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(E)-N,N-bis(3-phenyl-2-propenyl)-1-naphthalenemethanamine | 98977-80-1

中文名称
——
中文别名
——
英文名称
(E)-N,N-bis(3-phenyl-2-propenyl)-1-naphthalenemethanamine
英文别名
(E)-N-(naphthalen-1-ylmethyl)-3-phenyl-N-[(E)-3-phenylprop-2-enyl]prop-2-en-1-amine
(E)-N,N-bis(3-phenyl-2-propenyl)-1-naphthalenemethanamine化学式
CAS
98977-80-1
化学式
C29H27N
mdl
——
分子量
389.54
InChiKey
MRIOCSXWLDBPRT-OTYYAQKOSA-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:
    586.2±50.0 °C(Predicted)
  • 密度:
    1.123±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.3
  • 重原子数:
    30
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.1
  • 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:
    1-萘甲基胺 在 sodium tetrahydroborate 、 sodium carbonate 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 0.33h, 生成 (E)-N,N-bis(3-phenyl-2-propenyl)-1-naphthalenemethanamine
    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

  • N-Heterocyclic Carbene C,S Palladium(II) π-Allyl Complexes: Synthesis, Characterization, and Catalytic Application In Allylic Amination Reactions
    作者:Deepa Krishnan、Meiyi Wu、Minyi Chiang、Yongxin Li、Pak-Hing Leung、Sumod A. Pullarkat
    DOI:10.1021/om400110t
    日期:2013.4.22
    carbene C,S palladium(II) π-allyl complexes were successfully developed and characterized. Structural analyses of these complexes revealed that the organopalladium chelates adopt a skew-envelope conformation with a trans disposition of the substituents on the metal chelate rings. Utilizing these C,S palladium(II) π-allyl complexes as catalysts, a catalytic system for the allylic amination reaction has
    成功开发并表征了一系列五元N-杂环卡宾C,S钯(II)π-烯丙基配合物。对这些配合物的结构分析表明,有机钯螯合物采用偏斜包络构象,且金属螯合物环上的取代基发生转位。利用这些C,S钯(II)π-烯丙基络合物作为催化剂,已经开发出用于烯丙基胺化反应的催化体系。胺与不对称取代的烯丙基碳酸酯之间的一系列C–N键形成可通过区域选择性方式的复杂(±)-9高效催化。
  • Direct Use of Allylic Alcohols for Platinum-Catalyzed Monoallylation of Amines
    作者:Masaru Utsunomiya、Yoshiki Miyamoto、Junji Ipposhi、Takashi Ohshima、Kazushi Mashima
    DOI:10.1021/ol071365s
    日期:2007.8.1
    A new direct catalytic amination of allylic alcohols promoted by the combination of platinum and a large bite-angle ligand DPEphos was developed in which the allylic alcohol was effectively converted to a pi-allylplatinum intermediate without the use of an activating reagent. The use of the DPEphos ligand was essential for obtaining high catalyst activity and high monoallylation selectivity of primary
    通过铂和大咬角配体DPEphos的结合促进了新的烯丙基醇的直接催化胺化反应,其中不使用活化剂就将烯丙基醇有效地转化为π-烯丙基铂中间体。DPEphos配体的使用对于获得高催化剂活性和伯胺的高单烯丙基化选择性至关重要,从而可以形成多种单烯丙基化产物,收率良好。
  • 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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