Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives
Preparation of 4-benzyl-2-substituted phthalazin-1-one derivatives 2-8 is reported. Condensation of 4-benzyl-1-chlorophthalazine (9) with a series of different nucleophiles gave 4-benzylphthalazin-1-ylamino derivatives (10-13 and 16) and 4-amino-2-[N'-(4-benzylphthalazin-1-yl)-hydrazino]-6-aryl...
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doaj-ed35a450f4904ed1b17aed08804830c02020-11-25T02:50:42ZengMDPI AGPharmaceuticals1424-82472011-08-01481158117010.3390/ph4081158Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine DerivativesAhmed H. BedairAhmed M. El-AgrodyMohammed A. El-NassagAshraf H.F. Abd El-WahabHany M. MohamedPreparation of 4-benzyl-2-substituted phthalazin-1-one derivatives 2-8 is reported. Condensation of 4-benzyl-1-chlorophthalazine (9) with a series of different nucleophiles gave 4-benzylphthalazin-1-ylamino derivatives (10-13 and 16) and 4-amino-2-[N'-(4-benzylphthalazin-1-yl)-hydrazino]-6-arylpyrimidine-5-carbonitriles (14a,b). Interaction of 9 with ambident anions was also studied. 5-Benzyl-6,6a,12-triazobenzo[a]-anthracen-7-one (15) is obtained from 9 and anthranilic acid derivatives. Treatment of 16 with (EtO)3CH/Ac2O under reflux afforded the corresponding ethoxymethylene derivative 17, while aqueous ammonium hydroxide treatment afforded carboxamide derivative 18. The structures of the newly synthesized derivatives were confirmed by their elemental analysis, IR, 1H NMR, 13C NMR and mass spectral studies. Antimicrobial activities of some selected compounds were also studied and some of these were found to exhibit promising effects against Gram-positive and Gram-negative bacteria and fungi.http://www.mdpi.com/1424-8247/4/8/1158/phthalazine derivativesanthracene derivativessynthesisantimicrobial activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ahmed H. Bedair Ahmed M. El-Agrody Mohammed A. El-Nassag Ashraf H.F. Abd El-Wahab Hany M. Mohamed |
spellingShingle |
Ahmed H. Bedair Ahmed M. El-Agrody Mohammed A. El-Nassag Ashraf H.F. Abd El-Wahab Hany M. Mohamed Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives Pharmaceuticals phthalazine derivatives anthracene derivatives synthesis antimicrobial activity |
author_facet |
Ahmed H. Bedair Ahmed M. El-Agrody Mohammed A. El-Nassag Ashraf H.F. Abd El-Wahab Hany M. Mohamed |
author_sort |
Ahmed H. Bedair |
title |
Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives |
title_short |
Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives |
title_full |
Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives |
title_fullStr |
Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives |
title_full_unstemmed |
Synthesis and Biological Screening of 4-Benzyl-2H-phthalazine Derivatives |
title_sort |
synthesis and biological screening of 4-benzyl-2h-phthalazine derivatives |
publisher |
MDPI AG |
series |
Pharmaceuticals |
issn |
1424-8247 |
publishDate |
2011-08-01 |
description |
Preparation of 4-benzyl-2-substituted phthalazin-1-one derivatives 2-8 is reported. Condensation of 4-benzyl-1-chlorophthalazine (9) with a series of different nucleophiles gave 4-benzylphthalazin-1-ylamino derivatives (10-13 and 16) and 4-amino-2-[N'-(4-benzylphthalazin-1-yl)-hydrazino]-6-arylpyrimidine-5-carbonitriles (14a,b). Interaction of 9 with ambident anions was also studied. 5-Benzyl-6,6a,12-triazobenzo[a]-anthracen-7-one (15) is obtained from 9 and anthranilic acid derivatives. Treatment of 16 with (EtO)3CH/Ac2O under reflux afforded the corresponding ethoxymethylene derivative 17, while aqueous ammonium hydroxide treatment afforded carboxamide derivative 18. The structures of the newly synthesized derivatives were confirmed by their elemental analysis, IR, 1H NMR, 13C NMR and mass spectral studies. Antimicrobial activities of some selected compounds were also studied and some of these were found to exhibit promising effects against Gram-positive and Gram-negative bacteria and fungi. |
topic |
phthalazine derivatives anthracene derivatives synthesis antimicrobial activity |
url |
http://www.mdpi.com/1424-8247/4/8/1158/ |
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