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Pharmaceutical compound
Diaza-2C-DFLY
Clinical data
Other names8-(Aminoethyl)-1,5-dihydropyrrolo[2,3-f]indole; Dipyrrolophenethylamine; Dipyrrolo-PEA
ATC code
  • None
Chemical and physical data
FormulaC12H13N3
Molar mass199.257 g·mol−1
3D model (JSmol)
  • N([H])([H])CCC1=C2C=CNC2=CC2=C1NC=C2
  • InChI=1S/C12H13N3/c13-4-1-10-9-3-6-14-11(9)7-8-2-5-15-12(8)10/h2-3,5-7,14-15H,1,4,13H2
  • Key:DVHVDLRBBZVUJL-UHFFFAOYSA-N

Diaza-2C-DFLY, also known as 8-(aminoethyl)-1,5-dihydropyrrolo[2,3-f]indole, is a chemical compound of the phenethylamine family related to the FLY group of psychedelic drugs.[1] It is a tricyclic benzodipyrrole or pyrroloindole derivative.[1] The compound is the analogue of 2C-DFLY in which the oxygen atoms within the dihydrofuran rings have been replaced with nitrogen atoms.[1] Diaza-2C-DFLY is a sort of hybrid chemical structure between the phenethylamine FLY compounds and tryptamines.[1] In addition, it may be considered a substituted partial ergoline.[1] Diaza-2C-DFLY does not yet appear to have been synthesized or studied.[1] It was first described in the scientific literature, as a theoretical compound of interest, by Daniel Trachsel in 2013.[1] Various related theoretical compounds were also discussed.[1]

See also

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References

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  1. 1 2 3 4 5 6 7 8 Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 502–503. ISBN 978-3-03788-700-4. OCLC 858805226. Archived from the original on 21 August 2025. Es gabe noch eine große Anzahl an potenziell interessanten Verbindungen, so z. B. die Substanzen 30a-30b. Die Substanzen des Typs 30a tragen eine Indolstruktur, was insofern interessant ist, als sie ein neues Verschmelzen zwischen Phenethylaminen und Tryptaminen darstellen. Die Substanzen des Typs 30b tragen in den zwei Pyridin-Strukturelementen zwar Heteroatome an den richtigen Stellen, haben aber, verglichen mit 30a komplett andere Säure-Base-Eigenschaften, da Pyridinderivate im Gegensatz zu Indolen basischer Natur sind.
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