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7-bromo-2,4-dichloro-3-nitroquinoline | 879004-45-2

中文名称
——
中文别名
——
英文名称
7-bromo-2,4-dichloro-3-nitroquinoline
英文别名
7-Bromo-2,4-dichloro-3-nitroquinoline
7-bromo-2,4-dichloro-3-nitroquinoline化学式
CAS
879004-45-2
化学式
C9H3BrCl2N2O2
mdl
——
分子量
321.945
InChiKey
SLVKQLWNNSMKFQ-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):
    4.3
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    58.7
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    7-bromo-2,4-dichloro-3-nitroquinoline4-二甲氨基吡啶铁粉溶剂黄146三乙胺三氟乙酸 作用下, 以 甲醇二氯甲烷N,N-二甲基甲酰胺乙腈 为溶剂, 反应 28.17h, 生成 2-(4-((4-amino-1-(2-hydroxy-2-methylpropyl)-2-(pentan-2-yl)-1H-imidazo[4,5-c]quinolin-7-yl)methyl)phenyl)acetonitrile
    参考文献:
    名称:
    [EN] CONJUGATE COMPRISING TOLL-LIKE RECEPTOR AGONIST
    [FR] CONJUGUÉ COMPRENANT UN AGONISTE DU RÉCEPTEUR DE TYPE TOLL
    摘要:
    Disclosed herein are compounds that are Toll-like receptor (TLR) agonist, conjugates comprising these compounds and cell targeting moiety, pharmaceutical compositions thereof, method of activating toll-like receptors 7 and/or 8 and method for the treatment of diseases or disorders mediated by toll-like receptors 7 and/or 8, in particular viral infections and proliferative disorders, such as cancer.
    公开号:
    WO2023198195A1
  • 作为产物:
    参考文献:
    名称:
    [EN] CONJUGATE COMPRISING TOLL-LIKE RECEPTOR AGONIST
    [FR] CONJUGUÉ COMPRENANT UN AGONISTE DU RÉCEPTEUR DE TYPE TOLL
    摘要:
    Disclosed herein are compounds that are Toll-like receptor (TLR) agonist, conjugates comprising these compounds and cell targeting moiety, pharmaceutical compositions thereof, method of activating toll-like receptors 7 and/or 8 and method for the treatment of diseases or disorders mediated by toll-like receptors 7 and/or 8, in particular viral infections and proliferative disorders, such as cancer.
    公开号:
    WO2023198195A1
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文献信息

  • 2-Amino 1H-Imidazo Ring Systems and Methods
    申请人:Kshirsagar Tushar A.
    公开号:US20090023720A1
    公开(公告)日:2009-01-22
    1H-Imidazo ring systems (e.g., imidazopyridines, imidazoquinolines, imidazonaphthyridines, 6,7,8,9-tetrahydro imidazoquinolines and imidazonaphthyridines) with an amino substituent at the 2-position, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.
    本发明揭示了在2-位置具有氨基取代基的咪唑环系统(例如咪唑吡啶,咪唑喹啉,咪唑萘啉,6,7,8,9-四氢咪唑喹啉和咪唑萘啉),含有这些化合物的制药组合物,制备这些化合物的方法,中间体以及这些化合物作为免疫调节剂的用途,用于调节动物细胞因子生物合成以及治疗包括病毒和肿瘤性疾病在内的疾病的方法。
  • 2-amino 1H-in-imidazo ring systems and methods
    申请人:3M Innovative Properties Company
    公开号:US08143270B2
    公开(公告)日:2012-03-27
    1H-Imidazo ring systems (e.g., imidazopyridines, imidazoquinolines, imidazonaphthyridines, 6,7,8,9-tetrahydro imidazoquinolines and imidazonaphthyridines) with an amino substituent at the 2-position, pharmaceutical compositions containing these compounds, methods of making the compounds, intermediates, and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.
    本发明公开了在2位具有氨基取代基的1H-咪唑环系(例如咪唑吡啶、咪唑喹啉、咪唑萘啉、6,7,8,9-四氢咪唑喹啉和咪唑萘啉)及其制药组合物、制备上述化合物的方法、中间体以及这些化合物的用途,包括作为免疫调节剂,调节动物的细胞因子生物合成,用于治疗包括病毒和肿瘤疾病在内的疾病。
  • [EN] 2-AMINO 1H IMIDAZO RING SYSTEMS AND METHODS<br/>[FR] SYSTEMES CYCLIQUES DE 2-AMINO 1H-IMIDAZO ET PROCEDES CORRESPONDANTS
    申请人:3M INNOVATIVE PROPERTIES CO
    公开号:WO2006029115A3
    公开(公告)日:2007-06-28
  • EP1784180A4
    申请人:——
    公开号:EP1784180A4
    公开(公告)日:2009-07-22
  • 2-AMINO 1H IMIDAZO RING SYSTEMS AND METHODS
    申请人:3M INNOVATIVE PROPERTIES COMPANY
    公开号:EP1784180A2
    公开(公告)日:2007-05-16
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