Making a Stronger Methaqualone Analog (PPQ)
22,079
Published 2024-07-18
Intro largely written and idea by Quinazolineking (discord: tangramexcerpt)
YT:@Quinazolineking
All Comments (21)
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My man out here reviving ludes, so our generation can finally start accurately cosplaying wolf of wall street.
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NileRed is like the first boss you encounter in a game. Chemiolis is like the end-game boss.
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My MAN. A Methaqualone analogue? After PCMo, you're the guy.
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A request for next one is 5-minute craft antipsychotic medication that'll get me out of manic behavior into the real world somehow
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This workup really revived my faith in purification methods
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I can BARELY recall ludes . It was a long time ago . Yeah , that's it ...
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As someone who has chosen to do adv chem this year (6th year chemistry) i can proudly say i am starting to understand some terms used in this vid
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If the estimate of an active dose of this is 0.5mg, this synthesis at 13.5g is 27,000 doses! More importantly, it's not hard to absorb such small quantities through the skin or mucous membranes, so PPE would be absolutely essential in replicating this.
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i realy like how for the end you just speedrun the proces, stil explaing thu also i would like to see more crystalization processing from you❤
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And we never heard from him ever again.
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Can’t wait to see one of the many, many LSD analogues.
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Have you seen any literature on the reaction straight to the benzoxazinone with anthranilic acid, benzoyl chloride, and pyridine? I have tried this reaction but was not able to get a product with the correct melting point. Eliminates the need for DCM and triethylamine based on multiple papers I’ve seen, but I haven’t gotten it to work after a couple goes. Great work on this stuff man!
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Hey thats me
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Really enjoyed the video keep it up cant wait for the next one
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Yo my name is Quandale Dingle, and this is my cousin Quinaziline Methaqualone!
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Funny how none of the darknet markets seem to sell Methaqualone, but here a YouTuber is making analogues
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how about Arecoline from the Betel nut next?
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is the molecule excited to see me
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I’m excited to watch this, I saw the paper on this compound about a year ago and I’ve been curious
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8:19 - It wouldn't surprise me if the acetic anhydride acetylates the carboxylic acid first to form the mixed anhydride, which is then more susceptible to the intramolecular cyclisation. Acetic anhydride seems like an odd choice of solvent otherwise. I wonder if it's possible to use excess benzoyl chloride to acetylate the nitrogen, form the mixed anhydride and then cyclise all in one step...
