## Abstract Phenazopyridine hydrochloride (**1**), a drug in clinical use for many decades, and some derivatives were studied by one‐ and two‐dimensional ^1^H, ^13^C and ^15^N NMR methodology. The assignments, combined with DFT calculations, reveal that the preferred protonation site of the drug is
Derivatives of pyrazinecarboxylic acid: 1H, 13C and 15N NMR spectroscopic investigations
✍ Scribed by Wolfgang Holzer; Gernot A. Eller; Barbara Datterl; Daniela Habicht
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 159 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2437
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
NMR spectroscopic studies are undertaken with derivatives of 2‐pyrazinecarboxylic acid. Complete and unambiguous assignment of chemical shifts (^1^H, ^13^C, ^15^N) and coupling constants (^1^H,^1^H; ^13^C,^1^H; ^15^N,^1^H) is achieved by combined application of various 1D and 2D NMR spectroscopic techniques. Unequivocal mapping of ^13^C,^1^H spin coupling constants is accomplished by 2D (δ,J) long‐range INEPT spectra with selective excitation. Phenomena such as the tautomerism of 3‐hydroxy‐2‐pyrazinecarboxylic acid are discussed. Copyright © 2009 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## REFERENCE DATA carbons, for various substituent groups and positions were carried out by gated decoupling with NOE. ## RESULTS AND DISCUSSION The I3C NMR chemical shifts of the compounds are shown in Tables 123; 'J(CH) and long-range coupling constants of 2, 9, 13 and 18, measured by gated d
## Abstract ^1^H, ^13^C, and ^15^N NMR chemical shifts for pyridazines 4–22 were measured using 1D and 2D NMR spectroscopic methods including ^1^H^1^H gDQCOSY, ^1^H^13^C gHMQC, ^1^H^13^C gHMBC, and ^1^H^15^N CIGAR–HMBC experiments. Copyright © 2010 John Wiley & Sons, Ltd.
## Abstract ^1^H NMR assignment, including the values of δ~H~ and __J__(H,H) for the cyclopropane moiety, and ^13^C NMR and ^15^N NMR spectral data for ciprofloxacin are presented. Copyright © 2004 John Wiley & Sons, Ltd.
We report a 1 H, 13 C and 15 N NMR investigation of one symmetrically substituted 2,7-dichloro and two unsymmetrically substituted 2-chloro and 4-bromo DMAN [1,8-bis(dimethylamino)naphthalene] proton sponges and their protonated salts. From a consideration of the NMR data reported we conclude, that
## Abstract Mesomeric heteropentalene betaines are conjugated fused polyheterocyclic structures that represent interesting intermediates for organic synthesis. Five such structures, containing at least four nitrogen atoms and various substituents, have been characterized by ^1^H, ^13^C and ^15^N NM