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3-phenyl-2-(pyridin-3-yl)-2,3-dihydroquinazolin-4(1H)-one | 1429192-02-8

中文名称
——
中文别名
——
英文名称
3-phenyl-2-(pyridin-3-yl)-2,3-dihydroquinazolin-4(1H)-one
英文别名
3-Phenyl-2-pyridin-3-yl-1,2-dihydroquinazolin-4-one;3-phenyl-2-pyridin-3-yl-1,2-dihydroquinazolin-4-one
3-phenyl-2-(pyridin-3-yl)-2,3-dihydroquinazolin-4(1H)-one化学式
CAS
1429192-02-8
化学式
C19H15N3O
mdl
——
分子量
301.348
InChiKey
GBOAOGPUWZZDAT-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

物化性质

  • 沸点:
    535.5±50.0 °C(Predicted)
  • 密度:
    1.248±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    45.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    N-phenyl-2-[(3-pyridinylmethylene)amino]benzamide 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 以144 mg的产率得到3-phenyl-2-(pyridin-3-yl)-2,3-dihydroquinazolin-4(1H)-one
    参考文献:
    名称:
    N-Methyldihydroquinazolinone Derivatives of Retro-2 with Enhanced Efficacy against Shiga Toxin
    摘要:
    The Retro-2 molecule protects cells against Shiga toxins by specifically blocking retrograde transport from early endosomes to the trans-Golgi network A SAR study has been carried out to identify more potent compounds. Cyclization and modifications of Retro-2 led to a compound with roughly 100 fold improvement of the EC50 against Shiga toxin cytotoxicity measured in a cell protein synthesis assay. We also demonstrated that only one enantiomer of the dihydroquinazolinone reported herein is bioactive.
    DOI:
    10.1021/jm4002346
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文献信息

  • Microwave-promoted one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions
    作者:Yang Yang、Renzhong Fu、Yang Liu、Jing Cai、Xiaojun Zeng
    DOI:10.1016/j.tet.2020.131312
    日期:2020.7
    3-dihydroquinazoline-4(1H)-one derivatives have been synthesized via one-pot three-component reaction using isatoic anhydrides, amines and aldehydes (or ketones) catalyzed by heteropolyanion-based ionic liquids under microwave-promoted conditions. The practical protocol was found to tolerate a wide range of substrates with different functional groups. Moderate to excellent yields, solvent-free media and operational
    在微波促进下,通过杂多阴离子基离子液体催化的等位酸酐,胺和醛(或酮)通过一锅三组分反应合成了一系列2,3-二氢喹唑啉-4(1 H)-one衍生物。条件。发现该实用方案可耐受具有不同官能团的多种底物。中等至极好的产量,无溶剂介质和操作简便是主要亮点。此外,催化剂可以回收和再利用而没有明显的反应性损失。与现有方法相比,该方法提供了绿色且经过改进的协议。
  • CuO nanoparticles catalyzed simple and efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones under ultrasound irradiation in aqueous ethanol under ultrasound irradiation in aqueous ethanol
    作者:Jin Zhang、Decheng Ren、Yangmin Ma、Weitao Wang、Hao Wu
    DOI:10.1016/j.tet.2014.05.059
    日期:2014.8
    A CuO nanoparticle-catalyzed one-pot process has engineered for the preparation of diverse quinazolinones from the readily available isatoic anhydride, aldehydes and amine or ammonium. For amine substrates the reactions afford 2,3-dihydroquinazolin-4(1H)-ones in aqueous ethanol promoted by ultrasound irradiation. However, the ammonium substrates undergo intramolecular electron transfer and rearrangement
    一种由CuO纳米颗粒催化的一锅法,经设计可从容易获得的等角酸酐,醛和胺或制备各种喹唑啉酮。对于胺底物,反应得到在乙醇溶液中由超声辐射促进的2,3-二氢喹唑啉-4(1 H)-one。然而,底物经历分子内电子转移和重排产生喹唑啉-4(3 H)一。该催化剂可循环使用四次而不会损失任何实质活性。其他显着特征还包括广泛的官能团耐受性(合成了46种喹唑啉酮,首先报道了其中的9种),并在温和条件下提供了中等至优异的收率。
  • Corrigendum to “Microwave-promoted one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions” [Tetrahedron Lett. 76/27 (2020) 131312]
    作者:Yang Yang、Renzhong Fu、Yang Liu、Jing Cai、Xiaojun Zeng
    DOI:10.1016/j.tet.2020.131419
    日期:2020.9
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