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Homarylamine

From Wikipedia, the free encyclopedia
(Redirected fromMethylenedioxymethylphenethylamine)
Chemical compound
Pharmaceutical compound
Homarylamine
Clinical data
Other names1,3-benzodioxolyl-N-methyl-5-ethanamine;
3,4-methylenedioxy-N-methyl-2-phenylethylamine;
Norlobivine
Routes of
administration
Various
Legal status
Legal status
  • US-SCHEDULE I DRUG as Positional isomer of MDA
Identifiers
  • 2-(1,3-Benzodioxol-5-yl)-N-methylethanamine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC10H13NO2
Molar mass179.219 g·mol−1
3D model (JSmol)
  • CNCCC1=CC2=C(C=C1)OCO2
  • InChI=1S/C10H13NO2/c1-11-5-4-8-2-3-9-10(6-8)13-7-12-9/h2-3,6,11H,4-5,7H2,1H3
  • Key:OPJOMVMFYOUDPK-UHFFFAOYSA-N
  (verify)

Homarylamine (INN;[1] also known as3,4-methylenedioxy-N-methylphenethylamine andMDMPEA) is anantitussive (anti-cough) drug[2] which was patented in 1956 byMerck & Co.,[3] but has never been used medically as such.

Chemically it is asubstituted phenethylamine. It is theN-methylatedanalog ofmethylenedioxyphenethylamine (MDPEA). It is a schedule I drug in the USA as a positional isomer of MDA.

Reactions

[edit]

Reaction of homoarylamine withformaldehyde giveshydrastinine.

A practical application of homarylamine is in the synthesis ofRoemerin [de].[4]

See also

[edit]

References

[edit]
  1. ^"International Non-Proprietary Names for Pharmaceutical Preparations"(PDF).Chronicle of the World Health Organization.12 (3). 1958.
  2. ^Stefko PL, Denzel J, Hickey I (March 1961). "Experimental Investigation of Nine Antitussive Drugs".Journal of Pharmaceutical Sciences.50 (3):216–221.Bibcode:1961JPhmS..50..216S.doi:10.1002/jps.2600500309.
  3. ^U.S. patent 2,820,739
  4. ^Marion, L., Grassie, V. (August 1944). "The Synthesis of l-Roemerine 1".Journal of the American Chemical Society.66 (8):1290–1292.Bibcode:1944JAChS..66.1290M.doi:10.1021/ja01236a024.


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