Method of reducing α, β unsaturated ketones in opioid compositions
The present invention is directed to a process for reducing the level of α, β-unsaturated ketone in an opioid analgesic composition by hydrogenation the opioid analgesic composition with diimide or a diimide progenitor.
1. A process for reducing a level of α, β-unsaturated ketone in an opioid analgesic composition comprising
hydrogenating a starting opioid analgesic composition having an α, β-unsaturated ketone impurity with diimide, a diimide progenitor, or a combination thereof in a suitable solvent, to produce a resultant opioid analgesic composition having a level of α, β-unsaturated ketone less than the starting composition,
wherein the opioid analgesic is selected from the group consisting of oxycodone, hydrocodone, hydromorphone, pharmaceutically acceptable salts thereof and mixtures thereof.
2. The process of claim 1 , wherein the diimide progenitor is dipotassium azodicarboxylate.
3. The process of claim 1 , wherein said hydrogenation is performed under reflux.
4. The process of claim 1 , wherein the solvent is an alcohol, selected from the group consisting of methanol, ethanol and isopropanol.
5. The process of claim 1 , further comprising recovering the hydrogenated opioid analgesic composition.
6. The process of claim 1 , wherein the opioid analgesic is oxycodone or a pharmaceutically acceptable salt thereof.
7. The process of claim 1 , wherein the opioid analgesic is hydrocodone or a pharmaceutically acceptable salt thereof.
8. The process of claim 1 , wherein the opioid analgesic is hydromorphone or a pharmaceutically acceptable salt thereof.
9. The process of claim 1 , wherein the hydrogenation produces an opioid analgesic composition having an α, β-unsaturated ketone level of less than 25 ppm, less than about 15 ppm, less than about 10 ppm, or less than about 5 ppm.
10. The process of claim 1 , wherein the α, β-unsaturated ketone is a compound of formula (II):
wherein:
R is selected from the group consisting of hydrogen; C 1-8 alkyl; C 3-6 cycloalkyl; (C 3-6 )cycloalkyl(C 1-3 )alkyl; phenyl(C 1-3 )alkyl; and phenyl(C 1-3 )alkyl substituted with 1-3 members of the group consisting of C 1-8 alkyl, trifluoromethyl, nitro, dialkylamino and cyano;
R 1 is selected from the group consisting of hydrogen; C 1-8 alkyl; C 3-6 cycloalkyl; C 1-8 alkoxy; C 3-6 cycloalkoxy; 2-(4-morpholinyl)ethyl; benzyloxycarbonyl; (R 8 ) 3 C(O)—; phenyl(C 1-3 )alkyl; and phenyl(C 1-3 )alkyl substituted with 1-3 members of the group consisting of C 1-8 alkyl, trifluoromethyl, nitro, dialkylamino and cyano;
R 3 is hydrogen, hydroxyl or alkoxy;
each R 8 is independently hydrogen, a C 1-4 alkyl, a C 3-6 cycloalkyl, phenyl or benzyl
or a pharmaceutically acceptable salt thereof.
11. A process for producing an opioid analgesic composition comprising
hydrogenating an α, β-unsaturated ketone composition, with diimide, a diimide progenitor or a combination thereof in a suitable solvent, to form the opioid analgesic composition,
wherein the opioid analgesic is selected from the group consisting of oxycodone, hydrocodone, hydromorphone, pharmaceutically acceptable salts thereof and mixtures thereof.
12. The process of claim 11 , wherein the diimide progenitor is dipotassium azodicarboxylate.
13. The process of claim 11 , wherein said hydrogenation is performed under reflux.
14. The process of claim 11 , wherein the solvent is an alcohol selected from the group consisting of methanol, ethanol and isopropanol.
15. The process of claim 11 , further comprising recovering the hydrogenated opioid analgesic composition.
16. The process of claim 11 , wherein the α, β-unsaturated ketone is a compound of formula (II):
wherein:
R is selected from the group consisting of hydrogen; C 1-8 alkyl; C 3-6 cycloalkyl; (C 3-6 )cycloalkyl(C 1-3 )alkyl; phenyl(C 1-3 )alkyl; and phenyl(C 1-3 )alkyl substituted with 1-3 members of the group consisting of C 1-8 alkyl, trifluoromethyl, nitro, dialkylamino and cyano;
R 1 is selected from the group consisting of hydrogen; C 1-8 alkyl; C 3-6 cycloalkyl; C 1-8 alkoxy; C 3-6 cycloalkoxy; 2-(4-morpholinyl)ethyl; benzyloxycarbonyl; (R 8 ) 3 C(O)—; phenyl(C 1-3 )alkyl; and phenyl(C 1-3 )alkyl substituted with 1-3 members of the group consisting of C 1-8 alkyl, trifluoromethyl, nitro, dialkylamino and cyano;
R 3 is hydrogen, hydroxyl or alkoxy;
each R 8 is independently hydrogen, a C 1-4 alkyl, a C 3-6 cycloalkyl, phenyl or benzyl
or a pharmaceutically acceptable salt thereof.
17. The process of claim 16 , wherein the opioid analgesic is hydromorphone or a pharmaceutically acceptable salt thereof.
18. The process of claim 16 , wherein the opioid analgesic is hydrocodone or a pharmaceutically acceptable salt thereof.
19. The process of claim 11 , wherein the opioid analgesic is oxycodone or a pharmaceutically acceptable salt thereof.
20. The process of claim 11 , wherein the hydrogenation produces an opioid analgesic composition having an α, β-unsaturated ketone level of less than 25 ppm, less than about 15 ppm, less than about 10 ppm, or less than about 5 ppm.
21. The process of claim 5 , wherein the recovery step comprises crystallizing the hydrogenated opioid analgesic composition.
22. The process of claim 15 , wherein the recovery step comprises crystallizing the hydrogenated opioid analgesic composition.