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Befuraline

From Wikipedia, the free encyclopedia
Psychoactive drug of the piperazine chemical class

Pharmaceutical compound
Befuraline
Clinical data
ATC code
  • none
Identifiers
  • 1-benzofuran-2-yl(4-benzylpiperazin-1-yl)methanone
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC20H20N2O2
Molar mass320.392 g·mol−1
3D model (JSmol)
  • O=C(N1CCN(CC1)CC2=CC=CC=C2)C3=CC4=C(C=CC=C4)O3
  • InChI=1S/C20H20N2O2/c23-20(19-14-17-8-4-5-9-18(17)24-19)22-12-10-21(11-13-22)15-16-6-2-1-3-7-16/h1-9,14H,10-13,15H2 checkY
  • Key:SRIJFPBZWUFLFD-UHFFFAOYSA-N checkY
  (verify)

Befuraline (DIV-154) is apsychoactive drug and member of thepiperazinechemical class which wasdeveloped inGermany in the 1970s.[1] Befuraline hasstimulant andantidepressant effects and has seen some use in Germany andFrance, although it has never become widely used.[2] Befuraline's activemetabolitebenzylpiperazine is likely to contribute to its effects.

Synthesis

[edit]
Synthesis:[1] Patent:[3]

A one-step coupling between coumarilic acid (benzofuran-2-carboxylic acid) [496-41-3] (1) andbenzylpiperazine (BzP) (2) gives an amide, and henceBefuraline (3).

See also

[edit]

References

[edit]
  1. ^abBoksay IJ, Popendiker K, Weber RO, Söder A (1979). "Synthesis and pharmacological activity of befuraline (N-benzo[b]furan-2-ylcarbonyl-N'-benzylpiperazine), a new antidepressant compound".Arzneimittel-Forschung.29 (2):193–204.PMID 582130.
  2. ^Gastpar M, Gastpar G, Gilsdorf U (November 1985). "Befuraline, its safety and efficacy in depressed inpatients".Pharmacopsychiatry.18 (6):351–5.doi:10.1055/s-2007-1017396.PMID 4089015.S2CID 9322026.
  3. ^DE2157424 idem Rolf-Ortwin Weber, Alfons Soder, Istvan Boksay,U.S. patent 4,374,990 (1980 to Hoechst Aktiengesellschaft).
SSRIsTooltip Selective serotonin reuptake inhibitors
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Others/uncategorized


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