Chemistry:Manifaxine

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Short description: Chemical compound
Manifaxine
Manifaxine.svg
Clinical data
Other namesGW-320,659
Routes of
administration
Oral
ATC code
  • none
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC12H15F2NO2
Molar mass243.254 g·mol−1
3D model (JSmol)
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Manifaxine (developmental code name GW-320,659) is a norepinephrine–dopamine reuptake inhibitor developed by GlaxoSmithKline through structural modification of radafaxine, an isomer of hydroxybupropion and one of the active metabolites of bupropion.[1] Manifaxine was researched for treatment of attention deficit hyperactivity disorder (ADHD) and obesity and was found to be safe, reasonably effective, and well-tolerated for both applications.[2][3] However, no results were reported following these initial trials and development was discontinued.[1]

Synthesis

Synthesis:[4] Patent:[5] See also:[6][7]

The Grignard reaction between 3,5-difluorobenzonitrile [64248-63-1] (1) and ethylmagnesium bromide gives 3,5-difluoropropiophenone [135306-45-5] (2). Halogenation with molecular bromine occurs at the alpha-keto position providing 2-bromo-3',5'-difluoropropiophenone [135306-46-6] (3). Intermolecular ring formation with DL-Alaninol (2-Aminopropanol) [6168-72-5] completed the synthesis of Manifaxine (4).

See also

References

  1. 1.0 1.1 "Manifaxine - AdisInsight". https://adisinsight.springer.com/drugs/800006906. 
  2. "GW320659 for the treatment of attention-deficit/hyperactivity disorder in children". Journal of the American Academy of Child and Adolescent Psychiatry 41 (8): 914–20. August 2002. doi:10.1097/00004583-200208000-00009. PMID 12162627. 
  3. "Pharmacogenetics and obesity: common gene variants influence weight loss response of the norepinephrine/dopamine transporter inhibitor GW320659 in obese subjects". Pharmacogenetics and Genomics 15 (12): 883–9. December 2005. doi:10.1097/01213011-200512000-00006. PMID 16272960. 
  4. "(2 S ,3 S ,5 R )-2-(3,5-Difluorophenyl)-3,5- dimethyl-2-morpholinol: A Novel Antidepressant Agent and Selective Inhibitor of Norepinephrine Uptake". Journal of Medicinal Chemistry 39 (2): 347–349. 1 January 1996. doi:10.1021/jm950630p. PMID 8558500. 
  5. James Leroy Kelley, et al. EP0426416 (1991 to Wellcome Foundation Ltd).
  6. Frank Ivy Carroll, et al. US9562001 (2012 to Research Triangle Institute).
  7. Frank Ivy Carroll, et al. US20180215701 (Research Triangle Institute).