Aminolysis of 2-Aryl-5-R-5,6-dihydro-7H-[1,2,4]triazolo[5,1-b]1,3]thiazin-7-ones |
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Authors: | V. N. Britsun A. N. Esipenko V. V. Pirozhenko M. O. Lozinskii |
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Affiliation: | (1) Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, 02094, Ukraine |
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Abstract: | We have established that the products of aminolysis of 2-aryl-5-R-5,6-dihydro-7H-[1,2,4]triazolo-[5,1-b][1,3]thiazin-7-ones in boiling ethanol are 3-R-3-(5-aryl-4H-1,2,4-triazol-3-ylsulfanyl)-propanamides, and at 180°C–210°C (depending on the structure of the substituent R): 3-phenyl-4,5-dihydro-1H-1,2,4-triazoline-5-thione and 3-arylacrylamides or 3-(3-aryl-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)propanamides. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1587–1592, October, 2005. |
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Keywords: | 3-arylacrylamides 3-aryl-4,5-dihydro-1H-1,2,4-triazoline-5-thiones 2-aryl-5-R-5,6-dihydro-7H-[1,2,4]triazolo[5,1-b][1,3]thiazin-7-ones 3-(3-aryl-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)propanamides 3-R-3-(5-aryl-4H-1,2,4-triazol-3-ylsulfanyl)propanamides aminolysis |
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