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[(2-hydroxy-naphthalen-1-yl)-phenyl-methyl]-urea | 3686-36-0

中文名称
——
中文别名
——
英文名称
[(2-hydroxy-naphthalen-1-yl)-phenyl-methyl]-urea
英文别名
N-[(2-hydroxynaphthalen-1-yl)(phenyl)methyl]urea;1-((2-hydroxynaphthalen-1-yl)(phenyl)methyl)urea;1-(alpha-Ureidobenzyl)-2-naphthol;[(2-hydroxynaphthalen-1-yl)-phenylmethyl]urea
[(2-hydroxy-naphthalen-1-yl)-phenyl-methyl]-urea化学式
CAS
3686-36-0
化学式
C18H16N2O2
mdl
——
分子量
292.337
InChiKey
IOVHREABHCCJQS-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:
    22
  • 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:
    75.4
  • 氢给体数:
    3
  • 氢受体数:
    2

上下游信息

  • 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:
    参考文献:
    名称:
    1,2-二氢-1-芳基萘并[1,2-e][1,3]恶嗪-3-酮衍生物在微波辅助和热无溶剂条件下的新型三组分一锅法合成
    摘要:
    1,2-Dihydro-1-arylnaphtho[1,2-e] [1,3]oxazine-3-one 衍生物使用一种新颖、简便的 β-萘酚一锅缩合方法以中等至高产率合成,芳香醛和尿素在微波辅助和热无溶剂条件下。
    DOI:
    10.1055/s-2007-970763
  • 作为产物:
    描述:
    1-Benzylidenenaphthalen-2-one 、 尿素 在 nanocrystalline iron oxychloride grafted MCM-41 作用下, 以 neat (no solvent) 为溶剂, 生成 [(2-hydroxy-naphthalen-1-yl)-phenyl-methyl]-urea
    参考文献:
    名称:
    Nanocrystalline FeOClx grafted MCM-41 as active mesoporous catalyst for the solvent-free multi-condensation reaction
    摘要:
    使用热活化的FeC13/MCM-41催化剂,芳香醛、萘酚和尿素(或酰胺)的多组分缩合反应可催化转化为具有药用价值的酰胺基烷基萘酚。
    DOI:
    10.1039/c6ra14736d
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文献信息

  • Preparation and characterization of Fe3O4@SiO2@PMA:AS an efficient and recyclable nanocatalyst for the synthesis of 1-amidoalkyl-2-naphthols
    作者:Mohsen Esmaeilpour、Jaber Javidi、Maryam Zandi
    DOI:10.1016/j.materresbull.2014.04.019
    日期:2014.7
    superparamagnetic Fe 3 O 4 @SiO 2 that is synthesized based on several stages. First of all, the Fe 3 O 4 @SiO 2 nanosphere core-shell is synthesized. Then, H 3 PMo 12 O 40 nanoparticles were synthesized by the treatment of H 3 PMo 12 O 40 with n -Octane as solvent by a solvothermal method and this nano hetero polyacid immobilized onto the imidazole functionalized Fe 3 O 4 @SiO 2 nanoparticles. The
    摘要 在本文中,我们报道了一种基于多个阶段合成的功能化超顺磁性 Fe 3 O 4 @SiO 2 的制备方法。首先,合成了Fe 3 O 4 @SiO 2 纳米球核壳。然后,通过溶剂热法用正辛烷作为溶剂处理H 3 PMo 12 O 40 合成H 3 PMo 12 O 40 纳米颗粒,并将该纳米杂多酸固定在咪唑官能化的Fe 3 O 4 @SiO 2 纳米颗粒上。样品的结构通过XRD、TEM、DLS、FE-SEM、FT-IR、N 2 吸附-解吸等温线分析和VSM表征。此外,还描述了一种使用 β-萘酚、醛和乙酰胺的多组分、一锅缩合反应制备酰胺烷基萘酚的有效和直接的方案,在无溶剂和微波条件下,在 Fe 3 O 4 @SiO 2 -imid-PMA n 存在下苯甲酰胺和尿素。此外,纳米催化剂可以很容易地通过磁场回收并在接下来的反应中重复使用至少 5 次,而不会明显降低催化活性。
  • Solvent-free, highly efficient one-pot multi-component synthesis of 1-amido- and 1-carbamato-alkyl naphthols/phenols catalyzed by ethylammonium nitrate as reusable ionic liquid under neat reaction condition at ambient temperature
    作者:Shafeek A.R. Mulla、Tarek A. Salama、Mohsinkhan Y. Pathan、Suleman M. Inamdar、Santosh S. Chavan
    DOI:10.1016/j.tetlet.2012.12.004
    日期:2013.2
    developed for the efficient synthesis of 1-amido- and 1-carbamato-alkyl naphthols/phenols in excellent yields via one-pot three-component condensation of various aldehydes, amides/carbamates/urea, and naphthols/phenols using ethylammonium nitrate (EAN) as a reusable ionic liquid catalyst under neat reaction condition at ambient temperature.
    已开发出一种无溶剂,环境清洁,温和且简单的单锅多组分方案,可通过一锅三组分高效合成1-酰胺基和1-氨基甲酰基烷基萘酚/苯酚,且产率高在室温下纯净的反应条件下,使用硝酸乙铵(EAN)作为可重复使用的离子液体催化剂,将各种醛,酰胺/氨基甲酸酯/脲和萘酚/酚缩合。
  • Brønsted acidic ionic liquid as an efficient and reusable catalyst for one-pot synthesis of 1-amidoalkyl 2-naphthols under solvent-free conditions
    作者:Abdol R. Hajipour、Yosof Ghayeb、Nafisehsadat Sheikhan、Arnold E. Ruoho
    DOI:10.1016/j.tetlet.2009.07.116
    日期:2009.10
    amidoalkyl naphthols from condensation of aldehydes with amides or urea and 2-naphthol in the presence of a catalytic amount of Brønsted acidic ionic liquid ([TEBSA][HSO4]) under thermal solvent-free conditions. High yields, short reaction time, easy work-up and reusability of the catalyst are advantages of this procedure.
    已经开发了一种温和有效的方法,在催化量的布朗斯台德酸性离子液体([TEBSA] [HSO 4 ])存在下,由醛与酰胺或尿素和2-萘酚缩合制备酰胺基烷基萘酚无条件。该方法的优点是高产率,短反应时间,易于后处理和催化剂的可重复使用性。
  • Synthesis of Novel Thioamidoalkyl- and Thiocarbamidoalkyl Naphthols via a Three-Component Condensation Reaction Using Heterogeneous Catalyst of Ferric Hydrogensulfate
    作者:Hossein Eshghi、Gholam Hossein Zohuri、Saman Damavandi
    DOI:10.1080/00397911.2010.526281
    日期:2012.2.15
    heterogeneous catalyst for the one-pot multicomponent reaction of β-naphthol, aromatic aldehydes, and thioamide derivatives to obtain the corresponding thioamidoalkyl naphthols. Various novel thioamidoalkyl naphthols and thiocarbamidoalkyl naphthols were synthesized in good yields from thioacetamide and thiourea. The heterogeneous nature of the catalyst made it reusable for further chemical reactions. GRAPHICAL
    摘要 以硫酸氢铁[Fe(HSO4)3]为合适的多相催化剂,用于β-萘酚、芳香醛和硫代酰胺衍生物的一锅多组分反应,得到相应的硫代酰胺基烷基萘酚。以硫代乙酰胺和硫脲为原料,以良好的收率合成了各种新型硫代氨基烷基萘酚和硫代氨基烷基萘酚。催化剂的多相性质使其可重复用于进一步的化学反应。图形概要
  • Magnetite (Fe3O4) nanoparticles-supported dodecylbenzenesulfonic acid as a highly efficient and green heterogeneous catalyst for the synthesis of substituted quinolines and 1-amidoalkyl-2-naphthol derivatives
    作者:Deepak Katheriya、Nipun Patel、Harsh Dadhania、Abhishek Dadhania
    DOI:10.1007/s13738-020-02069-9
    日期:2021.4
    The methodology provides a facile approach for the synthesis of targeted compounds with excellent isolated yields. Additionally, the catalyst can be recovered through external magnet and reused up to five reaction cycles with prominent reactivity. The present approach offers many advantages such as green and mild reaction condition, facile catalyst recovery and excellent isolated yield of final products
    摘要 磁性可回收磁铁矿(Fe 3 O 4)合成并通过不同的分析技术(如TEM,XRD,FTIR,TGA,SEM,EDX和VSM)对纳米颗粒负载的十二烷基苯磺酸(DDBSA @ MNP)进行了表征。通过一锅缩合反应,评估了合成的DDBSA @ MNP的催化效率,用于合成取代的喹啉和1-酰胺基-2-萘。该方法为合成目标化合物提供了简便的方法,具有优异的分离收率。另外,可以通过外部磁体回收催化剂,并以显着的反应性重复使用多达五个反应周期。本方法提供了许多优点,例如绿色和温和的反应条件,容易的催化剂回收以及优异的最终产物分离产率。 图形摘要
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