A new heterocyclic ring closure in ferricyanide oxidation of 2,4,6-triphenylpyridinium salts

1983 ◽  
Vol 48 (11) ◽  
pp. 3307-3314 ◽  
Author(s):  
Petr Nesvadba ◽  
Petr Štrop ◽  
Josef Kuthan
Keyword(s):  
Alkaline Solution ◽  
Heterocyclic Ring ◽  
Potassium Ferricyanide ◽  
Probable Mechanism ◽  
Ring Closure ◽  
Pyridinium Salts ◽  
Mechanism Of Formation ◽  
Pyrrole Derivatives ◽  
Quaternary Pyridinium Salts ◽  
Heterocyclic Derivatives

The quaternary pyridinium salts Ia-Ic react with alkaline solution of potassium ferricyanide to give the condensed heterocyclic derivatives IIIa, b, IV, whereas the salts Id-If give the pyrrole derivatives IIa-IIc under the same conditions. The diaza heterocycle IIIa reacts with methyl iodide to give methoiodide V, whereas by action of bromine it produces two monobromo derivatives VIa, b. The pyrrole derivatives IIa, b give monobromo derivatives IId, e on bromination. A probable mechanism of formation of the heterocyclic derivatives is discussed.

Oxidation of 1,2,3,4,6-substituted pyridinium salts with ferricyanide

1984 ◽  
Vol 49 (2) ◽  
pp. 543-548 ◽  
Author(s):  
Petr Nesvadba ◽  
Josef Kuthan
Keyword(s):  
Reaction Mechanism ◽  
Alkaline Solution ◽  
Quaternary Salt ◽  
Spectral Characteristics ◽  
Potassium Ferricyanide ◽  
Pyridinium Salts ◽  
Pyrrole Derivatives ◽  
Quaternary Pyridinium Salts ◽  
Pyrrole Derivative

Quaternary pyridinium salts IIa-IId are oxidized with alkaline solution of potassium ferricyanide to give a mixture of pyrrole derivatives Ia-Ib and IVa-IVd. The quaternary salt IIe under the same conditions affords a mixture of compounds IVe and V whereas IId gives only the pyrrole derivative IVd. The reaction mechanism is discussed and spectral characteristics of the products are interpreted.

Sterically Crowded Heterocycles. III. A General Approach to Imidazo[1,2-a]pyridines by Ferricyanide Oxidation of Quaternary Pyridinium Salts

1996 ◽  
Vol 61 (1) ◽  
pp. 126-138 ◽  
Author(s):  
Richard Kubík ◽  
Stanislav Böhm ◽  
Iveta Ruppertová ◽  
Josef Kuthan
Keyword(s):  
Potassium Hydroxide ◽  
Potassium Ferricyanide ◽  
Pyridinium Salts ◽  
Oxidizing Agents ◽  
Quaternary Pyridinium Salts ◽  
Substituted 1

Substituted 1-(pyridin-2-yl)-2,4,6-triphenylpyridinium perchlorates 1b-1e were converted with potassium ferricyanide and potassium hydroxide to sterically crowded 2-phenyl-3-[(Z)-1,3-diphenyl-3-oxopropenyl]imidazo[1,2-a]pyridines 2b-2e accompanied by minor isomeric 2-benzoyl-3,5-diphenyl-1-(pyridin-2-yl)pyrroles 3c-3e. 4-Phenyl-2,6-di(4-substituted phenyl)-1-(pyridin-2-yl)pyridinium salts 4a, 4b gave exclusively corresponding imidazo[1,2-a]pyridines 5a, 5b while the ferricyanide oxidation of 1-(5-iodo- and 5-cyanopyridin-2-yl)-2,4,6-triphenylpyridinium perchlorates 6a, 6b led to mixtures of major imidazo[1,2-a]pyridines 7a-7c and minor pyrroles 8a-8c. Some mechanistic aspects of the oxidation procedure are discussed in connection with a resistance of 2,6-diphenyl-1,3,5-trimethylpyridinium perchlorate (9c) towards the oxidizing agents.

Untersuchungen an quartären Pyridinium-Salzen, XV [1] Pseudobasen und Redoxprodukte bei der Umsetzung von Pyridinium-Salzen mit Alkoholat / Investigations of Quaternary Pyridinium Salts, XV [1] Pseudobases and Redox Products in the Reaction of Pyridinium Salts with Alcoxides

1983 ◽  
Vol 38 (7) ◽  
pp. 873-883 ◽  
Author(s):  
Wolf-H. Gündel
Keyword(s):  
Alkaline Solution ◽  
Redox Reaction ◽  
Pyridinium Salts ◽  
Aqueous Alkaline Solution ◽  
Quaternary Pyridinium Salts

Abstract Mono-and diquaternary pyridinium salts substituted in 3-position with electron with-drawing groups, react with alcohols under basic conditions to give 6-alcoxy-1,6-dihydro-pyridines. Symmetric dipyridinium salts react in aqueous alkaline solution to products with 6-pyridone and dihydropyridine moiety. This redox reaction depends on the length of the bridge connecting the pyridinium rings. Pyridinium salts can be reduced by aluminiumtriisopropoxide to 1,4-dihydropyridines.

Oxidation of polysubstituted pyridinium salts

1982 ◽  
Vol 47 (5) ◽  
pp. 1494-1502 ◽  
Author(s):  
Petr Nesvadba ◽  
Josef Kuthan
Keyword(s):  
Alkaline Medium ◽  
Electrophilic Substitution ◽  
Pyridine Ring ◽  
Potassium Ferricyanide ◽  
Pyridinium Salts ◽  
Complex Reaction

Oxidation of 1-substituted 2,4,6-triphenylpyridinium salts Ia-Ij with potassium ferricyanide in an alkaline medium was accompanied by contraction of the pyridine ring and formation of 1,2,3,5-tetrasubstituted pyrroles II. The derivative IIf underwent facile electrophilic substitution in the position 4. Contrary to compounds Ia-Ij, the 1-substituted-2,6-diphenylpyridinium salts IIIa,b were oxidized to give a complex reaction mixture containing 4-pyridones IVa,b.

Effect of micelle formation of quaternary pyridinium salts on their recyclization to anilines

1981 ◽  
Vol 17 (4) ◽  
pp. 367-369 ◽  
Author(s):  
T. V. Stupnikova ◽  
A. I. Serdyuk ◽  
V. N. Kalafat ◽  
R. S. Sagitullin ◽  
V. P. Marshtupa
Keyword(s):  
Micelle Formation ◽  
Pyridinium Salts ◽  
Quaternary Pyridinium Salts

scholarly journals Synthesis and Evaluation Antibacterial Activity of Some New Substituted 5-Bromoisatin Containing Five, Six Heterocyclic Ring

2016 ◽  
Vol 13 (2) ◽  
pp. 345-359
Author(s):  
Baghdad Science Journal
Keyword(s):  
Heterocyclic Ring ◽  
Absolute Ethanol ◽  
Synthesis Process ◽  
Triazole Derivatives ◽  
Amide Derivatives ◽  
Heterocyclic Derivatives ◽  
Acid Anhydrides ◽  
Specific Reactions ◽  
Derivatives Of ◽  
Product Compound

This research includes the synthesis of some new different heterocyclic derivatives of 5-Bromoisatin. New sulfonylamide, diazine, oxazole, thiazole and 1,2,3-triazole derivatives of 5-Bromoisatin have been synthesized. The synthesis process started by the reaction of 5-Bromoisatin with different reagents to obtain schiff bases of 5-Bromoisatin intermediate compounds(1, 8, 19) by using glacial acetic acid as a catalyst in three routes. The first route, 5-Bromoisatin reacted with p-aminosulfonylchloride to product compound(1), then converted to sulfonyl amide derivatives(2-7) by the reaction of compound(1) with different substituted primary aromatic amine in absolute ethanol. The second route includes the reaction of 5-Bromoisatin reacted with ethyl glycinate to give 5-bromo-3-(Ethyl imino acetate)-2-oxo indole(8), which undergo react with hydrazine hydrate 80% to obtain hydrazine derivatives(9) that react with different acid anhydrides to obtain diazine derivatives(10-14). Also compound(8) reacts with urea and thiourea to give compounds(15,16) which undergo cyclization with p-bromophenacylbromide in absolute ethanol as a solvent to obtain oxazole (17) and thiazole (18), respectively. The third route included the reaction of 5-Bromoisatin with p-phenylenediamine in ethanol to obtain compound(19) which is converted to new substitutes 1,2,3-triazole derivatives(22,23) by diazotation of compound(19) and treating the resulted salt(20) with sodium azid, then acetylaceton or ethylacetoacetate, respectively. Newly synthesized compounds were identified by spectral methods. (FTIR, 1H-NMR, 13C-NMR) and measurements of some of its physical properties and also some specific reactions. Furthermore the effects of the synthesized compounds were studied on some strains of bacteria.

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