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萘替芳Z异构体 | 65473-08-7

中文名称
萘替芳Z异构体
中文别名
——
英文名称
(Z)-N-methyl-N-(3-phenyl-2-propenyl)-1-naphthalenemethanamine
英文别名
cis-naftifine;(Z)-N-methyl-N-(naphthalen-1-ylmethyl)-3-phenylprop-2-en-1-amine
萘替芳Z异构体化学式
CAS
65473-08-7
化学式
C21H21N
mdl
——
分子量
287.404
InChiKey
OZGNYLLQHRPOBR-FLIBITNWSA-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

物化性质

  • 沸点:
    440.1±24.0 °C(Predicted)
  • 密度:
    1.082±0.06 g/cm3(Predicted)
  • 溶解度:
    氯仿(少量溶解)、DMSO(少量溶解)、乙酸乙酯(少量溶解)、甲醇(少量溶解)

计算性质

  • 辛醇/水分配系数(LogP):
    5.1
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

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

反应信息

  • 作为产物:
    描述:
    N-methyl-N-(3-phenyl-2-propynyl)-1-naphthalenemethanamine 在 Pd-BaSO4 氢气 作用下, 以 吡啶 为溶剂, 以44%的产率得到萘替芳Z异构体
    参考文献:
    名称:
    Synthesis and structure-activity relationships of naftifine-related allylamine antimycotics
    摘要:
    Naftifine (1) is the first representative of the new antifungal allylamine derivatives. Its biological activity is strictly bound to specific structural requirements that are unrelated to those of known antifungals. A tertiary allylamine function seems to be a prerequisite for activity against fungi. By systematic variation of the individual structural elements in 1, detailed structure-activity relationships are defined in which the phenyl ring is the structural feature permitting the widest variations. Versatile synthetic routes to allylamine derivatives and comparative biological data are presented.
    DOI:
    10.1021/jm00151a019
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文献信息

  • One-Pot Multicomponent Synthesis of Allyl and Alkylamines Using a Catalytic System Composed of Ruthenium Nanoparticles on Copper <i>N</i>-Heterocyclic Carbene-Modified Silica
    作者:Deepti Kalsi、Savarithai J. Louis Anandaraj、Manisha Durai、Claudia Weidenthaler、Meike Emondts、Steven P. Nolan、Alexis Bordet、Walter Leitner
    DOI:10.1021/acscatal.2c04044
    日期:2022.12.16
    integrated one-pot synthesis of valuable allylamines and alkylamines from amines, formaldehyde, and terminal alkynes is achieved using a single catalyst material. This multifunctional catalytic system is composed of a silica support on which are jointly assembled ruthenium nanoparticles and covalently functionalized copper N-heterocyclic carbene (NHC) complexes, introducing a new generation of nanoparticles
    使用单一催化剂材料实现了从胺、甲醛和末端炔烃中一锅法合成有价值的烯丙胺和烷基胺。这种多功能催化系统由二氧化硅载体组成,在其上共同组装了钌纳米粒子和共价功能化的铜N-杂环卡宾 (NHC) 配合物,引入了新一代固定在分子修饰表面上的纳米粒子。通过多种技术研究了所得 Ru@SiO 2 -[Cu-NHC] 材料的结构、结构、形态和电子特性,包括 N 2吸附、固态核磁共振、电子显微镜和 X 射线光电子能谱. Ru@SiO 2-[Cu-NHC] 被发现对一系列烯丙胺和烷基胺的一锅法合成具有活性和选择性,这些产品在精细化工和制药工业中非常重要。详细研究表明,固定化分子 Cu(I)–NHC 络合物负责胺、甲醛和末端炔烃的原子高效 A 3偶联,而所得炔丙基胺的选择性氢化由 Ru(0) 纳米粒子催化. 在单个载体上结合分子和纳米粒子位点的设计策略和制备方法非常灵活,为开发能够在一锅中进行复杂反应序列的多功能催化系统开辟了道路。
  • Thoma; Kuebler; Reimann, Pharmazie, 1997, vol. 52, # 5, p. 362 - 373
    作者:Thoma、Kuebler、Reimann
    DOI:——
    日期:——
  • BERNEY, D.
    作者:BERNEY, D.
    DOI:——
    日期:——
  • Synthesis and structure-activity relationships of naftifine-related allylamine antimycotics
    作者:Anton Stuetz、Apostolos Georgopoulos、Waltraud Granitzer、Gabor Petranyi、Daniel Berney
    DOI:10.1021/jm00151a019
    日期:1986.1
    Naftifine (1) is the first representative of the new antifungal allylamine derivatives. Its biological activity is strictly bound to specific structural requirements that are unrelated to those of known antifungals. A tertiary allylamine function seems to be a prerequisite for activity against fungi. By systematic variation of the individual structural elements in 1, detailed structure-activity relationships are defined in which the phenyl ring is the structural feature permitting the widest variations. Versatile synthetic routes to allylamine derivatives and comparative biological data are presented.
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