Catalytic acidic deep eutectic mixture for efficient and promising synthesis of quinazolinone and quinoxaline derivatives

A facilitated and economical protocol was designed to synthesize novel acidic deep eutectic mixture (ADEM) from urea/SbCl<sub>3</sub>/HCl as commercially available substrates for the first time. Urea acts as a hydrogen bond donor, SbCl<sub>3</sub> serves as a Lewis acid catalyst, and HCl provides ionic conductivity and an acidic environment. The architectural chemical composition of acidic deep eutectic mixture was confirmed using EDX and FT-IR spectroscopy. This approach led to performing the quinazolinone synthesis with remarkable yield under moderate conditions in a short time and excellent functional group tolerance. Furthermore, in another reaction <i>via</i> a one-pot strategy, π-conjugated polycyclic quinoxaline frameworks were successfully synthesized. Moreover, ADEM demonstrated the capability of being reused and recycled for up to five terms while not decreasing the efficiency or impacting chemical performance regarding the reaction. Besides, the exploitation of inexpensive materials, time-saving reactions, and broad substrate range are prominent attributes of the designed procedure.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra03346b
Citations
2
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
1.87
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article

Catalytic acidic deep eutectic mixture for efficient and promising synthesis of quinazolinone and quinoxaline derivatives

Zohreh Mirjafari, Javad Mokhtari, Najmedin Azizi, Faqeer Mohammad
2 citations
RSC Advances
Quinazolinone synthesis and applications
1.87
article

Catalytic acidic deep eutectic mixture for efficient and promising synthesis of quinazolinone and quinoxaline derivatives

Zohreh Mirjafari, Javad Mokhtari, Najmedin Azizi, Faqeer Mohammad
article en
2 citations

Abstract

A facilitated and economical protocol was designed to synthesize novel acidic deep eutectic mixture (ADEM) from urea/SbCl<sub>3</sub>/HCl as commercially available substrates for the first time. Urea acts as a hydrogen bond donor, SbCl<sub>3</sub> serves as a Lewis acid catalyst, and HCl provides ionic conductivity and an acidic environment. The architectural chemical composition of acidic deep eutectic mixture was confirmed using EDX and FT-IR spectroscopy. This approach led to performing the quinazolinone synthesis with remarkable yield under moderate conditions in a short time and excellent functional group tolerance. Furthermore, in another reaction <i>via</i> a one-pot strategy, π-conjugated polycyclic quinoxaline frameworks were successfully synthesized. Moreover, ADEM demonstrated the capability of being reused and recycled for up to five terms while not decreasing the efficiency or impacting chemical performance regarding the reaction. Besides, the exploitation of inexpensive materials, time-saving reactions, and broad substrate range are prominent attributes of the designed procedure.

RSC AdvancesVol. 15(32)
Islamic Azad University, Science and Research Branch (IR), Chemistry and Chemical Engineering Research Center of Iran (IR)
Openalex Percentile: Top 14%
Quinazolinone synthesis and applications
1.87
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