2012
DOI: 10.4314/bcse.v27i1.9
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Use of transesterified 1,3-diketoesters in the synthesis of trisubstituted pyrazoles and their biological screening

Abstract: ABSTRACT. Starting from 2-acetylbenzofuran derivatives 1a-d, methyl/ethyl 4-substituted/unsubstituted benzofuran-2-yl)-2,4-dioxobutanoate 2a-d and 3a-d have been synthesized by Claisen's condensation reaction with diethyloxalate. The transesterified product, 1,3-diketoester 2a-d on condensation with phenyl hydrazine undergo cyclization to afford the corresponding methyl 5-(substituted/unsubstituted benzofuran-2-yl)-1-phenyl-1H-pyrazole-3-carboxylate 4a-d, which upon further condensation with hydrazine hydrate … Show more

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Cited by 7 publications
(8 citation statements)
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“…In 13 C NMR spectra signals appeared at δ 151.00 and 165.56 indicates 3 rd and 5 th Carbon of triazole moiety respectively, other signals were appeared at the presupposed chemical shifts. As per the general methods reported, compound ( 5 ) was reacted with substituted benzoic/pyridinyl acids in phosphorous oxychloride at reflux temperature for 8–10 h to gives 6‐substituted‐3‐[5‐(3‐fluoro‐4‐methoxy‐phenyl)‐1 H ‐pyrazol‐3‐yl]‐[1, 2,4]triazolo[3, 4‐b][1, 3,4]thiadiazole derivatives ( 6 a‐l ). IR spectra with absence of NH 2 and SH stretching vibrations and absence of NH 2 and SH protons in NMR suggesting formation of 6‐substituted‐3‐[5‐(3‐fluoro‐4‐methoxy‐phenyl)‐1 H ‐pyrazol‐3‐yl]‐[1, 2,4]triazolo[3, 4‐b][1, 3,4]thiadiazole derivatives ( 6 a‐l ).…”
Section: Resultsmentioning
confidence: 99%
“…In 13 C NMR spectra signals appeared at δ 151.00 and 165.56 indicates 3 rd and 5 th Carbon of triazole moiety respectively, other signals were appeared at the presupposed chemical shifts. As per the general methods reported, compound ( 5 ) was reacted with substituted benzoic/pyridinyl acids in phosphorous oxychloride at reflux temperature for 8–10 h to gives 6‐substituted‐3‐[5‐(3‐fluoro‐4‐methoxy‐phenyl)‐1 H ‐pyrazol‐3‐yl]‐[1, 2,4]triazolo[3, 4‐b][1, 3,4]thiadiazole derivatives ( 6 a‐l ). IR spectra with absence of NH 2 and SH stretching vibrations and absence of NH 2 and SH protons in NMR suggesting formation of 6‐substituted‐3‐[5‐(3‐fluoro‐4‐methoxy‐phenyl)‐1 H ‐pyrazol‐3‐yl]‐[1, 2,4]triazolo[3, 4‐b][1, 3,4]thiadiazole derivatives ( 6 a‐l ).…”
Section: Resultsmentioning
confidence: 99%
“…Analytical and spectral data of 3a was in full agreement with proposed structure. 5-(H/Br benzofuran-2-yl)-1-phenyl-1H-pyrazole-3-carbohydrazides (1a-b) 24 and 4-(arylidene)-2-phenyloxazol-5(4H)-ones (2a-g) were synthesized in quantitative yields by adopting the literature method 25 and their confirmation were done on the basis of m.p. determination.…”
Section: Resultsmentioning
confidence: 99%
“…[ 16 ] Several benzofuran derivatives have been prepared and introduced as antibacterial agents. [ 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 ] Renuka et al . [ 17 ] designed and synthesized a series of substituted benzofurans as DNA gyrase B inhibitors of Mycobacterium tuberculosis (MTB).…”
Section: Benzofuran As Antibacterial and Antifungal Agentmentioning
confidence: 99%