Pazinaclone (DN-2327) is a sedative and anxiolytic drug in the cyclopyrrolone family of drugs. Some other cyclopyrrolone drugs include zopiclone and eszopiclone.
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| Formula | C25H23ClN4O4 |
| Molar mass | 478.93 g·mol−1 |
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Pazinaclone has a very similar pharmacological profile to the benzodiazepines including sedative and anxiolytic properties, but with less amnestic 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 a partial agonist at GABAA benzodiazepine receptors, although pazinaclone is more subtype-selective than most benzodiazepines.[3]
Synthesis
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Reaction of 2-amino-7-chloro-1,8-naphthyridine with phthalic anhydride leads to the corresponding phthalimide. Selective reduction of one of the imide carbonyl groups in essence converts that to an aldehyde. Condensation with tert-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
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edit- ^ 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 20581568.573-9&rft.date=1992-03&rft_id=https://api.semanticscholar.org/CorpusID:20581568#id-name=S2CID&rft_id=info:pmid/1350101&rft_id=info:doi/10.1016/0091-3057(92)90375-p&rft.aulast=Wada&rft.aufirst=T&rft.au=Fukuda, N&rfr_id=info:sid/en.wikipedia.org:Pazinaclone" class="Z3988">
- ^ 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 35222663.442-50&rft.date=1995-10&rft_id=https://api.semanticscholar.org/CorpusID:35222663#id-name=S2CID&rft_id=info:pmid/8619007&rft_id=info:doi/10.1007/BF02246492&rft.aulast=Suzuki&rft.aufirst=M&rft.au=Uchiumi, M&rft.au=Murasaki, M&rfr_id=info:sid/en.wikipedia.org:Pazinaclone" class="Z3988">
- ^ 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 22793644.601-18&rft.date=2005-05&rft_id=https://api.semanticscholar.org/CorpusID:22793644#id-name=S2CID&rft_id=info:pmid/15926867&rft_id=info:doi/10.1517/13543784.14.5.601&rft.aulast=Atack&rft.aufirst=JR&rfr_id=info:sid/en.wikipedia.org:Pazinaclone" class="Z3988">