Differential protonation and dynamic structure of doxylamine succinate in solution using 1H and 13C NMR

Copyright 2004 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 42(2004), 7 vom: 15. Juli, Seite 636-40
1. Verfasser: Somashekar, B S (VerfasserIn)
Weitere Verfasser: Nagana Gowda, G A, Ramesha, A R, Khetrapal, C L
Format: Aufsatz
Sprache:English
Veröffentlicht: 2004
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Comparative Study Journal Article Research Support, Non-U.S. Gov't Carbon Isotopes Protons Solutions Doxylamine 95QB77JKPL doxylamine succinate V9BI9B5YI2
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245 1 0 |a Differential protonation and dynamic structure of doxylamine succinate in solution using 1H and 13C NMR 
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520 |a A protonation and dynamic structural study of doxylamine succinate, a 1:1 salt of succinic acid with dimethyl-[2-(1-phenyl-1-pyridin-2-yl-ethoxy)ethyl]amine, in solution using one- and two-dimensional 1H and 13C NMR experiments at variable temperature and concentration is presented. The two acidic protons of the salt doxylamine succinate are in 'intermediate' exchange at room temperature, as evidenced by the appearance of a broad signal. This signal evolves into two distinct signals below about -30 degrees C. A two-dimensional 1H-1H double quantum filtered correlation experiment carried out at -55 degrees C shows protonation of one of the acidic protons to the dimethylamine nitrogen. A two-dimensional rotating frame 1H-1H NOE experiment at the same temperature reveals that the other proton remains with the succinate moiety. Comparison of the 1H and 13C chemical shifts and the 13C T1 relaxation times of the salt with those of the free base further substantiate the findings 
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650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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700 1 |a Ramesha, A R  |e verfasserin  |4 aut 
700 1 |a Khetrapal, C L  |e verfasserin  |4 aut 
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