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2,3-Dichlorophenylpiperazine

2,3-Dichlorophenylpiperazine (2,3-DCPP or DCPP) is a chemical compound from the phenylpiperazine family. It is both a precursor in the synthesis of aripiprazole and one of its metabolites. It is unclear whether 2,3-DCPP is pharmacologically active as a serotonin receptor agonist similar to its close analogue 3-chlorophenylpiperazine (mCPP), though it has been shown to act as a partial agonist of the dopamine D<sub>2</sub> and D<sub>3</sub> receptors.

Legality

2,3-DCPP has been made illegal in Japan and Hungary after having been identified in seized designer drug samples.

List of derivatives

  1. Aripiprazole
  2. Cariprazine
  3. BAK 2-66
  4. Brilaroxazine (formally RP5063)
  5. FAUC-365 [474432-66-1]
  6. CJB-090 2xHCl [595584-40-0]
  7. NGB 2849 [189061-11-8]
  8. NGB 2904 Fb: [189061-11-8] HCl: [189060-98-8]
  9. PG-01037 2xHCl: [675599-62-9]
  10. PG648
  11. Aripiptranyl (Abilifarnate)
  12. PGX-2000001
  13. So-called R-22
  14. So-called JJC 7−065
  15. R-PG-648

Positional Isomer

The positional isomer 3,4-dichlorophenylpiperazine (3,4-DCPP) is also known, and acts as both a serotonin releaser via the serotonin transporter, and a β<sub>1</sub>-adrenergic receptor blocker, though with relatively low affinity at both targets.

Triple Substituted

The 3,4,5-Trichlorophenylpiperazine [67305-64-0] ("3 stripes") is also a highly regarded arrangement & has been awarded the Beecham patent of . Such 3,4,5-Trisubstituted aromatic entities is already known from clenbuterol. Leading to CID:151687078 (Ex 6 is a concrete example of this) i.e. 1-(4-Amino-3,5-dichlorophenyl)-4-(4-phthalimido-1- butyl)piperazine.

See also

References

External links