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2,6-diphenylpiperidin-4-one thiosemicarbazone | 502960-94-3

中文名称
——
中文别名
——
英文名称
2,6-diphenylpiperidin-4-one thiosemicarbazone
英文别名
Hydrazinecarbothioamide, 2-(2,6-diphenyl-4-piperidinylidene)-;[(2,6-diphenylpiperidin-4-ylidene)amino]thiourea
2,6-diphenylpiperidin-4-one thiosemicarbazone化学式
CAS
502960-94-3
化学式
C18H20N4S
mdl
——
分子量
324.45
InChiKey
TXVGSYASCIKJMI-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

物化性质

  • 熔点:
    180-184 °C (decomp)(Solv: methanol (67-56-1))
  • 沸点:
    514.0±60.0 °C(Predicted)
  • 密度:
    1.26±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    94.5
  • 氢给体数:
    3
  • 氢受体数:
    3

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:
    2,6-diphenylpiperidin-4-one thiosemicarbazone双氧水 作用下, 以 氯仿 为溶剂, 反应 3.0h, 以87%的产率得到7,9-diphenyl-1,2,4,8-tetraazaspiro[4.5]decan-3-thione
    参考文献:
    名称:
    Synthesis of 6-Substituted/Unsubstituted- 7,9-diaryl-1,2,4,8-tetraazaspiro[4.5]- decan-3-thiones
    摘要:
    Some 2,6-diarylpiperidin-4-one thiosemicarbazones (1a-8a), obtained from the corresponding 2,6-diarylpiperidin-4-ones (1-8) on oxidative cyclization with H2O2 at OdegreesC provide 7,9-diaryl-1,2,4,8-tetraaza spiro[4.5]decan-3-thiones(1b-8b) in excellent yields. The structures of these compounds have been established on the basis of their elemental, analytical and spectral data.
    DOI:
    10.1081/scc-120018753
  • 作为产物:
    描述:
    苯甲醛 在 ammonium acetate 作用下, 以 乙醇 为溶剂, 反应 2.0h, 生成 2,6-diphenylpiperidin-4-one thiosemicarbazone
    参考文献:
    名称:
    A facile microwave assisted green chemical synthesis of novel piperidino 2-thioxoimidazolidin-4-ones and theirin vitromicrobiological evaluation
    摘要:
    A series of novel hybrid heterocyclic compounds, 3-(3-alkyl-2,6-diarylpiperin-4-ylidene)-2-thioxoimidazolidin-4-ones were synthesised and a comparative study was also carried out under microwave irradiation. The synthesised compounds were characterised by their melting points, elemental analysis, MS, FT-IR, one-dimensional NMR (1H, D2O exchanged 1H and
    DOI:
    10.3109/14756361003691878
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文献信息

  • Synthesis, spectral analysis and in vitro microbiological evaluation of 3-(3-alkyl-2,6-diarylpiperin-4-ylidene)-2-thioxoimidazolidin-4-ones as a new class of antibacterial and antifungal agents
    作者:J. Thanusu、V. Kanagarajan、M. Gopalakrishnan
    DOI:10.1016/j.bmcl.2009.11.074
    日期:2010.1
    In the present work, a new series of bis hybrid heterocycle comprising both piperidine and thiohydantoin nuclei together namely 3-(3-alkyl-2,6-diarylpiperin-4-ylidene)-2-thioxoimidazolidin-4-ones 46-60 was synthesized by the treatment of the respective thiosemicarbazones 31-45 with chloroethyl acetate and anhydrous sodium acetate in refluxing ethanol for 4 h and were characterized by melting point, elemental analysis, MS, FT-IR, one-dimensional NMR (H-1, D2O exchanged H-1 and C-13), two dimensional HOMOCOSY and NOESY spectroscopic data. In addition, the title compounds were screened for their antimicrobial activities against a spectrum of clinically isolated microbial organisms. Compounds 47-50, 52-55 and 57-60 with fluoro, chloro, methoxy or methyl functions at the para position of phenyl rings attached to C-2 and C-6 carbons of piperidine moiety along with and without methyl substituent at position C-3 of the piperidine ring exerted potent biological activities againstStaphylococcus aureus, beta-Hemolytic streptococcus, Vibrio cholerae, Escherichia coli, Pseudomonas aeruginosa, Aspergillus flavus, Candida albicans, Candida 6 and Candida 51 at a minimum inhibitory concentration. (C) 2009 Elsevier Ltd. All rights reserved.
  • Balasubramanian; Ramalingan; Kabilan, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2002, vol. 41, # 11, p. 2402 - 2404
    作者:Balasubramanian、Ramalingan、Kabilan
    DOI:——
    日期:——
  • Synthesis and Microbiological Evaluation of Novel [N-Acetyl-2,6-Diarylpiperidin-4-YL]-5-Spiro-4-Acetyl-2-(Acetylamino)-Δ2-1,3,4-Thiadiazolines
    作者:S. Balasubramanian、C. Ramalingan、G. Aridoss、P. Partiban、S. Kabilan
    DOI:10.1007/s00044-004-0035-5
    日期:2004.6
    Some novel spiropiperidinyl thiadiazolines have been synthesized and their bacterial activity against Streptococcus faecalis, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and Klepsiella pneumoniae and antifungal activity against Cryptococcus neoformans, Candida-6, Candida-51, Aspergillus niger and Aspergillusflavus were evaluated. Compound 23 exhibited potent antibacterial activity in vitro against Klepsiella pneumoniae while compound 24 exerted potent antifungal activity in vitro against Cryptococcus neoformans.
  • Fazal Mohamed; Seema Mubarak; Dar, Mukhtar Ahmad, Oriental Journal of Chemistry, 2011, vol. 27, # 1, p. 333 - 335
    作者:Fazal Mohamed、Seema Mubarak、Dar, Mukhtar Ahmad、Abuthair、Ramani Devi
    DOI:——
    日期:——
  • A facile microwave assisted green chemical synthesis of novel piperidino 2-thioxoimidazolidin-4-ones and their<i>in vitro</i>microbiological evaluation
    作者:V. Kanagarajan、J. Thanusu、M. Gopalakrishnan
    DOI:10.3109/14756361003691878
    日期:2011.2.1
    A series of novel hybrid heterocyclic compounds, 3-(3-alkyl-2,6-diarylpiperin-4-ylidene)-2-thioxoimidazolidin-4-ones were synthesised and a comparative study was also carried out under microwave irradiation. The synthesised compounds were characterised by their melting points, elemental analysis, MS, FT-IR, one-dimensional NMR (1H, D2O exchanged 1H and
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