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2-(4-methoxyphenyl)-4-phenylthiazol-5-ylamine | 53628-47-0

中文名称
——
中文别名
——
英文名称
2-(4-methoxyphenyl)-4-phenylthiazol-5-ylamine
英文别名
2-(4-methoxyphenyl)-4-phenylthiazol-5-amine;2-(4-methoxy-phenyl)-4-phenyl-thiazol-5-ylamine;5-Amino-2-anisyl-4-phenyl-thiazol;2-(4-Methoxyphenyl)-4-phenyl-1,3-thiazol-5-amine;2-(4-methoxyphenyl)-4-phenyl-1,3-thiazol-5-amine
2-(4-methoxyphenyl)-4-phenylthiazol-5-ylamine化学式
CAS
53628-47-0
化学式
C16H14N2OS
mdl
——
分子量
282.366
InChiKey
DUAHRZJXYJCNQT-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):
    3.9
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    76.4
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-(4-methoxyphenyl)-4-phenylthiazol-5-ylamine1,3-苯并噻唑-2-羰酰氯吡啶 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以46%的产率得到N-(2-(4-methoxyphenyl)-4-phenylthiazol-5-yl)benzo[d]thiazole-2-carboxamide
    参考文献:
    名称:
    Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives
    摘要:
    A series of Ugi reactions has been successfully performed using ammonia as the amine component, employing 2,2,2-trifluoroethanol its a non-nucleophilic solvent in order to suppress known side reactions. Utilizing concentrated aqueous ammonia its it convenient Source, this approach offered a simple, one-step assembly of Ugi adducts suitable for elaboration into it variety of 5-aminoazole compounds through postcondensation modifications. Free or N-substituted 5-aminothiazoles and 5-(trifluoroacetamido)oxazoles were all prepared by this improved methodology. The scope of the synthetic route developed and application of the different products are discussed.
    DOI:
    10.1021/jo9014529
  • 作为产物:
    描述:
    参考文献:
    名称:
    Gewald,K. et al., Journal fur praktische Chemie (Leipzig 1954), 1974, vol. 316, p. 299 - 303
    摘要:
    DOI:
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文献信息

  • Synthesis of 5-aminothiazoles as building blocks for library synthesis
    作者:Mark J. Thompson、William Heal、Beining Chen
    DOI:10.1016/j.tetlet.2006.02.004
    日期:2006.4
    A convenient route to 4-phenyl-5-aminothiazoles is described, which offers control over Substitution at the 2-position. 2-N-Acylglycinamides were dithionated and a subsequent TFAA-mediated cyclisation step was followed by removal of the 5-N-trifluoroacetyl group providing the free amines. Though applicable generally the method was found to be most effective when introducing aromatic substituents at the 2-position, whereupon moderate overall yields of the 5-amino compounds were obtained. (c) 2006 Elsevier Ltd. All rights reserved.
  • Versatile assembly of 5-aminothiazoles based on the Ugi four-component coupling
    作者:Mark J. Thompson、Beining Chen
    DOI:10.1016/j.tetlet.2008.06.067
    日期:2008.9
    A flexible route to novel 5-aminothiazoles has been developed based on cyclisation of diamide adducts, prepared using the Ugi reaction, in the presence of Lawesson's reagent. The Walborsky reagent ( 1,1,3,3-tetramethylbutyl isocyanide) was used as the isonitrile component, facilitating subsequent deprotection of the N-alkyl group to yield free 5-aminothiazoles, which were prepared with a variety of substituents at the 2- and 4-positions. (C) 2008 Elsevier Ltd. All rights reserved.
  • [EN] THIAZOLE AND OXAZOLE DERIVATIVES FOR USE IN THE TREATMENT OF PRION DISEASES, CANCER AND CONDITIONS OF THE CENTRAL NERVOUS SYSTEM AS WELL AS IN THE REGULATION OF STEM CELLS<br/>[FR] DÉRIVÉS DE THIAZOLE ET D'OXAZOLE S'UTILISANT DANS LE TRAITEMENT DE MALADIES À PRIONS, DU CANCER ET DE TROUBLES DU SYSTÈME NERVEUX CENTRAL, ET DANS LA RÉGULATION DE CELLULES SOUCHES
    申请人:UNIV SHEFFIELD
    公开号:WO2008090382A1
    公开(公告)日:2008-07-31
    [EN] Compounds of the formula (I) are provided: Fomula (I) wherein X, Y, R1, R2 and R3 are as defined in the specification. The compounds may be useful in the treatment of various diseases and conditions, in particular prion diseases.
    [FR] L'invention concerne des composés représentés par la formule (I), dans laquelle X, Y, R1, R2 et R3 sont tels que définis dans la description. Ces composés peuvent être utiles dans le traitement de diverses maladies et affections, en particulier les maladies à prions.
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