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

Halogenated biaryl heterocyclic compounds and methods of making and using the same

a technology of biaryl heterocyclic compounds and biaryl heterocyclic compounds, which is applied in the field of antiinfective, antiproliferative, antiinflammatory, and prokinetic agents, can solve the problems of drug compositions, serious and even fatal results for patients infected with such resistant bacteria, and antibiotic agents developed for clinical use ultimately encounter problems

Inactive Publication Date: 2006-07-06
CHEN SHILI +8
View PDF32 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0011] In addition, the invention provides methods of synthesizing the foregoing compounds. Following synthesis, an effective amount of one or more of the compounds can be formulated with a pharmaceutically acceptable carrier for administration to a mammal for use as an anti-cancer, anti-microbial, anti-biotic, anti-fungal, anti-parasitic or anti-viral agent, or to treat a proliferative disease, an inflammatory disease or a gastrointestinal motility disorder. The compounds or formulations can be administered, for example, via oral, parenteral, or topical routes, to provide an effective amount of the compound to the mammal.

Problems solved by technology

However, such beliefs have been shaken by the fact that strains of cells or microorganisms resistant to currently effective therapeutic agents continue to evolve.
In fact, virtually every antibiotic agent developed for clinical use has ultimately encountered problems with the emergence of resistant bacteria.
For example, resistant strains of Gram-positive bacteria such as methicillin-resistant staphylocci, penicillin-resistant streptococci, and vancomycin-resistant enterococci have developed, which can cause serious and even fatal results for patients infected with such resistant bacteria.
Unfortunately, linezolid-resistant strains of organisms are already being reported.

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
  • Halogenated biaryl heterocyclic compounds and methods of making and using the same
  • Halogenated biaryl heterocyclic compounds and methods of making and using the same
  • Halogenated biaryl heterocyclic compounds and methods of making and using the same

Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis of Aryl Iodide 101

Method A

[0134] Scheme 1 depicts the synthesis of aryl iodide 101, an intermediate useful in producing compounds of the present invention.

Synthesis of Amine 91

[0135] A solution of 3-fluoroanaline 90 (18.7 g, 168.3 mmol) in tetrahydrofuran (THF, 150 mL) was treated with potassium carbonate (K2CO3, 46.45 g, 336.6 mmol, 2.0 equiv) and water (H2O) (150 mL) before a solution of benzyl chloroformate (CBZCl, 31.58 g, 185.1 mmol, 26.1 mL, 1.1 equiv) in THF (50 mL) was dropwise added into the reaction mixture at room temperature under nitrogen (N2). The resulting reaction mixture was stirred at room temperature for 2 hours (h). When thin layer chromatography (TLC) showed the reaction was complete, the reaction mixture was treated with H2O (100 mL) and ethyl acetate (EtOAc, 100 mL). The two layers were separated, and the aqueous layer was extracted with EtOAc (2×100 mL). The combined organic extracts were washed with H2O (2×100 mL) and saturated aqueous sodiu...

example 2

Synthesis of Compounds 1 and 2

[0148] Scheme 3 illustrates the synthesis of amine 105, an intermediate used in the synthesis of compounds 1 and 2. Aryl iodide 101 is coupled to a substituted aryl boronic acid (the Suzuki reaction) to produce N-[3-(2-fluoro-4′-hydroxymethyl-biphenyl-4-yl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide (biaryl alcohol 102). Other coupling reactions (for example, the Stille reaction), using alternate coupling intermediates easily obtained or synthesized by those skilled in the art, could also be employed to synthesize target biaryl intermediates similar to biaryl alcohol 102. Biaryl alcohol 102 is then converted to amine 105 by chemistry well known to those skilled in the art.

[0149] Scheme 4 illustrates the synthesis of compounds 1 and 2. Amine 105 is alkylated with the requisite bromides to afford compounds 1 and 2.

Synthesis of Amine 105

[0150] A suspension of aryl iodide 101 (14.0 g, 37 mmol) in toluene (120 mL) was treated with 4-(hydroxymethyl)phenylb...

example 3

Synthesis of Amine 3

[0156] Scheme 5 illustrates the synthesis of amine 3. 3-fluoropropylamine hydrochloride (amine hydrochloride 106) was synthesized from 1-bromo-3-fluoropropane 139 and then alkylated with benzyl chloride 107 to afford amine 3.

Synthesis of Benzyl Chloride 107

[0157] To a solution of 3-(3-fluoro-4-iodo-phenyl)-5-hydroxymethyl-oxazolidin-2-one (1.0 g, 2.97 mmol), isoxazol-3-ol (0.30 g, 3.56 mmol) and triphenylphosphine (1.02 g, 3.86 mmol) in THF (15 mL) was added diisopropyl azodicarboxylate (DIAD, 0.74 mL, 3.56 mmol) dropwise at 0° C. The reaction was warmed to room temperature and stirring was continued for 2 h. The solvent was evaporated and the crude was purified on silica gel, eluting with hexanes / EtOAc 2:1 to 3:2, to give 3-(3-fluoro-4-iodo-phenyl)-5-(isoxazol-3-yloxymethyl)-oxazolidin-2-one (1.01 g; 84% yield).

[0158] A degassed mixture containing 3-(3-fluoro-4-iodo-phenyl)-5-(isoxazol-3-yloxymethyl)-oxazolidin-2-one (1.0 g, 2.48 mmol), 4-(hydroxymethyl)ph...

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

PropertyMeasurementUnit
Fractionaaaaaaaaaa
Massaaaaaaaaaa
Massaaaaaaaaaa
Login to View More

Abstract

The present invention relates generally to the field of anti-infective anti-proliferative, anti-inflammatory, and prokinetic agents. More particularly, the invention relates to a family of compounds having at least one halogenated hydrocarbon moiety, a biaryl moiety, and at least one heterocyclic moiety, that are useful as such agents.

Description

RELATED APPLICATION [0001] This application claims the benefit of and priority to U.S. Patent Application Nos. 60 / 530,371, filed Dec. 17, 2003, and 60 / 576,267, filed Jun. 2, 2004, the disclosures of which are incorporated by reference herein.FIELD OF THE INVENTION [0002] The present invention relates generally to the field of anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents. More particularly, the invention relates to a family of halogenated biaryl heterocyclic compounds, comprising at least one halogenated hydrocarbon moiety, a biaryl moiety, and at least one heterocyclic moiety, that are useful as therapeutic agents. BACKGROUND [0003] Since the discovery of penicillin in the 1920s and streptomycin in the 1940s, many new compounds have been discovered or specifically designed for use as antibiotic agents. It was once believed that infectious diseases could be completely controlled or eradicated with the use of such therapeutic agents. However, such belie...

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): A61K31/421A61K31/42A61K31/365A61K31/506A61K31/501A61K31/497A61K31/4439C07D263/20C07D263/24C07D413/02C07D413/06C07D413/12
CPCC07D263/20A61P21/00A61P29/00A61P31/00A61P31/10A61P31/12A61P33/00A61P35/00A61P43/00
Inventor CHEN, SHILIZHOU, JIACHENGWU, YUSHENGWANG, DEPINGSALVINO, JOSEPHOYELERE, ADEGBOYEGALOU, RONGLIANGBHATTACHARJEE, ASHOKECHEN, YI
Owner CHEN SHILI
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