Pyrimidinesulfonic acids

Pyrimidine-4-sulfonic acid, 2,6-dimethyl-reactions, 3, 97 Pyrimidinesulfonic acids acidic pif 3, 60 reactions, 3, 96 synthesis, 3, 138 Pyrimidine-2-sulfonic acids acidic pK, 3, 60 reactions, 3, 97 Pyrimidine-4-sulfonic acids hydrolysis, 3, 97 Pyrimidine-2-sulfonyl chloride synthesis, 3, 138... 

To investigate thiamine metabolism in mammals, thiamine (Rf values 0.16, 0.04, and 0.03), urinary excretion of thiamine metabolites [thiochirome (Rf values 0.31, 0.28, and 0.33), thiazole (Rf values 0.85, 0.79, and 0.81), and 2-methyl-4-amino-pyrimidinecarboxylic acid (Rf values 0.42, 0.21, and 0.26)], and related compounds [pyrimidinesulfonic acid (Rf values 0.48, 0.39, and 0.46), a-hydroxyethylthiamine (Rf values 0.23, 0.09, and 0.06), A -methylnicotinamide (Rf values 0.31, 0.06, and 0.05)] were analyzed and identified by TLC on silica gel with acetonitrile-water (40 10 vol/vol) adjusted to a pH of 2.54, 4.03, and 7.85 with formic acid as solvents, respectively.Although A -methylnicotinamide and thio-chrome could not be separated in single-phase chromatography at pH 2.54, a second phase at right angle, with a pH 4.03 solvent, separated these quite clearly without affecting the resolution of the other compounds. 

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