Synthesis, Biological Evaluation of Some Arylsulfonyl, Carboxamide Derivatives of 3-Methyl-1H-pyrazol-5(4H)-one

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Authors: Sabahat Sardar, Tashfeen Akhtar, Shahid Hameed and Khalid Mohammed Khan
Date: Dec. 31, 2012
From: Journal of the Chemical Society of Pakistan(Vol. 34, Issue 6)
Publisher: Knowledge Bylanes
Document Type: Report
Length: 4,380 words

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Summary: Synthesis of pyrazolone, its derivatives is of particular interest in heterocyclic chemistry due to their pharmaceutical importance. In the present study arylsulfonyl (1a-f , 2a-f) , carboxamide (3a-e) derivatives of 3-methyl-1H-pyrazol-5(4H)-one were synthesized. The reaction of pyrazolone with arylsulfonyl chlorides resulted in mono (1a-f) , disubstituted (2a-f) arylsulfonyl derivatives of 3-methyl-1H-pyrazol-5(4H)-one. On the other h,, the pyrazolone on treatment with different isocyanates yielded respective carboxamides (3a-e). The synthesized compounds were screened for urease inhibition, antibacterial, antioxidant assays, exhibit promising urease inhibition. Compound 1e was observed to be most active urease inhibitor in the series with 91.9 % inhibition. However, the antioxidant, antibacterial activities of all the compounds were non-significant at non-toxic concentration.

Keywords: Pyrazolone derivatives, Carboxamides, Urease inhibition, Antibacterial, Antioxidant.


Pyrazolone moiety is an appealing template for medicinal chemistry as it has been a part of many drugs [1]. Pyrazolone derivatives have been the interest of research owing to diverse applications such as antioxidant, antimicrobial, cytotoxic, anticancer, antiviral, anticonvulsant, antibacterial , molluscicidal activities [2-7]. They also exhibit antitumor, antihypoglycemic, antifungal, analgesic, antipyretic , anti-inflammatory activities [8] besides being used as dyes as well [9-11]. Pyrazolones have also been employed in the synthesis of other heterocycles [12], in the separation of lanthanides , dyes preparation [13]. They gave a great impetus to the research for potential pharmacological drugs carrying pyrazolone substituents. The pyrazolone nucleus exhibits structural feature to be a potential urease inhibitor, which is not an explored area of the pyrazolone chemistry.

The urease is a nickel-dependent metalloenzyme that catalyzes the hydrolysis of urea into an ammonium ion, carbamate which spontaneously breaks down to form ammonia , carbon dioxide [14]. The inhibitors of urease have been extensively studied because of their potential use in diseases such as Helicobacter pylori-induced peptic ulcer [15], urinary lithiasis, pyelonephritis , hepatic coma [16]. Urease has been reported to be responsible for the development of acute pyelonephritis by participating in urolithiasis , is also involved in infection-induced arthritis [17]. In order to control the urease activity, urease inhibitors have also been used along with fertilizers to control the rate of urea-hydrolysis in soil [18].

Heterocycles exhibiting urease inhibition have also been synthesized , reported by our group in the past few years [19-23]. We herein report some new pyrazolone derivatives, synthesized to explore their potential urease inhibition properties.

Results , Discussion


The reaction sequences employed for the synthesis of target pyrazolone derivatives is illustrated in Scheme-1. All the synthesized compounds were characterized using modern spectroscopic techniques, screened for their antibacterial, antioxidant , urease inhibition assays.

Arylsulfonyl derivatives of 3-methyl-1H- pyrazol-5(4H)-one were synthesized by the reaction of pyrazolone with various arylsulfonyl chlorides in the presence of triethylamine [21]. On TLC two products were observed, which were separated by silica gel column chromatography , identified as mono- , disubstituted pyrazolones. The synthesis was later optimized by 1:1 , 1:2 molar equivalents of pyrazolone , arylsulfonyl chloride to afford mono- (1a-f) , disubstituted (2a-f)...

Source Citation

Source Citation
Sardar, Sabahat, et al. "Synthesis, Biological Evaluation of Some Arylsulfonyl, Carboxamide Derivatives of 3-Methyl-1H-pyrazol-5(4H)-one." Journal of the Chemical Society of Pakistan, vol. 34, no. 6, 31 Dec. 2012. Accessed 12 Aug. 2022.

Gale Document Number: GALE|A319199513