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Syntheses based on 2-ethoxycarbonylmethyl-7-methyl-1,3,4-thiadiazolo[3,2-a]pyrimidin-5(5H)-one
Authors:M. A. Kukaniev  S. Sh. Shukurov  Yu. Khodzhibaev  N. Kurbonova  S. G. Bandaev
Affiliation:(1) V. I. Nikitin Institute of Chemistry, Academy of Sciences of Republic Tajikistan, 299 ul. Aini, 734069 Dushanbe, Tajikistan
Abstract:2-Ethoxycarbonylmethyl-7-methyl-1,3,4-thiadiazolo[3,2-a]pyrimidin-5(5H)-one containing the active methylene group reacts easily with carbon disulfide and phenyl isothiocyanate in the presence of sodium hydride. Further alkylation of the reaction product by alkyl halides results in the formation of the corresponding 1,3,4-thiadiazolo[3,2-a]pyrimidine derivatives containing a ketene dithioacetal fragment. Deceased. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2371–2373, November, 1998.
Keywords:2-ethoxycarbonylmethyl-7-methyl-1,3,4-thiadiazolo[3,2-a]pyrimidin-5(5H)-one  1,3,4-thiadiazolo[3,2-a]pyrimidines  ethyl (7-methyl-5-oxo-5H-1,3,4-thiadiazolo-[3,2-a]pyrimidin-2-yl)methylthiothiocarbonylacetate  ethyl 2-(7-methyl-5-oxo-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-2-yl)-3,3-bis(methylthio)acrylate
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