Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
 Pages:  1  2
Author: Subject: Warfarin syntheses
DocX
Hazard to Others
***




Posts: 179
Registered: 22-10-2015
Member Is Offline

Mood: No Mood

[*] posted on 26-4-2023 at 11:47


Quote: Originally posted by Mateo_swe  

I have seen what Warfarin does to rats, it doesnt seem nice at all, there must be better ways.


Really? Pray tell, how and when did you see this?
A warfarin overdose should most likely result in gastrointestinal bleeding. The gut of mammals has a HUGE, extremely vasculated surface area, and bleeding disorders generally start there. To sieve blood into the gut is a pretty painless thing, you get tired, drowsy, shot of breath and faint.

Or it's a haemorrhage stroke. That can be painful, but not for long. Not like drowning.
Bleeding is sort of painless. So I really wonder what you saw?

And regarding the chemistry I have actually reached a dead end when it comes to the reagents. My hope was there would be a route with affordable and accessible precursors, but I still haven't found one.

[Edited on 20232323/4/26 by DocX]
View user's profile View All Posts By User
Fery
National Hazard
****




Posts: 990
Registered: 27-8-2019
Location: Czechoslovakia
Member Is Offline


[*] posted on 28-5-2023 at 12:47


Reviving the thread. Did anyone succeed in 4-hydroxycoumarin synthesis?
Here I found a German page with coumarin synthesis:
http://forum.lambdasyn.org/index.php/topic,1471.0.html
I synthesized the second reactant (benzylideneacetone) here:
https://www.sciencemadness.org/whisper/viewthread.php?tid=15...
View user's profile Visit user's homepage View All Posts By User
Fery
National Hazard
****




Posts: 990
Registered: 27-8-2019
Location: Czechoslovakia
Member Is Offline


[*] posted on 10-10-2023 at 06:27


This seems to be a suitable home lab way for warfarin. But only racemic product. For obtaining stereoisomers it would be necessary to have (R,R)- or (S,S)-1,2-diphenylethylenediamine:
https://pubs.acs.org/doi/10.1021/ed800040m

Benzalacetone synthesis is here:
https://www.sciencemadness.org/whisper/viewthread.php?tid=15...

The 4-hydroxycoumarin may be obtained from phenol and meldrum acid:

Quote:
Treatment of phenol with meldrum acid under solvent-free condition at 90°C afforded 3-oxo-3-phenoxypropanoic acid in 92% isolated yield, that transformed to 4-hydroxycoumarin in 75 % and 48% isolated yield, upon treatment with Eaton’s reagent or polyphosphoric acid (PPA)


Attachment: j.arabjc.2015.06.012.pdf (1.6MB)
This file has been downloaded 104 times

The meldrum acid may be obtained by reacting malonic acid + acetone + acetic anhydride + cat. H2SO4

Attachment: CT9089300598.pdf (244kB)
This file has been downloaded 101 times
View user's profile Visit user's homepage View All Posts By User
 Pages:  1  2

  Go To Top