Difemetorex

Source: Wikipedia, the free encyclopedia.
Difemetorex
Clinical data
Routes of
administration		Oral
ATC code
  • none
Legal status
Legal status
  • Withdrawn
Identifiers
  • 2-[2-(diphenylmethyl)piperidin-1-yl]ethanol
JSmol)
  • OCCN1C(CCCC1)C(c2ccccc2)c3ccccc3

Difemetorex (

Ciba-Geigy in 1966 but is now no longer marketed.[6]

Synthesis

Alkylation of desoxypipradrol with ethylene oxide gives difemetorex.[7]

Synthesis of difemetorex

See also

References

  1. PMID 4949109
    .
  2. PMID 5089225
    .
  3. PMID 5072180
    .
  4. ISBN 0-7514-0499-3
    .
  5. ^ "The use of common stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances" (PDF). Retrieved 2010-03-23.[dead link]
  6. ISBN 2-8290-0039-0
    .
  7. ^ GB 861815, "New hydroxyalkyl-piperidines", issued 1961, assigned to CIBA Ltd 
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