Na2SiO3/SnFe2O4催化体系通过四组分反应制备骨架多样的喹唑啉-2,4(1H,3H)-二酮

IF 1.8 3区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Fazilat Ayambekam, M. Ghashang
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引用次数: 0

摘要

摘要采用Na2SiO3型硅酸钠进行酮、醛和氰基乙酰胺的四组分反应。研究了SnFe2O4纳米粒子对Na2SiO3催化电位的影响。通过该方法合成的所需产物是5-氨基-7-芳基-2,4-二氧代-2,3,4,4a,7,7a,8,9,10,11-十氢-1H-苯并[i]喹唑啉-6-腈,5-氨基-2,4-二氧代-7-芳基-1,2,3,4,4a、7,7a、8,10,11-十氢吡并[3,4-i]喹唑林-6-腈,8,9,10,11-十氢-1H-吡啶并[3,4-i]喹唑啉-6-腈和5-氨基-2,4-二氧代-7-芳基-1,2,3,4,4,4a,7,7a,8,10,11-十氢吡喃并[3,4-i]喹唑林-6-腈衍生物。该方法具有收率高、操作简便、后处理方便等优点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation of skeletally diverse quinazoline-2,4(1H,3H)-diones using Na2SiO3/SnFe2O4 catalytic system through a four-component reaction
Abstract Sodium silicate with the formula of Na2SiO3 was used for the four-component reaction of ketones, aldehydes and cyanoacetamide. The effect of SnFe2O4 nano-particles on the catalytic potential of Na2SiO3 was investigated. The desired products synthesized by this method are 5-amino-7-aryl-2,4-dioxo-2,3,4,4a,7,7a,8,9,10,11-decahydro-1H-benzo[i]quinazoline-6-carbonitriles, 5-amino-2,4-dioxo-7-aryl-1,2,3,4,4a,7,7a,8,10,11-decahydropyrano[3,4-i] quinazoline-6-carbonitrile, 5-amino-9-methyl-2,4-dioxo-7-aryl-2,3,4,4a,7,7a,8,9,10,11-decahydro-1H-pyrido[3,4-i] quinazoline-6-carbonitrile and 5-amino-2,4-dioxo-7-aryl-1,2,3,4,4a,7,7a,8,10,11-decahydrothiopyrano[3,4-i]quinazo-line-6-carbonitrile derivatives. This method has advantages of high yields, simple procedure and easy work-up.
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来源期刊
Main Group Metal Chemistry
Main Group Metal Chemistry CHEMISTRY, INORGANIC & NUCLEAR-CHEMISTRY, ORGANIC
CiteScore
4.10
自引率
27.80%
发文量
21
审稿时长
4 weeks
期刊介绍: This journal is committed to the publication of short communications, original research, and review articles within the field of main group metal and semi-metal chemistry, Main Group Metal Chemistry is an open-access, peer-reviewed journal that publishes in ongoing way. Papers addressing the theoretical, spectroscopic, mechanistic and synthetic aspects of inorganic, coordination and organometallic main group metal and semi-metal compounds, including zinc, cadmium and mercury are welcome. The journal also publishes studies relating to environmental aspects of these metals, their toxicology, release pathways and fate. Articles on the applications of main group metal chemistry, including in the fields of polymer chemistry, agriculture, electronics and catalysis, are also accepted.
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