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2,4(1H,3H)-Pyrimidinedione, 5-fluoro-6-methyl- (9CI) synthesis

3synthesis methods
-

Yield:1480-99-5 37%

Reaction Conditions:

with Selectfluor in water at 80; for 4 h;

Steps:



General procedure: Fluorination of 6-methyl- and 1,3,6-trimethyluracils1 and 2 (general procedure). A solution ofuracil 1 or 2 and F-TEDA-BF4 in water was stirredunder the conditions indicated in table, the solvent waspurged off with a stream of air, the residue was dissolvedin DMSO-d6, and 1H and 19F NMR spectra wererecorded. In some cases (see table), excess F-TEDABF4was removed by adding KI and Na2S2O3 to thereaction mixture before purging with air.

References:

Borodkin;Elanov;Shubin [Russian Journal of Organic Chemistry,2015,vol. 51,# 7,p. 1003 - 1007][Zh. Org. Khim.,2015,vol. 51,# 7,p. 1021 - 1025,5]