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1.
The reaction between p-(dimethylamino)benzaldehyde and 2-acylmethyl-1H-benzimidazoles and 6-amino-1,3-dimethylpyrimidino-2,4(1H,3H)-dione
has given previously unknown 5-unsubstituted 6-(1H-benzimidazol-2-yl)pyrido[2,3-d]pyrimidino-2,4(1H,3H)-diones. The reaction
occurs on boiling in acetic and acid and includes the formation of 1,4-dihydropyridine-bearing compounds in accordance with
the Hantzsch reaction scheme and aromatization as a result of cleavage of N,N-dimethylaniline.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 585–589, April 2007. 相似文献
2.
I. B. Dzvinchuk A. N. Chernega M. O. Lozinskii 《Chemistry of Heterocyclic Compounds》2007,43(12):1519-1524
A three component cyclocondensation of p-(dimethylamino)benzaldehyde with 3,5-dimethoxyaniline and 2-phenacyl-1H-benzimidazoles
gives previously unknown 2-aryl-3-(1H-benzimidazol-2-yl)-5,7-dimethoxyquinolines. The Hanztsch type reaction occurs in refluxing
acetic acid and is accompanied by aromatization of the 1,4-dihydroquinolines formed through loss of N,N-dimethylaniline.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1792–1798, December, 2007. 相似文献
3.
M. V. Vovk N. V. Mel’nichenko V. A. Sukach N. G. Chubaruk 《Chemistry of Heterocyclic Compounds》2004,40(11):1485-1489
6-Azido-1H-pyrazolo[3,4-b]pyridino-5-carbaldehydes react with aromatic amines to give the corresponding N-arylimines which cyclize on heating in boiling toluene to give 6-aryl-1,6-dihydrodipyrazolo[3,4-b:4,3-e]pyridines.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, 1717–1722, November, 2004. 相似文献
4.
T. E. Khoshtariya M. M. Matnadze N. T. Mirziashvili L. N. Kurkovskaya M. I. Sikharulidze T. O. Dzhashi 《Chemistry of Heterocyclic Compounds》2004,40(11):1454-1459
The Sandmeyer reaction was used to prepare 2,3-dioxo-2,3-dihydrobenzo[b]furoindoles which could be reduced with diborane or with complex hydrides to give the corresponding unsubstituted as well as the 3-hydroxybenzo[b]furoindoles.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No 11, pp. 1683–1689, November, 2004. 相似文献
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6.
E. A. Kaigorodova V. K. Vasilin M. M. Lipunov V. E. Zavodnik G. D. Krapivin 《Chemistry of Heterocyclic Compounds》2004,40(12):1600-1608
Iminophosphoranes containing a thieno[2,3-b]pyridine fragment were obtained through a sequence of reactions: 1) alkylation of 3-cyano-2(1H)-pyridinethiones in alkaline medium by an -halocarbonyl compound with subsequent Thorpe-Ziegler cyclization of the resultant 2-thioalkylpyridines to give 3-aminothieno[2,3-b]pyridines, 2) diazotization of the amino group and nucleophilic substitution of the diazonium group by an azido group without isolation of the diazonium salts, and 3) reaction of the 3-azidothieno[2,3-b]pyridines with triphenylphosphine.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1853–1862, December, 2004. 相似文献
7.
I. B. Dzvinchuk N. A. Tolmachova A. N. Chernega M. O. Lozinskii 《Chemistry of Heterocyclic Compounds》2009,45(2):194-200
The Hantzsch three-component cyclization of 4-(dimethylamino)benzaldehyde, cyclohexane-1,3-diones, and some 1,3-[N,C]-dinucleophiles
(5-amino-3-methyl-1-phenylpyrazole, 3,5-dimethoxyaniline, and 4-amino-1,3-dimethylpyrimidine-2,6-dione) proceeds in boiling
acetic acid with the splitting off N,N-dimethylaniline and the formation of polycondensed heterocyclic sytems with a γ-unsubstituted
pyridine ring (pyrazolo[3,4-b]quinoline, acridine, and pyrimido[4,5-b]quinoline).
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 244-251, February, 2009. 相似文献
8.
The interaction of 6-allylthio-4-imino-1-methyl-3-methylthio-5-phenyl-1,5-dihydro-4H-pyrazolo[3,4-d]-pyrimidine with bromine
leads to the formation of 8-bromomethyl-4-imino-1-methyl-3-methylthio-5-phenyl-4,5,7,8-tetrahydro-1H-pyrazolo[4,3-e][1,3]thiazolo[3,2-a]
pyrimidinium tribromide.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 602–604. April, 2007. 相似文献
9.
M. A. Metwally H. A. Etman H. E. Gafer A. M. Khalil 《Chemistry of Heterocyclic Compounds》2008,44(6):715-721
3-Amino-4,6-dimethylpyrazolo[3,4-b]pyridine was used for the preparation of some novel heterocycles of pharmaceutical interest.
The starting material reacted with 2-cyano-3,3-bis(methylthio)acrylate, chloroacetyl chloride, phenyl isothiocyanate, carbon
disul-fide, and aromatic aldehydes to give the novel heterocycles. The structures of the hitherto unknown ring systems have
been confirmed by analytical and spectral methods.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 891–898, June, 2008. 相似文献
10.
R. I. Yurchenko A. D. Ponomarenko N. N. Svarovskaya A. A. Tolmachev 《Chemistry of Heterocyclic Compounds》2005,41(5):656-661
A series of 1-adamantylimidazo[1,2-a]pyridines has been synthesized. The negative influence of electron-acceptor substituents in the pyridine ring on the alkylation of substituted 2-aminopyridines with bromomethyl (adamantan-1-yl) ketone has been demonstrated. Bromination of adamantylimidazo-[1,2-a]pyridines on boiling in liquid bromine or in the presence of a Lewis acid resulted in insertion of a bromine atom in the imidazole ring without affecting the adamantane nucleus. The compounds studied take part in the Ritter reaction despite the absence of an easily removed groups in the adamantane nucleus.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, 761–766, May, 2005. 相似文献
11.
O. A. Abd Allah 《Chemistry of Heterocyclic Compounds》2005,41(8):1076-1084
7-[1,3-Dithiolan-2-ylidene]-3-phenyl-5,6,7,8-tetrahydro[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine-6,8-dione and 7-[5-oxo-1,3-dithiolan-2-ylidene]-3-phenyl-5,6,7,8-tetrahydro[1,2,4]triazolo[3,4-b][1,3,4]-thiadiazepine-6,8-diones
were obtained by treating 3-phenyl-5,6,7,8-tetrahydro[1,2,4]triazolo-[3,4-b][1,3,4]thiadiazepine-6,8-diones with CS2 and chloroacetyl chloride, respectively. Treatment of the above compounds with mercaptoacetic acid gave 1,2-dibromoethane
or the corresponding spiro polyfused heterocycles. Some other triazolothiadiazepine derivatives including spiro polyfused
compounds were also synthesized.
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Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 8, 1256–1264, August, 2005. 相似文献
12.
B. Vigante G. Tirzitis D. Tirzite B. Chekavichus J. Uldrikis A. Sobolev G. Duburs 《Chemistry of Heterocyclic Compounds》2007,43(2):225-232
Different modifications of the Hantzsch synthesis using 10-methyl-10H-phenothiazine-3-carbaldehyde gave 4-(10-methyl-10H-phenothiazin-3-yl)-substituted
1,4-dihydropyridine-3,5-di-, 5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-, and 5,5-dioxo-4,5-dihydro-1H-5λ6-benzo[4,5]thieno[3,2-b]pyridine-3-carboxylic esters.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 280–288, February, 2007. 相似文献
13.
L. G. Voskressensky T. N. Borisova T. A. Vorob’eva A. I. Chernyshev A. V. Varlamov 《Russian Chemical Bulletin》2005,54(11):2594-2601
Reactions of substituted tetrahydropyrrolo[3,2-c]pyridines with dimethyl acetylenedicarboxylate in protic and aprotic solvents were studied. A novel single-step method for
the synthesis of pyrrolo[2,3-d]azocine derivatives was developed.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2513–2519, November, 2005. 相似文献
14.
E. V. Mironova A. T. Gubaidullin A. M. Murtazina I. A. Litvinov V. A. Mamedov 《Journal of Structural Chemistry》2008,49(1):95-101
Three tetrahydrobenzo[e]pyrano[4,3-b]pyridines formed in a diethyl 2,4,6-trioxoheptanedicarboxylic ether-substituted salicylic aldehyde-ammonium acetate system were studied by single crystal X-ray diffraction. After the introduction of a methoxy group in the tricyclic system, the tetrahydropyridine and pyrane rings adopted the half-chair conformation, while in the unsubstituted compound, the tetrahydropyridine ring has a distorted boat conformation, and the pyrane ring has a C-envelope conformation. In the compounds, the N-H?O and O-H?O intermolecular hydrogen bonds give rise to the development of chain structures. In two of the three compounds examined, the hydrogen atoms at the chiral centers are in the trans-position, as in the structure of natural tetrahydrocannabinols. 相似文献
15.
V. V. Lyaskovskyy Z. V. Voitenko V. A. Kovtunenko 《Chemistry of Heterocyclic Compounds》2007,43(3):253-276
Data on methods for the synthesis of isoindolo[2,1-a]benzimidazole and its derivatives and their chemical characteristics
are reviewed. Data from quantum-chemical calculations of certain structures are presented. Possible practical applications
of the compounds are indicated.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 323–351, March, 2007. 相似文献
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T. S. Safonova M. P. Nemeryuk N. A. Grineva A. F. Keremov O. S. Anisimova N. P. Solov’eva 《Chemistry of Heterocyclic Compounds》2004,40(12):1609-1617
We have studied some properties and conversions of pyrimido[4,5-b]-1,4-benzothiazepines: reduction, oxidation, reactions with nucleophilic reagents (methanol, hydrazine, hydroxylamine, o-methylhydroxylamine, and thiosemicarbazide). We have synthesized derivatives of a novel heterocyclic system: pyrimido[5,4-c]isoquinoline.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1863–1872, December, 2004.For Communication 53, see [1]. 相似文献