1953 年 73 巻 4 号 p. 379-382
3-(2′-Methyl-4′-aminopyrimidyl-5′)-methyl-4-methyl-5-β-hydroxyethylthiazol-2-thion was treated with hydrogen peroxide at pH 7.0, 8.0 and in a strongly alkaline range to examine the difference in the products obtained at different pH ranges. At the same time, the formation mechanism was also assumed. Confirmation of the products was made chiefly by the paper partition chromatography, with isolation of some of the products. The products formed were as follows:
At pH 7.0-Vitamin B1 disulfide (VI), vitamin B1 (II) (in minute amount), thiochrome (IV) (in minute amount).
At pH 8.0-Thiamine-thiazolone (III) (in large amount), vitamin B1 disulfide (VI), thiochrome (IV), vitamin B1 (II) (in minute amount).
In strongly alkaline range-Thiamine-thiazolone (III) (in extremely large amount), thiochrome (IV), 2-methyl-4-amino-5-aminomethylpyrimidine (VII) (in minute amount).