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Eterobarb

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Eterobarb
Clinical data
Routes of
administration
Oral
ATC code
  • none
Identifiers
  • 5-ethyl-1,3-bis(methoxymethyl)-5-phenyl-1,3-diazinane-2,4,6-trione
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H20N2O5
Molar mass320.345 g·mol−1
3D model (JSmol)
  • CCC1(C(=O)N(C(=O)N(C1=O)COC)COC)C2=CC=CC=C2
  • InChI=1S/C16H20N2O5/c1-4-16(12-8-6-5-7-9-12)13(19)17(10-22-2)15(21)18(11-23-3)14(16)20/h5-9H,4,10-11H2,1-3H3 ☒N
  • Key:DACOQFZGGLCXMA-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Eterobarb (Antilon) is abarbiturate derivative. It has mainlyanticonvulsant action with lesssedative effects than the closely related compoundphenobarbital. It saw reasonable success in clinical trials, but is not in widespread medical use.[1][2]

Synthesis

[edit]

Eterobarb can be synthesized by reactingphenobarbital withchloromethyl methyl ether in presence of a base.[3]

Eterobarb synthesis

References

[edit]
  1. ^Gallagher BB, Baumel IP, Woodbury SG, Dimicco JA (May 1975). "Clinical evaluation of eterobarb, a new anticonvulsant drug".Neurology.25 (5):399–404.doi:10.1212/wnl.25.5.399.PMID 1094318.S2CID 35510833.
  2. ^Smith DB, Goldstein SG, Roomet A (1986). "A comparison of the toxicity effects of the anticonvulsant eterobarb (antilon, DMMP) and phenobarbital in normal human volunteers".Epilepsia.27 (2):149–55.doi:10.1111/j.1528-1157.1986.tb03518.x.PMID 3956454.S2CID 20206800.
  3. ^Vida JA, Wilber WR, Reinhard JF (March 1971). "Anticonvulsants. 2. Acyloxymethyl and halomethyl derivatives of barbituric acid and diphenylhydantoin".Journal of Medicinal Chemistry.14 (3):187–9.doi:10.1021/jm00285a002.PMID 5552206.
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