نتایج جستجو برای: 5 substituted 1h tetrazoles

تعداد نتایج: 1266962  

Journal: :journal of pharmaceutical and health sciences 0

a simple, fast, efficient and environmentally friendly method for synthesis of benzimidazole and its 2-alkyl, aryl and heteroaryl substituted derivatives was developed using zeolite hy. two component cyclolcondensation of 1,2-phenylenediamine (o-phenylenediamine) and commercially available carboxylic acids catalyzed by zeolite hy without any solvent, under microwave irradiation led to formation...

Journal: :Journal of combinatorial chemistry 2009
Juliya V Kharchenko Oleksandr S Detistov Valeriy D Orlov

We have developed a liquid-phase route for combinatorial synthesis of novel substituted 5-(1,2,4-oxadiazol-5-yl)-3,4-dihydropyrimidine-2(1H)-thiones. Biginelli-type three-component condensation of 1-(3-aryl-1,2,4-oxadiazol-5-yl)acetones, thiourea, and benzaldehydes is shown to result in new 5-(1,2,4-oxadiazol-5-yl)-3,4-dihydropyrimidine-2(1H)-thione heterocyclic system. If salicylaldehydes are ...

Journal: :European Journal of Organic Chemistry 2021

The azotetrazole moiety represents a great platform for energetic materials, it offers planar and nitrogen-rich backbone, combined with high heat of formation, which easily can be functionalized tuned. Herein, we start from sodium 5-aminotetrazolate obtain two isomers by substitution reaction 2-chloroethanol. Azidoethyl nitratoethyl substituted azo- tetrazoles were finally synthesized oxidative...

Journal: :Molecules 2015
Baskar Nammalwar Nagendra Prasad Muddala Rajasekar Pitchimani Richard A Bunce

OSU-6, an MCM-41 type hexagonal mesoporous silica with mild Brönsted acid properties, has been used as an efficient, metal-free, heterogeneous catalyst for the click synthesis of 5-benzyl and 5-aryl-1H-tetrazoles from nitriles in DMF at 90 °C. This catalyst offers advantages including ease of operation, milder conditions, high yields, and reusability. Studies are presented that demonstrate the ...

2014
Barbara Palka Angela Di Capua Maurizio Anzini Gyté Vilkauskaité Algirdas Šačkus Wolfgang Holzer

A straightforward synthesis of 6-substituted 1-phenyl-3-trifluoromethyl-1H-pyrazolo[4,3-c]pyridines and the corresponding 5-oxides is presented. Hence, microwave-assisted treatment of 5-chloro-1-phenyl-3-trifluoromethylpyrazole-4-carbaldehyde with various terminal alkynes in the presence of tert-butylamine under Sonogashira-type cross-coupling conditions affords the former title compounds in a ...

Journal: :Acta poloniae pharmaceutica 2010
Rakesh Chawla Ujjwal Sahoo Anshu Arora Prabodh Chander Sharma Vijayaraj Radhakrishnan

Some new [3-(4-phenyl)-5-phenyl-4,5-dihydropyrazol-1-yl](pyridine-4-yl)methanones and 3-substituted phenyl-5-substituted phenyl-4,5-dihydro-pyrazole-1-carbothioamides have been synthesized employing microwave techniques and evaluated for antimicrobial activity. Substituted acetophenones (1) were reacted with appropriately substituted benzaldehydes (2) in the presence of ethanol to furnish subst...

2005
P. D. Gokulan B. Jayakar

A new series of 5-substituted-3-methylsulfanyl-1-(2,4-dinitro phenyl)-1H-pyrazole-4-carboxylic acid ethyl esters were synthesized by reacting the amino group of 5-amino-3-methylsulfanyl-1-(2,4-dinitro phenyl)-1H-pyrazole-4carboxylic acid ethyl ester with acid anhydrides, acid chlorides and phenyl dithiocarbamates. The title compounds were investigated for analgesic, anti-inflammatory and ulcero...

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