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2-methyl-6-phenyl-1,3,7-triazapyrene | 1020166-31-7

中文名称
——
中文别名
——
英文名称
2-methyl-6-phenyl-1,3,7-triazapyrene
英文别名
2-Methyl-6-phenyl-1,3,7-triazapyrene;6-methyl-12-phenyl-5,7,13-triazatetracyclo[6.6.2.04,16.011,15]hexadeca-1(14),2,4(16),5,7,9,11(15),12-octaene
2-methyl-6-phenyl-1,3,7-triazapyrene化学式
CAS
1020166-31-7
化学式
C20H13N3
mdl
——
分子量
295.343
InChiKey
JXDDUFBYTASRRF-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):
    4.5
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    38.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    甲醇2-methyl-6-phenyl-1,3,7-triazapyrene 在 potassium hydroxide 、 potassium hexacyanoferrate(III) 作用下, 以 为溶剂, 反应 9.0h, 以67%的产率得到6-methoxy-2-methyl-8-phenyl-1,3,7-triazapyrene
    参考文献:
    名称:
    Synthesis and cleavage of 1,3,7-triazapyrene ethers
    摘要:
    Oxidative alkoxylation of 1,3,7-triazapyrenes in the system ROH-H2O-KOH-K3Fe(CN)(6) leads via a tandem S (N) (H)-S (N) (H) process to the formation of 6,8-dialkoxy-1,3,7-triazapyrenes. Hydrolytic cleavage of these ethers leads to products of single or double dealkylation, depending on the reaction conditions.
    DOI:
    10.1007/s10593-013-1168-6
  • 作为产物:
    描述:
    1,3,5-三嗪6(7)-benzoyl-2-methylperimidine 在 PPA 作用下, 反应 3.0h, 以47%的产率得到2-methyl-6-phenyl-1,3,7-triazapyrene
    参考文献:
    名称:
    Reaction of 6(7)-acyl-and 6(7)-formylperimidines with 1,3,5-triazines in poly-phosphoric acid
    摘要:
    A method has been developed for the synthesis of 1,3,7-triazapyrenes using the reaction of 6(7)-formyl- and 6(7)-benzoylperimidines with 1,3,5-triazines in PPA. Under these conditions, 6(7)-formylperimidine reacts with 2,4,6-trimethyl-1,3,5-triazine to give 6-hydroxy-1,3-diazapyrene.
    DOI:
    10.1007/s10593-008-0121-6
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文献信息

  • Novel three-component reaction of perimidines with 1,3,5-triazines and carbonyl compounds in polyphosphoric acid. an efficient method for peri-annelation of a carbocyclic and pyridine ring
    作者:A. V. Aksenov、N. A. Aksenov、A. S. Lyakhovnenko、A. B. Kumshaeva、I. V. Aksenova
    DOI:10.1007/s10593-012-1037-8
    日期:2012.7
    Methods have been developed for the synthesis of 1,3-diazapyrenes, 8(6)-aryl-6(8)-oxo-1,6,7,8-tetra-hydro-1,3-diazapyrenes, and 1,3,7-triazapyrenes based on a three-component reaction of perimidines with 1,3,5-triazines and carbonyl compounds, benzonitrile, or vinyl butyl ether in polyphosphoric acid.
    已经开发出用于合成1,3-二氮杂戊烯,8(6)-芳基-6(8)-氧代-1,6,7,8-四氢-1,3-二氮杂戊烯和1,3的方法,7-三氮杂py烯基于多im啶与1,3,5-三嗪和羰基化合物,苄腈乙烯基丁基醚在多磷酸中的三组分反应。
  • Novel three-component peri-annelation reactions of carbocyclic and pyridine rings with perimidines—synthesis of 1,3-diazapyrenes and 1,3,7-triazapyrenes
    作者:Alexander V. Aksenov、Alexander S. Lyahovnenko、Inna V. Aksenova、Oleg N. Nadein
    DOI:10.1016/j.tetlet.2008.01.064
    日期:2008.3
    A new effective synthetic method for 1,3-diazapyrenes and 1,3,7-triazapyrenes is developed based on the three-component reaction of perimidines or 1,8-diaminonaphthalene with 1,3,5-triazines and carbonyl compounds or benzonitrile in polyphosphoric acid (PPA).
    基于环二嘧啶1,8-二氨基萘1,3,5-三嗪和羰基化合物或苄腈的三组分反应,提出了一种有效的1,3-二氮杂戊烯和1,3,7-三氮杂戊烯的合成新方法。多磷酸PPA)。
  • Synthesis of 1,3-diazapyrenes and 1,3,7-triazapyrenes by the reaction of 1,8-naphthalenediamine with triazine in the presence of carbonyl compounds or benzonitrile in polyphosphoric acid
    作者:A. V. Aksenov、I. V. Aksenova、A. S. Lyakhovnenko、N. A. Aksenov
    DOI:10.1007/s10593-009-0192-z
    日期:2008.11
    A novel three-component synthesis has been developed for 1,3-diazapyrenes based on the reaction of 1,8-naphthalenediamine with triazine and carbonyl compounds in polyphosphoric acid (PPA). The use of benzonitrile in place of the carbonyl compounds in this reaction gives 6-phenyl-1,3,7-triazapyrenes.
  • Unexpected reaction of 1,8-naphthylenediamine and perimidines with 1,3,5-triazine in the presence of benzonitrile in polyphosphoric acid
    作者:I. V. Aksenova、A. V. Aksenov、A. S. Lyakhovnenko、I. V. Borovlev
    DOI:10.1007/s10593-008-0127-0
    日期:2008.7
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