Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Prolyl Hydroxylase Inhibitors

a technology of prolyl hydroxylase and inhibitor, which is applied in the direction of biocide, drug composition, extracellular fluid disorder, etc., can solve the problems of reduced oxygen levels in the blood, ubiquitination of hif-alpha and subsequent degradation, and achieve the effect of increasing the production of erythropoietin and epo

Inactive Publication Date: 2007-09-13
SMITHKLINE BECKMAN CORP
View PDF0 Cites 81 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0018]In a second aspect of the present invention, there is provided a compound of formula (I) or a salt or solvate thereof for use in mammalian therapy, e.g. treating amenia. An example of this therapeutic approach is that of a method for treating anemia caused by increasing the production of erythropoietin (Epo) by inhibiting HIF prolyl hydroxylases comprising administering a compound of formula (I) to a patient in need thereof, neat or admixed with a pharmaceutically acceptable excipient, in an amount sufficient to increase production of Epo.

Problems solved by technology

Anemia occurs when there is a decrease or abnormality in red blood cells, which leads to reduced oxygen levels in the blood.
This leads to ubiquitination of HIF-alpha and subsequent degradation.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Prolyl Hydroxylase Inhibitors
  • Prolyl Hydroxylase Inhibitors
  • Prolyl Hydroxylase Inhibitors

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0088]

N-{[1-(2-Cyclopropylethyl)-4-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]carbonyl}glycine

[0089]A mixture of 1-(2-cyclopropylethyl)-2H-pyrido [2,3-d][1,3]oxazine-2,4(1H)-dione (Prepared according to PCT Int. Appl. (2003), WO 2003059356 A2)(0.232 g, 1.00 mmol) and diethylmalonate (0.152 mL, 1.00 mmol) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (0.300 mL, 2.00 mmol). 1,4-dioxane (1.0 mL) was added and the solution was heated to 150° C. for 20 min. in a Biotage Initiator microwave synthesizer (http: / / www.biotage.com). Following cooling, glycine (0. 113 g, 1.50 mmol) was added and the solution was heated to 200° C. for 20 min. in a Biotage Initiator microwave synthesizer. The reaction mixture was then cooled, treated with 6M aqueous sodium hydroxide (2.0 mL), diluted with water and extracted with diethyl ether. The aqueous layer was then acidified with 6M aqueous hydrochloric acid and extracted twice with ethyl acetate. The organic solution was dried over MgSO4, filte...

example 2

[0090]

N-{[4-hydroxy-1-(3-methylbutyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]carbonyl}glycine

2a) Ethyl 2-[(3-methylbutyl)amino]-3-pyridinecarboxylate

[0091]A mixture of ethyl-2-chloronicotinic carboxylate (2.00 g, 10.8 mmol) and 3-(methylbutyl)amine (1.88 mL, 16.1 mmol) in ethanol (3.0 mL) was heated to 180° C. for 40 min. in a Biotage Initiator microwave synthesizer. The mixture was added to a solution of saturated aqueous sodium bicarbonate and extracted twice with ethyl acetate. The combined organic portions were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified via flash column chromatography (60% ethyl acetate in hexanes) to afford the title compound as a clear oil (2.05 g, 80%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.30 (dd, J=4.7, 1.9 Hz, 1 H), 8.13 (dd, J=7.6, 2.0 Hz, 1 H), 7.94 (br. s., 1 H), 6.51 (dd, J=7.8, 4.8 Hz, 1 H), 4.33 (q, J=7.2 Hz, 2 H), 3.48-3.58 (m, 2 H), 1.68-1.82 (m, 1 H), 1.51-163 (m, 2 H), 1.39 (t, J=7.2 Hz, 3 H), 0...

example 3

[0094]

N-{[1-(3,3-dimethylbutyl)-4-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]carbonyl}glycine

3a) Ethyl 2-[(3,3-dimethylbutyl)amino]-3-pyridinecarboxylate

[0095]A mixture of ethyl-2-chloronicotinic carboxylate (0.518 g, 2.79 mmol) and (3,3-dimethylbutyl)amine (0.560 mL, 4.18 mmol) in ethanol (3.0 mL) was heated to 180° C. for 40 min. in a Biotage Initiator microwave synthesizer. The mixture was concentrated and the residue was diluted in water, treated with saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The combined organic portions were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified via flash column chromatography (60% ethyl acetate in hexanes) to afford the title compound as a clear oil (0.655 g, 94%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.31 (dd, J=4.8, 2.0 Hz, 1 H), 8.12 (dd, J=7.6, 2.0 Hz, 1 H), 7.87 (br. s., 1 H), 6.51 (dd, J=7.6, 4.8 Hz, 1 H), 4.33 (q, J=7.2 Hz, 2 H), 3.30-3.61 (m, 2 H), 1.55-1.68 (m, ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention described herein relates to certain bicyclic heteroaromatic N-substituted glycine derivatives of formula (I)which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.

Description

CROSS REFERENCE TO PRIOR APPLICATION[0001]This application claims the benefit of U.S. provisional 60 / 779737 filed 7 Mar. 2006.FIELD OF THE INVENTION[0002]This invention relates to certain bicyclic heteroaromatic N-substituted glycine derivatives that are inhibitors of HIF prolyl hydroxylases, and thus have use in treating diseases benefiting from the inhibition of this enzyme, anemia being one example.BACKGROUND OF THE INVENTION[0003]Anemia occurs when there is a decrease or abnormality in red blood cells, which leads to reduced oxygen levels in the blood. Anemia occurs often in cancer patients, particularly those receiving chemotherapy. Anemia is often seen in the elderly population, patients with renal disease, and in a wide variety of conditions associated with chronic disease.[0004]Frequently, the cause of anemia is reduced erythropoietin (Epo) production resulting in prevention of erythropoiesis (maturation of red blood cells). Epo production can be increased by inhibition of p...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61K31/495A61K31/47C07D487/08
CPCC07D471/04A61P43/00A61P7/06A61P9/00A61P9/10
Inventor FITCH, DUKE M.COLON, MARIELA
Owner SMITHKLINE BECKMAN CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com