156112-54-8Relevant articles and documents
Alkylation of 6-Polyfluoroalkyl-2-thiouracils with Haloalkanes
Khudina,Ivanova,Burgart, Ya. V.,Pervova,Shatunova,Borisevich,Khursan,Saloutin
, p. 782 - 791 (2019)
The structure of 6-polyfluoroalkyl-2-thiouracils and reactivity of nucleophilic centers in their molecules were analyzed by quantum chemical calculations. According to the experimental data, methylation of 6-polyfluoroalkyl-2-thiouracils with methyl iodide initially gives 2-methylsulfanyl-substituted pyrimidin-4-one and then S,N3- and S,O-dimethyl derivatives. The optimal conditions for the selective formation of the S, N3- isomer were heating in tert-butyl alcohol in the presence of cesium carbonate as a base. Ethylation of 6-polyfluoroalkyl-2-thiouracils afforded approximately equal amounts of S,N3- and S,O-dimethyl derivatives. S,N3-Dimethyl-substituted pyrimidines in boiling ethanol in the presence of potassium carbonate were converted into uracil potassium salts as a result of nucleophilic substitution of the methylsulfanyl group by ethoxy and subsequent dealkylation of the latter.
2-arylaminopyrimidinone derivative, and herbicide and plant growth regulator
-
, (2008/06/13)
Disclosed are a herbicide and a plant growth regulator comprising a 2-arylaminopyrimidinone derivative represented by the formula (1): STR1 (wherein Q represents various kinds of aromatic ring or heterocyclic ring). This compound can be used safely to mai