GC-MS and GC-IR analysis of regioisomeric cannabinoids related to 1-(5-fluoropentyl)-3-(1-naphthoyl)-indole

• NCJ Number: 253186
• Date Published: January 2021
• Length: 10 pages
• Award: Forensic Chemistry of Substituted 1-Alkyl-3-Acylindoles: Isomeric Synthetic Cannabinoids.

Abstract

The compounds in this study are the regioisomeric 2-, 3-, 4-, 5-, 6- and 7-(1-naphthoyl) substituted 1-(5-fluoropentyl)-indoles and the 3-(1-naphthoyl) substituted isomer in this series is also known as AM-2201. These compounds are structurally similar to JWH-018 except for the additional fluorine at the terminal end of the n-pentyl side-chain. These six regioisomeric compounds have the identical elemental composition (C24H22FNO) and differ in the position of attachment of the 1-napthoyl group on the indole ring. The electron ionization mass spectra showed similar major fragment ions with a molecular radical cation of significant abundance at m/z 359. The six compounds have similar fragment ions at m/z 127 and 155 for the naphthyl and naphthoyl cations. There is a prominent fragment ion at m/z 342 [M-17](+) in the EI-MS of 1-(5-fluoropentyl)-3-, 4-, 5- and 6-(1-naphthoyl)-indoles due to the loss of the hydroxyl group and this ion is most prominent in the 3-(1-naphthoyl) substituted isomer (AM-2201). The six compounds were separated using gas chromatography on a capillary column containing a trifluoropropylmethyl polysiloxane (Rtx-200) stationary phase. The elution order appears to be related to the steric crowding of the indole ring substituents. The 7- and 2-(1-naphthoyl) substituted isomers eluted first due to the possibility for maximum interactions between the naphthyol and alkyl side-chains. The vapor phase infrared spectra differentiate among these six compounds based on the position of the 1-naphthoyl group on the indole ring. The vapor phase spectra for these compounds are compared to the non-fluorinated analogues, JWH-018 and its regioisomeric equivalents. (C) 2018 Published by Elsevier B.V.