Synthesis of 1-substituted 5-acetyl (ethoxycarbonyl)-2,3-dihydropyrazolo-[3,4-b]pyridin-3-ones

Lebed, P. S.; Mozgovaya, N. G.; Манойленко, О. В.; Tolmachova, V. S.; Вовк, М. В.

doi:10.1007/s10593-012-1099-7

Cited by 4 publications

(1 citation statement)

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“…In particular, they play key role as intermediates in the synthesis of pyridines and pyrimidines (Dyachenko, 2005;Habashi et al, 1986;Lebed et al, 2012;Kumar et al, 2009;Riad et al, 1989;Sadek et al, 2011;Viale et al, 2011;Yadav et al, 2003;Yadav et al, 2011). They are prepared by the two component reaction of alkyl acetoacetate and different aromatic /hetero aromatic amines (Desai et al, 2001).…”

Section: Introductionmentioning

confidence: 99%

Process optimization and eco-friendly/greener synthesis of some n-aryl/heteryl acetoacetamides

Sirisha¹,

Rajyalaxmi²,

Olivia³

2013

Int Curr Pharm J

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N-aryl/heteryl acetoacetamides are the intermediates used in the synthesis of various heterocyclic compounds like 1,4-dihydropyridines, pyrimidines etc. Three different substituted N-aryl/heteryl acetoacetamide derivatives (I-III) have been prepared from the reaction of ethylacetoacetate and three different aryl/heteryl primary amines under solvent free conditions using potassium tert-butoxide as catalyst. The reactions were carried out by two different methods (viz., Conventional and Microwave irradiation) and they are simple, eco-friendly and economical. All reactions were processed for optimization with different ratios of aryl/heteryl amine and ethylacetoacetate like1:1,1:1.2,1:1.4,1:1.6,1:1.8,1:2 and a comparison was made between the percentage yields with each ratio. Highest percentage yield was observed with 1:1.8 ratio for I & II and 1:1.6 ratio for III in both the methods. However, the microwave irradiation method was found to be superior to the conventional method. The newly synthesized compounds have been purified by recrystallization and characterized by physical and spectral data.DOI: http://dx.doi.org/10.3329/icpj.v2i11.16533 International Current Pharmaceutical Journal, October 2013, 2(11): 189-192

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