Infrared Spectra of Sulfonamide Derivatives. I. Pyridine, Thiazole, and Pyrimidine Derivatives

29Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

The infrared spectra of N-(2-pyridyl)-, N-(2-thiazolyl)-, N-(2-pyrimidinyl)- and N-phenyl-sulfonamide derivatives and their N-deuterated compounds, as well as N1- or ring N-methylsulfonamide derivatives were measured. The spectral changes on N-deuteration suggest that pyrimidine derivatives take the amido form, while pyridine and thiazole derivatives take the imido form. The SO2 symmetric stretching bands of sulfanilamide derivatives may be divided into the two regions, 1170 to 1145 cm-1 and 1145 to 1130 cm-1, according to the amido form and the imido form, respectively. © 1963, The Pharmaceutical Society of Japan. All rights reserved.

Cite

CITATION STYLE

APA

Uno, T., Machida, K., Hanai, K., Ueda, M., & Sasaki, S. (1963). Infrared Spectra of Sulfonamide Derivatives. I. Pyridine, Thiazole, and Pyrimidine Derivatives. Chemical and Pharmaceutical Bulletin, 11(6), 704–708. https://doi.org/10.1248/cpb.11.704

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free