Author Topic: 3-methylfentanyl  (Read 2273 times)

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Cyrax

  • Guest
3-methylfentanyl
« on: January 26, 2002, 08:33:00 AM »
What is the chemical structure of 3-methylfentanyl?  Can someone draw me a structure formule?

Thx

altair

  • Guest
Re: 3-methylfentanyl
« Reply #1 on: January 26, 2002, 10:38:00 AM »
EtCo   Ph
       \ /
        N
    Me  |  
     \/   \
      |   |
      \   /
        N
        |
        \
      |
        Ph

something like this perhaps?

btw
this was then what now

slappy

  • Guest
Re: 3-methylfentanyl
« Reply #2 on: January 26, 2002, 07:17:00 PM »
That is correct. It should also be noted that only (-)-cis-3-Methylfentanyl holds the extreme potency. Fentanyl is achiral, when you introduce that methyl group, you end up with 4 enantiomers.

Cyrax

  • Guest
Re: 3-methylfentanyl
« Reply #3 on: January 27, 2002, 04:20:00 AM »
Isn't it amazing that 3-methylfentanyl is 30 times more potent than fentanyl ?

What about an enamine alkylation a la Stork to make the
3-methyl-4-piperidone?

Does anyone has refs. about the synthesis of 4-piperidone?

slappy

  • Guest
Re: 3-methylfentanyl
« Reply #4 on: January 27, 2002, 08:10:00 AM »
Let me put it this way...

Attempted synthesis of 3-Methylfentanyl without a glovebox == Death