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4-(4-chlorophenoxy)-6,7-dimethoxyquinazoline | 1593235-80-3

中文名称
——
中文别名
——
英文名称
4-(4-chlorophenoxy)-6,7-dimethoxyquinazoline
英文别名
——
4-(4-chlorophenoxy)-6,7-dimethoxyquinazoline化学式
CAS
1593235-80-3
化学式
C16H13ClN2O3
mdl
——
分子量
316.744
InChiKey
OYCYLNWTKGHMPA-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):
    4.09
  • 重原子数:
    22.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    53.47
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    4-(4-chlorophenoxy)-6,7-dimethoxyquinazoline 、 (3β,17β)-17-(benzoylthio)-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-androst-5-ene 在 hydridotetakis(triphenylphosphine)rhodium(I)1,2-双(二苯基膦基)苯 作用下, 以 氯苯 为溶剂, 反应 6.0h, 以73%的产率得到(3β,17β)-17-[4-(6,7-dimethoxyquinazolinyl)thio]-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]androst-5-ene
    参考文献:
    名称:
    Synthesis of Cycloalkyl/Steroidal Heteroaryl Sulfides Using Rhodium-Catalyzed Heteroaryl Exchange Reaction
    摘要:
    Cycloalkyl heteroaryl sulfides are efficiently synthesized by the single -bond cleavage and exchange reaction of S-cycloalkyl thioesters and heteroaryl ethers without using a base. The method is applicable to steroids at the A- and D -rings, and provides diverse heteroarylthiolated steroids with five- and six -membered heteroarenes.
    DOI:
    10.3987/com-19-14147
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文献信息

  • Rhodium-catalyzed synthesis of unsymmetric di(heteroaryl) compounds via heteroaryl exchange reactions
    作者:Mieko Arisawa
    DOI:10.1080/10426507.2019.1602621
    日期:2019.7.3
    activities by interacting with proteins and nucleic acids. Then, synthesis of such compounds is critical for the development of drugs. Unsymmetric HetAr-X-HetAr′ compounds were efficiently synthesized by rhodium-catalyzed heteroaryl exchange reactions, which involved equilibrium control by judicious design of organic heteroaryl reagents. This method allows synthesis of unsymmetric HetAr–O–HetAr′, HetAr–S–HetAr′
    摘要 不对称二(杂芳基)HetAr-X-HetAr'化合物具有柔性和刚性基团,有望通过与蛋白质和核酸相互作用而表现出多种生物活性。然后,此类化合物的合成对于药物开发至关重要。不对称 HetAr-X-HetAr' 化合物是通过催化的杂芳基交换反应有效合成的,该反应涉及通过有机杂芳基试剂的明智设计来控制平衡。该方法允许从杂芳基芳基醚和杂芳基试剂合成不对称 HetAr-O-HetAr'、HetAr-S-HetAr' 和 HetAr-CH2-HetAr' 化合物以及 HetAr-F 化合物。催化的杂芳基交换反应也用于从 N-苯甲酰基杂芳烃和杂芳基芳基醚合成 C-N 连接的二(杂芳基)化合物。该合成具有广泛的适用性,提供了多种新型不对称 HetAr-X-HetAr' 和 C-N 连接的二(杂芳基)化合物,其中含有五元和六元杂芳烃。图形概要
  • Rhodium-catalyzed synthesis of unsymmetrical di(aryl/heteroaryl)methanes using aryl/heteroarylmethyl ketones via CO–C bond cleavage
    作者:Guangzhe Li、Mieko Arisawa、Masahiko Yamaguchi
    DOI:10.1039/c4cc00816b
    日期:——
    RhH(PPh3)4 and 1,2-bis(diphenylphosphino)benzene catalyze the reaction of aryl/heteroarylmethyl ketones and aryl heteroaryl ethers giving unsymmetrical diarylmethanes containing one or two heteroarenes in high yields. The reaction does not use alkali metal bases, and therefore does not form large amounts of metal waste.
    RhH(PPh3)4和1,2-双(二苯基膦基)苯催化芳基/杂芳基甲基酮与芳基杂芳基醚的反应,从而高收率得到不对称的包含一个或两个杂芳烃的二芳基甲烷。该反应不使用碱属碱,因此不会形成大量的属废料。
  • Thieme Chemistry Journals Awardees – Where Are They Now? Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Ethers Using Heteroaryl Exchange Reaction
    作者:Mieko Arisawa、Masahiko Yamaguchi、Saori Tanii、Takaya Tougo、Kiyofumi Horiuchi
    DOI:10.1055/s-0036-1588801
    日期:2017.8
    di(heteroaryl) ethers were synthesized by the rhodium-catalyzed heteroaryl exchange reaction of heteroaryl aryl ethers and heteroaryl esters at equilibrium. Diverse unsymmetric di(heteroaryl) ethers containing five- and six-membered heteroarenes were obtained. Di(heteroaryl) ethers can be synthesized starting from diaryl ethers, because heteroaryl aryl ethers are obtained by the heteroaryl exchange reaction
    不对称二(杂芳基)醚是通过杂芳基芳基醚和杂芳基酯在平衡时的催化杂芳基交换反应合成的。获得了包含五元和六元杂芳烃的多种不对称二(杂芳基)醚。二(杂芳基)醚可以从二芳基醚开始合成,因为杂芳基芳基醚是通过二芳基醚的杂芳基交换反应获得的。
  • Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides
    作者:Mieko Arisawa、Saori Tanii、Takeru Tazawa、Masahiko Yamaguchi
    DOI:10.1039/c6cc05400e
    日期:——

    A rhodium complex catalyzed the conversion of the C–O bond of heteroaryl aryl ethers to the C–F bond.

    一种配合物催化了杂芳基芳基醚的C-O键转化为C-F键。
  • Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Sulfides Using Heteroaryl Ethers and <i>S</i>-Heteroaryl Thioesters via Heteroarylthio Exchange
    作者:Mieko Arisawa、Takeru Tazawa、Saori Tanii、Kiyofumi Horiuchi、Masahiko Yamaguchi
    DOI:10.1021/acs.joc.6b02585
    日期:2017.1.6
    Unsymmetric di(heteroaryl) sulfides were synthesized by a rhodium-catalyzed heteroarylthio exchange reaction of heteroaryl aryl ethers and S-(heteroaryl) thioesters. The reaction has broad applicability, giving diverse unsymmetric di(heteroaryl) sulfides containing five- and six-membered heteroarenes. No base is required in this reaction, which has been developed by the judicious design of organic substrates.
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