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Substituted phenylmorpholine

In this article, we will delve into the topic of Substituted phenylmorpholine, which has aroused great interest and debate in different areas. Substituted phenylmorpholine is a topic that has become the focus of attention of experts, academics and specialists in the field, due to its relevance and impact in different sectors. Over the last decades, Substituted phenylmorpholine has been acquiring greater importance and relevance, generating endless questions and concerns about its influence on today's society. In this article, we will analyze in detail and exhaustively the different facets of Substituted phenylmorpholine, with the aim of providing a complete and well-founded overview of this topic.

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Various phenmetrazine derivatives

Substituted phenylmorpholines, or substituted phenmetrazines alternatively, are chemical derivatives of 2-phenylmorpholine or of the psychostimulant drug phenmetrazine.

Most such compounds act as releasers of monoamine neurotransmitters, and have stimulant effects. Some also act as agonists at serotonin receptors, and compounds with an N-propyl substitution act as dopamine receptor agonists.

A number of derivatives from this class have been investigated for medical applications, such as for use as anorectics or medications for the treatment of ADHD. Some compounds have also become subject to illicit use as designer drugs.[1][2][3][4]

List of phenylmorpholines

List of phenmetrazine analogues and related compounds
Substance Structure CAS #
2-phenylmorpholine 23972-41-0
2-phenyl-3-methylmorpholine (phenmetrazine) 134-49-6
2-phenyl-3,4-dimethylmorpholine (phendimetrazine) 634-03-7
2-phenyl-5-methylmorpholine (isophenmetrazine) 80123-66-6
2-phenyl-3-ethylmorpholine (phenetrazine) 100368-98-7
2-phenyl-3-methyl-4-ethylmorpholine (phenmetetrazine) 92196-09-3
2-phenyl-3,5-dimethylmorpholine (PDM-35) 1218345-44-8
2-phenyl-3,6-dimethylmorpholine (6-methylphenmetrazine, 3,6-DMPM) 92902-99-3
2-phenyl-5,5-dimethylmorpholine (G-130) 42013-48-9
2-phenyl-3-methylmorpholin-5-one (fenmetramide) 5588-29-4
4-isopropyl-2-phenylmorpholine[5] 23222-62-0
Fenbutrazate 4378-36-3
Morazone 6536-18-1
2-Fluorophenmetrazine 1533654-24-8
3-fluorophenmetrazine (PAL-593) 1350768-28-3
4-Fluorophenmetrazine (PAL-748) 1097796-73-0
3-fluorophenetrazine
3-chlorophenmetrazine (PAL-594) 1097796-78-5
3-Methoxyphenmetrazine
2-Methylphenmetrazine 1507705-48-7
3-methylphenmetrazine (PAL-773) 1350768-41-0
4-methylphenmetrazine (PAL-747) 1998216-41-3
4-methylphendimetrazine 1445576-23-7
3-Iodophenmetrazine
2-(4-Bromo-2,5-dimethoxyphenyl)morpholine (2C-B-morpholine)
3,4-Methylenedioxyphenmetrazine[6]
Naphthylmetrazine (PAL-704)
2-(thiophen-2-yl)-3-methylmorpholine
2-(3-(Trifluoromethyl)phenyl)morpholine (flumexadol)[7] 30914-89-7
Oxaflozane 26629-87-8
Phenmetrazol 1350768-19-2
N-Ethylphenmetrazol 97630-98-3
(+)-(2S,3S)-2-(3-chlorophenyl)-3,5,5-trimethylmorpholin-2-ol (radafaxine) 106083-71-0
(2S,3S,5R)-2-(3,5-difluorophenyl)-3,5-dimethylmorpholin-2-ol (manifaxine) 135306-39-7
PF-219,061[8] 710654-74-3
PF-592,379 710655-15-5
OSU-6162 156907-84-5
LPH-5[9] 2641630-97-7
2-Methyl-3-phenylpiperidine 70769-67-4
2-Phenyl-3-methyl-thiomorpholine
4-Methyl-5-phenyl-1,3-oxazolidine[10] 42794-92-3
Picilorex 62510-56-9
Butyltolylquinuclidine
3-benzylmorpholine (3-BZM)[11] 7684-27-7
3-Benzhydrylmorpholine (3-BZHM) 93406-27-0

Additional phenylmorpholines and their activities as monoamine releasing agents (MRAs) have been described.[12]

See also

References

  1. ^ Boswell GE (1997). "Synthesis, stereochemistry and anti-tetrabenazine activity of bicyclo analogues of 2-phenylmorpholines". Journal of Heterocyclic Chemistry. 34 (6): 1813–1820. doi:10.1002/jhet.5570340629.
  2. ^ US 20130203752, Blough BE, Rothman R, Landavazo A, Page KM, Decker AM, "Phenylmorpholines and analogues thereof", published 8 August 2013 
  3. ^ Mayer FP, Burchardt NV, Decker AM, Partilla JS, Li Y, McLaughlin G, et al. (May 2018). "Fluorinated phenmetrazine "legal highs" act as substrates for high-affinity monoamine transporters of the SLC6 family". Neuropharmacology. 134 (Pt A): 149–157. doi:10.1016/j.neuropharm.2017.10.006. PMC 7294773. PMID 28988906.
  4. ^ McLaughlin G, Baumann MH, Kavanagh PV, Morris N, Power JD, Dowling G, et al. (September 2018). "Synthesis, analytical characterization, and monoamine transporter activity of the new psychoactive substance 4-methylphenmetrazine (4-MPM), with differentiation from its ortho- and meta- positional isomers". Drug Testing and Analysis. 10 (9): 1404–1416. doi:10.1002/dta.2396. PMC 7316143. PMID 29673128.
  5. ^ Chem-Sink (chemicals that are Sn2 products & Friedel-Crafts alkylation reactants)
  6. ^ Swist M, Wilamowski J, Zuba D, Kochana J, Parczewski A (May 2005). "Determination of synthesis route of 1-(3,4-methylenedioxyphenyl)-2-propanone (MDP-2-P) based on impurity profiles of MDMA". Forensic Science International. 149 (2–3): 181–92. doi:10.1016/j.forsciint.2004.06.016. PMID 15749360.
  7. ^ Chemicalbook dot com: Flumexadol
  8. ^ Morpholine Dopamine Agonists For The Treatment Of Pain. Michael Andrew Ackley US 2009/0318451 AI Dec., 24th 2009. 1st Page.
  9. ^ Kristensen J, et al. 5-HT2A Agonists for Use in Treatment of Depression. Patent US 2021/0137908
  10. ^ Valter K, Arrizabalaga P (1998). Designer Drugs Directory. Elsevier. pp. 129, 135. ISBN 0-444-20525-X.
  11. ^ NIH PubChem Compound Summary for CID 3283983
  12. ^ "Phenylmorpholines and analogues thereof". Google Patents. 20 May 2011. Retrieved 7 December 2024. Table 3. Monoamine Release and 5HT2B Activity of a Series of Phenmetrazine Analogs Table 4. Comparison of the DA, 5-HT, and NE Releasing Activity of a Series of Phenmetrazine Analogs Table 5. Comparison of the DA, 5-HT, and NE Releasing Activity of a Series of (2S,5S)-5-methyl-2-phenylmorpolines
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