Synthesis, Characterization and Anti-Microbial Activity of Novel Pyramidine Derivatives
Abstract
Pyrimidine is a heterocyclic aromatic organic compound similar to benzene and pyridine, containing two nitrogen atoms at positions 1 and 3 of the six-member ring. Three nucleobases found in nucleic acids, cytosine (C), thymine (T), and uracil (U), are pyrimidine derivatives. A pyrimidine has many properties in common with pyridine, as the number of nitrogen atoms in the ring increases the ring pi electrons become less energetic and electrophilic aromatic substitution gets more difficult while nucleophilic aromatic substitution gets easier. Chalcones react with aminoguanidine to give intermediate compounds which on further reacts with substituted ketones to give Pyramidine derivatives. A total of 6 compounds were synthesized from one scheme and they were recrystallized by appropriate solvents. They were identified and characterized by various spectral methods. In the present study, all synthesized compounds tested for anti bacterial activity and anti-fungal activity. They shown significant activity when compared with standard drug Streptomycin and Miconazole respectively.
Keywords: Pyramidines, Characterization, Streptomycin, Miconazole, Anti-microbial activity.
Keywords:
Pyramidines, Characterization, Streptomycin, Miconazole, Anti-microbial activityDOI
https://doi.org/10.22270/jddt.v11i2-S.4693References
Chaithanya MS, Vaidya VP, Nagendrappa G; “Synthesis and biological activity of 2-amino-4H-pyrimido [2, 1-b][1,3]benzothiazoles-3-carboxylates”, Asian journal of chemistry, apr 2011; 23(4):1618-1620.
Rajendra Prasad Y, Bhaskar Rao B, Agarwal NK, Srinivasa Rao A, “Synthesis and Antimicrobial activity of some new 2, 4, 6- trisubstituted pyrimidines”, Asian journal of chemistry , feb 2011; 23(2):641-644.
Babu AN, Nadendla RR; “Synthesis and Antimicrobial activity of 1-substituted phenyl -3-substituted phenyl-4-[(3, 4, 5-trimethoxy)-5-benzyl]-4-aminopyrimidine formazans” Asian journal of chemistry, jan 2011; 23(1):278-280.
Thore SN; “Synthesis of some 3, 5-bis-1, 4-dihydro-4-phenyl 2, 6-dimethyl pyridine-21-amino-61-phenyl pyrimidines”, Asian journal of chemistry, jan 2007; 19(6):4429-4432.
Mobinikhaledi A, Forughifar N, Shariatzadeh SM, Ghaznavi E; “Synthesis and biological activities of some oxazolo and oxothiazolo pyrimidines”, Asian journal of chemistry, 2007; 19(1):228-232.
Kumar N, Tiwari S, Yadav AK; “Pyrido [2, 3-d] pyrimidines and their ribofuranosides: Synthesis and antimicrobial investigations”, Indian journal of chemistry, april 2007; 46:702-706.
Akbari JD, Mehta KB, Pathak SJ, Joshi HS; “synthesis and antimicrobial activity of some new pyrazolo [3, 4-d] pyrimidines and thiazolo [4, 5-d] pyrimidines”, Indian journal of chemistry, March 2008; 47B:477-480.
Vijaya Kumar P, Manohar Reddy K, Rajeswar Rao V; “Synthesis of some 7-methyl-3-(2-oxo-2H-chromen-3-yl)-5H [1, 3] thiazolo[3,2-a-]-pyrimidine-5-ones”, Indian journal of chemistry, May 2008; 47B:759-763.
Sondhi SM, Dinodia M, Rani R, Shukla R, Raghubir R; “Synthesis, anti-inflammatory and analgesic activity evaluation of some pyrimidine derivatives”, Indian journal of chemistry, feb 2009; 49B:273-281.
Rashinkar GS, Pore SB, Mote KB, Salunkhe RS; “An efficient synthesis of novel 2-amino-4-aryl-6-ferrocenyl pyrimidines”, Indian journal of chemistry, April 2009; 48B:606-610.
Rana PB, Patel JA, Mistry BD, Desai KR; “Microwave and conventional techniques for the synthesis of a series of pyrazolo[5,4-d]-pyrimidine derivatives and their antimicrobial screening”, Indian journal of chemistry, NOV 2009; 48B:1601-1608.
Lanjewar KR, Rahatgaonkar AM, Chorghade MS, Saraf BD; “Synthesis and antimicrobial activity of 5-(2-aminothiazol-4-yl)-3,4-dihydro-4-phenyl pyrimidin-2(1H)-one”, Indian journal of chemistry, DEC 2009; 48B:1732-1737.
Chattopadhyay G, Saha D, Ray PS, Naskar S, Sarkar S; “Synthesis of novel thiazolo[5,4-d]pyrimidines” Indian journal of chemistry, Sep 2010; 49B:1229-1234.
Rajanarendar E, Raju S, Nagi Reddy M, Rama Murthy K, “An elegant one-pot synthesis of isoxazolo [2, 3-a] pyrimidines”, Indian journal of chemistry, oct 2010; 49B:1422-1427
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