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Aromatic sulfone hydroxamic acid metalloprotease inhibitor

a technology of metalloprotease and aromatic sulfone, which is applied in the direction of amide active ingredients, drug compositions, cardiovascular disorders, etc., can solve the problems of low side effects, poor repair, and number of disease states, and achieve the effect of minimal side effects

Inactive Publication Date: 2006-04-20
BARTA THOMAS +19
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0094] An advantage of the invention is the provision of compounds, compositions and methods effective for treating such pathological conditions by selective inhibition of a metalloproteinase such as MMP-2, MMP-9 or MMP-13 associated with such conditions with minimal side effects resulting from inhibition of other metalloproteinases, such as MMP-1, whose activity is necessary or desirable for normal body function.

Problems solved by technology

The loss of this balance for whatever reason leads to a number of disease states.
This can produce improper wound healing leading to weak repairs, adhesions and scarring.
These latter defects can lead to disfigurement and / or permanent disabilities as with post-surgical adhesions.
Chronic release of active TNF can cause cachexia and anorexia.
One possible problem associated with known MMP inhibitors is that such compounds often exhibit the same or similar inhibitory effects against each of the MMP enzymes.
Although marimastat exhibited some measure of efficacy via these markers, toxic side effects were noted.
The most common drug-related toxicity of marimastat in those clinical trials was musculoskeletal pain and stiffness, often commencing in the small joints in the hands, spreading to the arms and shoulder.
It is thought that the lack of specificity of inhibitory effect among the MMPs may be the cause of that effect.
Although many of the known MMP inhibitors such as batimastat, marimastat and the hydroxamates of WO 98 / 37877 and WO 98 / 38163 exhibit a broad spectrum of activity against MMPS, those compounds are not particularly selective in their inhibitory activity.
This lack of selectivity may be the cause of the musculoskeletal pain and stiffness observed with their use.

Method used

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  • Aromatic sulfone hydroxamic acid metalloprotease inhibitor
  • Aromatic sulfone hydroxamic acid metalloprotease inhibitor
  • Aromatic sulfone hydroxamic acid metalloprotease inhibitor

Examples

Experimental program
Comparison scheme
Effect test

example 1

Preparation of N-hydroxy-2-[(4-phenoxyphenyl)sulfonyl]acetamide

[0504]

[0505] Part A: To a solution of 3-bromopyruvic acid hydrate (1.95 g, 11.7 mmol) cooled to zero degrees Celsius in methanol (50 mL) was added 4-(phenoxy)benzenethiol (2.35 g, 11.7 mmol). The solution was stirred for 15 minutes followed by concentration in vacuo. The residue was partitioned between ethyl acetate and H2O and the organic layer was dried over magnesium sulfate. Concentration in vacuo provided the crude sulfide as a yellow solid that was used without any additional purification.

[0506] Part B: To a solution of the crude sulfide of part A (1.2 g, 2O cooled to zero degrees Celsius was added Oxone® (3.5 g, 5.72 mmol). The solution was stirred for 1 hour followed by removal of excess Oxone® by filtration. The filtrate was concentrated and the residue was dissolved into ethyl acetate and washed with saturated NaHCO3 and saturated NaCl and dried over magnesium sulfate. After concentration in vacuo the resulti...

example 2

Preparation of N-hydroxy-2-methyl-2-[(4-phenoxyphenyl)sulfonyl]propanamide

[0508]

[0509] Part A: To a solution of 4-(phenoxy)benzenethiol (3.8 g, 18.8 mmol) in methanol (60 mL) cooled to zero degrees Celsius was added t-butyl bromoacetate (2.8 mL, 18.8 mmol) and triethylamine (2.6 mL, 19.0 mmol). The solution was stirred for 30 minutes and was then concentrated in vacuo. The residue was partitioned between ethyl acetate and H2O and the organic layer was washed with saturated NaCl and dried over magnesium sulfate. Concentration in vacuo provided the sulfide as an oil. To a solution of the sulfide in dichloromethane (85 mL) was added m-chloroperbenzoic acid (13.8 g, 43.2 mmol) over 15 minutes. The solution was stirred at ambient temperature for 2 hours. The reaction was quenched by the addition of aqueous Na2SO3. After 30 minutes the solution was filtered through Celite®. The filtrate was washed with 25 percent aqueous hydroxylamine, 1N HCl, and saturated NaCl and dried over magnesium ...

example 3

Preparation of 1,1-dimethylethyl ester 4-[(hydroxyamino)carbonyl]-4-[(phenoxyphenyl)-sulfonyl]-1-piperidinecarboxylic acid

[0513]

[0514] Part A: A solution of 4-(phenoxy)benzenethiol (2.03 g, 10.0 mmol) in DMSO (DMSO; 20 mL) was heated to sixty-five degrees Celsius for 5 hours. The solution remained at ambient temperature for 18 hours. The solution was extracted with ethyl acetate and the combined organic layers were washed with H2O and saturated NaCl and dried over magnesium sulfate. Concentration in vacuo provided the disulfide as a yellow oil (2.3 g, quantitative yield).

[0515] Part B: To a solution of ethyl isonipecotate (15.7 g, 0.1 mol) in THF (100 mL) was added a solution of di-tert-butyl dicarbonate (21.8 g, 0.1 mol) in THF (5 mL) dropwise over 20 minutes. The solution was stirred overnight at ambient temperature and concentrated in vacuo to yield a light oil. The oil was filtered through silica gel (7:3 ethyl acetate / hexanes) and concentrated in vacuo to give the BOC-piperid...

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Abstract

A treatment process is disclosed that comprises administering an effective amount of an aromatic sulfone hydroxamic acid that exhibits excellent inhibitory activity of one or more matrix metalloprotease (MMP) enzymes, such as MMP-2, MMP-9, and MMP-13, while exhibiting substantially less inhibition at least of MMP-1 to a host having a condition associated with pathological matrix metalloprotease activity. The administered enzyme inhibitor corresponds in structure to formula (I), below, or a pharmaceutically acceptable salt thereof, wherein R1 and R2 are both hydrido or R1 and R2 together with the atoms to which they are bonded form a 5- to 8-membered ring containing one, two, or three heteroatoms in the ring that are oxygen, sulfur, or nitrogen. R3 in formula (I) is an optionally substituted aryl or optionally substituted heteroaryl radical. Also disclosed are metalloprotease inhibitor compounds having those selective activities, processes for manufacture of such compounds and pharmaceutical compositions using an inhibitor.

Description

TECHNICAL FIELD [0001] This invention is directed to proteinase (protease) inhibitors, and more particularly to the use of aromatic sulfone hydroxamic acid compounds that, inter alia, are selective inhibitors of matrix metalloproteinases in a process for treating conditions associated with pathological matrix metalloproteinase activity, the selective inhibitors themselves, compositions of proteinase inhibitors, intermediates for the syntheses of proteinase inhibitors, and processes for the preparation of proteinase inhibitors. BACKGROUND OF THE INVENTION [0002] Connective tissue, extracellular matrix constituents and basement membranes are required components of all mammals. These components are the biological materials that provide rigidity, differentiation, attachments and, in some cases, elasticity to biological systems including human beings and other mammals. Connective tissues components include, for example, collagen, elastin, proteoglycans, fibronectin and laminin. These bio...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/426A61K31/421A61K31/4166A61K31/19A61K31/16A61K31/167A61K31/27A61K31/35A61K31/351A61K31/357A61K31/366A61K31/38A61K31/381A61K31/382A61K31/39A61K31/4427A61K31/443A61K31/4433A61K31/444A61K31/445A61K31/4465A61K31/4525A61K31/454A61K31/496A61K31/505A61K31/506A61K31/5375A61K31/54A61K31/541A61P1/02A61P1/04A61P9/10A61P13/00A61P19/00A61P19/02A61P25/28A61P27/02A61P29/00A61P35/00A61P35/04A61P43/00C07C317/44C07C319/06C07D211/66C07D211/94C07D211/96C07D239/04C07D279/06C07D309/08C07D309/12C07D319/06C07D327/02C07D333/38C07D335/02C07D337/04C07D401/06C07D401/12C07D405/12C07D405/14C07D407/12C07D409/12C07D409/14C07D413/06C07D413/12C07D413/14C07D417/12C07D521/00
CPCA61K31/19A61K31/4166A61K31/421A61K31/426C07C317/44C07D207/48C07D211/54C07D211/66C07D211/86C07D211/94C07D211/96C07D225/02C07D231/12C07D233/56C07D239/04C07D249/08C07D263/06C07D265/06C07D279/06C07D281/08C07D309/08C07D309/28C07D319/06C07D325/00C07D335/02C07D337/04C07D401/06C07D401/12C07D405/12C07D407/12C07D409/12C07D409/14C07D413/12C07D413/14C07D417/12A61P1/02A61P1/04A61P13/00A61P19/00A61P19/02A61P25/28A61P27/02A61P29/00A61P35/00A61P35/04A61P43/00A61P9/10
Inventor BARTA, THOMASBECKER, DANIELBEDELL, LOUISBOEHM, TERRICARROLL, JEFFERYDECRESCENZO, GARYFLETCHER, THERESAFRESKOS, JOHNGETMAN, DANIELHANSON, GUNNARHOCKERMAN, SUSANHOWARD, CAROLKOLODZIEJ, STEPHENLI, MADELEINEMCDONALD, JOSEPHMISCHKE, DEBORAHMULLINS, PATRICKRICO, JOSEPHSTEHLE, NATHANVILLAMIL, CLARA
Owner BARTA THOMAS
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