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1.
Reactions of aromatic aldehydes with cyanothioacetamide and dimethyl malonate in the presence ofN-methylmorpholine affordedN-methylmorpholinium 4-aryl-5-cyano-3-methoxycarbonyl-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates. The latter were used to
synthesize substituted 6-(alkylthio)-2-oxo-1,2,3,4-tetrahydropyridines.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 485–487, March, 2000. 相似文献
2.
Condensation of isovaleraldehyde with cyanothioacetamide and ethyl acetoacetate (or its enamine) gives 3-cyano-5-ethoxycarbonyl-4-isobutyl-6-methyl-3,4-dihydropyridine-2(1H)-thione. This compound was used in the synthesis of substituted 1,4-dihydropyridin-2-yl sulfides.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 166–168, January, 1999. 相似文献
3.
Ya. Yu. Yakunin V. D. Dyachenko V. P. Litvinov 《Chemistry of Heterocyclic Compounds》2000,36(12):1431-1436
By reaction of ethoxymethylene derivatives of trifluorothenoyl- and trifluorobenzoylacetone with cyanothioacetamide in the presence of excess N-methylmorpholine, we have obtained the corresponding N-methylmorpholinium 5-acyl-3-cyano-6-trifluoromethylpyridine-2-thiolates and have studied their alkylation. 相似文献
4.
Condensation of 2-chlorobenzaldehyde with cyanothioacetamide and ethyl butyroylacetate results in 4-(2-chlorophenyl)-3-cyano-5-ethoxycarbonyl-6-propyl-3,4-dihydropyridine-2(1H)-thione, whose further transformation affords the corresponding substituted 2-methylthio-1,4-dihydropyridine.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 173–175, January, 2000. 相似文献
5.
Condensation of 2-chlorobenzaldehyde with cyanothioacetamide and ethyl butyroylacetate results in 4-(2-chlorophenyl)-3-cyano-5-ethoxycarbonyl-6-propyl-3,4-dihydropyridine-2(1H)-thione, whose further transformation affords the corresponding substituted 2-methylthio-1,4-dihydropyridine.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 173–175, January, 2000. 相似文献
6.
A. V. Samet A. M. Shestopalov M. I. Struchkova V. V. Semenov V. N. Nesterov Yu. T. Struchkov 《Russian Chemical Bulletin》1996,45(8):1945-1951
Previously unknown 5-azolylpyrans were obtained by reactions ofN-acetonyl- andN-phenacylimidazoles, -triazoles, and -tetrazoles with arylmethylenemalononitriles. The structure of 2-amino-3-cyano-6-methyl-5-(5-nitrotetrazol-2-yl)-4-phenyl-4H-pyran was established by X-ray structural analysis.Deceased.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 2050–2055, August, 1996. 相似文献
7.
L. B. Kulikova G. I. Ezhova N. E. Kravchenko O. V. Dorofeeva A. S. Kulikov A. G. Zavozin 《Russian Chemical Bulletin》2007,56(8):1631-1636
Conditions for N-acylation of 2-amino-5-aryl-6H-1,3,4-thiadiazines with trifluoroacetic anhydride and halogen-substituted carboxylic acid halides with retention of the initial
heterocyclic system were found. 5-Aryl-2-haloacylamino-6H-1,3,4-thiadiazines were obtained in preparative yields. Their reactions with hetarenethiols afforded N-hetarylthioacyl derivatives.
Dedicated to Academician V. A. Tartakovsky on the occasion of his 75th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1570–1575, August, 2007. 相似文献
8.
The reactions of 3- or 4-hydroxybenzaldehydes with cyanothioacetamide and Meldrum's acid in the presence ofN-methylmorpholine affordedN-methylmorpholinium 5-cyano-4-(3-or 4-hydroxyphenyl)-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates, respectively. The resulting
compounds were used in the synthesis of substituted 6-alkylthio-1,2,3,4-tetrahydropyridin-2-ones.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2333–2336. December, 1999. 相似文献
9.
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
10.
S. G. Krivokolysko V. D. Dyachenko A. N. Chernega V. P. Litvinov 《Chemistry of Heterocyclic Compounds》2001,37(10):1208-1215
The condensation of 2-chlorobenzaldehyde with cyanothioacetamide and 2-thenoyltrifluoroacetone in the presence of N-methylmorpholine takes place stereoselectively and leads to the formation of N-methylmorpholinium 4,5-trans-4-(2-chlorophenyl)-3-cyano-6-hydroxy-5-(2-thenoyl)-6-trifluoromethyl-1,4,5,6-tetrahydropyridine-2-thiolate. The latter was used to synthesize the corresponding 2-alkylthiotetrahydropyridines. The structure of 4,5-trans-4-(2-chlorophenyl)-3-cyano-6-hydroxy-2-methallylthio-5-(2-thenoyl)-6-trifluoromethyl-1,4,5,6-tetrahydropyridine was determined by X-ray crystallographic analysis. 相似文献
11.
K. S. Chunikhin L. A. Rodinovskaya A. M. Shestopalov 《Chemistry of Heterocyclic Compounds》2007,43(10):1247-1251
The Michael addition of cyanothioacetamide to nitrostyrenes was investigated. Previously unknown 2-amino-4-aryl-3-cyano-5-hydroxyimino-4,5-dihydrothiophenes
were obtained.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1472–1477, October, 2007. 相似文献
12.
S. G. Krivokolysko V. D. Dyachenko E. B. Rusanov V. P. Litvinov 《Chemistry of Heterocyclic Compounds》2001,37(8):987-992
4-(2-Chlorophenyl)-3-cyano-6-hydroxy-5-(2-thienoyl)-6-trifluoromethylpiperidin-2-thione, which was used for the synthesis of 2-allylthio-4-(2-chlorophenyl)-3-cyano-6-hydroxy-5-(2-thienoyl)-6-trifluoromethyl-1,4,5,6-tetrahydropyridine, was obtained by the reaction of 2-thienoyltrifluoroacetone with 2-chlorophenylphenylmethylenecyanothioacetamide or with a mixture of 2-chlorobenzaldehyde and cyanothioacetamide in the presence of N-methylmorpholine. The molecular and crystal structure of the piperidinthione have been established by X-ray crystallography. 相似文献
13.
Synthesis and reactions of 1-R-3-benzoyl-5-ethoxycarbonyl-6-oxo-1,2,3,6-tetrahydropyridine-2-thiones
V. N. Britsun A. N. Esipenko A. N. Chernega E. B. Rusanov M. O. Lozinskii 《Chemistry of Heterocyclic Compounds》2007,43(11):1411-1419
Cycloacylation of N-R-3-oxo-3-phenylpropanethioamides by diethyl ethoxymethylenemalonate occurs selectively to form 1-R-3-benzoyl-5-ethoxycarbonyl-6-oxo-1,2,3,6-tetrahydropyridine-2-thiones
which are convenient starting materials for the synthesis of bi-and tricyclic hetero systems including the previously unknown
9-R-7-ethoxycarbonyl-5-phenyl-8,9-dihydropyrido[2,3-d][1,2,4]triazolo[1,5-a]-pyrimidin-8-ones.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1660–1669, November, 2007. 相似文献
14.
A. A. Krauze É. É. Liepin'sh Yu. É. Pelcher Z. A. Kalme I. V. Dipan G. Ya. Dubur 《Chemistry of Heterocyclic Compounds》1985,21(1):77-83
The condensation of ethyl arylidenacetoacetate with cyanothioacetamide and of arylidenecyanothioacetamides with ethyl acetoacetate or of arylidenecyanothioacetamides with ethyl -aminocrotonate gave 3-cyano-4-aryl-5-ethoxycarbonyl-6-methyl-3,4-dihydropyridine-2-thiones. PMR spectroscopy showed that the 3-cyano-4-aryl-3,4-dihydropyridine-2-thiones are formed as a mixture of cis and trans isomers.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 95–102, January, 1985. 相似文献
15.
N-Methylmorpholinium 4-aryl-5-cyano-2-oxo-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates were obtained by the condensation of
aromatic aldehydes, cyanothioacetamide, and Meldrum's acid in the presence ofN-methylmorpholine. They were then used in the syntheses of substituted 6-alkylthio-3,4-dihydropyridin-2(1H)-ones and 4,5-dihydrothieno[2,3-b]pyridin-6(7H)-ones.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1852–1856, October, 1997. 相似文献
16.
S. I. Moryashova L. K. Salamandra A. E. Fedorov L. A. Rodinovskaya A. M. Shestopalov V. V. Semenov 《Russian Chemical Bulletin》1998,47(2):357-360
Reactions of sodium derivatives of 2- and 3-thenoylacetaldehydes with cyanothioacetamide gave 2- and 3-cyano-6-thienylpyridine-2(1H)-thiones, which were used in the synthesis of substituted 2-alkylthiopyridines, thieno[2,3-b]pyridines, and other fused heterocycles.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 365–368, February, 1998. 相似文献
17.
A. D. Dyachenko S. M. Desenko V. D. Dyachenko 《Chemistry of Heterocyclic Compounds》2004,40(8):1017-1023
Treatment of monothiomalonodiamide with cyclohexylidenemalononitrile or cyclohexylidenecyanoacetic ester in the presence of sodium ethylate gave 6-amino-3-carbamoyl-5-cyano-3,4-dihydrospirocyclohexane-4-pyridine-2-thiol and 5-cyano-3-thiocarbamoyl-4-spirocyclohexanepiperidine-2,6-dione. Their alkylation and hydrolysis have been studied. 相似文献
18.
Multi-component condensation of cyanoselenoacetamide with ethyl 2-furfuryl-idenacetoacetate and liquid alkyl halides, catalyzed
byN-methylmorpholine, affords 7-alkylseleno-5-amino-8-cyano-3-ethoxycarbonyl-4-(2-furyl)-2-methyl-1,4-dihydro-1,6-naphthyridines,
which have not been described hitherto.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 121–124, January, 2000. 相似文献
19.
Multi-component condensation of cyanoselenoacetamide with ethyl 2-furfuryl-idenacetoacetate and liquid alkyl halides, catalyzed
byN-methylmorpholine, affords 7-alkylseleno-5-amino-8-cyano-3-ethoxycarbonyl-4-(2-furyl)-2-methyl-1,4-dihydro-1,6-naphthyridines,
which have not been described hitherto.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 121–124, January, 2000. 相似文献
20.
V. N. Nesterov S. G. Krivokolysko V. V. Dotsenko V. P. Litvinov 《Russian Chemical Bulletin》1997,46(5):990-996
The reaction of arylcyanomethylenethiocetamides with Meldrum, acid gave Michael adducts as ammonium salts. When heated in
alcohol, these salts undergo cyclization to ammonium 4-aryl-5-cyano-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolates. The structure
ofN-methylmorpholinium 4-(2′-chlorophenyl)-5-cyano-2-oxo-1,2,3,4-tetrahydropyridine-6-thiolate was established by X-ray structural
analysis.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1029–1034, May, 1997. 相似文献