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A. A. Avetisyan I. L. Aleksanyan L. P. Ambartsumyan 《Russian Journal of Organic Chemistry》2005,41(5):772-773
Synthesis was performed of 4-(4-ethoxycarbonylphenylamino)- and 4-(2-carboxyphenylamino)-2-methylquinolines by reaction of 2-methyl-4-chloroquinoline with anesthesin and anthranilic acid. In concentrated sulfuric acid 4-(2-carboxyphenylamino)-2-methylquinoline underwent cyclization into 6-hydroxy-7-methylquinolino[3,2-c]quinoline, and the alkaline hydrolysis of 4-(4-ethoxycarbonylphenyl-amino)quinoline afforded 2-methyl-4-(4-carboxyphenylamino)quinoline.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 5, 2005, pp. 786–787.Original Russian Text Copyright © 2005 by Avetisyan, Aleksanyan, Ambartsumyan. 相似文献
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4-(4-PhenyI-3-pyrazolyl)-4H-1,2,4-triazoles and 4-phenyl-5-(4H-1,2,4-triazol4-yl)-3-pyrazolols were prepared by the reaction of formylhydrazine on α-phenyl-α-cyanoacetaldehydes and ethyl α-phenyl-α-cyanoacetates. 相似文献
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R. C. Arora V. K. Rastogi A. K. Agrawal S. S. Parmar 《Journal of heterocyclic chemistry》1978,15(5):869-871
Some substituted 2-ethyl-3-(4-hydrazinocarbonylphenyl)-4-quinazolones and 2-ethyl-3-(4-hydrazinocarbonylmethylphenyl)-4-quinazolones were synthesized and characterized by their sharp melting points, elemental analyses and spectral data. 相似文献
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Burmistrov V. A. Syrbu S. A. Novikov I. V. 《Russian Journal of General Chemistry》2002,72(7):1099-1103
The temperature dependences of the dielectric permittivity of 4-(2,3-epoxypropoxy)-4'-alkoxyazoxybenzenes (n = 1-10) and 4-propoxy-4'-alkoxyazoxybenzenes (n = 1-10) with mesomorphic properties were measured by dielectrometry. The introductrion of the terminal epoxy group increases the dielectric permittivity and its anisotropy. The dipole moments of molecules of 4-(2,3-epoxypropoxy)-4'-alkoxyazoxybenzenes (n = 1-10) and 4-propoxy-4'-alkoxyazoxybenzenes (n = 1-10) were determined by the second Debye method. The epoxy-substituted azoxybenzenes have higher dipole moments than their structural analogs. 相似文献
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Harutyunyan A. A. Israyelyan S. G. Panosyan H. A. Safaryan M. S. Dilanyan S. V. 《Russian Journal of Organic Chemistry》2020,56(9):1588-1594
Russian Journal of Organic Chemistry - 4-(4-Aminophenyl)-2,6-diphenylpyrimidine was synthesized by reaction of (E)-1-(4-aminophenyl)-3-phenylprop-2-en-1-one with benzamidine and was involved in a... 相似文献
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Yun Gen LIU Shao Bai LI* National Laboratory of Applied Organic Chemistry Lanzhou University Lanzhou 《中国化学快报》2001,(12)
Natural diarylheptanoids have significant bioactivities. Some of them are potent inhibitors against prostaglandin biosynthesizing enzyme (PG synthetase) and 5-lipoxygenase (LT synthetase)1-2. Compound 1 was firstly isolated from Alnus rubra bark3. So far its synthesis has not been reported yet. Herein, we report the synthesis of compound 1. Meantime, compound 24 was also obtianed as an intermediate. Compound 7 and 16 were converted to compound 10 and 18 respectively, because compound 1… 相似文献
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Kiran S. Hon Hemantkumar N. Akolkar Bhausaheb K. Karale 《Journal of heterocyclic chemistry》2020,57(4):1692-1697
Novel 1-benzyl-3-(4-fluorophenyl)-1H-pyrazole-4-carbaldehydes 3a to 3e were synthesized via Vilsmeier-Haack reaction of the appropriate 1-benzyl-2-(1-(4-fluorophenyl)ethylidene)hydrazines, derived from 4-fluoroacetophenone 1 with substituted 2-benzylhydrazines 2a to 2e . The base catalyzed condensation of 1-benzyl-3-(4-fluorophenyl)-1H-pyrazole-4-carbaldehydes 3a to 3e with 1-(4-fluoro-2-hydroxyphenyl)ethanone 4 gave (E)-3-(1-benzyl-3-(4-fluorophenyl)-1H-pyrazol-4-yl)-1-(4-fluoro-2-hydroxyphenyl)prop-2-en-1-ones 5a to 5e . On cyclization with dimethyl sulfoxide (DMSO)/I2, compounds 5a to 5e gave 2-(1-benzyl-3-(4-fluorophenyl)-1H-pyrazol-4-yl)-7-fluoro-4H-chromen-4-ones 6a to 6e . Structures of all novel compounds were confirmed by infrared (IR), proton nuclear magnetic resonance (1H NMR), carbon nuclear magnetic resonance (13C NMR), and mass spectral data. All the synthesized compounds were screened for their antibacterial activities. 相似文献
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Starting from readily available 2-substituted-4-formylthiazoles and selenazoles, a series of 4-(2-aryl-4-selenazolyl)-1,2,3-selenadiazoles I and 4-(2-substituted-4-thiazolyl)-1,2,3-selenadiazoles II were prepared. Pyrolysis of compound II afforded (2-substituted-4-thiazolyl) acetylenes VII. Addition of potassium hydroxide pellets to an alcoholic solution of II gave 2-substituted-1,4-diselenafulvenes VIII. Decomposition of compound II with base followed by the addition of carbon disulfide gave 5-substituted 2-thioxo-1,3-thiaselenoles XI. 相似文献
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On the aromaticity of square planar Ga4(2-) and In4(2-) in gaseous NaGa4- and NaIn4- clusters 总被引:1,自引:0,他引:1
Kuznetsov AE Boldyrev AI Li X Wang LS 《Journal of the American Chemical Society》2001,123(36):8825-8831
We investigated the electronic structure and chemical bonding of two bimetallic clusters NaGa4- and NaIn4-. Photoelectron spectra of the anions were obtained and compared with ab initio calculations. We found that the ground state of the two anions contains a square planar dianion interacting with a Na+ cation. The Ga4(2-) and In4(2-) dianions both possess two delocalized pi electrons and are considered to be aromatic, similar to that recently found in Al4(2-). Using calculations for a model compound, we showed that a recently synthesized Ga4-organometallic compound also contains an aromatic -Ga4(2-)- unit, analogous to the gaseous clusters. 相似文献
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A. Ya. Strakov N. N. Tonkikh M. V. Petrova I. A. Strakova 《Chemistry of Heterocyclic Compounds》1997,33(4):441-444
Reactions of 4-hydrazinobenzoic acid with 2-formyl- and 2-acetyldimedones were utilized to synthesize 6,6-dimethyl- and 3,6,6-trimethyl-1-(4-hydroxycarbonylphenyl)-4-oxo-4,5,6,7-tetrahydroindazoles
corre-spondingly, and the reaction with 2-cyano-3-ethoxy-5,5-dimethylcyclohex-2-en-1-one gave 2-(4-hydroxy-carbonylphenyl)-3-amino-4-oxo-6,6-dimethyl-4,5,6,7-tetrahydroindazole.
Riga Technical University, Riga LV-1658. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 516–519, April,
1997. 相似文献
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A. I. Pavlyuchenko N. I. Smirnova E. I. Kovshev 《Chemistry of Heterocyclic Compounds》1985,21(10):1145-1147
New liquid-crystalline 2-(4-cyanophenyl)-5-(4-alkyl- and alkoxyphenyl)pyridines were obtained by condensation of 1-dimethylamino-3-dimethylimmonia-2-(4-alkyl- or alkoxyphenyl)-1-propene perchlorates with 4-cyanoacetophenone and subsequent conversion of the 1-dimethylamino-2-(p-alkyl- or alkoxyphenyl)-4-(p-cyanobenzoyl)-1,3-butadienes to 5-(4-alkyl- or alkoxyphenyl)-2-(4-cyanophenyl)pyrylium perchlorates and refluxing of the latter with ammonium acetate in acetic acid.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1392–1394, October, 1985. 相似文献
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Dz. Sile V. A. Slavinska G. Rozental J. Popelis Yu. Balodis E. Lukevics 《Chemistry of Heterocyclic Compounds》2002,38(3):287-291
We have developed a method for the synthesis of ethyl 4-(3-pyridyl)- and 4-(4-pyridyl)-2-oxobutenoates by condensation of 3-pyridinecarbaldehyde and 4-pyridinecarbaldehyde monohydrate respectively with ethyl pyruvate, esterifiction of the target acids, and hydrolysis of the corresponding ethyl ester ketals in the presence of FeCl3·6H2O. 相似文献
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N. Saemian G. Shirvani H. Matloubi 《Journal of Radioanalytical and Nuclear Chemistry》2006,268(3):545-548
Summary Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3-triazole and 1-(4-sulfonamide-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-fluoro-benzonitrile-[cyano-14C]. 相似文献
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Methyl aroylpyruvates reacted with 4-amino-N-carbamimidoylbenzene-1-sulfonamide in acetic acid–ethanol (1: 1) to give methyl 4-aryl-2-{[4-(carbamimidoylsulfamoyl)phenyl]amino}-4-oxobut-2-enoates which were found to exist in solution as mixtures of Z and E isomers. 相似文献
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R. S. Baltrushis Z. -I. G. Beresnevichyus V. Yu. Mitskyavichyus 《Chemistry of Heterocyclic Compounds》1982,18(9):967-971
Bromination of 1-(4-hydroxyphenyl)dihydrouracil and its 6-methyl derivative with bromine in refluxing acetic acid gave 1-(3,5-dibromo-4-hydroxyphenyl)-5-bromo-, 1-(3,5-dibromo-4-hydroxyphenyl)-5-bromo-, and 1-(3,5-dibromo-4-hydroxyphenyl)-5-bromo-6-methyldihydrouracils and 1-(3,5-dibromo-4-hydroxyphenyl)-5-methyluracil. 5-Bromo- and 5,5-dibromodihydrouracils were dehydrobrominated, and the same compounds undergo decomposition to 3,5-dibromo-4-hydroxyphenylurea upon alkaline hydrolysis.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1251–1254, September, 1982. 相似文献
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1 INTRODUCTION The triazole derivatives were widely studied because they represent the largest group of modern fungicides and extensively used in both human and veterinary therapy and in agriculture[1~3]. For exam- ple, there are commercially available … 相似文献
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Wolff-Kishner reduction of 3-amino-4-(o-chlorobenzoyl)pyridine ( 3 ) afforded 3-amino-4-(o-chlorobenzyl)pyridine ( 5 ), which on subsequent reaction with triethyl orthoformate and then acetyl hydrazide yielded 1-acetyl-2-[N-[4-(o-chlorobenzyl)pyridin-3-yl]formimidoyl]hydrazone ( 7 ). Cyclization of hydrazone 7 gave 3-(3-methyl-4H-1,2,4-triazol-4-yl)-4-(o-chlorobenzyl)pyridine ( 8 ), which on Jones oxidation yielded 3-(3-methyl-4H-1,2,4-triazol-4-yl)-4-(o-chlorobenzyl)pyridine ( 9 ). The Mannick reaction of 3-(3-methyl-4H-l,2,4-triazol-4-yl)-4-(o-chlorobenzyl)pyridine ( 9 ) with aqueous formalin and dimethylamine hydrochloride afforded 3-[3-[(dimethylamino)methyl]-5-methyl-4H-1,2,4-triazol-4-yl]-4-(o-chlorobenzoyl)-pyridine ( 10 ). 3-[3-[(Dimethylamino)methyl]-5-methyl-4H-1,2,4-triazol-4-yl]-4-(o-chlorobenzoyl)pyridine ( 10 ) exhibited good anticonvulsant activity in the subcutaneous pentylenetetrazole anticonvulsant screen indi cating that an appropriately substituted-pyridine ring moiety can serve as a bioisostere of a chlorobenzene ring with respect to anticonvulsant activity. 相似文献