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2-[(methylthio)(piperidin-1-yl)methylene]malononitrile | 3012-89-3

中文名称
——
中文别名
——
英文名称
2-[(methylthio)(piperidin-1-yl)methylene]malononitrile
英文别名
2-[methylthio(piperidin-1-yl)methylene]malononitrile;1-Piperidino-1-methylmercapto-2.2-dicyan-aethylen;2-[Methylsulfanyl(piperidin-1-yl)methylidene]propanedinitrile
2-[(methylthio)(piperidin-1-yl)methylene]malononitrile化学式
CAS
3012-89-3
化学式
C10H13N3S
mdl
——
分子量
207.299
InChiKey
XUVREQPIGIZEHA-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):
    1.8
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    76.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Synthesis, antibacterial activity and cytotoxicity of new fused pyrazolo[1,5-a]pyrimidine and pyrazolo[5,1-c][1,2,4]triazine derivatives from new 5-aminopyrazoles
    作者:Wedad M. Al-Adiwish、M.I.M. Tahir、A. Siti-Noor-Adnalizawati、Siti Farah Hashim、Nazlina Ibrahim、W.A. Yaacob
    DOI:10.1016/j.ejmech.2013.04.029
    日期:2013.6
    with hydrazine hydrate under reflux in ethanol. These compounds were utilized as intermediates to synthesize pyrazolo[1,5-a]-pyrimidines 3a–c, 4a–d, 5a–c, and 6a–c, as well as pyrazolo[5,1-c][1,2,4]triazines 7a–c and 8a–c, by the reaction of 2-[bis(methylthio)methylene]malononitrile, α,α-dicyanoketene-N,S-acetals 1a–b, acetylacetone, acetoacetanilide as well as acetylacetone, and malononitrile, respectively
    在已知的α,α-二氰基t烯-N,S-乙缩醛1a - c与水合肼在乙醇中回流的反应中,高产率地制备了新的5-氨基吡唑2a - c。这些化合物被用作合成吡唑并[1,5- a ]-嘧啶3a – c,4a – d,5a – c和6a – c以及吡唑并[5,1- c ] [1,2 ,4]三嗪7a – c和8a – c,分别通过2- [双(甲硫基)亚甲基]丙二腈,α,α-二氰基ene烯-N,S-乙缩醛1a - b,乙酰丙酮,乙酰乙酰苯胺以及乙酰丙酮和丙二腈反应。此外,用戊丹-2,5-二酮环化2a - c可以得到相应的5-吡咯基吡唑9a - c。此外,2a – c与乙酸酐的融合导致相应的1-乙酰基-1 H-吡唑类10a – c。还报道了几种选择的化合物对Vero细胞的抗菌活性和细胞毒性。
  • A one-pot, three-component, microwave-assisted synthesis of novel 7-amino-substituted 4-aminopyrazolo[1,5-a][1,3,5]triazine-8-carbonitriles
    作者:Felicia Phei Lin Lim、Giuseppe Luna、Anton V. Dolzhenko
    DOI:10.1016/j.tetlet.2015.11.006
    日期:2015.12
    The synthesis of novel 7-amino-substituted pyrazolo[1,5-a][1,3,5]triazine-8-carbonitriles was achieved via a three-component reaction of 3-amino-substituted 5-aminopyrazole-4-carbonitriles, cyanamide and triethyl orthoformate under microwave irradiation. Under catalyst-free conditions, this three-component reaction accommodated a generous diversity of amino substituents making it ideal for the generation
    新型7-氨基取代的吡唑并[1,5- a ] [1,3,5]三嗪-8-腈的合成是通过3-氨基取代的5-氨基吡唑-4-腈的三组分反应实现的,微波辐射下的氰胺和原甲酸三乙酯。在无催化剂的条件下,该三组分反应可容纳大量的氨基取代基,因此非常适合用于药物开发过程的化合物库的生成。
  • SYNTHESIS OF THIENO[3,2-<i>b</i>]PYRIDINES
    作者:Masataka Yokoyama、Masanori Tohnishi、Akemi Kurihara、Tsuneo Imamoto
    DOI:10.1246/cl.1982.1933
    日期:1982.12.5
    Several thieno[3,2-b]pyridines could be easily synthesized by methallation using LDA directly from 3-(disubstituted amino)-2-cyano-3-methylthioacrylonitriles.
    通过使用 LDA 直接从 3-(二取代氨基)-2-氰基-3-甲硫基丙烯腈进行甲氧基化,可以轻松合成多种噻吩并[3,2-b]吡啶。
  • One-pot synthesis of new tetrasubstituted thiophenes and selenophenes
    作者:David Thomae、Enrico Perspicace、Dorothée Henryon、Zhanjie Xu、Serge Schneider、Stéphanie Hesse、Gilbert Kirsch、Pierre Seck
    DOI:10.1016/j.tet.2009.10.021
    日期:2009.12
    In this work, we described the synthesis of new tetrasubstituted thiophenes and selenophenes achieved by an easy one-pot four-step procedure. Expected compounds were obtained in good yield from ketene dithioacetals.
    在这项工作中,我们描述了通过简单的一锅四步法实现的新的四取代噻吩和硒代苯的合成。从乙烯酮二硫缩醛以高收率获得预期的化合物。
  • Synthesis of New Multi-Functionalised 1,1′-Carbonylbispyrazole Derivatives
    作者:Manijeh Mohadeszadeh、Hossein Eshghi、Sattar Saberi、Mostafa Gholizadeh
    DOI:10.3184/174751915x14271377629065
    日期:2015.4
    A new series of multi-functionalised 1,1′-carbonylbispyrazole derivatives were synthesised through cyclisation of pyrazole carbohydrazides with some substituted methylene malononitriles in very good yields. The structures of all synthesised compounds were established on the basis of NMR, IR, MS and elemental analysis.
    通过吡唑碳酰肼与一些取代的亚甲基丙二腈的环化,合成了一系列新的多功能化 1,1'-羰基双吡唑衍生物,收率非常好。所有合成化合物的结构均在NMR、IR、MS和元素分析的基础上建立。
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