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3-benzylamino-2-phenylquinazolinone | 81107-41-7

中文名称
——
中文别名
——
英文名称
3-benzylamino-2-phenylquinazolinone
英文别名
3-(benzylamino)-2-phenylquinazolin-4(3H)-one;3-(Benzylamino)-2-phenylquinazolin-4-one
3-benzylamino-2-phenylquinazolinone化学式
CAS
81107-41-7
化学式
C21H17N3O
mdl
——
分子量
327.385
InChiKey
DXHSEUQUNQRHMX-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):
    3.8
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    44.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Pd-Catalyzed Intramolecular Aerobic Oxidative C–H Amination of 2-Aryl-3-(arylamino)quinazolinones: Synthesis of Fluorescent Indazolo[3,2-b]quinazolinones
    摘要:
    A palladium-catalyzed intramolecular aerobic oxidative C-H amination of 2-aryl-3-(arylamino)quinazolinones has been developed, providing a variety of substituted indazolo[3,2-b]quinazolinone derivatives in moderate to excellent yields. Preliminary mechanistic studies suggested that a palladacycle dimer could be the key intermediate, which underwent a cascade "rollover" cyclometalation and C-H amination sequence. Furthermore, the potential utility of these products has been demonstrated as a new class of blue fluorophores for fluorescent materials.
    DOI:
    10.1021/ol5026553
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文献信息

  • QUINAZOLINONE MODULATORS OF TGR5
    申请人:Pinkerton Anthony B.
    公开号:US20090035306A1
    公开(公告)日:2009-02-05
    The present invention relates to quinazolinone compounds useful as modulators of TGR5 and methods for the treatment or prevention of metabolic, cardiovascular, and inflammatory diseases.
    本发明涉及喹唑酮类化合物,可用作TGR5调节剂,并用于治疗或预防代谢性、心血管和炎症性疾病的方法。
  • Palladium-Catalyzed Cascade Reaction of 2-Amino-<i>N</i>′-arylbenzohydrazides with Triethyl Orthobenzoates To Construct Indazolo[3,2-<i>b</i>]quinazolinones
    作者:Weiguang Yang、Rui Qiao、Jiuxi Chen、Xiaobo Huang、Miaochang Liu、Wenxia Gao、Jinchang Ding、Huayue Wu
    DOI:10.1021/jo5024848
    日期:2015.1.2
    A palladium-catalyzed sequential cyclization/C-H activation cascade reaction of 2-amino-N'-arylbenzohydrazides with triethyl orthobenzoates has been developed, providing indazolo[3,2-b]quinazolinones in good to high yields. Two key intermediates of the reaction, 2-phenyl-3-(phenylamino)quinazolinone and C-H insertion palladacycle, were isolated, and their structures were unambiguously confirmed by X-ray crystallography. This method represents an unprecedented example of a halogen-free protocol to access indazolo[3,2-b]quinazolinones. Moreover, this chemistry also provides a useful tool for the discovery of fluorescent materials.
  • ABOUL-ENEIN M. N.; EID A. I., PHARMAC. ACTA HELV., 1981, 56, NO 8, 239-240
    作者:ABOUL-ENEIN M. N.、 EID A. I.
    DOI:——
    日期:——
  • [EN] QUINAZOLINONE MODULATORS OF TGR5<br/>[FR] MODULATEURS QUINAZOLINONES DE TGR5
    申请人:KALYPSYS INC
    公开号:WO2008067219A2
    公开(公告)日:2008-06-05
    [EN] The present invention relates to quinazolinone compounds useful as modulators of TGR5 and methods for the treatment or prevention of metabolic, cardiovascular, and inflammatory diseases.
    [FR] Cette invention concerne des composés quinazolinones utilisés en tant que modulateurs de TGR5 ainsi que des méthodes permettant de traiter ou de prévenir des maladies métaboliques, cardiovasculaires et inflammatoires.
  • Pd-Catalyzed Intramolecular Aerobic Oxidative C–H Amination of 2-Aryl-3-(arylamino)quinazolinones: Synthesis of Fluorescent Indazolo[3,2-<i>b</i>]quinazolinones
    作者:Weiguang Yang、Jiuxi Chen、Xiaobo Huang、Jinchang Ding、Miaochang Liu、Huayue Wu
    DOI:10.1021/ol5026553
    日期:2014.10.17
    A palladium-catalyzed intramolecular aerobic oxidative C-H amination of 2-aryl-3-(arylamino)quinazolinones has been developed, providing a variety of substituted indazolo[3,2-b]quinazolinone derivatives in moderate to excellent yields. Preliminary mechanistic studies suggested that a palladacycle dimer could be the key intermediate, which underwent a cascade "rollover" cyclometalation and C-H amination sequence. Furthermore, the potential utility of these products has been demonstrated as a new class of blue fluorophores for fluorescent materials.
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