Issue 0, 1971

Heterocyclic studies. Part XV. Synthesis and covalent hydration of pteridine-4-carboxylic acid, -4-carboxamide, and -4-carbonitrile

Abstract

Hydrolysis of ethyl pteridine-4-carboxylate gave the corresponding carboxylic acid as a 5,6:7,8-dihydrated species which could not be dehydrated without decomposition. Syntheses of pteridine-4-carboxamide, N-ethylpteridine-4-carboxamide, 6,7-dimethylpteridine-4-carboxamide, and pteridine-4-carbonitrile are described and the covalent hydration behaviour of these compounds is discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 375-378

Heterocyclic studies. Part XV. Synthesis and covalent hydration of pteridine-4-carboxylic acid, -4-carboxamide, and -4-carbonitrile

J. Clark, W. Pendergast, F. S. Yates and A. E. Cunliffe, J. Chem. Soc. C, 1971, 375 DOI: 10.1039/J39710000375

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements