School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China; Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, Guangxi University, Nanning, Guangxi 530004, P. R. China.
School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China.
J Pharm Biomed Anal. 2023 Sep 20;234:115525. doi: 10.1016/j.jpba.2023.115525. Epub 2023 Jun 12.
Gas chromatography-mass spectrometry (GC-MS) is the first choice for law enforcement agencies in various countries to analyze new psychoactive substances (NPS) because of its advantages and complete databases. For synthetic cathinone-type NPS (SCat), alkalization and extraction processes before GC-MS analysis are essential. However, the base form of SCat is unstable, causing it to quickly degrade in solution and cause pyrolysis at the GC-MS injection inlet. In this study, we investigated the degradation of ethyl acetate and pyrolysis at the GC-MS injection inlet of 2-fluoromethcathinone (2-FMC), the most unstable SCat. Using gas chromatography-quadruple/time-of-flight mass spectrometry (GC-Q/TOF-MS) combined with the predicted data from theoretical calculations and the analysis of mass spectrometry (MS) fragmentation, the structures of 15 2-FMC degradation and pyrolysis products were identified. Among them, 11 products were produced during degradation, and six products were obtained from pyrolysis (two of which were the same as the degradation products). At the same time, the degradation and pyrolysis pathways of 2-FMC were provided. The balance between keto-enol and enamine-imine tautomerism triggered the primary degradation pathway of 2-FMC. The subsequent degradation started from the tautomer with a hydroxyimine structure, including imine hydrolysis, oxidation, imine-enamine tautomerism, intramolecular ammonolysis of halobenzene, and hydration to generate a series of degradation products. The secondary degradation reaction was the ammonolysis of ethyl acetate to yield N-[1-(2'-fluorophenyl)-1-oxopropan-2-yl]-N-methylacetamide and the byproduct, N-[1-(2'-fluorophenyl)-1-oxopropan-2-yl]-N-methylformamide. In the pyrolysis of 2-FMC, the major reactions were dehydrogenation, intramolecular ammonolysis of halobenzene, and defluoromethane. The achievements of this manuscript not only study 2-FMC degradation and pyrolysis but also lay the foundation for the study of SCat stability and their accurate analysis by GC-MS.
气相色谱-质谱联用技术(GC-MS)因其优势和完整的数据库,成为各国执法机构分析新型精神活性物质(NPS)的首选。对于合成卡西酮类 NPS(SCat),GC-MS 分析前的碱化和提取过程是必不可少的。然而,SCat 的碱基形式不稳定,导致其在溶液中迅速降解,并在 GC-MS 进样口发生热解。在本研究中,我们研究了最不稳定的 SCat-2-氟甲卡西酮(2-FMC)在乙酸乙酯中的降解和在 GC-MS 进样口的热解。使用气相色谱-四极杆/飞行时间质谱联用技术(GC-Q/TOF-MS),结合理论计算预测数据和质谱(MS)碎片分析,鉴定了 15 种 2-FMC 降解和热解产物的结构。其中,降解过程中生成了 11 种产物,热解过程中得到了 6 种产物(其中 2 种与降解产物相同)。同时,提供了 2-FMC 的降解和热解途径。酮-烯醇和烯胺-亚胺互变异构平衡触发了 2-FMC 的主要降解途径。随后的降解从具有羟亚胺结构的互变异构体开始,包括亚胺水解、氧化、亚胺-烯胺互变异构、卤代苯的分子内氨解以及水合作用,生成一系列降解产物。二次降解反应是乙酸乙酯的氨解,生成 N-[1-(2'-氟苯基)-1-氧代丙-2-基]-N-甲基乙酰胺和副产物 N-[1-(2'-氟苯基)-1-氧代丙-2-基]-N-甲基甲酰胺。在 2-FMC 的热解中,主要反应是脱氢、卤代苯的分子内氨解和脱氟甲烷。本研究的成果不仅研究了 2-FMC 的降解和热解,还为 SCat 稳定性的研究及其通过 GC-MS 进行准确分析奠定了基础。