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3a,5,5-Trimethyl-1,3-diphenyl-3a,4,5,6-tetrahydro-3H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine | 106366-67-0

中文名称
——
中文别名
——
英文名称
3a,5,5-Trimethyl-1,3-diphenyl-3a,4,5,6-tetrahydro-3H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine
英文别名
3a,4,5,6-Tetrahydro-3a,5,5-trimethyl-1,3-diphenyl-3H-1,2,4-triazolo<4,3a><1,5>benzodiazepine;3a,5,5-Trimethyl-1,3-diphenyl-4,6-dihydro-[1,2,4]triazolo[4,3-a][1,5]benzodiazepine
3a,5,5-Trimethyl-1,3-diphenyl-3a,4,5,6-tetrahydro-3H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine化学式
CAS
106366-67-0
化学式
C25H26N4
mdl
——
分子量
382.508
InChiKey
UMKOKNZULZFIBL-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):
    5.9
  • 重原子数:
    29
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    30.9
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2,2,4-三甲基-2,3-二氢-1H-1,5-苯并二氮杂卓N-苯基苯羰基亚肼酰氯三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 12.0h, 以70%的产率得到3a,5,5-Trimethyl-1,3-diphenyl-3a,4,5,6-tetrahydro-3H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine
    参考文献:
    名称:
    A Convenient Synthesis of Novel [1,2,4]Triazolo[4,3-a][1,5]benzodiazepine Derivatives
    摘要:
    本论文描述了一种通过腈亚胺与 2, 3-二氢-1H-1,5-苯并二氮杂卓的 [3 + 2] - 环加成,合成以前未知的 3a,4,5,6-四氢-3H-双[1,2,4]三唑并[4,3-a][1,5]苯并二氮杂卓系统的方法。以类似的方法,从 3H-1,5-苯并二氮杂卓制备了 3a,4,4a,5-四氢-3H-双[1,2,4]三唑并[4,3-a:3′,4′-d][1,5]苯并二氮杂卓体系。
    DOI:
    10.1055/s-1986-31628
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文献信息

  • AVERSA, M. C.;FERLAZZO, A.;GIANNETTO, P.;KOHNKE, F. H., SYNTHESIS, BRD, 1986, N 3, 230-231
    作者:AVERSA, M. C.、FERLAZZO, A.、GIANNETTO, P.、KOHNKE, F. H.
    DOI:——
    日期:——
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同类化合物

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