Synthesis of 4‐(Phenylamino)quinazoline‐2(<i>1H</i>)‐thiones Using Green Solvents

Given the importance of quinazolines and quinazolinethiones in therapeutic and Food and Drug Administration (FDA)-approved molecules, we thought interesting to consider their synthesis in green solvents. We have shown that obtain 4-(arylamino)quinazoline-2-(1H)-thiones and 4-(arylamino)pteridine-2-(1H)-thiones analogues was efficient in green solvents derived from biomass, especially eucalyptol. Although reaction times are somewhat long to achieve good yields, the products were obtained by simple filtration. This considerably limited the loss of atoms due to the use of large quantities of solvents for purification on silica gel columns, and makes our route a sustainable one.

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-08-12
DOI
https://doi.org/10.1002/chem.202402136
Citations
3
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.75
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article

Synthesis of 4‐(Phenylamino)quinazoline‐2(1H)‐thiones Using Green Solvents

Gatien Messire, Sabine Berteina‐Raboin, Claudie Adolf
3 citations
Chemistry - A European Journal
Quinazolinone synthesis and applications
0.75
article

Synthesis of 4‐(Phenylamino)quinazoline‐2(1H)‐thiones Using Green Solvents

Gatien Messire, Sabine Berteina‐Raboin, Claudie Adolf
article en
3 citations

Abstract

Given the importance of quinazolines and quinazolinethiones in therapeutic and Food and Drug Administration (FDA)-approved molecules, we thought interesting to consider their synthesis in green solvents. We have shown that obtain 4-(arylamino)quinazoline-2-(1H)-thiones and 4-(arylamino)pteridine-2-(1H)-thiones analogues was efficient in green solvents derived from biomass, especially eucalyptol. Although reaction times are somewhat long to achieve good yields, the products were obtained by simple filtration. This considerably limited the loss of atoms due to the use of large quantities of solvents for purification on silica gel columns, and makes our route a sustainable one.

Chemistry - A European JournalVol. 30(63)
Université d'Orléans (FR), Centre National de la Recherche Scientifique (FR), Institut de Chimie Organique et Analytique (FR)
Responsible consumption and production
Openalex Percentile: Top 33%
Quinazolinone synthesis and applications
0.75
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