Volume 21, Issue 1 pp. 41-48
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Pyridinethiones. IX preparation of ricinidine, thioricinidine and other 2(1H)-pyridones and -thiones related to nicotinic acid

Jan Becher

Corresponding Author

Jan Becher

Department of Chemistry, Odense University, Campusvej 55, DK5230 Odense M, Denmark

Department of Chemistry, Odense University, Campusvej 55, DK5230 Odense M, DenmarkSearch for more papers by this author
Tea Johansen

Tea Johansen

Department of Chemistry, Odense University, Campusvej 55, DK5230 Odense M, Denmark

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Maged Aziz Michael

Maged Aziz Michael

Department of Chemistry, Odense University, Campusvej 55, DK5230 Odense M, Denmark

A DANIDA grant to M.A.M is greatfully acknowledged.

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First published: January/February 1984
Citations: 12

Abstract

2(1H)-Pyridones and -thiones related to 1-substituted nicotinic acid derivatives have been prepared via the corresponding l-substituted-3-formyl-2(1H)-pyridones and -thiones. A number of synthetic procedures for the interconversion of functional groups in these nicotinic acid derivatives are given i.e. preparation of the aldoximes, nitriles, carboxamides and carboxylic acids as well as the 3- hydroxyalkyl derivatives. The course of the basic peroxide oxidation of the l-substituted-3-formyl-2(1H)-pyridinethiones is found to be very dependent upon the electronegativity of the 1-substituent. A preparation of ricinidine is also described.

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