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3',7',7'-trimethyl-1'-phenyl-1',7',8',9'-tetrahydrospiro[indoline-3,4'-pyrazolo[3,4-b]quinoline]-2,5'(6'H)-dione | 1231744-19-6

中文名称
——
中文别名
——
英文名称
3',7',7'-trimethyl-1'-phenyl-1',7',8',9'-tetrahydrospiro[indoline-3,4'-pyrazolo[3,4-b]quinoline]-2,5'(6'H)-dione
英文别名
3',7',7'-trimethyl-1'-phenyl-6',7',8',9'-tetrahydro-spiro[indoline-3,4'-pyrazolo[3,4-b]quinoline]-2,5'(1'H)-dione;(+/-)-3,7,7-trimethyl-1-phenyl-6,7,8,9-tetrahydrospiro[pyrazolo[3,4-b]quinoline-4,3'-indoline]-2',5(1H)-dione;3',7',7'-trimethyl-1'-phenylspiro[1H-indole-3,4'-8,9-dihydro-6H-pyrazolo[3,4-b]quinoline]-2,5'-dione
3',7',7'-trimethyl-1'-phenyl-1',7',8',9'-tetrahydrospiro[indoline-3,4'-pyrazolo[3,4-b]quinoline]-2,5'(6'H)-dione化学式
CAS
1231744-19-6
化学式
C26H24N4O2
mdl
——
分子量
424.502
InChiKey
PYUXAPPAVXKBQC-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):
    3.8
  • 重原子数:
    32
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    76
  • 氢给体数:
    2
  • 氢受体数:
    4

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

反应信息

点击查看最新优质反应信息

文献信息

  • An efficient synthesis of pyrazolo[3,4-b]pyridine-4-spiroindolinones by a three-component reaction of 5-aminopyrazoles, isatin, and cyclic β-diketones
    作者:Jairo Quiroga、Sandra Portillo、Alfredo Pérez、Jaime Gálvez、Rodrigo Abonia、Braulio Insuasty
    DOI:10.1016/j.tetlet.2011.03.067
    日期:2011.5
    Novel pyrazolopyridine-spiroindolinones were prepared by the three-component reaction of 5-aminopyrazoles, isatin, and cyclic β-diketones in aqueous media and catalyzed by p-TSA. This protocol provides a simple one-step procedure with the advantages of easy work-up, mild reaction conditions and environmentally benign.
    新型吡唑吡啶-螺并吲哚满酮是通过5-吡唑靛红和环状β-二酮性介质中的三组分反应制备的,并通过p -TSA催化。该协议提供了一个简单的一步程序,具有易于处理,反应条件温和且对环境无害的优点。
  • New four-component reactions in water: a convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4-b]pyridine derivatives
    作者:Kamaraj Balamurugan、Subbu Perumal、J. Carlos Menéndez
    DOI:10.1016/j.tet.2011.03.020
    日期:2011.5
    New four-component domino reactions are described that allow the one-pot synthesis of spiro[indoline/acenaphthylene-3,4'-pyrazolo[3,4-b]pyridine derivatives from the reaction of phenylhydrazine, 3-aminocrotononitrile, isatin/acenaphthylene-1,2-dione, and cyclic 1,3-dicarbonyl compounds, including cyclohexane-1,3-diones, barbituric acid, and 2-thioxodihydropyrimidine-4,6(1H,5H)-dione, in the presence of (+/-)-camphor-10-sulfonic acid (CSA). These processes take place in water and involve the generation of two rings and five new bonds (two C-C, two C-N and one C = N) in a single synthetic operation, with expedient work-up and diminished waste generation due to the absence of extraction and purification steps. (C) 2011 Elsevier Ltd. All rights reserved.
  • One-pot construction of spirooxindole backbone via biocatalytic domino reaction
    作者:Yi-Ru Liang、Yu-Jing Hu、Xue-Han Zhou、Qi Wu、Xian-Fu Lin
    DOI:10.1016/j.tetlet.2017.06.031
    日期:2017.7
    A simple and environmentally friendly method to synthesize spiropyrazolo[3,4-b]pyridines derivatives starting from isatin, cyclic-1,3-diketone and 3-methyl-5-aminopyrazole was developed. With the optimized conditions for enzymes, solvents, enzyme loading and reaction time in hand, 9 compounds were obtained in acceptable yields. Moreover, the investigation in fluorescent properties of these products showed their potential application in the field of new fluorescent material. (C) 2017 Elsevier Ltd. All rights reserved.
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