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3,6,8-trimethyl-4-(4-nitrophenyl)-1-phenyl-8,9-dihydro-1H-pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine-5,7(4H,6H)-dione | 1571869-88-9

中文名称
——
中文别名
——
英文名称
3,6,8-trimethyl-4-(4-nitrophenyl)-1-phenyl-8,9-dihydro-1H-pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine-5,7(4H,6H)-dione
英文别名
3,6,8-trimethyl-4-(4-nitrophenyl)-1-phenyl-8,9-dihydro-1H-pyrazolo[4',3':5,6]pyrido[2,3-d]pyrimidine-5,7(4H,6H)-dione
3,6,8-trimethyl-4-(4-nitrophenyl)-1-phenyl-8,9-dihydro-1H-pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine-5,7(4H,6H)-dione化学式
CAS
1571869-88-9
化学式
C23H20N6O4
mdl
——
分子量
444.45
InChiKey
KWTMLLZPCSBDLL-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

  • 沸点:
    614.9±65.0 °C(predicted)
  • 密度:
    1.48±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.72
  • 重原子数:
    33.0
  • 可旋转键数:
    3.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    116.99
  • 氢给体数:
    1.0
  • 氢受体数:
    9.0

反应信息

点击查看最新优质反应信息

文献信息

  • A Novel and Efficient Five-Component Synthesis of Pyrazole Based Pyrido[2,3-d]pyrimidine-diones in Water: A Triply Green Synthesis
    作者:Majid Heravi、Mansoureh Daraie
    DOI:10.3390/molecules21040441
    日期:——
    A novel one pot synthesis of pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine-diones, via a five-component reaction, involving, hydrazine hydrate, ethyl acetoacetate, and 1,3-dimethyl barbituric acid, an appropriate aryl aldehydes and ammonium acetate catalyzed via both of heterogeneous and homogeneous catalysis in water, is reported.
    吡唑并[4',3':5,6]吡啶并[2,3-d]嘧啶-二酮的新型一锅合成,通过五组分反应,涉及乙酰乙酸乙酯和1,3-据报道,二甲基巴比妥酸是一种合适的芳基醛和乙酸铵,可通过中的非均相和均相催化进行催化。
  • Catalytic regioselective synthesis of pyrazole based pyrido[2,3-d]pyrimidine-diones and their biological evaluation
    作者:Shailesh P. Satasia、Piyush N. Kalaria、Dipak K. Raval
    DOI:10.1039/c3ob42132e
    日期:——
    A new type of biopolymer-based heterogeneous catalyst, cellulose supported acidic ionic liquid (Cell-IL), which was developed earlier in our lab, has been found to be very effective for the regioselective synthesis of pyrazole based pyrido[2,3-d]pyrimidine-diones. Its regioselectivity was confirmed by 1H NMR spectroscopy. All the newly synthesized compounds were characterized by LC-MS, 1H NMR, 13C NMR, IR spectroscopy and elemental analysis. The newly synthesized compounds were evaluated for their in vitro antimalarial activity against Plasmodium falciparum, in vitro antitubercular activity against Mycobacterium tuberculosis H37Rv strain and also for their antibacterial activity against a panel of pathogenic strains of bacteria and fungi. Some of them exhibited excellent activity when compared with first line drugs.
    我们实验室早先开发的一种新型生物聚合物基异相催化剂--纤维素支撑的酸性离子液体(Cell-IL)被发现对吡唑吡啶并[2,3-d]嘧啶二酮的区域选择性合成非常有效。1H NMR 光谱证实了它的区域选择性。所有新合成的化合物都通过 LC-MS、1H NMR、13C NMR、IR 光谱和元素分析进行了表征。对新合成的化合物进行了评估,以确定它们对恶性疟原虫的体外抗疟活性、对结核分枝杆菌 H37Rv 株的体外抗结核活性,以及对细菌和真菌致病菌株的抗菌活性。与一线药物相比,其中一些药物表现出卓越的活性。
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