Methods of making bempedoic acid and compositions of the same
The invention provides methods of preparing 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid and methods of making a pharmaceutical material comprising a purified amount of 8-hydroxy-2,2,14, 14-tetramethylpentadecanedioic acid. Also provided are compositions and pharmaceutical materials including a purified amount of 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid as well as methods of treating various diseases and conditions using the compositions and pharmaceutical materials.
1. A method of preparing a pharmaceutical material comprising a compound of formula (V):
the method comprising:
(a) contacting ethyl isobutyrate with a substituted 5-chloropentane in the presence of a first base to form a compound of formula (I):
wherein the substituted 5-chloropentane is selected from the group consisting of 1-bromo-5-chloropentane and 1-iodo-5-chloropentane;
(b) contacting the compound of formula (I) with a salt of formula [M]+[X] − to form a compound of formula (II):
wherein [M] + is selected from the group consisting of Li + , Na + and K + , and [X] − is I − ;
(c) contacting the compound of formula (II) with toluenesulfonylmethyl isocyanide in the presence of a second base to form a first intermediate, and contacting the first intermediate with an acid to form a compound of formula (IV):
and
(d) contacting the compound of formula (IV) with a reducing agent to form a second intermediate, and contacting the second intermediate with a hydrolyzing base to form a compound of formula (V),
wherein the pharmaceutical material comprises 0.0001% to less than or equal to 0.15% of the compound of formula (VI):
based on the total weight of the pharmaceutical material.
2. The method of claim 1 , wherein in step (a), less than about 1% by weight of the substituted 5-chloropentane remains after forming the compound of formula (I).
3. The method of claim 1 , wherein in step (a), the molar ratio of ethyl isobutyrate to the substituted 5-chloropentane is from about 1.1:1 to about 1.21:1.
4. The method of claim 1 , wherein in step (b), the salt of formula [M] + [X] − is sodium iodide.
5. The method of claim 1 , wherein in step (c), the molar ratio of the compound of formula (II) to toluenesulfonylmethyl isocyanide is about 1.9:1.
6. The method of claim 1 , wherein in step (d), contacting the compound of formula (IV) with a reducing agent comprises contacting the compound of formula (IV) with about 0.35 molar equivalents of the reducing agent based on the molar amount of the compound of formula (IV).
7. The method of claim 1 , wherein in step (d), contacting the compound of formula (IV) with a reducing agent to form a second intermediate, and contacting the second intermediate with a hydrolyzing base to form a compound of formula (V) is conducted in a single reaction vessel.
8. The method of claim 1 , further comprising:
(e) purifying the compound of formula (V) to provide the pharmaceutical material comprising a purified amount of the compound of formula (V).
9. The method of claim 8 , wherein in step (e), purifying the compound of formula (V) comprises crystallizing the compound of formula (V) from a solvent, wherein the solvent comprises ethyl acetate.
10. The method of claim 8 , wherein in step (e), purifying the compound of formula (V) comprises crystallizing the compound of formula (V) to provide a crystalline form of the compound of formula (V), and the method further comprises recrystallizing the crystalline form of the compound of formula (V).
11. The method of claim 8 , wherein the purified amount of the compound of formula (V) is greater than 99.0% by weight of the total weight of the pharmaceutical material.
12. A method of preparing a pharmaceutical material comprising a compound of formula (V):
the method comprising:
(a) contacting 1-bromo-5-chloropentane with about 1.1 molar equivalents of ethyl isobutyrate in the presence of lithium diisopropylamide at a temperature in the range of about−20° C. to about 0° C. to form a compound of formula (I):
(b) contacting the compound of formula (I) with about 1.1 molar equivalents of sodium iodide in 2-butanone at a temperature in the range of about 78° C. to about 82° C. to form a compound of formula (IIa):
(c) contacting the compound of formula (IIa) with toluenesulfonylmethyl isocyanide in the presence of sodium tert-pentoxide in dimethylacetamide at a temperature in the range of about −20° C. to about 10° C. to form a first intermediate, and contacting the first intermediate with an acid at a temperature in the range of about −10° C. to about 35° C. to form a compound of formula (IV):
and
(d) contacting the compound of formula (IV) with about 0.35 molar equivalents of sodium borohydride to form a second intermediate, and contacting the second intermediate with sodium hydroxide in a solution to form a compound of formula (V).
13. The method of claim 12 , wherein in step (c), the molar ratio of the compound of formula (IIa) to toluenesulfonylmethyl isocyanide to sodium tert-pentoxide is about 1.9:1:2.1.
14. The method of claim 12 , further comprising:
(f) adjusting the pH of the solution comprising the compound of formula (V) to about 5 to about 6;
(g) extracting the compound of formula (V) from the solution using methyl tert-butyl ether to provide a methyl tert-butyl ether solution comprising the compound of formula (V);
(h) exchanging the methyl tert-butyl ether of the methyl tert-butyl ether solution with ethyl acetate to provide an ethyl acetate solution comprising the compound of formula (V);
(i) filtering the ethyl acetate solution comprising the compound of formula (V) through silica gel;
(j) crystallizing the compound of formula (V) using ethyl acetate and water to provide a crystalline form of the compound of formula (V); and
(k) recrystallizing the crystalline form of the compound of formula (V) using ethyl acetate and water to provide the pharmaceutical material comprising a purified amount of the compound of formula (V).
15. The method of claim 14 wherein in step (g), extracting the compound of formula (V) from the solution using methyl tert-butyl ether is conducted at a temperature less than or equal to about 50° C.
16. The method of claim 14 , wherein in step (j), crystallizing the compound of formula (V) using ethyl acetate and water is conducted over a temperature range of about 50° C. to about −5° C.
17. The method of claim 14 , wherein in step (k), recrystallizing the crystalline form of the compound of formula (V) using ethyl acetate and water is conducted over a temperature range of about 70° C. to about 5° C.
18. The method of claim 14 , further comprising:
(l) dissolving the crystalline form of the compound of formula (V) in acetonitrile, thereby forming a solution;
(m) contacting the solution with charcoal;
(n) filtering the charcoal to provide a purified solution comprising the compound of formula (V); and
(o) crystallizing the compound of formula (V) from the purified solution to provide the pharmaceutical material comprising a purified amount of the compound of formula (V).
19. The method of claim 14 , wherein the purified amount of the compound of formula (V) is greater than 99.0% by weight of the total weight of the pharmaceutical material.
20. The method of claim 12 , wherein the pharmaceutical material comprises 0.0001% to less than or equal to 0.15% of the compound of formula (VI):
based on the total weight of the pharmaceutical material.