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2-甲基苯并唑 | 1033202-12-8

中文名称
2-甲基苯并唑
中文别名
3-(3-溴苯基)-1,2,4-噁二唑;3-(3-溴苯基)-1,2,4-恶二唑
英文名称
3-(3-bromophenyl)-1,2,4-oxadiazole
英文别名
——
2-甲基苯并唑化学式
CAS
1033202-12-8
化学式
C8H5BrN2O
mdl
MFCD10699671
分子量
225.044
InChiKey
NJOGUMIPSJIRBL-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):
    2.5
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    38.9
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

反应信息

  • 作为反应物:
    描述:
    2-甲基苯并唑联硼酸频那醇酯1,1'-双(二苯基膦)二茂铁(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloridepotassium acetate 作用下, 以 1,4-二氧六环 为溶剂, 以53.8%的产率得到3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,2,4-oxadiazole
    参考文献:
    名称:
    WO2019180646A5
    摘要:
    公开号:
    WO2019180646A5
  • 作为产物:
    描述:
    间溴苯甲腈盐酸羟胺sodium carbonate对甲苯磺酸 作用下, 以 乙醇 为溶剂, 反应 22.0h, 生成 2-甲基苯并唑
    参考文献:
    名称:
    [EN] PYRAZOLO[1,5-A]PYRIMIDINYL CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS
    [FR] COMPOSÉS DE PYRAZOLO[1,5-A]PYRIMIDINYL CARBOXAMIDE ET LEUR UTILISATION DANS LE TRAITEMENT DE TROUBLES MÉDICAUX
    摘要:
    本发明提供了取代的吡唑[1,5-a]嘧啶基甲酰胺及其相关有机化合物,包含此类化合物的组合物,医疗包,以及使用此类化合物和组合物治疗医疗障碍的方法,例如,戈谢病,帕金森病,路易体病,痴呆症或多系统萎缩症。所述的代表性的取代吡唑[1,5-a]嘧啶基甲酰胺化合物包括2-杂环基-4-烷基-吡唑[1,5-a]嘧啶-3-甲酰胺化合物及其变体。
    公开号:
    WO2017176960A1
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文献信息

  • [EN] 5-SUBSTITUTED IMINOTHIAZINES AND THEIR MONO-AND DIOXIDES AS BACE INHIBITORS,COMPOSITIONS,AND THEIR USE<br/>[FR] IMINOTHIAZINES 5-SUBSTITUÉES ET LEUR MONOXYDES ET DIOXYDES COMME INHIBITEURS DE BACE, LEURS COMPOSITIONS ET LEUR UTILISATION
    申请人:SCHERING CORP
    公开号:WO2012139425A1
    公开(公告)日:2012-10-18
    The present invention discloses certain iminothiazine compounds and mono- and dioxides thereof, including compounds Formula (I): and tautomers and stereoisomers thereof, and pharmaceutically acceptable salts of said compounds, said tautomers and said stereoismers, wherein each of variables shown in the formula are as defined herein. The compounds of the invention may be useful as BACE inhibitors and/or for the treatment and prevention of various pathologies related thereto. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and uses, including Alzheimer's disease, are also disclosed.
    本发明揭示了某些咪唑啉化合物及其单体和二氧化物,包括化合物Formula (I):及其互变异构体和立体异构体,以及所述化合物、所述互变异构体和所述立体异构体的药用盐,其中公式中显示的各变量如本文所定义。本发明的化合物可能作为BACE抑制剂,用于治疗和预防与之相关的各种病理。还公开了包括一种或多种这样的化合物(单独和与一种或多种其他活性剂组合)的药物组合物,以及它们的制备和用途方法,包括阿尔茨海默病。
  • 5-SUBSTITUTED IMINOTHIAZINES AND THEIR MONO- AND DIOXIDES AS BACE INHIBITORS, COMPOSITIONS, AND THEIR USE
    申请人:Wu Wen-Lian
    公开号:US20140128382A1
    公开(公告)日:2014-05-08
    The present invention discloses certain iminothiazine compounds and mono- and dioxides thereof, including compounds Formula (I): and tautomers and stereoisomers thereof, and pharmaceutically acceptable salts of said compounds, said tautomers and said stereoisomers, wherein each of variables shown in the formula are as defined herein. The compounds of the invention may be useful as BACE inhibitors and/or for the treatment and prevention of various pathologies related thereto. Pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other active agents), and methods for their preparation and uses, including Alzheimer's disease, are also disclosed.
    本发明揭示了某些亚胺噻唑化合物及其单体和二氧化物,包括化合物公式(I):及其互变异构体和立体异构体,以及所述化合物、所述互变异构体和所述立体异构体的药学上可接受的盐,其中公式中所示的每个变量如本文所定义。本发明的化合物可用作BACE抑制剂和/或用于治疗和预防与之相关的各种病理学。本发明还揭示了包括一种或多种此类化合物(单独和与一种或多种其他活性剂组合)的制药组合物,以及其制备和用途的方法,包括阿尔茨海默病。
  • Substituted pyrazolo[1,5-a]pyrimidines for the treatment of medical disorders
    申请人:BIAL—BioTech Investments, Inc.
    公开号:US10934298B2
    公开(公告)日:2021-03-02
    The invention provides substituted pyrazolo[1,5-a]pyrimidinyl carboxamide and related organic compounds, compositions containing such compounds, medical kits, and methods for using such compounds and compositions to treat medical disorders, e.g., Gaucher disease, Parkinson's disease, Lewy body disease, dementia, or multiple system atrophy, in a patient. Exemplary substituted pyrazolo[1,5-a]pyrimidinyl carboxamide compounds described herein include 2-heterocyclyl-4-alkyl-pyrazolo[1,5-a]pyrimidine-3-carboxamide compounds and variants thereof. The invention provides, in part, a compound of formula (I-A): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined herein.
    本发明提供了取代的吡唑并[1,5-a]嘧啶基羧酰胺及相关有机化合物、含有此类化合物的组合物、医用试剂盒以及使用此类化合物和组合物治疗患者的内科疾病(如戈谢病、帕森病、路易体病、痴呆症或多系统萎缩)的方法。 本文所述的示例性取代吡唑并[1,5-a]嘧啶基羧酰胺化合物包括2-杂环-4-烷基吡唑并[1,5-a]嘧啶-3-羧酰胺化合物及其变体。 本发明部分提供了式(I-A)化合物:或其药学上可接受的盐,其中变量如本文所定义。
  • Triazolone derivatives or salts thereof and pharmaceutical compositions comprising the same
    申请人:YUHAN CORPORATION
    公开号:US10995086B2
    公开(公告)日:2021-05-04
    The present technology provides triazolone derivatives or pharmaceutically acceptable salts thereof, preparation processes thereof, pharmaceutical compositions comprising the same, and the use thereof. The triazolone derivatives or their pharmaceutically acceptable salts exhibit selective inhibitory activity on VAP-1 and therefore can be usefully applied, e.g., for the treatment and prophylaxis of nonalcoholic hepatosteatosis (NASH).
    本技术提供了三唑酮生物或其药学上可接受的盐、其制备工艺、包含三唑酮生物或其药学上可接受的盐的药物组合物及其用途。三唑酮生物或其药学上可接受的盐类对 VAP-1 具有选择性抑制活性,因此可用于治疗和预防非酒精性肝病(NASH)等。
  • 5-SUBSTITUTED IMINOTHIAZINES AND THEIR MONO-AND DIOXIDES AS BACE INHIBITORS, COMPOSITIONS, AND THEIR USE
    申请人:Merck Sharp & Dohme Corp.
    公开号:EP2697210B1
    公开(公告)日:2017-03-01
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