IP Library Granted Patent US 8,008,502
Granted Patent B2
US 8,008,502 · App. 12/383,854 · Granted Aug 30, 2011

Thiazoline acid derivatives

Assignee: University of Florida Research Foundation, Inc.
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Quick Facts
Patent No.
US 8,008,502
App. No.
12/383,854
Granted
Aug 30, 2011
Kind
B2
Abstract

The present invention relates to novel thiazoline acids and derivatives thereof useful as chelators of trivalent metals in therapeutic applications. For example, the thiazoline acid derivatives are useful in diagnosing and treating pathological conditions associated with an excess of trivalent metals in humans and animals.

Claims (25)

1. A method of preparing a compound of the formula:

wherein:

Z is CH or N;

R is H or acyl;

R 1 , R 2 , R 3 and R 5 may be the same or different and represent H, alkyl or hydrocarbyl arylalkyl having up to 14 carbon atoms;

R 4 is H or alkyl having 1-4 carbon atoms, and salts thereof with a pharmaceutically acceptable acid, comprising reacting a first reagent of the formula:

with a second reagent of the formula:

or a salt thereof with a pharmaceutically acceptable acid.

2. The method of claim 1 , wherein the first and second reagents are reacted in an inert solvent or a mixture of inert solvents.

3. The method of claim 2 , wherein the inert solvent or the mixture is aqueous.

4. The method of claim 2 , wherein the mixture comprises an aqueous solvent and an alcohol.

5. The method of claim 4 , wherein the aqueous solvent is a phosphate buffer.

6. The method of claim 4 , wherein the alcohol is methanol.

7. The method of claim 4 , wherein the mixture comprises a phosphate buffer and methanol.

8. The method of claim 2 , wherein the first and second reagents are reacted at ambient temperature.

9. The method of claim 2 , wherein the first and second reagents are reacted at a temperature from about ambient temperature to about 80° C.

10. The method of claim 9 , wherein the temperature is from about 50° C. to about 80° C.

11. The method of claim 10 , wherein the temperature is about 70° C.

12. The method of claim 2 , wherein the first and second reagents are reacted under an inert gas atmosphere.

13. The method of claim 1 , wherein the first and second reagents are reacted in the presence of a base.

14. The method of claim 13 , wherein the base is NaHCO 3 .

15. The method of claim 1 , wherein Z is CH.

16. The method of claim 15 , wherein R═R 1 ═R 2 ═R 4 ═R 5 ═H.

17. The method of claim 1 , wherein Z is N.

18. The method of claim 1 , wherein Z is CH and R 3 is an alkyl having 1-4 carbon atoms.

Assignments (1)
CONFIRMATORY LICENSE Recorded Dec 15, 2016
From: UNIVERSITY OF FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040982/0531 →
Continuity (6)
Continuation 11522299 · Sep 15, 2006
Continuation 10944150 · Sep 17, 2004
Continuation 10300071 · Nov 20, 2002
Continuation 09531753 · Mar 20, 2000
Continuation 09144103 · Aug 31, 1998
Related Publication 20100094016A1 · Apr 15, 2010