Using of modified sugarcane bagasse as a green and inexpensive catalyst for the synthesis of indeno[1,2-b]quinolin-8-one derivatives

被引:0
作者
Zare, Samaneh Hamidi [1 ]
Rostami, Esmael [1 ]
机构
[1] Payame Noor Univ, Dept Chem, POB 19395-3697, Tehran, Iran
来源
IRANIAN JOURNAL OF CATALYSIS | 2020年 / 10卷 / 04期
关键词
Sugarcane bagasse; Solid acid catalyst; Heterogeneous catalyst; Indenoquinolin; ONE-POT SYNTHESIS; ANTITUMOR-ACTIVITY; SOLID ACID; 3-COMPONENT SYNTHESIS; REUSABLE CATALYST; EFFICIENT; INHIBITORS; NANOCOMPOSITE; DISCOVERY;
D O I
暂无
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Chemical grafting of 3-aminipropyl triethoxysilane to carbonized bagasse and acidification of amino groups leads us to introduce a new, efficient and green solid acid catalyst. We used the Fourier-transform infrared spectroscopy (FT-IR), X-Ray Diffraction (XRD), Thermogravimetric analysis (TGA), Field Emission Scanning Electron Microscope (FE-SEM), elemental-mapping and Energy Dispersive X-ray spectroscopy (EDX) for the characterization of the catalyst. This novel catalyst efficiently used to the synthesis of benzo [h]indenoquinolin derivatives and the products were obtained with 80-95% of yields at 3-5 h with high purity. All of the products were characterized by FT-IR, H-1 and (CNMR)-C-13 spectroscopies and compared with authentic samples. Our protocol offers several significant advantages, such as easy preparation of catalyst, green nature of catalyst and reaction media, high yields, good reaction times and easy workup.
引用
收藏
页码:277 / 282
页数:6
相关论文
共 38 条
[1]   p-TSA-catalyzed one-pot synthesis and docking studies of some 5H-indeno[1,2-b]quinoline-9,11(6H,10H)-dione derivatives as anticonvulsant agents [J].
Ahmed, Kamaal ;
Dubey, Balkrishna ;
Nadeem, Sayyed ;
Shrivastava, Birendra ;
Sharma, Pankaj .
CHINESE CHEMICAL LETTERS, 2016, 27 (05) :721-725
[2]   Introducing of a New Bio-inspired Hierarchical Porous Silica as an Inorganic Host for Ni-Pd Alloy Nanoparticles for the Synthesis of Aminobiphenyls from the One-Pot Suzuki-Miyaura Coupling-Nitro Reduction [J].
Beigbaghlou, Somayyeh Sarvi ;
Kalbasi, Roozbeh Javad ;
Marjani, Katayoun ;
Habibi, Azizollah .
CATALYSIS LETTERS, 2018, 148 (08) :2446-2458
[3]   Sugarcane bagasse and leaves: foreseeable biomass of biofuel and bio-products [J].
Chandel, Anuj K. ;
da Silva, Silvio S. ;
Carvalho, Walter ;
Singh, Om V. .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2012, 87 (01) :11-20
[4]   Preparation of solid acid catalyst from glucose-starch mixture for biodiesel production [J].
Chen, Guo ;
Fang, Baishan .
BIORESOURCE TECHNOLOGY, 2011, 102 (03) :2635-2640
[5]   Synthesis and antitumor activity of some indeno[1,2-b]quinoline-based bis carboxamides [J].
Deady, LW ;
Desneves, J ;
Kaye, AJ ;
Finlay, GJ ;
Baguley, BC ;
Denny, WA .
BIOORGANIC & MEDICINAL CHEMISTRY, 2000, 8 (05) :977-984
[6]  
Dehghanpoor S., 2018, BULG CHEM, V50, P18
[7]   A Au(I)-catalyzed hydrogen bond-directed tandem strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives [J].
Jiang, Chongguo ;
Xiong, Zhiling ;
Jin, Shengfei ;
Gao, Peng ;
Tang, Yingzhan ;
Wang, Yanshi ;
Du, Chuan ;
Wang, Xiaoyu ;
Liu, Yang ;
Lin, Bin ;
Liu, Yongxiang ;
Cheng, Maosheng .
CHEMICAL COMMUNICATIONS, 2016, 52 (77) :11516-11519
[8]   Fe3O4@urea/HITh-SO3H as an efficient and reusable catalyst for the solvent-free synthesis of 7-aryl-8H-benzo[h]indeno-[1,2-b]quinoline-8-one and indeno[2′,1′:5,6]pyrido[2,3-d] pyrimidine derivatives [J].
Jiang, Shenghao ;
Shen, Macheng ;
Sheylchahmad, Fatima Rashid .
OPEN CHEMISTRY, 2020, 18 (01) :648-662
[9]   Three-component, one-pot synthesis of benzo[f]indenoquinoline derivatives catalyzed by poly(4-vinylpyridinium) hydrogen sulfate [J].
Khaligh, Nader Ghaffari .
CHINESE JOURNAL OF CATALYSIS, 2014, 35 (04) :474-480
[10]   Condensation of fluorosubstituted benzaldehydes with amines and cyclic 1,3-diketones [J].
Kozlov, N. G. ;
Gusak, K. N. .
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 42 (11) :1668-1674