WO2007025798A2 - 4-aryloxy quinoline derivatives as 5-ht6 modulators - Google Patents
4-aryloxy quinoline derivatives as 5-ht6 modulators Download PDFInfo
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/40—Nitrogen atoms attached in position 8
Definitions
- This invention relates to aryloxy quinoline compounds, and associated compositions, methods for use as therapeutic agents, and methods of preparation thereof.
- n is an integer from 0 to 3;
- Ar is optionally substituted aryl or optionally substituted heteroaryl
- R 3 is hydrogen, or alkyl; s is from 0 to 2; and each of R c and R d is independently hydrogen or alkyl; and a is 1 or 2; each of R 5 and R 6 is independently hydrogen or alkyl;
- R 7 is hydrogen, alkyl, alkoxy, or -NR 8 R 9 ; and each of R 8 and R 9 is independently hydrogen or alkyl, or a pharmaceutically acceptable salt thereof.
- the present invention also provides methods for preparing, compositions comprising, and methods for using the aforementioned compounds.
- 5-hydroxytryptamine (5-HT) as a major modulatory neurotransmitter in the brain are mediated through a number of receptor families termed 5-HT1, 5-HT2, 5- HT3, 5-HT4, 5-HT5, 5-HT6, and 5-HT7. Based on a high level of 5- HT6 receptor mRNA in the brain, it has been stated that the 5-HT6 receptor may play a role in the pathology and treatment of central nerve system disorders.
- 5- HT2-selective and 5-HT6 selective ligands have been identified as potentially useful in the treatment of certain CNS disorders such as Parkinson's disease, Huntington's disease, anxiety, depression, manic depression, psychoses, epilepsy, obsessive compulsive disorders, mood disorders, migraine, Alzheimer's disease (enhancement of cognitive memory), sleep disorders, feeding disorders such as anorexia, bulimia and obesity, panic attacks, akathisia, attention deficit hyperactivity disorder (ADHD), attention deficit disorder (ADD), withdrawal from drug abuse such as cocaine, ethanol, nicotine and benzodiazepines, schizophrenia, and also disorders associated with spinal trauma and/or head injury such as hydrocephalus.
- CNS disorders such as Parkinson's disease, Huntington's disease, anxiety, depression, manic depression, psychoses, epilepsy, obsessive compulsive disorders, mood disorders, migraine, Alzheimer's disease (enhancement of cognitive memory), sleep disorders, feeding disorders such as anorexia, bulimia and obesity, panic
- Such compounds are also expected to be of use in the treatment of certain gastrointestinal (GI) disorders such as functional bowel disorder.
- GI gastrointestinal
- Such compounds are also expected to be of use in the treatment of certain gastrointestinal (GI) disorders such as functional bowel disorder.
- GI gastrointestinal
- Such compounds are also expected to be of use in the treatment of certain gastrointestinal (GI) disorders such as functional bowel disorder.
- GI gastrointestinal
- the invention provides substituted quinoline compounds, associated compositions, methods for use as therapeutic agents, and methods of preparation thereof.
- One embodiment of the present invention provides piperazinyl- substituted quinoline compounds and associated pharmaceutical compositions, and methods for using the same in the treatment of central nervous system (CNS) diseases and gastrointestinal tract disorders.
- CNS central nervous system
- Alkyl means the monovalent linear or branched saturated hydrocarbon moiety, consisting solely of carbon and hydrogen atoms, having from one to twelve carbon atoms.
- “Lower alkyl” refers to an alkyl group of one to six carbon atoms (i.e., "Ci-C ⁇ alkyl”). Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, isobutyl, sec-butyl, tert-butyl, pentyl, n-hexyl, octyl, dodecyl, and the like.
- Alkoxy means a moiety of the formula -OR, wherein R is an alkyl moiety as defined herein.
- alkoxy moieties include, but are not limited to, methoxy, ethoxy, isopropoxy, and the like.
- Antagonist refers to a compound that diminishes or prevents the action of another compound or receptor site.
- Aryl means a monovalent cyclic aromatic hydrocarbon moiety consisting of a mono-, bi- or tricyclic aromatic ring.
- the aryl group can be optionally substituted as defined herein.
- aryl moieties include, but are not limited to, phenyl, naphthyl, naphthalenyl, phenanthryl, fluorenyl, indenyl, pentalenyl, azulenyl, oxydiphenyl, biphenyl, methylenediphenyl, aminodiphenyl, diphenylsulfidyl, diphenylsulfonyl, diphenylisopropylidenyl, benzodioxanyl, benzofuranyl, benzodioxylyl, benzopyranyl, benzoxazinyl, benzoxazinonyl, benzopiperadinyl, benzopiperazinyl, benzopyrrolidinyl, benzomorpholin
- Cycloalkyl means a saturated carbocyclic moiety consisting of mono- or bicyclic rings. Cycloalkyl can optionally be substituted with one or more substituents, wherein each substituent is independently hydroxy, alkyl, alkoxy, halo, haloalkyl, amino, monoalkylamino, or dialkylamino, unless otherwise specifically indicated. Examples of cycloalkyl moieties include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and the like, including partially unsaturated derivatives thereof such as cyclohexenyl, cyclopentenyl, and the like. "Cycloalkylalkyl” means a moiety of the formula -R'-R", where R' is alkylene and R" is cycloalkyl as defined herein.
- Heteroalkyl means an alkyl radical as defined herein wherein one, two or three hydrogen atoms have been replaced with a substituent independently selected from the group consisting of -OR a , -NR b R c , and -S(O) n R d (where n is an integer from 0 to 2), with the understanding that the point of attachment of the heteroalkyl radical is through a carbon atom, wherein R a is hydrogen, acyl, alkyl, cycloalkyl, or cycloalkylalkyl; R b and R c are independently of each other hydrogen, acyl, alkyl, cycloalkyl, or cycloalkylalkyl; and when n is 0, R d is hydrogen, alkyl, cycloalkyl, or cycloalkylalkyl, and when n is 1 or 2, R d is alkyl, cycloalkyl, cycloalkylalkyl, amino, acyl
- Representative examples include, but are not limited to, 2-hydroxyethyl, 3- hydroxypropyl, 2-hydroxy- l-hydroxymethylethyl, 2,3-dihydroxypropyl, 1- hydroxymethylethyl, 3-hydroxybutyl, 2,3-dihydroxybutyl, 2-hydroxy- l-methylpropyl, 2- aminoethyl, 3-aminopropyl, 2-methylsulfonylethyl, aminosulfonylmethyl, aminosulfonylethyl, aminosulfonylpropyl, methylaminosulfonylmethyl, methylaminosulfonylethyl, methylaminosulfonylpropyl, and the like.
- Heteroaryl means a monocyclic or bicyclic monovalent radical of 5 to 12 ring atoms having at least one aromatic ring containing one, two, or three ring heteroatoms selected from N, O, or S, the remaining ring atoms being C, with the understanding that the attachment point of the heteroaryl radical will be on an aromatic ring.
- the heteroaryl ring may be optionally substituted as defined herein.
- heteroaryl moieties include, but are not limited to, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, oxadiazolyl, thiadiazolyl, pyrazinyl, thienyl, benzothienyl, thiophenyl, furanyl, pyranyl, pyridyl, pyridinyl, pyridazyl, pyrrolyl, pyrazolyl, pyrimidyl, quinolinyl, isoquinolinyl, benzofuryl, benzothiophenyl, benzothiopyranyl, benzimidazolyl, benzooxazolyl, benzooxadiazolyl, benzothiazolyl, benzothiadiazolyl, benzopyranyl, indolyl, isoindolyl, triazolyl, triazinyl, quinoxalinyl,
- Haloalkyl means alkyl as defined herein in which one or more hydrogen has been replaced with same or different halogen.
- exemplary haloalkyls include -CH 2 Cl, -CH 2 CF 3 , -CH 2 CCl 3 , perfluoroalkyl (e.g., -CF 3 ), and the like.
- Optionally substituted when used in association with "aryl", or “heteroaryl” means an aryl, or heteroaryl that is optionally substituted independently with one or more, e.g., one to four substituents, preferably one or two substituents, selected from alkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, hydroxyalkyl, halo, nitro, cyano, hydroxy, alkoxy, amino, acylamino, mono-alkylamino, di-alkylamino, haloalkyl, haloalkoxy, heteroalkyl, -COR (where R is hydrogen, alkyl, phenyl or phenylalkyl), - (CR'R") n -COOR (where n is an integer from 0 to 5, R' and R" are independently hydrogen or alkyl, and R is hydrogen, alkyl, cycloalkyl, cycloalkylalkyl,
- leaving group means the group with the meaning conventionally associated with it in synthetic organic chemistry, i.e., an atom or group displaceable under substitution reaction conditions.
- Examples of leaving groups include, but are not limited to, halogen, alkane- or arylenesulfonyloxy, such as methanesulfonyloxy, ethanesulfonyloxy, thiomethyl, benzenesulfonyloxy, tosyloxy, and thienyloxy, dihalophosphinoyloxy, optionally substituted benzyloxy, isopropyloxy, acyloxy, and the like.
- Module means a molecule that interacts with a target. The interactions include, but are not limited to, agonist, antagonist, and the like, as defined herein.
- Disease state means any disease, condition, symptom, or indication.
- Inert organic solvent or “inert solvent” means the solvent is inert under the conditions of the reaction being described in conjunction therewith, including for example, benzene, toluene, acetonitrile, tetrahydrofuran, N,N-dimethylformamide, chloroform, methylene chloride or dichloromethane, dichloroethane, diethyl ether, ethyl acetate, acetone, methyl ethyl ketone, methanol, ethanol, propanol, isopropanol, tert- butanol, dioxane, pyridine, and the like.
- the solvents used in the reactions of the present invention are inert solvents.
- “Pharmaceutically acceptable” means useful in preparing a pharmaceutical composition that is generally safe, non-toxic, and neither biologically nor otherwise undesirable and includes that which is acceptable for veterinary as well as human pharmaceutical use.
- “Pharmaceutically acceptable salts” of a compound means salts that are pharmaceutically acceptable, as defined herein, and that possess the desired pharmacological activity of the parent compound.
- Such salts include: acid addition salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or formed with organic acids such as acetic acid, benzenesulfonic acid, benzoic, camphorsulfonic acid, citric acid, ethanesulfonic acid, fumaric acid, glucoheptonic acid, gluconic acid, glutamic acid, glycolic acid, hydroxynaphtoic acid, 2- hydroxyethanesulfonic acid, lactic acid, maleic acid, malic acid, malonic acid, mandelic acid, methanesulfonic acid, muconic acid,
- inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like
- organic acids such as acetic acid, benzenesulfonic acid, benzoic, camphorsulfonic acid, citric acid,
- Acceptable organic bases include diethanolamine, ethanolamine, N-methylglucamine, triethanolamine, tromethamine, and the like.
- Acceptable inorganic bases include aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate and sodium hydroxide.
- the preferred pharmaceutically acceptable salts are the salts formed from acetic acid, hydrochloric acid, sulfuric acid, methanesulfonic acid, maleic acid, phosphoric acid, tartaric acid, citric acid, sodium, potassium, calcium, zinc, and magnesium.
- pro-drug and “prodrug”, which maybe used interchangeably herein, refer to any compound which releases an active parent drug according to formula I in vivo when such prodrug is administered to a mammalian subject.
- Prodrugs of a compound of formula I are prepared by modifying one or more functional group(s) present in the compound of formula I in such a way that the modification(s) maybe cleaved in vivo to release the parent compound.
- Prodrugs include compounds of formula I wherein a hydroxy, amino, or sulfhydryl group in a compound of Formula I is bonded to any group that may be cleaved in vivo to regenerate the free hydroxyl, amino, or sulfhydryl group, respectively.
- prodrugs include, but are not limited to, esters (e.g., acetate, formate, and benzoate derivatives), carbamates (e.g., N ,N- dimethylaminocarbonyl) of hydroxy functional groups in compounds of formula I, N- acyl derivatives (e.g. N-acetyl) N-Mannich bases, Schiff bases and enaminones of amino functional groups, oximes, acetals, ketals and enol esters of ketone and aldehyde functional groups in compounds of Formula I, and the like, see Bundegaard, H. "Design of Prodrugs" pl-92, Elesevier, New York-Oxford (1985), and the like.
- esters e.g., acetate, formate, and benzoate derivatives
- carbamates e.g., N ,N- dimethylaminocarbonyl
- N- acyl derivatives e.g. N-acetyl
- Protecting group means the group which selectively blocks one reactive site in a multifunctional compound such that a chemical reaction can be carried out selectively at another unprotected reactive site in the meaning conventionally associated with it in synthetic chemistry. Certain processes of this invention rely upon the protective groups to block reactive nitrogen and/or oxygen atoms present in the reactants.
- the terms "amino-protecting group” and “nitrogen protecting group” are used interchangeably herein and refer to those organic groups intended to protect the nitrogen atom against undesirable reactions during synthetic procedures.
- Exemplary nitrogen protecting groups include, but are not limited to, triflu or o acetyl, acetamido, benzyl (Bn), benzyloxycarbonyl (carbobenzyloxy, CBZ), p- methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, t ⁇ t-butoxycarbonyl (BOC), and the like.
- Bn benzyloxycarbonyl
- CBZ benzyloxycarbonyl
- p- methoxybenzyloxycarbonyl p-nitrobenzyloxycarbonyl
- t ⁇ t-butoxycarbonyl BOC
- Solidvates means solvent addition forms that contain either stoichiometric or non stoichiometric amounts of solvent. Some compounds have a tendency to trap a fixed molar ratio of solvent molecules in the crystalline solid state, thus forming a solvate. If the solvent is water the solvate formed is a hydrate, when the solvent is alcohol, the solvate formed is an alcoholate. Hydrates are formed by the combination of one or more molecules of water with one of the substances in which the water retains its molecular state as H 2 O, such combination being able to form one or more hydrate.
- Subject means mammals and non-mammals. Mammals means any member of the mammalia class including, but not limited to, humans; non-human primates such as chimpanzees and other apes and monkey species; farm animals such as cattle, horses, sheep, goats, and swine; domestic animals such as rabbits, dogs, and cats; laboratory animals including rodents, such as rats, mice, and guinea pigs; and the like. Examples of non-mammals include, but are not limited to, birds, and the like. The term "subject” does not denote a particular age or sex.
- “Therapeutically effective amount” means an amount of a compound that, when administered to a subject for treating a disease state, is sufficient to effect such treatment for the disease state.
- the “therapeutically effective amount” will vary depending on the compound, disease state being treated, the severity or the disease treated, the age and relative health of the subject, the route and form of administration, the judgement of the attending medical or veterinary practitioner, and other factors.
- treating when referring to a chemical reaction means adding or mixing two or more reagents under appropriate conditions to produce the indicated and/or the desired product. It should be appreciated that the reaction which produces the indicated and/or the desired product may not necessarily result directly from the combination of two reagents which were initially added, i.e., there may be one or more intermediates which are produced in the mixture which ultimately leads to the formation of the indicated and/or the desired product.
- One aspect of the present invention provides compounds of the formula I:
- m is an integer from 0 to 3;
- X is -CH- or -N-;
- Ar is optionally substituted aryl or optionally substituted heteroaryl;
- R 1 is hydrogen, halo, alkyl, haloalkyl, heteroalkyl, alkoxy, cyano, -S(O) 8 -R 0 ,
- R 3 is hydrogen, or alkyl; s is from 0 to 2; and each of R c and R d is independently hydrogen or alkyl; and a is 1 or 2; each of R 5 and R 6 is independently hydrogen or alkyl;
- R 7 is hydrogen, alkyl, alkoxy, or -NR 8 R 9 ; and each of R 8 and R 9 is independently hydrogen or alkyl, or a pharmaceutically acceptable salt thereof.
- scope of the present invention encompasses not only the various isomers which may exist but also the various mixture of isomers which may be formed. Furthermore, the scope of the present invention also encompasses prodrugs, solvates and salts of compounds of formula I.
- X is N.
- R 1 is hydrogen, alkyl, or halo.
- R 1 is alkyl.
- R 1 is methyl.
- each R 2 is independently hydrogen, alkyl or halo. In some embodiments, R 2 is hydrogen.
- R 3 is hydrogen or alkyl. In specific embodiments, R 3 is hydrogen or methyl.
- m is 0.
- R c and R d are independently hydrogen or alkyl.
- compounds of Formula I is more specifically of the Formula IA:
- n is an integer from 0 to 5; and each R 4 is independently halo, alkyl, haloalkyl, heteroalkyl, alkoxy, cyano,
- each of R c and R d is independently hydrogen or alkyl; and a is 1 or 2; each of R 5 and R 6 is independently hydrogen or alkyl; R 7 is hydrogen, alkyl, alkoxy, or -NR 8 R 9 ; and each of R 8 and R 9 is independently hydrogen or alkyl; and m, R 1 , R 2 , and R 3 are as defined herein.
- n 0, 1 or 2.
- each R 4 is independently alkyl, alkoxy, or halo. Still in other embodiments, each R 4 is independently alkoxy or halo.
- each R 4 is independently methoxy, chloro or fluoro.
- compounds of Formula I is more specifically of the Formula IB:
- compositions comprising a therapeutically effective amount of at least one compound of Formula I and a pharmaceutically acceptable carrier.
- Yet another aspect of the invention provides a method for treating a central nervous system (CNS) disease state in a subject comprising administering to the subject a therapeutically effective amount of a compound of Formula I.
- the disease state may comprise, for example, psychoses, schizophrenia, manic depressions, neurological disorders, memory disorders, attention deficit disorder, Parkinson's disease, amyotrophic lateral sclerosis, Alzheimer's disease or Huntington's disease.
- Still another aspect of the present invention provides a method for treating a disorder of the gastrointestinal tract in a subject comprising administering to the subject a therapeutically effective amount of a compound of Formula I.
- Another aspect of the present invention provides a method for producing a compound of Formula I.
- the subject methods may comprise, in certain embodiments, reacting a quinoline compound of the formula:
- the starting materials and reagents used in preparing these compounds generally are either available from commercial suppliers, such as Aldrich Chemical Co., or are prepared by methods known to those skilled in the art following procedures set forth in references such as Fieser and Fieser's Reagents for Organic Synthesis; Wiley & Sons: New York, 1991, Volumes 1-15; Rodd's Chemistry of Carbon Compounds, Elsevier Science Publishers, 1989, Volumes 1-5 and Supplemental; and Organic Reactions, Wiley & Sons: New York, 1991, Volumes 1-40.
- the following synthetic reaction schemes are merely illustrative of some methods by which the compounds of the present invention can be synthesized, and various modifications to these synthetic reaction schemes can be made and will be suggested to one skilled in the art having referred to the disclosure contained in this Application.
- the starting materials and the intermediates of the synthetic reaction schemes can be isolated and purified if desired using conventional techniques, including but not limited to, filtration, distillation, crystallization, chromatography, and the like. Such materials can be characterized using conventional means, including physical constants and spectral data.
- the reactions described herein preferably are conducted under an inert atmosphere at atmospheric pressure at a reaction temperature range of from about -78 °C to about 150 °C, more preferably from about 0 °C to about 125 °C, and most preferably and conveniently at about room (or ambient) temperature, e.g., about 20 °C.
- Scheme A illustrates one synthetic procedure usable to prepare compounds of the invention, wherein m, Ar, R 1 , R 2 , and R 3 are as defined herein, and each of X and Yis independently a leaving group.
- X and Yare different leaving groups e.g., different halides, to allow selective reaction.
- X or Y selectively depending on the desired reaction.
- Numerous synthetic routes to quinolines are known and may be used in preparation of the subject compounds, and the procedure of Scheme A is only exemplary. Specific examples of the procedure of Scheme A are provided in the following Experimental section.
- a hydroxyl aryl compound A-I is deprotonated with a base, e.g., potassium tert-butoxide.
- a base e.g., potassium tert-butoxide.
- this deprotonation reaction is conducted under an inert aprotic solvent, such as THF.
- Reacting the resulting deprotonated aryloxide with quinoline compound A-2 then affords an aryloxy-substituted quinoline compound A-3.
- This latter reaction may be effected by heating under polar aprotic solvent conditions.
- deprotonation can be conducted in situ in the presence of the quinoline compound A-2.
- the aryloxy-substituted quinoline compound A-3 can be prepared from the hydroxyl aryl compound A- 1 is then coupled with a piperazinyl compound A-4, typically in the presence of a palladium coupling catalyst.
- R 3 is hydrogen or an amino-protecting group, it maybe replaced with other R 3 group, such as an alkyl group, following the coupling step to introduce a desired R 3 substituent of Formula I.
- the compounds of the invention have selective affinity for 5-HT receptors, including 5-HT 6 , and as such are expected to be useful in the treatment of certain CNS disorders such as Parkinson's disease, Huntington's disease, anxiety, depression, manic depression, psychosis, epilepsy, obsessive compulsive disorders, mood disorders, migraine, Alzheimer's disease (enhancement of cognitive memory), sleep disorders, feeding disorders such as anorexia, bulimia, and obesity, panic attacks, akathisia, attention deficit hyperactivity disorder (ADHD), attention deficit disorder (ADD), withdrawal from drug abuse such as cocaine, ethanol, nicotine and benzodiazepines, schizophrenia, and also disorders associated with spinal trauma and/or head injury such as hydrocephalus.
- CNS disorders such as Parkinson's disease, Huntington's disease, anxiety, depression, manic depression, psychosis, epilepsy, obsessive compulsive disorders, mood disorders, migraine, Alzheimer's disease (enhancement of cognitive memory), sleep disorders, feeding disorders such as anorexia,
- the pharmacology of the compounds of this invention was determined by art recognized procedures.
- the in vitro techniques for determining the affinities of test compounds at the 5-HT6 receptor in radioligand binding and functional assays are described in Example 9.
- the present invention includes pharmaceutical compositions comprising at least one compound of the present invention, or an individual isomer, racemic or non- racemic mixture of isomers or a pharmaceutically acceptable salt or solvate thereof, together with at least one pharmaceutically acceptable carrier, and optionally other therapeutic and/or prophylactic ingredients.
- the compounds of the present invention will be administered in a therapeutically effective amount by any of the accepted modes of administration for agents that serve similar utilities. Suitable dosage ranges are typically 1-500 mg daily, preferably 1-100 mg daily, and most preferably 1-30 mg daily, depending upon numerous factors such as the severity of the disease to be treated, the age and relative health of the subject, the potency of the compound used, the route and form of administration, the indication towards which the administration is directed, and the preferences and experience of the medical practitioner involved.
- One of ordinary skill in the art of treating such diseases will be able, without undue experimentation and in reliance upon personal knowledge and the disclosure of this Application, to ascertain a therapeutically effective amount of the compounds of the present invention for a given disease.
- compounds of the present invention will be administered as pharmaceutical formulations including those suitable for oral (including buccal and sublingual), rectal, nasal, topical, pulmonary, vaginal, or parenteral (including intramuscular, intraarterial, intrathecal, subcutaneous and intravenous) administration or in a form suitable for administration by inhalation or insufflation.
- oral including buccal and sublingual
- parenteral including intramuscular, intraarterial, intrathecal, subcutaneous and intravenous
- administration by inhalation or insufflation is generally oral using a convenient daily dosage regimen which can be adjusted according to the degree of affliction.
- a compound or compounds of the present invention, together with one or more conventional adjuvants, carriers, or diluents, may be placed into the form of pharmaceutical compositions and unit dosages.
- the pharmaceutical compositions and unit dosage forms maybe comprised of conventional ingredients in conventional proportions, with or without additional active compounds or principles, and the unit dosage forms may contain any suitable effective amount of the active ingredient commensurate with the intended daily dosage range to be employed.
- compositions may be employed as solids, such as tablets or filled capsules, semisolids, powders, sustained release formulations, or liquids such as solutions, suspensions, emulsions, elixirs, or filled capsules for oral use; or in the form of suppositories for rectal or vaginal administration; or in the form of sterile injectable solutions for parenteral use.
- Formulations containing about one ( 1) milligram of active ingredient or, more broadly, about 0.01 to about one hundred ( 100) milligrams, per tablet, are accordingly suitable representative unit dosage forms.
- the compounds of the present invention may be formulated in a wide variety of oral administration dosage forms.
- the pharmaceutical compositions and dosage forms may comprise a compound or compounds of the present invention or pharmaceutically acceptable salts thereof as the active component.
- the pharmaceutically acceptable carriers may be either solid or liquid. Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules.
- a solid carrier may be one or more substances which may also act as diluents, flavouring agents, solubilizers, lubricants, suspending agents, binders, preservatives, tablet disintegrating agents, or an encapsulating material.
- the carrier In powders, the carrier generally is a finely divided solid which is a mixture with the finely divided active component.
- the active component In tablets, the active component generally is mixed with the carrier having the necessary binding capacity in suitable proportions and compacted in the shape and size desired.
- the powders and tablets preferably contain from about one (1) to about seventy (70) percent of the active compound.
- Suitable carriers include but are not limited to magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatine, tragacanth, methylcellulose, sodium carboxymethylcellulose, a low melting wax, cocoa butter, and the like.
- the term "preparation" is intended to include the formulation of the active compound with encapsulating material as carrier, providing a capsule in which the active component, with or without carriers, is surrounded by a carrier, which is in association with it.
- cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges maybe as solid forms suitable for oral administration.
- liquid form preparations including emulsions, syrups, elixirs, aqueous solutions, aqueous suspensions, or solid form preparations which are intended to be converted shortly before use to liquid form preparations.
- Emulsions may be prepared in solutions, for example, in aqueous propylene glycol solutions or may contain emulsifying agents, for example, such as lecithin, sorbitan monooleate, or acacia.
- Aqueous solutions can be prepared by dissolving the active component in water and adding suitable colorants, flavors, stabilizers, and thickening agents.
- Aqueous suspensions can be prepared by dispersing the finely divided active component in water with viscous material, such as natural or synthetic gums, resins, methylcellulose, sodium carboxymethylcellulose, and other well known suspending agents.
- Solid form preparations include solutions, suspensions, and emulsions, and may contain, in addition to the active component, colorants, flavors, stabilizers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.
- the compounds of the present invention maybe formulated for parenteral administration (e.g., by injection, for example bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre- filled syringes, small volume infusion or in multi-dose containers with an added preservative.
- the compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, for example solutions in aqueous polyethylene glycol.
- oily or nonaqueous carriers, diluents, solvents or vehicles examples include propylene glycol, polyethylene glycol, vegetable oils (e.g., olive oil), and injectable organic esters (e.g., ethyl oleate), and may contain formulatory agents such as preserving, wetting, emulsifying or suspending, stabilizing and/or dispersing agents.
- the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilization from solution for constitution before use with a suitable vehicle, e.g., sterile, pyrogen-free water.
- the compounds of the present invention maybe formulated for topical administration to the epidermis as ointments, creams or lotions, or as a transdermal patch.
- Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
- Lotions may be formulated with an aqueous or oily base and will in general also containing one or more emulsifying agents, stabilizing agents, dispersing agents, suspending agents, thickening agents, or coloring agents.
- Formulations suitable for topical administration in the mouth include lozenges comprising active agents in a flavored base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert base such as gelatine and glycerine or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.
- the compounds of the present invention may be formulated for administration as suppositories.
- a low melting wax, such as a mixture of fatty acid glycerides or cocoa butter is first melted and the active component is dispersed homogeneously, for example, by stirring. The molten homogeneous mixture is then poured into convenient sized molds, allowed to cool, and to solidify.
- the compounds of the present invention may be formulated for vaginal administration. Pessaries, tampons, creams, gels, pastes, foams or sprays containing in addition to the active ingredient such carriers as are known in the art to be appropriate.
- the compounds of the present invention may be formulated for nasal administration.
- the solutions or suspensions are applied directly to the nasal cavity by conventional means, for example, with a dropper, pipette or spray.
- the formulations may be provided in a single or multidose form. In the latter case of a dropper or pipette, this may be achieved by the patient administering an appropriate, predetermined volume of the solution or suspension. In the case of a spray, this may be achieved for example by means of a metering atomizing spray pump.
- the compounds of the present invention may be formulated for aerosol administration, particularly to the respiratory tract and including intranasal administration. The compound will generally have a small particle size for example of the order of five (5) microns or less.
- Such a particle size may be obtained by means known in the art, for example by micronization.
- the active ingredient is provided in a pressurized pack with a suitable propellant such as a chlorofluorocarbon (CFC), for example, dichlorodifluoromethane, trichlorofluoromethane, or dichlorotetrafluoroethane, or carbon dioxide or other suitable gas.
- CFC chlorofluorocarbon
- the aerosol may conveniently also contain a surfactant such as lecithin.
- the dose of drug may be controlled by a metered valve.
- the active ingredients may be provided in a form of a dry powder, for example a powder mix of the compound in a suitable powder base such as lactose, starch, starch derivatives such as hydroxypropylmethyl cellulose and polyvinylpyrrolidine (PVP).
- the powder carrier will form a gel in the nasal cavity.
- the powder composition may be presented in unit dose form for example in capsules or cartridges of e.g., gelatine or blister packs from which the powder may be administered by means of an inhaler.
- formulations can be prepared with enteric coatings adapted for sustained or controlled release administration of the active ingredient.
- the compounds of the present invention can be formulated in transdermal or subcutaneous drug delivery devices.
- transdermal delivery systems are advantageous when sustained release of the compound is necessary and when patient compliance with a treatment regimen is crucial.
- Compounds in transdermal delivery systems are frequently attached to an skin-adhesive solid support.
- the compound of interest can also be combined with a penetration enhancer, e.g., Azone (l-dodecylazacycloheptan-2-one).
- Azone l-dodecylazacycloheptan-2-one
- Sustained release delivery systems are inserted subcutaneously into the subdermal layer by surgery or injection.
- the subdermal implants encapsulate the compound in a lipid soluble membrane, e.g., silicone rubber, or a biodegradable polymer, e.g., polylactic acid.
- the pharmaceutical preparations are preferably in unit dosage forms.
- the preparation is subdivided into unit doses containing appropriate quantities of the active component.
- the unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, such as packeted tablets, capsules, and powders in vials or ampoules.
- the unit dosage form can be a capsule, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.
- This example illustrates a process for preparing intermediate 8-bromo-3- methyl-4-phenoxyquinoline.
- This example illustrates a process for preparing intermediate 4-(3-methyl-4- phenoxy-quinolin-8-yl)-piperazine- 1-carboxylic acid tert-butyl ester.
- Example 3 This example illustrates a process for preparing 3-methyl-8-piperazin- l-yl-4-
- This example illustrates a process for preparing 4-(3-fluoro- 1-vinyl-penta- l,3-dienyloxy)-3-methyl-8-piperazin-l-yl-quinoline dihydrochloride.
- This example illustrates a process for preparing 4-(3-methoxy- 1-vinyl-penta- l,3-dienyloxy)-3-methyl-8-piperazin- 1-yl-quinoline hydrochloride.
- This example illustrates a process for preparing 4-(4-fluoro- 1-vinyl-penta- l,3-dienyloxy)-3-methyl-8-piperazin-l-yl-quinoline dihydrochloride.
- This example illustrates a process for preparing 4-(3,4,-difluoro- 1-vinyl- penta- l,3,-dienyloxy)-3-methyl-8-piperazin- 1-yl-quinoline trihydrochloride.
- This example illustrates a variety of formulation compositions.
- the ingredients are mixed and dispensed into capsules containing about 100 mg each; one capsule would approximate a total daily dosage.
- the ingredients are combined and granulated using a solvent such as methanol.
- the formulation is then dried and formed into tablets (containing about 20 mg of active compound) with an appropriate tablet machine.
- the active ingredient is dissolved in a portion of the water for injection. A sufficient quantity of sodium chloride is then added with stirring to make the solution isotonic. The solution is made up to weight with the remainder of the water for injection, filtered through a 0.2 micron membrane filter and packaged under sterile conditions.
- the ingredients are melted together and mixed on a steam bath, and poured into molds containing 2.5 g total weight.
- nasal spray formulations Several aqueous suspensions containing from about 0.025-0.5 percent active compound are prepared as nasal spray formulations.
- the formulations optionally contain inactive ingredients such as, for example, microcrystalline cellulose, sodium carboxymethylcellulose, dextrose, and the like. Hydrochloric acid may be added to adjust pH.
- the nasal spray formulations may be delivered via a nasal spray metered pump typically delivering about 50- 100 microliters of formulation per actuation. A typical dosing schedule is 2-4 sprays every 4- 12 hours.
- This example illustrates in vitro radioligand binding studies of compound of formula I.
- the binding activity of compounds of this invention in vitro was determined as follows. Duplicate determinations of ligand affinity are made by competing for binding of [ 3 H]LSD in cell membranes derived from HEK293 cells stably expressing recombinant human 5-HT6 receptor. This cell line was prepared by the method described by Monsma et al., Molecular Pharmacology, Vol. 43 pp. 320-327 (1993). All determinations were made in assay buffer containing 50 mM Tris-HCl, 10 mM MgSO 4 , 0.5 mM EDTA, 1 mM ascorbic acid, pH 7.4 at 37 0 C, in a 250 microliter reaction volume.
- Assay tubes containing [ 3 H] LSD (5 nM), competing ligand, and membrane were incubated in a shaking water bath for 60 min. at 37 0 C, filtered onto Packard GF-B plates (pre-soaked with 0.3% PEI) using a Packard 96 well cell harvester and washed 3 times in ice cold 50 mM Tris-HCl. Bound [ 3 H] LSD was determined as radioactive counts per minute using Packard TopCount.
- binding basal + where Hill is the Hill slope, [ligand] is the concentration of competing radioligand and IC 50 is the concentration of radioligand producing half-maximal specific binding of radioligand.
- the specific binding window is the difference between the Bmax and the basal parameters.
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Abstract
Description
Claims
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IL188927A IL188927A0 (en) | 2005-07-27 | 2008-01-21 | Aryloxy quinolines and uses thereof as 5-ht6 modulators |
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US7531553B2 (en) * | 2003-03-21 | 2009-05-12 | Amgen Inc. | Heterocyclic compounds and methods of use |
AU2008231787A1 (en) * | 2007-03-23 | 2008-10-02 | Abbott Gmbh & Co. Kg | Quinoline compounds suitable for treating disorders that respond to modulation of the serotonin 5-HT6 receptor |
ES2574154T3 (en) * | 2007-08-07 | 2016-06-15 | Abbvie Deutschland Gmbh & Co Kg | Quinoline compounds suitable for treating disorders that respond to serotonin 5-HT6 receptor modulation |
US10572665B2 (en) * | 2012-12-28 | 2020-02-25 | Fireeye, Inc. | System and method to create a number of breakpoints in a virtual machine via virtual machine trapping events |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0349062A1 (en) | 1988-06-27 | 1990-01-03 | Merck Frosst Canada Inc. | Quinoline ether alkanoic acid |
WO1990009787A1 (en) | 1989-02-27 | 1990-09-07 | The Du Pont Merck Pharmaceutical Company | Novel sulfonamides as radiosensitizers |
WO1991004027A1 (en) | 1989-09-15 | 1991-04-04 | Pfizer Inc. | New n-aryl and n-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme a: cholesterol acyl transferase (acat) |
MX9200299A (en) | 1991-02-07 | 1992-12-01 | Roussel Uclaf | NEW NITROGENATED BICYCLE DERIVATIVES, THEIR PROCEDURE FOR PREPARING THE NEW INTERMEDIATE COMPOUNDS OBTAINED THEIR APPLICATION AS MEDICINES AND THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM. |
ATE156120T1 (en) | 1991-02-07 | 1997-08-15 | Roussel Uclaf | BIZYCLIC NITROGEN COMPOUNDS, THEIR PRODUCTION, INTERMEDIATE PRODUCTS OBTAINED, THEIR USE AS MEDICINAL PRODUCTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
GB9125485D0 (en) | 1991-11-29 | 1992-01-29 | Merck Sharp & Dohme | Therapeutic agents |
GB9125515D0 (en) | 1991-11-29 | 1992-01-29 | Merck Sharp & Dohme | Therapeutic agents |
GB9510757D0 (en) | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
JPH08311032A (en) | 1995-05-18 | 1996-11-26 | Eisai Co Ltd | Alpha,beta-unsaturated ketone derivative |
IL135495A (en) | 1995-09-28 | 2002-12-01 | Hoechst Ag | Intermediate compounds for the preparation of substituted quinoline-2-carboxylic acid amides |
EP0912559B1 (en) * | 1996-07-13 | 2002-11-06 | Glaxo Group Limited | Fused heterocyclic compounds as protein tyrosine kinase inhibitors |
TW521072B (en) | 1997-06-02 | 2003-02-21 | Meiji Seika Kaisha | 4-quinolinol derivatives and fungicides containing the same as an active ingredient used for agriculture and horticulture |
US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
JP4548642B2 (en) | 1998-09-29 | 2010-09-22 | アメリカン・サイアナミド・カンパニー | Substituted 3-cyanoquinolines as protein tyrosine kinase inhibitors |
GB0023918D0 (en) | 2000-09-29 | 2000-11-15 | King S College London | Antiparasitic compounds |
KR20080079341A (en) | 2001-01-16 | 2008-08-29 | 아스트라제네카 아베 | Therapeutic heterocyclic compounds |
KR20030070916A (en) | 2001-01-16 | 2003-09-02 | 아스트라제네카 아베 | Therapeutic Chromone Compounds |
AR035898A1 (en) | 2001-05-25 | 2004-07-21 | Wyeth Corp | ARIL-8-AZABICICLO [3.2.1] OCTANS, A PROCESS FOR THEIR PREPARATION, A FORMULATION AND THE USE OF SUCH COMPOUNDS FOR THE MANUFACTURE OF A MEDICINAL PRODUCT FOR THE TREATMENT OF DEPRESSION |
WO2003080608A2 (en) * | 2002-03-27 | 2003-10-02 | Glaxo Group Limited | Quinoline and aza-indole derivatives and their use as 5-ht6 ligands |
GB0322510D0 (en) * | 2003-09-25 | 2003-10-29 | Glaxo Group Ltd | Novel compounds |
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003080580A2 (en) | 2002-03-27 | 2003-10-02 | Glaxo Group Limited | Quinoline derivatives and their use as 5-ht6 ligands |
Non-Patent Citations (4)
Title |
---|
A J. SLEIGHT ET AL., SEROTONIN ID RESEARCH ALERT, vol. 2, no. 3, 1997, pages 115 - 8 |
A.J. SLEIGHT ET AL., NEUROTRANSMISSION, vol. 11, 1995, pages 1 - 5 |
B.L ROTH ET AL., J PHARMAML EXP. THER., vol. 268, 1994, pages 1403 - 14120 |
D. R. SIBLEY ET AL., MOL PHARMACOL., vol. 43, 1993, pages 320 - 327 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2016943A1 (en) * | 2007-07-19 | 2009-01-21 | Laboratorios del Dr. Esteve S.A. | Substituted tetrahydro-quinoline-sulfonamide compounds, their preparation and use as medicaments |
US7964603B2 (en) | 2007-07-19 | 2011-06-21 | Laboratorios Del Dr. Esteve, S.A. | Substituted tetrahydro-quinoline-sulfonamide compounds, their preparation and use as medicaments |
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CN101228130A (en) | 2008-07-23 |
JP2009502853A (en) | 2009-01-29 |
ES2341489T3 (en) | 2010-06-21 |
ATE465151T1 (en) | 2010-05-15 |
CA2616473A1 (en) | 2007-03-08 |
BRPI0614483A2 (en) | 2011-03-29 |
EP1910296B1 (en) | 2010-04-21 |
IL188927A0 (en) | 2008-08-07 |
WO2007025798A3 (en) | 2007-07-26 |
DE602006013828D1 (en) | 2010-06-02 |
AU2006286654A1 (en) | 2007-03-08 |
US7307089B2 (en) | 2007-12-11 |
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