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1,3-dibenzyl-1,5-dihydro-imidazo[2,1-b]quinazolin-2-one | 832676-81-0

中文名称
——
中文别名
——
英文名称
1,3-dibenzyl-1,5-dihydro-imidazo[2,1-b]quinazolin-2-one
英文别名
Imidazo[2,1-b]quinazolin-2(3H)-one, 1,5-dihydro-1,3-bis(phenylmethyl)-;1,3-dibenzyl-3,5-dihydroimidazo[2,1-b]quinazolin-2-one
1,3-dibenzyl-1,5-dihydro-imidazo[2,1-b]quinazolin-2-one化学式
CAS
832676-81-0
化学式
C24H21N3O
mdl
——
分子量
367.45
InChiKey
JNUFSYMQUWVTEG-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
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    35.9
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    N-芴甲氧羰基-DL-苯丙氨酸异硫氰酸苯甲酯邻硝基苯甲醛 以55%的产率得到1,3-dibenzyl-1,5-dihydro-imidazo[2,1-b]quinazolin-2-one
    参考文献:
    名称:
    Solid-phase synthesis of imidazoquinazolinone derivatives with three-point diversity
    摘要:
    A novel imidazoquinazolinone-based tricyclic structure with three-point diversity has been synthesized using solid-phase methodology. The compounds were obtained by treating the amino group of polymer-linked amino acids with 2-nitrobenzaldehyde followed by reduction of the nitro group to an amine. Derivatization of amine with isothiocyanates and cyclization of the resulting thioureas with DIC followed by acidolytic cleavage yielded the desired imidazoquinazolinone based compounds in high purity and moderate to high yield. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2004.10.090
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文献信息

  • Solid-phase synthesis of imidazoquinazolinone derivatives with three-point diversity
    作者:Amit P. Kesarwani、Rajesh K. Grover、Raja Roy、Bijoy Kundu
    DOI:10.1016/j.tet.2004.10.090
    日期:2005.1
    A novel imidazoquinazolinone-based tricyclic structure with three-point diversity has been synthesized using solid-phase methodology. The compounds were obtained by treating the amino group of polymer-linked amino acids with 2-nitrobenzaldehyde followed by reduction of the nitro group to an amine. Derivatization of amine with isothiocyanates and cyclization of the resulting thioureas with DIC followed by acidolytic cleavage yielded the desired imidazoquinazolinone based compounds in high purity and moderate to high yield. (C) 2004 Elsevier Ltd. All rights reserved.
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