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2-bromo-8-methylbenzimidazo[2,1-b]quinazolin-12(5H)-one

中文名称
——
中文别名
——
英文名称
2-bromo-8-methylbenzimidazo[2,1-b]quinazolin-12(5H)-one
英文别名
2-bromo-8-methyl-6H-benzimidazolo[2,1-b]quinazolin-12-one
2-bromo-8-methylbenzimidazo[2,1-b]quinazolin-12(5H)-one化学式
CAS
——
化学式
C15H10BrN3O
mdl
——
分子量
328.168
InChiKey
XNPTUVSDNUBDJI-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
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    44.7
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    methyl 5-bromo-2-isothiocyanatobenzoate3,4-二氨基甲苯达卡巴嗪barium hydroxide octahydrate 作用下, 以 二氯甲烷1,4-二氧六环 为溶剂, 反应 16.43h, 以95%的产率得到2-bromo-8-methylbenzimidazo[2,1-b]quinazolin-12(5H)-one
    参考文献:
    名称:
    Microwave-Mediated Heterocyclization to Benzimidazo[2,1-b]quinazolin-12(5H)-ones
    摘要:
    An effective route to benzimidazo[2,1-b]quinazolin-12(5H)-ones from commercially available o-aryl isothiocyanate esters and o-phenylenediamines is reported. This method accommodates a variety of substituents on either starting material and proceeds under microwave irradiation in the presence of barium hydroxide, conditions that do not hydrolyze methyl ester substituents. The pharmacologically pertinent benzimidazoquinazolinone heterocycle is delivered in excellent yield and purity via both solution- and solid-phase protocols, the latter involving traceless release from the resin.
    DOI:
    10.1021/jo0618066
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文献信息

  • Microwave-Mediated Heterocyclization to Benzimidazo[2,1-<i>b</i>]quinazolin-12(5<i>H</i>)-ones
    作者:Richard D. Carpenter、Kit S. Lam、Mark J. Kurth
    DOI:10.1021/jo0618066
    日期:2007.1.1
    An effective route to benzimidazo[2,1-b]quinazolin-12(5H)-ones from commercially available o-aryl isothiocyanate esters and o-phenylenediamines is reported. This method accommodates a variety of substituents on either starting material and proceeds under microwave irradiation in the presence of barium hydroxide, conditions that do not hydrolyze methyl ester substituents. The pharmacologically pertinent benzimidazoquinazolinone heterocycle is delivered in excellent yield and purity via both solution- and solid-phase protocols, the latter involving traceless release from the resin.
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