Morforex

In today's world, Morforex has become a topic of utmost importance and relevance. Whether in the personal, professional, political or social sphere, Morforex has gained great relevance and has generated a wide debate among experts and society in general. The importance of Morforex lies in its direct impact on different aspects of daily life, as well as its influence on the development and evolution of different areas of knowledge and culture. This is why it is essential to analyze and understand in depth the importance and impact that Morforex has on our current reality, as well as to anticipate possible future scenarios that may arise as a result of its presence in various areas.

Morforex
Clinical data
ATC code
  • None
Identifiers
  • 4-ethyl]morpholine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC15H24N2O
Molar mass248.370 g·mol−1
3D model (JSmol)
  • CC(Cc1ccccc1)NCCN2CCOCC2
  • InChI=1S/C15H24N2O/c1-14(13-15-5-3-2-4-6-15)16-7-8-17-9-11-18-12-10-17/h2-6,14,16H,7-13H2,1H3
  • Key:ISEKMORYCCULAL-UHFFFAOYSA-N

Morforex (INN; Bo 637), also referable to as N-morpholinoethylamphetamine, is an anorectic which was never marketed.[1][2]

It produces amphetamine as an active metabolite.[3]

Synthesis

Patent:[4]

Amphetamine is reacted with N-Chloroethylmorpholine in the presence of IPA solvent.

See also

References

  1. ^ Ganellin CR, Triggle DJ (21 November 1996). Dictionary of Pharmacological Agents. CRC Press. pp. 1377–. ISBN 978-0-412-46630-4.
  2. ^ World Health Organization (2000). International Nonproprietary Names (INN) for Pharmaceutical Substances. World Health Organization. ISBN 978-0-11-986227-0.
  3. ^ Goodwin BL (10 November 2004). Handbook of Biotransformations of Aromatic Compounds. CRC Press. pp. 13–. ISBN 978-0-203-64196-5.
  4. ^ FR 2199M, "N-morpholino-1 n-phénylisopropylamino-2 éthane ", published 1963-12-09, assigned to Brevets Pharmaceutiques et Cosmetologiques