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4-[2-(5,6-Dichloro-1H-benzoimidazol-2-ylamino)-6-methyl-pyrimidin-4-ylamino]-2-(4-methyl-piperazin-1-ylmethyl)-phenol | 86260-57-3

中文名称
——
中文别名
——
英文名称
4-[2-(5,6-Dichloro-1H-benzoimidazol-2-ylamino)-6-methyl-pyrimidin-4-ylamino]-2-(4-methyl-piperazin-1-ylmethyl)-phenol
英文别名
4-[[2-[(5,6-dichloro-1H-benzimidazol-2-yl)amino]-6-methylpyrimidin-4-yl]amino]-2-[(4-methylpiperazin-1-yl)methyl]phenol
4-[2-(5,6-Dichloro-1H-benzoimidazol-2-ylamino)-6-methyl-pyrimidin-4-ylamino]-2-(4-methyl-piperazin-1-ylmethyl)-phenol化学式
CAS
86260-57-3
化学式
C24H26Cl2N8O
mdl
——
分子量
513.429
InChiKey
JBAPGDQNYCBYNF-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):
    4.8
  • 重原子数:
    35
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    105
  • 氢给体数:
    4
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    4-amino-2-<(4-methyl-1-piperazinyl)methyl>phenol trihydrochloride 、 [(4-氯-6-甲基-2-嘧啶基)硫代]乙腈N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以18%的产率得到4-[2-(5,6-Dichloro-1H-benzoimidazol-2-ylamino)-6-methyl-pyrimidin-4-ylamino]-2-(4-methyl-piperazin-1-ylmethyl)-phenol
    参考文献:
    名称:
    N2-1H-Benzimidazol-2-yl-N4-phenyl-2,4-pyrimidinediamines and N2-1H-benzimidazol-2-yl-5,6,7,8-tetrahydro-N4-phenyl-2,4-quinazolinediamines as potential antifilarial agents
    摘要:
    A series of N2-1H-benzimidazol-2-yl-N4-phenyl-2,4-pyrimidinediamines and N2-1H-benzimidazol-2-yl-5,6,7,8-tetrahydro-N4-phenyl-2,4-quinazolinediamines (XI) was synthesized for antifilarial evaluation. Condensation of the requisite beta-keto ester (VI) with N-cyanoguanidine afforded 2-pyrimidinylcyanamides (VIIa,b) and (5,6,7,8-tetrahydro-4-hydroxy-2-quinazolinyl)cyanamide (VIIc). Reaction of VII with a substituted o-phenylenediamine gave 2-(1H-benzimidazol-2-ylamino)-4-pyrimidinols and 2-[(5,6-dichloro-1H-benzimidazol-2-yl)amino]-5,6,7, 8-tetrahydro-4-quinazolinol (IX). Chlorination with phosphoryl chloride, followed by condensation with the appropriate substituted benzenamine, gave the desired N2-1H-benzimidazol-2-yl-N4-phenyl-2,4-pyrimidinediamines and N2-1H-benzimidazol-2-yl-5,6,7,8-tetrahydro-N4-phenyl-2,4-quinazolinediamines (XI). None of these compounds possessed antifilarial activity against Litomosoides carinii or Brugia pahangi infections in jirds.
    DOI:
    10.1021/jm00363a017
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文献信息

  • N2-1H-Benzimidazol-2-yl-N4-phenyl-2,4-pyrimidinediamines and N2-1H-benzimidazol-2-yl-5,6,7,8-tetrahydro-N4-phenyl-2,4-quinazolinediamines as potential antifilarial agents
    作者:Mario M. Angelo、Daniel Ortwine、Donald F. Worth、Leslie M. Werbel
    DOI:10.1021/jm00363a017
    日期:1983.9
    A series of N2-1H-benzimidazol-2-yl-N4-phenyl-2,4-pyrimidinediamines and N2-1H-benzimidazol-2-yl-5,6,7,8-tetrahydro-N4-phenyl-2,4-quinazolinediamines (XI) was synthesized for antifilarial evaluation. Condensation of the requisite beta-keto ester (VI) with N-cyanoguanidine afforded 2-pyrimidinylcyanamides (VIIa,b) and (5,6,7,8-tetrahydro-4-hydroxy-2-quinazolinyl)cyanamide (VIIc). Reaction of VII with a substituted o-phenylenediamine gave 2-(1H-benzimidazol-2-ylamino)-4-pyrimidinols and 2-[(5,6-dichloro-1H-benzimidazol-2-yl)amino]-5,6,7, 8-tetrahydro-4-quinazolinol (IX). Chlorination with phosphoryl chloride, followed by condensation with the appropriate substituted benzenamine, gave the desired N2-1H-benzimidazol-2-yl-N4-phenyl-2,4-pyrimidinediamines and N2-1H-benzimidazol-2-yl-5,6,7,8-tetrahydro-N4-phenyl-2,4-quinazolinediamines (XI). None of these compounds possessed antifilarial activity against Litomosoides carinii or Brugia pahangi infections in jirds.
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