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1.
D. Zicane Z. Tetere I. Rijkure M. V. Petrova E. Gudriniece U. Kalejs 《Chemistry of Heterocyclic Compounds》2000,36(7):792-795
Monohydrazides of 2-R-4-methyl-4-cyclohexene-1,1-dicarboxylic acids react with trifluoroacetic acid anhydride to give 4-substituted 3,5-dioxopyrazolidines, with phosphorus trichloride to give 4-(2-R-5-chloro-4-methylcyclohexane)-3,5-dioxopyrazolidines, and with acetic anhydride to give 4-(2-R-4-methyl-4-cyclohexene)-3,5-diacetoxypryazoles.For Communication 4, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 903–907, July, 2000. 相似文献
2.
V. N. Britsun 《Chemistry of Heterocyclic Compounds》2008,44(10):1262-1266
The cyclocondensation products of N-aryl-3-oxobutanethioamides with 5-amino-3-R-4-R1-pyrazoles are 4-(arylamino)-2-methyl-7-R-8-R1-pyrazolo[1,5-a]pyrimidine and pyrazolo[1,5-a]pyrimidine-4-thione derivatives, the ratio of which depends on the nucleophilicity of the starting 5-amino-3-R-4-R1-pyrazoles and the presence of a proton donor solvent.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1550-1555, October, 2008. 相似文献
3.
2-R-7a-Methyl-3-(spirocyclohexa-2,5-dien-4-one)perhydro-1-indolines were obtained by the reactions of 1-(4-ethoxyphenyl)-2-methylcyclohexanol with nitriles (RCN) in dichloromethane in the presence of concentrated sulfuric acid. 相似文献
4.
I. V. Ukrainets N. L. Bereznyakova V. A. Parshikov S. V. Shishkina 《Chemistry of Heterocyclic Compounds》2007,43(6):722-728
In acid medium ethyl 1-R-4-dicyanomethyl-2-oxo-1,2-dihydroquinoline-3-carboxylates are hydrated in the ketenimine tautomer
form exclusively to the corresponding quinolylcyanoacetamides.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 856–863, June, 2007. 相似文献
5.
I. V. Ukrainets N. L. Bereznyakova V. A. Parshikov S. V. Shishkina 《Chemistry of Heterocyclic Compounds》2007,43(5):608-616
Hydration of ethyl 1-R-4-dicyanomethyl-2-oxo-1,2-dihydroquinoline-3-carboxylate gives the corresponding substituted cyanoacetamides
which are readily and quantitatively cyclized to 6-R-5-hydroxy-2,4-dioxo-2,3,4,6-tetrahydrobenzo[c][2,7]naphthyridine-1-carbonitriles
in the presence of aqueous base.
For Communication 113 see [1].
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 726–735, May, 2007. 相似文献
6.
Synthesis and Some Chemical Properties of 2,2-Dimethyl-4-R-1-oxa-4-aza-2-sila-5-benzocycloheptanones
O. A. Zamyshlyaeva A. G. Shipov E. P. Kramarova Vad. V. Negrebetsky A. N. Shumskii S. N. Tandura S. Yu. Bylikin Yu. E. Ovchinnikov S. A. Pogozhikh Yu. I. Baukov 《Chemistry of Heterocyclic Compounds》2002,38(1):116-127
One-pot synthesis of 2,2-dimethyl-4-R-1-oxa-4-aza-2-sila-5-benzocycloheptanones (R = Me, CH2SiMe2Cl) from the N-methylamide of salicylic acid and salicylamide, respectively, by treatment of these amides with a mixture of hexamethyldisilazane and dimethylchloromethylchlorosilane was developed. The hydrolysis and other nucleophilic substitution reactions of the resultant seven-membered silacyclanes were studied. In the case of the silacyclane with R = Me, hydrolysis leads to the corresponding disiloxane, while the silacyclane with R = CH2SiMe2Cl gives either 2,2,6,6-tetramethyl-4-(2-hydroxybenzoyl)-2,6-disilamorpholine or its hydrochloride, depending on the reaction conditions. The chlorine atom was replaced by fluorine in the silacyclane with R = CH2SiMe2Cl. The structures of 2,2,6,6-tetramethyl-4-(2-hydroxybenzoyl)-2,6-disilamorpholine and its hydrochloride as well as 2,2-dimethyl-4-R-1-oxa-4-az! a-2-sila-5-benzocycloheptanones (R = CH2SiMe2Cl, CH2SiMe2F) were confirmed by X-ray diffraction. 相似文献
7.
T. V. Shokol V. V. Semenyuchenko V. P. Khilya 《Chemistry of Heterocyclic Compounds》2005,41(5):673-678
By recyclization of 2-R-6-ethyl-7-hydroxy(methoxy)-3-(5-phenyl-1,3,4-thiadiazol-2-yl)chromones when treated with hydrazine hydrate and phenylhydrazine, we synthesized 5-phenyl-2-(3-R-5-R1-1H-pyrazol-4-yl)-1H-1,3,4-thiadiazoles and 2-(3-R-5-R1-1-phenyl-1H-pyrazol-4-yl)-5-phenyl-1H-1,3,4-thiadiazoles. We confirmed the structure of the latter from 1H NMR spectra.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 781–787, May, 2005. 相似文献
8.
Kh. S. Shikhaliev A. V. Falaleev D. V. Krylsky A. S. Solov'ev G. V. Shatalov 《Chemistry of Heterocyclic Compounds》2002,38(11):1368-1370
We synthesized 2-(6-R-4-methyl-2-quinazolyl)amino-1,4-dihydropyrimid-4-ones by reaction of 6-R-4-methyl-2-quinazolylguanidines with acylacetic esters. 相似文献
9.
S. G. Taran I. V. Ukrainets L. V. Sidorenko O. V. Gorokhova N. A. Jaradat 《Chemistry of Heterocyclic Compounds》2000,36(8):944-947
Treatment of 1-R-2-oxo-4-hydroxyquinolin-3-ylamides of -halogen-substituted carboxylic acids with sodium methoxide leads to the formation of 2-R-3-oxomorpholino-[5,6-c]-6-R-quinolin-5-ones. The antituberculosis activity of the compounds synthesized was studied.For Communication 43, see [1].National Pharmaceutical Academy of Ukraine, Kharkov 310002; e-mail: igor@uiv.kharkov.ua. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1080–1083, August, 2000. 相似文献
10.
N. T. Pokhodylo O. Ya. Shiika V. S. Matiichuk N. D. Obushak 《Russian Journal of Organic Chemistry》2010,46(3):417-421
2-, 3-, and 4-[5-(1-Aryl-5-R-1H-1,2,3-triazol-4-yl)-1,3,4-oxadiazol-2-yl]pyridines were synthesized from the corresponding 1-aryl-5-R-1H-1,2,3-triazole-4-carbonyl chlorides and 2-, 3-, and 4-(1H-tetrazol-5-yl)-pyridines. 相似文献
11.
R. R. Shakirov L. I. Vlasova D. V. Shishkin N. N. Yarmukhamedov N. Z. Baybulatova D. G. Semesko V. A. Dokichev Yu. V. Tomilov 《Russian Chemical Bulletin》2005,54(7):1737-1743
5-Nitropentan-2-one reacts with methylamine and formaldehyde according to the Mannich reaction pattern to give 5-hexahydropyrimidinylcarbonyl-substituted
1-nitro-3,7-diazabicyclo[3.3.1]nonane in one experimental stage. When methyl 3-R-4-nitrobutanoates are used, the reaction
stops after the formation of substituted 5-nitrohexahydropyrimidines in 40–98% yields.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1687–1693, July, 2005. 相似文献
12.
Sergii Golota Ivan Sydorenko Roman Surma Olexandr Karpenko Andrzej Gzella 《合成通讯》2017,47(11):1071-1076
A multicomponent synthetic approach for 5-aryl/heterylidene-2-(2-hydroxyethylamino)- and 2-(3-hydroxypropylamino)-thiazol-4-ones starting from 2-thioxothiazolidin-4-one or 2-methylsulfanylthiazol-4-one was developed. The proposed method involves simultaneous aminolysis of 2-thioxo- or 2-methylsulfanyl groups and Knoevenagel condensation with (hetero)aromatic aldehydes using 2-aminoethanol or 3-aminopropan-1-ol as catalysts. Side-chain prototropic amino–imino tautomerism was observed for target 5-ylidene-2-alkylaminothiazol-4-ones. 相似文献
13.
A synthesis and study of the spatial structure of 3-acetyl-4-hydroxy-2-oxo-1,2-dihydroquinoline have been carried. 1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic
acids [1-(4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)ethylidene]hydrazides were prepared from this compound by two routes. A
comparative analysis of the antitubercular properties of the synthesized compounds and of the closely structurally related
N,N′-di(1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carbonyl)hydrazines has been performed.
*For Communication 151 see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 214–222, February, 2009. 相似文献
14.
Reaction with acetylacetone in the series of 3-arylmethylene-substituted furan-2-ones and pyrrol-2-ones was studied. 8-R-4-Acyl-5-aryl-3-oxo-9-oxabicyclo[4.3.0]nona-1,7-dienes
and N-tolyl-8-R-4-acyl-5-aryl-3-oxo-9-azabicyclo[4.3.0]nona-1,7-dienes were synthesized.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, 1457–1462, October, 2007. 相似文献
15.
I. V. Ukrainets M. Amer P. A. Bezuglyi O. V. Gorokhova L. V. Sidorenko A. V. Turov 《Chemistry of Heterocyclic Compounds》2002,38(5):571-575
The synthesis, antitubercular, anti-HIV, and antitumor activity of the 4-(adamant-1-yl)thiazolyl-2-amides of 1-R-4-hydroxy-2-oxoquinoline-3-carboxylic acids have been studied. An efficient method for purifying the 4-hydroxy-2-oxoquinoline derivatives from their metal salts is proposed. 相似文献
16.
L. M. Potikha A. R. Turelyk V. A. Kovtunenko A. V. Turov 《Chemistry of Heterocyclic Compounds》2010,46(1):82-95
The interaction of (Z)-1,3-diaryl-4-bromo-2-buten-1-ones with 1-substituted (benz)imidazoles in benzene gave (Z)-1-R-3-(2,4-diaryl-4-oxo-2-butenyl)-1H-imidazolium
bromides and (Z)-1-R-3-(2,4-diaryl-4-oxo-2-butenyl)-1H-benzimidazolium bromides which readily cyclize in the presence of base
to form derivatives of 7,9-diarylpyrido[1,2-a]benzimidazole and 6,8-diarylpyrimidazo[1,2-a]pyridine. The effects of the nature of substituents in the benzene ring of the diarylbutenones and the substituent at N(1)
in the (benz)imidazoles on the alkylation and cyclization reactions has been studied. The optimum conditions for the synthesis
of the 5-R-4-hydroxy-2,4-diphenyl-4,5-dihydro-1H-pyrido[1,2-a]benz-imidazol-10-ium, 5-R-2,4-diaryl-4-hydroxy-4,5-dihydro-3H-pyrido[1,2-a]benzimidazol-10-ium, and 5-R-2,4-diaryl-5H-pyrido[1,2-a]benzimidazol-10-ium
have been found. 相似文献
17.
It has been found that malonodinitrile and 2-(6-R1-oxo-3,4-dihydro-2-quinazolyl)acetonitrile in the presence of triethylamine undergo hetarylation by 5,6-dichloro-2,3-pyrazinedicarbonitrile at the active methylene group to give the triethylammonium salt of 2-(3-chloro-5,6-dicyano-2-pyrazinyl)malononitrile or 5-chloro-6-cyano(6-R1-4-oxo-1,2,3,4-tetrahydro-2-quinazolylidene)methyl-2,3-pyrazinedicarbonitriles. Reaction of these with primary amines leads to annelation of the pyrrole ring at the pyrazine [b] edge to give 6-amino-5-R-5H-pyrrolo[2,3-b]pyrazine-2,3,7-tricarbonitriles and 6-amino-5-R2-7-(6-R1-4-oxo-3,4-dihydro-2-quinazolyl)-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitriles respectively. 相似文献
18.
Zhidovinova M. S. Fedorova O. V. Rusinov G. L. Ovchinnikova I. G. 《Russian Chemical Bulletin》2003,52(11):2527-2528
The ultrasound effect accelerates the Biginelli reaction 40 and more times. A sonochemical method for the synthesis of ethyl 4-R-6-methyl-2-oxo- and 4-R-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylates was developed. The target products were obtained within 2 to 5 min in 90—95% yields. 相似文献
19.
A new effective approach to the synthesis of some new (Z)-5-(substituted)-2-thioxothiazolidin-4-one 3a–l and (Z)-5-(substituted)-2-(methylthio)thiazol-4(5H)-one 5a–l is reported under microwave irradiation as well as conventional conditions. 相似文献
20.
I. V. Ukrainets E. A. Taran O. V. Shishkin O. V. Gorokhova S. G. Taran N. A. Jaradat A. V. Turov 《Chemistry of Heterocyclic Compounds》2000,36(4):443-448
Ethyl esters of 1-R-2-oxo-4-hydroxyquinoline-3-carboxylic acids under thermolysis conditions are converted to 5,9-di-R-6,7,8-trioxodiquinolino[3,4-b;3,4-e]-4H-pyrans. One of the synthesized compounds was studied by X-ray diffraction.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 516–522, April, 2000. 相似文献