could this shit exist? 4-AcO-DAT

[danceofdays]

we have 5-MeO-DALT with allyl groups on the N... could replacing the methyl groups on 4-AcO-DMT with acetyl groups be possible, and if so, what could the effect potentially be? higher potency or a rush from different metabolization? or just a different trip in the same way 4-AcO-DMT and 4-PO-DMT are different.

 

[fastandbulbous]

Yes it's possible. So far there's people with it but I've heard nmothing about it from them


Sorry was talking about 4-acetoxydiallyltryptamine

 

[hugo24]

Umm, you put Chloroacetone on that 4-HO (first) and second, while its chemically possible to put two acetyls on the nitrogen, the formed (at least the aliphatic) imides are usually very unstable towards hydrolytic conditions. Plus, the nitrogen is no more basic which is a prerequisite to bind to 5-HT receptors.

 

[fastandbulbous]

^ Why ALD-52 is so unstable and degrades to LSD very quickly

 

[dread]

Short answer, no.

 

[nuke]

Also you've drawn an ether with a carbonyl group instead of the acetyl ester there.

 

[hugo24]

Altough ALD-52 is not an imide in the strict sense...

 

[Phener]

would the acetyl groups just not get removed straight away in the GI, leading to some generally unpleasant GI type compound?

 

[Aloysius]

would the acetyl groups just not get removed straight away in the GI, leading to some generally unpleasant GI type compound?

I second that, my guess would be very rapid generation of acetic acid and the primary amine, leading to something that is likely inactive. Depending on how you define unpleasant, this might be unpleasant, I don't think it will kill you however...