2-methoxymethylquinazolin-4(3H)-one | 21721-76-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 2-methoxymethylquinazolin-4(3H)-one
• 英文别名: 2-(methoxymethyl)-3H-quinazolin-4-one
• CAS: 21721-76-6
• 化学式: C₁₀H₁₀N₂O₂
• mdl: MFCD28011030
• 分子量: 190.202
• InChiKey: VBDBTBAAJPBZAI-UHFFFAOYSA-N

物化性质

• 沸点：
  328.5±44.0 °C(Predicted)
• 密度：
  1.27±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.6
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  50.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-methoxymethylquinazolin-4(3H)-one 在 四溴化碳 、 氢溴酸 、 三苯基膦 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 22.0h， 生成 2-(bromomethyl)-4(3H)-quinazolinone
  参考文献：
  名称：

  Chemical Probes to Study ADP-Ribosylation: Synthesis and Biochemical Evaluation of Inhibitors of the Human ADP-Ribosyltransferase ARTD3/PARP3

  摘要：

  The racemic 3-(4-oxo-3,4-dihydroquinazolin-2-yl)-N-[1-(pyridin-2-yl)ethyl]propanamide, 1, has previously been identified as a potent but unselective inhibitor of diphtheria toxin-like ADP-ribosyltransferase 3 (ARTD3). Herein we describe synthesis and evaluation of SS compounds in this class. It was found that the stereochemistry is of great importance for both selectivity and potency and that substituents on the phenyl ring resulted in poor solubility. Certain variations at the meso position were tolerated and caused a large shift in the binding pose. Changes to the ethylene linker that connects the quinazolinone to the amide were also investigated but proved detrimental to binding. By combination of synthetic organic chemistry and structure-based design, two selective inhibitors of ARTD3 were discovered.

  DOI：

  10.1021/jm401394u
• 作为产物：
  描述：

  2-methoxyacetamidobenzonitrile 在 过氧化脲素 、 potassium carbonate 作用下， 以 水 、 丙酮 为溶剂， 以77%的产率得到2-methoxymethylquinazolin-4(3H)-one
  参考文献：
  名称：

  Chemical Probes to Study ADP-Ribosylation: Synthesis and Biochemical Evaluation of Inhibitors of the Human ADP-Ribosyltransferase ARTD3/PARP3

  摘要：

  The racemic 3-(4-oxo-3,4-dihydroquinazolin-2-yl)-N-[1-(pyridin-2-yl)ethyl]propanamide, 1, has previously been identified as a potent but unselective inhibitor of diphtheria toxin-like ADP-ribosyltransferase 3 (ARTD3). Herein we describe synthesis and evaluation of SS compounds in this class. It was found that the stereochemistry is of great importance for both selectivity and potency and that substituents on the phenyl ring resulted in poor solubility. Certain variations at the meso position were tolerated and caused a large shift in the binding pose. Changes to the ethylene linker that connects the quinazolinone to the amide were also investigated but proved detrimental to binding. By combination of synthetic organic chemistry and structure-based design, two selective inhibitors of ARTD3 were discovered.

  DOI：

  10.1021/jm401394u

文献信息

• Metal- and Oxidant-Free Synthesis of Quinazolinones from <i>β</i>-Ketoesters with <i>o</i>-Aminobenzamides via Phosphorous Acid-Catalyzed Cyclocondensation and Selective C–C Bond Cleavage
  作者：Zhongwen Li、Jianyu Dong、Xiuling Chen、Qiang Li、Yongbo Zhou、Shuang-Feng Yin

  DOI：10.1021/acs.joc.5b00937

  日期：2015.10.2

  and efficient phosphorous acid-catalyzed cyclocondensation of β-ketoesters with o-aminobenzamides via selective C–C bond cleavage leading to quinazolinones is developed. This reaction proceeds smoothly under metal- and oxidant-free conditions, giving both 2-alkyl- and 2-aryl-substituted quinazolinones in excellent yields. This strategy can also be applied to the synthesis of other N-heterocycles, such

  通过选择性的CC键裂解产生喹唑啉酮，开发了一种通用且有效的亚磷酸催化β-酮酯与邻氨基苯甲酰胺的环缩合反应。该反应在无金属和无氧化剂的条件下顺利进行，从而以优异的收率得到2-烷基和2-芳基取代的喹唑啉酮。该策略也可以用于合成其他N-杂环，例如苯并咪唑和苯并噻唑。
• Phosphorous acid functionalized polyacrylonitrile fibers with a polarity tunable surface micro-environment for one-pot C–C and C–N bond formation reactions
  作者：Gang Xu、Lu Wang、Mengmeng Li、Minli Tao、Wenqin Zhang

  DOI：10.1039/c7gc02935g

  日期：——

  hydrophobic surface micro-environment of the fiber catalysts is proven to promote the catalytic activities impressively in cyclocondensation of β-ketoesters with 2-aminobenzamides, the Knoevenagel condensation as well as the multi-component Biginelli reactions in green solvents. Both the surface synergy of the catalytic sites and hydrophobic auxiliary groups (benzyl or n-butyl) in the surface of fiber catalysts

  纤维催化剂的制备和应用引起了人们的广泛关注。然而，尽管特别重要，但是关于纤维催化剂的微环境对催化活性的影响的研究是有限的。在这项工作中，报道了一种通过疏水基团合成极性可调的表面微环境的磷酸官能化聚丙烯腈纤维的新策略，用于一锅式C–C和C–N键形成反应。事实证明，纤维催化剂的特殊疏水表面微环境可显着提高β-酮酸酯与2-氨基苯甲酰胺的环缩合，Knoevenagel缩合以及在绿色溶剂中的多组分Biginelli反应的催化活性。催化位点的表面协同作用和疏水性辅助基团（苄基或纤维催化剂表面的正丁基）和反应介质中的界面加速在高效提高催化活性方面起着重要作用。因此，提出了一种表面协同机理来解释微环境效应。另外，可以使用镊子将纤维催化剂简单地从反应体系中分离出来，并直接用于下一循环而无需进一步处理。重要的是，即使在水或乙醇中进行10个反应循环后，其催化活性也不会显着降低。结果表明，磷酸功能化纤维显示出绿色和可持续的工业生产潜力。
• Disubstituted 6-aminoquinazolinones
  申请人：Merck & Co., Inc.

  公开号：US05385894A1

  公开（公告）日：1995-01-31

  Novel disubstituted 6-aminoquinazolinones of the Formula (I), are useful as angiotensin II antagonists: ##STR1##

  式(I)中的新型双取代6-氨基喹唑啉酮化合物是一种有效的血管紧张素II拮抗剂：##STR1##
• AT-2 antagonist inhibition of vascular restenosis
  申请人：Merck & Co., Inc.

  公开号：US05409926A1

  公开（公告）日：1995-04-25

  Novel disubstituted 6-aminoquinazolinones of the Formula ##STR1## are useful as angiotensin-II receptor (subtype 2) antagonists (AT.sub.2 antagonists) alone or in combination with heparin, and can act to suppress the vascular stenosis which commonly occurs during the development of atherosclerosis and the restenosis following arterial angioplasty, stent placement, bypass surgery, heart transplantation or endarterectomy.

  公式为##STR1##的新型二取代6-氨基喹唑啉酮化合物可作为血管紧张素-II受体（亚型2）拮抗剂（AT.sub.2拮抗剂）单独或与肝素联合使用，并可抑制动脉粥样硬化发展过程中常见的血管狭窄和动脉成形术、支架置入、搭桥手术、心脏移植或内膜切除术后的再狭窄。
• A Facile Route to Quinazolin-4(3<i>H</i>)-ones Functionalised at the 2-Position
  作者：V. Bavetsias

  DOI：10.1080/00397919808004519

  日期：1998.12

  Treatment of 2-methoxyacetamidobenzonitriles or 2-chloroacetamidobenzonitrile with UHP and K2CO3 provides a convenient route to 2-methoxymethyl- or 2-chloromethylquinazolin-4(3H)-ones. In addition, demethylation of 2-methoxymethylquinazolin-4(3H)-ones with 48% HBr gives 2-hydroxymethylquinazolin-4(3H)-ones.