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3,3-dimethyl-13-propyl-3,4-dihydro-1H-indazolo[1,2-b]phthalazine-1,6,11(2H,13H)-trione | 1245471-26-4

中文名称
——
中文别名
——
英文名称
3,3-dimethyl-13-propyl-3,4-dihydro-1H-indazolo[1,2-b]phthalazine-1,6,11(2H,13H)-trione
英文别名
3,3-dimethyl-13-propyl-2,3,4,13-tetrahydro-1Hindazolo[1,2-b]phthalazine-1,6,11-trione;2,3,4,13-tetrahydro-3,3-dimethyl-13-propyl-1H-indazolo[1,2-b]phthalazine-1,6,11-trione;3,4-dihydro-3,3-dimethyl-13-n-propyl-2H-indazolo[2,1-b]phthalazine-1,6,11(13H)-trione;3,3-dimethyl-13-propyl-4,13-dihydro-2H-indazolo[1,2-b]phthalazine-1,6,11-trione
3,3-dimethyl-13-propyl-3,4-dihydro-1H-indazolo[1,2-b]phthalazine-1,6,11(2H,13H)-trione化学式
CAS
1245471-26-4
化学式
C20H22N2O3
mdl
——
分子量
338.406
InChiKey
GCGHETNQEDNWJU-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):
    2.8
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    57.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    邻苯二甲酰肼5,5-二甲基-1,3-环己二酮正丁醛乙醇 作用下, 以 neat (no solvent) 为溶剂, 以63%的产率得到3,3-dimethyl-13-propyl-3,4-dihydro-1H-indazolo[1,2-b]phthalazine-1,6,11(2H,13H)-trione
    参考文献:
    名称:
    高效可回收磁性钴纳米催化剂通过一锅法三组分反应合成酞嗪衍生物
    摘要:
    摘要 1 H -Indazolo [2,1- b ]phthalazine-1,6,11-trione 衍生物通过邻苯二甲酰肼、双甲酮和芳香醛在 80°C 无溶剂条件下的一锅三组分缩合合成在新型 Co 纳米颗粒催化剂的存在下。该催化剂的制备方法是用原硅酸四乙酯包覆 Fe 3 O 4磁性纳米粒子,然后用 3-氯丙基(三甲氧基)硅烷和 2-氨基-1,3,4-噻二唑-5(4 H )-硫酮进行功能化,并与乙酸钴(II)。超顺磁性催化剂可以通过应用外部超级磁铁很容易地回收,并且可以使用多次而不会显着损失催化活性。
    DOI:
    10.1134/s1070428022100141
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文献信息

  • One-pot synthesis of aliphatic and aromatic 2H-indazolo[2,1-b]phthalazine-triones catalyzed by N-halosulfonamides under solvent-free conditions
    作者:Ramin Ghorbani-Vaghei、Rahman Karimi-Nami、Zahra Toghraei-Semiromi、Mostafa Amiri、Mehdi Ghavidel
    DOI:10.1016/j.tet.2011.01.024
    日期:2011.3
    N, N, N′, N′-Tetrabromobenzene-1,3-disulfonamide and poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) were used as efficient catalysts for the one-pot synthesis of aliphatic and aromatic 2H-indazolo[2,1-b]phthalazine-triones in excellent yields from aldehydes, phthalhydrazide, and dimedone at 80–100 °C under solvent-free conditions.
    N,N,N ',N'-四溴苯-1,3-二磺酰胺和聚(N--N-乙基苯-1,3-二磺酰胺)被用作一锅合成脂肪族和芳香族2的有效催化剂在80–100°C的无溶剂条件下,H-吲哚并[2,1- b ]酞嗪三酮以优异的产率从醛,邻苯二甲酰二甲基酮产生。
  • Phosphomolybdic Acid (PMA)-SiO2 as a Heterogeneous Solid Acid Catalyst for the One-Pot Synthesis of 2H-Indazolo[1,2-b]phthalazine-triones
    作者:Gowravaram Sabitha、Chitti Srinivas、Avula Raghavendar、Jhillu Singh Yadav
    DOI:10.1002/hlca.200900378
    日期:——
    Phosphomolybdic acid (PMA)–SiO2 was found to be an efficient catalyst for the three‐component condensation reaction of phthalhydrazide, 1,3‐diketone, and aldehydes to produce 2H‐indazolo[1,2‐b]phthalazine‐triones in excellent yields. The catalyst can be recovered and reused without significant loss of activity.
    酸(PMA)-SiO 2被发现是邻苯二甲酰,1,3-二酮和醛的三组分缩合反应产生2 H-吲唑并[1,2 - b ]邻苯二甲腈-三酮的有效催化剂。优异的产量。催化剂可被回收和再利用而没有明显的活性损失。
  • Phthalazine-trione as a blue-green light-emitting moiety: crystal structures, photoluminescence and theoretical calculations
    作者:Felipe Terra Martins、Lauro June Queiroz Maia、Gisane Gasparotto、Ana Karoline Silva Medanha Valdo、José Antônio Nascimento Neto、Leandro Ribeiro、Yuri de Freitas Rego、Cleiton Moreira da Silva、Ângelo de Fátima
    DOI:10.1039/c8nj02976h
    日期:——
    study (4-chlorophenyl, 3-methoxyphenyl and 4-nitrophenyl derivatives) and for those available in literature (4-fluorophenyl and 4-bromophenyl derivatives). Electronic transitions with the largest oscillator strengths were near 360 nm and were in excellent agreement with the experimental excitation energy (UV-visible and photoluminescence spectra). Lifetime values of selected samples could also be determined
    酞嗪2,3-二氮杂萘)和邻苯二甲酰2,3-二氢-1,4-酞嗪二酮)化合物是具有几种生物学特性的杂环。最近,类似的酞嗪三酮也出现了作为候选药物。在本文中,我们在蓝色和绿色光谱区域中引入了一种有前途的荧光团酞嗪-三酮部分。根据其晶体结构和随时间变化的密度泛函理论(TD-DFT)计算,可以合理化所需的光学特性。在紫外线(UV)激发(约360 nm)下,两个发光最大值约为。十个酞嗪三酮的取代度分别为460 nm和480 nm。通过我们的时间依赖性DFT计算,对于在本研究中还确定了晶体几何形状的三种邻苯二氮杂三酮(4-氯苯基,3-甲氧基苯基和4-硝基苯基衍生物)和可用的那些进行了时变DFT计算,使这种发光性质的守恒合理化。在文献中(4-氟苯基和4-溴苯基衍生物)。具有最大振荡器强度的电子跃迁接近360 nm,并且与实验激发能(紫外可见光谱和光致发光光谱)非常吻合。还可以确定所选样本的寿命值,该值在1
  • Microwave-assisted, montmorillonite K-10 catalyzed three-component synthesis of 2H-indazolo[2,1-b]phthalazine-triones under solvent-free conditions
    作者:Mudumala Veeranarayana Reddy、Gangireddy Chandra Sekhar Reddy、Yeon Tae Jeong
    DOI:10.1016/j.tet.2012.06.045
    日期:2012.8
    An efficient, rapid, and green synthesis of 2H-indazolo[2,1-b]phthalazine-triones has been accomplished under solvent-free conditions by the reaction of phthalhydrazide, aldehydes and 5,5-dimethylcyclohexane-1,3-dione. This approach exploits the synthetic potential of microwave irradiation and Montmorillonite K-10 combination and offers many advantages, such as excellent product yields, shorter reaction
    通过邻苯二甲酰,醛与5,5-二甲基环己烷-1,3-二酮的反应,在无溶剂条件下完成了2H-吲唑并[2,1 - b ]邻苯二甲酰基三酮的高效,快速和绿色合成。这种方法利用了微波辐射和蒙脱石K-10组合的合成潜力,并提供了许多优势,例如出色的产品收率,更短的反应时间,可重复使用的催化剂,易于分离的产品以及对环境无害的反应条件。
  • Synthesis and characterization of Ni(<scp>ii</scp>)–Vanillin–Schiff base–MCM-41 composite as an efficient and reusable nanocatalyst for multicomponent reactions
    作者:Mohsen Nikoorazm、Arash Ghorbani-Choghamarani、Maryam Khanmoradi
    DOI:10.1039/c6ra09371j
    日期:——

    Ni(ii)–Vanillin–Schiff base–MCM-41 has been synthesized and characterized by XRD, TGA, BET, EDS, SEM, ICP-OES, TEM and FT-IR spectroscopy. This nanostructural catalyst has been applied for multicomponent reactions.

    Ni(ii)-香草醛-席夫碱-MCM-41已经通过XRD、TGA、BET、EDS、SEM、ICP-OES、TEM和FT-IR光谱进行合成和表征。这种纳米结构催化剂已经应用于多组分反应。
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