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5-chloro-6-(2,6-dichlorophenyl)-7-(2-methylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrimidine | 187233-76-7

中文名称
——
中文别名
——
英文名称
5-chloro-6-(2,6-dichlorophenyl)-7-(2-methylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrimidine
英文别名
5-chloro-6-(2,6-dichlorophenyl)-7-(2-methyl-1-pyrrolidinyl)[1,2,4]triazolo[1,5-a]pyrimidine
5-chloro-6-(2,6-dichlorophenyl)-7-(2-methylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrimidine化学式
CAS
187233-76-7
化学式
C16H14Cl3N5
mdl
——
分子量
382.68
InChiKey
FXYRPYPEWDTROQ-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):
    5.3
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    46.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    5-chloro-6-(2,6-dichlorophenyl)-7-(2-methylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrimidine氰化四丁基铵乙腈 为溶剂, 反应 64.0h, 生成 5-cyano-6-(2,6-dichlorophenyl)-7-(2-methylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrimidine
    参考文献:
    名称:
    [DE] 6-(2,6-DICHLORPHENYL)-TRIAZOLOPYRIMIDINE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ZUR BEKÄMPFUNG VON SCHADPILZEN SOWIE SIE ENTHALTENDE MITTEL
    [EN] 6-(2,6-DICHLOROPHENYL)-TRIAZOLOPYRIMIDINES, METHODS FOR THE PRODUCTION THEREOF, USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI, AND AGENTS CONTAINING THE SAME
    [FR] 6-(2,6-DICHLORPHENYL)-TRIAZOLOPYRIMIDINES, LEUR PROCEDE DE PRODUCTION ET LEUR UTILISATION POUR LUTTER CONTRE LES CHAMPIGNONS NUISIBLES ET PRODUITS LES CONTENANT
    摘要:
    公开号:
    WO2005095405A3
  • 作为产物:
    描述:
    5,7-dichloro-6-(2,6-dichlorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine 、 2-甲基吡咯烷三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 14.0h, 生成 5-chloro-6-(2,6-dichlorophenyl)-7-(2-methylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrimidine
    参考文献:
    名称:
    [DE] 6-(2,6-DICHLORPHENYL)-TRIAZOLOPYRIMIDINE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ZUR BEKÄMPFUNG VON SCHADPILZEN SOWIE SIE ENTHALTENDE MITTEL
    [EN] 6-(2,6-DICHLOROPHENYL)-TRIAZOLOPYRIMIDINES, METHODS FOR THE PRODUCTION THEREOF, USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI, AND AGENTS CONTAINING THE SAME
    [FR] 6-(2,6-DICHLORPHENYL)-TRIAZOLOPYRIMIDINES, LEUR PROCEDE DE PRODUCTION ET LEUR UTILISATION POUR LUTTER CONTRE LES CHAMPIGNONS NUISIBLES ET PRODUITS LES CONTENANT
    摘要:
    公开号:
    WO2005095405A3
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文献信息

  • Substituted-triazolopyrimidines as anticancer agents
    申请人:American Home Products Corporation
    公开号:US20020068744A1
    公开(公告)日:2002-06-06
    The invention provides a method of treating or inhibiting the growth of cancerous tumour cells and associated diseases in a mammal in need thereof which comprises administering to said mammal an effective amount of a substituted triazolopyrimidine derivative or a pharmaceutically acceptable salt thereof and further provides a method of treating or inhibiting the growth of cancerous tumour cells and associated diseases in a mammal in need thereof by interacting with tubulin and microtubules and promoting microtubule polymerization which comprises administering to said mammal an effective amount of a substituted triazolopyrimidine derivative or a pharmaceutically acceptable salt thereof.
    该发明提供了一种治疗或抑制哺乳动物体内癌症肿瘤细胞及相关疾病的方法,包括向该哺乳动物体内施用有效量的取代三唑吡啶衍生物或其药学上可接受的盐,并进一步提供了一种通过与微管蛋白和微管相互作用并促进微管聚合的方法,治疗或抑制哺乳动物体内癌症肿瘤细胞及相关疾病,包括向该哺乳动物体内施用有效量的取代三唑吡啶衍生物或其药学上可接受的盐。
  • SUBSTITUTED-TRIAZOLOPYRIMIDINES AS ANTICANCER AGENTS
    申请人:Wyeth
    公开号:EP1307200A2
    公开(公告)日:2003-05-07
  • US5593996A
    申请人:——
    公开号:US5593996A
    公开(公告)日:1997-01-14
  • US7329663B2
    申请人:——
    公开号:US7329663B2
    公开(公告)日:2008-02-12
  • [EN] SUBSTITUTED-TRIAZOLOPYRIMIDINES AS ANTICANCER AGENTS<br/>[FR] TRIAZOLOPYRIMIDINES SUBSTITUES COMME AGENTS ANTICANCEREUX
    申请人:AMERICAN HOME PROD
    公开号:WO2002002563A2
    公开(公告)日:2002-01-10
    The invention provides a method of treating of inhibiting the growth of cancerous tumour cells and associated diseases in a mammal in need thereof which comprises administering to said mammal an effective amount of a substituted triazolopyrimidine derivative or a pharmaceutically acceptable salt thereof and further provides a method of treating or inhibiting the growth of cancerous tumour cells and associated diseases in a mammal in need thereof by interacting with tubulin and microtubules and promoting microtubule polymerization which comprises administering to said mammal an effective amount of a substituted triazolopyrimidine derivative or a pharmaceutically acceptable salt thereof.
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