Chemistry:Α-D2PV

From HandWiki

α-D2PV (DPPE) is a substituted cathinone derivative which has been sold as a designer drug. It was invented in the 1950s,[1] and first identified by forensic laboratories as a designer drug in 2020, though anecdotal reports suggest it may have emerged earlier than this. It is similar in structure to the potent designer stimulant drug alpha-PVP but with the propyl side chain replaced by a phenyl ring, and while it is less potent than alpha-PVP itself, Alpha-D2PV is still a reasonably potent stimulant and has been known to cause poisoning when misrepresented as less potent drugs such as MDMA. While it is also similar in structure to the dissociative drug diphenidine, Alpha-D2PV appears to produce only stimulant effects.[2][3][4]

In terms of the synthesis, it is made in a one-step Voight reaction between benzoin and pyrrolidine.[1]

See also

References

  1. 1.0 1.1 Heinzelman RV, Aspergren BD, "1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings", US patent 2773069, issued 4 December 1956
  2. "A review of synthetic cathinones emerging in recent years (2019-2022)". Forensic Toxicology 41 (1): 25–46. 2023. doi:10.1007/s11419-022-00639-5. PMID 36124107. 
  3. "Characterising differences between self-reported and wastewater-identified drug use at two consecutive years of an Australian music festival". The Science of the Total Environment 921. April 2024. doi:10.1016/j.scitotenv.2024.170934. PMID 38360330. Bibcode2024ScTEn.92170934P. 
  4. "Crystal structure and analytical profile of 1,2-diphenyl-2-pyrrolidin-1-ylethanone hydrochloride or 'α-D2PV': a synthetic cathinone seized by law enforcement, along with its diluent sugar, myo-inositol". Acta Crystallographica Section C 80 (4): 91–97. April 2024. doi:10.1107/S2053229624000561. PMID 38441142.