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Irina V. Ledenyova Vitaly V. Didenko Alexander S. Shestakov Khidmet S. Shikhaliev 《Journal of heterocyclic chemistry》2013,50(3):573-578
Diazotization of 3‐methyl‐4‐phenyl‐1H‐pyrazol‐5‐amine 1 in hydrochloric acid has been reported to afford the corresponding diazonium salt 2 . The latter underwent azocoupling with a variety of active methylene compounds (barbituric 3a and thiobarbituric 3b acid, 2‐hetarylpyrimidine‐4,6‐dione 6a , 6b , 4‐hydroxy‐6‐methylpyridin‐2(1H)‐one 10a , 4‐hydroxy‐6‐methyl‐2H‐pyran‐2‐one 10b , 4‐hydroxy‐1‐p‐tolyl‐1H‐pyrazole‐3‐carboxylic acid ethyl ester 14 , 1,3‐thiazolidine‐2,4‐dione 16a , 2‐thioxo‐1,3‐thiazolidin‐4‐one 16b ) to yield new pyrazolylazo derivatives. Fused pyrazolo[5,1‐c][1,2,4]triazines 5 , 9a , 9b , 12 , 13 were obtained by heterocyclization reactions. Copyright © 2013 HeteroCorporation 相似文献
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Mawlood Mohammad N. Potapov Andrei Yu. Vandyshev Dmitriy Yu. Shikhaliev Khidmet S. Potapov Mikhail А. Ledenyova Irina V. Kosheleva Evgeniya А. 《Chemistry of Heterocyclic Compounds》2019,55(11):1075-1079
Chemistry of Heterocyclic Compounds - Condensation of 1H-1,2,4-triazolo-5-diazonium salts with 1,3-cyclohexanedione, accompanied by cascade processes of cyclization and oxidative aromatization,... 相似文献
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I. V. Ledenyova P. A. Kartavtsev Kh. S. Shikhaliev A. Yu. Egorova 《Russian Journal of Organic Chemistry》2016,52(9):1316-1321
Coupling of 3-alkyl-4-aryl-1H-pyrazole-5-diazonium chlorides with methylene-active methyl phenacyl sulfones afforded new pyrazolo[5,1-c][1,2,4]triazine derivatives via cyclization of the corresponding intermediate 1-aryl-2-(hetarylhydrazinylidene)-2-(methanesulfonyl)ethanones. The reactivity of the methanesulfonyl group on C3 of pyrazolo[5,1-c][1,2,4]triazines toward some nucleophiles was studied. 相似文献
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I. V. Ledenyova A. V. Falaleev Kh. S. Shikhaliev E. A. Ryzhkova F. I. Zubkov 《Russian Journal of General Chemistry》2018,88(1):73-79
The reaction of ethyl 4-(chloromethyl)pyrazolo[5,1-c][1,2,4]triazine-3-carboxylates with thiourea in dimethylformamide involves ANRORC rearrangement (Addition of the Nucleophile, Ring Opening, and Ring Closure) followed by N-formylation to give N-{5-(4-oxo-8-phenyl-1,4-dihydropyrazolo[5,1-c][1,2,4]-triazin-3-yl)-1,3-triazol-2-yl}formamides whose structure was confirmed by X-ray analysis. The reaction mechanism has been studied by HPLC/MS. 相似文献
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Novichikhina N. P. Skoptsova A. A. Shestakov A. S. Potapov A. Yu. Kosheleva E. A. Kozaderov O. A. Ledenyova I. V. Podoplelova N. A. Panteleev M. A. Shikhaliev Kh. S. 《Russian Journal of Organic Chemistry》2020,56(9):1550-1556
Russian Journal of Organic Chemistry - The reaction of pyrrolo[3,2,1-ij]quinoline-1,2-diones with methyl (het)aryl ketones gave the corresponding 1-(het)arylmethylidenepyrroloquinolin-2-ones, and... 相似文献
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Irina V. Ledenyova Vitaly V. Didenko Victor V. Dotsenko Khidmet S. Shikhaliev 《Tetrahedron letters》2014
Cyanothioacetamide reacts with pyrazole-3(5)-diazonium chlorides to afford pyrazolo[5,1-c][1,2,4]triazine-3-carbothioamides 5. The latter can be oxidized with H2O2 to give either pyrazolo[5,1-c][1,2,4]triazine-3-carboxamides or 1,2,4-thiadiazole derivatives, depending on the reaction conditions. The Hantzsch-type reaction of thioamides 5 with α-bromo ketones leads to 3-(thiazol-2-yl)pyrazolo[5,1-c][1,2,4]triazines. 相似文献