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Pazinaclone

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Pazinaclone
Clinical data
ATC code
  • none
Identifiers
  • 2-(7-chloro-1,8-naphthyridin-2-yl)-3-[2-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-2-oxoethyl]-3H-isoindol-1-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC25H23ClN4O4
Molar mass478.93 g·mol−1
3D model (JSmol)
  • Clc1nc2nc(ccc2cc1)N4C(=O)c3ccccc3C4CC(=O)N6CCC5(OCCO5)CC6
  • InChI=1S/C25H23ClN4O4/c26-20-7-5-16-6-8-21(28-23(16)27-20)30-19(17-3-1-2-4-18(17)24(30)32)15-22(31)29-11-9-25(10-12-29)33-13-14-34-25/h1-8,19H,9-15H2 checkY
  • Key:DPGKFACWOCLTCA-UHFFFAOYSA-N checkY
  (verify)

Pazinaclone (DN-2327) is asedative andanxiolytic drug in thecyclopyrrolone family of drugs. Some other cyclopyrrolone drugs includezopiclone andeszopiclone.

Pazinaclone has a very similar pharmacological profile to thebenzodiazepines including sedative and anxiolytic properties, but with lessamnestic effects,[1] and at low doses it is a relatively selective anxiolytic, with sedative effects only appearing at higher doses.[2]

Pazinaclone produces its sedative and anxiolytic effects by acting as apartial agonist atGABAA benzodiazepine receptors, although pazinaclone is more subtype-selective than most benzodiazepines.[3]

Synthesis

[edit]
Pazinaclone synthesis:U.S. patent 4,778,801

Reaction of 2-amino-7-chloro-1,8-naphthyridine withphthalic anhydride leads to the corresponding phthalimide. Selective reduction of one of the imide carbonyl groups in essence converts that to an aldehyde. Condensation withtert-butyl(triphenylphosphoranylidene)acetate gives the Wittig product.

The carboxylic acid is then treated with diethyl cyanophosphonate to convert that to an activated acid cyanide; reaction with 1,4-dioxa-8-azaspiro[4.5]decane results in formation of the corresponding amide, pazinaclone.

See also

[edit]

References

[edit]
  1. ^Wada T, Fukuda N (March 1992). "Effect of a new anxiolytic, DN-2327, on learning and memory in rats".Pharmacology, Biochemistry, and Behavior.41 (3):573–9.doi:10.1016/0091-3057(92)90375-p.PMID 1350101.S2CID 20581568.
  2. ^Suzuki M, Uchiumi M, Murasaki M (October 1995). "A comparative study of the psychological effects of DN-2327, a partial benzodiazepine agonist, and alprazolam".Psychopharmacology.121 (4):442–50.doi:10.1007/BF02246492.PMID 8619007.S2CID 35222663.
  3. ^Atack JR (May 2005). "The benzodiazepine binding site of GABA(A) receptors as a target for the development of novel anxiolytics".Expert Opinion on Investigational Drugs.14 (5):601–18.doi:10.1517/13543784.14.5.601.PMID 15926867.S2CID 22793644.
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