EP1066035A2 - Substituted aromatic compounds for treatment of antibiotic resistant infections - Google Patents

Substituted aromatic compounds for treatment of antibiotic resistant infections

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Publication number
EP1066035A2
EP1066035A2 EP99911497A EP99911497A EP1066035A2 EP 1066035 A2 EP1066035 A2 EP 1066035A2 EP 99911497 A EP99911497 A EP 99911497A EP 99911497 A EP99911497 A EP 99911497A EP 1066035 A2 EP1066035 A2 EP 1066035A2
Authority
EP
European Patent Office
Prior art keywords
alkyl
carbons
halo
alkenyl
ring system
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP99911497A
Other languages
German (de)
French (fr)
Other versions
EP1066035A4 (en
Inventor
William Y. Ellis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Department of Army
US Army Medical Research and Materiel Command USAMRMC
Original Assignee
US Department of Army
US Army Medical Research and Materiel Command USAMRMC
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Filing date
Publication date
Application filed by US Department of Army, US Army Medical Research and Materiel Command USAMRMC filed Critical US Department of Army
Publication of EP1066035A2 publication Critical patent/EP1066035A2/en
Publication of EP1066035A4 publication Critical patent/EP1066035A4/en
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
    • C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
    • C07C215/30—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings containing hydroxy groups and carbon atoms of six-membered aromatic rings bound to the same carbon atom of the carbon skeleton
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4458—Non condensed piperidines, e.g. piperocaine only substituted in position 2, e.g. methylphenidate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
    • C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
    • C07C2603/24—Anthracenes; Hydrogenated anthracenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
    • C07C2603/26—Phenanthrenes; Hydrogenated phenanthrenes

Definitions

  • compositions of the invention contain as active agents compounds containing aryl ring systems, including phenyl, naphthyl and anthracene ring systems, substituted by a carbon bound to an oxygen which is also bound to a nitrogen through a saturated carbon or carbon chain which may be substituted with halo, hydroxy, alkoxy, amino or alkylamino are disclosed,
  • the aryl ring system is further substituted by at least two halo substituents or halo-substituted substituents.
  • Halofantrine is a known antimalarial having a phenan- threne ring system substituted by a carbon bound to an oxygen which is also bound to a nitrogen through a saturated CH 2 -CH 2 chain to tertiary nitrogen having two butyl substituents.
  • the phenanthrene ring system is further substituted with 2 chlorines and one trifluoromethyl.
  • This invention relates to compounds of the general formula: wherein A is a aromatic hydrocarbon ring system and R 1 is a carbon bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon and wherein at least one of R 2 , R 3 and R is an electron-rich substituent.
  • the active agents are useful for treating patients suffering from infections including gram positive organisms, such as streptococcus, staphylococcus, anthracis, gram negative bacteria such as neisseria species, yeasts and mycobacterium. These compounds are effective against strains which have shown resistance to other antimicrobial agents .
  • infections including gram positive organisms, such as streptococcus, staphylococcus, anthracis, gram negative bacteria such as neisseria species, yeasts and mycobacterium.
  • This invention relates to compounds that have use in treating several infectious diseases which are now resistant to treatment to conventionally used antibiotics. Some of the compounds described herein have had previously been suggested for use in treating malaria. Some of the compounds are newly discovered. Most of the compounds are lipophilic. The lipid solubility of these compounds should permit the drugs to enter into cells, including cells of the central nervous system. Many of the compounds could be also be absorbed from the intestinal tract when given orally. They may be administered as cyclodextrin inclusion complexes to increase bioavailability. They may also be administered transdermally. Using patches for transdermal administration makes it possible to more easily control dosage.
  • R 1 is of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carbox- yl , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, a ino, or alkyl a ino group, X is (CH 2 ) L N( (CH2) n (CH 3 ) ) m wherein is 1-3, n is ⁇ 6, m is 1 v or 2 with the proviso that when m is 2, at least one n is ⁇ 3, or X may
  • R 2 , R 3 and R 4 may be alkyl (including cycloalkyl) , a saturated, nitrogen-containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl , carboxyalkyl, hydroxy, halo, alkenyl, alkenyloxy, haloalkyl (including perhaloalkyl) , wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings with the provision that
  • Z and X may be linked to form a heterocylic ring system.
  • any alkyl or aryl at R 2 , R 3 and R 4 may be further substituted with aryl of 1-2 rings, halo, (including multiple halo substitutions) alkyl, haloalkyl or alkoxy.
  • Preferred halo substituents are chloro or bromo and a preferred haloalkyl is trifluoromethyl .
  • Particularly useful compounds are those of Formulas I, II, III and IV.
  • any of R 28 may be substituents designated under R 2 , R 3 and R in the general formula above, with the proviso that at least one of R 2 _ 8 is an electron- rich substituent and any one of R ]( R 9 or R 10 is a substituent as defined as R 1 in the general formula.
  • Preferred compounds are those having at least two halos groups on the compound, with chloro or trifluoromethyl being particularly preferred groups.
  • any of R 2 _ 8 may be substituents identified as R 2 , R 3 or R in the general formula with the proviso that at least one substituents is an electron-rich moiety and R 1 is as designated for R 1 (CHOZX) for the general formula above.
  • R 1 is as designated for R 1 (CHOZX) for the general formula above.
  • Many of the preferred compounds have at least two halo or halo-substituted substituents.
  • R 1 is defined as in the general formula and R 2.6 is defined in the same manner as R 2 , R 3 and R 4 in the general formula. May of the preferred compounds have least two halo or halo-substituted substituents.
  • a particularly valuable compound of Formula II is of the formula:
  • R 1 is a carbon bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon and is of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxyl , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group, X is (CH 2 ) ,N ( (CH2) n (CH 3 ) ) m wherein , is 1-3, n is ⁇ 6, m is 1 or 2 with the proviso that when m is 2 , at least one n is ⁇ 3, or X may be (CH 2 ) o J as defined in the
  • halo substituents are chloro or bromo and preferred haloalkyl is tri- fluoromethyl .
  • a particularly useful member of this group of compounds is desbutylhalofantrin, a compound of the formula: which has now been found to be superior to halofantrine for treatment of malaria. (See U.S. Patent 5,711,966, which is incorporated herein by reference in its entirety.)
  • the phenanthrenes may be made by several methods, including the following scheme:
  • the phenanthrene compounds may also be prepared using the phenanthroic acid chlorides.
  • Example 1 The phenanthrene compounds may also be prepared using the phenanthroic acid chlorides.
  • the strains were streaked on blood agar plates (trypti- case soy broth containing 5% sheep cells) .
  • a single colony was isolated and grown in Mueller-Hinton Broth (MHB) as recommended by the national Committee for Clinical Laboratory Standards for rapidly growing bacteria.
  • MHB Mueller-Hinton Broth
  • Candida species and related yeasts were isolated in a similar manner on brain-heart infusion agar (BHI) .
  • Susceptibility tests The antibiotic susceptibility profile of each strain was determined using standard microtiter dilution plates obtained from the Clinical Microbiology Laboratory at Ohio State University Hospitals. The Inocula were prepared by suspending a 4 hour log phase growth in MHB visually egual in turbidity of an 0.5 McFarland standard.
  • Inocula were further diluted and added to microdilution trays to achieve a final density of approximately 1 x 10 5 CFU/ml .
  • the trays were incubated for 16 to 20 hours at 35 °C.
  • the highest dilution at which wells remained clear was considered to be the minimum inhibitory concentration (MIC) .
  • the MIC and minimum bacterial concentration (MBC) of the strains to the active agents were determined by two-fold dilutions in Mueller-Hinton broth.
  • Susceptibility tests for ATCC-obtained microorganisms and clinical isolates of gram positive bacteria including methicillin-susceptible and resistant staphylococci , streptococci, pneumococci and gram negative bacteria, including Enterobacteriaceae, Pseudomo- nas, Hemophilus and Neisseria were performed in microtiter plates as described above.
  • Compounds of the invention were dissolved in 1 ml of methanol and stored in aliguots at -70 °C. They were diluted in Mueller-Hinton broth for final screening. Compositions were tested in 0.1 ml volumes by serial dilution in microtiter plates against Staphylococcus aureus methicillin- sensitive ATCC 29213 and the ethicillin-resistant wild type T67738, as described above. The T67738 was resistant to most antimicrobial drugs, including ciprofloxacin.
  • the dosage and method of administration will depend on the location of the infection, the condition of the patient and the availability of professional supervision. Methods of administration include parenteral, oral, buccal, nasal or endotracheal routes.
  • the active agents may be administered as sprays.
  • the active agent may be delivered as a powder that is snorted. Inclusion complexes such as cyclodextrin inclusion complexes would be particularly useful for buccal administration of these active agents.
  • the compounds of the invention may also be admin- istered topically by any means, including by rectal route.
  • Suppositories, solutions for use as retention enemas, and creams or jellies are appropriate carriers for use in rectal administration.
  • the agents may be administered directly to infected tissue.
  • the active agents may be administered in the form of sprays or ointments.
  • Compounds of the invention may be applied to the skin or mucosa, including the vaginal mucosa, using creams, jellies, suppositories, or solutions.
  • the active agents of the invention may be delivered directly to the epithelial tissue topically.
  • compositions containing the active agents of the invention to the applied directly to target tissues and prosthetic devices could be given by aerosol into the trachea or administered in mist along with other agents into the respiratory tract.
  • the compositions of the invention may also be used prophylactically to protect from infection by pathogenic organisms .
  • Capsules of a formulation of active agent designated #184366 for oral administration are prepared by containing 250 mg. of the active agent, 100 mg. starch, and 5 mg. magnesium stearate. The capsules are administered daily or twice a day to achieve a daily dosage of 500 mg. per day.
  • Example 3
  • a preparation for application to the skin or mucosa may be prepared in the following manner: Ingredient %w/w
  • Example 4 A formulation for administration as a retention enema may be formulated in the following manner:
  • the active agent When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
  • Example 5 When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
  • Example 6 To 15 ml of phosphate buffered saline is added 3 mg of compound #185308. The composition is placed in a bottle having a stopper with a smooth glass rod extending into the solution. The composition is applied to boils using the smooth glass rod as an applicator. The composition may also be administered as a spray from a bottle with an atomizer.
  • Example 6 To 15 ml of phosphate buffered saline is added 3 mg of compound #185308. The composition is placed in a bottle having a stopper with a smooth glass rod extending into the solution. The composition is applied to boils using the smooth glass rod as an applicator. The composition may also be administered as a spray from a bottle with an atomizer.
  • Example 6 Example 6 :
  • a composition is prepared for use on the skin or mucosa in the following manner:
  • Phosphate buffered saline 86.5% When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
  • composition prepared as a gel for application to the skin :
  • composition prepared for administration as a supposi- tory is a composition prepared for administration as a supposi- tory:
  • Active agent #185308 0.5 mg glyceryl monosterate 1.0 Gm hydrogenated coconut oil 1.0 Gm glyceryl monopalmitate 1.0 Gm
  • Active agent #185308 0.5 mg glyceryl monosterate 1.0 Gm hydrogenated coconut oil 1.0 Gm glyceryl monopalmitate 1.0 Gm
  • Example 10
  • composition for intravenous administration comprising:
  • Example 11 Capsules of a formulation of active agent designated
  • Example 12 For oral administration are prepared by containing 250 mg. of the active agent, 100 mg. starch, and 5 mg. magnesium stearate. The capsules are administered daily or twice a day to achieve a daily dosage of 500 mg. per day.
  • Example 12 Example 12
  • a preparation for application to the skin or mucosa may be prepared in the following manner: Ingredient %w/w
  • Example 13 A formulation for administration as a retention enema may be formulated in the following manner:
  • Example 14 When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
  • Example 14 When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
  • Example 15 To 15 ml of phosphate buffered saline is added 3 mg of compound #11. The composition is placed in a bottle having a stopper with a smooth glass rod extending into the solution. The composition is applied to boils using the smooth glass rod as an applicator. The composition may also be administered as a spray from a bottle with an atomizer.
  • Example 15 To 15 ml of phosphate buffered saline is added 3 mg of compound #11. The composition is placed in a bottle having a stopper with a smooth glass rod extending into the solution. The composition is applied to boils using the smooth glass rod as an applicator. The composition may also be administered as a spray from a bottle with an atomizer.
  • Example 15 Example 15:
  • Example 16 To a 4 X 4 inch bandage having a smooth surface on one side there is applied to the smooth surface .02 ml of the solution prepared as a 2 ⁇ M solution of active agent designated # 4 in PBS . The prepared bandage is then enclosed in a foil covering which is made air-tight. For application, the bandage is unwrapped and is applied smooth side down on the wound .
  • Example 16 To a 4 X 4 inch bandage having a smooth surface on one side there is applied to the smooth surface .02 ml of the solution prepared as a 2 ⁇ M solution of active agent designated # 4 in PBS . The prepared bandage is then enclosed in a foil covering which is made air-tight. For application, the bandage is unwrapped and is applied smooth side down on the wound .
  • Example 16 Example 16:
  • a composition is prepared for use on the skin or mucosa in the following manner: Ingredient %w/w
  • Phosphate buffered saline 86.5% When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
  • composition prepared as a gel for application to the skin :
  • composition prepared for administration as a supposi- tory is a composition prepared for administration as a supposi- tory:
  • composition for intravenous administration comprising:
  • Desbutylhalofantrine 300 mg. 10% glucose in 1/2 normal saline to 300 ml.
  • compositions for intravenous administration are particularly valuable for administration intravenously during heart surgery and to patients suffering from endocar- ditis.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

This invention relates to compounds of general formula (Y) wherein A is an aromatic hydrocarbon ring system and R1 is a carbon bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon and wherein at least one of R2, R3 and R4 is an electron-rich substituent. The active agents are useful for treating patients suffering from infections including gram positive organisms, such as streptococcus, staphylococcus, anthracis, gram negative bacteria such as neisseria species, yeasts and mycobacterium. They are effective against strains which have shown resistance to other antimicrobial agents.

Description

Title: Substituted Aromatic Compounds for Treatment of Antibiotic Resistant Infections
Field of the Invention:
This invention relates to the treatment of antibiotic- resistant infections, including particularly infections caused by bacteria, mycobacteria , fungi and yeasts. A preferred group of compositions of the invention contain as active agents compounds containing aryl ring systems, including phenyl, naphthyl and anthracene ring systems, substituted by a carbon bound to an oxygen which is also bound to a nitrogen through a saturated carbon or carbon chain which may be substituted with halo, hydroxy, alkoxy, amino or alkylamino are disclosed, In preferred embodiments, the aryl ring system is further substituted by at least two halo substituents or halo-substituted substituents. Background of the Invention:
The benefit from use of antibiotics as a means of treating infections has been increasingly compromised by the development of resistant strains of microorganisms. Most of the new drugs are derivatives of older compounds. It is necessary to develop new agents that will respond to the current needs for medicinals that will effectively control pathogenic microbial populations that are resistant to antibiotics.
Halofantrine is a known antimalarial having a phenan- threne ring system substituted by a carbon bound to an oxygen which is also bound to a nitrogen through a saturated CH2-CH2 chain to tertiary nitrogen having two butyl substituents. The phenanthrene ring system is further substituted with 2 chlorines and one trifluoromethyl. Summary of the Invention:
This invention relates to compounds of the general formula: wherein A is a aromatic hydrocarbon ring system and R1 is a carbon bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon and wherein at least one of R2, R3 and R is an electron-rich substituent.
The active agents are useful for treating patients suffering from infections including gram positive organisms, such as streptococcus, staphylococcus, anthracis, gram negative bacteria such as neisseria species, yeasts and mycobacterium. These compounds are effective against strains which have shown resistance to other antimicrobial agents . Detailed Description of the invention:
This invention relates to compounds that have use in treating several infectious diseases which are now resistant to treatment to conventionally used antibiotics. Some of the compounds described herein have had previously been suggested for use in treating malaria. Some of the compounds are newly discovered. Most of the compounds are lipophilic. The lipid solubility of these compounds should permit the drugs to enter into cells, including cells of the central nervous system. Many of the compounds could be also be absorbed from the intestinal tract when given orally. They may be administered as cyclodextrin inclusion complexes to increase bioavailability. They may also be administered transdermally. Using patches for transdermal administration makes it possible to more easily control dosage.
The active agents for use in accord with the teachings of this disclosure are of the general formula:
wherein A is an aromatic ring system and R1 is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon. R1 is of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carbox- yl , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, a ino, or alkyl a ino group, X is (CH2) LN( (CH2) n(CH3) )m wherein is 1-3, n is <6, m is 1 vor 2 with the proviso that when m is 2, at least one n is <3, or X may be (CH2)oJ wherein 0 is 0-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phe- noxy, phenylalkyl, phenylalkoxy , carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, including keto or ester moieties with alkyl groups of 1-4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons. Regarding substituents of R2(a) , R3(a) and R4(a), a may be 0-4 with the proviso that at least one a is not 0. R2, R3 and R4 may be alkyl (including cycloalkyl) , a saturated, nitrogen-containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl , carboxyalkyl, hydroxy, halo, alkenyl, alkenyloxy, haloalkyl (including perhaloalkyl) , wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings with the provision that at least one of R2, R3 and R is an electron-rich substituent. Z and X may be linked to form a heterocylic ring system. Furthermore, any alkyl or aryl at R2, R3 and R4 may be further substituted with aryl of 1-2 rings, halo, (including multiple halo substitutions) alkyl, haloalkyl or alkoxy. Preferred halo substituents are chloro or bromo and a preferred haloalkyl is trifluoromethyl .
Compounds wherein X is (CH2)oJ and o is 2-4 are novel.
Particularly useful compounds are those of Formulas I, II, III and IV.
Formula I
In compounds of Formula I, any of R28 may be substituents designated under R2, R3 and R in the general formula above, with the proviso that at least one of R2_8 is an electron- rich substituent and any one of R]( R9 or R10 is a substituent as defined as R1 in the general formula. Preferred compounds are those having at least two halos groups on the compound, with chloro or trifluoromethyl being particularly preferred groups.
Formula II
In compounds of Formula II, any of R2_8 may be substituents identified as R2, R3 or R in the general formula with the proviso that at least one substituents is an electron-rich moiety and R1 is as designated for R1 (CHOZX) for the general formula above. Many of the preferred compounds have at least two halo or halo-substituted substituents.
Formula III
wherein R1 is defined as in the general formula and R2.6 is defined in the same manner as R2, R3 and R4 in the general formula. May of the preferred compounds have least two halo or halo-substituted substituents.
A particularly valuable compound of Formula II is of the formula:
Compounds of Formulas I, II and III can be made using the following methods: 3,5 -3ιs(Aryl)pheπyltoluene
Ar : Where X is mono- or di- halo, alkoxy, or halogen substituted alkyl. Otherwise X ishydrogen. Preparing starting materials :
PPA -H20
A general method for production:
0 O Li I I I I I CH-.C -NHR ÷ CH,CH2CH2CH2ϋ CH,C-NP nBu
NBS/CCI4 (PhVjP © <P) 1 )KO(Bu
ArCH, _ ArCH2Br : ArCH2P(Ph)3 Br 2 )HCHQ > ArCH=CH2
m-CI-Ph-COOH
R2NH
ArCHOHCH2NR2 ArCH CH2 Side Chain Introductions
NBS/CCI4 AgNO, ArCH3 >~ ArCH2Br *► ArCHO
(1)
Cf03 BH3 Pb(OAc),
ArCH3 — *- ArCOOH ^ ArCH2OH *- ArCHO
(2) PyrN2 (1)
BH,
(1) + Lι(CH nCN *- ArCHOH(CH2)ηCN *~ ArCHOH(CH2)nCH; H2 n=12
(1) + ArCHOHCH2CH2NHR
O \\ O u RH '
<1> + BrZnCH2CNR2 - ArCHOHCH2CNHR2 *~ ArCHOHCH2CH2NHR2
(2) EtQHH® » π Clasen j|
ArC— OEt *- ArCCH2C02Et
-CH2Br
ArCHOHCH2NR2
ArCHOHCH2NR2 -(Z-FIPERIDYL)-4, 5-DICHLORO-9 -ANTKR ACENEME THA OL ( R 2183^4)
CH,OCHCl,
2 -Pyrid ylhthium
AlClj, CH2C12
Compounds of the general formula wherein A is a phenan- threne ring are known. Compounds of the following formula:
Formula IV
wherein R1 is a carbon bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon and is of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxyl , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group, X is (CH2) ,N ( (CH2) n(CH3) )m wherein , is 1-3, n is <6, m is 1 or 2 with the proviso that when m is 2 , at least one n is <3, or X may be (CH2)oJ as defined in the general formula, wherein R2 and R3 are as defined in the general formula and a is 0 to 3 , with the proviso that for at least one of R2 or R3 a is 1 - 3. Preferred halo substituents are chloro or bromo and preferred haloalkyl is tri- fluoromethyl . A particularly useful member of this group of compounds is desbutylhalofantrin, a compound of the formula: which has now been found to be superior to halofantrine for treatment of malaria. (See U.S. Patent 5,711,966, which is incorporated herein by reference in its entirety.)
The phenanthrenes may be made by several methods, including the following scheme:
The phenanthrene compounds may also be prepared using the phenanthroic acid chlorides. Example 1:
To a solution of 2g of 10- (ω-bromoacetyl) -2 , 7- dichlorophenanthrene in 25 ml of THF is added 2.9 g. of di- n-heptylamine in 5 ml of THF at ambient temperature. After one hour, the THF is evaporated, the residue triturated with pentane, and filtered. The pentane residue is dissolved in EtOH/THF and reacted with 0.42 g of NaBH4 for 1.5 hours. The resulting reaction mixture is concentrated, the diluted with H2H, extracted with Et20, and acidified with gaseous HC1 to yield the dichlorophenanthraceneaminoalcohol HC1 salt.
Several active agents of the invention were tested for activity against several infectious organisms. Some of the methods used in testing are described below. Media:
The strains were streaked on blood agar plates (trypti- case soy broth containing 5% sheep cells) . A single colony was isolated and grown in Mueller-Hinton Broth (MHB) as recommended by the national Committee for Clinical Laboratory Standards for rapidly growing bacteria. Candida species and related yeasts were isolated in a similar manner on brain-heart infusion agar (BHI) . Susceptibility tests: The antibiotic susceptibility profile of each strain was determined using standard microtiter dilution plates obtained from the Clinical Microbiology Laboratory at Ohio State University Hospitals. The Inocula were prepared by suspending a 4 hour log phase growth in MHB visually egual in turbidity of an 0.5 McFarland standard. Inocula were further diluted and added to microdilution trays to achieve a final density of approximately 1 x 105 CFU/ml . The trays were incubated for 16 to 20 hours at 35 °C. The highest dilution at which wells remained clear was considered to be the minimum inhibitory concentration (MIC) .
The MIC and minimum bacterial concentration (MBC) of the strains to the active agents were determined by two-fold dilutions in Mueller-Hinton broth. Susceptibility tests for ATCC-obtained microorganisms and clinical isolates of gram positive bacteria including methicillin-susceptible and resistant staphylococci , streptococci, pneumococci and gram negative bacteria, including Enterobacteriaceae, Pseudomo- nas, Hemophilus and Neisseria, were performed in microtiter plates as described above.
Compounds of the invention were dissolved in 1 ml of methanol and stored in aliguots at -70 °C. They were diluted in Mueller-Hinton broth for final screening. Compositions were tested in 0.1 ml volumes by serial dilution in microtiter plates against Staphylococcus aureus methicillin- sensitive ATCC 29213 and the ethicillin-resistant wild type T67738, as described above. The T67738 was resistant to most antimicrobial drugs, including ciprofloxacin.
The most active compounds were studied further by time and dose-related killing curve analysis using large inocula (1 X 107 CFU/ml) .
The dosage and method of administration will depend on the location of the infection, the condition of the patient and the availability of professional supervision. Methods of administration include parenteral, oral, buccal, nasal or endotracheal routes. The active agents may be administered as sprays. For nasal administration, the active agent may be delivered as a powder that is snorted. Inclusion complexes such as cyclodextrin inclusion complexes would be particularly useful for buccal administration of these active agents.
The compounds of the invention may also be admin- istered topically by any means, including by rectal route.
Suppositories, solutions for use as retention enemas, and creams or jellies are appropriate carriers for use in rectal administration. The agents may be administered directly to infected tissue. For example, in case of open wounds, the active agents may be administered in the form of sprays or ointments.
Compounds of the invention may be applied to the skin or mucosa, including the vaginal mucosa, using creams, jellies, suppositories, or solutions. The active agents of the invention may be delivered directly to the epithelial tissue topically. For example, during surgery compositions containing the active agents of the invention to the applied directly to target tissues and prosthetic devices. The compositions could be given by aerosol into the trachea or administered in mist along with other agents into the respiratory tract. The compositions of the invention may also be used prophylactically to protect from infection by pathogenic organisms .
Dosage forms containing about 25 to 1000 mg for administration by mouth are suggested for use in adults. Howev- er, because the condition and size of the patient and the infectring organisms may differ greatly, eventual dosage requirements must be adjusted by the physician. Hence, dosage suggestions are provided to give general guidance to those of skill in the art. In accord with the purposes of providing such guidance, the following data is provided. The information provided is useful
The concentration required to provide benefit was studied in culture and provides guidance for effective concentration in the blood of the infected animal. The results of these studies may be seen in Tables I and II
TABLE I:
Active agent: Effective Concentration
R1 CHOZX other substitutions: S. Aureous (Resist).
Formula I
Z=H, X=CH2-(2-piperidinyl) R2 and R4 are Cl 3.1 μg/ml ( R 218394)
Formula II
Z=H, X=CH2-(2-piperidinyl) R, = Cl R7 = OCH,
(WR 184366) R, 4-Cl-phenyl 3 . 13 μg/ml (the acetate)
Z=H, X=CH2-(2-piperidinyl) R6 = Cl , R7 = 0CH3 ,
(WR 185308) R, = 3 , 4 dichloro-phenyl 6 . 25 μg/ml (the acetate)
The above compounds are also important for use in treatment of mycobacterial and fungal infections. Other compounds include those of the formula:
Formula I
R1 is CHOZX and Z=H, X=CH2-N (C H9) (C3H7) R5 and R6 are Cl (WR 201674)
R1 is CHOZX and Z=H, X= (CH2) 2NHC3H7 R, is Cl (WR 198118)
R1 is CHOZX and Z=H, X= (CH2) 2NHC3H7 R, is Cl, R. is CF, (WR 201683)
Formula II
Z=H, X=CH2-(2-piperidinyl) R6=C1, R7=CF3, R3=4-C1 -phenyl Z=H, X=CH2-(2-piperidinyl) R6=CF3, R7=OCH3, R3=3,4 dichloro-phenyl Formula III
Z=H, X=CH2-(2-piperidinyl) R3 and R5 are 4-Cl-phenyl Z=H, X=CH2-(2-piperidinyl) R3=C1, R5=4-OCH3-phenyl Z=H, X=CH2CH2(2-piperidinyl) R3=C1, R5=4-OCH3-phenyl
Formula IV
Active agent: Effective Concentration
Aureous
Sens. Resist. Mycobacteria
H piperidinyl (#1) CF3 1 CF3 1 1.56
H piperidinyl (#2) Cl 1 CF3 1 3.3
H piperidinyl (#3) Cl 2 CF3 1 3.0
H piperidinyl (#4) Br 1 Br 1 1.5
HH p piippeerriiddiinnyyll ( (##55)) CCll 11 CCll 11 .75
H CH2-piperidinyl (#6) Cl 1 Cl 1 1.56
H piperidinyl (#7) CF3 2 Cl 2 3.0
H piperidinyl (#8) CF3 1 CF3 1 6.2
H CH2-piperidinyl ( #9 ) Cl 2 CF3 1 0.8
H CH2NHCH(CH2CH3)2 (#11) CF3 1 CF3 1 3.3 H (CH2)NH(CH2)3CH3 (#12) CF3 1 Cl 2 1.56
Example 2 :
Capsules of a formulation of active agent designated #184366 for oral administration are prepared by containing 250 mg. of the active agent, 100 mg. starch, and 5 mg. magnesium stearate. The capsules are administered daily or twice a day to achieve a daily dosage of 500 mg. per day. Example 3 :
A preparation for application to the skin or mucosa may be prepared in the following manner: Ingredient %w/w
Compound #185308 15.0% glyceryl monostearate 3.0%
Petrolatum 83.5%
Example 4 : A formulation for administration as a retention enema may be formulated in the following manner:
Ingredient w/w %
Compound #218394 15%
Propylene glycol 85%
When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities. Example 5:
To 15 ml of phosphate buffered saline is added 3 mg of compound #185308. The composition is placed in a bottle having a stopper with a smooth glass rod extending into the solution. The composition is applied to boils using the smooth glass rod as an applicator. The composition may also be administered as a spray from a bottle with an atomizer. Example 6 :
To a 4 X 4 inch bandage having a smooth surface on one side there is applied to the smooth surface .02 ml of the solution prepared as a 2 μM solution of active agent designated # 183308 in PBS. The prepared bandage is then enclosed in a foil covering which is made air-tight. For application, the bandage is unwrapped and is applied smooth side down on the wound. Example 7:
A composition is prepared for use on the skin or mucosa in the following manner:
Ingredient %w/w
Agent designated #201683 0.5% propylene glycol 13.0%
Phosphate buffered saline 86.5% When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
Example 8 :
A composition prepared as a gel for application to the skin:
Ingredient %w/w active agent #1843660 0.5% propylene glycol 10.0%
Polyethylene glycol 89.5% Example 9 :
A composition prepared for administration as a supposi- tory:
Ingredient (%w/w)
Active agent #185308 0.5 mg glyceryl monosterate 1.0 Gm hydrogenated coconut oil 1.0 Gm glyceryl monopalmitate 1.0 Gm Example 10:
A composition for intravenous administration is prepared comprising:
184366 300 mg. 10% glucose in 1/2 normal saline to 300 ml.
Regarding the compounds of Formula IV (Phenanthrenes) , the following examples are provided: Example 11: Capsules of a formulation of active agent designated
#1 for oral administration are prepared by containing 250 mg. of the active agent, 100 mg. starch, and 5 mg. magnesium stearate. The capsules are administered daily or twice a day to achieve a daily dosage of 500 mg. per day. Example 12 :
A preparation for application to the skin or mucosa may be prepared in the following manner: Ingredient %w/w
Compound #3 15.0% glyceryl monostearate 3.0%
Petrolatum 83.5%
Example 13 : A formulation for administration as a retention enema may be formulated in the following manner:
Ingredient w/w %
Compound #10 15%
Propylene glycol 85%
When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities. Example 14:
To 15 ml of phosphate buffered saline is added 3 mg of compound #11. The composition is placed in a bottle having a stopper with a smooth glass rod extending into the solution. The composition is applied to boils using the smooth glass rod as an applicator. The composition may also be administered as a spray from a bottle with an atomizer. Example 15:
To a 4 X 4 inch bandage having a smooth surface on one side there is applied to the smooth surface .02 ml of the solution prepared as a 2 μM solution of active agent designated # 4 in PBS . The prepared bandage is then enclosed in a foil covering which is made air-tight. For application, the bandage is unwrapped and is applied smooth side down on the wound . Example 16:
A composition is prepared for use on the skin or mucosa in the following manner: Ingredient %w/w
Agent designated #9 0.5% propylene glycol 13.0%
Phosphate buffered saline 86.5% When the active agent is administered to the mucosa of the oral cavity, it may be administered as a buccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
Example 17 :
A composition prepared as a gel for application to the skin:
Ingredient %w/w active agent designated #3 0.5% propylene glycol 10.0%
Polyethylene glycol 89.5% Example 18:
A composition prepared for administration as a supposi- tory:
Ingredient (%w/w)
Active agent #8 0.5 mg glyceryl monosterate 1.0 Gm hydrogenated coconut oil 1.0 Gm glyceryl monopalmitate 1.0 Gm Example 19:
A composition for intravenous administration is prepared comprising:
Desbutylhalofantrine: 300 mg. 10% glucose in 1/2 normal saline to 300 ml.
The compositions for intravenous administration are particularly valuable for administration intravenously during heart surgery and to patients suffering from endocar- ditis.

Claims

What we claim is:
1. A method of treating or preventing infection caused by bacteria, mycobacterium or fungi by administration of a composition containing as an active agent a bacteria, mycobacterium or yeast growth-inhibiting effective amount of a compound of the formula:
wherein A is a hydrocarbon aromatic ring system, R1 is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon or carbon chain, with R1 being of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be car- boxyl , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, addi- tionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group and X is (CH2) t N( (CH2) n(CH3) ) m wherein , is 1 to 3 , n is <6, m is 1 or 2 with the proviso that when m is 2, at least one of n is <3, or X may be (CH2)oJ wherein o is 0-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, and wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phenoxy, phenylalkyl, phenylalkoxy, carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, including keto or ester moieties, with alkyl groups having 1-4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons and, further, wherein X and Z may be linked to form a heterocyclic ring system and (a) is 0- 4 with the proviso that at least one of (a) is not 1, R2, R3 and R4 may be alkyl (including cycloalkyl) , a saturated, nitrogen-containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl , amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl , arylalkylaminoalkyl , carboxyalkyl, hydroxy, halo, alkenyl, or alkenyloxy, halo-substituted alkyl, wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings and wherein any alkyl or aryl at R2, R3 and R4 may be further substituted with halo (including multiple halo subtitutions) , aryl of 1-2 rings, alkyl, haloalkyl or alkoxy, with the proviso that at least one of R2, R3 and R4 is an electron-rich substituent.
A method of claim 1 of treating or preventing infection caused by bacteria, mycobacterium or fungi by administration of a composition containing as an active agent a bacteria, mycobacterium or yeast growth-inhibiting effective amount of a compound of the formula:
Formula I
wherein any of R2, R3, R4, B^ , R6, R7 and R8 may be H, alkyl (including cycloalkyl) , a saturated, nitrogen- containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl, carboxyalkyl, hydroxy, halo, alkenyl, or alkenyloxy, halo-substituted alkyl, wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings and wherein any alkyl or aryl may be further substituted with halo (including multiple halo subtitutions) , aryl of 1-2 rings, alkyl, haloalkyl or alkoxy, with the proviso that at least one of R2, R3, R, R5, R6, R7 and R8 is an electron-rich substituent and one of R1 , Rg or R10 is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon or carbon chain, being of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxy1 , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group and X is (CH2) tN( (CH2)n(CH3) )m wherein , is 1-3, n is <6 , m is
1 or 2 with the proviso that when m is 2 , at least one n is <3, or X may be (CH2)oJ wherein o is 0-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, and wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phe- noxy, phenylalkyl, phenylalkoxy, carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, includ- ing keto or ester moieties, with alkyl groups having 1-
4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons and, furthermore, X and Z may be linked to form a heterocyclic ring system.
3. A method of claim 2 wherein at least two of R2, R3, R4, Rc5 ' , R ^6, ' , R-, and R„ are Cl or F3C .
4. A method of claim 2 wherein Z=H, X=CH2~ (2-piperidine) R2 and R4 are Cl .
5. A method of claim 2 wherein Rg is CHOZX and Z=H, X=CH2- N(C4H9) (C3H7) and R5 and R6 are Cl .
A method of claim 2 wherein R1 is CHOZX and Z=H, X=(CH2)2NH(C3H7) and R3 is Cl .
A nethod of claim 2 wherein R1 is CHOZX and Z=H, X=(CH2)2NH(C3H7) , R3 is Cl and R5 is CF3.
A method of of claim 1 of treating or preventing infection caused by bacteria, mycobacterium or fungi by administration of a composition containing as an active agent a bacteria, mycobacterium or yeast growth-inhibiting effective amount of a compound of the formula:
Formula II
wherein any of R2, R3, R4, R5, R6, R7 and R8 may be H, alkyl (including cycloalkyl) , a saturated, nitrogen- containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl, carboxyalkyl, hydroxy, halo, alkenyl, or alkenyloxy, halo-substituted alkyl, wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings and wherein any alkyl or aryl may be further substi- tuted with halo (including multiple halo subtitutions) , aryl of 1-2 rings, alkyl, haloalkyl or alkoxy, with the proviso that at least one of R2, R3, R4, R5, R6, R7 and R8 is an electron-rich substituent and one of R1 , is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon or carbon chain, being of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxyl , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group and X is (CH2) (N( (CH2)n(CH3) )m wherein L is 1-3, n is <6 , m is 1 or 2 with the proviso that when m is 2 , at least one n is <3, or X may be (CH2)oJ wherein o is 0-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, and wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phe- noxy, phenylalkyl, phenylalkoxy, carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, includ- ing keto or ester moieties, with alkyl groups having 1-
4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons and, furthermore, X and Z may be linked to form a heterocyclic ring system.
9. A method of claim 8 wherein Z=H, X=CH2- (2-piperidine) R6 = Cl, R7 = OCH3, R3 = 4-Cl-phenyl.
10. A method of claim 8 wherein Z=H, X=CH2- (2-piperidine) R6 = Cl, R7 = 0CH3, R3 = 3,4 dichloro-phenyl .
11. A method of claim 8 wherein Z=H, X=CH,- (2-piperidine) R6=C1 , R7=CF3 , R3=4 -C1 -phenyl .
12 . A method of claim 8 wherein Z=H, X=CH2~ ( 2-piperidine) R6=CF3 , R7=OCH3 , R3=3 , 4-diclhoro-phenyl .
13. A method of claim 1 of treating or preventing infection caused by bacteria, mycobacterium or fungi by administration of a composition containing as an active agent a bacteria, mycobacterium or yeast growth-inhibiting effective amount of a compound of the formula:
Formula III
wherein any of R2, R3, R4, R5, and R6, may be H, alkyl (including cycloalkyl) , a saturated, nitrogen-containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl, carboxyalkyl, hydroxy, halo, alkenyl, or alkenyloxy, halo-substituted alkyl, wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings and wherein any alkyl or aryl may be further substituted with halo (including multiple halo subtitutions) , aryl of 1-2 rings, alkyl, haloalkyl or alkoxy, with the proviso that at least one of R2, R3, R4, Rg, R6, R7 and R8 is an electron-rich substituent and one of R1 , is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon or carbon chain, being of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxyl, ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group and X is (CH2) tN( (CH2)n(CH3) )m wherein ^ is 1-3, n is <6, m is 1 or 2 with the proviso that when m is 2 , at least one n is <3, or X may be (CH2)oJ wherein o is 0-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, and wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phe- noxy, phenylalkyl, phenylalkoxy, carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, including keto or ester moieties, with alkyl groups having 1- 4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons, and, furthermore, X and Z may be linked to form a heterocyclic ring system.
14. A method of claim 13 wherein Z=H, X=CH2- (2-piperidine) R3 and R5 are 4-Cl-phenyl.
15. A method of claim 13 wherein Z=H, X=CH2~ (2-piperidine) R3=C1, R5=4-OCH3-phenyl.
16. A method of claim 13 wherein Z=H, X=CH2CH2 (2-piperidine) R3=C1, R5=4-OCH3-phenyl
17. A method of of claim 1 of treating or preventing infec- tion caused by bacteria, mycobacterium or fungi by administration of a composition containing as an active agent a bacteria, mycobacterium or yeast growth-inhibiting effective amount of a compound of the formula: Formula IV
wherein any (a) is 1-3 and R2, and R3, may be H, alkyl
(including cycloalkyl) , a saturated, nitrogen-containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl-aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl, carboxy- alkyl, hydroxy, halo, alkenyl, or alkenyloxy, halo- substituted alkyl, wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings and wherein any alkyl or aryl may be further substituted with halo (including multiple halo subtitutions) , aryl of 1-2 rings, alkyl, haloalkyl or alkoxy, with the proviso that at least one of R2, R3, R4, R5, R6, R7 and R8 is an electron-rich substituent and one of R1 , is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon or carbon chain, being of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxy1 , ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group and X is (CH2)tN( (CH2)n(CH3) ) m wherein , is 1-3, n is <6, m is 1 or 2 with the proviso that when m is 2 , at least one n is <3, or X may be (CH2)0J wherein o is 0-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, and wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phe- noxy, phenylalkyl, phenylalkoxy, carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, including keto or ester moieties, with alkyl groups having 1- 4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons, and, furthermore,
X and Z may be linked to form a heterocyclic ring system.
18. A method of claim 17 wherein the active agent is desbutyl- halofantrine.
19. A method of claim 17 wherein the active agent is chosen from among compounds wherein
H piperidinyl (#1) CF3 1 CF3 1
H piperidinyl (#2) Cl 1 CF3 1
H piperidinyl (#3) Cl 2 CF3 1
H piperidinyl (#4) Br 1 Br 1 H piperidinyl (#5) Cl 1 Cl 1
H CH2-piperidinyl (#6) Cl 1 Cl 1
H piperidinyl (#7) CF3 2 Cl 2
H piperidinyl (#8) CF3 1 CF3 1
H CH2-piperidinyl(#9) Cl 2 CF3 1
H CH2NHCH(CH2CH3)2 (#11) CF3 1 CF3 1
H (CH2)NH(CH2)3CH3 (#12) CF3 1 Cl 2
0. A compound of the formula:
wherein A is a hydrocarbon aromatic ring system, R1 is bound directly to an oxygen and is also bound to a nitrogen through a saturated carbon or carbon chain, with R1 being of the structure CHOZX wherein Z may be hydrogen, a second bond to the oxygen, or may be carboxy1, ether or ester moiety wherein the ether or ester moiety may be alkyl of 1-8 carbons, phenyl, phenylalkyl, wherein the alkyl moiety consists of 1-4 carbons and wherein any said alkyl or phenyl group may, additionally, be substituted with hydroxy, alkyl of 1-2 carbons, alkenyl of 2-3 carbons, halo, amino, or alkyl amino group and X (CH2)oJ wherein o is 2-4 and J is a saturated nitrogen-containing ring system with up to 10 carbon atoms in the ring system and may have up to 4 bridge carbons, and wherein any saturated ring system may be substituted with alkyl, alkenyl, halo, alkoxy or haloalkyl moieties of 1-5 carbons or with phenyl, phenoxy, phenylalkyl, phenylalkoxy, carboxy or carbonyl groups, wherein the carboxy or carbonyl groups, including keto or ester moieties, with alkyl groups having 1-4 carbons, alkenyl groups of 2-5 carbons or phenylalkyl wherein the alkyl is of 1-3 carbons or phenylalkoxy wherein the alkyl is of 1-3 carbons, and (a) is 0-4 with the proviso that at least one of (a) is not 1, R2, R3 and R4 may be alkyl (including cycloalkyl) , a saturated, nitrogen-containing ring of 4-10 atoms, alkoxy, aryl, aryloxy, aryloxyalkyl, amino, amino-alkyl, alkyl- aminoalkyl, arylamino, alkenyl, arylalkenyl, arylalkylaminoalkyl, carboxyalkyl, hydroxy, halo, alkenyl, or alkenyloxy, halo-substituted alkyl, wherein any alkyl has 1-8 carbons, alkenyl has 2-8 carbons, wherein halo is chloro, fluoro or bromo and aryl is a ring system of 1-3 rings and wherein any alkyl or aryl at R2, R3 and R may be further substituted with halo (including multiple halo subtitutions) , aryl of 1-2 rings, alkyl, haloalkyl or alkoxy, with the proviso that at least one of R2, R3 and R4 is an electron-rich substituent.
21. A compound of claim 20 wherein A is a benzene ring.
22. A compound of claim 20 wherein A is a phenanthrene ring.
23. A compound of claim 20 wherein A is naphthalene ring.
24. A compound of claim 20 wherein A is anthracene ring.
EP99911497A 1998-03-26 1999-03-25 Substituted aromatic compounds for treatment of antibiotic resistant infections Withdrawn EP1066035A4 (en)

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