Demethylation of 14-hydroxy substituted alkaloid derivatives
The present invention is directed to a method for demethylating 14-hydroxy substituted alkaloid derivatives, in particular of 14-hydroxy-17-methyl-4,5-epoxymorphinane-6-on-derivatives. This is achieved by reacting a starting compound with a compound of general formula R 1 OOC—N═N—COOR 2 in a suitable solvent.
1. A method of producing a compound of formula (I)
or a salt thereof, comprising:
reacting a compound of formula (II)
with an azodicarboxylic acid dialkyl ester of general formula R 1 OOC—N═N—COOR 2 in a suitable solvent, and at least one antioxidant, wherein
X is selected from H, alkyl, silyl or acetyl; and
R 1 and R 2 are independently selected from a linear or branched substituted or unsubstituted alkyl, and
wherein the bond between atoms 7 and 8 is single or a double bond.
2. The method according to claim 1 , wherein the solvent is an aprotic dipolar solvent.
3. The method according to claim 1 , wherein the reaction is performed at a temperature in the range of from 20° C. to 100° C.
4. The method of claim 3 , wherein the temperature is maintained for at least one hour.
5. The method of claim 1 , wherein after reacting the compound of formula (II) with an azodicarboxylic acid dialkyl ester, the reaction solution is supplemented with 5,5-dimethylcyclohexane-1,3-dione (dimedone) and methanol or hydrazines and methanol.
6. The method of claim 5 , wherein the reaction solution is maintained at a temperature in the range of from 20° C. to 100° C. over a time of 1-10 hours after adding dimedone and methanol.
7. The method according to claim 5 , wherein following reacting the compound of formula (II) and optionally reacting with dimedone/hydrazines and methanol, an acid is added to the reaction solution.
8. The method of claim 7 , wherein the acid is a hydrochloric acid.
9. The method according to claim 8 , wherein the hydrochloric acid has a concentration of about 5% V/V.
10. The method according to claim 1 , wherein the antioxidant is selected from the group consisting of ascorbic acid and its derivatives, citric acid, tartric acid, polyhydroxy butyric acid (PHB) esters, butylated hydroxyanisol (BHA) and butylated hydroxytoluene (BHT).
11. The method according to claim 1 , wherein R 1 and/or R 2 are independently selected from a linear or branched, substituted or unsubstituted, C 1 -C 6 alkyl.
12. The method according to claim 11 , wherein R 1 and/or R 2 are independently selected from methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, pentyl, and hexyl.
13. The method according to claim 12 , wherein R 1 and/or R 2 are independently selected from isopropyl and ethyl.
14. The method according to claim 13 , wherein R 1 and/or R 2 are identical.
15. The method according to claim 2 , wherein the aprotic dipolar solvent is selected from the group consisting of methanol, ethanol, acetone, toluene, dimethylformamide, N,N-dimethylacetamide, acetonitrile, acetic acid ethylester and methyl-tert-butylether.
16. The method of claim 15 , wherein the solvent is dimethylformamide.
17. The method according to claim 3 , wherein the reaction is performed at a temperature in the range of from 30-90° C.
18. The method according to claim 3 , wherein the reaction is performed at a temperature in the range of from 40-80° C.
19. The method according to claim 3 , wherein the reaction is performed at a temperature in the range of from 50-70° C.
20. The method of claim 4 , wherein the temperature is maintained for at least two hours.
21. The method of claim 4 , wherein the temperature is maintained for at least three hours.
22. The method of claim 4 , wherein the temperature is maintained for at least four hours.
23. The method of claim 6 , wherein the reaction solution is maintained at a temperature in the range of from 20° C. to 100° C. for a period of time of from 2 to 5 hours after adding dimedone and methanol.
24. The method of claim 5 , wherein the reaction solution is maintained at a temperature in the range of from 30 to 80° C. for a period of time of from 1 to 10 hours after adding dimedone and methanol.
25. The method of claim 24 , wherein the reaction solution is maintained at a temperature in the range of from 30 to 80° C. for a period of time of from 2 to 5 hours after adding dimedone and methanol.
26. The method of claim 5 , wherein the reaction solution is maintained at a temperature in the range of from 40 to 70° C. for a period of time of from 1 to 10 hours after adding dimedone and methanol.
27. The method of claim 26 , wherein the reaction solution is maintained at a temperature in the range of from 40 to 70° C. for a period of time of from 2 to 5 hours after adding dimedone and methanol.
28. The method according to claim 10 , wherein the antioxidant is 2,6-di-tert-butyl-4-methylphenol.