Author Topic: Naloxone aka Narcan ---> Oxymorphone ??  (Read 1751 times)

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nowaynohow

  • Guest
Naloxone aka Narcan ---> Oxymorphone ??
« on: August 26, 2003, 10:13:00 AM »
If Naloxone is made from Oxymorphone, can the process be easily reveresed?  Thank You.

"Naloxone hydrochloride in structure differs from oxymorphone in that the methyl group on the nitrogen atom is replaced by an allyl group."

http://opioids.com/oxymorphone/structure.html


http://opioids.com/naloxone/structure.html


slappy

  • Guest
I think that this is very easily be done.
« Reply #1 on: August 26, 2003, 10:46:00 PM »
This can very easily be done. I see this happening by quaternizing the amine with Methyl Iodide, then treatment of that salt with a Palladium0 species to deallylate. Careful handling will be required to achive high yields though.

In the methylation step, you would need to make the competition favor the alkylation of the amine. This is not that hard because the rate of alkylation is:

kR3N/kROH @ pH7 = ~500-1000

This means keeping the raction neutral, and using <=1eq. MeI. Otherwise, you would need to protect the alcohol and phenol as the acetate esters (Ac2O), and then saponify afterwards (K2CO3). The removal of the acetates might not be neccisary because that compound is probably just as active.

The quaternary salt from the previous reactiong will need to be dissolved in a solvent like DMF, and deallylated with a Palladium compound like Pd(PPh3)4 or Pd2(dba)3.

nowaynohow

  • Guest
Do you guys find this exciting or not?
« Reply #2 on: August 28, 2003, 07:25:00 AM »
Could someone else please agree or disagree with what he said.  How long would this take?

morpheus

  • Guest
Reversal
« Reply #3 on: September 08, 2003, 01:17:00 AM »
Are you sure its oxymorphone its made from and not
amomorphine which is like syrup of ipecac in that
it makes you puke your guts out.Amomorphine has no high
your too sick to feel it.Its used as a emetic.Swim is not always right though.