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1,1-Dimethyl-3-(1-naphthalen-1-yl-3-oxo-3-phenylpropyl)urea

中文名称
——
中文别名
——
英文名称
1,1-Dimethyl-3-(1-naphthalen-1-yl-3-oxo-3-phenylpropyl)urea
英文别名
1,1-dimethyl-3-(1-naphthalen-1-yl-3-oxo-3-phenylpropyl)urea
1,1-Dimethyl-3-(1-naphthalen-1-yl-3-oxo-3-phenylpropyl)urea化学式
CAS
——
化学式
C10H19N2O4PolS
mdl
——
分子量
346.4
InChiKey
AVQSMXNOWAIDEQ-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):
    3.6
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    49.4
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1,1-Dimethyl-3-(1-naphthalen-1-yl-3-oxo-3-phenylpropyl)urea三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 生成 tert-butyl (2S)-5-(3-azidopropylamino)-2-[[4-[(2,4-diaminopteridin-6-yl)methyl-methylamino]benzoyl]amino]-5-oxopentanoate
    参考文献:
    名称:
    Solid-phase synthesis of skeletally diverse benzofused sultams via palladium-catalyzed cyclization
    摘要:
    The solid-phase synthesis of sultams from resin-bound amino acids is described. The sulfonylation of the resin-bound primary amines afforded the requisite secondary amines, after which the intramolecular Buchwald-Hartwig-type coupling forms the C-S bond. A final alkylation on the sulfonamides followed by cleavage provided the corresponding seven-membered sultams. (c) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.01.055
  • 作为产物:
    描述:
    参考文献:
    名称:
    Solid-phase synthesis of skeletally diverse benzofused sultams via palladium-catalyzed cyclization
    摘要:
    The solid-phase synthesis of sultams from resin-bound amino acids is described. The sulfonylation of the resin-bound primary amines afforded the requisite secondary amines, after which the intramolecular Buchwald-Hartwig-type coupling forms the C-S bond. A final alkylation on the sulfonamides followed by cleavage provided the corresponding seven-membered sultams. (c) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.01.055
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文献信息

  • An efficient synthesis of β-acylureas via a three-component, one-pot synthesis using TCS/ZnCl2
    作者:Tamer K. Khatab、Khairy A.M. El-Bayouki、Wahid M. Basyouni
    DOI:10.1016/j.tetlet.2011.01.066
    日期:2011.3
    A simple and efficient one-pot, three-component synthesis of new trisubstituted ureas containing diastereotopic protons is achieved via the reaction of aromatic aldehydes, aromatic ketones, and dimethyl cyanamide using a TCS/ZnCl2 reagent mixture at room temperature.
    通过在室温下使用TCS / ZnCl 2试剂混合物使芳族醛,芳族酮和二甲基氰胺反应,可以简单,高效地一锅三组分合成新的含非对映体质子的三取代脲。
  • Solid-phase synthesis of skeletally diverse benzofused sultams via palladium-catalyzed cyclization
    作者:Wenteng Chen、Zhi Li、Lili Ou、Marc A. Giulianott、Richard A. Houghten、Yongping Yu
    DOI:10.1016/j.tetlet.2011.01.055
    日期:2011.3
    The solid-phase synthesis of sultams from resin-bound amino acids is described. The sulfonylation of the resin-bound primary amines afforded the requisite secondary amines, after which the intramolecular Buchwald-Hartwig-type coupling forms the C-S bond. A final alkylation on the sulfonamides followed by cleavage provided the corresponding seven-membered sultams. (c) 2011 Elsevier Ltd. All rights reserved.
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