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13-(4-fluorophenyl)-3,3-dimethyl-2,3,4,6,11,13-hexahydro-1H-indazolo[1,2-b]phthalazine-1,6,11-trione | 1017238-96-8

中文名称
——
中文别名
——
英文名称
13-(4-fluorophenyl)-3,3-dimethyl-2,3,4,6,11,13-hexahydro-1H-indazolo[1,2-b]phthalazine-1,6,11-trione
英文别名
3,4-dihydro-3,3-dimethyl-13-(4-fluorophenyl)-2H-indazolo[2,1-b]phthalazine-1,6,11(13H)-trione;13-(4-fluorophenyl)-3,3-dimethyl-2,3,4,13-tetrahydro-1H-indazolo[1,2-b]phthalazine-1,6,11-trione;2,3,4,13-Tetrahydro-3,3-dimethyl-13-(4-fluorophenyl)-indazolo[2,1-b]phthalazine-1,6,11-trione;13-(4-fluorophenyl)-3,3-dimethyl-4,13-dihydro-2H-indazolo[1,2-b]phthalazine-1,6,11-trione
13-(4-fluorophenyl)-3,3-dimethyl-2,3,4,6,11,13-hexahydro-1H-indazolo[1,2-b]phthalazine-1,6,11-trione化学式
CAS
1017238-96-8
化学式
C23H19FN2O3
mdl
——
分子量
390.414
InChiKey
BWEUXNGEHACUGR-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):
    3.3
  • 重原子数:
    29
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    57.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    SO 3 H-官能化介孔二氧化硅材料作为固体酸催化剂,可轻松,无溶剂地合成2 H-吲唑并[ 2,1- b ]酞嗪-1,6,11-三酮衍生物
    摘要:
    SO 3 H-官能化介孔二氧化硅材料(SO 3 H-FMSM)作为一种高效,温和,可回收和环保的非均相介孔纳米催化剂,被用于合成2 H-吲唑并[ 2,1 - b ]邻苯二甲酰1.6。 1,11-三酮衍生物在无溶剂热(SF)条件下的2,3-二氢邻苯二甲酸-1,4-二酮,二甲酮和苯甲醛衍生物的一锅三组分缩合反应中,具有优异的收率和较短的反应时间。
    DOI:
    10.1039/c5nj01733e
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文献信息

  • An efficient and green one-pot synthesis of indazolo[1,2-b]-phthalazinetriones via three-component reaction of aldehydes, dimedone, and phthalhydrazide using Fe3O4@SiO2 core–shell nanoparticles
    作者:Boshra Mirhosseini-Eshkevari、Mohammad Ali Ghasemzadeh、Javad Safaei-Ghomi
    DOI:10.1007/s11164-014-1854-8
    日期:2015.10
    An efficient and eco-friendly procedure for the one-pot synthesis of biologically active heterocyclic compounds including indazolo[1,2- b ]-phthalazinetriones has been developed in the presence of Fe3O4@SiO2 nanoparticles. The multicomponent reactions of aldehydes, dimedone, and phthalhydrazide were carried out under solvent-free conditions to obtain some indazolo[1,2- b ]-phthalazinetrione derivatives
    在Fe 3 O 4 @SiO 2纳米粒子的存在下,已经开发出了一种有效且环保的方法,用于一锅合成生物活性杂环化合物,包括吲哚并[1,2- b ]-酞嗪三酮。在无溶剂条件下进行醛,二甲酮和邻苯二甲酰肼的多组分反应,得到一些吲唑并[1,2- b ]-酞嗪三酮衍生物。本方法提供了许多优点,例如优异的收率,简单的后处理,低的反应时间,容易的催化剂分离和很少的催化剂负载。
  • Novel ionic liquid <i>N,N</i>-diethyl-<i>N</i>-sulfoethanaminium hydrogen sulfate: Design, characterization, and application as a highly efficient catalyst for the production of triazolo[1,2-<i>a</i>]indazole-triones and 2<i>H</i>-indazolo[2,1-<i>b</i>]phthalazine-triones
    作者:Abdolkarim Zare、Fatemeh Masihpour
    DOI:10.1080/10426507.2016.1149853
    日期:2016.8.2
    mass data. Then, its catalytic activity was examined for the preparation of triazolo[1,2-a]-indazole-triones and 2H-indazolo[2,1-b]phthalazine-triones by the one-pot multi-component condensation of arylaldehydes with dimedone and 4-phenylurazole/2,3-dihydrophthalazine-1,4-dione under solvent-free conditions. [Et3N-SO3H]HSO4 efficiently promoted the reaction to afford the products in high yields and
    图形摘要 摘要合成了一种新型布朗斯台德酸性离子液体,即 N,N-二乙基-N-磺胺硫酸氢盐 ([Et3N-SO3H]HSO4),并使用 FT-IR、1H NMR、13C NMR 和质谱数据进行表征。然后,通过芳醛与二甲酮的一锅多组分缩合反应制备三唑并[1,2-a]-吲唑-三酮和2H-吲唑并[2,1-b]酞嗪-三酮的催化活性和 4-苯基脲唑/2,3-二氢酞嗪-1,4-二酮在无溶剂条件下。[Et3N-SO3H]HSO4 有效地促进了反应,以高产率和短反应时间提供了产物。
  • Efficient synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives using succinimidinium N-sulfonic acid hydrogen sulfate as a new ionic liquid catalyst
    作者:Masoumeh Abedini、Farhad Shirini、Javad Mohammad-Alinejad Omran
    DOI:10.1016/j.molliq.2015.09.014
    日期:2015.12
    Succinimidinium N-sulfonic acid hydrogen sulfate is prepared as a new ionic liquid and characterized with a variety of techniques including FT-IR, 1H and 13C NMR, SEM, mass spectra method as well as Hammett acidity function. After identification, this reagent was used as an efficient catalyst for the multi-component synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives. The simple work-up, mild
    琥珀酰亚胺N-磺酸硫酸氢盐被制备为新型离子液体,并通过多种技术进行表征,包括FT-IR,1 H和13 C NMR,SEM,质谱法以及哈米特酸度函数。鉴定后,该试剂用作2 H-吲哚并[ 2,1 - b ]邻苯二甲腈-三酮衍生物的多组分合成的有效催化剂。简单的后处理,温和的反应条件,优异的收率和相对较短的反应时间是该方案的显着优势。另外,该离子液体可以循环使用几次而其催化活性没有明显降低。
  • Solvent-free, sonochemical, one-pot, four-component synthesis of 2H-indazolo[2,1-b]phthalazine-triones and 1H-pyrazolo[1,2-b]phthalazine-diones catalyzed by Fe3O4@SiO2-imid-PMAn magnetic nanoparticles
    作者:Mohsen Esmaeilpour、Jaber Javidi、Fatemeh Nowroozi Dodeji、Saeed Zahmatkesh
    DOI:10.1007/s11164-016-2462-6
    日期:2021.6
    A practical and green method for the synthesis of 2H-indazolo[2,1-b]phthalazine-triones and 1H-pyrazolo[1,2-b]phthalazine-diones using Fe3O4@SiO2-imid-PMAn nanoparticles as an eco-friendly magnetic catalyst from the four-component condensation, solvent-free reaction of phthalic anhydride, hydrazinium hydroxide, 1,3-diketones, and aldehydes under thermal or ultrasound irradiation at room temperature
    一种使用 Fe 3 O 4 @SiO 2 -imid-PMA合成 2 H -吲唑并[2,1- b ]酞嗪三酮和 1 H -吡唑并[1,2- b ]酞嗪二酮的实用绿色方法n描述了纳米粒子作为一种环保磁性催化剂,来自邻苯二甲酸酐、氢氧化肼、1,3-二酮和醛的四组分缩合、无溶剂反应,在室温下进行热或超声辐照。这种新方法具有显着的优点,例如操作简单、产率高、反应时间短以及没有任何繁琐的后处理或纯化。此外,催化剂的热稳定性、易于制备和分离使其成为一种良好的多相体系,是其他多相催化剂的有用替代品。此外,催化剂可以很容易地通过磁场回收并重复使用八个连续的反应循环而不会显着损失活性。
  • Magnetic Nanoparticle Immobilized N-Propylsulfamic Acid as a Recyclable and Efficient Nanocatalyst for the Synthesis of 2H-indazolo[2,1-b]phthalazine-triones in Solvent-Free Conditions: Comparison with Sulfamic Acid
    作者:Amin Rostami、Bahman Tahmasbi、Ako Yari
    DOI:10.5012/bkcs.2013.34.5.1521
    日期:2013.5.20
    N-Propylsulfamic acid supported onto magnetic $Fe_3O_4$ nanoparticles (MNPs-PSA) was used as an efficient and magnetically recoverable catalyst for synthesis of 2H-Indazolo[2,1-b]phthalazine-1,6,11(13H)-trione derivatives from the three-component, one-pot condensation reaction of phthalhydrazide, aromatic aldehydes and cyclic 1,3-diones, in good to excellent yields at $100^\circ}C$ under solvent-free conditions. The catalyst was easily separated with the assistance of an external magnetic field from the reaction mixture and reused for several consecutive runs without significant loss of its catalytic efficiency. In order to compare, the synthesis of 2H-Indazolo[ 2,1-b]phthalazine-1,6,11(13H)-trione derivatives in the presence of catalytic amount of sulfamic acid (SA) under same reaction condition was also reported.
    负载在磁性$Fe_3O_4$纳米颗粒上的N-丙基磺酸胺(MNPs-PSA)被用作一种高效且可磁性回收的催化剂,用于从酞酰肼、芳香醛和环状1,3-二酮的三组分一锅法缩合反应中合成2H-吲唑[2,1-b]酞嗪-1,6,11(13H)-三酮衍生物,在无溶剂条件下于$100^\circ}C$下得到良好至优异的产率。催化剂借助外部磁场轻松地从反应混合物中分离出来,并在连续多次循环使用中保持其催化效率无显著损失。为了进行比较,同样反应条件下使用硫酸胺(SA)催化量的2H-吲唑[2,1-b]酞嗪-1,6,11(13H)-三酮衍生物的合成也进行了报道。
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