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https://eu.docworkspace.com/d/sIEyBj6iWAunHybgG

There are way better and easier preparations for both the nitrostyrene and its reduction for which I kindly recommend Al/Hg or even better, Red-Al.

You mean like LSZ? or otherwise I already see the molecules I imagine you meant 2-benzyl substituted azetidines would be potentially active... I personally love aziridines but know they're not healthy. Thank's for the inspiration, is this hot now or? P.S. I wonder if by any chance in the method...

you will need a big-enough reactor with all it''s accessories first.

This one is easier extracted from plant source but it's extremely poisonous in pure form.

did it work? the stuff involved are a real danger or at least very unpleasant to interact with.

Well I made several that have superpotent radiolabeled ligand displacement behavior but this is in between my own self that didn't have enough so far (too much would be scary) and independently by the Prof. Nichols the one from the picture above and a handful of people inside a research...

I tend to give off this particular one for free every time, and show them how it's done.

It's synthesis starts with hydrolysis of melatonin and subjecting the resulting 5-MeO-tryptamine to reductive amination with formaldehyde and STAB.

you will have to read out loud PROPIONIC ACID CHLORIDE several times and then read about the chlorinating reagent...it's unwise to attempt this as a beginner.

It's all just straight forward but does need time and patience to grow crystals of.

It just can't work out for you this way if you're a beginner... unfortunately.

Yes, this could be interesting.

"solution phase synthesis of the cyclic heptapeptide melanotan II in 2.6% overall yield for 12 steps" https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2587946/

Hi this is absolutely not how you want to start practical chemistry since it's obvious to me that the procedures are super dangerous and the whole thing will be frustrating.

You need to distill and also dry the solvent with anhydrous MgSO4, Na2SO4 or CaCL2. Normally there is one simple and then a fractional distillation to perform for purity.

As most commercial sources of P2NP have a clean product it's nowadays pointless to synthesise it yourself but the whole journey of multistep syntheses can be a good quest to learn a lot from. One thing I wish you would do different from the plan you made, for the final reduction please don't try...

got one of those close at hand but if there is trouble drying it...

Place it in a sealed container alongside an open jar with hydroxide or concentrated sulfuric acid or some drying agent.

How many of each of the pills do you have and it will be an answerable question, as it is it's not bad to say the amount of active compound in each. Lets see first if there interest in extracting it and then see what comes out because some may be difficult to isolate.