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Piberaline

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Piberaline
Clinical data
Trade namesTrelibet
ATC code
  • none
Identifiers
  • [4-(Phenylmethyl)piperazin-1-yl]-pyridin-2-ylmethanone
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC17H19N3O
Molar mass281.359 g·mol−1
3D model (JSmol)
  • C1CN(CCN1CC2=CC=CC=C2)C(=O)C3=CC=CC=N3
  • InChI=1S/C17H19N3O/c21-17(16-8-4-5-9-18-16)20-12-10-19(11-13-20)14-15-6-2-1-3-7-15/h1-9H,10-14H2
  • Key:TZFUBYYADABEAV-UHFFFAOYSA-N
  (verify)

Piberaline (EGYT-475;Trelibet) is apsychoactive drug and member of thepiperazinechemical class which wasdeveloped in the 1980s. It hasstimulant andantidepressant effects which are thought to be due largely to its active metabolitebenzylpiperazine.[1] It was studied to a limited extent in Hungary and Spain, but was not widely accepted and does not seem to be in current use, although a closely related drugbefuraline with similar effects has been slightly more successful.

Synthesis

[edit]

Piberaline can be prepared by reaction ofpicolinic acid with benzylpiperazine.[2][3][4]

Synthesis of piberaline

Alternatively, it can be synthesized from2-chloropyridine, carbon monoxide, and benzylpiperazine.

See also

[edit]

References

[edit]
  1. ^Tekes K, Tóthfalusi L, Malomvölgyi B, Hermán F, Magyar K (1987). "Studies on the biochemical mode of action of EGYT-475, a new antidepressant".Polish Journal of Pharmacology and Pharmacy.39 (2):203–211.PMID 2448760.
  2. ^DE 2215545, Korösi J, Erdelyi L, Balla I, Lay A, Szabo G, Kiszelly E, "Pyridinderivate und ihre Salze sowie ihre Verwendung und Verfahren zur Herstellung derselben [Pyridine derivatives and their salts and their use and processes for the preparation thereof]", issued 11 March 1976, assigned to Egyt Gyogyszervegyeszeti Gyar, Budapest. 
  3. ^Kumar K, Michalik D, Garcia Castro I, Tillack A, Zapf A, Arlt M, et al. (February 2004). "Biologically Active Compounds through Catalysis: Efficient Synthesis ofN -(Heteroarylcarbonyl)-N ′-(arylalkyl)piperazines".Chemistry: A European Journal.10 (3):746–757.doi:10.1002/chem.200305327.PMID 14767940.
  4. ^Younes S, Labssita Y, Baziard-Mouysset G, Payard M, Rettori M, Renard P, et al. (January 2000). "Synthesis and structure-activity relationships of novel arylalkyl 4-benzyl piperazine derivatives as sigma site selective ligands".European Journal of Medicinal Chemistry.35 (1):107–121.doi:10.1016/S0223-5234(00)00113-6.PMID 10733608.
Adamantanes
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Phenylpiperazines
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