Pharmacology - Synthetic Super Cocaine

[Jasim]

MOD EDITED : links to commercial sites are not allowed

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I was doing some research about cocaine analogs and found this:


This is not really a reference and could be complete BS, but note the comment about a cocaine analog with 40x the potency, could this be cocaethylene?

Has anyone ever done any work on making cocaine more potent? I know a lot of work has went into making it less potent (psychoactive wise) for medicinal purposes.

I know cocaethylene is more potent, but I'm having trouble finding specifically how much more potent than cocaine it is.

Any help, sources, or comments would be much appreciated. Thanks.

EDIT:
Here's something comparing cocaine and cocaethylene, but interestingly this says that for several effects listed cocaine is the more potent one. However it does say this with regards to potentiation: "During cocaine-alcohol consumption, both cocaine and cocaethylene will cause increases in dopamine availability, resulting in greater dopamine than with either drug alone, causing greater euphoria."
and....
"Cocaine is also a potent activator of the neurotransmitter serotonin, which has an inhibiting effect on dopamine activity. Thus, cocaine stimulates dopamine activity (causing euphoria), but also stimulates serotonin activity (which partially inhibits dopamine activity, thus modifying the euphoric effect). In contrast, cocaethylene is about 40 times less potent than cocaine in stimulating serotonin, thus causing greater euphoria than cocaine."

http://www.allbusiness.com/health-ca.../458004-1.html

[90%.]

swims good guess this is what the pdf they send swiy when you order the "COCAINE BOOK" from that site




The basic formula for cocaine starts by purchasing or making tropinone, converting the tropinone into 2- carbomethoxytropinone (also known as methyl-tropan-3-one-2-carboxylate), reducing this to ecgonine, and changing that to cocaine. Sounds easy? It really is not very simple, but with Reagan's new drug policies, cracking down on all of the drug smuggling at the borders, this synthetic cocaine may be the source of the future. This synthesis is certainly worth performing with the high prices that cocaine is now commanding. As usual, I will start with the precursors and intermediates leading up to the product.
Succindialdehyde
This can be purchased, too. 23.2 g of succinaldoxime powder in 410 ml of 1 N sulfuric acid and add dropwise with stirring at 0°C a solution of 27.6 g of sodium nitrite in 250 ml of water over 3 hours. After the addition, stir and let the mixture rise to room temp for about 2 hours, taking care not to let outside air into the reaction. Stir in 5 g of Ba carbonate and filter. Extract the filtrate with ether and dry, evaporate in vacuo to get the succindialdehyde. This was taken from JOC, 22, 1390 (1957). To make succinaldoxime, see JOC, 21, 644 (1956).
Complete Synthesis of Succindialdehyde
JACS, 68, 1608 (1946)
In a 2 liter 3 necked flask equipped with a stirrer, reflux condenser, and an addition funnel, is mixed 1 liter of ethanol, 67 g of freshly distilled pyrrole, and 141 g of hydroxylamine hydrochloride. Heat to reflux until dissolved, add 106 g of anhydrous sodium carbonate in small portions as fast as reaction will allow. Reflux for 24 hours and filter the mixture. Evaporate the filtrate to dryness under vacuo. Take up the residue in the minimum amount of boiling water, decolorize with carbon, filter and allow to recrystallize in refrigerator. Filter to get product and concentrate to get additional crop. Yield of succinaldoxime powder is a little over 40 g, mp is 171-172°C.
5.8 g of the above powder is placed in a beaker of 250 ml capacity and 54 ml of 10% sulfuric acid is added. Cool to 0°C and add in small portions of 7 g of sodium nitrite (if you add the nitrite too fast, nitrogen dioxide fumes will evolve). After the dioxime is completely dissolved, allow the solution to warm to 20°C and effervescence to go to completion. Neutralize the yellow solution to litmus by adding small portions of barium carbonate. Filter off the barium sulfate that precipitates. The filtrate is 90% pure succindialdehyde and is not purified further for the reaction to create tropinone. Do this procedure 3 more times to get the proper amount for the next step, or multiply the amounts given by four and proceed as described above.
Take the total amount of succinaldehyde (obtained from 4 of the above syntheses combined) and without further treatment or purification (this had better be 15.5 g of succindialdehyde) put into an Erlenmeyer flask of 4-5 liters capacity. Add 21.6 g of methylamine hydrochloride, 46.7 g of acetonedicarboxylic acid, and enough water to make a total volume of 2 liters. Adjust the pH to 8-10 by slowly adding a saturated solution of disodium phosphate. The condensate of this reaction (allow to set for about 6 days) is extracted with ether, the ethereal solution is dried over sodium sulphate and distilled, the product coming over at 113°C at 25 mm of pressure is collected. Upon cooling, 14 g of tropinone crystallizes in the pure state. Tropinone can also be obtained by oxidation of tropine with potassium dichromate, but I could not find the specifics for this operation.
2-Carbomethoxytropinone
A mixture of 1.35 g of sodium methoxide (this is sodium in a minimum amount of methanol), 3.5 g of tropinone, 4 ml of dimethylcarbonate and 10 ml of toluene is refluxed for 30 min. Cool to 0°C and add 15 ml of water that contains 2.5 g of ammonium chloride. Extract the solution after shaking with four 50 ml portions of chloroform, dry, evaporate the chloroform in vacuo. Dissolve the oil residue in 100 ml of ether, wash twice with a mixture of 6 ml of saturated potassium carbonate and three ml of 3 N KOH. Dry and evaporate in vacuo to recover the unreacted tropinone. Take up the oil in a solution of aqueous ammonium chloride and extract with chloroform, dry, and evaporate in vacuo to get an oil. The oil is dissolved in hot acetone, cool, and scratch inside of flask with glass rod to precipitate 2-carbomethoxytropinone. Recrystallize 16 g of this product in 30 ml of hot methyl acetate and add 4 ml of cold water and 4 ml of acetone. Put in freezer for 2.5-3 hours. Filter and wash the precipitate with cold methyl acetate to get pure product.
Methylecgonine
0.4 mole of tropinone is suspended in 80 ml of ethanol in a Parr hydrogenation flask (or something that can take 100 psi and not react with the reaction, like stainless steel or glass). 10 g of Raney Nickle is added with good agitation (stirring or shaking) followed by 2-3 ml of 20% NaOH solution. Seal vessel, introduce 50 psi of hydrogen atmosphere (after flushing vessel with hydrogen) and heat to 40-50°C. After no more uptake of hydrogen (pressure gauge will hold steady after dropping to its lowest point) bleed off pressure and filter the nickle off, rinse out bottle with chloroform and use this rinse to rinse off the nickle while still on the filter paper. Make the filtrate basic with KOH after cooling to 10°C. Extract with chloroform dry, and evaporate the chloroform in vacuo to get an oil. Mix the oil plus any precipitate with an equal volume of dry ether and filter. Add more dry ether to the filtrate until no more precipitate forms, filter and add to the rest of the precipitate. Recrystallize from isopropanol to get pure methylecgonine. Test for activity. If active, skip down to the step for cocaine. If not active, proceed as follows. Stir with activated carbon for 30 min, filter, evaporate in vacuo, dissolve the brown liquid in methanol, and neutralize with 10% HCl acid in dry ether. Evaporate the ether until the two layers disappear, and allow to stand for 2 hours at 0°C to precipitate the title product. There are many ways to reduce 2-carbomethoxytropinone to methylecgonine. I chose to design a Raney Nickle reduction because it is cheap and not as suspicious as LAH and it is much easier than zinc or sodium amalgams.
Cocaine
4.15 g of methylecgonine and 5.7 g of benzoic anhydride in 150 ml of dry benzene are gently refluxed for 4 hours taking precaution against H2O in the air (drying tube). Cool in an ice bath, acidify carefully with hydrochloric acid, dry, and evaporate in a vacuum to get a red oil which is treated with a little portion of isopropanoi to precipitate cocaine.
As you can see, this is quite a chore. The coca leaves give ecgonine, which as you can see, is only a jump away from cocaine. If you can get egconine, then dissolve 8.5 g of it in 100 ml of ethanol and pass (bubble) dry HCl gas through this solution for 30 min. Let cool to room temp and let stand for another 1.5 hours. Gently reflux for 30 min and evaporate in vacuo. Basify the residue oil with NaOH and filter to get 8.4 g of methylecgonine, which is converted to cocaine as in the cocaine step above.
Below is given a somewhat easier method of producing tropinone by the general methods of Willstatter, who was instrumental in the first synthetic production of cocaine and several other alkaloids. After reviewing this method, I found it to be simpler than the above in many respects.
Tropinone
10 g of pyrrolidinediethyl diacetate are heated with 10 g of cymene and 2 g of sodium powder, the reaction taking place at about 160°C. During the reaction (which is complete in about 10 min) the temp should not exceed 172°C. The resulting reaction product is dissolved in water, then saturated with potassium carbonate, and the oil, which separates, is boiled with dilute sulfuric acid. 2.9 g of tropinone picrate forms and is filtered.
Here are two more formulas devised by Willstatter that produce tropinone from tropine. Take note of the yield differences.
Tropinone
To a solution of 25 g tropine, dissolved in 10 times its weight of 20% sulfuric acid are added 25 g of a 4% solution of potassium permanganate in 2 or 3 g portions over 45 min while keeping the temp at 10-12°C. The addition of permanganate will cause heat (keep the temp 10-12°C) and precipitation of manganese dioxide. The reaction mixture is complete in I hour. A large excess of NaOH is added and the reaction is steam distilled until I liter of distillate has been collected. The tropinone is isolated as the dibenzal compound by mixing the distillate with 40 g of benzaldehyde in 500 cc of alcohol and 40 g of 10% sodium hydroxide solution. Let stand several days to get dibenzaltropinone as yellow needles. Yield: 15.5 g, 28%. Recrystallize from ethanol to purify.
Tropinone
A solution of 12 g of chromic acid in the same amount of water (12 g) and 60 g of glacial acetic acid is added dropwise with stirring over a period of 4 hours to a solution of 25 g of tropine in 500 mL of glacial acetic acid that has been warmed to 60-70°C and is maintained at this temp during the addition. Heat the mixture for a short time on a steam bath until all the chromic acid has disappeared, cool and make strongly alkaline with NaOH. Extract with six 500 mL portions of ether and evaporate the ether in vacuo to get an oil that crystallizes readily. Purify by converting to the picrate or fractionally distill, collecting the fraction at 224-225°C at 714 mm vacuo.
The tropinones can be used in the above formula (or in a formula that you have found elsewhere) to be converted to cocaine. Remember to recrystallize the 2-carbomethoxytropinone before converting to methylecgonin

[Jasim]

I don't see anything there regarding a more potent form of cocaine though. Thanks btw.

[Boca Bitch]

Originally Posted by Jasim

"Cocaine is also a potent activator of the neurotransmitter serotonin, which has an inhibiting effect on dopamine activity. Thus, cocaine stimulates dopamine activity (causing euphoria), but also stimulates serotonin activity (which partially inhibits dopamine activity, thus modifying the euphoric effect). In contrast, cocaethylene is about 40 times less potent than cocaine in stimulating serotonin, thus causing greater euphoria than cocaine."

http://www.allbusiness.com/health-ca.../458004-1.html

I really don't think that's true...

To me it doesn't make sense as they're both excitatory neurotransmitters. Triggering the release of several neurotransmitters similar in effect, act complimentary to each other. This is why caffeine enhances the effects of amphetamines and cocaine.

For another, MDMA acts almost solely as a serotonin re-uptake inhibitor; however, it indirectly releases dopamine, because high amounts of serotonin in the brain, results in an elevated amount dopamine as well. The University of Utah's Genetics Department clearly states this in a presentation of drug effects, by showing how it works within the mouse on "Ecstasy." http://learn.genetics.utah.edu/conte...ugs/mouse.html

[Jasim]

Thanks Boca Bitch. I didn't think that sounded correct. I wish I could find some papers on cocethylene regarding pharmcokinetics. I will keep looking.

[Boca Bitch]

Originally Posted by Jasim

Thanks Boca Bitch. I didn't think that sounded correct. I wish I could find some papers on cocethylene regarding pharmcokinetics. I will keep looking.

Sure, no problem.

The problem is that there's not been enough research done, and most articles presented as "research" is really just bias bullshit published by the Fed., based on theory.

Good luck sorting through the mountains of crap!