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Cimoxatone

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Cimoxatone
Clinical data
ATC code
  • none
Identifiers
  • 3-[[4-[5-(methoxymethyl)-2-oxo-oxazolidin-3-yl]phenoxy]methyl]benzonitrile
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.070.537 Edit this at Wikidata
Chemical and physical data
FormulaC19H18N2O4
Molar mass338.363 g·mol−1
  • InChI=1S/C19H18N2O4/c1-23-13-18-11-21(19(22)25-18)16-5-7-17(8-6-16)24-12-15-4-2-3-14(9-15)10-20/h2-9,18H,11-13H2,1H3 checkY
  • Key:MVVJINIUPYKZHR-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Cimoxatone (MD 780515) is a reversible inhibitor of MAO-A (RIMA).[1] It has a significant food interaction–related adverse effect in combination with tyramine.[2] It was never marketed.

Synthesis

Synthesis:[3] Patent:[4]

The condensation of 4-benzyloxyaniline [6373-46-2] (1) with 1-chloro-3-methoxy-2-propanol [4151-97-7] (2) in ethanol alcohol gave (3); cyclization with diethylcarbonate in toluene in the presence of NaOMe gave 5-(methoxymethyl)-3-(4-phenylmethoxyphenyl)-1,3-oxazolidin-2-one, CID:19781994 (4). Debenzylation gives 3-(4-hydroxyphenyl)-5-(methoxymethyl)-1,3-oxazolidin-2-one [135605-66-2] (5). which is alkylated with 3-cyanobenzyl bromide [28188-41-2] (6) to give cimoxatone (7).

See also

References

  1. ^ Nair NP, Ahmed SK, Kin NM, West TE (1995). "Reversible and selective inhibitors of monoamine oxidase A in the treatment of depressed elderly patients". Acta Psychiatr Scand Suppl. 386: 28–35. doi:10.1111/j.1600-0447.1995.tb05921.x. PMID 7717092. S2CID 9100689.
  2. ^ Nair NP, Ahmed SK, Kin NM (November 1993). "Biochemistry and pharmacology of reversible inhibitors of MAO-A agents: focus on moclobemide". J Psychiatry Neurosci. 18 (5): 214–25. PMC 1188542. PMID 7905288.
  3. ^ Ancher, J.F.; Cimoxatone. Drugs Fut 1984, 9, 6, 412.
  4. ^ DE2923295 idem Guy R. Bourgery et al. U.S. patent 4,287,351 (1981 to Delalande S.A.). See for compound 200.