Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Effect of Conformation of Molecules on Molecular Interaction. II. Nicotinamides and Pyridine Esters
掛見 喜一郎瀬崎 仁大菅 喜一郎中野 真汎
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1968 年 16 巻 5 号 p. 819-821

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In a series of solubility studies of pyridine derivatives with 8-methoxycaffeine in aqueous solution, an extent of molecular interaction of N, N-dimethylnicotinamide (I) was found to be much less than those of unsubstituted and N-monomethylnicotinamide. Degree of complexation of 3-acetoxypyridine (II) was revealed to be much less than that of methyl nicotinate. Reduced complexing tendencies of I and II were attributed to nonplanar structures of these compounds in solution.
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© The Pharmaceutical Society of Japan
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