## L-dihydroxyphenytalanine-H3 L-tyrwsine-2HZ dopamine-H 3methoxytyramine-H3 ' H 5 and vanillylmzndetic acid H2 were prepared by hydrogen-deuterium exchange under acidic o r basic conditions. 4-hydroxy-3methoxy phenylethyleneglycol-H3 was prepared f m m vanillylman-2 2 d e t i c acid-H by reductio
Synthesis of CD3-labelled 3-methoxytyramine, normetanephrine and metanephrine for use as internal standards in mass fragmentographic analyses
✍ Scribed by Frits A. J. Muskiet; Stanislav Pavel; Gerrie J. Stob; Henk Elzinga
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 328 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The preparation of CD~3~‐labelled 3‐methoxytyramine, normetanephrine and metanephrine from their parent catecholamines is described. The syntheses include N‐maleylation, O‐methylation by dimethylsulfate‐D~6~, removal of the protecting group by acid hydrolysis and partial purification of the reaction product. Examples of the use of the deuterium labelled O‐methylated catecholamine metabolites as internal standards for the ammonia chemical ionisation mass fragmentographic determination of their naturally occurring analogs in urine, are given.
📜 SIMILAR VOLUMES
Trideuterated 3,4-dihydroxyphenylglycolaldehyde (DOPEGAL-d 3 ) was synthesized from tetradeuterated catechol. After derivatization with N-methyl-N-trimethylsilyltrifluoroacetamide, the identity of DOPEGAL-d 3 was confirmed by comparison with unlabeled DOPEGAL by gas chromatography-mass spectrometry
## Abstract Four deuterium‐labelled benzodiazepines were prepared for use as internal standards in the quantification of chlordiazepoxide, demethyldiazepam, diazepam, and oxazepam at low levels in body fluids by selected ion monitoring. The method described provides a way to introduce cleanly and i