Chemical profiling of the synthetic cannabinoid MDMB-CHMICA: Identification, assessment, and stability study of synthesis-related impurities in seized and synthesized samples

被引:10
作者
Muenster-Mueller, Sascha [1 ,2 ]
Hansen, Steven [3 ]
Opatz, Till [3 ]
Zimmermann, Ralf [2 ,4 ]
Puetz, Michael [1 ]
机构
[1] Fed Criminal Police Off, Forens Sci Inst, Wiesbaden, Germany
[2] Univ Rostock, Joint Mass Spectrometry Ctr, Inst Chem, Chair Analyt Chem, Rostock, Germany
[3] Johannes Gutenberg Univ Mainz, Inst Organ Chem, Mainz, Germany
[4] Helmholtz Zentrum Muenchen, Joint Mass Spectrometry Ctr, Cooperat Grp Comprehens Mol Analyt, Neuherberg, Germany
关键词
controlled synthesis; impurity profiling; LC-MS; MDMB-CHMICA; new psychoactive substances (NPS); REDUCTIVE AMINATION; HARMONIZED METHOD; AMPHETAMINE; ROUTE; METHYLAMPHETAMINE; FORMYLKYNURENINE; PHARMACOLOGY; DERIVATIVES; TRYPTOPHAN; FUBINACA;
D O I
10.1002/dta.2652
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, the most discriminating synthesis-related impurities found in samples from seizures and controlled synthesis of the synthetic cannabinoid MDMB-CHMICA (methyl (S)-2-(1-(cyclohexylmethyl)-1H-indole-3-carboxamido)-3,3-dimethylbutanoate) were characterized. Based on 61 available powder samples of MDMB-CHMICA, 15 key-impurities were assessed, isolated in larger quantities via flash chromatography and structurally elucidated and characterized via high resolution mass spectrometry and nuclear magnetic resonance spectroscopy. Apart from verifying the relation of the impurities to the major component, the interpretation of their chemical structures with distinct structural elements provided first insights into the manufacturing process and the precursor compounds used. Following liquid chromatography mass spectrometry analysis of the 15 key-impurities, the 61 seized samples of MDMB-CHMICA were evaluated and classified via multivariate data analysis based on the corresponding relative peak areas. In a second part of this work, stability tests and multiple controlled syntheses of MDMB-CHMICA were carried out to better understand variations in impurity signatures and to assess the significance of variations in the impurity patterns of seized samples. The last coupling step of the amino acid with 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid was performed using the coupling agents oxalyl chloride, thionyl chloride, and HATU. Furthermore, the impact of reaction time and temperature on the impurity profile were investigated. Overall, eight new impurities were found in the controlled syntheses and two degradation products of MDMB-CHIMCA were found in the course of the stability tests. Replicates of a synthesis conducted on the same day showed similar impurity signatures; on different days they showed discriminable signatures. The use of different coupling reagents or conditions gave clearly distinguishable impurity signatures.
引用
收藏
页码:1192 / 1206
页数:15
相关论文
共 56 条
[1]   Development of a harmonised method for the profiling of amphetamines -: II.: Stability of impurities in organic solvents [J].
Aalberg, L ;
Andersson, K ;
Bertler, C ;
Cole, MD ;
Finnon, Y ;
Huizer, H ;
Jalava, K ;
Kaa, E ;
Lock, E ;
Lopes, A ;
Poortman-van der Maar, A ;
Sippola, E ;
Dahlén, J .
FORENSIC SCIENCE INTERNATIONAL, 2005, 149 (2-3) :231-241
[2]   Development of a harmonised method for the profiling of amphetamines -: I.: Synthesis of standards and compilation of analytical data [J].
Aalberg, L ;
Andersson, K ;
Bertler, C ;
Borén, H ;
Cole, MD ;
Dahlén, J ;
Finnon, Y ;
Huizer, H ;
Jalava, K ;
Kaa, E ;
Lock, E ;
Lopes, A ;
Poortman-van der Meer, A ;
Sippola, E .
FORENSIC SCIENCE INTERNATIONAL, 2005, 149 (2-3) :219-229
[3]   Absolute configuration of the synthetic cannabinoid MDMB-CHMICA with its chemical characteristics in illegal products [J].
Andernach, Lars ;
Pusch, Stefan ;
Weber, Carina ;
Schollmeyer, Dieter ;
Muenster-Mueller, Sascha ;
Puetz, Michael ;
Opatz, Till .
FORENSIC TOXICOLOGY, 2016, 34 (02) :344-352
[4]   Isomeric discrimination of synthetic cannabinoids by GC-EI-MS: 1-adamantyl and 2-adamantyl isomers of N-adamantyl carboxamides [J].
Asada, Akiko ;
Doi, Takahiro ;
Tagami, Takaomi ;
Takeda, Akihiro ;
Sawabe, Yoshiyuki .
DRUG TESTING AND ANALYSIS, 2017, 9 (03) :378-388
[5]   'Spice' and other herbal blends: harmless incense or cannabinoid designer drugs? [J].
Auwaerter, Volker ;
Dresen, Sebastian ;
Weinmann, Wolfgang ;
Mueller, Michael ;
Puetz, Michael ;
Ferreiros, Nerea .
JOURNAL OF MASS SPECTROMETRY, 2009, 44 (05) :832-837
[6]   Development of a harmonised pan-European method for the profiling of amphetamines [J].
Ballany, J ;
Caddy, B ;
Cole, M ;
Finnon, Y ;
Aalberg, L ;
Janhunen, K ;
Sippola, E ;
Andersson, K ;
Bertler, C ;
Dahlén, J ;
Kopp, I ;
Dujourdy, L ;
Lock, E ;
Margot, P ;
Huizer, H ;
Poortman, A ;
Kaa, E ;
Lopes, A .
SCIENCE & JUSTICE, 2001, 41 (03) :193-196
[7]   Pharmacology of Valinate and tert-Leucinate Synthetic Cannabinoids 5F-AMBICA, 5F-AMB, 5F-ADB, AMB-FUBINACA, MDMB-FUBINACA, MDMB-CHMICA, and Their Analogues [J].
Banister, Samuel D. ;
Longworth, Mitchell ;
Kevin, Richard ;
Sachdev, Shivani ;
Santiago, Marina ;
Stuart, Jordyn ;
Mack, James B. C. ;
Glass, Michelle ;
McGregor, Iain S. ;
Connor, Mark ;
Kassiou, Michael .
ACS CHEMICAL NEUROSCIENCE, 2016, 7 (09) :1241-1254
[8]  
Bowden JPB., 2014, Patent, Patent No. [WO02014167530A1, 02014167530, 2014167530 A1, 2014167530]
[9]  
Buchler I. P., 2009, Patent No. [WO2009106980A2, 2009106980]
[10]   Gas chromatographic-mass spectrometric analysis of residual solvent trapped into illicit cocaine exhibits using head-space solid-phase microextraction [J].
Chiarotti, M ;
Marsili, R ;
Moreda-Piñeiro, A .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2002, 772 (02) :249-256