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8,9-dihydrobenzo[4,5]imidazo[1,2-a]pyridin-6(7H)-one | 1314243-70-3

中文名称
——
中文别名
——
英文名称
8,9-dihydrobenzo[4,5]imidazo[1,2-a]pyridin-6(7H)-one
英文别名
8,9-dihydro-7H-pyrido[1,2-a]benzimidazol-6-one
8,9-dihydrobenzo[4,5]imidazo[1,2-a]pyridin-6(7H)-one化学式
CAS
1314243-70-3
化学式
C11H10N2O
mdl
——
分子量
186.213
InChiKey
AYQKCRYULHVSIY-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):
    2.2
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    34.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1,2-环己二酮 作用下, 以 乙醚乙醇 为溶剂, 反应 15.0h, 生成 8,9-dihydrobenzo[4,5]imidazo[1,2-a]pyridin-6(7H)-one
    参考文献:
    名称:
    3-溴环己烷-1,2-二酮可作为Hantzsch合成噻唑和相关杂环的有用试剂
    摘要:
    我们描述了使用3-溴环己烷-1,2-二酮(一种空气稳定的通用试剂)用于汉茨噻唑的合成以及其他紧密相关的杂环的合成。
    DOI:
    10.1016/j.tetlet.2011.05.028
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文献信息

  • Molecular Iodine-Catalyzed Aerobic α,β-Diamination of Cyclohexanones with 2-Aminopyrimidine and 2-Aminopyridines
    作者:Thanh Binh Nguyen、Ludmila Ermolenko、Pascal Retailleau、Ali Al-Mourabit
    DOI:10.1021/acs.orglett.6b00823
    日期:2016.5.6
    oxygen molecules and releasing three water molecules as the only byproduct. In addition, the functionalized products including protected 2-aminoimidazoles introduced without aromatization can serve as useful building blocks for natural product synthesis and medicinal chemistry.
    分子被证明是用2-氨基嘧啶/ 2-氨基吡啶环己酮进行好化α,β-双基化环己酮的极佳催化剂。这种α,β-C–H官能化在底物和条件下都非常简单,涉及一个半分子并释放三个分子作为唯一的副产物。此外,包括未经芳香化处理引入的受保护的2-氨基咪唑在内的功能化产品可以用作天然产物合成和药物化学的有用组成部分。
  • [EN] BENZ- OR PYRIDO-IMIDAZOLE DERIVATIVES<br/>[FR] DERIVES DE BENZO- OU PYRIDO-IMIDAZOLE
    申请人:YUNGJIN PHARMACEUTICAL CO., LTD.
    公开号:WO1997003077A1
    公开(公告)日:1997-01-30
    (EN) A benz- or pyrido-imidazole compounds represented by general formula (I), wherein R is hydrogen atom, a hydroxy group, a C1-C6 lower alkyl group, a C1-C6 lower alkoxy group, a substituted or unsubstituted phenyl or pyridyl group, a substituted or unsubstituted guanidino group, or an amino group having a general formula: NR3R4 in which R3 and R4, identical to or different from each other, represent hydrogen atom, a C1-C6 lower alkyl group, a C3-C6 cyclic alkyl group, a substituted or unsubstituted phenyl or pyridyl group, a C1-C6 lower alkoxy group, a C2-C6 alkyl group, or phenyl alkyl group; R1 and R2, identical to or different from each other, are hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 lower alkoxy group, an amino group which may be substituted with a C1-C2 alkyl group, a C1-C6 alkoxy carbonyl group, a halogen atom, a cyano group, a C1-C6 alkylthio group, or a C1-C6 acyl group; R6 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C3 lower alkoxy group, a halogen atom, or a hetero atom; n is an integer from 0 to 4, inclusive; and X is a nitrogen atom or CR5 wherein R5 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 lower alkoxy group, or a halogen atom, or its pharmaceutically acceptable salts are disclosed. These compounds show excellent anti-ulcer activity.(FR) L'invention porte sur des composés benzo- ou pyrido-imidazole de formule générale (I) dans laquelle, R est un atome d'hydrogène, un groupe hydroxy, alkyle inférieur C1-C6, alcoxy inférieur C1-C6, phényle ou pyridyle substitué ou non substitué, guanidino substitué ou non substitué, ou un groupe amino de formule générale NR3R4, dans laquelle R3 et R4 qui peuvent être identiques ou différents, représentent un atome d'hydrogène, un groupe alkyle inférieur C1-C6, alkyle cyclique C3-C6, phényle ou pyridyle substitué ou non substitué, alcoxy inférieur C1-C6, alkyle C2-C6 ou phényle alkyle; et dans laquelle R1 et R2, qui peuvent être identiques ou différents, représentent un atome d'hydrogène, un groupe alkyle inférieur C1-C6, alcoxy inférieur C1-C6, un groupe amino pouvant être substitué par alkyle C1-C6, alcoxy carbonyl C1-C6, un atome d'halogène, un groupe cyano, alkylthio C1-C6, ou acyle C1-C6; R6 est un atome d'hydrogène, un groupe alkyle inférieur C1-C6, alcoxy inférieur C1-C3, un atome d'halogène, ou un hétéroatome; n est un entier de 0 à 4, compris; X est un atome d'azote ou CR5 dans lequel R5 est un atome d'hydrogène, un groupe alkyle inférieur C1-C6, alcoxy inférieur C1-C6, ou un atome d'halogène; ainsi que leurs sels pharmacocompatibles. Ces composés présentent une excellente activité anti-ulcères.
    一种由通式(I)表示的并或吡啶咪唑化合物,其中R为原子、羟基、C1-C6低烷基、C1-C6低烷基、取代或未取代的基或吡啶基、取代或未取代的鸟氨酸基或具有一般式NR3R4的基基团,其中R3和R4,相同或不同,表示原子、C1-C6低烷基、C3-C6环烷基、取代或未取代的基或吡啶基、C1-C6低烷基、C2-C6烷基或基烷基;R1和R2,相同或不同,为原子、C1-C6低烷基、C1-C6低烷基、基基团,可用C1-C2烷基取代、C1-C6烷羰基、卤素原子、基、C1-C6烷基或C1-C6酰基;R6为原子、C1-C6低烷基、C1-C3低烷基、卤素原子或杂原子;n为0到4的整数,包括4;X为原子或CR5,其中R5为原子、C1-C6低烷基、C1-C6低烷基或卤素原子,或其药学上可接受的盐。这些化合物表现出优异的抗溃疡活性。
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