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Synthesis and Identification of Urinary Metabolites of 4-Lodo-2,5-Dimethoxyphenethylamine

NCJ Number
236211
Journal
Journal of Forensic Sciences Volume: 56 Issue: 5 Dated: September 2011 Pages: 1319-1323
Author(s)
Tatsuyuki Kanamori, Ph.D.; Kenji Kuwayama, Ph.D.; Kenji Tsujikawa, Ph.D.; Hajime Miyaguchi, Ph.D.; Yuko T. Iwata, Ph.D.; Hiroyuki Inoue, Ph.D.
Date Published
September 2011
Length
5 pages
Annotation
This article describes the synthesis and identification of urinary metabolites of 4-iodo-2,5-dimethoxyphenethylamine (2C-I), a new psychoactive drug.
Abstract
2C-I hydrochloride was administered orally to male Sprague-Dawley rats, and the urinary extracts were analyzed by gas chromatography/mass spectrometry (GC/MS), then five putative 2C-I metabolites were synthesized in the authors'laboratory. In the synthetic process of the 2C-I metabolites, iodination of the aromatic ring was successfully carried out using iodine and orthoperiodic acid as the iodination reagent, and selective debenzylation of aryl benzyl ether was accomplished by the acid hydrolysis method using trifluoroacetic acid and thioanisole. The synthesized metabolites were well separated and detected by GC/MS after valeryl derivatization. The results showed that 2C-I underwent O-demethylation, N-acetylation, and deamination, followed by oxidation to the corresponding carboxylic acid in rats. The data presented in this study will be very useful for the analysis of 2C-I and its metabolites in forensic samples. (Published Abstract)