Synthesis of Xanthene and Dihydroquinazolin-4(1H)-ones by fructose catalyst

Publish Year: 1397
نوع سند: مقاله کنفرانسی
زبان: English
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شناسه ملی سند علمی:

IRANCC20_782

تاریخ نمایه سازی: 28 اردیبهشت 1398

Abstract:

Xanthene, Benzoxanthene and 2-Amino-chromene and its derivatives represent an important class and very useful compounds in various fields of chemistry. These molecules are biologically active and find application in pharmacological, medicinal [1]. Also, Dihydroquinazolin-4 (1H) -ones constitute an important class of heterocycliccompounds that have been widely exhibited spectrum of biological, physiological activities and pharmacological properties [2], such as anticancer, antidiuretic, anticonvulsant, antibacterial, antifungal activity [3] and mono-amine oxidase inhibition and are also used as 5-hydroxytryptamine (5-HT) receptor ligands. Recently,Lindsley and coworkers observed the metabotropic glutamate receptor (mGluR) properties of this class of compounds. In this project, sulfonated fructose used as a new, non-toxic and effective catalyst for benzaldehyde, 2-naphthol and dimedone for the synthesis of tetrahydrobenzo [a] xanthene-11-one and the reaction of aldehyde and 2-naphthol to synthesize 14H-DI benzo [a, j] Xanthene. Advantages of this method are: the use of inexpensive, affordable and non-toxic catalyst, high efficiency, relatively short response times, simple product purifications, good to excellent yields.

Authors

Ashraf Moradi

Department of Chemistry, Faculty of Science, University of Zabol, Zabol, Iran

Ali Kakeshpour

Department of Chemistry, Faculty of Science, University of Tehran, Tehran, Iran

Fatemeh Pirani

Department of Chemistry, Faculty of Science, University of Zabol, Zabol, Iran