IP Library Granted Patent US 11,566,005
Granted Patent B2
US 11,566,005 · App. 17/747,656 · Granted Jan 31, 2023

Highly pure phentolamine mesylate and methods for making same

Inventor: Daniela Carmen Oniciu (Gainesville, FL)
Assignee: Ocuphire Pharma, Inc.
C07D233/24
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Quick Facts
Patent No.
US 11,566,005
App. No.
17/747,656
Granted
Jan 31, 2023
Kind
B2
Abstract

This invention provides methods for synthesizing phentolamine mesylate from phentolamine and methanesulfonic acid in the presence of acetone and water. The methods of the present invention provide highly pure phentolamine mesylate. The invention also provides highly pure phentolamine mesylate.

Claims (27)

1. A method for making phentolamine mesylate, comprising:

(a) allowing Compound 1

to react with methanesulfonic acid in the presence of acetone and water under conditions effective to make a first mixture comprising phentolamine mesylate;

(b) admixing the first mixture and methyl t-butyl ether to make a second mixture; and

(c) allowing the phentolamine mesylate to precipitate from the second mixture.

2. The method of claim 1 , wherein allowing the phentolamine mesylate to precipitate from the second mixture comprises cooling the second mixture to a temperature of 15° C. to −25° C.

3. The method of claim 1 , further comprising the step of:

(d) isolating the phentolamine mesylate from the second mixture, wherein the isolating provides isolated phentolamine mesylate.

4. The method of claim 3 , wherein the isolating is filtering, and the isolated phentolamine mesylate is filtered phentolamine mesylate.

5. The method of claim 3 , further comprising the step of:

(e) drying the isolated phentolamine mesylate to provide dried phentolamine mesylate.

6. The method of claim 1 , wherein the acetone and water are present in the first mixture of step (a) in a ratio of 10 (plus or minus up to 20%):1 acetone:water by volume to 12 (plus or minus up to 20%):1 acetone:water by volume.

7. The method of claim 1 , wherein Compound 1 is present in the first mixture of step (a) at a concentration of 0.2 (plus or minus up to 20%) moles/liter of the acetone and water to 0.4 (plus or minus up to 20%) moles/liter of the acetone and water.

8. The method of claim 5 , wherein the dried phentolamine mesylate has purity of at least 98% by weight of the dried phentolamine mesylate.

9. The method of claim 5 , wherein the dried phentolamine mesylate has a purity of 99.0% to 100% by weight of the dried phentolamine mesylate.

10. The method of claim 5 , wherein the dried phentolamine mesylate comprises less than 0.5% of an impurity by weight of the dried phentolamine mesylate.

11. The method of claim 5 , wherein the dried phentolamine mesylate is not subject to further purification.

12. Phentolamine mesylate that exhibits an X-ray powder diffraction (XRPD) pattern comprising a peak at 6.87±0.2 degrees 2-theta, a peak at 20.32±0.2 degrees 2-theta, and a peak at 21.36±0.2 degrees 2-theta.

13. The phentolamine mesylate of claim 12 , wherein the XRPD pattern further comprises a peak at 18.86±0.2 degrees 2-theta and a peak at 21.07±0.2 degrees 2-theta.

14. The phentolamine mesylate of claim 13 , wherein the XRPD pattern further comprises a peak at 11.65±0.2 degrees 2-theta, at 13.15±0.2 degrees 2-theta, and a peak at 20.85±0.2 degrees 2-theta.

15. The phentolamine mesylate of claim 12 , wherein the phentolamine mesylate comprises less than 1% of an impurity by weight of the phentolamine mesylate.

16. The phentolamine mesylate of claim 12 having a molar ratio of crystalline phentolamine mesylate to amorphous phentolamine mesylate of at least 9:1.

17. A composition comprising an effective amount of the phentolamine mesylate of claim 12 and a pharmaceutically acceptable carrier or excipient.

18. The composition of claim 17 , wherein the composition is an ophthalmic solution.

19. The composition of claim 17 , wherein the composition comprises the phentolamine mesylate in an amount of 1% by weight or volume of the composition.

20. A method for a) inhibiting contraction of smooth muscle of a subject's iris, b) reducing a subject's pupil diameter, or c) improving visual contrast sensitivity or visual acuity, comprising administering to a subject in need of a) inhibition of iris smooth muscle contraction, b) reduction of pupil diameter or c) improvement of visual contrast sensitivity or improvement of visual acuity, an effective amount of the phentolamine mesylate of claim 12 .

21. A method for a) treating a dim or night vision disturbance, b) treating or reversing pharmacologically induced mydriasis, or c) treating presbyopia, comprising administering to a subject in need of a) treatment of dim or night vision disturbance, b) treatment or reversal of pharmacologically induced mydriasis or c) treatment of presbyopia, an effective amount of the phentolamine mesylate of claim 12 .

Assignments (3)
SECURITY INTEREST Recorded Apr 21, 2026
From: OPUS GENETICS, INC.
To: OPCM SA LLC, AS PURCHASER AGENT FOR THE SECURED PARTIES
Reel/Frame 075478/0138 →
CHANGE OF NAME Recorded Dec 27, 2024
From: OCUPHIRE PHARMA, INC.
To: OPUS GENETICS, INC.
Reel/Frame 069793/0460 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 9, 2022
From: ONICIU, DANIELA CARMEN
To: OCUPHIRE PHARMA, INC.
Reel/Frame 060756/0383 →
Priority Claims (1)
CN 202110679032.9 · Jun 18, 2021 · national
Continuity (2)
Provisional Application 63189839 · May 18, 2021
Related Publication 20220388965A1 · Dec 8, 2022
Cited By (5)
US 12,201,615 US 12,201,616 US 12,312,308 US 12,576,066 US 12,576,067