Acetate salt of buprenorphine and methods for preparing buprenorphine
The present disclosure provides acetate salts of buprenorphine, and its anhydrates, solvates, hydrates, and crystalline forms thereof, where the acetate salts of buprenorphine are essentially free of impurities. The disclosure further provides method of preparing the acetate salts, buprenorphine free base prepared from the acetate salts, other salts prepared from the free base, and pharmaceutical compositions thereof essentially free of impurities.
1. A method for preparing buprenorphine free base comprising:
(a) agitating an admixture comprising an acetate salt of buprenorphine, a solution, and a basic material at a temperature of from about 20° C. to about 90° C. to provide buprenorphine free base; and
(b) isolating the buprenorphine free base from the admixture.
2. The method of claim 1 , wherein the admixture comprises at least about 1 mass equivalent of the solution relative to the starting mass of the acetate salt of buprenorphine.
3. The method of claim 1 , wherein the solution comprises water and an alcohol.
4. The method of claim 3 , wherein the solution comprises from about 30 wt % to about 70 wt % alcohol in water.
5. The method of claim 3 , wherein the alcohol is selected from methanol, ethanol, isopropyl alcohol, and combinations thereof.
6. The method of claim 5 , wherein the alcohol is isopropyl alcohol.
7. The method of claim 1 , wherein the basic material comprises a hydroxide, a carbonate, an alkoxide, a hydride, a phosphate, a borate, an oxide, a cyanide, a silicate, or an amine, or combinations thereof.
8. The method of claim 1 , wherein the basic material comprises ammonium hydroxide.
9. The method of claim 1 , wherein the admixture comprises from about 0.5 molar equivalents to about 20 molar equivalents of basic material relative to starting moles of the acetate salt of buprenorphine.
10. The method of claim 1 , wherein the admixture is agitated for from about 1 hour to about 36 hours.
11. The method of claim 1 , wherein the admixture is agitated at a temperature of from about 30° C. to about 45° C.
12. The method of claim 1 , wherein isolating the buprenorphine free base in (b) comprises (i) forming a slurry comprising buprenorphine free base with a slurrying solution comprising water and an alcohol; and (ii) filtering the buprenorphine free base from the slurry.
13. A buprenorphine free base product obtained from the method of claim 1 , wherein the buprenorphine free base product comprises about 0.10 wt % or less of a compound of formula (12):
14. A buprenorphine free base product obtained from the method of claim 13 , wherein the buprenorphine free base product comprises between about 0.05 wt % and 0.08 wt % of the compound of formula (12).
15. A buprenorphine free base product obtained from the method of claim 1 , wherein the buprenorphine free base product comprises about 0.05 wt % or less of a compound of formula (13):
16. A method for preparing buprenorphine free base comprising:
(a) agitating an admixture comprising an acetate salt of buprenorphine, a solution comprising from about 30 wt % to about 70 wt % of an alcohol in water, and ammonium hydroxide at a temperature of from about 20° C. to about 90° C., to provide buprenorphine free base; and (b) isolating the buprenorphine free base of (a).
17. The method of claim 16 , where the alcohol is isopropyl alcohol.
18. The method of claim 16 , wherein the admixture is agitated at a temperature of from about 30° C. to about 45° C.
19. A method for preparing buprenorphine free base comprising:
(a) converting an acetate salt of buprenorphine to a buprenorphine free base product in the presence of a basic material; and
(b) isolating the buprenorphine free base product of (a) without chromatography, wherein the buprenorphine free base product comprises about 0.05 wt % to about 0.10 wt % of a compound of formula (12)
and about 0.05 wt % or less of a compound of formula (13)
20. The method of claim 19 , wherein the buprenorphine free base product comprises about 0.05 wt % to about 0.08 wt % of a compound of formula (12).