WO2008002621A2

WO2008002621A2 - Benzyl-substituted quinolone m1 receptor positive allosteric modulators

Info

Publication number: WO2008002621A2
Application number: PCT/US2007/014943
Authority: WO
Inventors: Craig Lindsley; William D. Shipe; Feng Yang; Jaime Lynn Bunda
Original assignee: Merck & Co., Inc.
Priority date: 2006-06-28
Filing date: 2007-06-27
Publication date: 2008-01-03
Also published as: EP2037739B1; WO2008002621A3; EP2037739A4; AU2007265412A1; US8178667B2; ATE530544T1; EP2037739A2; CA2655787A1; JP2009542663A; US20100009962A1

Abstract

The present invention is directed to benzyl-substituted quinolone compounds of general formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the treatment of diseases in which the M1 receptor is involved.

Description

TITLE OF THE INVENTION

BENZYL-SUBSTITUTED QUlNOLONE Ml RECEPTOR POSITIVE ALLOSTERIC

MODULATORS

FIELD OF THE INVENTION

The invention is directed to a class of benzyl-substituted quinolone compounds, their salts, pharmaceutical compositions comprising them and their use in therapy of the human body. In particular, the invention is directed to a class of benzyl-substituted quinolone compounds which are muscarinic Ml receptor positive allosteric modulators, and are useful in the treatment of Alzheimer's Disease and other diseases mediated by the muscarinic Ml receptor.

BACKGROUND OF THE INVENTION

Alzheimer's Disease is a common neurodegenerative disease affecting the elderly, resulting in progressive memory impairment, loss of language and visuospatial skills, and behavior deficits. Characteristics of the disease include degeneration of cholinergic neurons in the cerebral cortex, hippocampus, basal forebrain, and other regions of the brain, neurofibrillary tangles, and accumulation of the amyloid β peptide (Aβ). Aβ is a 39-43 amino acid produced in the brain by processing of the beta-amyloid precursor protein (APP) by the beta-amyloid protein cleaving enzyme ("beta secretase" or "BACE") and gamma-secretase. The processing of APP leads to accumulation of Aβ in the brain.

Cholinergic neurotransmission involves the binding of acetylcholine either to the nicotinic acetycholine receptor (nAChR) or to the muscarinic acetycholine receptor (mAChR). It has been hypothesized that cholinergic hypofunction contributes to the cognitive deficits of patients suffering from Alzheimer's Disease. Consequently, acetylcholinesterase inhibitors, which inhibit acetylcholine hydrolysis, have been approved in the United States for use in the treatment of the cognitive impairments of Alzheimer's Disease patients. While acetylcholinesterase inhibitors have provided some cognitive enhancement in Alzheimer's Disease patients, the therapy has not been shown to change the underlying disease pathology. A second potential pharmacotherapeutic target to counteract cholinergic hypofunction thesis is the activation of muscarinic receptors. Muscarinic receptors are prevalent throughout the body, and in the central nervous system are involved in cognitive, behavior, sensory, motor and autonomic functions. Five distinct muscarinic receptors (M1-M5) have been identified in mammals.

The muscarinic Ml receptor, which is prevalent in the cerebral cortex, hippocampus and striatum, has been found to have a major role in cognitive processing and is believed to have a role in the pathophysiology of Alzheimer's Disease. See Eglen et al, TRENDS in Pharmacological Sciences, 2001, 22:8, 409-414. However, Ml ligands which have been developed and studied for Alzheimer's Disease have produced side effects common to other muscarinic receptor ligands, such as sweating, nausea and diarrhea. See Spalding et al, MoI Pharmacol, 2002, 61:6, 1297-1302.

In addition, unlike acetylcholinesterase inhibitors, which are known to provide symptomatic treatment, Ml agonists also have the potential to treat the underlying disease mechanism of Alzheimer's Dieasease. The cholinergic hypothesis of Alzheimer's Disease is linked to both β-amyloid and hyperphosphorylated tau protein. Formation of β-amyloid may impair the coupling of the muscarinic receptor with G-proteϊns. Stimulation of the Ml muscarinic receptor has been shown to increase formation of the neuroprotective αAPPs fragment, thereby preventing the formation of the Aβ peptide. Thus, Ml agonists may alter APP processing and enhance αAPPs secretion. See Fisher, Jpn J Pharmacol, 2000, 84:101-112.

The muscarinic receptors are known to contain one or more allosteric sites, which may alter the affinity with which muscarinic ligands bind to the primary binding or orthosteric sites. See, e.g., S. Lazareno et al, MoI Pharmacol, 2002, 62:6, 1491-1505; S. Lazareno et al, MoI Pharmacol, 2000, 58, 194-207.

Thus the compounds of the invention, which are muscarinic Ml receptor positive allosteric modulators, are believed to be useful in the treatment of Alzheimer's Disease and other diseases mediated by the muscarinic Ml receptor.

SUMMARY OF THE INVENTION

The present invention is directed to compounds of general formula (I)

or a pharmaceutically acceptable salt thereof, or an enantiomer or diastereomer thereof, which are useful as Ml receptor positive allosteric modulators. The compounds are useful for treating mammals for diseases or disorders in which the Ml receptor is involved, such as Alzheimer's disease, cognitive impairment, pain disorders and sleep disorders, to a patient in need thereof, by administering to the patient a compound of general formula (I).

The invention is also directed to pharmaceutical compositions which include an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt or an enantiomer or diastereomer thereof, and a pharmaceutically acceptable carrier, and the use of the compounds and pharmaceutical compositions of the invention in the treatment of such diseases.

DETAILED DESCRIPTION OF THE INVENTION

In one embodiment, the invention is directed compounds of general formula (I)

and pharmaceutically acceptable salts thereof, and enantiomers and diastereomers thereof, wherein

Rl is selected from the group consisting of (1) hydrogen,

(2) -Ci_6 alkyl, and

(3) -CH₂-aryl, wherein said Rl alkyl or aryl moiety is optionally substituted with one or more

(a) halogen, (b) cyano, and

(c) — O-Ci_6 alkyl, wherein said alkyl is optionally substituted with one or more halo;

R2, R3_; R4 and R5 are independently selected from the group consisting of (1) hydrogen,

(2) -Ci.₆ alkyl,

(3) -C3-7 cycloalkyl,

(4) halogen,

(5) cyano, (6) -0-RlO₅ and

(7) -S(O)_n-RH,

(8) -NR¹⁰R¹¹ wherein said R2, R3_S R4 and R5 alkyl or cycloalkyl is optionally substituted with one or more

(a) halogen,

(b) hydroxy, and (c) -O-Ci-6 alkyl;

R6, R7₃ R8 and R9 are independently selected from the group consisting of (1) hydrogen, (2) -O- Cl -6 alkyl, (3) -Ci_₆ alkyl,

(4) halogen, and

(5) cyano;

Rl 0 and Rl 1 are selected from the group consisting of (l) -Ci-6 alkyl, and

(2) -(CH2)m-aryl, wherein said RlO and Rl 1 alkyl or aryl moiety is optionally substituted with one or more

(a) halogen,

(b) cyano, and (c) — O-Cl-6 alkyl, wherein said alkyl is optionally substituted with one or more halo, provided that when RlO and Rl 1 are bonded to a single nitrogen atom, then RlO and Rl 1 may be linked together to form a 4, 5 or 6 atom carbocyclic chain, wherein one or more of the ring carbon atoms may be replaced with a nitrogen or oxygen atom;

HET is selected from the group consisting of

wherein X I₃ χ2, χ3_? χ4 and χ5 together form a 5- or 6-membered aromatic ring, wherein each of Xl, χ2, χ3₃ χ4 and X5 is independently selected from the group consisting of

(1) CR12,

(2) N,

(3) NRl 3, (4) O, and provided that X4 may alternatively be a bond, and further provided that two Rl2 groups, or one Rl2 group and one Rl3 group, when positioned at neighboring X atoms on the ring, may be linked together to form a group selected

5 from

(1) -O-CH2-CH2-O-,

(2) -CRl4=CRl4-CRl4=CRl4-₅ and (3) -NRl5-CRl4=CRl4-;, or (2)

wherein X^ is selected from the group consisting of (1 ) CR14R14'_S

(2) NRl 5, and

(3) O,

15 provided that when p is 0, then X6 is CR14R14'_;

Rl2 and Rl2' are selected from the group consisting of (1) hydrogen, (2) Ci-₆ alkyl, 0 (3) -O-Ci-6 alkyl,

(4) cyano,

(5) halogen, and (6) -(CH2)m-aryl, wherein said Rl2 and Rl2'alkyl or aryl moiety is optionally substituted with one or more 5 (a) halogen,

(b) cyano, (c) -Ci-6 alkyl, and (d) -O-Ci_6 alkyl, wherein said alkyl moiety is optionally substituted with one or more halo; $0

Rl 3 is selected from the group consisting of (1) hydrogen, (2) -Ci-₆ alkyl, (3) -C3-8 cycloalkyl,

15 wherein said alkyl and cycloalkyl Rl 3 moiety is optionally substituted with one or more

(a) halogen,

- 5 - (b) cyano, or

(c) hydroxy;

Rl 4 and R.14' are independently selected from the same group as Rl2 and Rl2';

Rl 5 is selected from the same group as Rl 3;

m is 1 , 2, 3 or 4; n is 0, 1 or 2, and p is O, l or 2.

The invention is also directed to methods of treating mammals for diseases in which the

Ml receptor is involved, such as Alzheimer's disease, cognitive impairment, pain disorders and sleep disorders, to a patient in need thereof, by administering to the patient an effective amount of a compound of general formula (T). The invention is also directed to pharmaceutical compositions which include an effective amount of a compound of formula (T), or pharmaceutically acceptable salts thereof, and a pharmaceutically acceptable carrier.

The invention is further directed to a method for the manufacture of a medicament or a composition for treating diseases or disorders in which the Ml receptor is involved, such as Alzheimer's disease, cognitive impairment, pain disorders and sleep disorders, comprising combining a compound of the present invention with a pharmaceutically acceptable carrier or diluent.

In one embodiment of compounds of formula (I), Rl is hydrogen or -C\-6 alkyl. More preferably, Rl is hydrogen. In preferred embodiments of the compounds of formula (T), R2, R3_} R4 and R5 are independently selected from the group consisting of hydrogen and halogen. Preferred R2_ RS₅ R4 and R5 halogens are fluoro or bromo.

In preferred embodiments of the compounds of formula (I), R6, R7₅ R8 and R9 are independently selected from the group consisting of hydrogen and halogen. Preferred R^₃ R7_S R8 and R9 halogens are fluoro or bromo. In one embodiment, each of R6, R7₅ R8 and R9 are hydrogen. In another embodiment, R8 is halogen, and Rβ, R7, and R9 are hydrogen.

In one sub-genus of the invention, HET is the 5- or 6- membered aromatic ring of structure

In one embodiment of this sub-genus, each of Xl, χ2, χ3₅ χ4 and χ5 i_s CRl2₅ wherein Rl 2 is preferably selected from the group consisting of hydrogen, halogen, cyano, -O-Cl_6 alkyl or optionally substituted -Ci -6 alkyl. hi another embodiment, one of Xl₅ χ2, X3, χ4 and X^ is N and the others are each CRl2, wherein each Rl2 is preferably selected from the group consisting of hydrogen, halogen, cyano or optionally substituted C 1-6 alkyl. hi another embodiment, two of Xl, X2, χ3₅ χ4 and χ5 are N and the others are each CRl 2, wherein each Rl 2 i_s preferably selected from the group consisting of hydrogen, halogen, cyano or optionally substituted C 1-6 alkyl.

Exemplary Xl, χ2, χ3_? χ4₅ χ5 groups in these embodiments include:

In another embodiment . χ4 is a bond, and one of Xl₃ X2, χ3 and X5 is N, one is NRl3, and the others are each CR12, wherein each Rl2 i_s preferably selected from the group consisting of hydrogen, halogen, cyano or optionally substituted Ci_6 alkyl. Exemplary Xl, X2, χ3, χ4_;

X5 groups in this embodiment include:

LQ another embodiment, two Rl 2 groups, or one Rl 2 group and one Rl 3 group, when positioned at neighboring X atoms on the ring, are linked together to form a group selected from

(1) -O-CH2-CH2-O-,

(2) -CRl4=CRl4-CRl4=CRl4-, and

(3) -NRl5-CRl4=CRl4..

Exemplary Xl, X2, χ3₅ χ4_} χ5 groups in this embodiment include:

In another sub-genus of the invention, HET is a 5- or 6- membered heterocyclic ring of structure

In one embodiment of this sub-genus, p is 2 and χ6 is selected from the group consisting of (1) CR14R14'_S (wherein RΪ4 and Rl4' are preferably hydrogen or optionally substituted alkyl),

(2) NRl 5 (wherein Rl 5 is preferably optionally substituted alkyl), or 0 (3) 0.

Where a variable occurs more than once in formula (I) or in a substituent thereof, the individual occurrences of that variable are independent of each other, unless otherwise specified.

As used herein, the term "alkyl," by itself or as part of another substituent, means a saturated straight or branched chain hydrocarbon radical having the number of carbon atoms 5 designated (e.g., Cl -10 alkyl means an alkyl group having from one to ten carbon atoms). Preferred alkyl groups for use in the invention are C 1-6 alkyl groups, having from one to six atoms. Exemplary alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-buryl, isobutyl, tert- butyl, pentyl, hexyl, and the like. Co alkyl means a bond.

As used herein, the term "cycloalkyl." by itself or as part of another substituent, means a .0 saturated cyclic hydrocarbon radical having the number of carbon atoms designated (e.g., C3-12 cycloalkyl means a cycloalkyl group having from three to twelve carbon atoms). The term cycloalkyl as used herein includes mono-, bi- and tricyclic saturated carbocycles, as well as bridged and fused ring carbocycles. such as spiro fused ring systems.

Preferred cycloalkyl groups for use in the invention are monocyclic C3_g cycloalkyl

'.5 groups, having from three to eight carbon atoms. Exemplary monocyclic cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like. Exemplary bridged cycloalkyl groups include adamantly and norbomyl. Exemplary fused cycloalkyl groups include decahydronaphthalene. As used herein, the term "aryl," by itself or as part of another substituent, means an aromatic cyclic hydrocarbon radical. Preferred aryl groups have from six to ten carbons atoms. The term "aryl" includes multiple ring systems as well as single ring systems. Preferred aryl groups for use in the invention include phenyl and naphthyl. The term "aryl" also includes fused cyclic hydrocarbon rings which are partially aromatic

(i.e., one of the fused rings is aromatic and the other is non-aromatic). An exemplary aryl group which is partially aromatic is indanyl.

The term "halo" or "halogen" includes fluoro, chloro, bromo and iodo. As used herein, the term "heteroaryl," by itself or as part of another substituent, means a cyclic or polycyclic group having ring carbon atoms and at least one ring heteroatom (O₅ N or S), wherein at least one of the constituent rings is aromatic. Preferred heteroaryl groups have from 5 to 12 ring atoms. More preferred heteroaryl groups have 5 or 6 ring atoms. Exemplary heteroaryl groups for use in the invention include carbazolyl, carbolinlyl, chromenyl, cinnolinyl, furanyl, benzofuranyl, benzofurazanyl, isobenzofuranyl, imidazolyl, benzimidazolyl, benzimidazolonyl, indazolyl, indolyl, isoindolyl, indolinyl, indolazinyl, ϊndynyl, oxadiazolyljoxazolyl, benzoxazolyl, isoxazolyl, pyranyl, pyrazinyl, pyrazolyl, benzopyrazolyl, pyridazinyl, pyridyl, pyrimidinyl, pyrrolyl, quinolyl, isoquinolyl, tetrazolyl, thiazolyl, isothiazolyl, thiadiazolyl, thienyl, thiophenyl, benzothiophenyl, triazinyl and triazolyl, and N- oxides thereof. The term "heteroaryl" also includes fused cyclic heterocyclic rings which are partially aromatic (i.e., one of the fused rings is aromatic and the other is non-aromatic). An exemplary heteroaryl group which is partially aromatic is benzodioxol.

When a heteroaryl group as defined herein is substituted, the substituent may be bonded to a ring carbon atom of the heteroaryl group, or on a ring heteroatom {i.e., a nitrogen, oxygen or sulfur), which has a valence which permits substitution. Preferably, the substituent is bonded to a ring carbon atom. Similarly, when a heteroaryl group is defined as a substituent herein, the point of attachment may be at a ring carbon atom of the heteroaryl group, or on a ring heteroatom (i.e., a nitrogen, oxygen or sulfur), which has a valence which permits attachment. Preferably, the attachment is at a ring carbon atom. Some of the compounds of the instant invention have at least one asymmetric center.

Additional asymmetric centers may be present depending upon the nature of the various substituents on the molecule. Compounds with asymmetric centers give rise to enantiomers (optical isomers), diastereomers (confϊgurational isomers) or both, and it is intended that all of the possible enantiomers and diastereomers in mixtures and as pure or partially purified compounds are included within the scope of this invention. The present invention is meant to encompass all such isomeric forms of these compounds. Compounds described herein may contain one or more double bonds, and may thus give rise to cisltrans isomers as well as other conformational isomers. The present invention includes all such possible isomers as well as mixtures of such isomers.

Formula (I) is shown above without a definite stereochemistry at certain positions. The present invention includes all stereoisomers of Formula (I) and pharmaceutically acceptable salts thereof.

The independent syntheses of the enantiomerically or diastereomerically enriched compounds, or their chromatographic separations, may be achieved as known in the art by appropriate modification of the methodology disclosed herein. Their absolute stereochemistry may be determined by the x-ray crystallography of crystalline products or crystalline intermediates that are derivatized, if necessary, with a reagent containing an asymmetric center of known absolute configuration.

If desired, racemic mixtures of the compounds may be separated so that the individual enantiomers are isolated. The separation can be carried out by methods well known in the art, such as the coupling of a racemic mixture of compounds to an enantiomerically pure compound to form a diastereomeric mixture, followed by separation of the individual diastereomers by standard methods, such as fractional crystallization or chromatography. The coupling reaction is often the formation of salts using an enantiomerically pure acid or base. The diastereomeric derivatives may then be converted to the pure enantiomers by cleavage of the added chiral residue. The racemic mixture of the compounds can also be separated directly by chromatographic methods using chiral stationary phases, which methods are well known in the art.

Alternatively, any enantiomer of a compound may be obtained by stereoselective synthesis using optically pure starting materials or reagents of known configuration by methods well known in the art.

General Preparation

Compounds of the invention may be prepared according to the general procedure outlined in Scheme 1.

Scheme 1

Microwave irradiation of a neat mixture of aniline A with diethyl ethoxymethylenemalonate at 180 °C yields enamine B. The mixture is diluted with phenyl ether and irradiated at 250 °C to produce the quinolone core C. Treatment with base in the presence of an alkylating agent gives N-substituted quinolones D, which are hydrolyzed with lithium hydroxide to generate carboxylic acids E after acidic workup. Compounds E are converted to compounds of the invention F by transition metal-catalyzed cross-coupling with the appropriate boronic acids. During any of the above synthetic sequences it may be necessary or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may.be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W.McOmie, Plenum Press, 1973, and T. W. Greene & P/G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups may be removed at a convenient sequent stage using methods known from the art.

Specific embodiments of the compounds of the invention, and methods of making them, are described in the Examples herein.

The term "substantially pure" means that the isolated material is at least 90% pure, and preferably 95% pure, and even more preferably 99% pure as assayed by analytical techniques known in the art.

As used herein, the term "muscarinic Ml receptor " refers to one of the five subtypes of the muscarinic acetylcholine receptor, which is from the superfamily of G-protein coupled receptors. The family of muscarinic receptors is described, for example, in Pharmacol Ther, 1993, 58:319-379; Eur J Pharmacol, 1996, 295:93-102, and MoI Pharmacol, 2002, 61 :1297- 1302. The muscarinic receptors are known to contain one or more allosteric sites, which, may alter the affinity with which muscarinic ligands bind to the primary binding or orthosteric sites. See, e.g., S. Lazareno et al, MoI Pharmacol, 2002, 62:6, 1491-1505. As used herein, the terms "positive allosteric modulator" and "allosteric potentiator" are used interchangeably, and refer to a ligand which interacts with an allosteric site of a receptor to activate the primary binding site. The compounds of the invention are positive allosteric modulators of the muscarinic Ml receptor. For example, a modulator or potentiator may directly or indirectly augment the response produced by the endogenous ligand (such as acetylcholine or xanomeline) at the orthosteric site of the muscarinic Ml receptor in an animal, in particular, a human.

The actions of ligands at allosteric receptor sites may also be understood according to the "allosteric ternary complex model," as known by those skilled in the art. The allosteric ternary complex model is described with respect to the family of muscarinic receptors in Birdsall et al, Life Sciences, 2001, 68:2517-2524. For a general description of the role of allosteric binding sites, see Christopoulos, Nature Reviews: Drug Discovery, 2002, 1:198- 210.

It is believed that the compounds of the invention bind to an allosteric binding site that is distinct from the orthosteric acetylcholine site of the muscarinic Ml receptor, thereby augmenting the response produced by the endogenous ligand acetylcholine at the orthosteric site of the Ml receptor. It is also believed that the compounds of the invention bind to an allosteric site which is distinct from the xanomeline site of the muscarinic Ml receptor, thereby augmenting the response produced by the endogenous ligand xanomeline at the orthosteric site of the Ml receptor. The term "pharmaceutically acceptable salts" refers to salts prepared from pharmaceutically acceptable non-toxic bases or acids including inorganic or organic bases and inorganic or organic acids. The compounds of the invention may be mono, di or tris salts, depending on the number of acid functionalities present in the free base form of the compound. Free bases and salts derived from inorganic bases include aluminum, ammonium, calcium, copper, ferric, ferrous, lithium, magnesium, manganic salts, manganous, potassium, sodium, zinc, and the like. Particularly preferred are the ammonium, calcium, magnesium, potassium, and sodium salts. Salts in the solid form may exist in more than one crystal structure, and may also be in the form of hydrates. Salts derived from pharmaceutically acceptable organic nontoxic bases include salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines, and basic ion exchange resins, such as arginine, betaine, caffeine, choline, N,N'-dibenzylethylene-diarnine, diethylamine, 2- diethylaminoethanol, 2-dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethyl- morpholine, N-ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, isopropylamine, lysine, methylglucamine, moφholine, piperazine, piperidine, polyamine resins, procaine, purines, theobromine, triethylamine, trimethylamine, tripropylamine, tromethamine, and the like. When the compound of the present invention is basic, salts may be prepared from pharmaceutically acceptable non-toxic acids, including inorganic and organic acids. Such acids include acetic, trifluoroacetic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethanesulfonic, fumaric, gluconic, glutamic, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic, pantothenic, phosphoric, succinic, sulfuric, tartaric, p- toluenesulfonic acid, and the like. Particularly preferred are citric, hydrobromic, hydrochloric, trifluoroacetic, maleic, phosphoric, sulfuric, fumaric and tartaric acids.

The present invention is directed to the use of the compounds of formula (I) disclosed herein as Ml allosteric modulators in a patient or subject such as a mammal in need of such activity, comprising the administration of an effective amount of the compound. In addition to humans, a variety of other mammals can be treated according to the method of the present invention.

The compounds of the present invention have utility in treating or ameliorating Alzheimer's disease. The compounds may also be useful in treating or ameliorating other diseases mediated by the muscarinic Ml receptor, such as sleep disorders, pain disorders (including acute pain, inflammatory pain and neuropathic pain) and cognitive disorders (including mild cognitive impairment). Other conditions that may be treated by the compounds of the invention include Parkinson's Disease, pulmonary hypertension, chronic obstructive pulmonary disease (COPD), asthma, urinary incontinence, glaucoma, schizophrenia (including cognitive deficits due to schizophrenia), Trisomy 21 (Down Syndrome), cerebral amyloid angiopathy, degenerative dementia, Hereditary Cerebral Hemorrhage with Amyloidosis of the Dutch-Type (HCHWA-D), Creutzfeld- Jakob disease, prion disorders, amyotrophic lateral sclerosis, progressive supranuclear palsy, head trauma, stroke, pancreatitis, inclusion body myositis, other peripheral amyloidoses, diabetes and atherosclerosis. hi preferred embodiments, the compounds of the invention are useful in treating Alzheimer's Disease, cognitive disorders, pain disorders and sleep disorders. For example, the compounds may be useful for the prevention of dementia of the Alzheimer's type, as well as for the treatment of early stage, intermediate stage or late stage dementia of the Alzheimer's type.

Potential sleep conditions or disorders for which the compounds of the invention may be useful include enhancing sleep quality; improving sleep quality; augmenting sleep maintenance; increasing the value which is calculated from the time that a subject sleeps divided by the time that a subject is attempting to sleep; decreasing sleep latency or onset (the time it takes to fall asleep); decreasing difficulties in falling asleep; increasing sleep continuity; decreasing the number of awakenings during sleep; decreasing nocturnal arousals; decreasing the time spent awake following the initial onset of sleep; increasing the total amount of sleep; reducing the fragmentation of sleep; altering the timing, frequency or duration of REM sleep bouts; increasing the amount and percentage of stage 2 sleep; promoting slow wave sleep; enhancing EEG-delta activity during sleep; increasing daytime alertness; reducing daytime drowsiness; treating or reducing excessive daytime sleepiness; insomnia; hypersomnia; narcolepsy; interrupted sleep; sleep apnea; wakefulness; nocturnal myoclonus; REM sleep interruptions; jet-lag; shift workers' sleep disturbances; dyssomnias; night terror; insomnias associated with depression, emotional/mood disorders, as well as sleep walking and enuresis, and sleep disorders which accompany aging; Alzheimer's sundowning; conditions associated with circadian rhythmicity as well as mental and physical disorders associated with travel across time zones and with rotating shift-work schedules; conditions due to drugs which cause reductions in REM sleep as a side effect; syndromes which are manifested by non-restorative sleep and muscle pain or sleep apnea which is associated with respiratory disturbances during sleep; and conditions which result from a diminished quality of sleep. Pain disorders for which the compounds of the invention may be useful include neuropathic pain (such as postherpetic neuralgia, nerve injury, the "dynias", e.g., vulvodynia, phantom limb pain, root avulsions, painful diabetic neuropathy, painful traumatic mononeuropathy, painful polyneuropathy); central pain syndromes (potentially caused by virtually any lesion at any level of the nervous system); postsurgical pain syndromes (eg, postmastectomy syndrome, postthoracotomy syndrome, stump pain); bone and joint pain (osteoarthritis), repetitive motion pain, dental pain, cancer pain, myofascial pain (muscular injury, fibromyalgia); perioperative pain (general surgery, gynecological), chronic pain, dysmennorhea, as well as pain associated with angina, and inflammatory pain of varied origins (e.g. osteoarthritis, rheumatoid arthritis, rheumatic disease, teno- synovitis and gout), headache, migraine and cluster headache, primary hyperalgesia, secondary hyperalgesia, primary allodynia, secondary allodynia, or other pain caused by central sensitization.

Compounds of the invention may also be used to treat or prevent dyskinesias. Furthermore, compounds of the invention may be used to decrease tolerance and/or dependence to opioid treatment of pain, and for treatment of withdrawal syndrome of e.g., alcohol, opioids, and cocaine.

The subject or patient to whom the compounds of the present invention is administered is generally a human being, male or female, in whom Ml allosteric modulation is is desired, but may also encompass other mammals, such as dogs, cats, mice, rats, cattle, horses, sheep, rabbits, monkeys, chimpanzees or other apes or primates, for which treatment of the above noted disorders is desired.

The compounds of the present invention may be used in combination with one or more other drugs in the treatment of diseases or conditions for which the compounds of the present invention have utility, where the combination of the drugs together are safer or more effective than either drug alone. Additionally, the compounds of the present invention may be used in combination with one or more other drugs that treat, prevent, control, ameliorate, or reduce the risk of side effects or toxicity of the compounds of the present invention. Such other drugs may be administered, by a route and in an amount commonly used therefor, contemporaneously or sequentially with the compounds of the present invention. Accordingly, the pharmaceutical compositions of the present invention include those that contain one or more other active ingredients, in addition to the compounds of the present invention. The combinations may be administered as part of a unit dosage form combination product, or as a kit or treatment protocol wherein one or more additional drugs are administered in separate dosage forms as part of a treatment regimen.

Examples of combinations of the compounds of the invention include combinations with anti- Alzheimer's Disease agents, for example beta-secretase inhibitors; alpha 7 nicotinic agonists, such as ABT089, SSR18O711 and MEM63908; gamma-secretase inhibitors, such as LY450139 and TAK 070; tau phosphorylation inhibitors; blockers of Aβ oligomer formation; 5-HT4 agonists, such as PRX-03140; 5-HT6 antagonists, such as GSK 742467, SGS-518, FK-962, SL- 65.0155, SRA-333 and xaliproden; 5-HT1 a antagonists, such as lecozotan; p25/CDK5 inhibitors; NKl /NK3 receptor antagonists; COX-2 inhibitors; HMG-CoA reductase inhibitors; NSAIDs including ibuprofen; vitamin E; anti-amyloid antibodies (including anti-amyloid humanized monoclonal antibodies), such as bapineuzumab, ACCOOl, CAD 106, AZD3102, Hl 2Al IVl; anti-inflammatory compounds such as (R)-flurbiprofen, nitroflurbiprofen, rosiglitazone, ND- 1251, VP-025, HT-0712 and EHT-202; CB-I receptor antagonists or CB-I receptor inverse agonists, such as AVE 1625; antibiotics such as doxycycline and rifampin; N-methyl-D-aspartate (NMD A) receptor antagonists, such as memantine, neramexane and EVTlOl ; cholinesterase inhibitors such as galantamine, rivastigmine, donepezil, tacrine, phenserine, ladostigil and ABT- 089; growth hormone secretagogues such as ibutamoren, ibutamoren mesylate, and capromorelin; histamine H3 receptor antagonists such as ABT-834, ABT 829, GSK 189254 and CEP16795; AMPA agonists or AMPA modulators, such as CX-717, LY 451395, LY404187 and S-18986; PDE IV inhibitors, including MEM1414, HT0712 and AVE8112; GABAA inverse agonists; GSK3β inhibitors, including AZD1080, SAR502250 and CEP16805; neuronal nicotinic agonists; selective Ml agonists; and microtubule affinity regulating kinase (MARK) ligands; or other drugs that affect receptors or enzymes that either increase the efficacy, safety, convenience, or reduce unwanted side effects or toxicity of the compounds of the present invention. Examples of combinations of the compounds of the invention include combinations with agents for the treatment of pain, for example non-steroidal anti-inflammatory agents, such as aspirin, diclofenac, duflunisal, fenoprofen, flurbiprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, naproxen, oxaprozin, piroxicam, sulindac and tolmetin; COX-2 inhibitors, such as celecoxib, rofecoxib, valdecoxib, 406381 and 644784; CB-2 agonists, such as 842166 and SAB378; VR-I antagonists, such as AMG517, 705498, 782443, PAC20030, Vl 14380 and A425619; bradykinin B 1 receptor antagonists, such as SSR240612 and NVPSAA164; sodium channel blockers and antagonists, such as VX409 and SPI860; nitric oxide synthase (NOS) inhibitors (including iNOS and nNOS inhibitors), such as SD6010 and 274150; glycine site antagonists, including lacosamide; neuronal nicotinic agonists, such as ABT 894; NMDA antagonists, such as AZD4282; potassium channel openers; AMPA/kainate receptor antagonists; calcium channel blockers, such as ziconotide and NMED 160; GABA-A receptor IO modulators (e.g., GABA- A receptor agonists); matrix metalloprotease (MMP) inhibitors; thrombolytic agents; opioid analgesics such as codeine, fentanyl, hydromorphone, levorphanol, meperidine, methadone, morphine, oxycodone, oxymorphone, pentazocine, propoxyphene; neutrophil inhibitory factor (NIF); pramipexole, ropinirole; anticholinergics; amantadine; monoamine oxidase B15 ("MAO-B") inhibitors; 5HT receptor agonists or antagonists; mGlu5 antagonists, such as AZD9272; alpha agonists, such as AGNXX/YY; neuronal nicotinic agonists, such as ABT894; NMDA receptor agonists or antagonists, such as AZD4282; NKI antagonists; selective serotonin reuptake inhibitors ("SSRI") and/or selective serotonin and norepinephrine reuptake inhibitors ("SSNRI"), such as duloxetine; tricyclic antidepressant drugs, norepinephrine modulators; lithium; valproate; gabapentin; pregabalin; rizatriptan; zolmitriptan; naratriptan and sumatriptan.

The compounds of the invention may be administered in combination with compounds useful for enhancing sleep quality and preventing and treating sleep disorders and sleep disturbances, including e.g., sedatives, hypnotics, anxiolytics, antipsychotics, antianxiety agents, antihistamines, benzodiazepines, barbiturates, cyclopyrrolones, orexin antagonists, alpha-1 antagonists, GABA agonists, 5HT-2 antagonists including 5HT-2A antagonists and 5HT-2A/2C antagonists, histamine antagonists including histamine H3 antagonists, histamine H3 inverse agonists, imidazopyridines, minor tranquilizers, melatonin agonists and antagonists, melatonergic agents, other orexin antagonists, orexin agonists, prokineticin agonists and antagonists, pyrazolopyrimidines, T-type calcium channel antagonists, triazolopyridines, and the like, such as: adinazolam, allobarbital, alonimid, alprazolam, amitriptyline, amobarbital, amoxapine, armodafinil, APD- 125, bentazepam, benzoctamine, brotizolam, bupropion, busprione, butabarbital, butalbital, capromorelin, capuride, carbocloral, chloral betaine, chloral hydrate, chlordiazepoxide, clomipramine, clonazepam, cloperidone, clorazepate, clorethate, clozapine, conazepam, cyprazepam, desipramine, dexclamol, diazepam, dichloralphenazone, divalproex, diphenhydramine, doxepin, EMD-281014, eplivanserin, estazolam, eszopiclone, ethchlorynol, etomidate, fenobam, flunitrazepam, flurazepam, fluvoxamine, fluoxetine, fosazepam, gaboxadol, glutethimide, halazepam, hydroxyzine, ibutamoren, imipramine, indiplon, lithium, lorazepam, lormetazepam, LY-156735, maprotiline, MDL-100907, mecloqualone, melatonin, mephobarbital, meprobamate, methaqualone, methyprylon, midaflur, midazolam, modafinil, nefazodone, NGD-2-73, nisobamate, nitrazepam, nortriptyline, oxazepam, paraldehyde, paroxetine, pentobarbital, perlapine, perphenazine, phenelzine, phenobarbital, prazepam, promethazine, propofol, protriptyline, quazepam, ramelteon, reclazepam, roletamide, secobarbital, sertraline, suproclone, TAK-375, temazepam, thioridazine, tiagabine, tracazolate, tranylcypromaine, trazodone, triazolam, trepipam, tricetamide, triclofos, trifluoperazine, trimetozine, trimipramine, uldazepam, venlafaxine, zaleplon, zolazepam, zopiclone, Zolpidem, and salts thereof, and combinations thereof, and the like, or the compound of the present invention may be administered in conjunction with the use of physical methods such as with light therapy or electrical stimulation.

In another embodiment, the subject compound may be employed in combination with levodopa (with or without a selective extracerebral decarboxylase inhibitor such as carbidopa or benserazide), anticholinergics such as biperiden (optionally as its hydrochloride or lactate salt) and trihexyphenidyl (benzhexol) hydrochloride, COMT inhibitors such as entacapone, MOA-B inhibitors, antioxidants, A2a adenosine receptor antagonists, cholinergic agonists and dopamine receptor agonists such as alentemol, bromocriptine, fenoldopam, lisuride, naxagolide, pergolide and pramipexole. The term "composition" as used herein is intended to encompass a product comprising specified ingredients in predetermined amounts or proportions, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts. This term in relation to pharmaceutical compositions is intended to encompass a product comprising one or more active ingredients, and an optional carrier comprising inert ingredients, as well as any product which results, directly or indirectly, from combination, complexation or aggregation of any two or more of the ingredients, or from dissociation of one or more of the ingredients, or from other types of reactions or interactions of one or more of the ingredients.

In general, pharmaceutical compositions are prepared by uniformly and intimately bringing the active ingredient into association with a liquid carrier or a finely divided solid carrier or both, and then, if necessary, shaping the product into the desired formulation. In the pharmaceutical composition the active compound, which is a compound of formula (I), is included in an amount sufficient to produce the desired effect upon the process or condition of diseases. Accordingly, the pharmaceutical compositions of the present invention encompass any composition made by admixing a compound of the present invention and a pharmaceutically acceptable carrier. The carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g., oral or parenteral (including intravenous). Thus, the pharmaceutical compositions of the present invention can be presented as discrete units suitable for oral administration such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient. Further, the compositions can be presented as a powder, as granules, as a solution, as a suspension in an aqueous liquid, as a non-aqueous liquid, as an oil- in-water emulsion or as a water-in-oil liquid emulsion, hi addition to the common dosage forms set out above, the compounds represented by Formula (T), or pharmaceutically acceptable salts thereof, may also be administered by controlled release means and/or delivery devices.

Pharmaceutical compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions. Pharmaceutical compositions may contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents and preserving agents, in order to provide pharmaceutically elegant and palatable preparations. Tablets may contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients may be, for example, inert diluents, such' as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example starch, gelatin or acacia, and lubricating agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period.

A tablet containing the composition of this invention may be prepared by compression or molding, optionally with one or more accessory ingredients or adjuvants. Compressed tablets may be prepared by compressing, in a suitable machine, the active ingredient in a free-flowing form such as powder or granules, optionally mixed with a binder, lubricant, inert diluent, surface active or dispersing agent. Molded tablets may be made by molding in a suitable machine, a mixture of the powdered compound moistened with an inert liquid diluent. Each tablet preferably contains from about 0.1 mg to about 500 mg of the active ingredient and each cachet or capsule preferably containing from about 0.1 mg to about 500 mg of the active ingredient. Compositions for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin, or olive oil.

Other pharmaceutical compositions include aqueous suspensions, which contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions. In addition, oily suspensions may be formulated by suspending the active ingredient in a vegetable oil, for example arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. Oily suspensions may also contain various excipients. The pharmaceutical compositions of the invention may also be in the form of oil-in- water emulsions, which may also contain excipients such as sweetening and flavoring agents. The pharmaceutical compositions may be in the form of a sterile injectable aqueous or oleaginous suspension, or in the form of sterile powders for the extemporaneous preparation of such sterile injectable solutions or dispersions. In all cases, the final injectable form must be sterile and must be effectively fluid for easy syringability. The pharmaceutical compositions must be stable under the conditions of manufacture and storage; thus, preferably should be preserved against the contaminating action of microorganisms such as bacteria and fungi.

Pharmaceutical compositions of the present invention can be in a form suitable for topical use such as, for example, an aerosol, cream, ointment, lotion, dusting powder, or the like. Further, the compositions can be in a form suitable for use in transdermal devices. These formulations may be prepared via conventional processing methods. As an example, a cream or ointment is prepared by mixing hydrophilic material and water, together with about 5 wt% to about 10 wt% of the compound, to produce a cream or ointment having a desired consistency.

Pharmaceutical compositions of this invention can also be in a form suitable for rectal administration wherein the carrier is a solid. It is preferable that the mixture forms unit dose suppositories. Suitable carriers include cocoa butter and other materials commonly used in the art.

By "pharmaceutically acceptable" it is meant the carrier, diluent or excipient must be compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.

The terms "administration of or "administering a" compound mean providing a compound of the invention to the individual in need of treatment in a form that can be introduced into that individual's body in a therapeutically useful form and therapeutically useful amount, including, but not limited to: oral dosage forms, such as tablets, capsules, syrups, suspensions, and the like; injectable dosage forms, such as FV, IM, or IP, and the like; transdermal dosage forms, including creams, jellies, powders, or patches; buccal dosage forms; inhalation powders, sprays, suspensions, and the like; and rectal suppositories.

The terms "effective amount" or "therapeutically effective amount" means the amount of the subject compound that will elicit the biological or medical response of a tissue, system, animal or human that is being sought by the researcher, veterinarian, medical doctor or other clinician.

As used herein, the term "treatment" or "treating" means any administration of a compound of the present invention and includes (1) inhibiting the disease in an animal that is experiencing or displaying the pathology or symptomatology of the diseased (i.e., arresting further development of the pathology and/or symptomatology), or (2) ameliorating the disease in an animal that is experiencing or displaying the pathology or symptomatology of the diseased (i.e., reversing the pathology and/or symptomatology).

The compositions containing compounds of the present invention may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. The term "unit dosage form" is taken to mean a single dose wherein all active and inactive ingredients are combined in a suitable system, such that the patient or person administering the drug to the patient can open a single container or package with the entire dose contained therein, and does not have to mix any components together from two or more containers or packages. Typical examples of unit dosage forms are tablets or capsules for oral administration, single dose vials for injection, or suppositories for rectal administration. This list of unit dosage forms is not intended to be limiting in any way, but merely to represent typical examples of unit dosage forms.

The compositions containing compounds of the present invention may conveniently be presented as a kit, whereby two or more components, which may be active or inactive ingredients, carriers, diluents, and the like, are provided with instructions for preparation of the actual dosage form by the patient or person administering the drug to the patient. Such kits may be provided with all necessary materials and ingredients contained therein, or they may contain instructions for using or making materials or components that must be obtained independently by the patient or person administering the drug to the patient.

When treating or ameliorating a disorder or diseases for which compounds of the present invention are indicated, generally satisfactory results are obtained when the compounds of the present invention are administered at a daily dosage of from about 0.1 mg to about 100 mg per kg of animal body weight, preferably given as a single daily dose or in divided doses two to six times a day, or in sustained release form. The total daily dosage is from about 1.0 mg to about 2000 mg, preferably from about 0.1 mg to about 20 mg per kg of body weight. In the case of a 70 kg adult human, the total daily dose will generally be from about 7 mg to about 1,400 mg. This dosage regimen may be adjusted to provide the optimal therapeutic response. The compounds may be administered on a regimen of 1 to 4 times per day, preferably once or twice per day.

The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. For example, a formulation intended for the oral administration to humans may conveniently contain from about 0.005 mg to about 2.5 g of active agent, compounded with an appropriate and convenient amount of carrier material. Unit dosage forms will generally contain between from about 0.005 mg to about 1000 mg of the active ingredient, typically 0.005, 0.01 mg, 0.05 mg, 0.25 mg, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 200 mg, 300 mg, 400 mg, 500 mg, 600 mg, 800 mg or 1000 mg, administered once, twice or three times a day.

It will be understood, however, that the specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the host undergoing therapy.

The utility of the compounds as Ml receptor positive allosteric modulators may be demonstrated by methodology known in the art, including by the assay described below. The assay is designed to select compounds that possess modulator activity at the acetylcholine muscarinic Ml receptor or other muscarinic receptors expressed in CHOnfat cells by measuring the intracellular calcium with a FLIPR384 Fluorometric Imaging Plate Reader System. The assay studies the effect of one or several concentrations of test compounds on basal or acetylcholine-stimulated Ca2+ levels using FLIPR. Compounds are prepared and subjected to a preincubation period of 4 min. Thereafter, a single EC20 concentration of acetylcholine is added to each well (3nM final). The intracellular

Ca2+ level of each sample is measured and compared to an acetylcholine control to determine any modulatory activity.

Cells: CHOnfat/hMl, hM2, hM3 or hM4 cells are plated 24 hr before the assay at a density of 18,000 cells/ well (100 μL) in a 384 well plate. CHOnfat/hMl and CHOnfat/hM3

Growth Medium: 90% DMEM (Hi Glucose); 10% HI FBS; 2mM L-glutamine; O.lmM NEAA; Pen-Strep; and lmg/ ml Geneticin, are added. For M2Gqi5CHOnfat and M4Gqi5CHOnfat cells, an additional 600ug/ml hygromycin is added.

Equipment: 384 well plate, 120 μL addition plate; 96-well Whatman 2ml Uniplate Incubator, 37 "C, 5% CO2; Skatron EMBLA-384 Plate Washer; Multimek Pipetting System;

Genesis Freedom 200 System; Mosquito System; Temo Nanolitfe Pipetting System; and FLTPR384 Fluorometric Imaging Plate Reader System are used.

Buffers. Assay Buffer: Hanks Balanced Salt Solution, with 2OmM Hepes, 2.5mM Probenecid (Sigma P-8761) first dissolved in IN NaOH, 1% Bovine Serum Albumin (Sigma A- 9647). Dye Loading Buffer: Assay Buffer plus 1% Fetal Bovine Serum and Fluo-4AM/Pluronic Acid Mixture. 2mM Fluo-4AM ester stock in DMSO (Molecular Probes F-14202) Concentration of 2uM in buffer for a final concentration of 1 μM in Assay. 20% Pluronic Acid Solution stock, with concentration of 0.04% in Buffer, 0.02% in Assay.

65 μL of 2 mM Fluo-4AM are mixed with 130 μL of 20% Pluronic Acid. The resulting solution and 650 μL FBS is added to the assay buffer for a total volume of 65 mL. Positive Controls: 4-Br-A23187: 10 mM in DMSO; final concentration 10 μM. Acetylcholine: 1OmM in water, working stock at both 2OuM and 3OuM in assay buffer, final concentration of 10 μM. This is used to check the maximum stimulation of the CHOKl/hMl cells. 2OuM (2x) acetylcholine is added in the preincubation part of the assay, and the 3OuM (3x) stock is added in the second part. (EC2θ)Acetylcholine: 1OmM in water, working stock of 9nM (3x), and final concentration in assay is 3nM. This is used after the preincubation with test compounds. Addition of the EC20 Acetylcholine to each well with a test compound will ascertain any modulator activity. 24 wells contain 3nM Acetylcholine alone as a control.

Determining Activity of Putative Compounds: Screening Plate: Compounds are titrated in 96-well plates (columns 2-11), 100% DMSO, started at a concentration of 15mM (15Ox stock concentration), and 3-fold serial dilutions using Genesis Freedom200 System. Four 96-well plates are combined into a 384-well plate using Mosquito Nanolitre Pipetting System by transferring IuI of serial diluted compounds to each well, and ImM acetylcholine (10Ox stock concentration) were added as a control. Using Temo, 49 μl assay buffer is added to each well of the 384- well plate right before assay. hi a 96-well Whatman 2ml Uniplate, 9nM Acetylcholine (3x) is pipetted into wells corresponding to the screening compounds, and into control wells. The 3OuM acetylcholine control (3x) is added into control wells, and the 3x agonist plate is transferred into a 384 well plate.

Cells are washed three times with 100 μL of buffer, leaving 30μL of buffer in each well. Using Multimek, 30 μL of Dye Loading Buffer is added into each well and incubated at 37°C, 5% CO2 for up to one hr.

After 60 min, the cells are washed three times with 100 μL of buffer, leaving 30 μL of buffer in each well. The cell plate, screening plate, and agonist addition plates are placed on the platform in the FLIPR and the door closed. A signal test to check background fluorescence and basal fluorescence signal is performed. Laser intensity is adjusted if necessary.

4 min of preincubation with the test compounds is provided to determine any agonist activity on the Ml receptor by comparison to the 1 mM acetylcholine control. After preincubation, the EC20 value of acetylcholine (3nM final) is added to determine any modulator activity. A further description of the muscarinic FLIPR assay can be found in International patent application WO2004/073639. In particular, the compounds of the following examples had activity in the aforementioned assay, generally with an EC50 value of 1 OμM of less. Such a result is indicative of the intrinsic activity of the compounds in use as Ml allosteric modulators.

Several methods for preparing the compounds of this invention are illustrated in the schemes and examples herein. Starting materials are made according to procedures known in the art or as illustrated herein. The following examples are provided so that the invention might be more fully understood. These examples are illustrative only and should not be construed as limiting the invention in any way.

EXAMPLE 1

1 -[4-(6-chloropyridin-3 -yl )-2-fiuoroben2yl] -5, 8-difiuoro-4-oxo- 1 ,4-dihydroquinoline-3 - carboxylic acid

1-2 diethyl 2-((2,5-difluorophenylamino)methylene)maIonate

Aniline 1-1 (1.07 g, 0.835 mL, 8.3 mmol) and diethyl ethoxymethylenemalonate (2.7 g, 2.5 mL, 12.5 mmol) were combined in a 5 mL vial. The mixture was irradiated in a Biotage Initiator microwave at 180 "C for 20 min. After cooling to ambient temperature, the adduct 1-2 precipitated from the mixture. The solid was collected by filtration and washed with hexanes, yielding 1.83 g (73%) of 1-2 as a crystalline white solid. Enamine 1-2 is slightly soluble in hexanes, so a minimum volume of solvent (—10 mL) was used for washing. The material was used in the next step without further purification. ¹H NMR (CDCl₃, 300 MHz): 11.07 (br d, J= 12.3 Hz, IH), 8.39 (d, J= 13.5 Hz, IH)₃ 7.11 (m, IH), 7.02 (m, IH), 6.78 (m, IH), 4.33 (q, 2H), 4.27 (q, 2H), 1.38 (t, 3H), 1.32 (t, 3H); MS (Electrospray): m/z 300.2 (MH⁺).

1-3 ethyl 5,8-difluoro-4-oxo-l,4-dihydroquinoline-3-carbθ3cylate Enamine 1-2 (0.46 g, 1.54 mmol) was placed in a 5 mL vial and dissolved in 2.5 mL of diphenyl ether. The mixture was irradiated in a Biotage Initiator microwave at 250 ⁰C for 6 h. After cooling to ambient temperature, the cyclization product 1-3 precipitated from the mixture. The solid was collected by filtration and washed with hexanes, yielding 115 mg (30%) of 1-3 as a crystalline white solid. Quinolone 1-3 is insoluble in hexanes, so a large volume of solvent (~100 mL) was used for washing. Highly pure recovered enamine 1-2 could be resubjected to heating to produce more 1-3. ¹HNMR (CDCl₃, 300 MHz): 9.14 (s, IH), 7.44 (m, IH), 7.15 (m, IH), 4.53 (q, 2H), 1.49 (t, 3H); MS (Electrospray): m/z 254.1 (MH⁺).

1-4 ethyl l-(4-bromo-2-fluorobenzyl)-5,8-difluoro-4-oxo-l,4-dihydroquinoline-3-carboxylate

Quinolone 1-3 (2.03 g, 8.0 mmol) was suspended in 40 mL anhydrous DMF and treated with potassium carbonate (3.32 g, 24.0 mmol), potassium iodide (66 mg, 0.4 mmol), and 4-bromo-l- (bromomethyl)-2-fluorobenzene (2.36 g, 8.8 mmol). After 24 h at ambient temperature, the reaction was partitioned in ethyl acetate and saturated aqueous NH₄Cl solution. The layers were separated, and the aqueous layer was extracted once with ethyl acetate. The ethyl acetate layers were combined and solvent was removed in vacuo. 1-4 was obtained as a pure white solid (2.28 g, 65%) after two washes with cold MeOH. ¹H NMR (CDCl₃, 300 MHz): 8.39 (s, IH), 7.31 (dd, IH), 7.28-7.20 (m, 2H)₅ 6.98 (m, IH)₅ 6.85 (app t, IH)₅ 5.49 (app d, 2H), 4.39 (q, 2H)₅ 1.40 (t, 3H); MS (Electrospray): m/z 441.1 (MH⁺).

1-5 l^-bromo^-fluorobenzyO-SjS-difluoro^-oxo-l^-dihydroquinoline-S-carboxylic acid

Ethyl ester 1-4 (880 mg, 2.0 mmol) was suspended in 10 mL of dioxane and treated with 2.0 mL of a saturated aqueous LiOH solution. After 16 h, the reaction was poured into a separatory funnel containing 20 mL of ethyl acetate and acidified with 3 N aq. HCl. The product was not appreciably soluble in either layer, but remained suspended in the ethyl acetate layer. The layers were separated and the aqueous layer was extracted with EtOAc (2 x 20 mL). The organic layers were combined and solvent was removed in vacuo to give carboxylic acid 1-5 (810 mg, 98%) as a white powder. ¹H NMR (CDCl₃, 300 MHz): 14.28 (s, IH), 8.76 (s, IH)₅ 7.44 (m₅ IH), 7.38- 7.24 (m, 2H), 7.16 (m, IH), 6.87 (app t, IH), 5.63 (app d, 2H); MS (Electrospray): m/z 413.0 (MH⁺).

1-6 (Example 1) l-^^-chloropyridin-S-y^-l-fluorobenzylJ-S-S-difluoro^-oxo-l^-dihydroquinoline-S- carboxylic acid

A vial was charged with aryl bromide 1-5 (150 mg, 0.364 mmol), boronate ester (105 mg; 0.437 mmol), 1 M cesium carbonate solution (0.73 mL), and 2 mL of THF. Catalytic Pd(P¹BUa)₂ (4 mg) was added and the reaction was heated under microwave irradiation at 160 °C for 10 min. After cooling, the reaction mixture was transferred to a separatory funnel with ~60 mL of CH2CI₂, 30 mL of pH 7 buffer, and 30 mL of water. The CH₂Cl₂ layer was removed and the aqueous layer was extracted with CH₂Cl₂ (2x more). The combined CH₂Cl₂ layers were filtered through a pad of Celite, dried over MgSO₄, filtered, and concentrated in vacuo yielding chloropyridine 1-6 (108 mg, 67%) as a yellow solid. ¹H NMR indicates a mixture of isomers. ¹H NMR (CDCl₃, 300 MHz): 14.29 (s, IH), 8.78 (s, IH), 8.56 (m, IH), 7.79 (m, IH), 7.45 (m, 2H), 7.33 (m, IH), 7.16 (m, 2H), 6.87 (app t, IH), 5.68 (br d, J= 3.0 Hz, 2H); MS (Electrospray): m/z 445.1 (MH⁺).

EXAMPLE 2

1 -(2-fluoro-4-( 1 -propyl- 1 H^r-pyrazol-4-yl)benzyl-5-fluoro- 1₅4-dihydrooxoquinoline-3-carboxylic acid

2-2 diethyl {[(2-bromo-5-fluorophenyI)amino]methyIene}malonate

2-1 (200 g, 1053 mmol) and diethyl ethoxymethylenemalonate (228 g, 1053 mmol) were combined neat and heated to 120 "C. After 2 h, the reaction was poured hot into 2 L of methanol. The resulting mixture was cooled to 10 °C and filtered, washing with methanol. The product was dried on the filter under N₂, yielding 320 g (84%) of 2-2 in two crops. MS (Electrospray): m/z 315.9 (MH⁺-CO₂)- 2-3 ethyl 8-bromo-5-fluoro-4-oxo-l,4-dihydroquinoline-3-carboxylate

Diphenyl ether (3.5 L) was heated to 250 "C₅ and 2-2 (320 g, 888 mmol) was added. After 2 h, the reaction was cooled to rt and 2 L of heptane were added. The mixture was filtered and washed with heptane. The product was dried on the filter under N₂, yielding 215 g (77%) of 2-3. MS (Electrospray): m/z 313.9 (Mtf).

2-4 ethyl 5-fluoro-4-oxo-l,4-dihydroquinoline-3-carboxylate Palladium on carbon (14 g, 13.2 mmol), sodium acetate trihydrate (30.3 g, 223 mmol), and 2-3 (70 g, 223 mmol) were combined in a 2 L Parr reactor. The mixture was degassed with vacuum/N₂ three times, and then charged with 100 psi of H₂. The reaction was stirred at rt overnight, after which time the reaction was complete. The mixture was filtered through a bed of Celite, washing with acetic acid. The filtrate was concentrated to remove acetic acid, and the residue was dissolved in ethyl acetate, washed with sat. aq. NaHCO₃, and dried over MgSO₄. The mixture was then filtered and concentrated to give 19 g (36%) of 2-4 as a tan solid. ¹H NMR (DMSO-^₅ 300 MHz): 12.27 (br s, IH), 8.42 (s, IH), 7.62 (m, IH), 7.39 (m, IH), 7.09 (m, IH), 4.20 (q, 2H), 1.24 (t, 3H); MS (Electrospray): m/z 236.1 (MH⁺).

2-5 ethyl 1-(4-bromo-2-fluorobenzyl)-5-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate

Quinolone 2-4 (3 g, 12.7 mmol) was suspended in 40 mL anhydrous DMF and treated with potassium carbonate (4.2 g, 15.0 mmol) and 4-bromo-2-fluoro-l-(bromomethyl)-2-fluorobenzene (3.5 g, 12.7 mmol). After 24 h at ambient temperature, the reaction was partitioned in ethyl acetate and saturated aqueous NH₄Cl solution. The layers were separated, and the aqueous layer was extracted once with ethyl acetate. The ethyl acetate layers were combined and solvent was removed in vacuo. 2-5 was obtained as a pure white solid (3.75g, 70%) after two washes with cold MeOH. ¹H NMR (CDCl₃, 300 MHz): 8.50 (s, IH), 7.41 (m, IH), 7.34 (dd, 2H), 7.25 (s, IH), 7.05 (m, 2H), 6.86 (m, IH), 5.49 (s, 2H), 4.39 (q, 2H), 1.40 (t, 3H); MS (Electrospray): m/z 422.1 (MH⁺). 2-6 l^-fluoro^-^-propyl-l/f-pyrazoI^-yObenzyl-S-fluoro-l^-dihydro-oxoquinoline-S- car boxy lie acid Aryl bromide 2-5 (100 mg, 0.23 mmol), pyrazole boronic acid (35 mg, 0.23 mmol), 1 M Cs₂CO₃ solution (0.5 mL), and catalytic Pd(t-BuP)₃ (3 mg) were combined in 1 mL of THF in a microwave vial. The mixture was heated under microwave irradiation at 160 ⁰C for 10 min and then the solvent evaporated. The crude product was suspended in 10 mL of dioxane and treated with 2.0 mL of a saturated aqueous LiOH solution. After 16 h, the reaction was poured into a separatory funnel containing 20 mL of ethyl acetate and acidified with 3 N aq. HCl. The product was not appreciably soluble in either layer, but remained suspended in the ethyl acetate layer. The layers were separated and the aqueous layer was extracted with EtOAc (2 x 20 mL). The organic layers were combined and solvent was removed in vacuo to give carboxylic acid 2-6 (70mg. 72%) as a white powder. ¹H NMR (DMSO-d6, 300 MHz): 8.97 (s, IH)₃ 8.2 (s, IH)₅ 7.88 (s, IH), 7.65 (m, IH)₅ 7.46 (m, 2H)₅ 7.32 (m, IH)₅ 7.11 (m, 3H)₅ 5.64 (s, IH)₅4.0 (q₅2H)₅ 1.77 (m₅ 2H)₅ 0.81 (t, 3H); MS (Electro spray): m/z 424.1 (MH⁺).

EXAMPLE 3

8-fluoro-l - {4-[6-(dimethylamino)pyridin-3-yl]benzyl} -4-oxo-l ,4-dihydroquinoline-3-carboxylic acid

3-1 3-2

3-2

8-fluoro-l-{4-[6-(dimethylamino)pyridin-3-yl]benzyl}-4-oxo-l,4-dihydroquinoline-3- carboxylic acid

Fluoropyridine 3-1, prepared according to Scheme 2, (200 mg, 0.51 mmol) and a 40 wt. % aqueous solution of dimethylamine (1 mL) were combined and heated under microwave irradiation at 150 ⁰C for 5 min. Solvent was removed under a stream of nitrogen and the crude product was purified by mass-guided HPLC to give 3-2 (152 mg, 71%) as a light tan solid. ¹H NMR (CDCl₃, 300 MHz): 8.84 (s, IH), 8.50 (d, J= 2.1 Hz₃ IH), 8.40 (m, IH)₅ 8.01 (dd, J= 9.3, 2.1 Hz, IH), 7.54-7.48 (m, 5H)₅ 7.24 (d, J= 8.7 Hz₅ IH)₅ 6.93 (d₅ J= 8.7 Hz₅ IH)₅ 5.71 (br d₅ J= 2.4 Hz₅ 2H)₅ 3.36 (s, 6H); MS (Electrospray): /w/z 418.2 (MH⁺).

Some primary and secondary amines not available as aqueous solutions were also compatible with the substitution chemistry described in Scheme 4. In these instances, excess amine was simply added to the fluoropyridine and 1 mL of water, and the same procedure was applied to afford diverse analogs of 3-2.

The compounds of the following examples were prepared in an analogous manner to that described in the Examples above.

W 2

The following abbreviations are used throughout the text: Me: methyl

Et: ethyl t-Bu: tert-butyl

Ar: aryl

Ph: phenyl

Bn: benzyl

Ac: acetyl aq : aqueous h: hour min: minute

MOH : metal hydroxide

THF: tetrahydrofuran

MH : metal hydride

MWI : microwave irradiation rt: room temperature

HPLC: high performance liquid chromatography While the invention has been described and illustrated with reference to certain particular embodiments thereof, those skilled in the art will appreciate that various adaptations, changes, modifications, substitutions, deletions, or additions of procedures and protocols may be made without departing from the spirit and scope of the invention. It is intended, therefore, that the invention be defined by the scope of the claims that follow and that such claims be interpreted as broadly as is reasonable.

Claims

WHAT IS CLAIMED IS:

1. A compound of formula (I):

Rl is selected from the group consisting of (1) hydrogen, (2) -Ci-6 alkyl, and (3) -CH2-aryl, wherein said Rl alkyl or aryl moiety is optionally substituted with one or more

(a) halogen,

(b) cyano, and

(c) -O-Ci-6 alkyl, wherein said alkyl is optionally substituted with one or more halo;

R2, R3₅ R4 and R5 are independently selected from the group consisting of (1) hydrogen, (2) -Ci-₆ alkyl, (3) -C3-7 cycloalkyl,

(4) halogen,

(5) cyano,

(6) -0-RlO₅ and (7) -S(O)n-Rl l, wherein said R2, R3₅ R4 and R5 alkyl or cycloalkylis optionally substituted with one or more

(a) halogen,

(b) hydroxy, and (c) -O-Ci_6 alkyl;

Re, R7₅ R8 and R9 are independently selected from the group consisting of

(1) hydrogen, (2) -O- Ci-6 alkyl,

(3) -Ci-6 alkyl,

(4) halogen, and

(5) cyano;

Rl 0 and Rl 1 are selected from the group consisting of (l) -Ci-6 alkyl, and (2) -(CH2)m-aryl, wherein said RlO and Rl 1 alkyl or aryl moiety is optionally substituted with one or more

(a) halogen, (b) cyano, and

(c) -O-Ci-6 alkyl, wherein said alkyl is optionally substituted with one or more halo, provided that when RlO and Rl 1 are bonded to a single nitrogen atom, then RlO and R) 1 may be linked together to form a 4, 5 or 6 atom carbocyclic chain, wherein one or more of the ring carbon atoms may be replaced with a nitrogen or oxygen atom;

HET is selected from the group consisting of

wherein Xl, X2_? χ3₅ χ4 and χ5 together form a 5- or 6-membered aromatic ring, wherein each of Xl, X2, χ3_} χ4 and X^ is independently selected from the group consisting of (I) CRl 2 (2) N,

(3) NRl3, (4) O, and (5) S₅ provided that X4 may alternatively be a bond, and further provided that two Rl2 groups, or one Rl2 group and one Rl3 group, when positioned at neighboring X atoms on the ring, may be linked together to form a group selected from - ■ - - - - . - ^■

(1) -O-CH2-CH2-O-, (2) -CR^=CRM-CRH=CRW-, and

(3) -NR 15-CRl4=CRl4-, or

(2)

wherein X6 is selected from the group consisting of

(1) CRl4Rl4\

(2) NRl 5, and

(3) O; provided that when p is 0, χ6 is CR14R14'_;

Rl 2 and Rl 2' are selected from the group consisting of

(1) hydrogen,

(2) Ci-₆ alkyl,

(3) -O-Ci-6 alkyl, (4) cyano,

(5) halogen, and

(6) -(CH2)m-aryl, wherein said Rl2 and Rl2' alkyl or aryl moiety is optionally substituted with one or more

(a) halogen, (b) cyano,

(c) -Ci-6 alkyl, and (d) -O-C 1-6 alkyl, wherein said alkyl moiety is optionally substituted with one or more halo;

R!3 is selected from the group consisting of (1) hydrogen, . (2) -Ci_₆ alkyl₃ wherein said alkyl and cycloalkyl Rl 3 moiety is optionally substituted with one or more

(a) halogen, (b) cyano, or

(c) hydroxy; Rl4 and R 14' are independently selected from the same group as Rl2 and Rl2';

Rl 5 is selected from the same group as Rl 3; 5 m is 1,

2, 3 or 4; n is 0, 1 or 2;, and p is 0, 1 or 2. 0 2. A compound of claim 1, wherein Rl is hydrogen.

3. A compound of claim 1, wherein R2, R3₃ R4 and R5 are independently selected from the group consisting of hydrogen and halogen. 5

4. A compound of claim 1 wherein R6, R7₅ R8 and R9 are independently selected from the group consisting of hydrogen and halogen.

5. A compound of claim 4 wherein R<>, R7_S R8 and R9 are hydrogen. 0

6. A compound of claim 4, wherein R8 is halogen, and R6, R7₃ and R9 are hydrogen.

7. A compound of claim I₅ wherein HET is

8. A compound of claim 7, wherein each of X 1 , χ2, χ3 , χ4 and X5 is CR 1² ₅ wherein Rl 2 is selected from the group consisting of hydrogen, halogen, cyano, -O-Ci-6 alkyl or optionally substituted -C 1-6 alkyl.

0

9. A compound of claim 7, wherein one of Xl , X2, χ3_? χ4 and χ5 is N and the others are each CRl 2₅ wherein Rl 2 is selected from the group consisting of hydrogen, halogen, cyano or optionally substituted Cl -6 alkyl.

10. A compound of claim 7, wherein two of Xl , X2, X3, χ4 and X5 are N and the others are each CR12, wherein Rl2 is selected from the group consisting of hydrogen, halogen, cyano or optionally substituted Ci-6 alkyl.

11. A compound of claim 7, wherein the χl , X2., χ3_? χ4_s χ5 group is selected from the

12. A compound of claim 7, wherein X4 is a bond, and one of Xl₉ X2, χ3 and X5 is N, one is NRl ^₅ and the others are each CRl 2, wherein Rl 2 is selected from the group consisting of hydrogen, halogen, cyano or optionally substituted Cj-6 alkyl.

13. A compound of claim 12, wherein the Xl, χ2, χ3₃ χ4_a χ5 group is selected from the group consisting of

14. A compound of claim 7, wherein two Rl2 groups, or one Rl 2 group and one Rl 3 group, when positioned at neighboring X atoms on the ring, are linked together to form a group selected from

(1) -O-CH2-CH2-O-,

(2) -CRl4=CRl4-CRl4=CRl4-, and

(3) -NRl5-CRl4=CRl4-.

15. A compound of claim 14, wherein the Xl, X², X3, χ4₅ χ5 group is selected from the group consisting of

16. A compound of claim I₅ wherein HET is

(2)

N *&1

17. A compound of claim 16, wherein p is 2 and X^ is selected from the group consisting of (1) CRHR14'₅

(2) NRl 5, or

(3) O.

18. A compound of claim 1, which is selected from the group consisting of

l-[4-(6-chloropyridin-3-yl)-2-fluorobenzyl]-5,8-difluoro-4-oxo-l,4-dihydroquinoline-3- carboxylic acid; l-(2-fluoro-4-(l-propyl-lH-pyrazol-4-yl)benzyl)-5-fluoro-l,4-dihydro-4-oxoquinoline-3- carboxylic acid;

8-fluoro-l-{4-[6-(dimethylamino)pyridin-3-yl]benzyl}-4-oxo-l,4-dihydroquinoline-3-carboxylic acid;

1 -(biphenyl-4-ylmethyl)-8-fluoro-4-oxo- 1 ^-dihydroquinoline-S-carboxylic acid; l-(biphenyl-4-ylmethyl)-5,8-difluoro-4-oxo-l,4-dihydroquinoIine-3-carboxylic acid;

1 -(biphenyl-4-ylmethyl)-4-oxo- 1 ,4-dihydroquinoline-3 -carboxylic acid;

1 -(biphenyl-4-ylrnethyl)-5-fluoro-4-oxo- 1 ,4-dihydroquinoline-3-carboxylic acid;

5,8-difluoro-l -[(2'-fluorobiphenyl-4-yl)methyl]-4-oxo- 1 ^-dihydroquinoline-S-carboxylic acid; 5 ,8-difluoro- 1 -[(3 ^r-fluorobiphenyl-4-yl)methyl]-4-oxo- 1 ,4-dihydroquinoline-3-carboxylic acid;

5,8-difluoro-l-[(4^t-methoxybiphenyl-4-yl)methyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid;

5₃8-difluoro-4-oxo- 1 - { [4'-(trifluoromethyl)biphenyl-4-yI]methyl} - 1 ,4-dihydroquinoline-3 - carboxylic acid; 5 1 -[4-(5-fluoropyridin-2-yl)benzyl]-4-oxo-l ,4-dihydroquinoline-3-carboxylic acid;

1 -[(3-chlorobiphenyl-4-yl)methyl]-4-oxo-l ,4-dihydroquinoline-3-carboxylic acid; l-[(3-fluorobiphenyl-4-yl)methyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid;

1 -[(2'-cyanobipheπyl-4-yl)methyl]-4-oxo-l ,4-dihydroquinoline-3-carboxylic acid;

5 , 8-difl uoro- 1 - [(3 -fluorobiphenyl-4-yl)methyl] -4-oxo- 1 ,4-dihydroquinol ine-3 -carboxylic acid;0 8-fluoro-l-[(3-fluorobiphenyl-4-yl)methyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid;

5,8-difluoro- 1 -[2-fluoro-4-(6-methoxypyridin-3 -yl)benzyl] -4-oxo- 1 ,4-dihydroquinoline-3 - carboxylic acid; l-[2-fluoro-4-(5-fluoro-6-methylpyridin-2-yl)benzyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; 5 l-[2-fluoro-4-(l-methyl-lH-pyrazol-4-yl)beπ2yl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; l-[4-(3-5-dimethyl-lH-pyrazol-4-yl)-2-fluorobenzyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; l-[2-fluoro-4-(lH-pyrazol-4-yl)benzyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; l-[2-fluoro-4-(2-fluoropyridin-4-yl)benzyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; 0 l-[2-fluoro-4-(3-fluoropyridin-4-yl)benzyl]-4-oxo- 1 ^-dihydroquinoline-S-carboxylic acid; l-[2-fluoro-4-(2-methoxypyrimidin-5-yl)ben2yl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid;

1 -[4-(2,3-dihydro- 1₅4-benzodioxin-6-yl)-2-fluorobenzyl]-5,8-difluoro-4-oxo- 1 ,A- dihydroquinoline-3-carboxylic acid;

1 -[4-(I -benzofuran-2-yl)-2-fluorobenzyl]-5,8-difluoro-4-oxo- 1 ^-dihydroquinoline-S-carboxylic S acid;

5,8-difluoro-l-[2-fluoro-4-(lH-indol-4-yl)benzyl]-4-oxo-l-4-dihydroquinoIine-3-carboxylic acid;

5₅8-difluoro- 1 -{2-fluoro-4-[6-(dimethylamino)pyridin-3-yl]benzyl}-4-oxo-l ,4-dihydroquinoline-

3-carboxylic acid;

5,8-difluoro-l-[2-fluoro-4-(3-fluoropyridin-4-yl)ben2yl]-4-oxo-l₅4-dihydroquinoline-3- I carboxylic acid;

5,8-difluoro-l-[2-fluoro-4-(6-fluoropyridin-3-yl)benzyl]-4-oxo-l,4-dihydroquinoline-3- carboxylic acid;

S.S-difluoro-l^-fluoro^-pyrimidm-S-ylbenzyO^-oxo-l^-dihydroquinoline-S-carboxylic acid; 5,8-difluoro-l-[2-fluoro-4-(2-fluoropyridin-4-yI)benzyl]-4-oxo-l₃4-dihydroquinoline-3- carboxylic acid; . .. . . ■

5₃8-difluoro-l-[2-fluoro-4-(5-methoxypyridin-3-yl)benzyl]-4-oxo-l_:>4-dihydroquinoline-3- carboxylic acid; 5,8-difluoro-l-(2-fluoro-4-pyridin-3-ylbenzyl)-4-oxo-l,4-dihydroquinoline-3-carboxylic acid;

1 -[(4'-methoxybiphenyl-4-yl)methyl]-4-oxo- 1 ,4-dihydroquinoline-3-carboxylic acid;

5-fluoro- 1 -[(4'-methoxybiphenyl-4-yl)methyl]-4-oxo- 1 ^-dihydroquinoline-S-carboxylic acid;

5 -fluoro- 1 -[2-fluoro-4-(l -isobutyl- 1 H-pyrazol-4-yl)benzyl]-4-oxo- 1 ,4-dihydroquinoline-3 - carboxylic acid; 5-fluoro-l-[2-fluoro-4-(lH-pyrazol-4-yl)benzyl]-4-oxo-l₅4-dihydroquinoline-3-carboxylic acid;

5-fluoro- 1 -[2-fluoro-4-(l -propyl- 1 H-pyrazol-4-yl)benzyI]-4-oxo- 1 ,4-dihydroquinoline-3- carboxylic acid;

5 -fluoro- 1 -[2-fluoro-4-( 1 -methyl- 1 H-pyrazol-4-yl)benzyl]-4-oxo- 1 ,4-dihydroquinoline-3- carboxylic acid; 8-fluoro-l-[(4'-methoxybiphenyl-4-yl)methyl]-4-oxo-l₅4-dihydroquinoline-3-carboxylic acid;

5₅8-difluoro-4-oxo-l-[4-(l,2,3-thiadiazol-4-yl)ben2yl]-l,4-dihydroquinoline-3-carboxylic acid;

4-oxo- 1 - [4-( 1 ,2,3 -thiadiazo l-4-yl)benzyl] - 1 ,4-dihydroquinoline-3 -carboxylic acid ;

8-fluoro-4-oxo-l -[4-(1 ,2,3~thiadiazol-4-yl)benzyl]-l ^-dihydroquinoline-S-carboxylic acid;

5-fluoro-4-oxo-l -[4-(l,2,3-thiadiazol-4-yl)benzyl]-l ,4-dihydroquinoline-3-carboxylic acid; 8-fluoro- 1 -[4-(I -isobutyl- 1 H-pyrazoI-4-yl)benzyl]-4-oxo- 1 ,4-dihydroquinoline-3 -carboxylic acid;

8-fluoro-l-{4-[6-(4-methylpiperazin-l-yl)pyridin-3-yl]ben2yl}-4-oxo-l,4-dihydroquinoline-3- carboxylic acid;

8-fluoro- l-[4-(6-methoxypyridin-3-yl)benzyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; 8-fluoro-l-[2-fluoro-4-(l-propyl-lH-pyrazol-4-yl)ben2yl]-4-oxo-l,4-dihydroquinoline-3- carboxylic acid;

8-fluoro- 1 -[2-fluoro-4-(6-methoxypyridin-3-yl)benzyl]-4-oxo- 1 ^-dihydroquinoline-S-carboxylic acid;

8-fluoro- 1 -(4-{6-[(2-hydroxyethyl)amino]pyridin-3-yl}benzyl)-4-oxo- 1 ,4-dihydroquinoline-3- carboxylic acid;

8-fluoro- 1 -[4-( 1 -methyl- 1 H-pyrazol-4-yl)ben2yl]-4-oxo- 1 ,4-dihydroq uinoline-3-carboxylic acid;

8-fluoro-4-oxo-l-(4-pyridin-3-ylben2yl)-l,4-dihydroquinoline-3-carboxylic acid; 8-fluoro-l-[4-(6-morphoHn-4-ylpyridin-3-yl)benzyl]-4-oxo-l_:(4-dihydroquinoline-3-carboxylic acid;

8-fluoro- 1 -[2-fluoro-4-(l H-pyrazol-4-yl)benzyl]-4-oxo- 1 ,4-dihydroquinoline-3-caxboxylic acid;

1 -[4-(I -benzyl-1 H-pyrazol-4-yl)-2-fluorobenzyl]-8-fluoro-4-oxo- 1 ,4-dihydroquinoIine-3- carboxylic acid;

8-£luoro-l-[4-(6-fluoropyridin-3-yl)benzyl]-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; l-[4-(6-chloropyridin-3-yl)benzyl]-8-fluoro-4-oxo-l,4-dihydroquinoline-3-carboxylic acid; l-{4-[6-(dimethylatnino)pyridin-3-yl]benzyl}-8-fluoro-4-oxo-l,4-dihydroquinolme-3-carboxylic acid; 1 -[4-(6-azetidin-l-ylpyridin-3-yl)ben2yl]-8-fluoro-4-oxo-l ,4-dihydroquinoline-3 -carboxylic acid;

1 -[4-(6-chloropyridin-3-yl)benzyl]-5-fluoro-4-oxo-l ,4-dihydroquinoline-3-carboxylic acid;

8-fluoro-l -{2-fluoro-4-[l -(3-methylbutyl)- 1 H-pyrazol-4-yl]benzyl} -4-oxo-l ,4-dihydroquinoline-

3 -carboxylic acid;

5-fluoro-l-[4-(6-fluoropyridin-3-yl)benzyl]-4-oxo-l,4-dihydroquinoliiie-3-carboxylic acid; 8-fluoro-4-oxo-l-[4-(6-pyrrolidin-l-ylpyridin-3-yl)benzyl]-l ,4-dihydroquinoline-3 -carboxylic acid;

8-fluoro-l -[2-fluoro-4-( 1 -methyl- 1 H-pyrazol-5-yl)benzyl] -4-oxo-l ,4-dihydroquinoline-3- carboxylic acid;

4-oxo-5-piperazin-l-yH-[4-(6-piperazin-l-ylpyridin-3-yl)benzyl]-l,4-dihydroquinoline-3- carboxylic acid;

5-morpholin-4-yl- 1 -[4-(6-moφholin-4-ylpyridin-3-yl)benzyl]-4-oxo- 1 ,4-dihydroquinoline-3- carboxylic acid;

5-(methylamino)-l-{4-[6-(methylarnino)pyridin-3-yl]ben2yl}-4-oxo-l,4-dihydroquinoline-3- carboxylic acid; 5-fluoro- 1 - {4-[6-(methylamino)pyridin-3-yl]benzyl } -4-oxo- 1 ^-dihydroquinoline-S-carboxylic acid;

5-fluoro-l-(4-{6-[(2-hydroxyethyl)amino]pyridin-3-yl>benzyl)-4-oxo-l,4-dihydroquinoline-3- carboxylic acid;

5-fluoro-4-oxo-l -(4-pyridin-3-ylbenzyl)- 1 ,4-dihydroquinoline-3-carboxylic acid; and enantiomers and diastereomers thereof, and pharmaceutically acceptable salts thereof.

19. A pharmaceutical composition comprising an effective amount of a compound of claim 1 or a pharmaceutically acceptable salts thereof, and a pharmaceutically acceptable carrier.

20. A method of treating Alzheimer's Disease, a cognitive impairment, a pain disorder or a sleep disorder in a patient in need thereof, by administering to the patient an effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof.

21. A method for the manufacture of a medicament for treating Alzheimer's Disease, a cognitive impairment, a pain disorder or a sleep disorder, comprising combining a compound of claim 1 with a pharmaceutical carrier or diluent.