    公开(公告)日:2018-04-11
  • METHODS OF USING SUBSTITUTED PYRAZOLE AND PYRAZOLE COMPOUNDS AND FOR TREATMENT OF HYPERPROLIFERATIVE DISEASES
    申请人:Bantam Pharmaceutical, LLC
    公开号:EP3548024A2
    公开(公告)日:2019-10-09
  • Substituted Pyrazole and Pyrrole Compounds and Methods for Using Them for Inhibition of Initiation of Translation and Treatment of Diseases and Disorders Relating Thereto
    申请人:Bantam Pharmaceutical, LLC
    公开号:US20180311218A1
    公开(公告)日:2018-11-01
    Disclosed are pyrazole compounds, as well as pharmaceutical compositions and methods of use thereof. One embodiment is a compound having the structure (I) and pharmaceutically acceptable salts and/V-oxides thereof, wherein X 1 , X 2 , Z 1 , Z 2 , the ring system denoted by “a”, R 1 , A 1A , L 1B , A 1B , L 1A , L 2 , Q, L 3 , R 3 , A 4A , L 4B , A 4B , L 4A , R 4 , L 5 , and R 5 are as described herein. In certain embodiments, compounds disclosed herein disrupt the elF4E/eiF4G interaction, and can be used to treat hyperproliferative disorder, a neurological disease or disorder, or autism.
  • Methods of Using Substituted Pyrazole and Pyrazole Compounds and for Treatment of Hyperproliferative Diseases
    申请人:Bantam Pharmaceutical, LLC
    公开号:US20200069656A1
    公开(公告)日:2020-03-05
    Disclosed are methods of treating hyperproliferative disorders such as cancer, methods of arresting the cell cycle in cancer cells, methods of inhibiting glutathione synthesis in cancer cells, and associated compounds for use and uses in medicaments. In certain embodiments, the methods, uses and compounds are provided with reference to compounds of the structural formula (I), in which X 1 , X 2 , Z 1 , Z 2 , the ring system denoted by “a”, R 1 , L 1 , L 2 , Q, L 3 , R 3 , L 4 , R 4 , L 5 , and R 5 are as described herein. In certain embodiments, compounds disclosed herein are especially active against cancers having a mutant KRAS gene.
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