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2-(1-oxo-[4-methoxyphenyl]methyl)-6-(4-methoxyphenyl)pyrazine | 700875-15-6

中文名称
——
中文别名
——
英文名称
2-(1-oxo-[4-methoxyphenyl]methyl)-6-(4-methoxyphenyl)pyrazine
英文别名
[6-(p-methoxyphenyl)pyrazin-2-yl](p-methoxyphenyl)methanone;6-(4-methoxyphenyl)-2-((4-methoxyphenyl)carbonyl)pyrazine;(4-methoxyphenyl)-[6-(4-methoxyphenyl)pyrazin-2-yl]methanone
2-(1-oxo-[4-methoxyphenyl]methyl)-6-(4-methoxyphenyl)pyrazine化学式
CAS
700875-15-6
化学式
C19H16N2O3
mdl
——
分子量
320.348
InChiKey
VKDMKEAQSHCXMX-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):
    3.1
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    61.3
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-(1-oxo-[4-methoxyphenyl]methyl)-6-(4-methoxyphenyl)pyrazine2,2,6,6-四甲基哌啶正丁基锂 、 APTS 作用下, 以 四氢呋喃正己烷甲苯 为溶剂, 反应 13.5h, 生成 2-(1-hydroxy-[4-methoxyphenyl]methyl)-3-(2-[4-methoxyphenyl]-1,3-dioxolan-2-yl)-5-(4-methoxyphenyl)pyrazine
    参考文献:
    名称:
    从葡萄灰霉病菌合成吡嗪生物碱。二嗪43
    摘要:
    吡嗪的区域选择性金属化和交叉偶联反应提供了容易获得硼替拉嗪A和B以及硼替拉嗪A的异构体的优点,并且氯吡嗪的收率很高。
    DOI:
    10.1021/jo0478196
  • 作为产物:
    描述:
    6-(4-Methoxy-phenyl)-pyrazine-2-carbonyl chloride 在 叔丁基锂 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 13.75h, 生成 2-(1-oxo-[4-methoxyphenyl]methyl)-6-(4-methoxyphenyl)pyrazine
    参考文献:
    名称:
    Synthesis of Naturally Occurring Pyrazine and Imidazole Alkaloids from Botryllus LeachiRID=?a?ID=?a? Dedicated to Prof. G . Märkl on the occasion of his 75 th birthday
    摘要:
    The synthesis of the naturally occurring and biologically active alkaloids 1 and 2, first isolated from the red ascidian Botryllus leachi by Duran et al. [1], is described and the structure proposed for Botryllazine B (1) is confirmed. The analytical data for 2-(p-hydroxybenzoyl)-4-(p-hydroxyphenyl)imidazole (2) are discussed and compared with the literature. With special emphasis of H-1 NMR data the tautomerism of aroylimidazolemethanones is described.
    DOI:
    10.1007/s00706-003-0085-2
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文献信息

  • Scope and Limitation for FeSO<sub>4</sub>-Mediated Direct Arylation of Heteroarenes with Arylboronic Acids and Its Synthetic Applications
    作者:Kimihiro Komeyama、Yuya Nagao、Manabu Abe、Ken Takaki
    DOI:10.1246/bcsj.20130166
    日期:2014.2.15
    FeSO4-mediated direct arylation of heteroarenes with arylboronic acids in the presence of K2S2O8 has been developed. A slow addition of an aqueous solution of an iron complex was crucial in the ary...
    已经开发了在 K2S2O8 存在下 FeSO4 介导的杂芳烃与芳基硼酸的直接芳基化。缓慢添加铁络合物的水溶液在 ary...
  • Synthesis and in vitro evaluation of botryllazine B analogues as a new class of inhibitor against human aldose reductase
    作者:Ryota Saito、Mai Tokita、Keisuke Uda、Chikako Ishikawa、Mitsutoshi Satoh
    DOI:10.1016/j.tet.2009.01.020
    日期:2009.4
    Botryllazine B analogues of diverse substitution patterns have been prepared, and their in vitro inhibitory activities against recombinant human aldose reductase (h-ALR2) evaluated. Among the 15 compounds tested, 6-(4-aminophenyl)-2-(4-hydroxyphenyl)carbonylpyrazine (7b) proved to be the most potent inhibitor, with IC50=0.91 mu M. Kinetic analyses of 7b and botryllazine B(1) revealed that these inhibitors exhibit an unprecedented mixed-type inhibition on h-ALR2 with respect to the substrate D,L-glyceraldehyde, in the presence of NADPH at inhibitor concentrations near the IC50 values. (C) 2009 Elsevier Ltd. All rights reserved.
  • Synthesis of Pyrazine Alcaloids from <i>Botryllus </i><i>leachi</i>. Diazines 43
    作者:Frédéric Buron、Nelly Plé,、Alain Turck、Guy Queguiner
    DOI:10.1021/jo0478196
    日期:2005.4.1
    Regioselective metalation of pyrazines and cross-coupling reactions provides an easy access to botryllazines A and B and to an isomer of botryllazine A with good yields from chloropyrazine.
    吡嗪的区域选择性金属化和交叉偶联反应提供了容易获得硼替拉嗪A和B以及硼替拉嗪A的异构体的优点,并且氯吡嗪的收率很高。
  • Synthesis of Naturally Occurring Pyrazine and Imidazole Alkaloids from Botryllus LeachiRID=?a?ID=?a? Dedicated to Prof. G . Märkl on the occasion of his 75 th birthday
    作者:Siavosh Mahboobi、Andreas Sellmer、Thomas Burgemeister、Alexei Lyssenko、Dieter Schollmeyer
    DOI:10.1007/s00706-003-0085-2
    日期:2004.3.1
    The synthesis of the naturally occurring and biologically active alkaloids 1 and 2, first isolated from the red ascidian Botryllus leachi by Duran et al. [1], is described and the structure proposed for Botryllazine B (1) is confirmed. The analytical data for 2-(p-hydroxybenzoyl)-4-(p-hydroxyphenyl)imidazole (2) are discussed and compared with the literature. With special emphasis of H-1 NMR data the tautomerism of aroylimidazolemethanones is described.
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