2004
DOI: 10.1081/scc-200043224
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Three‐Component One‐Pot Synthesis of 1,4‐Dihydropyrano[2,3‐c]pyrazole Derivatives in Aqueous Media

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Cited by 82 publications
(16 citation statements)
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“…We also examined the reaction of 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one with chalcone, but the desired product was not obtained even after prolonged reaction times ( Table 2, entry 13). When 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one was replaced by barbituric acid the related products (III) were obtained in good yields ( Table 2, entries [14][15][16][17][18].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…We also examined the reaction of 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one with chalcone, but the desired product was not obtained even after prolonged reaction times ( Table 2, entry 13). When 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one was replaced by barbituric acid the related products (III) were obtained in good yields ( Table 2, entries [14][15][16][17][18].…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the biological activity of fused azoles has led to intensive research on their synthesis [11][12][13]. Recently, three component one-pot condensation of 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one, aldehydes and malononitrile for the construction of 1,4-dihydropyrano [2,3-c]pyrazole derivatives has been reported under different conditions [14][15][16][17][18]. However, most of the reported methods have their drawbacks.…”
Section: Introductionmentioning
confidence: 99%
“…The synthesis of organic compounds include 1,4‐dihydropyrano[2,3‐ c ]pyrazoles, tetrahydrobenzo[ b ]pyran, pyrano[4,3‐ b ]pyrans, bispyrazole, 1 H ‐pyrazolo[3,4‐ b ]quinolones, hexahydroacridine‐1,8‐diones and methylenebis(3‐hydroxy‐5,5‐dimethylcyclohex‐2‐enones) has been considerable attention of organic chemists due to their broad range of pharmaceutical and biological properties include arisugacins, anti‐multidrug‐resistant, anti‐inflammatory, photodynamic therapy, inhibitors of human Chk1 kinase, spasmolytic and anti‐filarial agents . Literature survey shows that various processes and catalysts for the synthesis of these compounds include {[HIM]C(CN) 3 }, {[HMIM]C(CN) 3 },, [nano‐Fe 3 O 4 @SiO 2 @(CH 2 ) 3 ‐Imidazole‐SO 3 H]Cl, 2‐carbamoylhydrazine‐1‐sulfonic acid or carbamoylsulfamic acid, L ‐proline, eggshell (ES)‐supported Cu(OH) 2 nanoribbons, triethylbenzylammonium chloride, [2‐MPyH]OTf, ZnCl 2 , hexadecyltrimethylammonium bromide, phosphomolybdic acid and sodium acetate trihydrate urea …”
Section: Introductionmentioning
confidence: 99%
“…The first method has been reported by using the base-catalyzed cyclization of 4-aryliden-5-pyrazolone [32]. New approaches for the production of pyrazole include synthesis based process of β-cyclodextrin [33], cinchona alkaloid derivatives [34], Sc(OTf) 3 [35], triethylamine [36], water or ethanol media [37,38], imidazole [39], CuO/ZrO 2 [40] and triethylbenzylammonium chloride [41].…”
Section: Introductionmentioning
confidence: 99%