Aqueous-Mediated green synthesis of novel spiro[indole-quinazoline] derivatives using kit-6 mesoporous silica coated Fe3O4 nanoparticles as catalyst

被引:38
作者
Abdolmohammadi, Shahrzad [1 ]
Shariati, Shahab [2 ]
Fard, Narges Elmi [3 ]
Samani, Amir [1 ]
机构
[1] Islamic Azad Univ, Dept Chem, East Tehran Branch, POB 18735-138, Tehran, Iran
[2] Islamic Azad Univ, Dept Chem, Rasht Branch, Rasht, Iran
[3] Islamic Azad Univ, Young Researchers & Elite Club, South Tehran Branch, Tehran, Iran
关键词
IN-VITRO; ARYLMETHYLIDENEPYRUVIC ACIDS; CYCLOCONDENSATION REACTION; MAGNETITE NANOPARTICLES; TIO2; NANOPARTICLES; HIGHLY EFFICIENT; MILD SYNTHESIS; NANOCOMPOSITE; ANTICANCER; ROUTE;
D O I
10.1002/jhet.3981
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this work, a series of eight new spiro[3,4 ']1,3-dihydro-2H-indol-2-one-2 '-amino-4 ',6 ',7 ',8 '-tetrahydro-2 ',5'(1'H,3'H)-quinazoline-diones were successfully synthesized through a three-component reaction of 1H-indole-2,3-diones (isatins), guanidine nitrate, and 1,3-cyclohexanediones, by use of Kit-6 mesoporous silica coated Fe3O4 nanoparticles (Fe3O4@SiO2@KIT-6) as a highly efficient magnetically separable nanocatalyst in aqueous media at 60 degrees C. Several notable features of thiseco-friendly protocol are high yields of products, short reaction times, operational simplicity, and the use of easily available and recyclable catalyst.
引用
收藏
页码:2729 / 2737
页数:9
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