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4-phenyl-2H-pyrido [1,2-a]pyrimidine-2-one | 66156-19-2

中文名称
——
中文别名
——
英文名称
4-phenyl-2H-pyrido [1,2-a]pyrimidine-2-one
英文别名
4-phenyl-2H-pyrido[1,2-a]pyrimidin-2-one;4-phenyl-pyrido[1,2-a]pyrimidin-2-one;4-Phenyl-2H-pyrido<1,2-a>pyrimidin-2-on;4-phenylpyrido[1,2-a]pyrimidin-2-one
4-phenyl-2H-pyrido [1,2-a]pyrimidine-2-one化学式
CAS
66156-19-2
化学式
C14H10N2O
mdl
MFCD05149434
分子量
222.246
InChiKey
AHPOSBFUSLSSMD-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):
    1.8
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    32.7
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-ones utilizing activated alkynoates
    摘要:
    The synthesis of the biologically relevant, 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-one 7, is reported. Addition of substituted 2-aminopyridines 5 to activated alkynoates leads to the facile formation of a series of metabolically stable trifluoromethyl substituted pyrido[1,2-a]pyrimidines under mild conditions. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(03)00700-7
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文献信息

  • Metal and Solvent-Free Synthesis of 2<i>H</i>-Pyrido[1,2-<i>a</i>]pyrimidin-2-ones Catalyzed by Elemental Sulfur
    作者:Thangavel Pavithra、E. Sankari Devi、Subbiah Nagarajan、Vellaisamy Sridharan、C. Uma Maheswari
    DOI:10.1002/ejoc.201901356
    日期:2019.10.31
    method for the synthesis of 4‐methyl‐2H‐pyrido[1,2‐a]pyrimidin‐2one from β‐oxo esters and 2aminopyridine in the presence of sulfur was demonstrated. In this reaction, inexpensive and readily available starting materials and catalysts were employed. The advantages of this strategy are: (i) A neat, oxidant and metal free reaction. (ii) The reaction was tolerant to different β‐oxo esters and 2‐aminopyridines
    展示了一种在硫存在下由β-氧代酯和2-氨基吡啶合成4-甲基-2 H-吡啶并[1,2 - a ]嘧啶-2-酮的简单有效的方法。在该反应中,使用廉价且容易获得的起始原料和催化剂。该策略的优点是:(i)纯净,无氧化剂和无金属的反应。(ii)该反应可耐受不同的β-氧代酯和2-氨基吡啶
  • Copper(II)/Iron(III) Co-catalyzed Intermolecular Diamination of Alkynes: Facile Synthesis of Imidazopyridines
    作者:Jing Zeng、Yu Jia Tan、Min Li Leow、Xue-Wei Liu
    DOI:10.1021/ol301858j
    日期:2012.9.7
    A facile synthesis of imidazo[1,2-alpha]pyridines has been achieved by copper(II) and iron(III) co-catalyzed C-N bond formation. This reaction involves an intermolecular oxidative diamination of alkynes with high chemoselectivity and regioselectivity.
  • Palazzo; Tamburini, Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti, 1911, vol. <5> 20 I, p. 41
    作者:Palazzo、Tamburini
    DOI:——
    日期:——
  • Seide, Chemische Berichte, 1925, vol. 58, p. 354
    作者:Seide
    DOI:——
    日期:——
  • JPH04188068A
    申请人:——
    公开号:JPH04188068A
    公开(公告)日:1992-07-06
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