Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Studies on Coenzyme Analogs. XI. Synthesis of N-Methyl-and N, N-Dimethylcytidine 5'-Phosphate
池原 森男上田 亨池田 一芳
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1962 年 10 巻 9 号 p. 767-771

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Uridine was converted to 2', 3'-O-isopropylidene-5'-O-benzoyluridine and derived to 2', 3'-O-isopropylidene-4-methylthiouridine by successive thiolation and methylation. The latter compound was reacted with either CH3NH2 or (CH3)NH2 to produce 2', 3'-Oisopropylidene-N-methyl-or N, N-dimethylcytidine respectively. N-Methyl-and N, Ndimethylcytidine 5'-phosphate were synthesized by the poly-phosphoric acid method followed by the acidic removal of isopropylidene groups.
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© The Pharmaceutical Society of Japan
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