Phenmetrazine

Phenmetrazine was first patented in Germany in 1952 by Boehringer-Ingelheim,[1][2] with some pharmacological data published in 1954.[3] It was the result of a search by Thomä and Wick for an anorectic drug without the side-effects of amphetamine.[4] Phenmetrazine was introduced into clinical use in 1954 in Europe.[5]

In clinical use, phenmetrazine produces less nervousness, hyperexcitability, euphoria and insomnia than drugs of the amphetamine family.[6] It tends not to increase heart rate as much as other stimulants. Due to the relative lack of side effects, one study found it well tolerated in children.[4] In a study of the effectiveness on weight loss between phenmetrazine and dextroamphetamine, phenmetrazine was found to be slightly more effective.[7]

Phenmetrazine acts as a releasing agent of norepinephrine and dopamine with EC₅₀ values of 50.4 ± 5.4 nM and 131 ± 11 nM, respectively.[8] It has negligible efficacy as a releaser of serotonin, with an EC₅₀ value of only 7,765 ± 610 nM.[8]

After an oral dose, about 70% of the drug is excreted from the body within 24 hours. About 19% of that is excreted as the unmetabolised drug and the rest as various metabolites.[9]

In trials performed on rats, it has been found that after subcutaneous administration of phenmetrazine, both optical isomers are equally effective in reducing food intake, but in oral administration the levo isomer is more effective. In terms of central stimulation however, the dextro isomer is about 4 times as effective in both methods of administration.[10]

The salt which has been used for immediate-release formulations is phenmetrazine hydrochloride (Preludin). Sustained-release formulations were available as resin-bound, rather than soluble, salts. Both of these dosage forms share a similar bioavailability as well as time to peak onset, however, sustained-release formulations offer improved pharmacokinetics with a steady release of active ingredient which results in a lower peak concentration in blood plasma.

1105 g. of 2-phenyl-3-methyl-4-(B-hydroxy ethyl) tetrahydro-1,4-oxazine are dissolved in 4000 cc. of anhydrous toluene. 910 g. of a-phenyl-u-ethyl acetic acid chloride are dissolved in 400 cc. of anhydrous toluene and the resulting solution is slowly added to the heated solution of the tetrahydro-1,4-oxazine compound. The mixture is then heated to boiling for about 5 hours. About 1000 g. of ice are added to the cooled reaction mixture which is then rendered alkaline by the addition of 20% sodium carbonate solution to a pH of 9.0. Thereafter the mixture is vigorously stirred by means of a turbine mixer for one hour and the toluene phase is separated. The toluene solution is washed with 1000 cc. of saturated sodium chloride solution and is dried over anhydrous sodium sulfate. The toluene is then evaporated and the residue is subjected to high vacuum distillation. 1650 g. of a-phenyl-a-ethyl acetic acid-(Z-phenyl- 3-methyl tetrahydro-l,4-oxazine)-N-ethyl ester, boiling at 235-240 C./ 0.05 mm. are obtained thereby in a yield of 90.5% of the theoretical yield.[11]

Its structure incorporates the backbone of amphetamine, the prototypical CNS stimulant which, like phenmetrazine, is a releasing agent of dopamine and norepinephrine. The molecule also loosely resembles ethcathinone, the active metabolite of popular anorectic amfepramone (diethylpropion). Unlike phenmetrazine, ethcathinone (and therefore amfepramone as well) are mostly selective as noradrenaline releasing agents.

Phenmetrazine has been used recreationally in many countries, including Sweden. When stimulant use first became prevalent in Sweden in the 1950s, phenmetrazine was preferred to amphetamine and methamphetamine by users.[12] In the autobiographical novel Rush by Kim Wozencraft, intravenous phenmetrazine is described as the most euphoric and pro-sexual of the stimulants the author used.

Phenmetrazine was classified as a narcotic in Sweden in 1959, and was taken completely off the market in 1965. At first the illegal demand was satisfied by smuggling from Germany, and later Spain and Italy. At first, Preludin tablets were smuggled, but soon the smugglers started bringing in raw phenmetrazine powder. Eventually amphetamine became the dominant stimulant of abuse because of its greater availability.

Phenmetrazine was taken by the Beatles early in their career. Paul McCartney was one known user. McCartney's introduction to drugs started in Hamburg, Germany. The Beatles had to play for hours, and they were often given the drug (referred to as Prellies) by the maid who cleaned their housing arrangements, German customers, or by Astrid Kirchherr (whose mother bought them). McCartney would usually take one, but John Lennon would often take four or five.[13] Hunter Davies asserted, in his 1968 biography of the band,[14] that their use of such stimulants then was in response to their need to stay awake and keep working, rather than a simple desire for kicks.

Jack Ruby said he was on phenmetrazine at the time he killed Lee Harvey Oswald.[15]

Preludin was also used recreationally in the US throughout the 1960s and early 1970s. It could be crushed up in water, heated and injected. The street name for the drug in Washington, DC was "Bam".[16] Phenmetrazine continues to be used and abused around the world, in countries including South Korea.[17]

• Substituted phenylmorpholine
• 3-Benzhydrylmorpholine
• Fenbutrazate
• Edivoxetine
• Phendimetrazine
• Morazone
• Reboxetine
• The Beatles drug use in Hamburg
• 3-Fluorophenmetrazine