Journal of Combinatorial Chemistry 2008-01-01

Novel and efficient one-pot tandem synthesis of 2-styryl-substituted 4(3H)-quinazolinones.

Minoo Dabiri, Mostafa Baghbanzadeh, Akram Sadat Delbari

Index: J. Comb. Chem. 10(5) , 700-3, (2008)

Full Text: HTML

Abstract

A novel one-pot tandem synthesis of 2-styryl-4(3 H)-quinazolinones in an acidic ionic liquid is reported. In this procedure isatoic anhydride, a primary aniline or ammonium acetate, and triethylorthoacetate are reacted in the presence of imidazolium trifluoroacetate [Hmim]TFA. Subsequently an aromatic aldehyde is added to the mixture to afford the title compounds in high to excellent yields.


Related Compounds

Related Articles:

Hydrogen-bonding in 2-aminobenzoyl-alpha-chymotrypsin formed by acylation of the enzyme with isatoic anhydride: IR and mass spectroscopic studies.

2002-01-04

[ChemBioChem. 3(1) , 68-75, (2002)]

Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids.

2011-11-18

[Org. Lett. 13 , 6114-6117, (2011)]

1,3-Dipolar cycloaddition-decarboxylation reactions of an azomethine ylide with isatoic anhydrides: formation of novel benzodiazepinones.

2011-02-04

[Org. Lett. 13(3) , 486-9, (2011)]

Suicide enzyme inactivators.

1983-01-01

[Basic Life Sci. 25 , 287-305, (1983)]

Synthesis of 2,3-dihydroquinazolin-4(1H)-ones by three-component coupling of isatoic anhydride, amines, and aldehydes catalyzed by magnetic Fe(3)O(4) nanoparticles in water.

2010-09-13

[J. Comb. Chem. 12(5) , 643-6, (2010)]

More Articles...