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Identification of LSD Derivatives, 1cP-LSD, MIPLA and 1B-LSD in Illegal Products as Paper Sheet

Rie Tanaka, Maiko Kawamura, Takashi Hakamatsuka, Ruri Kikura-Hanajiri

Yakugaku Zasshi October 31, 2020 DOI: 10.1248/yakushi.20-00124 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Analytical identification study Peer reviewed
Population Three paper sheet products containing LSD derivatives
Topics LSD
Keywords Quinoline Isopropyl Stereochemistry
Citations 15
Key points Three additional LSD derivatives—1cP-LSD, MIPLA, and 1B-LSD—were detected in paper sheet products in Japan, and 1cP-LSD and 1B-LSD readily deacylate to LSD during GC-MS analysis.

Abstract

Lysergic acid diethylamide (LSD) is a hallucinogen, synthesized from ergot alkaloid, and controlled as a narcotic in Japan. Recently, LSD derivatives have appeared as designer drugs, all over the world. In previous study, we reported identification and analysis of four LSD derivatives in four paper sheet products. In this study, we detected three additional LSD derivatives from three paper sheet products, which were obtained from September 2019 to March 2020 in Japan. We extracted the compounds from paper sheet products with methanol for LC-MS, high-resolution MS and GC-MS analyses. The compounds were identified as 4-cyclopropionyl-N,N-diethyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide (1cP-LSD), N-methyl-N-isopropyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo-[4,3-fg]quinoline-9-carboxamide (MIPLA), 4-butyryl-N,N-diethyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide (1B-LSD), by GC-MS, LC-MS, LC-Q-TOF-MS and NMR analyses. As well as other N1-acylated LSD derivatives, 1cP-LSD and 1B-LSD were easily deacylated to LSD during GC-MS analysis, we have to be careful to analyze these compounds.

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