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5-alkoxy 1,2,4 triazolo 1,5-c pyrimidine-2 (3H) -thione compounds, and 2,2′-dithiobis (5-alkoxy 1,2,4 triazolo 1, 5-c pyrimidine) and their use in the preparation of 2-chlorosulfonyl-5-alkoxy 1,2,4 triazolo 1,5-c pyrimidine compounds
5-alkoxy 1,2,4 triazolo 1,5-c pyrimidine-2 (3H) -thione compounds, and 2,2′-dithiobis (5-alkoxy 1,2,4 triazolo 1, 5-c pyrimidine) and their use in the preparation of 2-chlorosulfonyl-5-alkoxy 1,2,4 triazolo 1,5-c pyrimidine compounds
2-Chlorosulfonyl-5-alkoxy[1,2,4]triazolo-[1,5-c]pyrimidine compounds, such as 2-chlorosulfonyl-5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine, that are useful for the preparation of 5-alkoxy[1,2,4]triazolo [1,5-c]pyrimidine-2-sulfonamide herbicides, were prepared in an improved manner from 5-alkoxy[1,2,4]triazolo [1,5-c]pyrimidine-2(3H)-thione compounds, such as 5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine-2(3H)-thione, by oxidation with hydrogen peroxide to obtain novel 2,2'-dithiobis(5-alkoxy[1,2,4]triazolo[1,5-c]pyrimidine) compounds, such as 2,2'-dithiobis (5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine), and subsequent chloroxidation of these intermediate compounds.
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