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2,4-bis(4-methoxyphenyl)-2,7,8-trimethyl-2,3-dihydro-1H-benzo[b][1,4]diazepine | 1369787-56-3

中文名称
——
中文别名
——
英文名称
2,4-bis(4-methoxyphenyl)-2,7,8-trimethyl-2,3-dihydro-1H-benzo[b][1,4]diazepine
英文别名
2,4-Bis(4-methoxyphenyl)-2,7,8-trimethyl-1,3-dihydro-1,5-benzodiazepine;2,4-bis(4-methoxyphenyl)-2,7,8-trimethyl-1,3-dihydro-1,5-benzodiazepine
2,4-bis(4-methoxyphenyl)-2,7,8-trimethyl-2,3-dihydro-1H-benzo[b][1,4]diazepine化学式
CAS
1369787-56-3
化学式
C26H28N2O2
mdl
——
分子量
400.521
InChiKey
PWKJQCNLKIFTJR-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):
    5.4
  • 重原子数:
    30
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    42.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    4,5-二甲基-1,2-苯二胺4-乙炔基苯甲醚 在 mercuric triflate 作用下, 以 乙醇 为溶剂, 反应 2.5h, 以62%的产率得到2,4-bis(4-methoxyphenyl)-2,7,8-trimethyl-2,3-dihydro-1H-benzo[b][1,4]diazepine
    参考文献:
    名称:
    Terminal alkynes as keto-methyl equivalent toward one pot synthesis of 1,5-benzodiazepine derivatives under catalysis of Hg(OTf)2
    摘要:
    Mercuric triflate catalyzes the reaction between 1,2-diaminobenzene and terminal alkynes to afford 2,4-disubstituted 2-methyl-2,3-dihydro-1H-benzo[b][1,4]diazepine in an excellent yield. The terminal alkynes function as a source of keto-methyl equivalent. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.01.036
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文献信息

  • Graphite oxide: a metal free highly efficient carbocatalyst for the synthesis of 1,5-benzodiazepines under room temperature and solvent free heating conditions
    作者:Ramen Jamatia、Ajay Gupta、Binoyargha Dam、Mithu Saha、Amarta Kumar Pal
    DOI:10.1039/c6gc03110b
    日期:——
    We report a sustainable and metal free carbocatalyst, graphite oxide, for the synthesis of 1,5-benzodiazepines under room temperature and solvent free heating conditions.
    我们报告了一种在室温和无溶剂加热条件下合成1,5-苯并二氮杂pine的可持续且无金属的碳催化剂,氧化石墨。
  • A green and sustainable approach for the synthesis of 1,5-benzodiazepines and spirooxindoles in one-pot using a MIL-101(Cr) metal–organic framework as a reusable catalyst
    作者:Fillip Kumar Sarkar、Ajay Gupta、Ramen Jamatia、Jasha Momo H. Anal、Amarta Kumar Pal
    DOI:10.1039/d1nj03176g
    日期:——
    MIL-101(Cr) has been efficiently utilized for the synthesis of biologically relevant heterocycles such as 1,5-benzodiazepines and spirooxindoles in one-pot. MIL-101(Cr) was prepared via a solvothermal method and characterized by FT-IR, PXRD, SEM, TEM, EDX, and ICP-OES analysis. Thermogravimetric analysis (TGA) described its high thermal stability. Low catalyst loading, easy separation, reusability, and high
    金属-有机骨架 MIL-101(Cr) 已被有效地用于合成生物相关的杂环,如 1,5-苯二氮卓类和螺环吲哚。MIL-101(Cr) 是通过溶剂热法制备的,并通过 FT-IR、PXRD、SEM、TEM、EDX 和 ICP-OES 分析进行表征。热重分析 (TGA) 描述了其高热稳定性。低催化剂负载、易于分离、可重复使用和高产率是该协议的一些显着特点。无溶剂反应条件 (SFRC) 或水作为溶剂是绿色和可持续工艺开发领域的一些额外优势。
  • Terminal alkynes as keto-methyl equivalent toward one pot synthesis of 1,5-benzodiazepine derivatives under catalysis of Hg(OTf)2
    作者:Gourhari Maiti、Utpal Kayal、Rajiv Karmakar、Rudraksha N. Bhattacharya
    DOI:10.1016/j.tetlet.2012.01.036
    日期:2012.3
    Mercuric triflate catalyzes the reaction between 1,2-diaminobenzene and terminal alkynes to afford 2,4-disubstituted 2-methyl-2,3-dihydro-1H-benzo[b][1,4]diazepine in an excellent yield. The terminal alkynes function as a source of keto-methyl equivalent. (C) 2012 Elsevier Ltd. All rights reserved.
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