Synthesis, Characterization and antimicrobial activity of azole-pyrazolidin-3-one derivatives
DOI:
https://doi.org/10.7439/ijpc.v5i12.2793Abstract
Pyrazole derivatives have attracted considerable attention in last decade in view of diverse chemotherapeutic potential including anti-cancer. In the present research work some derivatives of pyrazole, 4-(1H-imidazol-1-yl)-5-phenylpyrazolidin-3-one (4a-g) , were synthesized by treating the corresponding hydrazones with base in moderate yields. The synthesized derivatives were characterized by FT-IR, 1 H NMR and Mass spectroscopy and screened for in vitro antimicrobial activity. The compounds 4c, 4f and 4g showed significant antimicrobial activities.Downloads
References
Vijesh AM, Isloor AM, Telkar S, Peethambar Sk, Rai S, Isloor N. Synthesis, characterization and antimicrobial studies of some new pyrazole incorporated imidazole derivatives. Eur J Med Chem 2011; 46(8): 3531-3536.
Ucucu U, Karaburun NG, Isikdag I. Synthesis and analgesic activity of some 1-benzyl-2-substituted-4, 5-diphenyl-1H-imidazole derivatives. Farmaco 2001; 56(4): 285-290.
Alegaon SG, Alagawadi KR, Sonkusare PV, Chaudhary SM, Dadwe DH, Shah AS. Novel Imidazo[2,1-b][1,3,4]thiadiazole carrying rhodanine-3-acetic acid as potential antitubercular agents. Biorg Med Chem Lett 2012; 22(5): 1917-1921.
Hadizadeh F, Hosseinzadeh H, Motamed-Shariaty V-S, Seifi M, Kazemi S. Synthesis and antidepressant activity of N-substituted imidazole-5-carboxamides in forced swimming test model. Iranian J Pham Res 2008; 7(1): 29-33.
Kalaria PN, Satasia SP, Raval DK. Synthesis, characterization and biological screening of novel 5-imidazo-pyrazole incorporated fused pyran motif under microwave irradiation. New J Chem 2014; 38: 1512-1521.
Bektas H, Karaali N, Sachin D, Demirbas A, Karaoglu SA, Demirbas N. Synthesis and antimicrobial activities of some new 1,2,4-triazole derivatives. Molecules 2010; 15: 2427-2438.
Amir M, Kumar S. Synthesis and anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation activities of 3, 5-dimethyl pyrazoles, 3-methylpyrazol-5-ones and 3, 5-disubstituted pyrazolines. Ind J Chem 2005; 44(B): 2532-2537.
Nitulescu GM, Draghici C, Olaru OT. New potential antitumor pyrazole derivatives: Synthesis and cytotoxic evaluation. Int J Mol Sci 2013; 14: 21805-21818.
Kasiotis KM, Tzanetou EN, Haroutounian SA. Pyrazoles as potential anti-angiogenesis agents: A contemporary overview. Frontier in Chem 2014; 2(Article 78): 1-7.
Shelke SN, Dalvi NR, Kale SB, More MS, Gill CH, Karale BK. Environmentally benign synthesis of fluorinated pyrazolone derivatives and their antimicrobial activity. Ind J Chem 2007; 46(B): 1174-1178.
Bhanat K, Parashar B, Sharma VK. Microwave induced synthesis and antimicrobial activities of various substituted pyrazolidines from chalcones. Res J Chem Sci 2014; 4(2): 68-74.
Bhosale SK, Bhosale NS. Synthesis and antimicrobial activity of some pyrazolidin-3-ones derivatives. Int J Chem Sci 2008; 6(4): 2256-2263.
Amir M, Kumar H, Khan SA. Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents. Bioorg Med Chem Lett 2008; 18: 918-922.
Aziz MA, Rahma GEAA, Hassan AA. Synthesis of novel pyrazole derivatives and evaluation of their antidepressant and anticonvulsant activities. Eur J Med Chem 2009; 44: 3480-3487.
Khode S, Maddi V, Aragade P, Palkar M, Ronad PK, Mamledesai S, Thippeswamy AHM, Satyanarayana D. Synthesis and pharmacological evaluation of novel series of 5- (substituted) aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines as novel anti-inflammatory and analgesic agent. Eur J Med Chem 2009; 44: 1682-1688.
Park HJ, Lee K, Park SJ, Ahn B, Lee JC, Cho HY, Lee KI. Identification of antitumor activity of pyrazole oxime ethers. Bioorg Med Chem Lett 2005; 15: 3307-3312.
Subramanian S, Sharma VK, Yun J, Jung S-H. Exploration of isosteric replacement of Imidazolidinone motif in 4-phenyl-1-arylsulfonylimidazolidinone with pyrazole and pyrazolidinone for cytotoxicity. Bull Korean Chem Soc 2014; 35(10): 2922-2928.
Rajput AP, Gore RP. Synthesis, characterization and antimicrobial screening of some novel 2-(1H-azol-1-yl)-N-(2-substitutedphenyl)-4-oxothiazolidin-3-yl) acetamides. Int J Chem Tech Res 2012; 4(3): 1212-1217.
Downloads
Published
Issue
Section
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgment of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (SeeThe Effect of Open Access).
- The author must submit Copyright form After acceptance of the article.