Chemistry:Ciramadol

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Short description: Opioid analgesic drug
Ciramadol
Ciramadol.svg
Clinical data
Other namesCiramadol, WY-15705
Routes of
administration		Oral
ATC code
  • none
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC15H23NO2
Molar mass249.354 g·mol−1
3D model (JSmol)
  (verify)

Ciramadol (WY-15,705) is an opioid analgesic that was developed in the late 1970s[1] and is related to phencyclidine, tramadol, tapentadol and venlafaxine.[2] It is a mixed agonist-antagonist for the μ-opioid receptor with relatively low abuse potential[3] and a ceiling on respiratory depression[4] which makes it a relatively safe drug. It has a slightly higher potency and effectiveness as an analgesic than codeine,[5] but is weaker than morphine.[6] Other side effects include sedation and nausea but these are generally less severe than with other similar drugs.[7]

Synthesis

Ciramadol synthesis:[8][9] Patents:[10][11][12]

The Claisen-Schmidt condensation between 3-(methoxymethoxy)benzaldehyde [13709-05-2] (1) and cyclohexanone (2) afforded CID:54364197 (3). Michael addition of dimethylamine leads the aminoketone, i.e. 2-[dimethylamino-[3-(methoxymethoxy)phenyl]methyl]cyclohexan-1-one, CID21518320. Reduction of the ketone proceeds stereospecifically to afford the cis aminoalcohol [51356-58-2] (4). Mild hydrolysis of the product gives the free phenol ciramadol (5).

See also


References

  1. ↑ "Benzylamine Analgesics" US patent 3928626
  2. ↑ "Ciramadol. A new analgesic". The Medical Journal of Australia 2 (9): 501–2. November 1979. doi:10.5694/j.1326-5377.1979.tb125803.x. PMID 522808. 
  3. ↑ "Comparative evaluation of morphine, pentazocine and ciramadol in postaddicts". The Journal of Pharmacology and Experimental Therapeutics 240 (3): 900–10. March 1987. PMID 3559982. 
  4. ↑ "Low ceiling respiratory depression by ciramadol". International Journal of Clinical Pharmacology Research 6 (6): 451–5. 1986. PMID 3100462. 
  5. ↑ "Ciramadol--a new synthetic analgesic. A double-blind comparison with oral codeine for postoperative pain relief". South African Medical Journal = Suid-Afrikaanse Tydskrif vir Geneeskunde 64 (25): 978–82. December 1983. PMID 6359486. 
  6. ↑ "A double-blind comparison of multiple intramuscular doses of ciramadol, morphine, and placebo for the treatment of postoperative pain.". Anesthesia and Analgesia 64 (11): 1101–7. November 1985. doi:10.1213/00000539-198511000-00012. PMID 3901821. https://dx.doi.org/10.1213%2F00000539-198511000-00012. 
  7. ↑ "Comparison of the analgesic efficacy and safety oral ciramadol, codeine, and placebo in patients with chronic cancer pain". Journal of Clinical Pharmacology 27 (2): 162–6. February 1987. doi:10.1002/j.1552-4604.1987.tb02178.x. PMID 3680568. 
  8. ↑ Yardley, J. P.; Fletcher, H.; Russell, P. B. (1978). "A potent benzylamine analgesic:(−)cis-2(α-dimethylamino-m-hydroxybenzyl)cyclohexanol". Experientia 34(9): 1124–1125. doi:10.1007/BF01922905.
  9. ↑ Paton, D.M.; Castaner, J.; Ciramadol. Drugs Fut 1980, 5, 6, 283.
  10. ↑ Peter B Russell, John P Yardley, U.S. Patent 3,928,626, U.S. Patent 4,017,637 (1975 and 1977 to American Home Products Corporation).
  11. ↑ John Patrick Yardley, Peter Byrom Russell, DE patent 2317183 (1986 to American Home Prod).
  12. ↑ John P. Yardley & Peter B. Russell, U.S. Patent 4,155,935 (1979 to Wyeth LLC).




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