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Yu. I. Murinov T. R. Nugumanov S. P. Ivanov M. E. Kletskii I. F. Kamaletdinov V. I. Minkin 《Chemistry of Heterocyclic Compounds》2009,45(4):461-467
It has been discovered experimentally that 5,5,6-trihydroxy-6-methylpyrimidine-2,4-dione is formed on oxidizing 5-hydroxy-6-methyluracil
with molecular oxygen in aqueous medium in the presence of copper(II) chloride. Ab initio and DFT calculations on the 6-31G*
basis, both in the gas phase and allowing for solvent, showed that the process proceeds with the direct participation of an
activated oxygen molecule on the complex CuCl2·(5-hydroxy-6-methyluracil)2.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 586-593, April, 2009. 相似文献
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G. T. Sukhanov A. G. Sukhanova Yu. V. Sheikov 《Chemistry of Heterocyclic Compounds》2007,43(6):786-792
Interaction of N(1)-alkyl-substituted 3-nitro-5-R-1,2,4-triazoles with dialkyl sulphates proceeds selectively and results in the respective salts
of 1,4-dialkyl-, 1,4,5-trialkyl-3-nitro-1,2,4-triazoliums. The reaction of N(4)-alkyl-substituted 3-nitro-5-R-1,2,4-triazoles yields the mixtures of the salts of 1,4-dialkyl-, 1,4,5-trialkyl-3-nitro-1,2,4-triazoliums
and 1,4-dialkyl-, 1,3,4-trialkyl-1,2,4-triazol-5-ones with predominance of quaternary salts.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 927–934, June, 2007. 相似文献
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2-Polyfluoroalkylchromones. 6. Synthesis of substituted 2-morpholino-2-trifluoromethylchroman-4-ones
Morpholine adds smoothly at the double bond of substituted 5- and 8-nitro-2-trifluoromethylchromones to form the corresponding 2-morpholino-2-trifluoromethylchroman-4-ones. 6-Methoxy-5-nitro-2-trifluoromethylchromone adds also benzylamine, whereas 7-methoxy-8-nitro-2-trifluoromethylchromone undergoes ring opening under the action of benzylamine to give 3-benzylamino-4,4,4-trifluoro-1-(2-hydroxy-4-methoxy-3-nitrophenyl)but-2-en-1-one. 相似文献
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Stanislav A. Grabovskiy Yuri I. MurinovNatalia N. Kabal’nova 《Tetrahedron letters》2012,53(45):6025-6028
Dehydration of 5,6-dihydro-5,6-dihydroxy-6-methyl- and 5,6-dihydro-5,6-dihydroxy-1,3,6-trimethyl-uracil in 0.4 M aqueous sulfuric acid gives 5-hydroxy-6-methyl- and 5-hydroxy-1,3,6-trimethyluracil in quantitative yields. Two possible mechanisms have been examined using the mPW1k/6-311+G(2df,2pd)//mPW1k/6-31+G(d,p) method for the transformation of methylated and non-methylated 5,6-dihydro-5,6-dihydroxy-6-methyluracils into the corresponding 5-hydroxy-6-methyluracils. The first is a hydride C5-C6 shift occurring in concert with the loss of a water molecule and formation of the corresponding protonated 5,6-dihydro-5-oxo-6-methyluracils. The second is an acid-catalyzed dehydration reaction to yield 5-hydroxy-6-methyluracils. The calculations demonstrated that the second pathway was energetically most favorable. 相似文献
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A synthesis of novel derivatives of 6-methyluracil, 6-methyl-2-thioxo-, and 2-imino-6-methyl-2,3-dihydro-1H-pyrimidin-4-one
containing a 2-(phenoxy)ethyl substituent at position 5 of the pyrimidine ring has been carried out. It was found that 5-[2-(phenoxy)ethyl]
derivatives of 6-methyl-2-thioxo- and 2-imino-6-methyl-2,3-dihydro-1H-pyrimidin-4-one are obtained by the condensation of
the corresponding ethyl 3-oxo-2-(2-phenoxyethyl)butanoates with thiourea or guanidine. 6-Methyl-5-[2-(phenoxy)ethyl]uracils
can be prepared by treating 6-methyl-5-[2-(phenoxy)ethyl]-2-thioxo-2,3-dihydro-1H-pyrimidin-4-ones with an excess of aqueous
monochloroacetic acid solution.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1213–1217, August, 2005. 相似文献
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G. T. Sukhanov A. G. Sukhanova Yu. V. Ilyasova 《Chemistry of Heterocyclic Compounds》2006,42(9):1197-1199
The reaction of 3-nitro-5-R-1,2,4-triazoles with diethyl sulfate gives 1-ethyl-3-R-5-nitro-, 4-ethyl-3-nitro-5-R-1,2,4-triazoles,
1,4-diethyl-, 1,4-diethyl-3-methyl-1,2,4-triazol-5-ones, and 1,4-diethyl-3-nitro-5-R-1,2,4-triazolium salts. When compared
with the use of dimethyl sulfate as alkylating agent the ethylation products have a markedly increased fraction of triazolones
(up to 30–37%) and a somewhat lowered yield of nitrotriazolium salts (up to 6–10%). The reaction time is increased by an order.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1378–1381, September, 2006. 相似文献
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A. G. Sukhanova G. V. Sakovich G. T. Sukhanov 《Chemistry of Heterocyclic Compounds》2008,44(11):1368-1373
Reaction of 3-nitro-1,2,4-triazole and 5-methyl-3-nitro-1,2,4-triazole with secondary and tertiary alcohols in conc. H2SO4 takes place at the N(2) atom. Alkylation by 2-propanol occurs regioselectively to form the 1-isopropyl-3-nitro-and 1-isopropyl-3-methyl-5-nitro-1,2,4-triazoles.
As a consequence of isomerization the alkylation using cyclohexyl or tert-butyl alcohols gives respectively a mixture of regioisomers
substituted at atom N(1) (1-cyclohexyl-3-nitro-and 1-cyclohexyl-5-methyl-3-nitro-1,2,4-triazoles) and at atom N(2) (5-nitro-1-cyclohexyl-and
1-cyclohexyl-3-methyl-5-nitro-1,2,4-triazoles) and, in the second case, to 1-tert-butyl-3-nitro-1,2,4-triazole.
* For Communication 5 see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1680–1687, November, 2008. 相似文献
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1,3-Bis(4-bromobutyl)-6-methyluracil reacts with diethyl 2-(dimethylamino)ethylphosphonate to form a bisquaternary ammonium
salt, whereas the reaction of 1,3-bis-(6-bromohexyl)-6-methyluracil with diethyl 2-(diethylamino)ethyl phosphate gives 1,3-bis-[(6-diethoxyphosphoryloxy)hexyl]-6-methyluracil
and 1,1,4,4-tetraethylpiperazinium dibromide.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1130–1132, June, 2000. 相似文献
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The crystal structure of the title complex, [K2(5-nbdc)2Cd(Ⅱ)·imH·H2O]∞ (5-nbdc=5-nitro-1,3-benzenedicarbonate, imH=imidazole) has been determined by X-ray diffraction analysis. The crystal data are: tetragonal, space group P41, Mr=694.93 for CdC19H12N4O13K2, a=1.018 6(10) nm, b=1.018 6(10) nm, c=2.436 7(5) nm; Z=4, V=2.528 2(6) nm3, F(000)=1 376, Dc=1.826 Mg·m-3, μ=1.267 mm-1. The title polymeric complex exhibits a two-dimensional framework, in which adjacent Cd(Ⅱ) ions are bridged by μ-O4-5-nitro-1,3-benzenedicarbonate groups forming one-dimensional chains that are further linked by μ-O3-5-nitro-1,3-benzenedicarbonate groups into two-dimensional anion rectangle sheets with large 32-membered rings. The strong π-π stacks of the benzene rings link these adjacent sheets into a three-dimensional van der Waals network. CCDC: 245527. 相似文献
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Alkylation of 3-nitro-1,2,4-triazole and 5-methyl-3-nitro-1,2,4-triazole with dialkyl sulfates or alkyl halides in the presence
of alkali proceeds with a low selectivity for the alkylating agent with the formation of two regioisomers at the N(1) and N(2) atoms of the heterocycle. Depending on the reaction conditions the proportion of the N(2) isomer was 14.6-33.8%.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 1020–1025, July, 2005. 相似文献
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T. V. Rybalova V. F. Sedova Yu. V. Gatilov O. P. Shkurko 《Journal of Structural Chemistry》2004,45(2):287-292
The crystal structures of 5-nitro- and 5-ethoxycarbonyl-substituted 6-phenyl-4-(3-fluorophenyl)-3,4-dihydro-(1H)-pyrimidin-2-ones were determined by X-ray diffraction analysis. Conformational peculiarities of the structures have been revealed and compared with data for other biologically active dihydropyrimidinones. 相似文献
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The reactions of 1-substituted 2-nitro-3-phenylaminoprop-2-en-1-ones with cyanothioacetamide afforded the corresponding 6-substituted 3-cyano-5-nitropyridine-2(1H)-thiones, which were used for the synthesis of 6-substituted 3-cyano-2-methylthio-5-nitropyridines and 7-substituted 4-hydroxy-8-nitropyrido[2",3":4,5]thieno[2,3-b]pyridin-2(1H)-ones. 相似文献
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AGNTO的制备和分子结构 总被引:8,自引:0,他引:8
通过3-硝基-1,2,4-三唑-5-酮(NTO)与氨基胍重碳酸盐反应制备NTO氨基胍盐,并用X射线衍射、元素分析、红外光谱对其进行了表征.晶体属于单斜晶系,空间群为P21/n.晶体学参数为:a=0.67870(10)nm, b=2.7915(4)nm, c=1.2739(2)nm; β =96.930(10) V=2.3959(6)nm3, Z=12, Dc=1.698 g•cm -3, μ( Mo K )=1.47 cm -1, F(000)=1272.晶体结构经全矩阵最小二乘法修正,最终偏离因子R=0.0352, wR =0.0718.该盐是一种具有广泛应用前景的产气剂材料. 相似文献
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1-(3,4-二甲氧基)苯乙基-3-环氧丙基-5-氰基-6-甲基脲嘧啶的合成及晶体结构 总被引:1,自引:0,他引:1
标题化合物1-(3,4-二甲氧基)苯乙基-3-环氧丙基-5-氰基-6-甲基脲嘧啶是 由1-(3,4-二甲氧基)苯乙基-5-氰基-6-甲基脲嘧啶在NaOH水溶液中与环氧氯丙 烷反应制得。结构通过单晶X射线衍射分析确定,其晶体属于单斜晶系,空间群 P2_1/a, 晶胞参数:a = 1.09(10) nm, b = 1.43(10) nm, c = 1.20(8) nm, V = 1.868 nm~3,Z = 4, D_c = 1.32 Mg/m~3, F(000) = 784。并用波谱法对分离得 到的副产物进行了结构表征。 相似文献
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Treatment of 1-alkyl-4,5-dichloro-3-nitropyridazin-6-one with C-nucleophiles and with ambident nucleophiles (2-azahetarylacetonitriles)
leads to a selective substitution of a chorine atom by the quaternary carbon atom of the carbanion formed from a substituted
acetonitrile. The pKa of the CH-acid 2-(1-alkyl-5-chloro-3-nitro-6-oxo-1,6-dihydro-4-pyridazinyl)malononitrile was determined by potentiometric
titration. Reaction of 2-(1-alkyl-5-chloro-3-nitro-6-oxo-1,6-dihydro-4-pyridazinyl)-2-hetarylacetonitriles with primary amines
gives 6,7-dihydro-1H-pyrrolo[2,3-d]pyridazin-7-ones.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 556–564, April, 2006. 相似文献
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L. R. Yakupova A. V. Ivanova R. L. Safiullin A. R. Gimadieva Yu. N. Chernyshenko A. G. Mustafin I. B. Abdrakhmanov 《Russian Chemical Bulletin》2010,59(3):517-521
The antioxidation activity of 5-substituted 6-methyluracils was quantitatively estimated in the model system of initiated
radical-chain oxidation of 1,4-dioxane. The rate constants of the reactions of 1,4-dioxane peroxide radicals with 6-methyluracil
(1), 6-methyl-5-piperidinouracil (2), 6-methyl-5-morpholinomethyluracil (3), 6-methyl-5-morpholinouracil (4), 6-methyl-5-methylaminouracil
(5), 5-ethylamino-6-methyluracil (6), and 5-hydroxy-6-methyluracil (7) were measured. Among compounds 1–7, derivative 7 is
most efficient with an inhibition rate constant of (5.2±0.1) · 104 L mol-1 s-1 (60 °C). 相似文献