SnCl2-catalyzed Kabachnik-Fields of alfa-aminophosphonates with potent antioxidant activity

A novel and efficient method for synthesizing a-aminophosphonates was developed through a Kabachnik–Fields multicomponent reaction using 6-aminocoumarin or 6-aminobenzodioxane, benzaldehyde, triethylphosphite, and a catalytic amount of SnCl2 in ethanol. The resulting 25 compounds 1a–l (71–92%) and 6a–m (45–96%) were obtained in moderate to excellent yields. Antioxidant activity, assessed via the FRAP andCUPRAC assays, the results demonstrated that several of these compounds exhibit comparable or evensuperior reducing power to ascorbic acid, particularly at low concentrations. These findings underscorethe potential of these a-aminophosphonates as promising antioxidant agents for future applications.ADME analysis predicts good oral bioavailability, limited brain and skin penetration, and potential CYP450inhibition.

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Publication Details

Journal
Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)
Published
2025-12-12
Primary Topic
Organophosphorus compounds synthesis
Type
article
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article

SnCl2-catalyzed Kabachnik-Fields of alfa-aminophosphonates with potent antioxidant activity

Abderrafia Hafid, Achraf Hibot, Mostafa Khouili, Maria Dolors Pujol et al.
Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)
Organophosphorus compounds synthesis
article

SnCl2-catalyzed Kabachnik-Fields of alfa-aminophosphonates with potent antioxidant activity

Abderrafia Hafid, Achraf Hibot, Mostafa Khouili, Maria Dolors Pujol, Salha Hamri
article en

Abstract

A novel and efficient method for synthesizing a-aminophosphonates was developed through a Kabachnik–Fields multicomponent reaction using 6-aminocoumarin or 6-aminobenzodioxane, benzaldehyde, triethylphosphite, and a catalytic amount of SnCl2 in ethanol. The resulting 25 compounds 1a–l (71–92%) and 6a–m (45–96%) were obtained in moderate to excellent yields. Antioxidant activity, assessed via the FRAP andCUPRAC assays, the results demonstrated that several of these compounds exhibit comparable or evensuperior reducing power to ascorbic acid, particularly at low concentrations. These findings underscorethe potential of these a-aminophosphonates as promising antioxidant agents for future applications.ADME analysis predicts good oral bioavailability, limited brain and skin penetration, and potential CYP450inhibition.

Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)
Openalex Percentile: Top 31%
Organophosphorus compounds synthesis
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