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1-phenacyl-2-(2-chloroethylamino)benzimidazole | 154055-46-6

中文名称
——
中文别名
——
英文名称
1-phenacyl-2-(2-chloroethylamino)benzimidazole
英文别名
2-(2-chloroethylamino)-1-phenacylbenzimidazole;2-[2-(2-chloroethylamino)benzimidazol-1-yl]-1-phenylethanone
1-phenacyl-2-(2-chloroethylamino)benzimidazole化学式
CAS
154055-46-6
化学式
C17H16ClN3O
mdl
——
分子量
313.787
InChiKey
OXKGOORCLLAPFJ-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):
    3.9
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    46.9
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-phenacyl-2-(2-chloroethylamino)benzimidazole 以88%的产率得到9-phenacyl-2,3-dihydroimidazo[1,2-a]benzimidazole
    参考文献:
    名称:
    Benzimidazole compounds
    摘要:
    本发明公开了通式(I)的化合物:##STR1## 其中,A、B、C、D、n、R.sub.1、R.sub.2、R.sub.3、R.sub.4、X、Y和Z如描述中所定义,并公开了它们作为抗糖尿病药物的用途。
    公开号:
    US05623073A1
  • 作为产物:
    描述:
    1-phenacyl-2-(2-chloroethylamino)benzimidazole hydrochlorideammonium hydroxide 作用下, 以 为溶剂, 以87%的产率得到1-phenacyl-2-(2-chloroethylamino)benzimidazole
    参考文献:
    名称:
    Research in the field of imidazo[1,2-a]benzimidazole derivatives: XXVII. 1-acylmethyl-2-(ω-hydroxyalkylamino)-benzimidazoles and their transformation into derivatives of tricyclic systems
    摘要:
    1-Acylmethyl-2-(omega-hydroxyalkylamino)benzimidazoles were synthesized and their behavior under various conditions was investigated: at the thermolysis without solvent, at heating in DMF or in 2-aminoethanol, hydrohalic acids, and acetic anhydride, in the presence of chlorinating agents (SOCl(2), POCl(3)). Depending on the reaction conditions derivatives were obtained of 1H-imidazo[1,2-a]-benzimidazole, 9H-2,3-dihydroimidazo[1,2-a]benzimidazole, and 10H-2,3,4,10-tetrahydropyrimido[1,2-a]-benzimidazole that were suitable synthons for the synthesis of functionally substituted derivatives of these tricyclic systems.
    DOI:
    10.1134/s1070428010020223
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文献信息

  • Dérivés du benzimidazole à activité antidiabétique et antiagrégante plaquettaire
    申请人:ADIR ET COMPAGNIE
    公开号:EP0571253A1
    公开(公告)日:1993-11-24
    Dérivés de formule générale (I) : où A, B, C, D, n, R₁, R₂, R₃, R₄, X, Y, Z sont tels que définis dans la description. Médicaments.
    通式(I)的衍生物 : 其中 A、B、C、D、n、R₁、R₂、R₃、R₄、X、Y、Z 如描述中所定义。 药物。
  • US5623073A
    申请人:——
    公开号:US5623073A
    公开(公告)日:1997-04-22
  • US5639756A
    申请人:——
    公开号:US5639756A
    公开(公告)日:1997-06-17
  • Research in the field of imidazo[1,2-a]benzimidazole derivatives: XXVII. 1-acylmethyl-2-(ω-hydroxyalkylamino)-benzimidazoles and their transformation into derivatives of tricyclic systems
    作者:V. A. Anisimova、I. E. Tolpygin、G. S. Borodkin
    DOI:10.1134/s1070428010020223
    日期:2010.2
    1-Acylmethyl-2-(omega-hydroxyalkylamino)benzimidazoles were synthesized and their behavior under various conditions was investigated: at the thermolysis without solvent, at heating in DMF or in 2-aminoethanol, hydrohalic acids, and acetic anhydride, in the presence of chlorinating agents (SOCl(2), POCl(3)). Depending on the reaction conditions derivatives were obtained of 1H-imidazo[1,2-a]-benzimidazole, 9H-2,3-dihydroimidazo[1,2-a]benzimidazole, and 10H-2,3,4,10-tetrahydropyrimido[1,2-a]-benzimidazole that were suitable synthons for the synthesis of functionally substituted derivatives of these tricyclic systems.
  • Benzimidazole compounds
    申请人:Adir Et Compagnie
    公开号:US05623073A1
    公开(公告)日:1997-04-22
    Compounds of the general formula (I): ##STR1## wherein A, B, C, D, n, R.sub.1, R.sub.2, R.sub.3, R.sub.4, X, Y and Z are as defined in the description, and their use as antidiabetics are disclosed.
    本发明公开了通式(I)的化合物:##STR1## 其中,A、B、C、D、n、R.sub.1、R.sub.2、R.sub.3、R.sub.4、X、Y和Z如描述中所定义,并公开了它们作为抗糖尿病药物的用途。
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