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5-三氟甲氧基-1,3-二氢-2H-苯并咪唑-2-硫酮 | 97963-59-2

中文名称
5-三氟甲氧基-1,3-二氢-2H-苯并咪唑-2-硫酮
中文别名
——
英文名称
2-mercapto-5-trifluoromethoxy-1H-benzimidazole
英文别名
5-Trifluoromethoxy-1H-benzimidazole-2-thiol;5-Trifluoromethoxy-1,3-dihydro-2H-benzimidazol-2-thione;5-(trifluoromethoxy)-1,3-dihydrobenzimidazole-2-thione
5-三氟甲氧基-1,3-二氢-2H-苯并咪唑-2-硫酮化学式
CAS
97963-59-2
化学式
C8H5F3N2OS
mdl
——
分子量
234.202
InChiKey
LOXKKKCAYRCQMF-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

物化性质

  • 沸点:
    263.5±50.0 °C(Predicted)
  • 密度:
    1.60±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    65.4
  • 氢给体数:
    2
  • 氢受体数:
    5

安全信息

  • 海关编码:
    2933990090

SDS

SDS:40232bf3fe6fd3ea7afeaf5a61ca36cd
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反应信息

  • 作为反应物:
    描述:
    5-三氟甲氧基-1,3-二氢-2H-苯并咪唑-2-硫酮 在 sodium percarbonate 作用下, 以 为溶剂, 反应 5.0h, 以73.5%的产率得到5(6)-trifluoromethoxy-1H-benzoimidazol-2-sulfonic acid
    参考文献:
    名称:
    WO2006/50148
    摘要:
    公开号:
  • 作为产物:
    描述:
    4-trifluoromethoxy-1,2-phenylenediamine dihydrochloride 、 potassium ethyl xanthogenatesodium hydroxide 作用下, 以 乙醇 为溶剂, 以75%的产率得到5-三氟甲氧基-1,3-二氢-2H-苯并咪唑-2-硫酮
    参考文献:
    名称:
    Picoline derivative useful as gastric acid secretion inhibitors
    摘要:
    式I的吡啶醛衍生物##STR1##,其中取代基具有描述中给出的含义,它们的盐是一种对胃具有显著保护作用的新化合物。
    公开号:
    US04686230A1
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文献信息

  • Fluoroalkoxy substituted benzimidazoles useful as gastric acid secretion
    申请人:BYK Gulden Lomberg Chemische Fabrik GmbH
    公开号:US04758579A1
    公开(公告)日:1988-07-19
    Dialkoxypyridines of formula I ##STR1## wherein R1 is 1-3C-alkyl which is completely or predominantly substituted by fluorine, or a chlorodifluoromethyl radical and R1' is hydrogen, halo, trifluoromethyl, 1-3C-alkyl, or 1-3C-alkoxy which is optionally completely or predominantly substituted by fluorine, or R1 and R1', together with the oxygen atom to which R1 is bonded, are 1-2C-alkylenedioxy, which is optionally completely or partly substituted by fluorine, or chlorotrifluoroethylenedioxy, R3 is 1-3C-alkoxy, one of R2 and R4 is 1-3C-alkoxy and the other is a hydrogen atom or 1-3C-alkyl and n is 0 or 1, and salts thereof are new compounds with a pronounced protective action on the stomach. Processes for preparing these compounds, medicaments containing them and their use, as well as intermediate compounds and their use for preparing the subject dialkoxypyridines, are disclosed.
    式I的二烷氧基吡啶##STR1##其中R1是完全或主要由甲基取代的1-3C-烷基,R1'是氢、卤素、三甲基、1-3C-烷基或1-3C-烷氧基,后者可以选择性地完全或主要由取代,或R1和R1'连同与R1连接的氧原子一起,是1-2C-烷二氧基,后者可以选择性地完全或部分由取代,或三氟乙烯二氧基,R3是1-3C-烷氧基,R2和R4中的一个是1-3C-烷氧基,另一个是氢原子或1-3C-烷基,n为0或1,以及它们的盐是一种对胃具有显著保护作用的新化合物。揭示了制备这些化合物的方法,含有它们的药物及其用途,以及中间体化合物及其用途用于制备所述二烷氧基吡啶
  • 1,4-Dihydropyridine-Fused Heterocycles, Process for Preparing the Same, Use and Compositions Containing Them
    申请人:MAUGER Jacques
    公开号:US20080261969A1
    公开(公告)日:2008-10-23
    This invention relates to compounds of formula (I) to processes for the preparation of such compounds, to pharmaceutical compositions comprising such compounds, and to methods of treatment comprising administering of such compounds.
    本发明涉及式(I)化合物、制备该类化合物的方法、包含该类化合物的药物组合物,以及通过给予该类化合物的治疗方法。
  • 1,4-dihydropyridine-fused heterocycles, process for preparing the same, use and compositions containing them
    申请人:Aventis Pharma S.A..
    公开号:US08163768B2
    公开(公告)日:2012-04-24
    This invention relates to compounds of formula (I) to processes for the preparation of such compounds, to pharmaceutical compositions comprising such compounds, and to methods of treatment comprising administering of such compounds.
    本发明涉及公式(I)的化合物,以制备这些化合物的方法,包含这些化合物的药物组合物,以及包含给予这些化合物的治疗方法。
  • MYC MODULATORS AND USES THEREOF
    申请人:Massachusetts Institute of Technology
    公开号:US20160168165A1
    公开(公告)日:2016-06-16
    The present disclosure provides compounds of Formula (I-a), Formula (I), and Formula (II). The compounds described herein may be Myc modulators (e.g., Myc inhibitors) and may be useful in treating in a subject in need thereof diseases associated with Myc and proliferative diseases (e.g., cancer). Also provided in the present disclosure are pharmaceutical compositions, kits, methods, and uses including a compound described herein.
    本公开提供式(I-a)、式(I)和式(II)的化合物。本文所描述的化合物可能是Myc调节剂(例如Myc抑制剂),并且可能有用于治疗与Myc和增殖性疾病(例如癌症)相关的患者。本公开还提供了包括所述化合物的药物组合物、试剂盒、方法和用途。
  • Myc modulators and uses thereof
    申请人:Massachusetts Institute of Technology
    公开号:US10017520B2
    公开(公告)日:2018-07-10
    The present disclosure provides compounds of Formula (I-a), Formula (I), and Formula (II). The compounds described herein may be Myc modulators (e.g., Myc inhibitors) and may be useful in treating in a subject in need thereof diseases associated with Myc and proliferative diseases (e.g., cancer). Also provided in the present disclosure are pharmaceutical compositions, kits, methods, and uses including a compound described herein.
    本公开提供了式(I-a)、式(I)和式(II)化合物。本文所述的化合物可以是Myc调节剂(如Myc抑制剂),可用于治疗有需要的受试者与Myc相关的疾病和增殖性疾病(如癌症)。本公开还提供了包括本文所述化合物的药物组合物、试剂盒、方法和用途。
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