WO2011050200A1

WO2011050200A1 - Fused heterocyclic compounds as orexin receptor modulators

Info

Publication number: WO2011050200A1
Application number: PCT/US2010/053609
Authority: WO
Inventors: Bryan James Branstetter; Michael A. Letavic; Kiev S. Ly; Dale A. Rudolph; Brad M. Savall; Chandravadan R. Shah; Brock T. Shireman
Original assignee: Janssen Pharmaceutica Nv
Priority date: 2009-10-23
Filing date: 2010-10-21
Publication date: 2011-04-28
Also published as: EP2491034A1; US8680275B2; EP2491034B1; UY32968A; AR078733A1; HK1175461A1; US20120202783A1; JP5847087B2; TW201121966A; CL2010001159A1; JP2013508404A; PE20110296A1

Abstract

Disubstituted 3,8-diaza-bicyclo[4.2.0]octane and 3,6-diazabicyclo [3.2.0]heptane compounds are described, which are useful as orexin receptor modulators. Such compounds may be useful in pharmaceutical compositions and methods for the treatment of diseased states, disorders, and conditions mediated by orexin activity, such as insomnia.

Description

FUSED HETEROCYCLIC COMPOUNDS AS OREXIN RECEPTOR

MODULATORS Cross Reference to Related Application

This application claims the benefit of US provisional patent application serial number 61/254,529, filed October 23, 2009.

Field of the Invention

The present invention relates to certain disubstituted 3,8-diaza- bicyclo[4.2.0]octane and 3,6-diazabicyclo [3.2.0]heptane compounds, pharmaceutical compositions containing them, methods of making them, and methods of using them for the modulation of the orexin receptor and for the treatment of disease states, disorders, and conditions mediated by orexin receptor activity.

Background of the Invention

Orexin (or hypocretin) signaling is mediated by two receptors and two peptide agonists. The two orexin peptides (orexin A and orexin B) herein after referred to as orexins, bind to two high affinity receptors, termed orexin-1 and orexin-2 receptors. The orexin-1 receptor is selective in favor of orexin A, while the orexin-2 receptor binds both orexins with similar affinities. The orexins, are cleavage products of the same gene, prepro orexin. In the central nervous system neurons expressing prepro-orexin, the precursor from which orexin is produced, are found in the perifornical nucleus, the dorsal hypothalamus and the lateral hypothalamus (C. Peyron et al., J. Neurosci., 1998, 18(23), 9996- 10015). Orexinergic cells in these nuclei project to many areas of the brain, extending rostrally to the olfactory bulbs and caudally to the spinal cord (van den Pol, A.N. et al., J. Neuroscience., 1999, 19(8), 3171 -3182).

The broad CNS distribution of orexin projections and neurons

expressing orexin receptors is suggestive of orexin involvement in a number of physiological functions including; feeding, drinking, arousal, stress, reward, metabolism and reproduction (T. Sakurai, Nature Reviews Neuroscience, 2007, 8(3), 171 -181 ). The targeted necrosis of cells expressing prepro-orexin suggests the most physiologically important roles of the orexins are likely to be effects on arousal, feeding and metabolism (J. Hara et al., Neuron, 2001 , 30, 345-354). A prominent orexin neuronal projection via the vagus nerve probably mediates central orexin effects on cardiac parameters (W.K. Samson et al., Brain Res., 1999, 831 , 248-253; T. Shirasaka et al., Am. J. Physiol., 1999, 277, R1780- R1785; C.-T. Chen et al., Am. J. Physiol., 2000, 278, R692-R697), gastric acid secretion and gastric motility (A.L. Kirchgessner and M.-T. Liu, Neuron, 1999, 24, 941 -951 ; N. Takahashi et al., Biochem. Biophys. Res. Commun., 1999, 254, 623-627).

Several lines of evidence indicate that the orexin system is an important modulator of arousal. Rodents administered orexins intracerebroventricularly spend more time awake (Piper et al., J. Neurosci. 2000, 12, 726-730). Orexin- mediated effects on arousal have been linked to orexin neuronal projections to histaminergic neurons in the tuberomammillary nucleus (TMN) (Yamanaka et al., Biochem. Biophys. Res. Comm. 2002, 290, 1237-1245). TMN neurons express the orexin-2 receptor primarily, and the orexin-1 receptor to a lesser extent. Rodents whose prepro orexin gene has been knocked out, or whose orexigenic neurons have been lesioned, display altered sleep/wake cycles similar to narcolepsy (Chemelli et al., Cell 1999, 98, 437-451 ; Hara et al., 2001 , supra). Dog models of narcolepsy have been shown to have mutant or nonfunctional orexin-2 receptors (Lin et al., Cell 1999, 98, 365-376). Human narcolepsy appears to be linked to deficient orexin signaling, likely related to immune ablation of orexinergic neurons in the lateral hypothalamus (Mignot et al., Am. J. Hum. Genet. 2001 , 68: 686-699; Minot & Thorsby, New England J. Med. 2001 , 344, 692), or, in rare cases, to mutations in the orexin-2 gene (Peyron et al., Nature Med. 2000, 6, 991 -997). The disclosure that rats, dogs and humans treated with the dual orexin-1/2 receptor antagonist, ACT-078573 (Brisbare-Roch et al., Nature Medicine, 2007, 13, 150-155) exhibited

decreased alertness together with characteristic clinical and EEG

(electroencephalographic) signs of sleep provides evidence to support a role for the orexin system in the regulation of arousal, sleep and wake states. EEG data indicates that orexin-2 may be more important than orexin-1 in the modulation of sleep/wake (P. Malherbe et al., Molecular Pharmacology (2009) 76(3):618-31 ; C. Dugovic et al., J. Pharmacol. Exp. Then, 2009, 330(1 ), 142- 151 ). Disorders of the sleep-wake cycle are therefore likely targets for orexin-2 receptor antagonist therapy. Examples of such disorders include sleep-wake transition disorders, insomnia, restless legs syndrome, jet-lag, disturbed sleep, and sleep disorders secondary to neurological disorders (e.g., manias, depressions, manic depression, schizophrenia, and pain syndromes (e.g., fibromyalgia, neuropathic pain).

The orexin system also interacts with brain dopamine systems.

Intracerebroventricular injections of orexins in mice increase locomotor activity, grooming and stereotypy; these behavioral effects are reversed by

administration of D₂ dopamine receptor antagonists (Nakamura et al., Brain Research, 873(1 ), 181 -7). Therefore, orexin-2 modulators may be useful to treat various neurological disorders; e.g., agonists or up-regulators to treat catatonia, antagonists or down-regulators to treat Parkinson's disease,

Tourette's syndrome, anxiety, delerium and dementias.

Recent evidence indicates a role for orexin in the pathogenesis of Alzheimers disease (Kang et al, Science Express, 2009, 1 -10). Brain interstitial fluid levels of amyloid-beta were demonstrated to fluctuate diurnally in both humans and rodents with sleep deprivation in rodents leading to significant increases in brain interstitial fluid levels of amyloid-beta. Infusion of a dual orexin antagonist in rodents suppressed interstitial levels of amyloid-beta and abolished the natural diurnal variation of amyloid-beta. The reduction of interstitial fluid amyloid-beta levels is correlated with reduced amyloid plaque formation, a hallmark of Alzheimer's disease, and consequently the regulation of sleep time could potentially inhibit amyloid-beta aggregation and slow the progression of Alzheimer's disease.

Orexin neurons project to many regions of the brain associated with reward function (T. Sakurai, supra) and research, focusing on animal models of drug intake, reward, and reinstatement, has expanded the link between the orexin system and addiction. A comprehensive set of data suggest that drugs of abuse activate the orexin system, which in turn enhances drug reward or drug seeking (G. Aston-Jones et al., Neuropharmacology, 2009, 56 (Suppl 1 ) 1 12-121 . Thus interactions between nicotine (J. K. Kane et al., Endocrinology, 2000, 141 (10), 3623-3629; J. K. Kane et al., Neurosci. Lett, 2001 , 298(1 ), 1 -4), morphine (D. Georgescu, et al., J. Neurosci., 2003, 23(8), 3106-31 1 1 ) and amphetamine (C. J. Winrow et al., Neuropharmacology, 2010, 58(1 ), 185-94) and the orexin system have been demonstrated. Additional studies from a number of laboratories have demonstrated an important relationship between the Orexin system and ethanol consumption. As examples, ethanol

consumption in an alcohol-preferring strain of rat was shown to up regulate Orexin mRNA in the lateral hypothalamus and that an Orexin-1 receptor antagonist reduced operant responding for ethanol (Lawrence, et. al., Br. J. Pharmacol., 2006, 148, 752-759). Treatment with an orexin-1 antagonist has also been shown to decrease operant responding for ethanol (Richards, et. al., Psychopharmacology, 2008, 199 (1 ), 109-1 17). Other studies have

demonstrated increased Fos activation of orexin neurons following contextual reinstatement to ethanol seeking (Dayas, et. al., Biol. Psychiatry, 2008, 63 (2), 152-157 and Hamlin, et. al., Neuroscience, 2007, 146, 525-536). Studies have also shown increased ethanol consumption following Orexin infusion into the paraventricular nucleus of the hypothalamus or in the lateral hypothalamus (Schneider, et. al., Alcohol. Clin. Exp. Res., 2007, 37(1 1 ), 1858-1865). These studies provide evidence that modulation of the Orexin system effects alcohol preference and therefore Orexin receptor antagonists are likely to be useful for the treatment of alcoholism.

Orexins and their receptors have been found in both the myenteric and submucosal plexus of the enteric nervous system, where orexins have been shown to increase motility in vitro (Kirchgessner & Liu, Neuron 1999, 24, 941 - 951 ) and to stimulate gastric acid secretion in vitro (Takahashi et al., Biochem. Biophys. Res. Comm. 1999, 254, 623-627). Orexin mediated effects on the gut may be driven by a projection via the vagus nerve (van den Pol, 1999, supra), as vagotomy or atropine prevent the effect of an intracerebroventricular injection of orexin on gastric acid secretion (Takahashi et al., 1999, supra). Orexin receptor antagonists or other down-regulators of orexin receptor- mediated systems are therefore potential treatments for ulcers, irritable bowel syndrome, diarrhea and gastroesophageal reflux. Body weight may also be affected by orexin-mediated regulation of appetite and metabolism (T. Sakurai et al., Cell, 1998, 92(4), 573-585; T.

Sakurai, Reg. Pept, 1999, 85(1 ), 25-30). Some effects of orexin on

metabolism and appetite may be mediated in the gut, where, as mentioned, orexins alter gastric motility and gastric acid secretion. Orexin receptor antagonists therefore are likely to be useful in treatment of overweight or obesity and conditions related to overweight or obesity, such as insulin resistance, type II diabetes, hyperlipidemia, gallstones, angina, hypertension, breathlessness, tachycardia, infertility, sleep apnea, back and joint pain, varicose veins and osteoarthritis. Conversely, orexin receptor agonists are likely to be useful in treatment of underweight and related conditions such as hypotension, bradycardia, ammenorrhea and related infertility, and eating disorders such as anorexia and bulimia.

Intracerebroventricularly administered orexins have been shown to increase mean arterial pressure and heart rate in freely moving (awake) animals (Samson et al., Brain Res. 1999, 831 , 248-253; Shirasaka et al., Am. J.

Physiol. 1999, 277, R1780-R1785) and in urethane-anesthetized animals

(Chen et al., Am. J. Physiol. 2000, 278, R692-R697), with similar results.

Orexin receptor agonists may therefore be candidates for treatment of hypotension, bradycardia and heart failure related thereto, while orexin receptor antagonists may be useful for treatment of hypertension, tachycardia and other arrhythmias, angina pectoris and acute heart failure.

From the foregoing discussion, it can be seen that the identification of orexin receptor modulators, in one embodiment modulators of the orexin-2 receptor, will be of great advantage in the development of therapeutic agents for the treatment of a wide variety of disorders that are mediated through these receptor systems.

Citation of a reference herein shall not be construed as an admission that such reference is prior art to the present invention. All publications referred to herein are incorporated by reference in their entireties.

Various small-molecule orexin receptor modulators have been reported e.g., N-aroyl cyclic amine derivatives (International Publication No.

WO2003002561 , January 9, 3003), ethylene diamine derivatives (International Publication No. WO2003051872, June 26, 2003), sulfonylamino-acetic acid derivatives (International Publication No. WO2004033418, April 22, 2004), N- aryl acetyl cyclic amine derivatives (International Publication No.

WO2004041791 , May 21 , 2004), diazepan derivatives (International Publication No. WO2007126935, November 8, 2007), amidoethylthioether derivatives (International Publication No. WO2007126934, November 8, 2007), 2- substituted proline bis-amide derivatives (International Publication No.

WO2008008551 , January 17, 2008), bridged diazepan derivatives

(International Publication No. WO2008008517, January 17, 2008), substituted diazepan derivatives (International Publication No. WO2008008518, January 17, 2008; US20080132490, WO2009058238), oxo bridged diazepan

derivatives (International Publication No. WO2008143856, November 27, 2008), 1 ,2-diamido ethylene derivatives (International Publication No.

WO200902231 1 , February 19, 2009), heteroaryl derivatives (International Publication No. WO20090163485, June 25, 2009), methyl substituted piperidinyl derivatives (International Publication No. WO2009124956, October 15, 2009), N,N-disubstituted-1 ,4-diazepane derivatives (Cox et al, Bioorganic & Medicinal Chemistry Letters, 2009, 19(1 1 ), 2997-3001 ), Orexin /Hypocretin receptor ligands (Boss, et al., Journal of Medicinal Chemistry, 2009, 52(4), 891 -903) 3,9-diazabicyclo[4.2.1 ]nonanes (Coleman et al, Bioorganic &

Medicinal Chemistry Letters, 2010, 20(14), 4201 -4205), the dual orexin receptor antagonist, [(7R)-4-(5-Chloro-1 ,3-benzoxazol-2-yl)-7-methyl-1 ,4- diazepan-1 -yl][5-methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl]methanone, (Cox, et. al., Journal of Medicinal Chemistry, 2010 53(14) 5320-5332), pyridazine carboxamide derivatives (International Publication No. WO2010051238), 2,5- disubstituted benzamide derivatives (International Publication No

WO2010051237, May 6, 2010), isonicotinamides (International Publication No WO2010051236), heterocyclylbenzoylpiperazines derivatives (International Publication No WO201048012), substituted diazepane derivatives

(International Publication No WO2010048017), substituted pyrrolidine derivatives (International Publication No WO2010048014),

triazolylbenzoylpiperidine derivatives (International Publication No

WO2010048010), triazolylbenzoylmorpholine derivatives (WO2010048013), conformationally restrained N,N disubstituted 1 ,4-diazapane derivatives (Coleman et al, Bioorganic & Medicinal Chemistry Letters, 2010, 20(7), 231 1 - 2315), tripyridyl carboxamide derivatives (International Publication No

WO2010017260), imidazopyridylmethyl substituted piperidine derivatives (International Publication No WO2010072722), imidazopyrazine substituted piperidine derivatives (US2010160344, June 24, 2010; US20100160345, June 24, 2010; International Publication No WO2010060472, June 3, 2010), N- {[(1 R,4S,6R)-3-(2-pyridinylcarbonyl)-3-azabicyclo[4.1 .0]hept-4-yl]methyl}-2- heteroarylamine derivatives (International Publication No WO2010063663), N- {[(1 S,4S,6S)-3-(2-pyridinylcarbonyl)-3-azabicyclo[4.1 .0]hept-4-yl]methyl}-2- heteroarylamine derivatives (International Publication No WO2010063662), imidazopyrimidine derivatives (International Publication No WO2010060471 ), and imidazopyrazine derivatives (International Publication No

WO2010060470). There remains a need, however, for potent orexin receptor modulators with desirable pharmaceutical properties.

Substituted diaza-bicyclic compounds have been reported as active central nervous system agents (International Publication No. WO2001081347, November 1 , 2001 ; US2002/0019388, February 14, 2002), o7 acetylcholine receptor modulators (US2005/101602, May 12, 2005; US2005/0065178, March 24, 2005 and Frost et al, Journal of Medicinal Chemistry, 2006, 49(26), 7843- 7853), proline transporter inhibitors for the treatment of cognitive impairment (WO2008067121 , June 5, 2008) and for improving cognition (WO 2006

124897, November 23, 2006 and US20060258672, November 16, 2006), as androgen receptor ligands for the treatment of androgen receptor associated conditions including cancer (WO2009081 197, July 2, 2009), and as histone deacetylase inhibitors for the treatment of cancers, neurodegenerative diseases and autoimmune diseases (WO20060123121 , November 23, 2006).

SUMMARY OF THE INVENTION

Certain disubstituted 3,8-diaza-bicyclo[4.2.0]octane and 3,6-diazabicyclo

[3.2.0]heptane derivatives have been found to have orexin-modulating activity. Thus, the invention is directed to the general and preferred embodiments defined, respectively, by the independent and dependent claims appended hereto, which are incorporated by reference herein.

In one general aspect, the invention is directed to a chemical entity of Formula (I):

wherein:

n is 0-1 ;

R¹ is a member selected from the group consisting of:

A) phenyl substituted or unsubstituted with one or two R^a members, and substituted in the ortho position with R^b;

R^a is independently selected from the group consisting of: halo, -Ci- 4alkyl, and -Ci_-4alkoxy, wherein two adjacent R^a members may come together to form a six membered aromatic ring;

R^b is a member selected from the group consisting of:

a) halo, -Ci_-4alkoxy, -CF₃, or -CF₂CHF₂;

b) 5-membered heteroaryl ring containing one oxygen or one sulfur members;

c) 5-6 membered heteroaryl ring containing one to three nitrogen members, optionally containing one oxygen member, substituted or unsubstituted with halo, -Ci_-4alkyl,

tetrahydropyran-2-yl, or -N(CH₃)2; and

d) phenyl substituted or unsubstituted with -F, or -CH₃;

B) pyridine substituted or unsubstituted with one or two R^c members and substituted with R^d, wherein R^d is positioned adjacent to the point of attachment by R¹ ;

R^c is a member independently selected from the group consisting of:

-Ci_-4alkyl, -CF₃, and -Ci_-4alkoxy,

R^d is a member selected from the group consisting of:

a) 5-6 membered heteroaryl ring selected from the group

consisting of: 1 H-1 ,2,3-triazol-1 -yl, 2H-1 ,2,3-triazol-2-yl, 1 H- pyrazol-3-yl, and 6-methyl-pyridin-2-yl; and b) -CF₃, -Br, or -Ci_-4alkoxy;

C) 6-mennbered heteroaryl ring selected from the group consisting of: pyrimidin-yl and pyrazin-yl, substituted or unsubstituted with a member independently selected from -CH₃, -OCH₃, or phenyl;

D) 5-membered heteroaryl ring selected from the group consisting of: 2- methyl-1 ,3-thiazol-yl, 5-methyl-isoxazol-4-yl, 2H-pyrazol-3-yl, 1 H- pyrazol-4-yl, isoxazolyl, and 1 ,3-oxazol-4-yl, each substituted with phenyl substituted or unsubstituted with -F or -CI; and

E) 3-methylfuran-2-yl, 9H-fluorene, 9H-fluoren-9-one, 3,5'-biisoxazole,

[3-methyl-5-(4-methyl-1 ,2,3-thiadiazol-5-yl)isoxazol-4-yl], or naphthyridine;

is a member selected from the group consisting of:

A) 6-membered heteroaryl ring containing two nitrogen members

substituted or unsubstituted with one or more members independently selected from the group consisting of: halo, -Ci_-4alkyl, -Ci_-4alkoxy, -CF₃, -NH₂, -NHCH₃, -N(Ci_-4alkyl)_1-2, -NHcyclopropyl, and phenyl;

B) pyridine substituted or unsubstituted with one or two members

independently selected from the group consisting of: -Ci_-4alkyl, -N(Ci- 4alkyl)₂, and -CF₃; and

C) quinoxalin-2-yl, benzooxazol-2-yl, or 5-chloro-1 ,3-benzoxazole.

In another general aspect, the invention is directed to a chemical entity of

Formula (II):

wherein

R³ is phenyl substituted or unsubstituted with a member independently

selected from the group consisting of: -Ci_-4alkyl, -Ci_-4alkoxy, and ph and

R⁴ is a member selected from the group consisting of: (5-trifluoromethyl)- pyridin-2-yl, (5-trifluoromethyl)-pyrimidin-2-yl, 4,6-dimethylpyrinnidin-2-yl, 4- phenylpyrimidin-2-yl, and quinoxalin-2-yl.

Further embodiments are provided by pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II), pharmaceutically acceptable prodrugs of compounds of Formula (I) or Formula (II), and pharmaceutically active metabolites of compounds of Formula (I) or Formula (II).

In certain embodiments, the compound of Formula (I) or Formula (II) is a compound selected from those species described or exemplified in the detailed description below.

In a further aspect, the invention relates to pharmaceutical compositions for treating a disease, disorder, or medical condition mediated by orexin receptor activity, comprising an effective amount of at least one chemical entity selected from compounds of Formula (I) or Formula (II), pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II), pharmaceutically acceptable prodrugs of compounds of Formula (I) or Formula (II), and pharmaceutically active metabolites of Formula (I) or Formula (II).

Pharmaceutical compositions according to the invention may further comprise one or more pharmaceutically acceptable excipients.

In another aspect, the chemical embodiments of the present invention are useful as orexin receptor modulators. Thus, the invention is directed to a method for modulating orexin receptor activity, including when such receptor is in a subject, comprising exposing orexin receptor to an effective amount of at least one chemical entity selected from compounds of Formula (I) or Formula (II), pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II), pharmaceutically acceptable prodrugs of compounds of Formula (I) or Formula (II), and pharmaceutically active metabolites of compounds of Formula (I) or Formula (II).

In another aspect, the invention is directed to a method of treating a subject suffering from or diagnosed with a disease, disorder, or medical condition mediated by orexin receptor activity, comprising administering to the subject in need of such treatment an effective amount of at least one chemical entity selected from compounds of Formula (I) or Formula (II), pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II), pharmaceutically acceptable prodrugs of compounds of Formula (I) or Formula (II), and pharmaceutically active metabolites of compounds of Formula (I) or Formula (II). Additional embodiments of methods of treatment are set forth in the detailed description.

In another aspect, method of studying isotopically labeled compounds in metabolic studies (preferably with ¹⁴C), reaction kinetic studies (with, for example ²H or ³H), detection or imaging techniques [such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT)] including drug or substrate tissue distribution assays, or in radioactive treatment of patients. For example, an ¹⁸F or ¹¹C labeled compound may be particularly preferred for PET or an I¹²³ for SPECT studies.

An object of the present invention is to overcome or ameliorate at least one of the disadvantages of the conventional methodologies and/or prior art, or to provide a useful alternative thereto. Additional embodiments, features, and advantages of the invention will be apparent from the following detailed description and through practice of the invention.

DETAILED DESCRIPTION

The invention may be more fully appreciated by reference to the following description, including the following glossary of terms and the concluding examples. For the sake of brevity, the disclosures of the

publications, including patents, cited in this specification are herein

incorporated by reference.

As used herein, the terms "including", "containing" and "comprising" are used herein in their open, non-limiting sense.

The term "alkyl" refers to a straight- or branched-chain alkyl group having from 1 to 12 carbon atoms in the chain. Examples of alkyl groups include methyl (Me, which also may be structurally depicted by the symbol, 7"), ethyl (Et), n-propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl (tBu), pentyl, isopentyl, tert-pentyl, hexyl, isohexyl, and groups that in light of the ordinary skill in the art and the teachings provided herein would be considered equivalent to any one of the foregoing examples. The term "alkoxy" includes a straight chain or branched alkyl group with a terminal oxygen linking the alkyl group to the rest of the molecule. Alkoxy includes methoxy, ethoxy, propoxy, isopropoxy, butoxy, t-butoxy, pentoxy and so on. "Aminoalkyl", "thioalkyl", and "sulfonylalkyl" are analogous to alkoxy, replacing the terminal oxygen atom of alkoxy with, respectively, NH (or NR), S, and SO₂.

The term "cyano" refers to the group -CN.

The term "cycloalkyl" refers to a saturated or partially saturated, monocyclic, fused polycyclic, or spiro polycyclic carbocycle having from 3 to 12 ring atoms per carbocycle. Illustrative examples of cycloalkyl groups include the foll wing entities, in the form of properly bonded moieties:

A "heterocycloalkyl" refers to a monocyclic ring structure that is saturated or partially saturated and has from 4 to 7 ring atoms per ring structure selected from carbon atoms and up to two heteroatoms selected from nitrogen, oxygen, and sulfur. The ring structure may optionally contain up to two oxo groups on sulfur ring members. Illustrative entities, in the form of properly bonded moieties, include:

The term "aryl" refers to a monocyclic, or fused or spiro polycyclic, aromatic carbocycle (ring structure having ring atoms that are all carbon) having from 3 to 12 ring atoms per ring. (Carbon atoms in aryl groups are sp² hybridized.) Illustrative examples of aryl groups include the following moieties:

The term "heteroaryl" refers to a monocyclic, fused bicyclic, or fused polycyclic aromatic heterocycle (ring structure having ring atoms selected from carbon atoms and up to four heteroatoms selected from nitrogen, oxygen, and sulfur) having from 3 to 12 ring atoms per heterocycle. Illustrative examples of heteroaryl groups include the following entities, in the form of properly bonded moieties:

Those skilled in the art will recognize that the species of heteroaryl, cycloalkyl, aryl and heterocycloalkyl groups listed or illustrated above are not exhaustive, and that additional species within the scope of these defined terms may also be selected.

The term "halogen" represents chlorine, fluorine, bromine or iodine. The term "halo" represents chloro, fluoro, bromo or iodo.

The term "substituted" means that the specified group or moiety bears one or more substituents. The term "unsubstituted" means that the specified group bears no substituents. The term "optionally substituted" means that the specified group is unsubstituted or substituted by one or more substituents. Where the term "substituted" is used to describe a structural system, the substitution is meant to occur at any valency-allowed position on the system. In cases where a specified moiety or group is not expressly noted as being optionally substituted or substituted with any specified substituent, it is understood that such a moiety or group is intended to be unsubstituted.

The terms "para", "meta", and "ortho" have the meanings as understood in the art. Thus, for example, a fully substituted phenyl group has substituents at both "ortho"(o) positions adjacent to the point of attachment of the phenyl ring, both "meta" (m) positions, and the one "para" (p) position across from the point of attachment as illustrated below.

To provide a more concise description, some of the quantitative expressions given herein are not qualified with the term "about". It is understood that, whether the term "about" is used explicitly or not, every quantity given herein is meant to refer to the actual given value, and it is also meant to refer to the approximation to such given value that would reasonably be inferred based on the ordinary skill in the art, including equivalents and approximations due to the experimental and/or measurement conditions for such given value. Whenever a yield is given as a percentage, such yield refers to a mass of the entity for which the yield is given with respect to the maximum amount of the same entity that could be obtained under the particular stoichiometric conditions. Concentrations that are given as percentages refer to mass ratios, unless indicated differently.

The terms "buffered" solution or "buffer" solution are used herein interchangeably according to their standard meaning. Buffered solutions are used to control the pH of a medium, and their choice, use, and function is known to those of ordinary skill in the art. See, for example, G.D. Considine, ed., Van Nostrand's Encyclopedia of Chemistry, p. 261 , 5^th ed. (2005), describing, inter alia, buffer solutions and how the concentrations of the buffer constituents relate to the pH of the buffer. See also Handbook of Chemistry and Physics, 84 e<±, pp. 8-37 to 8-44. For example, a buffered solution is obtained by adding MgSO₄ and NaHCO3 to a solution in a 10:1 w/w ratio to maintain the pH of the solution at about 7.5.

Any formula given herein is intended to represent compounds having structures depicted by the structural formula as well as certain variations or forms. In particular, compounds of any formula given herein may have asymmetric centers and therefore exist in different enantiomeric forms. All optical isomers and stereoisomers of the compounds of the general formula, and mixtures thereof, are considered within the scope of the formula. Thus, any formula given herein is intended to represent a racemate, one or more enantiomeric forms, one or more diastereomeric forms, one or more

atropisomeric forms, and mixtures thereof. Furthermore, certain structures may exist as geometric isomers (i.e., cis and trans isomers), as tautomers, or as atropisomers.

The symbols and ""^- are used as meaning the same spatial arrangement in chemical structures shown herein. Analogously, the symbols and " are used as meaning the same spatial arrangement in chemical structures shown herein.

Additionally, any formula given herein is intended to refer also to hydrates, solvates, and polymorphs of such compounds, and mixtures thereof, even if such forms are not listed explicitly. Certain compounds of Formula (I) or Formula (II) or pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II) may be obtained as solvates. Solvates include those formed from the interaction or complexation of compounds of the invention with one or more solvents, either in solution or as a solid or crystalline form. In some embodiments, the solvent is water and then the solvates are hydrates. In addition, certain crystalline forms of compounds of Formula (I) or Formula (II) or pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II) may be obtained as co-crystals. In certain embodiments of the invention, compounds of Formula (I) or Formula (II) were obtained in a crystalline form. In other embodiments, crystalline forms of compounds of Formula (I) or Formula (II) were cubic in nature. In other embodiments, pharmaceutically acceptable salts of compounds of Formula (I) or Formula (II) were obtained in a crystalline form. In still other embodiments, compounds of Formula (I) or Formula (II) were obtained in one of several polymorphic forms, as a mixture of crystalline forms, as a polymorphic form, or as an amorphous form. In other

embodiments, compounds of Formula (I) or Formula (II) convert in solution between one or more crystalline forms and/or polymorphic forms.

Reference to a chemical entity herein stands for a reference to any one of: (a) the actually recited form of such chemical entity, and (b) any of the forms of such chemical entity in the medium in which the compound is being considered when named. For example, reference herein to a compound such as R-COOH, encompasses reference to any one of, for example, R-COOH_(S), R-COOH₍soi₎, and R-COO^" _(SOi₎- In this example, R-COOH_(s) refers to the solid compound, as it could be for example in a tablet or some other solid

pharmaceutical composition or preparation; R-COOH_(SOi₎ refers to the

undissociated form of the compound in a solvent; and R-COO^"(_SOi) refers to the dissociated form of the compound in a solvent, such as the dissociated form of the compound in an aqueous environment, whether such dissociated form derives from R-COOH, from a salt thereof, or from any other entity that yields R-COO^" upon dissociation in the medium being considered. In another example, an expression such as "exposing an entity to compound of formula R- COOH" refers to the exposure of such entity to the form, or forms, of the compound R-COOH that exists, or exist, in the medium in which such exposure takes place. In still another example, an expression such as "reacting an entity with a compound of formula R-COOH" refers to the reacting of (a) such entity in the chemically relevant form, or forms, of such entity that exists, or exist, in the medium in which such reacting takes place, with (b) the chemically relevant form, or forms, of the compound R-COOH that exists, or exist, in the medium in which such reacting takes place. In this regard, if such entity is for example in an aqueous environment, it is understood that the compound R-COOH is in such same medium, and therefore the entity is being exposed to species such as R-COOH(aq) and/or R-COO^"(_aq), where the subscript "(aq)" stands for

"aqueous" according to its conventional meaning in chemistry and

biochemistry. A carboxylic acid functional group has been chosen in these nomenclature examples; this choice is not intended, however, as a limitation but it is merely an illustration. It is understood that analogous examples can be provided in terms of other functional groups, including but not limited to hydroxyl, basic nitrogen members, such as those in amines, and any other group that interacts or transforms according to known manners in the medium that contains the compound. Such interactions and transformations include, but are not limited to, dissociation, association, tautomerism, solvolysis, including hydrolysis, solvation, including hydration, protonation, and

deprotonation. No further examples in this regard are provided herein because these interactions and transformations in a given medium are known by any one of ordinary skill in the art.

In another example, a zwitterionic compound is encompassed herein by referring to a compound that is known to form a zwitterion, even if it is not explicitly named in its zwitterionic form. Terms such as zwitterion, zwitterions, and their synonyms zwitterionic compound(s) are standard lUPAC-endorsed names that are well known and part of standard sets of defined scientific names. In this regard, the name zwitterion is assigned the name identification CHEBI:27369 by the Chemical Entities of Biological Inerest (ChEBI) dictionary of molecular entities. As generally well known, a zwitterion or zwitterionic compound is a neutral compound that has formal unit charges of opposite sign. Sometimes these compounds are referred to by the term "inner salts". Other sources refer to these compounds as "dipolar ions", although the latter term is regarded by still other sources as a misnomer. As a specific example, aminoethanoic acid (the amino acid glycine) has the formula H₂NCH₂COOH, and it exists in some media (in this case in neutral media) in the form of the zwitterion ⁺H₃NCH₂COO^". Zwitterions, zwitterionic compounds, inner salts and dipolar ions in the known and well established meanings of these terms are within the scope of this invention, as would in any case be so appreciated by those of ordinary skill in the art. Because there is no need to name each and every embodiment that would be recognized by those of ordinary skill in the art, no structures of the zwitterionic compounds that are associated with the compounds of this invention are given explicitly herein. They are, however, part of the embodiments of this invention. No further examples in this regard are provided herein because the interactions and transformations in a given medium that lead to the various forms of a given compound are known by any one of ordinary skill in the art.

Any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds. Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, fluorine, and chlorine, such as ²H, ³H, ¹¹C, ¹³C, ¹⁴C, ¹⁵N, ¹⁸O, ¹⁷O, ³¹ P, ³²P, ³⁵S, ¹⁸F, ³⁶CI, ¹²⁵l, respectively. Such isotopically labeled compounds are useful in metabolic studies (preferably with ¹⁴C), reaction kinetic studies (with, for example ²H or ³H), detection or imaging techniques [such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT)] including drug or substrate tissue distribution assays, or in radioactive treatment of patients. In particular, an ¹⁸F or ¹¹C labeled compound may be particularly preferred for PET or an I¹²³ for SPECT studies. Further, substitution with heavier isotopes such as deuterium (i.e., ²H) may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements.

Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.

When referring to any formula given herein, the selection of a particular moiety from a list of possible species for a specified variable is not intended to define the same choice of the species for the variable appearing elsewhere. In other words, where a variable appears more than once, the choice of the species from a specified list is independent of the choice of the species for the same variable elsewhere in the formula, unless stated otherwise.

By way of a first example on substituent terminology, if substituent

S¹exampie is one of Si and S2, and substituent S² _exampie is one of S3 and S₄, then these assignments refer to embodiments of this invention given according to

1 2 ■ 1 2 the Choices S example iS Si and S example iS S3; S example IS Si and S example IS S₄; S example IS S2 and S example IS S3; S example IS S2 and S example IS S₄; and

equivalents of each one of such choices. The shorter ternninology "S¹ _exam_Pie is one of Si and S₂, and S² _eXampie is one of S₃ and S₄" is accordingly used herein for the sake of brevity, but not by way of limitation. The foregoing first example on substituent terminology, which is stated in generic terms, is meant to illustrate the various substituent assignments described herein. The foregoing convention given herein for substituents extends, when applicable, to members such as R¹ , R², R³, R⁴, A, R^a, R^b, R^c, R^d, R^e, R^f, R^g, R^h, R', R^j, and R^k, and any other generic substituent symbol used herein.

Furthermore, when more than one assignment is given for any member or substituent, embodiments of this invention comprise the various groupings that can be made from the listed assignments, taken independently, and equivalents thereof. By way of a second example on substituent terminology, if it is herein described that substituent S_eXampie is one of Si , S2, and S3, this listing refers to embodiments of this invention for which S_eXampie is Si ; S_eXampie is S₂;

Sexample IS S3; Sexample IS ΟΠ^β Of Si and S2; Sexample IS ΟΠ^β Of Si and S3; Sexample IS one of S2 and S3; S_eXampie is one of Si , S2 and S3; and S_eXampie is any equivalent of each one of these choices. The shorter terminology "S_eXampie is one of Si , S2, and S3" is accordingly used herein for the sake of brevity, but not by way of limitation. The foregoing second example on substituent terminology, which is stated in generic terms, is meant to illustrate the various substituent

assignments described herein. The foregoing convention given herein for substituents extends, when applicable, to members such as R¹ , R², R³, R⁴, A, R^a, R^b, R^c, R^d, R^e, R^f, R⁹, R^h, R', R^j, and R^k, and any other generic substituent symbol used herein.

The nomenclature "C j" with j > i, when applied herein to a class of substituents, is meant to refer to embodiments of this invention for which each and every one of the number of carbon members, from i to j including i and j, is independently realized. By way of example, the term Ci-3 refers independently to embodiments that have one carbon member (Ci ), embodiments that have two carbon members (C2), and embodiments that have three carbon members (C₃). The term C_n-malkyl refers to an aliphatic chain, whether straight or branched, with a total number N of carbon members in the chain that satisfies n < N < m, with m > n. Any disubstituent referred to herein is meant to

encompass the various attachment possibilities when more than one of such possibilities are allowed. For example, reference to disubstituent -A-B-, where A≠ B, refers herein to such disubstituent with A attached to a first substituted member and B attached to a second substituted member, and it also refers to such disubstituent with A attached to the second substituted member and B attached to the first substituted member.

According to the foregoing interpretive considerations on assignments and nomenclature, it is understood that explicit reference herein to a set implies, where chemically meaningful and unless indicated otherwise, independent reference to embodiments of such set, and reference to each and every one of the possible embodiments of subsets of the set referred to explicitly.

In certain embodiments of compounds of Formula (I), n is 0.

In certain embodiments of compounds of Formula (I), n is 1 .

Some embodiments are given by compounds of Formula (I) where R¹ is phenyl substituted with R^a, and R^a is -F, -OCH₃, or -CH₃.

In some of these embodiments, R¹ is phenyl substituted with R^b, and R^b is -Br, -I, -OCH3, -CF2CHF2 or -CF₃.

In some of these embodiments, R^b is 2-pyrrol-1 -yl, pyridin-2-yl, 3- chloropyridin-2-yl, 3-fluoropyridin-2-yl, 3-methylpyridin-2-yl, 4-methylpyridin-2- yl, 5-methylpyridin-2-yl, 6-methylpyridin-2-yl, pyridin-3-yl, N,N-dimethylpyridin- 2-amine, pyrimidin-2-yl, pyrimidin-5-yl, 2H-1 ,2,3-triazol-2-yl, 1 H-1 ,2,3-triazol-1 - yl, 1 H-1 ,2,4-triazol-5-yl, 1 H-pyrazol-1 -yl, 1 H-pyrazol-3-yl, 1 -methyl-1 H-pyrazol- 3-yl, 1 -(tetrahydro-2H-pyran-2-yl)-1 H-pyrazol-5-yl, 1 H-pyrazol-5-yl, 3-methyl- 1 ,2,4-oxadiazol-5-yl, oxazol-2-yl, 2-thiophen-2-yl or 2-furan-2-yl.

In some of these embodiments, R^b is phenyl, 3-fluorophenyl or 4- methylphenyl.

Some embodiments are given by compounds of Formula (I) where R¹ is substituted pyridine, where R^c is -CH₃, -OCH₃, or -CF₃, and R^d is -Br, - OCH₂CH₂CH₃, -CF₃, 1 H-1 ,2,3-triazol-1 -yl, 2H-1 ,2,3-triazol-2-yl, or 3- methylpyridin-2-yl.

Some embodiments are given by compounds of Formula (I) where R¹ is

2- ethoxy-naphthalen-1 -yl, 4-phenyl-pyrimidin-2-yl, 5-(2-fluorophenyl)-2-methyl- 1 ,3-thiazol-4-yl, 2-phenyl-2H-pyrazol-3-yl, 5-phenyl-isoxazol-4-yl, 5-methoxy-2- methylpyrimidin-4-yl, 3-phenylpyrazin-2-yl, 5-phenyl-1 H-pyrazol-4-yl, 5-methyl-

3- phenylisoxazol-4-yl, 5-phenylisoxazol-4-yl, 5-(2-fluorophenyl)-1 ,3-oxazol-4-yl, 5-(3-chlorophenyl)-1 ,3-oxazol-4-yl, 3',5-dimethyl-3,5'-biisoxazole, 3-methyl-5- (4-methyl-1 ,2,3-thiadiazol-5-yl)isoxazol-4-yl, 5-methyl-3-phenylisoxazol-4-yl, or 3-methylfuran-2-yl.

In certain embodiments of compounds of Formula (I), wherein R¹ is phenyl substituted with R^b, wherein R^b is pyrimidin-2-yl, 2H-1 ,2,3-triazol-2-yl, 1 H-pyrazol-3-yl, or 2-thiophen-2-yl.

In certain embodiments of compounds of Formula (I), wherein R¹ is 2- (2H-1 ,2,3-triazol-2-yl)phenyl, 2-fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl, 3-fluoro-2- (2H-1 ,2,3-triazol-2-yl)phenyl, 3-methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 4-fluoro- 2-(2H-1 ,2,3-triazol-2-yl)phenyl, 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 5- fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 5-methoxy-2-(2H-1 ,2,3-triazol-2- yl)phenyl, 3-fluoro-2-(1 H-pyrazol-3-yl)phenyl, 5-fluoro-2-(1 -methyl-1 H-pyrazol- 3-yl, or 2-thiophen-2-yl-phenyl.

Some embodiments are given by compounds of Formula (I) where R² is pyrimidine, pyrazine or pyridazine, each substituted or unsubstituted with one or more -Ci_-4alkyl, -OCH₃, -CF₃, -CI, -N(CH₃)₂, -NH₂, -NHCH₃, or phenyl.

In some of these embodiments, R² is 2-dimethylamino-6-methyl- pyrimidin-4-yl, 2-dimethylamino-6-trifluoromethyl-pyrimidin-4-yl, 2-fluoro-6- pyrimidin-2-yl-phenyl, 2-methylpyrimidin-4-amine, 2-phenylpyrimidin-4-yl, 4,6- dimethoxypyrimidin-2-yl, 4,6-dimethylpyrimidin-2-yl, 4-methoxypyrimidin-2-yl, 4- methylpyrimidin-2-yl, 4-(trifluoromethyl)pyrimidin-2-yl, 4-phenylpyrimidin-2-yl, 5- (trifluoromethyl)pyrimidin-2-yl, 6-methyl-2-trifluoromethyl-pyrimidin-4-yl, 6- methylpyrimidin-4-yl, 6-methylpyrimidin-2-amine, N,6-dimethylpyrimidin-2- amine, N,N-dimethylpyrimidin-4-amine, N-cyclopropyl-pyrimidin-4-amine, N- methylpyrimidin-4-amine, pyrimidine-2,4-diamine, 3,6-dimethylpyrazin-2-yl, 3- methylpyrazin-2-yl, 5-methylpyrazin-2-yl, 5,6-dimethylpyrazin-2-yl, 6- methylpyrazin-2-yl, or 6-chloropyridazin-4-yl.

Some embodiments are given by compounds of Formula (I) where R² is pyridine substituted or unsubstituted with one or more -CH₃, -CF₃, or -N(CH₃)2- In some of these embodiments, R² is 4-methylpyridin-2-yl, 4-

(trifluoromethyl)pyridin-2-yl, 4,6-dimethylpyridin-2-yl, 5-(trifluoromethyl)pyridin- 2-yl, 5-methylpyridin-2-yl, 6-methylpyridin-2-yl, 6-(trifluoromethyl)pyridin-2-yl, or N,N-dimethylpyridin-4-amine.

In certain embodiments of compounds of Formula (I), R² is 2- dimethylamino-6-trifluoromethyl-pyrimidin-4-yl, 4,6-dimethylpyrimidin-2-yl, or 4- (trifluoromethyl)pyrimidin-2-yl.

In certain embodiments of compounds of Formula (I), R¹ is 2-(2H-1 ,2,3- triazol-2-yl)phenyl, 2-fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl, 3-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl, 3-methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 4-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)phenyl, 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 5-fluoro-2- (2H-1 ,2,3-triazol-2-yl)phenyl, 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 3- fluoro-2-(1 H-pyrazol-3-yl)phenyl, 5-fluoro-2-(1 -methyl-1 H-pyrazol-3-yl, or 2- thiophen-2-yl-phenyl and R² is 2-dimethylamino-6-trifluoromethyl-pyrimidin-4-yl, 4,6-dimethylpyrimidin-2-yl, or 4-(trifluoromethyl)pyrimidin-2-yl.

Some embodiments are given by compounds of Formula (II) where R³ is

2,5-dimethylphenyl, 2,4-dimethylphenyl, biphenyl or 2-methoxyphenyl and R⁴ is 4-phenylpyrimidin-2-yl, 4,6-dimethylpyrimidin-2-yl, (5-trifluoromethyl)-pyridin-2- yl, (5-trifluoromethyl)-pyrimidin-2-yl, or quinoxalin-2-yl.

Compounds of Formula (I) and Formula (II) and pharmaceutically acceptable salts thereof are used, alone or in combination with one or more additional active ingredients, to formulate pharmaceutical compositions. A pharmaceutical composition therefore comprises an effective amount of at least one a compound of Formula (I) and Formula (II) or a pharmaceutically acceptable salt thereof.

The invention includes also pharmaceutically acceptable salts of the compounds of Formula (I) and Formula (II), preferably of those described above and of the specific compounds exemplified herein, and methods of treatment using such salts. A "pharmaceutically acceptable salt" is intended to mean a salt of a free acid or base of a compound represented by Formula (I) and Formula (II), that is non-toxic, biologically tolerable, or otherwise biologically suitable for

administration to the subject. See, generally, G.S. Paulekuhn, et al., "Trends in Active Pharmaceutical Ingredient Salt Selection based on Analysis of the

Orange Book Database", J. Med. Chem., 2007, 50:6665-72, S.M. Berge, et al., "Pharmaceutical Salts", J Pharm Sci., 1977, 66:1 -19, and Handbook of

Pharmaceutical Salts, Properties, Selection, and Use, Stahl and Wermuth, Eds., Wiley-VCH and VHCA, Zurich, 2002. Examples of pharmaceutically acceptable salts are those that are pharmacologically effective and suitable for contact with the tissues of patients without undue toxicity, irritation, or allergic response. A compound of Formula (I) and Formula (II) may possess a sufficiently acidic group, a sufficiently basic group, or both types of functional groups, and accordingly react with a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt,

bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt.

Examples of pharmaceutically acceptable salts include sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, phosphates, monohydrogen- phosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyne-1 ,4-dioates, hexyne-1 ,6-dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates, methoxybenzoates, phthalates, sulfonates, xylenesulfonates, phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates, γ-hydroxybutyrates, glycolates, tartrates, methane-sulfonates, propanesulfonates, naphthalene-1 -sulfonates,

naphthalene-2-sulfonates, and mandelates.

When the compound of Formula (I) or Formula (II) contains a basic nitrogen, the desired pharmaceutically acceptable salt may be prepared by any suitable method available in the art, for example, treatment of the free base with an inorganic acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfamic acid, nitric acid, boric acid, phosphoric acid, and the like, or with an organic acid, such as acetic acid, phenylacetic acid, propionic acid, stearic acid, lactic acid, ascorbic acid, maleic acid, hydroxymaleic acid, isethionic acid, succinic acid, valeric acid, fumaric acid, malonic acid, pyruvic acid, oxalic acid, glycolic acid, salicylic acid, oleic acid, palmitic acid, lauric acid, a pyranosidyl acid, such as glucuronic acid or galacturonic acid, an alpha-hydroxy acid, such as mandelic acid, citric acid, or tartaric acid, an amino acid, such as aspartic acid, glutaric acidor glutamic acid, an aromatic acid, such as benzoic acid, 2- acetoxybenzoic acid, naphthoic acid, or cinnamic acid, a sulfonic acid, such as laurylsulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, ethanesulfonic acid, any compatible mixture of acids such as those given as examples herein, and any other acid and mixture thereof that are regarded as equivalents or acceptable substitutes in light of the ordinary level of skill in this technology.

When the compound of Formula (I) or Formula (II) is an acid, such as a carboxylic acid or sulfonic acid, the desired pharmaceutically acceptable salt may be prepared by any suitable method, for example, treatment of the free acid with an inorganic or organic base, such as an amine (primary, secondary or tertiary), an alkali metal hydroxide, alkaline earth metal hydroxide, any compatible mixture of bases such as those given as examples herein, and any other base and mixture thereof that are regarded as equivalents or acceptable substitutes in light of the ordinary level of skill in this technology. Illustrative examples of suitable salts include organic salts derived from amino acids, such as N-methyl-D-glucamine, lysine, choline, glycine and arginine, ammonia, carbonates, bicarbonates, primary, secondary, and tertiary amines, and cyclic amines, such as tromethamine, benzylamines, pyrrolidines, piperidine, morpholine, and piperazine, and inorganic salts derived from sodium, calcium, potassium, magnesium, manganese, iron, copper, zinc, aluminum, and lithium.

The invention also relates to pharmaceutically acceptable prodrugs of the compounds of Formula (I) and Formula (II), and treatment methods employing such pharmaceutically acceptable prodrugs. The term "prodrug" means a precursor of a designated compound that, following administration to a subject, yields the compound in vivo via a chemical or physiological process such as solvolysis or enzymatic cleavage, or under physiological conditions (e.g., a prodrug on being brought to physiological pH is converted to the compound of Formula (I) or Formula (II)). A "pharmaceutically acceptable prodrug" is a prodrug that is non-toxic, biologically tolerable, and otherwise biologically suitable for administration to the subject. Illustrative procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in "Design of Prodrugs" , ed. H. Bundgaard, Elsevier, 1985.

Exemplary prodrugs include compounds having an amino acid residue, or a polypeptide chain of two or more (e.g., two, three or four) amino acid residues, covalently joined through an amide or ester bond to a free amino, hydroxy, or carboxylic acid group of a compound of Formula (I) or Formula (II). Examples of amino acid residues include the twenty naturally occurring amino acids, commonly designated by three letter symbols, as well as 4- hydroxyproline, hydroxylysine, demosine, isodemosine, 3-methylhistidine, norvalin, beta-alanine, gamma-aminobutyric acid, citrulline homocysteine, homoserine, ornithine and methionine sulfone.

Additional types of prodrugs may be produced, for instance, by derivatizing free carboxyl groups of structures of Formula (I) or Formula (II) as amides or alkyl esters. Examples of amides include those derived from ammonia, primary C_halky! amines and secondary di(Ci-₆alkyl) amines.

Secondary amines include 5- or 6-membered heterocycloalkyl or heteroaryl ring moieties. Examples of amides include those that are derived from ammonia, C_halky! primary amines, and di(Ci-₂alkyl)amines. Examples of esters of the invention include Ci_-7alkyl, C_5-7cycloalkyl, phenyl, and phenyl(Ci- ₆alkyl) esters. Preferred esters include methyl esters. Prodrugs may also be prepared by derivatizing free hydroxy groups using groups including

hemisuccinates, phosphate esters, dimethylaminoacetates, and

phosphoryloxymethyloxycarbonyls, following procedures such as those outlined in Fleisher et al., Adv. Drug Delivery Rev. 1996, 19, 1 15-130. Carbamate derivatives of hydroxy and amino groups may also yield prodrugs. Carbonate derivatives, sulfonate esters, and sulfate esters of hydroxy groups may also provide prodrugs. Derivatization of hydroxy groups as (acyloxy)methyl and (acyloxy)ethyl ethers, wherein the acyl group may be an alkyl ester, optionally substituted with one or more ether, amine, or carboxylic acid functionalities, or where the acyl group is an amino acid ester as described above, is also useful to yield prodrugs. Prodrugs of this type may be prepared as described in Robinson et al., J Med Chem. 1996, 39(l),10-18. Free amines can also be derivatized as amides, sulfonamides or phosphonamides. All of these prodrug moieties may incorporate groups including ether, amine, and carboxylic acid functionalities.

The present invention also relates to pharmaceutically active metabolites of the compounds of Formula (I) or Formula (II), which may also be used in the methods of the invention. A "pharmaceutically active metabolite" means a pharmacologically active product of metabolism in the body of a compound of Formula (I) or Formula (II) or salt thereof. Prodrugs and active metabolites of a compound may be determined using routine techniques known or available in the art. See, e.g., Bertolini, et al., J Med Chem. 1997, 40, 201 1 -2016; Shan, et al., J Pharm Sci. 1997, 86 (7), 765-767; Bagshawe, Drug Dev Res. 1995, 34, 220-230; Bodor, Adv Drug Res. 1984, 13, 224-331 ; Bundgaard, Design of Prodrugs (Elsevier Press, 1985); and Larsen, Design and Application of Prodrugs, Drug Design and Development (Krogsgaard-Larsen, et al., eds., Harwood Academic Publishers, 1991 ).

The compounds of Formula (I) or Formula (II) and their pharmaceutically acceptable salts, pharmaceutically acceptable prodrugs, and pharmaceutically active metabolites of the present invention are useful as modulators of the orexin receptor in the methods of the invention. As such modulators, the compounds may act as antagonists, agonists, or inverse agonists. The term "modulators" include both inhibitors and activators, where "inhibitors" refer to compounds that decrease, prevent, inactivate, desensitize or down-regulate orexin receptor expression or activity, and "activators" are compounds that increase, activate, facilitate, sensitize, or up-regulate orexin receptor

expression or activity.

The term "treat" or "treating" as used herein is intended to refer to administration of an active agent or composition of the invention to a subject for the purpose of effecting a therapeutic or prophylactic benefit through

modulation of orexin receptor activity. Treating includes reversing,

ameliorating, alleviating, inhibiting the progress of, lessening the severity of, or preventing a disease, disorder, or condition, or one or more symptoms of such disease, disorder or condition mediated through modulation of orexin receptor activity. The term "subject" refers to a mammalian patient in need of such treatment, such as a human.

Accordingly, the invention relates to methods of using the compounds described herein to treat subjects diagnosed with or suffering from a disease, disorder, or condition mediated by orexin receptor activity, such as: disorders of the sleep-wake cycle, metabolic disorders, neurological disorders and other disorders (e.g., feeding, drinking, arousal, stress, addiction, metabolism and reproduction). Symptoms or disease states are intended to be included within the scope of "medical conditions, disorders, or diseases."

Sleep disorders include, but are not limited to, sleep-wake transition disorders, insomnia, restless legs syndrome, jet-lag, disturbed sleep, and sleep disorders secondary to neurological disorders (e.g., manias, depressions, manic depression, schizophrenia, and pain syndromes (e.g., fibromyalgia, neuropathic).

Metabolic disorders include, but are not limited to, overweight or obesity and conditions related to overweight or obesity, such as insulin resistance, type II diabetes, hyperlipidemia, gallstones, angina, hypertension, breathlessness, tachycardia, infertility, sleep apnea, back and joint pain, varicose veins and osteoarthritis.

Neurological disorders include, but are not limited to, Parkinson's disease, Alzheimer's disease, Tourette's Syndrome, catatonia, anxiety, delirium and dementias.

Other disorders include, but are not limited to, ulcers, irritable bowel syndrome, diarrhea and gastroesophageal reflux.

In treatment methods according to the invention, an effective amount of a pharmaceutical agent according to the invention is administered to a subject suffering from or diagnosed as having such a disease, disorder, or condition. An "effective amount" means an amount or dose sufficient to generally bring about the desired therapeutic or prophylactic benefit in patients in need of such treatment for the designated disease, disorder, or condition. Effective amounts or doses of the compounds of the present invention may be ascertained by routine methods such as modeling, dose escalation studies or clinical trials, and by taking into consideration routine factors, e.g., the mode or route of administration or drug delivery, the pharmacokinetics of the compound, the severity and course of the disease, disorder, or condition, the subject's previous or ongoing therapy, the subject's health status and response to drugs, and the judgment of the treating physician. An example of a dose is in the range of from about 0.001 to about 200 mg of compound per kg of subject's body weight per day, preferably about 0.05 to 100 mg/kg/day, or about 1 to 35 mg/kg/day, in single or divided dosage units (e.g., BID, TID, QID). For a 70-kg human, an illustrative range for a suitable dosage amount is from about 0.05 to about 7 g/day, or about 0.2 to about 2.5 g/day.

Once improvement of the patient's disease, disorder, or condition has occurred, the dose may be adjusted for preventative or maintenance treatment. For example, the dosage or the frequency of administration, or both, may be reduced as a function of the symptoms, to a level at which the desired therapeutic or prophylactic effect is maintained. Of course, if symptoms have been alleviated to an appropriate level, treatment may cease. Patients may, however, require intermittent treatment on a long-term basis upon any recurrence of symptoms.

In addition, the active agents of the invention may be used in

combination with additional active ingredients in the treatment of the above conditions. The additional active ingredients may be coadministered separately with an active agent of compounds of Table 1 or included with such an agent in a pharmaceutical composition according to the invention. In an exemplary embodiment, additional active ingredients are those that are known or discovered to be effective in the treatment of conditions, disorders, or diseases mediated by orexin activity, such as another orexin modulator or a compound active against another target associated with the particular condition, disorder, or disease. The combination may serve to increase efficacy (e.g., by including in the combination a compound potentiating the potency or effectiveness of an active agent according to the invention), decrease one or more side effects, or decrease the required dose of the active agent according to the invention. The active agents of the invention are used, alone or in combination with one or more additional active ingredients, to formulate pharmaceutical compositions of the invention. A pharmaceutical composition of the invention comprises: (a) an effective amount of at least one active agent in accordance with the invention; and (b) a pharmaceutically acceptable excipient.

A "pharmaceutically acceptable excipient" refers to a substance that is non-toxic, biologically tolerable, and otherwise biologically suitable for administration to a subject, such as an inert substance, added to a

pharmacological composition or otherwise used as a vehicle, carrier, or diluent to facilitate administration of a agent and that is compatible therewith.

Examples of excipients include calcium carbonate, calcium phosphate, various sugars and types of starch, cellulose derivatives, gelatin, vegetable oils, and polyethylene glycols.

Delivery forms of the pharmaceutical compositions containing one or more dosage units of the active agents may be prepared using suitable pharmaceutical excipients and compounding techniques known or that become available to those skilled in the art. The compositions may be administered in the inventive methods by a suitable route of delivery, e.g., oral, parenteral, rectal, topical, or ocular routes, or by inhalation.

The preparation may be in the form of tablets, capsules, sachets, dragees, powders, granules, lozenges, powders for reconstitution, liquid preparations, or suppositories. Preferably, the compositions are formulated for intravenous infusion, topical administration, or oral administration.

For oral administration, the compounds of the invention can be provided in the form of tablets or capsules, or as a solution, emulsion, or suspension. To prepare the oral compositions, the compounds may be formulated to yield a dosage of, e.g., from about 0.05 to about 100 mg/kg daily, or from about 0.05 to about 35 mg/kg daily, or from about 0.1 to about 10 mg/kg daily. For example, a total daily dosage of about 5 mg to 5 g daily may be accomplished by dosing once, twice, three, or four times per day.

Oral tablets may include a compound according to the invention mixed with pharmaceutically acceptable excipients such as inert diluents,

disintegrating agents, binding agents, lubricating agents, sweetening agents, flavoring agents, coloring agents and preservative agents. Suitable inert fillers include sodium and calcium carbonate, sodium and calcium phosphate, lactose, starch, sugar, glucose, methyl cellulose, magnesium stearate, mannitol, sorbitol, and the like. Exemplary liquid oral excipients include ethanol, glycerol, water, and the like. Starch, polyvinyl-pyrrolidone (PVP), sodium starch glycolate, microcrystalline cellulose, and alginic acid are suitable disintegrating agents. Binding agents may include starch and gelatin. The lubricating agent, if present, may be magnesium stearate, stearic acid or talc. If desired, the tablets may be coated with a material such as glyceryl

monostearate or glyceryl distearate to delay absorption in the gastrointestinal tract, or may be coated with an enteric coating.

Capsules for oral administration include hard and soft gelatin capsules. To prepare hard gelatin capsules, compounds of the invention may be mixed with a solid, semi-solid, or liquid diluent. Soft gelatin capsules may be prepared by mixing the compound of the invention with water, an oil such as peanut oil or olive oil, liquid paraffin, a mixture of mono and di-glycerides of short chain fatty acids, polyethylene glycol 400, or propylene glycol.

Liquids for oral administration may be in the form of suspensions, solutions, emulsions or syrups or may be lyophilized or presented as a dry product for reconstitution with water or other suitable vehicle before use. Such liquid compositions may optionally contain: pharmaceutically-acceptable excipients such as suspending agents (for example, sorbitol, methyl cellulose, sodium alginate, gelatin, hydroxyethylcellulose, carboxymethylcellulose, aluminum stearate gel and the like); non-aqueous vehicles, e.g., oil (for example, almond oil or fractionated coconut oil), propylene glycol, ethyl alcohol, or water; preservatives (for example, methyl or propyl p-hydroxybenzoate or sorbic acid); wetting agents such as lecithin; and, if desired, flavoring or coloring agents.

The active agents of this invention may also be administered by non-oral routes. For example, the compositions may be formulated for rectal

administration as a suppository. For parenteral use, including intravenous, intramuscular, intraperitoneal, or subcutaneous routes, the compounds of the invention may be provided in sterile aqueous solutions or suspensions, buffered to an appropriate pH and isotonicity or in parenterally acceptable oil. Suitable aqueous vehicles include Ringer's solution and isotonic sodium chloride. Such forms will be presented in unit-dose form such as ampules or disposable injection devices, in multi-dose forms such as vials from which the appropriate dose may be withdrawn, or in a solid form or pre-concentrate that can be used to prepare an injectable formulation. Illustrative infusion doses may range from about 1 to 1000 g/kg/minute of compound, admixed with a pharmaceutical carrier over a period ranging from several minutes to several days.

For topical administration, the compounds may be mixed with a pharmaceutical carrier at a concentration of about 0.1 % to about 10% of drug to vehicle. Another mode of administering the compounds of the invention may utilize a patch formulation to affect transdermal delivery.

Compounds of the invention may alternatively be administered in methods of this invention by inhalation, via the nasal or oral routes, e.g., in a spray formulation also containing a suitable carrier.

Exemplary compounds useful in methods of the invention will now be described by reference to the illustrative synthetic schemes for their general preparation below and the specific examples that follow. Artisans will recognize that, to obtain the various compounds herein, starting materials may be suitably selected so that the ultimately desired substituents will be carried through the reaction scheme with or without protection as appropriate to yield the desired product. Alternatively, it may be necessary or desirable to employ, in the place of the ultimately desired substituent, a suitable group that may be carried through the reaction scheme and replaced as appropriate with the desired substituent. Unless otherwise specified, the variables are as defined above in reference to Formula (I). Reactions may be performed between the melting point and the reflux temperature of the solvent, and preferably between 0 °C and the reflux temperature of the solvent. Reactions may be heated employing conventional heating or microwave heating. Reactions may also be conducted in sealed pressure vessels above the normal reflux temperature of the solvent. Abbreviations and acronyms used herein include the following:

SCHEME A

a

(IXa) (IXb) (X)

According to Scheme A, compound (IV) is obtained from treating compound (III), with hydrogen gas, di-terf-butyl dicarbonate (BOC₂O), in the presence of a Pd catalyst and a tertiary amine base in a suitable solvent such as ethanol. In a particularly preferred embodiment the Pd catalyst is Pd(OH)₂ on carbon (20% on dry basis-Pearlman's catalyst), the tertiary amine base is triethylamine, and the solvent is EtOH. The enamine compound of formula (VI) where R is H, is obtained by reacting a compound of formula (IV) with commercially available benzylamine (V), in a solvent such as toluene and the like, employing a Dean-Stark trap apparatus for the removal of water, at temperatures ranging from 1 15 °C to 125 °C. Alternatively, the enamine compound of formula (VI), where R is -CH₃, is obtained by reacting a

compound of formula (IV) with commercially available (S)- a- methylbenzylamine or (R)- a-methylbenzylamine as described in Frost et al., J. Med Chem, 2006, 49, Pgs 7843-53. Compounds of formula (Vila) and (VI lb) are obtained by reduction of the double bond in a compound of formula (VI), with a reducing agent such as sodium triacetoxyborohydride, and the like, in a solvent such as toluene, with or without the presence of a drying agent such as molecular sieves and acetic acid, at temperatures ranging from 0 °C to ambient temperature. Compounds of formula (Villa) and (VII lb) are obtained by reduction of the ester moiety in compounds of formula (Vila) and (Vllb) with a reducing agent such as lithium aluminum hydride, and the like, in a solvent such as THF, at 0 °C. Compounds of formula (IXa) and (IXb) are obtained by activation of the alcohol with a suitable activating agent such as MsCI, in a solvent such as DCM or THF at temperatures ranging from 0 °C to 23 °C in the presence of a suitable base such as triethylamine followed by heating the mixture to temperatures ranging from 35 °C to 60 °C in the presence of a suitable base such as cesium carbonate for 1 to 24 h. Compound (X) is obtained by treating compounds of formula (IXa) and (IXb) with hydrogen in the presence of a solvent, preferably an alcoholic solvent such as ethanol at hydrogen pressures from 1 atm to 50 psi at temperatures ranging from 23 °C to 50°C, preferably at 50°C. . Alternatively, compound (X) is obtained by treating compounds of formula (IXa) and (IXb) with hydrogen generated using a continous flow hydrogenation apparatus (ThalesNano H-cube apparatus) in the presence of a solvent, preferably ethyl acetate, acetic acid or an alcoholic solvent such as ethanol optionally in the presence of an acid such as HCI or HOAc at hydrogen pressures from 10 to 100 bar at temperatures ranging from 23 °C to 100°C, preferably at 23-50°C. The (3R,4R)-isomer or the (3S.4S)- isomer of compounds of formula (IXa) and (IXb) are prepared as described in Frost et al., J. Med Chem, 2006, 49, Pgs 7843-53.

SCHEME B

(XX) (XXI)

According to SCHEME B, connpound (XIV) is obtained by reaction of connpound (XIII) with benzyl chloroformate in a solvent such as toluene at temperatures ranging from 0 °C to 23 °C, preferably 0 °C for a period of 1 to 8 hours, preferably about 4 h. Compound (XV) is obtained from compound (XIV) by reaction with allyl bromide in the presence of a base, preferably sodium or potassium hydroxide, in a solvent such as toluene, in the presence of a tetra alkyl ammonium chloride such as triethyl benzyl ammonium chloride at temperatures ranging from 23 °C to 100 °C, preferably about 50 °C for a period of from 1 to 4 days, preferably about 2 days. Compound (XVI) is obtained from compound (XV) by reaction with an acid, preferably formic acid. Compound (XVII) is obtained from compound (XVI) by reaction with hydroxyl amine hydrochloride in a solvent such as acetonitrile in the presence of a suitable base agent such as sodium acetate trihydrate for a period ranging from 12 to 24 hours. Compound (XVIII) is obtained from compound (XVII) by heating the compound (XVII) in a solvent such as pentanol at temperatures ranging from 100 °C to 150 °C, preferably at about 135 °C, for 12 to 24 hours, preferably about 20 hours followed by reaction with hydrogen gas in the presence of a catalyst such as Raney Ni, in a solvent such as ethanol and pressures around 60 psi for 2 to 6 hours, preferably about 4 hours. Compound (XVIII) is then converted to compound (XIX) by treatment with di-terf-butyl dicarbonate (BOC2O) in a mixed solvent such as pentanol/ethanol/water in the presence of a base such as sodium bicarbonate for a period of 12 to 24 hours, preferably about 15 hours. Following this procedure, the resulting boc protected material is treated with methanesulfonyl chloride in a solvent such as DCM in the presence of a base such as triethylamine at temperatures ranging from 0 °C to 35 °C, preferably around 0 °C to 23 °C for a period of 1 to 24 hours to provide compound (XIX). Compound (XIX) is converted to compound (XX) by reaction with an acid, preferably TFA in the presence of a solvent, preferably DCM for a period ranging from 4 to 24 hours, preferably about 20 hours followed by reaction with a base, preferably sodium hydroxide, in a solvent such as ethanol/water at temperatures ranging from 23 °C to 80 °C, preferably about 60 °C, for 1 to 4 hours. Compound (XXI) is obtained from compound (XX) by the addition of di-te/f-butyl dicarbonate (BOC2O) to the above mixture followed by treating the resulting boc protected Intermediate with hydrogen in the presence of a catalyst such as palladium on carbon in a solvent such as methanol or ethanol at pressures ranging from 15 to 60 psi for a period of about 2 hours.

SCHEME C

(XXII) (XXIVa)

1 ) HET, K3CO3

(XXV) 2) NaOH, MeOH (XXIVb)

(I) (I)

Intermediate compounds of formulae (XXIVa) and (XXIVb) are readily prepared as outlined in Scheme C from a commercially available or

synthetically accessible compound of formula (XXII) or (XXV). Compounds of formula (XXIVa) are obtained by reacting a compound of formula (XXII), where R^a2 is -H, halo, -Ci_-4alkyl, -Ci_-4alkoxy, -NO2, or two R^a2 members may come together to form a 6-membered aryl ring, where X is C or N (with the proviso that only one X member can be N), with commercially available HET

compounds of formula (XXIII), where HET is a 5-6 membered heteroaryl ring containing one to three nitrogen members, in the presence of copper(l)iodide, Cs₂CO₃ and N,N'-dimethylcyclohexane-1 ,2-diamine; in a solvent such as DMF or dioxane, at temperatures ranging from 60 °C to 100 °C (using conventional or microwave heating). One skilled in the art will recognize that 1 ,2,3-triazole can exist in two tautomeric forms defined as 2H-[1 ,2,3]triazole and 1 H- [1 ,2,3]triazole thus accounting for the formation of two regioisomers.

Alternatively, compounds of formula (XXIVb) are prepared by the reaction of halobenzonitrile compounds of formula (XXV) with HET, where HET is a 5-membered heteroaryl ring selected from the group consisting of triazole or pyrazole, in a solvent such as DMF and the like, in the presence of an inorganic base such as K2CO3 and the like, at temperatures ranging from 100 °C to 130 °C. Subsequent hydrolysis of the nitrile using a base such as aqueous NaOH and the like, in a solvent such as methanol provides

compounds of formula (XXIVb).

Compounds of formula (XXIVb) are also prepared by the reaction of halobenzonitrile compounds of formula (XXV) with HET-Sn(alkyl)₃, where HET- Sn(alkyl)₃ is a commercially available or synthetically accessible

trial kyltinheteroaryl compound, in a solvent such as DME, in the presence of a palladium catalyst such as Pd(PPh₃)₄, in the presence or absence of a catalytic amount of copper iodide, at temperatures ranging from 100 °C to 160 °C, using conventional or microwave heating. Subsequent hydrolysis of the nitrile using a base such as aqueous NaOH and the like, in a solvent such as methanol provides compounds of formula (XXIVb).

Compounds of formula (XXIVb) are also prepared by the reaction of halobenzonitrile compounds of formula (XXV) with HET-boronic acid, where HET-boronic acid is a commercially available or synthetically accessible heteroarylboronic acid, in a solvent such as DME, in the presence of a base such as NaHCO3, a palladium catalyst such as Pd(PPh₃)₄, at temperatures ranging from 80 °C to the reflux temperature of the solvent. Subsequent hydrolysis using a base such as aqueous NaOH and the like, in a solvent such as methanol provides compounds of formula (XXIVb).

Compounds of formula (I), where R^b2 is -I, may be further elaborated to compounds of formula (I), where R^b2 is HET, where HET is a 5-6 membered heteroaryl ring containg one to three nitrogen atoms optionally containing one oxygen member. Reaction of compounds of formula (I), where R^b2 is -I, with HET-Sn(alkyl)₃, where HET-Sn(alkyl)₃ is a commercially available or synthetically accessible trialkyltinheteroaryl compound, in a solvent such as DME, in the presence of a palladium catalyst such as Pd(PPh₃) , in the presence or absence of a catalytic amount of copper iodide, at temperatures ranging from 100 °C to 160 °C, using conventional or microwave heating, may provide compounds of formula (I).

(XXII) (XXVI) (XXVII)

(XXVIII) (XXI Vc)

According to Scheme D, compounds of formula (XXIVc) are obtained from compounds of formula (XXII), by first converting a commercially available or synthetically accessible compound of formula (XXII), where R^a2 is -H, halo, - Ci_-4alkyl, -Ci_-4alkoxy, -CF₃, or -NO2, and where X is C or N (with the proviso that only one X may be N) to one of formula (XXVI) under esterification conditions, for example by treating an alcohol solution of a compound of formula (XXII) with an acid. In a preferred method the compound of formula (XXII) is dissolved in a solvent such as MeOH and treated with H₂SO₄ to afford a compound of formula (XXVI). A compound of formula (XXVII) is obtained by reacting a suitable compound of formula (XXVI) with pinacol borane in the presence of a phosphine and a palladium catalyst, in the presence of an amine base, in a solvent such as THF, at temperatures ranging from room

temperature to 70 °C. In a preferred method the phosphine is tri(o- tolyl)phosphine, the palladium catalyst is Pd(OAc)₂ and the amine base is triethylamine.

A compound of formula (XXIVc) is obtained by reacting a compound of formula (XXVIII) with a compound R^b2-CI, where R^b2-CI is a suitable

commercially available or synthetically accessible 6-membered chloro- substituted heteroaryl compound, in the presence of a palladium catalyst, a base such as Na₂CO3, and the like, in a solvent such as 2-methyl- tetrahydrofuran (2-methyl-THF), and the like, at temperatures ranging from room temperature to 80 °C. In a preferred method the palladium catalyst is PdCl₂(dppf)-dcm adduct , the base is Na₂CO₃ and the solvent is 2-methyl-THF. A compound of formula (XXIVc) is obtained from a compound of formula (XXVIII) via ester hydrolysis. In a preferred method of hydrolysis, a compound of formula (XXVIII) in methyl-THF is treated with aqueous NaOH to afford a compound of formula (XXIVc).

SCHEME E

(XXX) (XXXIa) (XXXIIa)

(XXXI b) (XXXIIb) (XXXIIIb)

According to SCHEME E, substituted heteroaryl compounds R²CI of formula (XXXIIa) and (XXXI I la) are prepared from commercially available or synthetically accessible compounds of formula (XXX). Pyrimidols of formula (XXXIa) and (XXXIb) are commercially available or are prepared by reacting substituted alkyl malonates of formula (XXX), where R^e is halo, with urea in the presence of a base such as sodium ethoxide and the like; in a suitable solvent such as ethanol, at temperatures between room temperature and the reflux temperature of the solvent. Chlorination of commercially available pyrimidinols of formula (XXXIb) or synthetically accessible compounds of formula (XXXIa) using a chlorinating agent such as oxalyl chloride and the like; in a solvent such as CH2CI2, in the presence of a base such as Ν,Ν-dimethylaniline and the like; at temperatures ranging between room temperature and the reflux temperature of the solvent provides chloropyrimidines of formula (XXXIIa) or (XXXIIb).

Additionally, chloropyrimidines of formula (XIV) are further elaborated.

Chloropyrimidines of formula (XXXIIa) or (XXXIIb) are reacted with alkyl Grignard reagents (R⁹MgBr); in the presence of a catalytic amount of

Fe(acac)3, in a solvent such as Et₂O at 0 °C, provides alkyl chloropyrimidines of formula (XXXIIIa) or (XXXIIIb).

3-Fluoro-2-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid and 2-fluoro-6-

(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid are prepared according to

SCHEME F. 3-Fluorophthalic anhydride was dissolved in a solvent such as MeOH, at temperatures ranging from room temperature to the reflux

temperature of the solvent, to provide acid-esters (XXXVIa) and (XXXVIb). Conversion of the acid to the acid chloride is accomplished under standard chlorination conditions. In a preferred method the acid is heated with oxalyl chloride in a solvent such as DCM. Subsequent reaction of the acid chloride with N-hydroxyacetamide in a solvent such as CH₂CI₂ provides a mixture of esters (XXXVI la) and (XXXVI lb). Finally, esters (XXXVI la) and (XXXVI lb) are converted to a mixtue of esters (XXXVIIIa) and (XXXVIIIb) and acids (XXXIXa) and (XXXIXb) by treatment with a base, preferably sodium acetate, in the presence of a solvent, preferably t-BuOH.

Alternately, acid (XXXIXa) is prepared by first converting 2-fluoro-6- iodobenzoic acid to the acid chloride by reaction with a chlorinating agent such as oxalyl chloride, in a solvent such as DCM, with a catalytic amount of DMF, at a temperature of 0 °C. Subsequent reaction of the acid chloride with N- hydroxyacetamide in a solvent such as CH₂CI₂ provides (Z)-N'-((2-fluoro-6- iodobenzoyl)oxy)acetimidamide. 5-(2-Fluoro-6-iodophenyl)-3-methyl-1 ,2,4- oxadiazole is prepared by reacting (Z)-N'-((2-fluoro-6- iodobenzoyl)oxy)acetimidamide with sodium acetate, in a solvent such as tert- butanol, at temperatures ranging from 100 °C to 1 10 °C. 3-Fluoro-2-(3-methyl- 1 ,2,4-oxadiazol-5-yl)benzoic acid (XXXIXa) is prepared by reacting 5-(2-fluoro- 6-iodophenyl)-3-methyl-1 ,2,4-oxadiazole with a grignard reagent such as i- PrMgCI, in a suitable solvent such as THF and the like, at a temperature of -78 °C. Subsequent addition of CO₂ gas, at a temperature of -78 °C provides 3- fluoro-2-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid (XXXIXa).

SCHEME G

(XXXX) (XXXXI)

EtOD

Deuterated pyrimidine compounds of formula (XXXXI) are prepared according to Scheme G. Acetylacetone is reacted with an inorganic base such as K2CO3 in deuterated water, at temperatures ranging from 100 °C to 120 °C to provide 1 ,1 ,1 ,3,3,3,5,5-octadeuteriopentane-2,4-dione. 1 ,1 ,1 ,3,3,3,5,5- Octadeuteriopentane-2,4-dione is subsequently reacted with deuterated urea, in a solvent such as deuterated ethanol, 35% wt. DCI in D₂O, at temperatures ranging from 90 °C to 100 °C to provide deuterated pyrimidinols of formula (XXXX). Chlorination under standard chlorinating conditions provides chlorodetuteratedpyrimidine compounds of formula (XXXXI).

SCHEME H

(XXXXII) (XXXXIII) (XXXXIV) (I)

A compound of formula (XXXXIII) is obtained by treating a compound of formula (XXXXII) with R²CI, where R² is as defined in a compound of formula (I). Commercially available or synthetically accessible suitably substituted heteroaryl compounds of formula R²CI are reacted with compounds of formula (XXXXIII), in the presence of a suitably selected tertiary organic or inorganic base such as CS2CO3, Na2CO3, TEA, DIPEA and the like; in a solvent such as DMF, dichloromethane, THF, acetonitrile and the like; using conventional heating or microwave heating at a temperatures between room temperature and 200 °C. In a preferred embodiment the base is CS2CO3 and the solvent is DMF. Removal of the terf-butylcarbamate (boc) in compounds of formula

(XXXXIII) is accomplished by using methods known to one skilled in the art, such as, HCI, TFA, or -toluenesulfonic acid, in a solvent such as CH₃OH, dioxane, or CH2CI2. In a preferred embodiment, a compound of formula (XXXXIII) is treated with TFA in DCM or HCI to afford a compound of formula

(XXXXIV) .

A compound of formula (I) is obtained from a compound of formula (XXXXIV) by reacting a compound of formula (XXXXIV) with a compound of formula R¹CO2H under amide formation conditions. Compounds of formula R¹CO2H, where R¹ is as defined in formula (I), are commercially available, as described, or synthetically accessible appropriately substituted aryl or heteroaryl carboxylic acids. In a preferred embodiment a compound of formula (XXXXIV), either as a free base or as an acid salt, is reacted with a compound of formula R¹CO2H, in the presence of a dehydrating agent such as

HOBt/EDAC, CDI, HATU, HOAT; a suitably selected base such as DIPEA, TEA, and the like; in an organic solvent or mixture thereof, such as toluene, acetonitrile, ethyl acetate, DMF, THF, methylene chloride, and the like; to afford a compound of formula (I). In a particularly preferred embodiment the dehydrating agent is HATU, and the base is DIPEA.

In an alternative embodiment, a compound of formula R¹CO2H (as described above) may be first converted to a compound of formula R¹COCI, or compound of formula R¹COCI is a commercially available substituted aryl sulfonyl chloride. In a preferred embodiment, a compound of formula R¹CO2H is treated with thionyl chloride in a solvent such as toluene to afford a

compound of formula R¹COCI. A compound of formula (I) is obtained by treating a compound of formula R¹COCI with a compound of formula (XXXXIV), a suitably selected tertiary organic base such as TEA, and the like, in a solvent such as dichloromethane, THF, and the like, at a temperature between room temperature and the reflux temperature of the solvent.

SCHEME I

(XXXXII) (XXXXV)

A compound of formula (II) is obtained by treating a commercially available aryl sulfonyl chloride compound of formula R³SO2CI, wherein R³ is as defined in formula (II), with a compound of formula (XXXXII), wherein R⁴ is as defined above in formula (II) (compound of formula (XXXXV) is prepared as described as in Scheme H from commercially available or synthetically accessible suitably substituted heteroaryl compounds of formula R⁴-CI), a tertiary organic base such as TEA, and the like, in a solvent such as

dichloromethane, THF, and the like, at a temperature between room

temperature and the reflux temperature of the solvent.

Compounds of formula (I) or formula (II) may be converted to their corresponding salts using methods known to those skilled in the art. For example, amines of formula (I) or formula (II) may be treated with trifluoroacetic acid (TFA), HCI, maleic acid, or citric acid in a solvent such as diethyl ether (Et₂O), CH₂CI₂, tetrahydrofuran (THF), or methanol (MeOH) to provide the corresponding salt forms.

Compounds prepared according to the schemes described above may be obtained as single enantiomers, diastereomers, or regioisomers, by enantio- , diastero-, or regiospecific synthesis, or by resolution. Where the compounds according to this invention have at least one chiral center, they may accordingly exist as enantiomers. Where the compounds possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention. Compounds prepared according to the schemes above may alternately be obtained as racemic (1 :1 ) or non-racemic (not 1 :1 ) mixtures or as mixtures of diastereomers or regioisomers. Where racemic and non-racemic mixtures of enantiomers are obtained, single enantiomers may be isolated using conventional separation methods known to one skilled in the art, such as chiral chromatography, recrystallization, diastereomeric salt formation, derivatization into diastereomeric adducts, biotransformation, or enzymatic transformation. Where regioisomeric or diastereomeric mixtures are obtained, single isomers may be separated using conventional methods such as chromatography or crystallization.

The following examples are provided to further illustrate the invention and various preferred embodiments.

EXAMPLES

Chemistry:

In obtaining the compounds described in the examples below and the corresponding analytical data, the following experimental and analytical protocols were followed unless otherwise indicated.

Unless otherwise stated, reaction mixtures were magnetically stirred at room temperature (rt) under a nitrogen atmosphere. Where solutions were "dried," they were generally dried over a drying agent such as Na2SO₄ or MgSO . Where mixtures, solutions, and extracts were "concentrated", they were typically concentrated on a rotary evaporator under reduced pressure. Reactions under microwave irradiation conditions were carried out in a Biotage Initiator or CEM Discover instrument.

Normal-phase flash column chromatography (FCC) was performed on silica gel (S1O2) using prepackaged cartridges, eluting with the indicated solvents.

Preparative reverse-phase high performance liquid chromatography (HPLC) was performed on a Gilson HPLC with an Xterra Prep RPi₈ or an XBridge C18 OBD (5 μητι, 30 x 100 mm, or 50 X 150 mm) column, and a gradient of 10 to 99% acetonitrile/water (20 mM NH₄OH) over 12 to 18 min, and a flow rate of 30 mL/min.

Mass spectra (MS) were obtained on an Agilent series 1 100 MSD using electrospray ionization (ESI) in positive mode unless otherwise indicated.

Calculated (calcd.) mass corresponds to the exact mass.

Nuclear magnetic resonance (NMR) spectra were obtained on Bruker model DRX spectrometers. The format of the ¹H NMR data below is: chemical shift in ppm downfield of the tetramethylsilane reference (multiplicity, coupling constant J in Hz, integration).

Chemical names were generated using ChemDraw Ultra 6.0.2

(CambridgeSoft Corp., Cambridge, MA) or ACD/Name Version 9 (Advanced Chemistry Development, Toronto, Ontario, Canada).

Int rmediate 1 : 3,8-Diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester.

Step A. 3-Oxo-piperidine-1 ,4-dicarboxylic acid 1 -tert-butyl ester 4-ethyl ester. A mixture of 1 -benzyl-3-oxo-piperidine-4-carboxylic acid ethyl ester (1 1 .31 g, 38 mmol), di-t-butyl dicarbonate (8.78 g, 40.2 mmol), Et₃N (5.4 ml_, 38.7 mmol) and Pd(OH)₂ on carbon (20% on dry basis-Pearlman's catalyst) (1 .3 g) were taken into EtOH (1 10 ml_). The mixture was hydrogenated at 60 psi for 24 h in a Parr bottle. The catalyst was removed by filtration and the filtrate was concentrated to dryness to tan solid. Crude residue was shaken well with hexane (100 ml_) and filtered. The filtrate was concentrated to yield the title compound (9.70 g, 94.25%). MS (ESI) mass calcd. for Ci₃H₂i NO₅, 271 .32; ¹H NMR (400 MHz, CDCI₃) 4.24 (q, J = 7.1 , 2H), 4.03 (s br, 2H), 3.49 (t, J = 5.6, 2H), 2.32 (m, 3H), 1 .47 (s, 9H), 1 .31 (t, J = 7.1 , 3H).

Step B. 5-Benzylamino-3,6-dihydro-2H-pyridine-1 ,4-dicarboxylic acid 1 - tert-butyl ester 4-ethyl ester. 3-Oxo-piperidine-1 ,4-dicarboxylic acid 1 -tert-butyl ester 4-ethyl ester (8.15 g, 30 mmol) from Step A and benzyl amine (3.43 g, 31 .8 mmol) were dissolved into toluene (150 ml_). The mixture was refluxed vigorously for 72 h and the generated water was collected into Dean-Stark apparatus. The residual solution was concentrated to yield the title compound (10.2 g, 92.5%). MS (ESI) mass calcd. for C₂oH28N₂O₄, 360.45, m/z found, 361 .2 [M+H]⁺. The crude product was carried to the next step without any purification.

Step C: 3-Benzylamino-piperidine-1 ,4-dicarboxylic acid 1 -tert-butyl ester 4-ethyl ester. To a mixture of 5-benzylamino-3,6-dihydro-2H-pyridine-1 ,4- dicarboxylic acid 1 -tert-butyl ester 4-ethyl ester (10.2 g, 28.9 mmol) in toluene (1 10 mL) was added NaBH(OAc)₃ (30 g, 141 .5 mmol) and freshly activated 4A° powder molecular sieve (24 g) with vigorous stirring. The reaction mixture was cooled to 0 °C, then acetic acid (32.5 mL, 566 mmol) was added drop-wise in such a way that reaction mixture temperature remained below 5 °C. After the addition of acetic acid was complete, the mixture was allowed to warm to ambient temperature and stirred for 16 h. The reaction mixture was filtered and concentrated to remove most of the acetic acid. The crude residue was dissolved in ethyl acetate (125 mL) and saturated aqueous NaHCO3 solution (100 mL) was slowly added to neutralize the residual acid under stirring. The layers were separated and the aqueous layer was extracted with ethyl acetate (2 x 100 mL). The combined organics were dried over Na₂SO₄, filtered, and concentrated under reduced pressure (1 1 .25 g, crude). The residue was purified (FCC, S1O2, ethyl acetate/hexanes, gradient 0-40%) to yield the title compound (4.59g, 45%). MS (ESI) mass calcd. for C20H30N2O2, 362.46; m/z found, 363.3 [M+H]⁺. ¹ H NMR (DMSO-c/₆): 7.53-6.76 (m, 5H), 4.10-3.96 (m, 3H), 3.89-3.87 (m, 1 H), 3.66 3.54 (m, 1 H), 3.05-2.60 (m, 4H), 1 .80-1 .65 (m, 2H), 1 .60-1 .45 (m, 1 H), 1 .40 (s, 9H), 1 .14 (t, J = 7.1 , 3H).

Step D: 3-Benzylamino-4-hydroxymethyl-piperidine-1 -carboxylic acid tert-butyl ester. To a solution of LiAIH₄ (2M in THF, 14 mmol in 25 ml THF), cooled to 0 °C, was slowly added a solution of 3-benzylamino-piperidine-1 ,4- dicarboxylic acid 1 -tert-butyl ester 4-ethyl ester (4.53g, 12.5 mmol) in THF (25 mL). The reaction mixture was stirred at 0 °C for 15 min and then at room temperature for 2 h. The reaction mixture was again cooled to 0 °C and quenched with Na₂SO , 10 H₂O and stirred for 16 h. The reaction mixture was filtered, washed with THF and concentrated to yield title compound (3.69 g, 92%). MS (ESI) mass calcd. for CisH slWs, 320.43; m/z found, 321 .3 [M+H]⁺. ¹ H NMR (CDCIs): 7.42-7.19 (m, 5H), 5.64-4.97 (m, 1 H), 4.57-4.0 (m, 1 H), 3.99- 3.82 (m, 2H), 3.79-3.56 (m, 3H), 3.04-2.58 (m, 3H), 1 .95-1 .79 (m, 2H), 1 .74- 1 .55 (m, 2H), 1 .47 (s, 9H).

Step E: 8-Benzyl-3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert- butyl ester. To a cooled to 0 °C solution of 3-benzylamino-4-hydroxymethyl- piperidine-1 -carboxylic acid tert-butyl ester (3.65 g, 1 1 .4 mmol) and

triethylamine (4.77 mL, 34.2 mmol) in THF (60 mL), was added drop-wise methane sulfonyl chloride (1 .7 g, 14.8 mmol) at 0 °C. The reaction mixture was warmed to room temperature and stirred for 1 h, then CS₂CO3 (5.0 g, 15.4 mmol) was added. The reaction mixture was heated to 60 °C for 18 h. The reaction mixture was cooled to ambient temperature and filtered. The filtrate was washed with H₂O (2 x 100 mL), the organic layer was separated and the aqueous layer was extracted with EtOAc (2 x 100 mL). The combined organics were dried (Na₂SO₄), filtered, and concentrated under reduced pressure to yield the crude title compound (3.38 g). The crude product was purified (FCC, S1O2, 4% acetone, dichloromethane) to yield pure title compound (2.88 g, 84%). MS (ESI) mass calcd. for C18H26N2O2, 302.42; m/z found, 303.2 [M+H]⁺. ¹ H NMR (CDCI3): 7.35-7.15 (m, 5H), 4.02-2.80 (m, 9H), 2.48-2.36 (m, 1 H), 1 .95-1 .65 (m, 2H), 1 .56-1 .32 (m, 10H).

Step F: 3,8-Diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester. A mixture of 8-benzyl-3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester (1 .34 g, 4.44 mmol) and wet Pd(OH)₂/C (20 wt%, 938 mg) in EtOH (30 mL) was shaken under 60 psi atmosphere of H₂ for 2 days at 50 °C. The reaction mixture was filtered and concentrated to give title compound (1 .0 g, 94%). MS (ESI) mass calcd. for C_{1 1}H₂0N₂O₂, 212.29; m/z found, 213.2 [M+H]⁺. ¹ H NMR (CDCI3): 4.32-4.0 (m, 1 H), 3.93-3.17 (m, 5H), 3.10-2.70 (m, 3H), 1 .98- 1 .67 (m, 2H), 1 .56-1 .36 (m, 9H).

Intermediate 2: 2-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline.

Step A: 8-Quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester. To a mixture of 3,8-diaza-bicyclo[4.2.0]octane-3- carboxylic acid tert-butyl ester (Intermediate 1 , 1 .07 g, 5.05 mmol) and 2- chloro-quinoxaline (1 .02 g, 6.06 mmol) in DMF (20.0 ml_) was added Cs₂CO₃ (3.95 g, 12.1 mmol). The reaction mixture was heated at 80 °C for 16 h then cooled to ambient temperature. The reaction mixture was partitioned between water (400 ml_) and ethyl acetate (50 ml_) twice. The organic layers were combined and washed with water. The organic layers were dried (Na₂SO ), filtered and concentrated under reduced pressure to yield crude title compound (1 .84 g) which was used in the next step without purification.

Step B: 2-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline. To a solution of 8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester (1 .84 g, 5.40 mmol) in dioxane (30 ml_) was added trifluoro acetic acid (8.0 ml_). The reaction mixture was stirred at rt for 16 h. The solvent and excess trifluoro acetic acid were removed under reduced pressure. The crude product was purified on HPLC (Agilent, basic system) to yield the title

compound (925 mg, 72%). MS (ESI) mass calcd. for d₄H₁₆N₄, 240.3; m/z found, 241 .2 [M+H]⁺. ¹ H NMR (CDCI₃): ¹ H NMR (400 MHz, CDCI₃) 8.12 (s, 1 H), 7.86 (dd, J = 8.4, 1 .0, 1 H), 7.67 (dd, J = 8.4, 1 .0, 1 H), 7.54 (dd, J = 8.4, 1 .5,

1 H), 7.37 (dd, J = 8.3, 1 .4, 1 H), 4.45-4.37 (m, 1 H), 4.17-4.03 (m, 1 H), 3.90-3.82 (m, 1 H), 3.57 (dd, J = 14.3, 2.0, 1 H), 3.19-3.04 (m, 2H), 2.98 (s, 1 H), 2.81 -2.62 (m, 2H), 2.14-2.03 (m, 1 H), 1 .85-1 .73 (m, 1 H).

Intermediate 3: (1 R, 6S)-2-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline.

H The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S) 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester in Step A. MS (ESI) mass calcd. for Ci₄Hi₆N₄, 240.3; m/z found, 241 .2 [M+H]⁺. ¹ H NMR (CDCIs): 8.15 (s, 1 H), 7.86 (dd, J = 8.4, 1 .0, 1 H), 7.67 (dd, J = 8.4, 1 .0, 1 H), 7.57-7.34 (m, 1 H), 7.40-7.34 (m, 1 H), 4.45-4.37 (m, 1 H), 4.17-4.10 (m, 1 H), 3.86 (dd, J = 7.5, 3.4, 1 H), 3.57 (dd, J = 14.3, 2.0, 1 H), 3.10-3.05 (m, 2H), 2.98 (s, 1 H), 2.81 -2.62 (m, 2H), 2.14-2.03 (m, 1 H), 1 .84-1 .73 (m, 1 H).

Intermediate 4: (1 R, 6S)-8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S) 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and 2- chloro-4,6-dimethyl-pyrimidine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for Ci₂H₁₈N₄, 218.3; m/z found, 219.2 [M+H]⁺. ¹ H NMR (CDCI₃): 6.32 (s, 1 H), 4.25-4.16 (m, 1 H), 4.03 (t, J = 7.6, 1 H), 3.75(dd, J = 7.9, 3.1 , 1 H), 3.62 (dd, J = 14.5, 1 .6, 1 H), 3.15-3.05 (m, 1 H), 2.94 (dd, J = 14.5, 3.8, 1 H), 2.67-2.56 (m, 2H), 2.28 (s, 6H), 2.1 1 -1 .98 (m, 2H), 1 .77-1 .64 (m, 1 H).

Intermediate 5: (1 R, 6S)-8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 S, 6R) 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and 2- chloro-4,6-dimethyl-pyrimidine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for Ci₂Hi₈N₄, 218.3; m/z found, 219.2[M+H]⁺. ¹H NMR (CDCI3): 6.31 (s, 1 H), 4.25-4.16 (m, 1 H), 4.02 (t, J = 7.6, 1 H), 3.71 (dd, J = 8.0, 3.1 , 1 H), 3.59 (dd, J = 14.5, 1 .5, 1 H), 3.14-3.05 (m, 1 H), 2.94 (dd, J = 14.5, 3.8, 1 H), 2.67-2.56 (m, 2H), 2.28 (s, 6H), 2.1 1 -1 .98 (m, 2H), 1 .76-1 .62 (m, 1 H).

Intermediate 6: 8-(4-Phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 2, substituting 2-chloro-4-phenyl-pyrimidine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for Ci₆Hi₈N₄, 266.34; m/z found, 267.2 [M+H]⁺. The compound was used as such in the subsequent reactions.

Intermediate 7: 2-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-benzooxazole.

H

The title compound was prepared in a manner analogous to Intermediate 2, substituting 2-chloro-benzooxazole for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for C13H1₅N3O, 229.28; m/z found, 230.2 [M+H]⁺. The compound was used as such in the subsequent reactions.

Intermediate 8: (1 R, 6S)-[2-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-6-methyl- pyrimidin-4-yl]-dimethyl-amine.

H

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S)-(3,8-diaza-bicyclo[4.2.0]octane-3-caboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and 4- chloro-2-dimethylamino-6-methyl pyrimidine for 2-chloro-quinoxaline in Step A. The residue was purified (FCC, SiO₂, MeOH (2M NH₃)/DCM, 0-10%). MS (ESI) mass calcd. for Ci₃H₂i N₅, 247.34; m/z found 248.1 [M+H]⁺. ¹ H NMR (CDCIs): 5.40 (s, 1 H), 4.21 -4.10 (m, 1 H), 3.85 (t, J = 7.4, 1 H), 3.63-3.49 (m, 2H), 3.33 (s, 1 H), 3.09 (d, J = 9.3, 7H), 2.97 (dd, J = 14.3, 3.8, 1 H), 2.71 -2.52 (m, 2H), 2.19 (s, 3H), 2.09-1 .97 (m, 1 H), 1 .77-1 .59 (m, 1 H).

Intermediate 9: (1 R, 6S)-8-(6-Methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane.

H

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S)-(3,8-diaza-bicyclo[4.2.0]octane-3-caboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and 4- chloro-2-trifluoromethyl-6-methyl-pyrimidine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for C12H15 F₃N₄, 272.27; m/z found 273.0 [M+H]⁺. ¹H

NMR (CDCI3): 6.29 (s, br, 1 H), 6.13 (s, 1 H), 4.52 (d, J = 8.0, 1 H), 4.08-3.94 (m, 1 H), 3.87-3.75 (m, 1 H), 3.64 (t, J = 19.8, 1 H), 3.39-3.26 (m, 1 H), 3.1 1 (dd, J = 14.2, 3.5, 1 H), 3.00-2.77 (m, 2H), 2.38 (s, 3H), 2.22-2.07 (m, 1 H), 1 .92-1 .79 (m, 1 H). Intermediate 10: (1 R, 6S)-8-(3,6-Dimethyl-pyrazin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane.

H

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S)-(3,8-diaza-bicyclo[4.2.0]octane-3-caboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and 3- chloro-2,5-dimethyl-pyrazine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for Ci₂Hi₈N , 218.30. The compound was used as such in the subsequent reactions.

Intermediate 1 1 : (1 R, 6S) [4-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-6-trifluoromethyl- pyrimidin-2-yl]-dimethyl-amine.

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S)-(3,8-diaza-bicyclo[4.2.0]octane-3-caboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and (4- chloro-6-trifluoromethyl-pyrimidin-2-yl)-dimethyl-amine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for Ci₃Hi₈ F₃N₅, 301 .31 . m/z found 302.1

[M+H]⁺. ¹H NMR (CDCI₃): 9.04 (s, 1 H), 5.98-5.63 (m, 1 H), 4.56 (dd, J = 4.9, 3.1 , 1 H), 3.99 (t, J = 7.8, 1 H), 3.88-3.70 (m, 2H), 3.68-3.37 (m, 2H), 3.33-3.17 (m, 1 H), 3.16-3.00 (m, 6H), 2.95-2.74 (m, 1 H), 2.33-1 .85 (m, 2H).

Intermediate 12: (1 R, 6S)-( [4-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-6-methyl- pyrimidin-2-yl]-dimethyl-amine.

The title compound was prepared in a manner analogous to Intermediate 2, substituting (1 R, 6S)-(3,8-diaza-bicyclo[4.2.0]octane-3-caboxylic acid tert-butyl ester for 3,8-diaza-bicyclo[4.2.0]octane-3-carboxylic acid tert-butyl ester and (4- chloro-6-methyl-pyrimidin-2-yl)-dimethyl-amine for 2-chloro-quinoxaline in Step A. MS (ESI) mass calcd. for Ci₃H₂i N_5> 247.34. m/z found 248.1 [M+H]⁺. ¹H NMR (CDCIs): 5.40 (s, 1 H), 4.21 -4.10 (m, 1 H), 3.85 (t, J = 7.4, 1 H), 3.63-3.49 (m, 2H), 3.33 (s, 1 H), 3.09 (d, J = 9.3, 7H), 2.972.52 (m, 2H), 2.19 (s, 3H), 2.09- 1 .97 (1 H), 1 .77-1 .59 (m, 1 H)

Intermediate 13: 5-Fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid.

5-Fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid. To a solution of 5-fluoro-2-iodo- benzoic acid (3.86 g, 14.65 mmol), 2H-[1 ,2,3]triazole (2.5 g, 36.2 mmol),

Cs₂CO₃ (8.62 g, 24.5 mmol), trans-N, N'-dimethyl-cyclohexane-1 ,2-diamine (0.4 ml_), Cul (244 mg) and DMF (13 ml_) were added to a microwave ready vessel and heated to 100 °C for 10 min. The mixture was cooled, diluted with water, and extracted with EtOAc. The aqueous layer was acidified and extracted with EtOAc. The organic layer was dried over Na₂SO and concentrated. The residue was purified by FCC (SiO₂, gradient DCM to 10% MeOH/1 %

HOAc/DCM) gave the product as a white powder, (2.14 g, 71 %). ¹H NMR (400 MHz, CD3OD): 7.91 (s, 2H), 7.76 (dd, J = 8.9, 4.8 Hz, 1 H), 7.59 (dd, J = 8.5, 2.9 Hz, 1 H), 7.49 - 7.42 (m, 1 H).

Intermediate 14: 2-[1 ,2,3]Triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting 2-iodo-benzoic acid for 5-fluoro-2-iodo-benzoic acid. ¹H NMR (400 MHz, CD₃OD): 7.91 (s, 2H), 7.85-7.82 (m, 1 H), 7.75 (dd, J = 8.1 , 1 .0 Hz, 1 H), 7.69 (td, J = 7.7, 1 .5 Hz, 1 H), 7.60-7.55 (m, 1 H).

Intermediate 15: 2-Fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting 6-fluoro-2-iodo-benzoic acid for 5-fluoro-2-iodo-benzoic acid. ¹H NMR (400 MHz, CD₃OD): 7.96 (s, 2H), 7.87-7.82 (m, 1 H), 7.70 (td, J = 8.1 , 5.1 Hz, 1 H), 7.59 (ddd, J = 9.7, 8.4, 1 .4 Hz, 1 H).

Intermediate 16: 4-Fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting 4-fluoro-2-iodo-benzoic acid for 5-fluoro-2-iodo-benzoic acid. ¹H NMR (400 MHz, CD₃OD): 7.93 (s, 2H), 7.88 (dd, J = 8.7, 5.9 Hz, 1 H), 7.56 (dd, J = 9.2, 2.5 Hz, 1 H), 7.38-7.30 (m, 1 H).

Intermediate 17: 5-Fluoro-2-pyrimidin-2-yl-benzoic acid.

Step A. 5-Fluoro-2-iodo-benzoic acid methyl ester. To a 500 mL round- bottomed flask was added 5-fluoro-2-iodo-benzoic acid (23 g, 86.5 mmol) in methanol (230 mL). To the resulting solution was added cone, sulfuric acid (2.3 mL, 43.2 mmol). The reaction mixture was warmed to 65 °C and stirred for 15 h. The resulting mixture was concentrated under reduced pressure to a crude which was then was partitioned between ethyl acetate (250 mL) and a half sat. Na2CO3(aq) solution (250 mL). The layers were thoroughly mixed and then separated. The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide a yellow oil (23 g, 95% yield). ¹ H NMR (400 MHz, CDCI₃): 7.94 (dd, J = 8.7, 5.4 Hz, 1 H), 7.54 (dd, J = 9.0, 3.1 Hz, 1 H), 6.93 (m, 1 H), 3.94 (s, 3H).

Step B: 5-Fluoro-2-(4,4,5,5-tetramethyl-[1 ,3,2]dioxaborolan-2-yl)-benzoic acid methyl ester. To a 1 L round-bottomed flask equipped with a reflux condenser, temperature probe, and nitrogen line, was added 5-fluoro-2-iodo- benzoic acid methyl ester (23 g, 82 mmol) in anhydrous THF (250 mL).

Anhydrous triethylamine (34 mL, 246.4 mmol) was added and the resulting mixture was degassed with a nitrogen sparge for 5 minutes. Pinacol borane (17.9 mL, 123.2 mmol) was added and the reaction mixture was degassed once more for 5 minutes. Lastly, tri(o-tolyl)phosphine (1 .25 g, 4.1 mmol) and palladium acetate (461 mg, 2.053 mmol) were added. Again, the reaction mixture was degassed with a nitrogen sparge. The mixture was heated to 65 °C and stirred for 1 h. After cooling to room temperature, the reaction mixture was quenched with half sat. ammonium chloride solution (250 mL), and the resulting layers were separated. The aqueous layer was extracted with additional ethyl acetate (250 mL) and the combined organics were dried over magnesium sulfate. After filtration and concentration, the crude product was obtained as a yellow oil (23 g). The crude product was then slurried in 25% EA/hexanes (250 mL). The resulting solids were not desired product and were removed by filtration. The resulting solution was then concentrated to a yellow oil (21 g, 75 wt% desired, 16.1 g actual product, 70% yield), which was used directly in the next step. By ¹H-NMR, the crude product was also found to contain 14 wt% pinacol, 6.5 wt% ligand, and 4 wt% des-iodo starting material. ¹ H NMR (400 MHz, CDCIs): 7.61 (dd, J = 9.5, 2.5 Hz, 1 H), 7.52 - 7.45 (m, 1 H), 7.21 (td, J = 8.3, 2.5 Hz, 1 H), 3.91 (s, 3H), 1 .41 (s, 12H).

Step C: 5-Fluoro-2-pyrimidin-2-yl-benzoic acid methyl ester. To a 250 mL round-bottomed flask, was added 5-fluoro-2-(4,4,5,5-tetramethyl- [1 ,3,2]dioxaborolan-2-yl)-benzoic acid methyl ester (5.9 g, 21 .06 mmol) in 2- methyl-THF (50 mL). To the resulting solution was added 2-chloropyrimidine (2.9 g, 25.28 mmol), sodium carbonate (6.7 g, 63.19 mmol), and water (17 mL). The mixture was degassed for 30 minutes. PdCl₂(dppf)-dcm adduct (0.688 g, 0.843 mmol) was added and the reaction mixture was degassed once more for 30 minutes. The reaction mixture was warmed to 74 °C and stirred overnight. To the resulting solution was added diethyl ether (100 mL) and water (100 mL). The layers were thoroughly mixed separated. The aqueous layer was extracted with additional diethyl ether (100 mL). The combined organics were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to a brown crude material (5.85 g, 49% desired, 2.87 actual product). The crude product was further purified through recrystallization in 10%

EA/hexanes. The mixture was warmed to 70 °C and cooled slowly to room temperature. After filtration, the desired product was obtained as a brown solid (1 .72 g actual product, 35% yield overall after recrystallization). ¹H NMR (400 MHz, CDCI3): 8.78 (d, J = 4.9 Hz, 2H), 8.09 (dd, J = 8.7, 5.5 Hz, 1 H), 7.39 (dd, J = 8.6, 2.7 Hz, 1 H), 7.30 - 7.20 (m, 2H), 3.77 (s, 3H).

Step D: 5-Fluoro-2-pyrimidin-2-yl-benzoic acid. To a solution of 5-fluoro- 2-pyrimidin-2-yl-benzoic acid methyl ester (1 .72 g, 7.407 mmol) in 2-methyl- THF (20 mL) was added sodium hydroxide (0.74 g, 18.517 mmol) and water (20 mL). The mixture was heated to 72 °C and stirred for 2 h. The layers were separated and the aqueous layer was extracted with additional MTBE. A 50% HCI(aq) solution was then dripped into the aqueous layer until a pH of 1 was reached. The resulting solids were filtered to provide the desired product as an off-white solid (1 .34 g, 83% yield). ¹ H NMR (400 MHz, CD₃OD): 8.82 (d, J = 5.0 Hz, 2H), 7.89 (dd, J = 8.6, 5.4 Hz, 1 H), 7.53 (dd, J = 9.0, 2.7 Hz, 1 H), 7.39 (m, 2H).

Intermediate 18. 3,6-Diaza-bicyclo[3.2.0]heptane-6-carboxylic acid tert-butyl ester.

Step A. (2,2-Dimethoxy-ethyl)-carbamic acid benzyl ester. To a 500 ml_ round-bottomed flask equipped with temperature probe and nitrogen inlet were added aminoacetaldehyde dimethyl acetal (25 g, 238 mmol) in aq. NaOH (4.85 M, 69 ml_) and toluene (125 ml_). The mixture was cooled to 0 °C in an ice bath and benzylchloroformate (40.6 g, 238 mmol) was added at such a rate that the internal temperature was maintained below 20°C. The reaction mixture was stirred for 4 h at room temperature. The layers were separated, and the organic layer was washed with brine (2 x 20 ml_), dried with sodium sulfate, filtered, and concentrated to a colorless oil (53.24 g, 93% yield). ¹H-NMR (CDCI₃, 500 MHz): 7.30 (m, 5H), 5.1 1 (s, 2H), 4.37 (t, J=6.0 Hz, 1 H), 3.39 (s, 6H), 3.33 (t, J=6.0 Hz, 2H). MS (electrospray): exact mass calculated for Ci₂Hi₇NO₄, 239.12; m/z found, 240 [M+H]⁺.

Step B. Allyl-(2,2-dimethoxy-ethyl)-carbamic acid benzyl ester. To a 500 ml_ round-bottomed flask equipped with thermocouple probe, nitrogen inlet, reflux condenser, heating mantle, and mechanical stirring was added (2,2- dimethoxy-ethyl)-carbamic acid benzyl ester (50 g, 209 mmol) in toluene (180 ml_). To the resulting solution was added powdered KOH (51 .6 g, 920 mmol) and triethylbenzylammonium chloride (0.810 g, 3.55 mmol). A solution of allyl bromide (33.0 g, 275 mmol) in toluene (50 ml_) was added dropwise over 10 minutes. The mixture was heated to 50 °C and stirred for 2 days. To the reaction mixture was added water (230 ml_) over ten minutes. The layers were separated and the aqueous was extracted with toluene (2 x 200 ml_). The combined organics were washed with brine (1 x 200 ml_), dried with

magnesium sulfate, filtered, and concentrated to afford the title compound (57.8 g, 98%). ¹ H-NMR (CDCI₃, 500 MHz): 7.31 (m, 5H), 5.76 (m, 1 H), 5.15 (m, 4H), 4.51 (m, 1 H), 3.98 (d, J=9.48, 2H), 3.36 (m, 8H).

Step C. Allyl-(2-oxo-ethyl)-carbamic acid benzyl ester. To a 250 mL round-bottomed flask equipped with nitrogen inlet and magnetic stirring, were added allyl-(2,2-dimethoxy-ethyl)-carbamic acid benzyl ester (57.2 g, 205 mmol) and formic acid (88%, 67 mL). The reaction mixture was stirred at room temperature overnight. After concentration under reduced pressure, the resulting residue was taken up in 100 mL EA, 50 mL hexane, and 90 mL water. After separation of the layers, the aqueous layer was additionally extracted three times with hexanes (50 mL)/ethyl acetate (100 mL). The combined organics were washed with brine until the wash had a pH=6. The organics were dried with magnesium sulfate, filtered, and concentrated under reduced pressure to an oil (45.2g, 95% yield). ¹ H-NMR (CDCI₃, 400 MHz): 9.57 (d, 1 H), 7.31 (m, 5H), 5.77 (m, 1 H). 5.15 (m, 4H), 4.05 (m, 4H).

Step D. Allyl-(2-hydroxyimino-ethyl)-carbamic acid benzyl ester. To a 1 L round-bottomed flask, were added allyl-(2-oxo-ethyl)-carbamic acid benzyl ester (45.2 g, 193.8 mmol) and hydroxylamine hydrochloride (17.5 g, 251 .9 mmol) in acetonitrile (260 mL). To the resulting mixture was added a solution of sodium acetate trihydrate (29.5 g, 217 mmol) in H₂O (130 mL). The reaction mixture was stirred at room temperature under nitrogen _(g) overnight. The mixture was concentrated under reduced pressure and the resulting residue was extracted with ethyl acetate (2 x 130 mL). The combined organics were washed with brine, dried with magnesium sulfate, filtered, and concentrated under reduced pressure to afford the title compound (46.5 g, 97%). ¹H-NMR (CDCIs, 400 MHz): 7.32 (m, 5H), 6.72 (m, 1 H), 5.77 (bs, 1 H), 5.16 (m, 4H), 4.19 (m, 1 H), 3.95 (m, 3H). MS (electrospray): exact mass calculated for

C13H16N2O3, 248.12; m/z found, 249.1 [M+H]⁺.

Step E. 3-Amino-4-hydroxymethyl-pyrrolidine-1 -carboxylic acid benzyl ester. To a 1 L round-bottomed flask equipped with reflux condenser, heating mantle, nitrogen inlet, and magnetic stir bar, were added allyl-(2-hydroxyimino- ethyl)-carbamic acid benzyl ester (45.5 g, 183.3 mmol) and pentanol (560 mL). The reaction mixture was warmed to 135 °C and stirred for 20 h. The reaction mixture was transferred to a 2.25 L Parr bottle. To the mixture were added ethanol (95 mL) and Raney Ni (1 1 .4 g). The slurry was shaken under an atmosphere of H₂(g) (60 psi) for 4 h. The resulting reaction mixture was filtered and taken on directly to the next step.

Step F. 3-te/t-Butoxycarbonylamino-4-hydroxymethyl-pyrrolidine-1 - carboxylic acid benzyl ester. To a 3L round-bottomed flask, was added the filtered reaction mixture of 3-amino-4-hydroxymethyl-pyrrolidine-1 -carboxylic acid benzyl ester in pentanol/ethanol mixture. To the mixture sodium

bicarbonate (30.8 g, 367 mmol), H₂O (655 mL), and Boc anhydride (38 g, 174.1 mmol) were added. The mixture was stirred under N₂(g) for 15 h at room temperature. The biphasic mixture was then separated and the organics were washed with brine (655 mL). The organics were dried with magnesium sulfate, filtered, and concentrated under reduced pressure. The material was warmed to 98 °C in toluene/heptanes (280 mL each) and then filtered. The filtrate was slowly cooled to room temeperature and stirred for 20 h. The resulting solids were filtered and washed with heptanes to provide the title compound (39.5 g, 64% over two steps). ¹H-NMR (CD₃OD, 400 MHz): 7.31 (m, 5H), 5.1 1 (s, 2H), 4.20 (m, 1 H), 3.50-3.70 (m, 4H), 3.34-3.42 (m, 1 H), 3.18-3.29 (m, 1 H), 2.49 (m, 1 H), 1 .44 (s, 9H).

Step G. 3-terf-Butoxycarbonylamino-4-methanesulfonyloxymethyl- pyrrolidine-1 -carboxylic acid benzyl ester. To a 2L round-bottomed flask equipped with temperature probe and nitrogen inlet, were added 3-tert- butoxycarbonylamino-4-hydroxymethyl-pyrrolidine-1 -carboxylic acid benzyl ester (39.5 g, 1 12.7 mmol) in dichloromethane (550 mL) and triethylamine (22.8 g, 225.4 mmol). The solution was cooled to 0 °C in an ice bath.

Methanesulfonyl chloride (16.8 g, 146.5 mmol) was added dropwise over 20 min. The reaction mixture was allowed to warm to room temperature over 2 h. After stirring for 20 h, the reaction mixture was quenched with H₂O (550 mL) and the resulting layers were separated. The aqueous was extracted with DCM and the combined organics were then washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to an oil (40.2 g, 83% yield). ¹H-NMR (CDCI₃, 400 MHz): 7.32 (m, 5H), 5.13 (s, 2H), 4.69 (m, 1 H), 4.38 (m, 2H), 4.19 (m, 1 H), 3.67 (m, 2H), 3.24-3.46 (m, 2H), 3.00 (s, 3H), 2.73 (m, 1 H), 1 .49 (s, 9H). Step H. 3-Benzyl, 6-tert-butyl-3,6-diazabicyclo[3.2.0]heptane-3,6- dicarboxylate. To a 1 L round-bottomed flask were added 3-tert- butoxycarbonylamino-4-hydroxymethyl-pyrrolidine-1 -carboxylic acid benzyl ester (44 g, 104 mmol) in dichloromethane (150 mL) and trifluoroacetic acid (51 mL). The reaction mixture was stirred for 20 h. The reaction mixture was concentrated under reduced pressure. The residual material was taken up in ethanol (250 mL) and basified with 25% NaOH_(aq) to pH ~ 12 (70 mL).

Additional 25% NaOH_(aq) (15 mL) was added and the resulting mixture was warmed to 60 °C for 1 .5 h. After cooling to room temperature, the resulting mixture was then slowly added to di-tert-butyl dicarbonate (22.7 g, 104 mmol) in ethanol (30 mL) at room temperature over 40 minutes. The reaction mixture was concentrated under reduced pressure, and the resulting residual was partitioned between H₂O and ethyl acetate (250 mL each). The aqueous layer was extracted one more time with ethyl acetate and the combined organics were washed with brine, dried over magnesium sulfate, filtered, and

concentrated under reduced pressure. The crude product was further purified by flash column chromatography (2 x 330 g silica, 15 to 45% EA hexanes) to provide the title compound (20.9 g, 67%). ¹H-NMR (CD₃OD, 400 MHz): 7.32 (m, 5H), 5.16 (s, 2H), 4.66 (m, 1 H), 4.04 (m, 2H), 3.86 (d, J=12.1 Hz, 1 H), 3.45 (m, 1 H), 3.25 (m, 1 H), 3.02-3.16 (m, 2H), 1 .41 (s, 9H). MS (electrospray): exact mass calculated for Ci₈H₂ N₂O₄, 332.17; m/z found, 233.1 [M+H]⁺.

Step I. 3,6-Diaza-bicyclo[3.2.0]heptane-6-carboxylic acid tert-butyl ester. 3-Benzyl, 6-tert-butyl-3,6-diazabicyclo[3.2.0]heptane-3,6-dicarboxylate (2.61 mmol) in a Parr bottle was taken up in MeOH (0.1 M). Pd/C (5%wt- 61 .1 % H₂O from Johnson Mathey, 60 mg) was added. The mixture was placed on the Parr shaker and air was removed via vacuum. The system was purged a few time with nitrogen and then allowed to shake at 15 PSI for ~1 .5 hr. TLC showed that all the starting material was consumed. The mixture was filtered through a pad of Celite^®. The filtrate was concentrated to provide a viscous clear residue, II in 66.1 %. Material was clean enough to carry forward without purification. MS (ESI) mass calcd. for Ci₀Hi₈N₂O₂, 198.26; m/z found, 199.2 [M+H]⁺. ¹H NMR (400 MHz, CDCI₃) 4.73 - 4.50 (m, 1 H), 3.98 (t, J = 8.3, 1 H), 3.46 - 3.15 (m, 2H), 3.09 - 2.99 (m, 1 H), 2.93 - 2.82 (m, 1 H), 2.73 - 2.62 (m, 1 H), 2.53 - 2.42 (m, 1 H), 2.31 (s, 1 H), 1 .43 (s, 9H).

Intermediate 19: Biphenyl-2-yl-(3,6-diaza-bicyclo[3.2.0]hept-3-yl)-methanone.

Intermediate 18 (0.72 mmol), biphenyl-2-carboxylic acid (0.72 mmol), and HATU (1 .66 mmol) were taken up in DMF at 0.2 M. DIPEA (2.17 mmol) was added. The mixture was allowed to stir at 23 °C for ~1 hr. The mixture was diluted water and extracted with diethyl ether. The aqueous was extracted with ether again. The other fractions were combined and concentrated to provide the crude product. The product was purified on the silica gel chromatography (30-100% ethyl acetate/hexanes) over 12 minutes, then flushed with 100% ethyl acetate for 20 minutes to provide 3-(Biphenyl-2-carbonyl)-3,6-diaza- bicyclo[3.2.0]heptane-6-carboxylic acid tert-butyl ester, 91 %. MS (ESI) mass calcd. for C23H26N2O3, 378.46; m/z found, 379.2 [M+H]⁺. This material was taken up in DCM and TFA was added. The mixture was allowed to stir at 23 °C for 1 hr. It was then concentrated after checking by MS and LCMS to provide a yellow viscous oil. The oil was taken up and DCM and 1 M NaOH were added, and the resulting solution was allowed to stirred for 5 minutes. The layers were separated, and the organic layer was concentrated to provide Intermediate 19 as a light yellow foamy solid. MS (ESI) mass calcd. for Ci8Hi₈N₂O, 278.35; m/z found, 279.2 [M+H]⁺.

Intermediate 20: (3,6-Diaza-bicyclo[3.2.0]hept-3-yl)-(2-thiophen-2-yl-phenyl)- methanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 2-thiophen-2-yl-benzoic acid for biphenyl-2-carboxylic acid. MS (ESI) mass calcd. for Ci₆Hi₆N₂OS, 284.38; m/z found, 285.1 [M+H]⁺.

Intermediate 21 : (3,6-Diaza-bicyclo[3.2.0]hept-3-yl)-[5-(2-fluoro-phenyl)-2- m thyl-thiazol-4-yl]-methanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 5-(2-fluoro-phenyl)-2-methyl-thiazole-4-carboxylic acid for biphenyl- 2-carboxylic acid. MS (ESI) mass calcd. for Ci₇Hi₈FN₃OS, 317.38; m/z found, 318.2 [M+H]⁺.

Intermediate 22: (3,6-Diaza-bicyclo[3.2.0]hept-3-yl)-(2-methoxy-phenyl)- methanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 2-methoxybenzoic acid for biphenyl-2-carboxylic acid. MS (ESI) mass calcd. for C13H16N2O2, 232.28; m/z found, 233.2 [M+H]⁺. Intermediate 23: (2-Bromo-phenyl)-(3,6-diaza-bicyclo[3.2.0]hept-3-yl)- m thanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 2-bromobenzoic acid for biphenyl-2-carboxylic acid. MS (ESI) mass calcd. for Ci₂Hi₃BrN₂O, 218.15; m/z found, 281 .1 [M+H]⁺.

Intermediate 24: (3,6-Diaza-bicyclo[3.2.0]hept-3-yl)-(2-ethoxy-naphthalen-1 -yl)- methanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 2-ethoxy-naphthalene-1 -carboxylic acid for biphenyl-2-carboxylic acid. MS (ESI) mass calcd. for C18H20N2O2, 296.37; m/z found, 297.2 [M+H]⁺.

Intermediate 25: (3,6-Diaza-bicyclo[3.2.0]hept-3-yl)-(2-[1 ,2,3]triazol-2-yl- henyl)-methanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 2-[1 ,2,3]triazol-2-yl-benzoic acid for biphenyl-2-carboxylic acid. MS (ESI) mass calcd. for Ci₄H₁₅N₅O, 269.31 ; m/z found, 270.2 [M+H]⁺.

Intermediate 26: (3,6-Diaza-bicyclo[3.2.0]hept-3-yl)-(5-methyl-2-[1 ,2,3]triazol-2- l-phenyl)-methanone.

The title compound was prepared in a manner analogous to Intermediate 19, substituting 5-methyl-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 59) for biphenyl-2-carboxylic acid. MS (ESI) mass calcd. for Ci₅Hi₇N₅O, 283.33; m/z found, 284.2 [M+H]⁺.

Intermediate 27: (1 R,6S)-8-(4-(Trifluoromethyl)pyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

Step A: (1 R,6S)-tert-butyl 8-(4-(trifluoromethyl)pyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane-3-carboxylate. To (1 R,6S)-tert-butyl 3,8- diazabicyclo[4.2.0]octane-3-carboxylate (166 mg, 0.8 mmol) and DIPEA (404 μΙ_, 2.3 mmol) in ACN (3.4 ml_) was added 2-chloro-4- (trifluoromethyl)pyrimidine (1 10 μΙ_, 0.9 mmol). The reaction mixture was heated at reflux for 2 h, cooled to rt, diluted with water and extracted with CH₂CI₂ (2X). The combined organics were dried (Na₂SO ) and concentrated to give 185 mg (66%) of the title compound as a clear oil which was used without further purification. MS (ESI) mass calcd. For Ci6H₂i F₃N₄O₂, 358.40; m/z found 359.1 [M+H]⁺

Step B: (1 R,6S)-8-(4-(trifluoromethyl)pyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane. To (1 R,6S)-tert-butyl 8-(4-(trifluoromethyl)pyrimidin- 2-yl)-3,8-diazabicyclo[4.2.0]octane-3-carboxylate (185 mg, 0.5 mmol) in DCM (3 ml_) was added TFA (3 ml_). After 3h, the reaction was concentrated, neutralized with 5% Na₂CO₃ (aq) and extracted with DCM (3 X). The combined organics were dried (Na₂SO₄) and concentrated to give the title compound that was used without further purification. MS (ESI) mass calcd. For C Hi₃F₃N , 258.2; m/z found 259.1 [M+H]⁺

Intermediate 28: (1 R,6S)-8-(5-Methylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 27, substituting 2-bromo-5-methylpyrazine for 2-chloro-4- (trifluoromethyl)pyrimidine.

Intermediate 29: (1 R,6S)-8-(6-Methylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 27, substituting 2-bromo-6-methylpyrazine for 2-chloro-4- (trifluoromethyl)pyrimidine. Intermediate 30: (1 R,6S)-8-(3-Methylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 27, substituting 2-chloro-3-methylpyrazine for 2-chloro-4- (trifluoromethyl)pyrimidine. In addition, DMF and K2CO3 at 95 °C was used in place of DIPEA and ACN.

Intermediate 31 : (1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

Intermediate 32: 2-((1 R,6S)-3,8-Diazabicyclo[4.2.0]octan-8-yl)-5- chlorobenzo[d]oxazole.

The title compound was prepared in a manner analogous to Intermediate 27, substituting 2,5-dichlorobenzo[d]oxazole for 2-chloro-4- (trifluoromethyl)pyrimidine. In addition, DMF and K₂CO₃ at 95 °C was substituted for DIPEA and ACN. ntermediate 33: 3-Fluoro-2-(1 H-pyrazol-1 -yl)benzoic acid.

To a mixture of 3-fluoro-2-iodobenzoic acid (1 .4 g, 5.26 mmol), 1 H-pyrazole (0.72 g, 10.5 mmol), trans-N, N'-dimethyl-cyclohexane-1 ,2-diamine (0.17 mL, 1 .05 mmol), Cul (50.1 mg, 0.26 mmol), dioxane (50 mL) and water (0.028 mL) was added CS₂CO3 (3.43 g, 10.5 mmol). The reaction mixture was heated to 100 °C for 1 h. The reaction mixture was cooled to ambient temperature then diluted with water. The aqueous layer was acidified to pH2 and extracted with EtOAc (30 mL) three times. The organic layers were combined, dried over Na₂SO₄, filtered and concentrated. Purification (FCC), (DCM to 10%

MeOH/1 %HOAC/DCM) afforded the title compound as a colorless oil (790 mg, 72%). ¹H NMR (400 MHz, CDCI₃): 7.85 - 7.73 (m, 1 H), 7.54 - 7.44 (m, 1 H), 7.44 - 7.34 (m, 1 H), 6.55 (s, 1 H).

Intermediate 34: 3-Methyl-2-(1 H-pyrazol-1 -yl)benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 33 substituting 3-methyl-2-iodobenzoic acid for 3-fluoro-2-iodobenzoic acid. ¹ H NMR (500 MHz, CDCI3): 7.79 (d, J = 7.4 Hz, 2H), 7.48 (d, J = 7.5 Hz, 1 H), 7, (t, J = 7.6 Hz, 1 H), 6.53 (s, 1 H), 2.07 (s, 3H).

Intermediate 35: 3-Methyl-2-(2H-1 ,2,3-triazol-2-yl)benzonitrile.

To a mixture of 2-fluoro-3-methylbenzonitrile (4.0 g, 29.6 mmol) and 2H-1 ,2,3- triazole (2.04 g, 29.6 mmol) in DMF (80 ml_) was added potassium carbonate (8.26 g, 59.2 mmol). The resulting mixture was heated to 120 °C for 2h. The mixture was cooled, diluted with water and extracted with EtOAc. The organic layers were combined, dried over Na2SO₄, filtered and concentrated. The residue was purified by FCC (S1O2, ethyl acetate/hexanes, gradient 0-50%) to yield the title compound (1 .5 g, 26%). MS (ESI) mass calcd. for Ci₀H₈N₄,

184.2; m/z found, 185.1 [M+H]+. ¹H NMR (500 MHz, CDCI3): 7.95 (s, 2H), 7.66 (d, J = 7.7, 0.7 Hz, 1 H), 7.59 (d, J = 7.8, 0.6 Hz, 1 H), 7.50 (dd, J = 9.8, 5.7 Hz, 1 H), 2.20 (s, 3H).

Intermediate 36: 3-Methyl-2-(1 H-1 ,2,3-triazol-1 -yl)benzonitrile.

The title compound was a byproduct of the synthesis of Intermediate 35 (3.1 g, 56%). MS (ESI) mass calcd. for CioH₈N₄, 184.2; m/z found, 185.1 [M+H]+. ¹ H NMR (500 MHz, CDCI₃): 7.94 (d, J = 2.1 Hz, 1 H), 7.87 (d, J = 1 .1 Hz, 1 H), 7.71 - 7.67 (m, 1 H), 7.67 - 7.62 (m, 1 H), 7.56 (dd, J = 9.7, 5.8 Hz, 1 H), 2.17 (s, 3H).

Intermediate 37: 3-Methyl-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid.

To a solution of 3-methyl-2-(2H-1 ,2,3-triazol-2-yl)benzonitrile (1 .4 g, 7.82 mmol) in MeOH (15 ml_) was added a 4N aqueous solution of NaOH (10 ml_). The resulting mixture was heated to 90 °C. After 15h the reaction mixture was cooled to ambient temperature then diluted with water (50 ml_). The aqueous layer was acidified to pH2 and extracted with EtOAc (50 ml_) three times. The organic layers were combined, dried over Na₂SO₄, filtered and concentrated. The residue was purified by FCC (S1O2, gradient DCM to 10% MeOH/1 %HOAc/DCM) to yield the title compound (1 .3 g, 78%). ¹ H NMR (500 MHz, CDCI3): 7.90 (d, J = 7.7, Hz, 1 H), 7.83 (s, 2H), 7.57 - 7.53 (m, 1 H), 7.49 (dd, J = 9.7, 5.8 Hz, 1 H), 2.10 (s, 3H).

Intermediate 38: 3-Methyl-2-(1 H-1 ,2,3-triazol-1 -yl)benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 37, substituting 3-methyl-2-(1 H-1 ,2,3-triazol-1 -yl)benzonitrile for 3-methyl-2-(2H- 1 ,2,3-triazol-2-yl)benzonitrile. ¹H NMR (500 MHz, CDCI3): 8.17 (s, 1 H), 7.94 (s, 1 H), 7.69 (d, J = 6.8 Hz, 1 H), 7.65 (d, J = 7.7 Hz, 1 H), 7.63 - 7.56 (m, 1 H), 2.06 (s, 3H).

Intermediate 39: (1 R,6S)-tert-Butyl 3,8-diazabicyclo[4.2.0]octane-3- carboxylate.

To a solution of (1 R,6S)-tert-butyl 8-((S)-1 -phenylethyl)-3,8- diazabicyclo[4.2.0]octane-3-carboxylate (1 .5 g, 75%) in EtOH (50 mL) was added AcOH (1 .5 mL). The resulting mixture was cycled through an H-Cube containing a 20% Pd(OH)₂/C catalyst cartridge at 50 °C and 100 bar of hydrogen pressure. After 16 hours the resulting mixture was removed from the H-Cube and poured over a saturated sodium carbonate solution (100 mL). The aqueous layer was extracted with DCM (50 mL) four times. The organic layers were combined, dried over Na₂SO₄, filtered and concentrated under reduced pressure to yield the title compound (755 mg, 75%) which was used in the next step without purification. MS (ESI) mass calcd. for C11 H20N2O2, 212.2; m/z found, 213.1 [M+H]⁺. ¹H NMR (500 MHz, CDCI₃): 4.21 - 4.02 (m, 1 H), 3.84 - 3.59 (m, 3H), 3.47 - 3.36 (m, 1 H), 3.33 (dd, J = 8.3, 4.4 Hz, 1 H), 3.28 - 3.20 (m, 1 H), 2.91 - 2.71 (m, 2H), 1 .94 - 1 .81 (m, 1 H), 1 .81 - 1 .68 (m, 1 H), 1 .46 (s, 9H).

Intermediate 40: (1 R,6S)-8-(6-Methylpyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

Step A: To a microwave safe vial was added Intermediate 39 (375 mg, 1 .77 mmol), 2-chloro-6-methylpyridine (0.39 mL, 3.53 mmol), CH₃CN (10 mL) and DIPEA (0.61 mL, 3.53 mmol). The resulting mixture was heated to 180 C in a microwave reactor. After 3h the crude mixture was concentrated and purified directly by FCC (SiO₂, ethyl acetate/hexanes, 0-40%) to yield (1 R,6S)- tert-butyl 8-(6-methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane-3-carboxylate (80 mg, 15%). MS (ESI) mass calcd. for C17H25N3O2, 303.2; m/z found, 304.1 [M+H]⁺. ¹ H NMR (500 MHz, CDCI3): 7.31 (t, J = 7.7 Hz, 1 H), 6.50 - 6.40 (m, 1 H), 6.09 (dd, J = 45.4, 8.1 Hz, 1 H), 4.44 - 4.27 (m, Hz, 2H), 4.04 - 3.89 (m, 1 H), 3.84 - 3.66 (m, 2H), 3.60 - 3.22 (m, 2H), 2.86 - 2.72 (m, 1 H), 2.37 (s, 3H), 2.07 - 1 .96 (m, 1 H), 1 .92 - 1 .80 (m, 1 H), 1 .44 - 1 .28 (m, 9H).

Step B: To a solution of (1 R,6S)-tert-butyl 8-(6-methylpyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane-3-carboxylate (80 mg, 0.26 mmol) in DCM (5 mL) was added TFA (2 mL). The resulting mixture was allowed to stir at ambient temperature. After 16h the mixture was concentrated under reduced pressure. The resulting trifluoroacetic acid salt of the title compound (80 mg) was used without further purification. MS (ESI) mass calcd. for C12H17N3, 203.2; m/z found, 204.1 [M+H]⁺. Intermediate 41 : (1 R,6S)-8-(4-Methylpyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 40, substituting 2-chloro-4-methylpyridine for 2-chloro-6-methylpyridine in step A. MS (ESI) mass calcd. for Ci₂Hi₇N₃, 203.2; m/z found, 204.1 [M+H]⁺.

Intermediate 42: (1 R,6S)-8-(5-Methylpyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 40, substituting 2-chloro-5-methylpyridine for 2-chloro-6-methylpyridine in step A. MS (ESI) mass calcd. for Ci₂Hi₇N₃, 203.2; m/z found, 204.1 [M+H]⁺.

Intermediate 43: (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 40, substituting 2-chloro-4,6-dimethylpyridine for 2-chloro-6-methylpyridine in step A. MS (ESI) mass calcd. for C13H19N3, 217.2; m/z found, 218.1 [M+H]⁺. Intermediate 44: (1 R,6S)-8-(4-(Trifluoromethyl)pyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 40, substituting 2-chloro-4-(trifluoromethyl)pyridine for 2-chloro-6-methylpyridine in step A. MS (ESI) mass calcd. for Ci₂Hi₄F₃N₃, 257.1 ; m/z found, 258.1 [M+H]⁺.

Intermediate 45: (1 R,6S)-8-(6-(Trifluoromethyl)pyridin-2-yl)-3,8- diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 40, subsituting 2-chloro-6-(trifluoromethyl)pyridine for 2-chloro-6-methylpyridine in step A. MS (ESI) mass calcd. for Ci₂Hi₄F₃N₃, 257.1 ; m/z found, 258.1 [M+H]⁺.

Intermediate 46: 2-((1 R,6S)-3,8-Diazabicyclo[4.2.0]octan-8-yl)-N,N- dimethylpyridin-4-amine

Step A: To a microwave safe vial was added Intermediate 40 (200 mg, 0.94 mmol), 2-chloro-N,N-dimethylpyridin-4-amine (134 mg, 0.85 mmol), chloro[(1 ,2,3-n)-3-phenyl-2-propenyl][1 ,3-bis(2,6-di-/^'-propylphenyl)-4,5- dihydroimidazol-2-ylidene]palladium(ll) (5.6 mg, 0.0086 mmol), potassium tert- butoxide (96.1 mg, 0.85 mmol) and DME (8 ml_). The resulting mixture was heated to 100 °C. After 1 hour the mixture was allowed to cool to ambient temperature at which time water (20 ml_) was added. The aqueous layer was extracted with DCM (15 ml_) three times. The organic layers were combined, dried over Na2SO₄, filtered, and concentrated under reduced pressure. The crude residue was purified by reverse-phase HPLC (basic) to yield (1 R,6S)-tert- butyl 8-(4-(dimethylamino)pyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane-3- carboxylate (150 mg, 52%). MS (ESI) mass calcd. for Ci₈H₂8N₄O₂, 332.2; m/z found, 333.2 [M+H]⁺. ¹H NMR (500 MHz, CDCI₃): 7.84 (d, J = 5.7 Hz, 1 H), 6.02 (d, J = 5.6 Hz, 1 H), 5.45 - 5.31 (m, 1 H), 4.47 - 4.35 (m, 1 H), 4.09 - 3.96 (m, 1 H), 3.91 (t, J = 7.7 Hz, 1 H), 3.86 - 3.72 (m, 2H), 3.55 - 3.26 (m, 2H), 2.95 (s, 6H), 2.85 - 2.70 (m, 1 H), 2.06 - 1 .95 (m, 1 H), 1 .90 - 1 .84 (m, 1 H), 1 .45 - 1 .29 (m, J = 52.5 Hz, 9H).

Step B: A solution of (1 R,6S)-tert-butyl 8-(4-(dimethylamino)pyridin-2- yl)-3,8-diazabicyclo[4.2.0]octane-3-carboxylate (150 mg, 0.45 mmol) in DCM (5 ml_) was added TFA (2 ml_). The resulting mixture was allowed to stir at ambient temperature. After 16 hours the crude mixture was concentrated under reduced pressure. The resulting trifluoroacetic acid salt of the title compound was used without further purification. MS (ESI) mass calcd. for Ci₃H₂₀N₄, 232.2; m/z found, 233.2 [M+H]⁺.

Intermediate 47: 6-Methyl-2-[1 ,2,3]triazol-2-yl-nicotinic acid.

To a 100 ml round bottom flask containing 2-chloro-6-methylnicotinic acid (3 g, 17.4 mmol), copper iodide (0.16 g, 0.5 mol%), and cesium carbonate (1 1 .4 g, 35 mmol) was added a mixture of dioxane (20 ml_) and H₂O (0.1 ml, 5.25 mmol). Next triazole (2.03 ml_, 35 mmol) and finally (R,R)-(-)-N,N'-dimethyl-1 ,2- cyclohexanediamine ligand (0.56 ml_, 3.5 mmol) were added. The resulting clumpy yellow slurry was stirred until evenly dispersed. Upon heating to 100°C the reaction mixture changed from a yellow slurry to pale green. As heating progressed the slurry became less thick and was stirred more easily. The light green slurry was stirred for 4 hr at 100°C and left to stir at room temp overnight. At this point the reaction mixture appeared as a cobalt blue slurry which was then diluted with 20 ml_ ether and 20 ml_ H₂O. The resulting solution was thoroughly stirred and transferred to a seperatory funnel then the RBF was subsequently rinsed with 20 ml_ ether and H₂O each. The aqueous layer was separated from the organic layer and acidified to pH 1 with 6 ml_ cone. HCI. The now brown/ lime green aqueous layer was extracted twice with EtOAc. The bright yellow organic layers were combined and dried with Na₂SO and then cone, into a yellow powder under reduced pressure. To the yellow powder was added EtOAc to form a yellow slurry. The solids were filtered off and washed with EtOAc to give a very pale yellow powder, which was found by ¹H NMR to be Intermediate 53 (25% yield). The filtrate was cone, into a yellow solid and purified by FCC using 0-5% MeOH in DCM w/ 0.5% AcOH to give the title compound in a 20% yield. MS (ESI): mass calculated for C₉H₈N₄O₂, 204.18; m/z found 205.3 [M+H]⁺ _. ¹ H NMR (400 MHz, CD₃OD): 8.21 - 8.18 (m, 1 H), 7.98 (s, 2H), 7.51 (d, J = 7.9 Hz, 1 H), 2.64 (s, 3H).

Intermediate 48: 2-Fluoro-6-(pyrimidin-2-yl)benzoic acid.

Step A: 2-Fluoro-6-iodo-benzoic acid methyl ester. To a 200 ml_ round- bottomed flask were added 2-fluoro-6-iodo-benzoic acid (7.5 g, 28.2 mmol), LiOH^»H₂O (1 .42 g, 33.8 mmol), and THF (100 ml_). The resulting mixture was warmed to 50 °C and stirred for 2 h. Dimethyl sulfate (4.03 ml_, 42.3 mmol) was then added and the mixture was warmed to 65 °C. After 2 h, the mixture was cooled to room temperature and NH₄CI_(aq) (50 ml_, 13 wt% solution) was added. The two resulting layers were thoroughly mixed and then separated. The organic layer was dried over MgSO₄, filtered, and concentrated under reduced pressure to a light brown oil (7.79 g, 99% yield). ¹H NMR (400 MHz, CDCIs): 7.68 - 7.60 (m, 1 H), 7.15 - 7.06 (m, 2H), 3.98 (s, 3H).

Step B: 2-Fluoro-6-(4,4,5,5-tetramethyl-[1 ,3,2]dioxaborolan-2-yl)- benzoic acid methyl ester. To a 500 mL round-bottomed flask were added 2- fluoro-6-iodo-benzoic acid methyl ester (7.29, 26.0 mmol) and anhydrous THF (150 mL). This mixture was cooled to 0 °C and /^'-PrMgCI (13.7 mL, 2 M in THF, 27.3 mmol) was added dropwise. After 10 min, 2-isopropoxy-4,4,5,5- tetramethyl-1 ,3,2-dioxaborolane (5.58 mL, 27.3 mmol) was added. The mixture was allowed to warm to room temperature, and after 30 min NH CI(_ac?) (150 mL, 13 wt% solution) was added. The layers were mixed and then separated, and the aqueous layer was extracted with 100 mL of MTBE. The combined organic layers were dried over Na₂SO₄, filtered, and concentrated to a final mass of 6.07 g (90% wt%, 75% yield). ¹ H NMR (400 MHz, CDCI3): 7.47 - 7.38 (m, 2H), 7.17 - 7.1 1 (m, 1 H), 3.92 (s, 3H), 1 .36 (s, 12H).

Step C: 2-Fluoro-6-pyrimidin-2-yl-benzoic acid methyl ester. To a 250 mL round-bottomed flask under nitrogen were added 2-fluoro-6-(4,4,5,5- tetramethyl-[1 ,3,2]dioxaborolan-2-yl)-benzoic acid methyl ester (5.46 g, 19.5 mmol) in 2-methyl-THF (50 mL), 2-chloropyrimidine (2.68 g, 23.4 mmol), and sodium carbonate (6.2 g, 58.5 mmol) in water (17 mL). PdCI₂(dppf)-dcm adduct (CAS#72287-26-4) (1 .27 g, 1 .56 mmol) was then added and the reaction mixture was warmed to 74 °C and stirred for 2.5 h. After cooling, the mixture was diluted with MTBE (50 mL) and water (80 mL). The layers were thoroughly mixed separated. The aqueous layer was extracted with additional MTBE (100 mL). The combined organics were dried over magnesium sulfate, filtered, concentrated and then purified by flash chromatography (0-25%

EA/hexanes) to provide the title compound (1 .72 g, 72 wt%, 30% yield). ¹ H NMR (400 MHz, CDCI₃): 8.79 (d, J = 4.9 Hz, 2H), 8.15 (d, J = 7.9 Hz, 1 H), 7.51 (td, J = 8.1 , 5.6 Hz, 1 H), 7.28-7.20 (m, 2H), 3.92 (s, 3H).

Step D: 2-Fluoro-6-pyrimidin-2-yl-benzoic acid. To a solution of 2-fluoro-

6-pyrimidin-2-yl-benzoic acid methyl ester (1 .36 g, 5.85 mmol) in 2-methyl-THF (20 mL) was added sodium hydroxide (2 M in water, 9.3 mL, 18.6 mmol). The mixture was heated to 72 °C and stirred for 9 h. The layers were separated and the aqueous layer acified to pH 2 by dropwise addition of 50% HCI(_ac?) (3.1 mL). The resulting solids were stirred for 1 h, filtered, washed with water, MTBE, and heptanes, and then dried to provide the desired product as a white solid (1 .12 g, 88% yield). ¹ H NMR (400 MHz, CD₃OD): 8.83 (d, J = 4.9 Hz, 2H), 8.03 (dd, J = 7.9, 0.8 Hz, 1 H), 7.59 (td, J = 8.1 , 5.6 Hz, 1 H), 7.40 (t, J = 4.9 Hz, 1 H), 7.34 (ddd, J = 9.4, 8.4, 1 .0 Hz, 1 H).

Intermediate 49: 4-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid.

To 2-bromo-4-methoxybenzoic acid (4g, 17.3 mmol), Cul (266 mg, 1 .4 mmol) and Cs₂CO₃ (1 1 .2 g, 34.6 mmol) was added dioxane (36 mL), water (94 μΐ, 5.1 mmol), 2H-1 ,2,3-triazole (2.0 mL, 34.6 mmol) and (1 R,2R)-N1 ,N2- dimethylcyclohexane-1 ,2-diamine (683 μί, 4.3 mmol). The reaction mixture was heated to 100 °C for 3 hr. The reaction mixture was cooled rt, then EtOAc and water were added. The mixture was transferred to a separatory funnel and the aqueous layer separated. The aqueous layer was acidified with cone. HCI to pH~2 and extracted with EtOAc (2X). The organic layers were washed with brine and dried (Na₂SO₄) to give a yellow solid. This material was slurried with EtOAc (-20 mL) and the solids filtered (>95% 4-methoxy-2-(1 H-1 ,2,3-triazol-1 - yl)benzoic acid by HPLC). Purification (FCC) (50% DCM to 100% DCM containing 10% (5% formic acid/MeOH)) gave the title compound (2.6 g) as a yellow solid. ¹H NMR (CDCI₃): 7.99 - 7.90 (m, 1 H), 7.83 (s, 2H), 7.20 (d, J = 2.5 Hz, 1 H), 7.03 (dd, J = 8.8, 2.6 Hz, 1 H), 3.89 (s, J = 17.6 Hz, 3H).

Intermediate 50: 3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid.

Step A: 3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzonitrile and 3-fluoro-2-(1 H- 1 ,2,3-thazol-1 -yl)benzonitrile. A mixture of 2,3-difluorobenzonitrile (4.0 g, 28.8 mmol), 2H-1 ,2,3-triazole (1 .9 g, 28.8 mmol) in DMF (85.0 mL) and K₂CO₃ (7.9 g, 57.5 mmol) were heated to 125 °C for 1 .5 h. After cooling to rt, water was added and the mixture extracted with EtOAc (2 X). The combined organics were washed with brine and dried (Na₂SO₄). Purification via FCC (10-100% EtOAc in hexanes) gave two products. 3-Fluoro-2-(2H-1 ,2,3-triazol-2- yl)benzonitrile (1 .6 g, 29%), ¹H NMR (CDCI₃): 7.99 (s, J = 6.6 Hz, 2H), 7.67 - 7.63 (m, 1 H), 7.61 - 7.53 (m, 2H), 7.26 (s, 6 H) and 3-fluoro-2-(1 H-1 ,2,3-triazol- 1 -yl)benzonitrile (2.0 g, 38%) ¹H NMR (CDCI₃): 7.97 (dd, J = 4.4, 2.8 Hz, 1 H), 7.95 (d, J = 1 .2 Hz, 1 H), 7.70 (tt, J = 5.7, 2.8 Hz, 1 H), 7.65 (td, J = 8.1 , 4.9 Hz, 1 H), 7.62 - 7.57 (m, 1 H).

Step B: 3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid. To 3-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)benzonitrile (1 .5 g, 8.0 mmol) in MeOH (30 mL) was added 2M aq. NaOH (10 mL). The reaction was heated at reflux for 15h, then cooled to rt, acidified with 1 N aq. HCI to pH=1 and extracted with DCM (2X). The combined organics were washed with brine and dried (Na₂SO₄). Purification via Agilent (Reverse-Phase HPLC, basic conditions) gave the title compound (290 mg, 18%). ¹H NMR (CDCIs): 7.90 (s, 2H), 7.89 - 7.85 (m, 1 H), 7.63 - 7.56 (m, 1 H), 7.50 - 7.44 (m, 1 H) and 3-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid

(Intermediate 64, 140 mg, 8%).

Intermediate 51 : 6-Methyl-2-[1 ,2,3]triazol-1 -yl-nicotinic acid

The title compound was isolated from the procedure used to prepare

Intermediate 47 with a 25% yield. MS (ESI): mass calculated for Ο₉Η₈Ν₄Ο₂, 204.18; m/z found 205.3 [M+H]^{+ 1}H NMR (400 MHz, CD₃OD): 8.48 (d, J = 1 Hz, 1 H), 8.25 (dd, J = 7.9, 3.8 Hz, 1 H), 7.88 (d, J = 1 .1 Hz, 1 H), 7.54 (d, J = Hz, 1 H), 2.64 (s, 3H).

Intermediate 52: 3-Fluoro-2-(pyrimidin-2-yl)benzoic acid.

Step A: 3-Fluoro-2-(pyrimidin-2-yl)benzonitrile. 2-lodo-4- fluorobenzonitrile (2.5 g, 10.3 mmol) and 2-tributylstannane pyrimidine (3.7g, 10.0 mmol) were combined and dissolved in degassed DME (18 ml) then purged with bubbling N₂ for 5 minutes. The reaction was treated with

Pd(PPh₃) (577 mg, 0.5 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated in microwave at 160 °C for 90 min. The reaction was cooled and filtered through celite and concentrated to minimum volume and the ppt the formed was diluted with hexanes (40 ml) and cooled to 0 °C then filtered. The solid purified (FCC) (20-100% EA / hex) to give 3-fluoro- 2-(pyrimidin-2-yl)benzonitrile. ¹ H NMR (400 MHz, CDCI₃): 8.93 (d, J = 4.9 Hz, 2H), 8.14 (dd, J = 9.6, 2.7 Hz, 1 H), 7.86 (dd, J = 8.6, 5.3 Hz, 1 H), 7.36 (t, J = 4.9 Hz, 1 H), 7.32 - 7.24 (m, 1 H).

Step B: 3-Fluoro-2-(pyrimidin-2-yl)benzoic acid. 3-Fluoro-2-(pyrimidin-2- yl)benzonitrile (98 mg, 0.5 mmol) was dissolved in MeOH (3 mL) and 2M NaOH (aq, 1 mL). The reaction was heated at reflux for 15 h, then cooled to 23 °C, acidified with 1 N aq. HCI to pH=1 and extracted with EtOAc (2 X). The combined organics were washed with brine and dried over sodium sulfate to give the title compound. ¹ H NMR (400 MHz, DMSO-c/₆): 8.89 (d, J = 4.9 Hz, 1 H), 7.74 (dd, J = 7.6, 1 .2 Hz, 1 H), 7.63 (td, J = 8.0, 5.5 Hz, 1 H), 7.60 - 7.53 (m, 1 H), 7.52 (t, J = 4.9 Hz, 1 H). ntermediate 53: 2-[1 ,2,3]Triazol-1 -yl-benzoic acid.

The title compound was isolated from the synthesis of Intermediate 13. ¹H NMR (400 MHz, CD₃OD): 6.70 (d, J = 0.9 Hz, 1 H), 6.50 (dd, J = 7.7, 1 .5 Hz, 1 H), 6.30 (d, J = 1 .0 Hz, 1 H), 6.24.6.18 (m, 1 H), 6.17 -6.1 1 (m, 1 H), 6.01 (dd, J = 7.8, 1 .0 Hz, 1 H).

Intermediate 54: (1 R,6S)-8-(2-Phenylpyrimidin-4-yl)-3,8- diazabicyclo[4.2.0]octane.

Step A: (1 R,6S)-tert-butyl 8-(2-phenylpyrimidin-4-yl)-3,8- diazabicyclo[4.2.0]octane-3-carboxylate. The title compound was prepared in a manner analogous to Intermediate 2 substituting 4-chloro-2-phenylpyrimidine for 2-chloro-quinoxaline. MS (ESI) mass calcd. for 02Ι Η₂ΘΝ₄Ο2, 366.2; m/z found, 367.2 [M+H]⁺. ¹H NMR (600 MHz, CDCI₃) δ 8.39 - 8.35 (m, 2H), 8.29 (d, J = 5.8 Hz, 1 H), 7.46 - 7.39 (m, 3H), 6.18 - 6.02 (m, 1 H), 4.67 - 4.20 (m, 2H), 4.07 - 3.90 (m, 2H), 3.86 - 3.62 (m, 1 H), 3.60 - 3.31 (m, 2H), 2.99 - 2.83 (m, 1 H), 2.10 - 2.00 (m, 1 H), 1 .94 - 1 .82 (m, 1 H), 1 .45 - 1 .20 (m, 9H).

Step B: (1 R,6S)-8-(2-phenylpyrimidin-4-yl)-3,8-diazabicyclo[4.2.0]octane. MS (ESI) mass calcd. for Ci₆Hi₈N₄, 266.2; m/z found; 267.2 [M+H]⁺.

Intermediate 55: 2-Chloro-4,4,4,5,6,6,6-septadeuteriopyrimidine.

Step A: 1 ,1 ,1 ,3,3,3,5,5-Octadeuteriopentane-2,4-dione. To a solution of acetylacetone (10 ml_, 95.1 mmol) in D₂O (90 ml_) was added K₂CO₃ (1 .0 g, 7.29 mmol). The mixture was heated at 120 °C overnight. The aqueous layer was extracted with DCM and the combined organic layers were dried over Na₂SO₄, filtered and concentrated in vacuo to an orange liquid (Frediani et. al., Catalysis Comm. 2, 2001 , 125).

Step B: 2-Deuteriohydroxy-4,4,4,5,6,6,6-septadeuteriopyrimidine. To a solution of 1 ,1 ,1 ,3,3,3,5,5-Octadeuteriopentane-2,4-dione (product of Step A) (1 .60 g, 14.82 mmol) in EtOD (7 mL) was added urea-d₄ (0.95 g, 14.82 mmol) followed by 35% wt. DCI in D₂O (2 mL, 23.71 mmol). The mixture was heated at 90 °C for 36 h, cooled to room temperature and then chilled in an ice bath before filtration and washing of the white solid with cold EtOD to afford the desired product as the HCI salt (1 .53 g, 61 %).

Step C: 2-Chloro-4,4,4,5,6,6,6-septadeuteriopyrimidine. To 2- deuteriohydroxy-4,4,4,5,6,6,6-septadeuteriopyrimidine (product of Step B) (1 .53 g, 9.04 mmol) was added POCI₃ (7.9 mL, 9.04 mmol) and the mixture was heated at reflux for 16 h. The mixture was allowed to cool to room temperature and then added to ice drop wise. The aqueous mixture was neutralized to pH 6 in an ice bath with 5 N NaOH. The aqueous layer was extracted with DCM and the combined organic layers were dried over Na₂SO , filtered and concentrated in vacuo to afford the desired product as a yellow solid (1 .3 g, 96%). (ESI): mass calculated for C₆D₇CIN₂, 149.07; m/z found, 150.1 .

Intermediate 56: 3-Fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting for 3-fluoro-2-iodo-benzoic acid for 5-fluoro-2-iodo-benzoic acid in Step A. ¹ H NMR (400 MHz, CD₃OD): 7.93 (s, 2H), 7.81 (d, J = 8.3 Hz, 1 H), 7.63-7.58 (m, 1 H), 7.29 (td, J = 8.9, 0.9 Hz, 1 H).

Intermediate 57: 4-Chloro-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting 4-chloro-2-iodo-benzoic acid for 5-fluoro-2-iodo-benzoic acid in Step A. ¹ H NMR (400 MHz, CD₃OD): 7.93 (s, 2H), 7.84 - 7.78 (m, 2H), 7.59 (dd, J = 8.3, 2.1 Hz, 1 H).

Intermediate 58: 5-lodo-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting 2-bromo-5-iodobenzoic acid for 5-fluoro-2-iodo-benzoic acid in Step A. ¹ H NMR (400 MHz, CD₃OD): 8.09 (d, J = 2.0, 1 H), 8.03 - 7.97 (m, 1 7.95 - 7.86 (m, 3H), 7.53 (d, J =8.4, 1 H).

Intermediate 59: 5-Methyl-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting for 2-iodo-5-methyl benzoic acid for 5-fluoro-2-iodo-benzoic acid Step A. ¹ H NMR (400 MHz, CD₃OD): 7.87 (s 2H), 7.66 (d, J = 1 .3 Hz, 1 H), 7.59 (d, J = 8.2 Hz, 1 H), 7.53 - 7.46 (m, 1 H), 2.45 (s, 3H).

Intermediate 60: 5-Chloro-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting 5-chloro-2-iodo-benzoic acid for 5-fluoro-2-iodo-benzoic acid in Step A. ¹ H NMR (400 MHz, CD₃OD): 7.91 (s, 2H), 7.82 - 7.74 (m, 2H), 7.71 - 7.66 (m, 1 H).

Intermediate 61 : 5-Methoxy-2-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting for 2-iodo-5-methoxy benzoic acid for 5-fluoro-2-iodo-benzoic acid in Step A. ¹H NMR (400 MHz, CD₃OD): 7.81 (s, J = 6.4, 2H), 7.55 (d, J = 8.8, 1 H), 7.33 (d, J = 2.9, 1 H), 7.18 (dd, J = 8.8, 2.9, 1 H), 3.85 (s, 3H). Intermediate 62: 5-Fluoro-2-(1 H-pyrazol-5-yl)benzoic acid.

Step A: Methyl 2-bromo-5-fluorobenzoate (1 .0 gram, 4.2 mmol) and (1 H- pyrazol-5-yl)boronic acid (485 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 ml) then treated with NaHCO3 (706 mg, 8.4 mmol) in water and the reaction purged with bubbling N₂ for 5 minutes. The reaction was treated with Pd(PPh₃) (243 mg (0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. The reaction mixture was cooled to 23 °C, filtered, and solid rinsed with EtOAc. The organic layers were separated, dried and concentrated. Purification via FCC (ethyl acatate/hexanes, 0-30%) afforded methyl 5-fluoro-2-(1 H-pyrazol-5-yl)benzoate (415 mg, 44%).

Step B: A solution of methyl 5-fluoro-2-(1 H-pyrazol-5-yl)benzoate (415 mg, 1 .9 mmol) in EtOH (10 ml) was treated with 4.0 eq of LiOH and stirred and monitored for two hours the reaction was complete. Reaction was made to pH = 5, and then the solution concentrated under reduced pressure, during which time a ppt formed. The solution was concentrated to minimum volume and cooled in ice, filtered and washed with ice water to give 5-fluoro-2-(1 H-pyrazol- 5-yl)benzoic acid (172 mg, 44%). ¹H NMR (400 MHz, DMSO-c/₆): 13.03 (s, 1 H), 7.71 (d, J = 2.0 Hz, 1 H), 7.67 (dd, J = 8.3, 5.6 Hz, 1 H), 7.37 (td, J = 8.6, 2.9 Hz, 2H), 6.44 (d, J = 2.2 Hz, 1 H).

Intermediate 63: 2-Methyl-6-[1 ,2,3]triazol-2-yl-benzoic acid.

The title compound was prepared in a manner analogous to Intermediate 13, substituting for 2-iodo-6-methyl benzoic acid for 5-fluoro-2-iodo-benzoic acid in Step A. ¹ H NMR (400 MHz, CD₃OD): 7.89 (s, 2H), 7.72 (d, J = 8.1 Hz, 1 H), 7.48 (t, J = 7.9 Hz, 1 H), 7.36 (d, J = 7.7 Hz, 1 H), 2.46 (s, 3H).

Intermediate 64: 3-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid.

The title compound was obtained during the synthesis of Intermediate 50, Step B. ¹ H NMR (CDCIs): 7.92 - 7.83 (m, 2H), 7.66 (dd, J = 7.9, 1 .3 Hz, 1 H), 7.61 - 7.54 (m, 1 H), 7.27 (dd, J = 8.4, 1 .2 Hz, 1 H), 3.82 (s, 3H).

Intermediate 65: 2-Chloro-5-fluoro-4-methylpyrimidine.

To a solution of 2,4-dichloro-5-fluoropyrimidine (1 .02 g, 6.08 mmol) in

THF/NMP (38 mL/3 mL) was added Fe(acac)₃ (215 mg, 0.61 mmol) and the mixture was cooled to 0 °C. 3.0 M methylmagnesium bromide in Et₂O (3.04 mL, 9.12 mmol) was added dropwise. After 30 min at 0 °C, the reaction was complete and quenched with saturated aqueous NH CI solution. Et₂O was added and the layers were separated and the aqueous layer was further extracted with several portions of Et₂O. The combined organic extracts were dried over Na₂SO₄, filtered and concentrated in vacuo. Chromatography (Hexanes to 10% EtOAc/Hexanes) gave the desired product as a waxy white solid (430 mg, 48%). ¹H NMR (400 MHz, CDCI₃): 8.35 (s, 1 H), 2.55 (d, J = 2.5 Hz, 3H).

Intermediate 66: 2-Chloro-4,5,6-trimethylpyrimidine.

To 4,5,6-trimethylpyrimidin-2-ol (3.69 g, 26.7 mmol) was added POCI₃ (21 .7 ml_, 26.7 mmol) followed by Et₂NPh (2.17 ml_, 13.6 mmol) dropwise. The mixture was heated at reflux for 48 h and then added to ice dropwise. The aqueous layer was extracted with EtOAc (2x). Extraction was difficult due to a large amount of precipitate. The aqueous layer pH was adjusted to pH 4-5 with 28% NH OH and was filtered through Celite®. The aqueous layer was then extracted with DCM and the combined organic extracts dried over Na₂SO , filtered and concentrated in vacuo to a yellow solid. Chromatography (FCC) (0 to 30% EtOAc/Hex) afforded 2-chloro-4,5,6-trimethylpyrimidine (4.26 g, 100%).

Intermediate 67: 2-Chloro-4,5-dimethylpyrimidine.

The title compound was prepared in a manner analogous to Intermediate 65, substituting 2,4-dichloro-5-methylpyrimidine for 2,4-dichloro-5-fluoropyrimidine. MS (ESI): mass calculated for C₆H₇CIN2, 142.03, m/z found 143.1 [M+1 ]⁺. ¹ H NMR (500 MHz, CDCI₃): 8.32 - 8.25 (m, 1 H), 2.52 - 2.46 (m, 3H), 2.28 - 2.22 (m, 3H).

Intermediate 68: 3-Fluoro-2-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid.

Method A:

Step A: 2-Fluoro-6-(methoxycarbonyl)benzoic acid. 3-Fluorophthalic anhydride (377 mg, 2.27 mmol) was dissolved in MeOH (6 ml_) and heated to reflux for 15 h. The mixture was concentrated in vacuo and the two products (400 mg, 89%), 2-fluoro-6-(methoxycarbonyl)benzoic acid and 3-fluoro-2- (methoxycarbonyl)benzoic acid, were taken on to the next step without purification.

Step B: (Z)-Methyl 2-((((1 -aminoethylidene)amino)oxy)carbonyl)-3- fluorobenzoate. To a heterogeneous mixture of the two acids from step A (400 mg, 2 mmol) at 0 °C in DCM (5 ml_) was added oxalyl chloride (0.244 ml_, 2.32 mmol) followed by DMF (0.05 ml_). Gas evolution commenced immediately and after 5 min the ice bath was removed. When gas evolution had ceased and the mixture was homogeneous an aliquot was removed and quenched with MeOH. Formation of the methyl ester was confirmed by HPLC and the mixture was concentrated in vacuo. The viscous liquid was dissolved in fresh DCM (5 ml_) and treated with solid N-hydroxyacetamidine (165 mg, 2.22 mmol) in several portions followed by TEA (0.351 ml_, 2.52 mmol). After stirring for 14 h at ambient temperature the mixture was concentrated in vacuo.

Chromatography (Hex to 100% EtOAc/Hex) afforded two products (477 mg, 94%), (Z)-methyl 2-((((1 -aminoethylidene)amino)oxy)carbonyl)-3- fluorobenzoate and (Z)-methyl 2-((((1 -aminoethylidene)amino)oxy)carbonyl)-6- fluorobenzoate, which were taken on to the next step as a mixture. MS (ESI) mass calculated for Cn H FN₂O₄, 254.07; m/z found, 255.0.

Step C: 3-Fluoro-2-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid. To the mixture of products from Step B (477 mg, 1 .88 mmol) in t-BuOH (9 ml_) was added NaOAc (156 mg, 1 .88 mmol). The mixture was heated at 90 °C for 50 h and then concentrated in vacuo. This resulted in four products. The residue was dissolved in 1 M aq. K2CO3 and extracted with DCM to isolate methyl 2- fluoro-6-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoate and methyl 3-fluoro-2-(3- methyl-1 ,2,4-oxadiazol-5-yl)benzoate along with unreacted (Z)-methyl 2-((((1 - aminoethylidene)amino)oxy)carbonyl)-3-fluorobenzoate. The aqueous layer was then acidified with concentrated HCI and extracted with DCM. The combined organic layers from this extraction were dried over Na2SO₄, filtered and concentrated in vacuo. The acid isomers were purified on a Prep Agilent system with a XBridge Ci₈ OBD 50x100 mm column eluting with 5 to 99% 0.05% NH₄OH in H₂O/ACN over 17 min to afford the desired product (63 mg, 15%) as a white solid after acidification with 1 M aq. HCI in Et₂O. MS (ESI) mass calculated for C10H₇FN2O3, 222.04; m/z found, 223.0.

Method B:

Step A: (Z)-N'-((2-Fluoro-6-iodobenzoyl)oxy)acetimidamide. To a heterogeneous mixture of 2-fluoro-6-iodobenzoic acid (1 .51 g, 5.66 mmol) at 0 °C in DCM (28 mL) was added oxalyl chloride (0.635 mL, 7.36 mmol) followed by DMF (0.15 mL). Gas evolution commenced immediately and after 5 min the ice bath was removed. When gas evolution had ceased and the mixture was homogeneous an aliquot was removed and quenched with MeOH. Formation of the methyl ester was confirmed by HPLC and the mixture was concentrated in vacuo. The viscous liquid was dissolved in fresh DCM (28 mL) and treated with solid N-hydroxyacetamidine (503 mg, 6.79 mmol) in several portions followed by TEA (1 .2 mL, 8.49 mmol) at 0 °C. After stirring for 14 h at ambient temperature the mixture was washed with saturated aqueous NaHCO₃ solution. The combined organic extracts were dried over Na2SO₄, filtered and

concentrated in vacuo. Chromatography (Hex to 100% EtOAc/Hex) afforded the desired product as a colorless oil (1 .57 g, 86%). MS (ESI) mass calculated for C9H8FIN2O2, 321 .96; m/z found, 323.0. 1 H NMR (500 MHz, CDCI3): 7.70 - 7.65 (m, 1 H), 7.15 - 7.1 1 (m, 2H), 4.87 (br s, 2H), 2.06 (s, 3H).

Step B: 5-(2-Fluoro-6-iodophenyl)-3-methyl-1 ,2,4-oxadiazole. To a heterogeneous mixture of the product of Step A in t-BuOH (24 mL) was added NaOAc(603 mg, 7.27 mmol) in H₂O (0.9 mL). The mixture was then heated to 1 10 °C for 12 days. The reaction was concentrated in vacuo and then dissolved in toluene. The toluene was then filtered to remove NaOAc and then concentrated in vacuo. Chromatography (Hex to 40% EtOAc/Hex) afforded the desired product as a colorless oil (1 .21 g, 82%). MS (ESI) mass calculated for C₉H₆FIN₂O, 303.95; m/z found, 304.9. 1 H NMR (500 MHz, CDCI3): 7.82 - 7.77 (m, 1 H), 7.29 - 7.20 (m, 2H), 2.55 (s, 3H).

Step C: 3-Fluoro-2-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid. To THF

(15 mL) was added 2 M i-PrMgCI in THF (2.2 mL, 4.47 mmol). This mixture was cooled to -78 °C and the product of Step B (1 .09 g, 3.58 mmol) was added dropwise in THF (20 mL). The mixture was stirred for 30 min at -78 °C and then CO2 from a lecture bottle was bubbled into the solution for 3 h while allowing the temperature to slowly rise. When the temperature reached -20 °C the dry ice bath was replaced with an ice bath, bubbling of CO₂ was ceased and the mixture was allowed to come to room temperature overnight. The mixture was quenched by the addition of H₂O and a small amount of Et₂O. The organic layer was washed 2x with 2N aq. NaOH and the combined aqueous layers were then washed 3x with Et₂O. The aqueous layer was then acidified with concentrated HCI and extracted with DCM. The combined organic layers were dried over Na₂SO₄, filtered and concentrated in vacuo to afford the desired product as a white solid (661 mg, 83%). MS (ESI) mass calculated for CioH₇FN₂O₃, 222.04; m/z found, 223.0. 1 H NMR (500 MHz, CDCI₃): 7.96 (d, J = 7.8, 1 H), 7.72 - 7.64 (m, 1 H), 7.50 - 7.44 (m, 1 H), 2.56 - 2.48 (m, 3H).

Intermediate 69: 2-Fluoro-6-(3-methyl-1 ,2,4-oxadiazol-5-yl)benzoic acid.

The title compound was isolated from the synthesis of Intermediate 68, Method A. MS (ESI) mass calculated for Ci₀H₇FN₂O₃, 222.04; m/z found, 223.0. ¹H NMR (500 MHz, CDCI3): 7.89 (d, J = 7.7, 1 H), 7.65 - 7.59 (m, 1 H), 7.44 - 7.38 (m, 1 H), 2.50 (s, 3H).

Intermediate 70: 2,5-Dichloro-4-methylpyrimidine.

The title compound was prepared in a manner analogous to Intermediate 65, substituting 2,4,5-trichloropyrimidine for 2,4-dichloro-5-fluoropyrimidine. ¹H NMR (500 MHz, CDCI₃): 8.47 (s, 1 H), 2.61 (s, 3H). ntermediate 71 : 2,5-Dichloro-4,6-dimethylpyrinnidine.

To 5-chloro-4,6-dimethylpyrinnidin-2-ol (992 mg, 6.26 mmol) was added POCI3 (2.22 ml_, 23.77 mmol) followed by Et₂NPh (0.75 ml_, 4.69 mmol) dropwise. The mixture was heated at 125°C for 2 h. At approximately 2 h the reaction became homogeneous and was checked by HPLC and it showed all starting material had been consumed. The mixture was allowed to cool to room temperature and was then added dropwise to ice. After the ice had melted there was a white solid in a pink liquid. The aqueous layer was extracted with DCM and the combined organic layers were dried over Na₂SO₄, filtered and concentrated in vacuo. Chromatography (Hex to 10% EtOAc/Hex) afforded the desired product as a white solid (915 mg, 83%). ¹ H NMR (500 MHz, CDCI₃): 2.57 (s, 6H).

Intermediate 72: 2-Chloro-5-ethyl-4,6-dimethylpyrimidine.

The title compound was prepared in a manner analogous to Intermediate 66, substituting 5-ethyl-4,6-dimethylpyrimidin-2-ol for 4,5,6-trimethylpyrimidin-2-ol. MS (ESI): mass calculated for C₈HnCIN_2> 170.06, m/z found 171 .1 [M+1]⁺. ¹H NMR (500 MHz, CDCI₃): 2.65 (q, J = 7.6 Hz, 2H), 2.50 (s, 6H), 1 .15 (t, J = 7.6 Hz, 3H).

Intermediate 73: 2-Chloro-5-fluoro-4,6-dimethylpyrimidine.

Step A: 5-Fluoropyrimidine-2,4,6-triol. To a heterogeneous mixture of urea (641 mg, 10.67 mmol) and diethylfluoromalonate (1 .96 g, 10.67 mmol) in EtOH (1 1 ml_) was added 2.68 M NaOEt in EtOH (7.96 ml_, 21 .34 mmol). The mixture was heated at reflux for 60 h and then allowed to cool to room temperature. The mixture was filtered and the cake was then dissolved in warm water and the resulting solution was acidified with concentrated HCI to pH 2. The mixture was allowed to cool to room temperature and then cooled in an ice bath before filtering. The cake was washed with water and dried to afford 5-fluoropyrimidine-2,4,6-triol as a slightly off white solid (1 .45 g, 93%).

Step B: 2,4,6-Trichloro-5-fluoropyrimidine. To POCI₃ (4.49 ml_, 48.15 mmol) was added 5-fluoropyrimidine-2,4,6-triol (1 .41 g, 9.63 mmol) in several portions. There was a 2 °C increase in temperature. The N,N-dimethylaniline (1 .23 ml_, 9.73 mmol) was then added dropwise and the mixture heated at 1 10 °C for 24 h. The reaction mixture was allowed to cool only briefly and then was quenched by dropwise addition onto ice. When the ice was melted the aqueous layer was extracted several times with Et₂O. The combined organic extracts were dried over Na₂SO₄, filtered and concentrated in vacuo to a yellow solid after storing in the refrigerator overnight. This material was not purified further, but taken on to the next step without further purification.

Step C: 2-Chloro-5-fluoro-4,6-dimethylpyrimidine was prepared in a manner analogous to Intermediate 65, substituting 2,4,6-trichloro-5- fluoropyrimidine for 2,4-dichloro-5-fluoropyrimidine. ¹ H NMR (500 MHz, CDCIs): 2.50 (d, J = 2.7 Hz, 6H).

Intermediate 74: 3-[1 ,2,3]Triazol-2-yl-pyridine-2-carboxylic acid.

The title compound was prepared in a manner analogous to Intermediate 47 substituting 3-bromo-2-pyridinecarboxylic acid for 2-chloro-6-methylnicotinic acid. MS (ESI): mass calculated for C₈H₆N₄O₂, 190.10; m/z found 191 .1 [M+H]⁺ _. ¹H NMR (400 MHz, CDCI3): 8.77 (d, J = 4.3 Hz, 1 H), 8.26 (dt, J = 6.5, 3.3 Hz, 1 H), 7.88 (s, 2H), 7.65 (dd, J = 8.2, 4.7 Hz, 1 H).

Intermediate 75: 1 -[1 ,2,3]Triazol-2-yl-naphthalene-2-carboxylic acid.

The title compound was prepared in a manner analogous to Intermediate 47 substituting 1 -bromo-2-napthoic acid for 2-chloro-6-methylnicotinic acid. The title compound was obtained (484 mg, 50%). MS (ESI): mass calculated for C13H9N3O2, 239.23; m/z found 240.3 [M+H]⁺. ¹ H NMR (400 MHz, CD₃OD): 8.19 (d, J = 8.7 Hz, 1 H), 8.09 - 8.03 (m, 4H), 7.70 - 7.66 (m, 1 H), 7.58 (ddd, J = 8.2, 6.9, 1 .2 Hz, 1 H), 7.25 (d, J = 8.6 Hz, 1 H).

Intermediate 76: 1 -[1 ,2,3]Triazol-1 -yl-naphthalene-2-carboxylic acid.

The title compound was isolated as a byproduct from the preparation of

Intermediate 75 (25% yield). MS (ESI): mass calculated for C13H9N3O2, 239.23; m/z found 240.3 [M+H]^{+ 1}H NMR (400 MHz, CD₃OD): 8.33 (d, J = 0.9 Hz, 1 H), 8.24 (d, J = 8.6 Hz, 1 H), 8.14 - 8.07 (m, 2H), 8.01 (d, J = 0.9 Hz, 1 H), 7.71 (t, J = 7.6 Hz, 1 H), 7.60 (t, J = 7.7 Hz, 1 H), 7.1 1 (d, J = 8.5 Hz, 1 H).

Intermediate 77: 8-[1 ,2,3]Triazol-2-yl-naphthalene-1 -carboxylic acid.

The title compound was prepared in a manner analogous to Intermediate 47 substituting 8-bromo-2-napthoic acid for 2-chloro-6-methylnicotinic acid. The desired 8-[1 ,2,3]triazol-2-yl-naphthalene-1 -carboxylic acid was obtained (474mg, 16%). MS (ESI): mass calculated for C1 H9N3O2, 239.20; m/z found 240.3 [M+H]⁺ _. ¹H NMR (400 MHz, CD₃OD): 8.13 (t, J = 9.0 Hz, 2H), 7.95 - 7.91 (m, 3H), 7.82 (dd, J = 7.4, 1 .0 Hz, 1 H), 7.70 (dd, J = 9.8, 5.8 Hz, 1 H), 7.64 - 7.59 (m, 1 H).

Intermediate 78: 5-[1 ,2,3]Triazol-2-yl-benzo[1 ,3]dioxole-4-carboxylic acid.

The title compound was prepared in a manner analogous to Intermediate 47 substituting 5-bromobenzo[1 ,3]dioxole-4-carboxylic acid for 2-chloro-6- methylnicotinic acid. MS (ESI): mass calculated for CioH₇N₃O₄, 233.18; m/z found 234.3 [M+H]⁺. ¹H NMR (400 MHz, CD₃OD): 7.85 (s, 2H), 7.23 (d, J = 8.4 Hz, 1 H), 7.04 (d, J = 8.4 Hz, 1 H), 6.16 (s, 2H).

Intermediate 79: 2,3-Dimethoxy-6-[1 ,2,3]triazol-2-yl-benzoic acid

To a 20 ml microwave vial containing 2-bromo-4,5-dimethoxybenzoic acid (3 g, 1 1 .5 mmol), copper iodide (0.04 g, 0.5 mol%), cesium carbonate (7.5 g, 23 mmol), triazole (1 .33 mL, 23 mmol) and finally (R,R)-(-)-N,N'-dimethyl-1 ,2- cyclohexanediamine ligand (0.36 mL, 2.3 mmol) was added DMF (12 mL). The resulting clumpy yellow slurry was stirred until evenly dispersed then heated to 120°C for 10-20 min using a microwave. At this point the reaction mixture appeared as a blue slurry which was then diluted with 20 mL ether and 20 mL H₂O. The resulting solution was thoroughly stirred and transferred to a seperatory funnel then the RBF was subsequently rinsed with 20 mL ether and H₂O each. The aqueous layer was separated from the organic layer and acidified to pH 1 with 6 mL cone. HCI. The now brown/ lime green aqueous layer was extracted twice with EtOAc. The bright yellow organic layers were combined and dried with Na₂SO₄ and then cone, into a yellow powder under reduced pressure which was purified by FCC (0-5% MeOH in DCM w/ 0.5% AcOH) to afford 2,3-dimethoxy-6-[1 ,2,3]triazol-2-yl-benzoic acid (60%) and 2,3- dimethoxy-6-[1 ,2,3]triazol-1 -yl-benzoic acid (20%). Data for 2,3-dimethoxy-6- [1 ,2,3]triazol-2-yl-benzoic acid, MS (ESI): mass calculated for CnHnN₃O₄, 249.23; m/z found 250.3 [M+H]⁺ _. ¹H NMR (400 MHz, CD₃OD): 7.87 (s, 2H), 7.47 (s, 1 H), 7.18 (s, 1 H), 3.94 (s, 3H), 3.91 (s, 3H).

Intermediate 80: 2,3-Dimethoxy-6-[1 , 2, 3]triazol-1 -yl-benzoic acid.

The title compound was isolated from the procedure used to prepare

Intermediate 79 with a 20% yield. MS (ESI): mass calculated for Cn Hn N₃O , 249.23; m/z found 250.3 [M+H]⁺ _. ¹H NMR (400 MHz, CD₃OD): 8.17 (d, J = 1 .0 Hz, 1 H), 7.82 (d, J = 1 .0 Hz, 1 H), 7.62 (s, 1 H), 7.09 (s, 1 H), 3.95 (s, 3H), 3.91 (s, 3H). Intermediate 81 : 4-(1 H-1 ,2,3-Triazol-1 -yl)nicotinic acid.

The title compound was prepared in a manner analogous to Intermediate 47 substituting 4-chloronicotinic acid for 2-chloro-6-methylnicotinic acid. MS (ESI): mass calculated for Cn HioN₄O₃, 246.22; m/z found 247.3 [M+H]⁺. ¹ H NMR (400 MHz, CD3OD): 8.09 (t, J = 2.8 Hz, 1 H), 7.92 - 7.86 (m, 3H), 7.66 (dd, J = 8.7, 3.3 Hz, 1 H), 2.17 (dd, J = 2.5, 1 .3 Hz, 3H).

Intermediate 83: 3-Fluoro-2-(1 H-pyrazol-5-yl)benzoic acid.

Method A:

Step A: 2-Bromo-3-fluorobenzonitrile (1 .0 g, 5.0 mmol) and (1 H-pyrazol-

5-yl)boronic acid (647 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 ml_) then treated with NaHCO₃ (1260 mg, 8.4 mmol) in water and the reaction purged with bubbling N₂ for 5 minutes. The reaction was treated with Pd(PPh₃) (288 mg, 0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. Cooled to 23 °C filtered and solid rinsed with EtOAc and the layers separated. The organic layers were combined, dried and concentrated under reduced pressure.

Chromatography (0-30% ethyl acatate / hexanes) afforded 3-fluoro-2-(1 H- pyrazol-5-yl)benzonitrile (178 mg,19%).

Step B: To 3-fluoro-2-(1 H-pyrazol-5-yl)benzonitrile in MeOH (3 ml_) was added 2M aq. NaOH (1 ml_). The reaction was heated at reflux for 15h, then cooled to rt, acidified with 1 N aq. HCI to pH=1 and extracted with EtOAc to give (210 mg, 99%) of 3-fluoro-2-(1 H-pyrazol-5-yl)benzoic acid which was used crude.

Method B:

The title compound was prepared in a manner analogous to

Intermediate 62, substituting methyl 2-iodo-3-fluorobenzoate for methyl 2- bromo-5-fluorobenzoate in Step A. MS (ESI): mass calculated for

CioH₇FN₂O₂, 206.05; m/z found 207.0 [M+1 ]⁺.

Intermediate 84: 2-(1 H-1 ,2,3-Triazol-1 -yl)-6-(trifluoromethyl)nicotinic acid.

The title compound was prepared in a manner analogous to Intermediate 17, substituting 2-chloro-6-(trifluoromethyl)nicotinic acid for 5-fluoro-2-iodo-benzoic acid in step A, and substituting 1 ,4-dioxane for MeOH as the solvent, with 0.3 eq of water as an additive. ¹H NMR (400 MHz, DMSO-c/₆): 8.64 (s, 1 H), 8.37 (d, J = 7.6 Hz, 1 H), 8.1 1 (d, J = 7.8 Hz, 1 H), 7.93 (s, 1 H).

Intermediate 85: 4-Fluoro-2-(pyrimidin-2-yl)benzoic acid.

Step A: 2-lodo-4-fluorobenzonitrile (2.54 g, 10.3 mmol) and 2- tributylstannane pyrimidine (3.69 g, 10.0 mmol) were dissolved in

domethoxyethane (18 ml_) and treated with tetrakistriphenylphosphine) palladium (0) (578 mg, 0.5 mmol) and copper (I) iodide (95 mg, 0.5 mmol). The reaction was then heated to 160 C for 90 minutes in the microwave. The reaction was cooled, concenctrated under reduced pressure. Chromatography (20-100% EA in hexanes gave the desired product. ¹H NMR (400 MHz, CDCIs): 8.93 (d, J = 4.9 Hz, 2H), 8.14 (dd, J = 9.6, 2.7 Hz, 1 H), 7.86 (dd, J = 8.6, 5.3 Hz, 1 H), 7.36 (t, J = 4.9 Hz, 1 H), 7.32 - 7.23 (m, 1 H).

Step B: 3-Fluoro-2-(pyrimidin-2-yl)benzonitrile (85 mg, 0.4 mmol) was hydrolyzed to the acid in water (1 mL) by addition of 18 M H₂SO₄ (1 mL). The reaction was heated at 100 °C for 10 min, then cooled to 23 °C, and extracted with EtOAc (3 x 5 mL). The combined organics were dried (Na₂SO ) and concentrated under reduced pressure. This material was used crude in subsequent reactions.

Intermediate 86: 4-Methoxy-2-(pyrimidin-2-yl)benzoic acid.

Step A: 3-Fluoro-2-(pyrimidin-2-yl)benzonitrile was prepared in a manner analogous to Intermediate 85. ¹H NMR (400 MHz, CDCI3): 8.93 (d, J = 4.9 Hz, 2H), 8.14 (dd, J = 9.6, 2.7 Hz, 1 H), 7.86 (dd, J = 8.6, 5.3 Hz, 1 H), 7.36 (t, J = 4.9 Hz, 1 H), 7.32 - 7.23 (m, 1 H).

Step B: 3-Fluoro-2-(pyrimidin-2-yl)benzonitrile (85 mg, 0.4 mmol) was dissolved in MeOH (20 mL) was treated with 2M aq NaOH (15 mL). The reaction was heated at reflux overnight, the reaction was cooled to room temperature and filtered to remove the solid (amide) and washed with cold MeOH. The filtrate was concentrated to minimum volume and then acidified to pH=3 with 6 N aq. HCI and cooled to 0 °C then filtered and washed with cold water. This material was used crude in subsequent reactions.

Example 1 : (1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-thiophen-2-yl-phenyl)-methanone.

A mixture of (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 4, 28 mg, 0.13 mmol), 2-thiophen-2-yl- benzoic acid (29 mg, 0.14 mmol), HATU (73.2 mg, 0.19 mmol),

diisopropylethylamine (50 mg, 0.38 mmol) was stirred in DMF (4 mL) at room temperature for 2 h. Then the reaction mixture was partitioned between water and ethyl acetate mixture. The organic phase was separated and washed with 1 N aq. NaOH (10 mL) and then with water (2 x 15 mL). The organic phase was dried (Na₂SO₄), filtered and concentrated under reduced pressure. The crude product was purified on HPLC (basic system) to yield the title compound (31 .0 mg, 59.8%). MS (ESI) mass calcd. for C₂₃H₂₄N₄OS, 404.53; m/z found, 405.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 7.60-6.75 (m, 7H), 6.43-6.10 (m, 1 H), 4.10- 1 .78 (m, 16H).

Example 2: (1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-furan-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 substituting 2-furan-2-yl-benzoic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂3H₂ N₄O2, 388.46; m/z found, 389.2 [M+H]⁺. ¹H NMR (400 MHz, CDCIs): 7.77-7.64 (m, 1 H), 7.49-7.27 (m, 2H), 7.25-6.60 (m, 2H), 6.56-6.30 (m, 2H), 6.29-5.76 (m, 1 H), 4.94-2.67 (m, 8H), 2.44-1 .86 (m, 8H). Example 3: (1 R, 6S)-Biphenyl-2-yl -[8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting biphenyl-2-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for 0₂5Η₂₆Ν₄Ο, 398.50; m/z found, 399.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 7.55-7.29 (m, 7H), 7.25-6.98 (m, 1 H), 6.95-6.74 (m, 1 H), 6.41 -6.20 (m, 1 H), 4.56-3.58 (m, 5H), 3.52-2.62 (m, 2H), 2.60-2.28 (m, 2H), 2.13 (s, br, 5H), 1 .84-1 .27 (m, 2H).

Example 4: (1 R, 6S) (8-Quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-(2- thiophen-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane. MS (ESI) mass calcd. for C₂₅H22N₄OS, 426.53; m/z found, 427.0 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.23-6.00 (m, 12 H), 4.80- 2.69 (m, 10 H).

Example 5: (1 R, 6S) Biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone.

A mixture of (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline (179 mg, 0.745 mmol), biphenyl-2-carbonyl chloride (210 mg, 0.97 mmol), Et₃N (196 mg, 1 .95 mmol) was stirred into DCM (7.0 mL) for 18 h at room temperature. Then reaction mixture was diluted with more DCM (25 mL) and washed successively with 1 N aq. NaOH (5 mL) and water (2 x 15 mL). The organic phase was concentrated under reduced pressure. The crude residue was purified on HPLC (basic system) to yield pure title compound (373 mg, 99%). MS (ESI) mass calcd. for C₂7H₂ N₄O, 420.52; m/z found, 421 .2 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 8.00-7.32 (m, 1 1 H), 7.29-7.18 (m, 1 H), 6.75 (dd, J = 9.9, 4.2, 2H), 4.70-4.42 (m, 1 H), 4.30-3.90 (m, 3H), 3.8-3.74 (m, 0.66H), 3.51 -3.30 (m, 1 .35H), 3.13-3.03 (m, 0.5H), 2.90-2.80 (m, 0.5H), 2.68-2.51 (m, 0.5H), 1 .96- 1 .68 (m, 2H), 1 .59 - 1 .43 (m, 0.5H).

Example 6: (1 R, 6S) (2-Furan-2-yl-phenyl)-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-furan-2-yl-benzoic acid for 2-thiophen-2-yl-benzoic acid and (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline (Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane. MS (ESI) mass calcd. for C₂5H₂2N₄O₂, 410.47; m/z found, 41 1 .2 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 8.00-7.17 (m, 9H), 6.69-6.28 (m, 3H), 4.98-4.38 (m, 1 H), 4.27-3.84 (m, 4H), 3.83-3.05 (m, 2H), 3.03-2.84 (m, 1 H), 2.32-1 .97 (m, 2H).

Example 7: (1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- icyclo[4.2.0]oct-3-yl]-(2-pyrrol-1 -yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-pyrrol-1 -yl-benzoic acid for 2-furan-2-yl-benzoic acid. MS (ESI) mass calcd. for C23H2₅N₅O, 387.48; m/z found, 388.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.47-7.29 (m, 3H), 7.13-7.07 (m, 1 H), 7.00-6.91 (m, 3H), 6.29 (dd, J = 4.7, 2.5, 2H), 4.24-4.18 (m, 1 H), 4.13-3.86 (m, 3H), 3.80 (dd, J = 14.0, 3.0, 1 H), 3.55-3.35 (m, 2H), 2.80-2.69 (m, 1 H), 2.53 (dd, J = 14.0, 2.1 , 1 H), 2.32 (d, J = 14.4, 1 H), 2.20-1 .99 (m, 6H).

Example 8: Biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)- methanone.

The title compound was prepared in a manner analogous to Example 5, substituting 2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline (Intermediate 2) for (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline. MS (ESI) mass calcd for C₂7H₂ N₄O, 420.51 ; m/z found, 421 .2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.00-7.12 (m, 1 1 H), 6.68-6.27 (m, 3H), 5.00-2.87 (m, 8H), 2.32-1 .94 (m, 2H). Example 9: Biphenyl-2-yl-[8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane

(Intermediate 6) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and biphenyl-2-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂9H₂6N₄O, 446.54; m/z found, 447.3 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.44-7.28 (m, 13H), 7.27-6.79 (m, 3H), 4.70-3.66 (m, 4H), 3.59-2.31 (m, 3H), 2.19-0.93 (M, 3H).

Example 10: (1 R, 6S) (4'-Methyl-biphenyl-2-yl)-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 4'-methyl-biphenyl-2-carboxylic acid for 2-thiophen-2-yl-benzoic acid and (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline (Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane. MS (ESI) mass calcd. for C₂₈H₂6N₄O, 434.53; m/z found, 435.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.03-7.83 (m, 2H), 7.80-7.49 (m, 2H), 7.47-7.29 (m, 5H), 7.25-7.06 (m, 2H), 6.75-6.45 (m, 2H), 4.69-4.45 (m, 1 H), 4.34-3.71 (m, 4H), 3.58-3.09 (m, 2H), 3.02-2.54 (m, 2H), 2.43-1 .98 (m, 3H), 1 .93-1 .79 (m, 1 H).

Example 1 1 : (8-Benzooxazol-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-biphenyl-2- -methanone.

The title compound was prepared in a manner analogous to Example 5, substituting the trifluoro acetic acid salt of 2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)- benzooxazole (Intermediate 7) for (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)- quinoxaline. MS (ESI) mass calcd. for C26H23N3O2, 409.48; m/z found, 410.3 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.62-7.00 (m, 1 1 H), 7.01 -6.66 (m, 2H), 4.83-3.94 (m, 3H), 3.89-2.35 (m, 5H), 2.12-1 .14 (m, 2H).

Example 12: (2,6-Dimethoxy-phenyl)-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone.

The title compound was prepared in a manner analogous to Example 5, substituting the trifluoro acetic acid salt of 2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)- quinoxaline (Intermediate 2) for (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)- quinoxaline and 2,6-dimethoxy benzoyl chloride for biphenyl-2-carbonyl chloride. MS (ESI) mass calcd. for C₂3H₂₄N₄O₃, 404.46; m/z found, 405.3

[M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.25 (s, 0.25H), 7.98 (s, 0.75H), 7.90-7.80 (m, 1 H), 7.60-7.47 (m, 1 H), 7.44-7.30 (m, 2H), 7.23 (t, J = 8.4, 0.25H), 7.13 (t, J = 8.4, 0.75H), 6.58-6.44 (m, 1 .25H), 6.03 (d, J = 8.4, 0.75H), 4.90-4.56 (m, 1 H), 4.32-3.84 (m, 3H), 3.81 (s, 6H), 3.78-3.56 (m, 1 H), 3.50-3.30 (m, 1 H), 3.17-2.91 (m, 1 H), 2.41 -1 .53 (m, 3H).

Example 13: (1 R, 6S) (2-Bromo-phenyl)-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone.

The title compound was prepared in a manner analogous to Example 5, substituting 2-bromobenzoyl chloride for biphenyl-2-carbonyl chloride. MS (ESI) mass calcd. for C₂i Hi₉BrN₄O, 423.31 ; m/z found, 423.1 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 8.29-7.99 (m, 1 H), 7.94-7.84 (m, 1 H), 7.78-7.08 (m, 5.5H), 7.08-6.99 (m, 0.5H), 6.62 (dd, J = 7.5, 1 .0, 0.5H), 6.52 (dd, J = 7.6, 1 .6, 0.5H), 4.97-4.52 (m, 1 H), 4.35-3.74 (m, 4H), 3.70-2.87 (m, 2H), 2.37-1 .56 (m, 3H).

Example 14: (1 R, 6S) (2-Pyridin-3-yl-phenyl)-(8-quinoxalin-2-yl-3,8-diaza- methanone.

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-pyridin-3-yl-benzoic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C26H23N₅O, 421 .49; m/z found, 422.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.79-8.44 (m, 2H), 8.27-8.26 (m, 9H), 6.83-6.13 (m, 2H), 4.78-3.77 (m, 4H), 3.73-3.32 (m, 2H), 3.18-2.58 (m, 2H), 2.00-1 .47 (m, 2H).

Example 15: (2,6-Dimethoxy-phenyl)-[8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-methanone.

(Intermediate 6) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2,6-dimethoxy-benzoic acid for 2-thiophen-2-yl- benzoic acid. MS (ESI) mass calcd. for C₂5H₂6N₄O₃, 430.50; m/z found, 431 .3 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.60-7.27 (m, 7H), 7.25-6.66 (m, 3H), 4.84- 2.46 (m, 12H), 2.18-1 .15 (m, 4H).

Example 16: (8-Benzooxazol-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-(2,6- dimethoxy-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 5, substituting 2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-benzooxazole (Intermediate 7) for (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline and 2,6-dimethoxy benzoyl chloride for biphenyl-2-carbonyl chloride. MS (ESI) mass calcd. for C2₂H23N₃O₄, 393.44; m/z found 394.3 [M+H]⁺. ¹H NMR (400 MHz, CDCI₃): 7.54- 7.27 (m, 2H), 7.25-7.06 (m, 3H), 6.57-6.01 (m, 2H), 5.12-4.00 (m, 5H), 3.98- 3.33 (m, 7H), 3.20-2.94 (m, 2H), 2.24-1 .72 (m, 2H).

Example 17: (1 S, 6R) Biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone.

The chiral separation of biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone (Example 8) was carried out using chiral column. The slower moving isomer having optical rotation at 20 °C [oc]₅₈9 nM = - 201 .77 was identified as the title compound. MS (ESI) mass calcd. for

C₂7H₂ N₄O, 420.51 ; m/z found 421 .2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.21 - 7.14 (m, 12H), 6.82-6.46 (m, 2H), 4.76-2.50 (m, 6H), 1 .97-1 .48 (m, 3H), 1 .23- 0.8 (m, 1 H).

Example 18: (1 S, 6R) Biphenyl-2-yl-[8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- ethanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 S, 6R) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and biphenyl-2-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C^H eNUO, 398.5; m/z found 399.2 [M+H]⁺. ¹H NMR (400 MHz, CDCI₃): 7.56-7.25 (m, 7H), 7.24-6.72 (m, 2H), 6.44-6.17 (m, 1 H), 4.57-3.20 (m, 6H), 3.01 -2.40 (m, 2.5H), 2.37-2.00 (m, 6H), 1 .38-1 .31 (m, 1 .5H).

Example 19: 3-(2,5-Dimethyl-benzenesulfonyl)-8-(4-phenyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane.

A mixture of 8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane

(Intermediate 6, 1 10 mg, 0.29 mmol), 2,5-dimethyl-benzenesulfonyl chloride (83 mg, 0.41 mmol) and Et₃N (91 mg, 0.9 mmol) was stirred in DCM (5.0 mL) at RT for 18 h. The reaction mixture was diluted with more DCM (15 mL) and washed with water. The organic layers were combined, dried, filtered and concentrated under reduced pressure to yield crude product. The crude product was purified on HPLC (basic system) to yield the title compound (40 mg, 35%). MS (ESI) mass calcd. for C₂ H26N₄O₂S, 434.55; m/z found 435.3 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.26 (s br, 1 H), 7.87 (s br, 2H), 7.70 (s, 1 H), 7.51 -7.34 (m, 3H), 6.94 (d, J = 5.3, 1 H), 6.91 -6.73 (m, 2H), 4.62-4.52 (m, 1 H), 4.16 (t, J = 8.3, 1 H), 4.04 (dd, J = 13.5, 2.9, 1 H), 3.93 (dd, J = 8.6, 3.9, 1 H), 3.85-3.73 (m, 1 H), 3.74-3.59 (m, 1 H), 3.40 (dd, J = 13.5, 2.8, 1 H), 2.95- 2.89 (m, 1 H), 2.45 (s, 3H), 2.28-2.12 (m, 1 H), 2.21 -1 .85 (m, 4H). Example 20: (1 R, 6S) 2-[3-(2,4-Dimethyl-benzenesulfonyl)-3,8-diaza- bicyclo[4.2.0]oct-8-yl]-quinoxaline.

The title compound was prepared in a manner analogous to Example 19 substituting (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline

(Intermediate 3) for 8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 2,4-dimethyl-benzenesulfonyl chloride for 2,5-dimethyl-benzenesulfonyl chloride. MS (ESI) mass calcd. for C22H₂₄N₄O₂S, 408.52; m/z found 409.2

[M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 7.96 (s, 1 H), 7.86 (dd, J = 8.2, 1 .3, 1 H), 7.66 (d, J = 1 .2, 1 H), 7.58-7.52 (m, 1 H), 7.49 (dd, J = 8.4, 1 .1 , 1 H), 7.43-7.37 (m, 1 H), 6.62-6.48 (m, 2H), 4.69-4.61 (m, 1 H), 4.22-3.95 (m, 4H), 3.85-3.74 (m, 1 H), 3.69-3.59 (m, 1 H), 3.41 (dd, J = 14.0, 2.8, 1 H), 3.05-2.89 (m, 1 H), 2.42 (s, 3H), 2.30-2.14 (m, 1 H), 2.09 (s, 3H), 2.05-1 .92 (m, 1 H).

Example 21 : 2-[3-(2,5-Dimethyl-benzenesulfonyl)-3,8-diaza-bicyclo[4.2.0]oct-8- -quinoxaline.

The title compound was prepared in a manner analogous to Example 19 substituting 2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline (Intermediate 2) for 8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane (Intermediate 6). MS (ESI) mass calcd. for C₂2H2 N₄O₂S, 408.52; m/z found 409.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 7.96 (s, 1 H), 7.86 (dd, J = 8.2, 1 .3, 1 H), 7.66 (d, J = 1 .2, 1 H), 7.60-7.45 (m, 2H), 7.44-7.35 (m, 1 H), 6.63-6.49 (m, 2H), 4.71 -4.62 (m, 1 H), 4.17 (t, J = 8.0, 1 H), 4.07-3.95 (m, 2H), 3.85-3.75 (m, 1 H), 3.69-3.59 (m, 1 H), 3.41 (dd, J = 14.0, 2.8, 1 H), 3.05-2.89 (m, 1 H), 2.42 (s, 3H), 2.31 -2.16 (m, 1 H), 2.09 (s, 3H), 2.06-1 .95 (m, 1 H).

Example 22: (1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- icyclo[4.2.0]oct-3-yl]-(2-fluoro-6-pyrimidin-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-fluoro-6-pyrimidin-2-yl-benzoic acid for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 15 minutes. MS (ESI) mass calcd. for C23H23FN6O, 418.47; m/z found, 419.2 [M+H]⁺. ¹H NMR (400 MHz, CDCI3): 8.82-8.73 (m, 1 H), 8.40 (d, J = 4.8, 1 H), 8.32-8.26 (m, 0.4H), 8.23-8.08 (m, 0.6H), 7.52-7.36 (m, 1 H), 7.26-7.16 (m, 1 H), 7.03-6.93 (m, 0.35H), 6.89-6.84 (m, 0.2H), 6.77-6.70 (m, 45H), 6.43-6.24 (m, 0.6H), 5.98-5.91 (m, 0.4H), 3.72-327 (m, 6H), 2.42-1 .96 (m, 10H).

Example 23: (1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- (5-fluoro-2-pyrimidin-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 3-fluoro-6-pyrimidin-2-yl-benzoic acid for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 15 minutes. MS (ESI) mass calcd. for C23H23FN6O, 418.47; m/z found, 419.2 [M+H]⁺. ¹H NMR (400 MHz, CDCI3): 8.90-8.05 (m, 3H), 7.24-5.90 (m, 4H), 4.80-3.60 (m, 6H), 3.28- 2.65 (m, 2H), 2.40-1 .78 (m, 8H).

Example 24: (1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- -yl]-(2-ethoxy-naphthalen-1 -yl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-ethoxy-naphthalene-1 -carboxylic acid for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 15 minutes. MS (ESI) mass calcd. for C₂5H₂8N₄O₂, 416.52; m/z found, 417.2 [M+H]⁺. ¹H NMR (400 MHz, CDCI3): 7.84-7.56 (m, 2H), 7.48-7.15 (m, 3H), 7.1 1 -6.97 (m, 0.5H), 6.90- 6.80 (m, 0.5H), 6.41 -6.21 (m, 0.5H), 5.92 (s, 0.5H), 5.1 1 -4.68 (m, 0.5H), 4.40- 3.68 (m, 7H), 3.65-3.00 (m, 1 .5H), 3.00-2.63 (m, 1 H), 2.40-1 .96 (m, 7H), 1 .78- 1 .58 (m, 1 H), 1 .62-0.96 (m, 3H).

Example 25: (1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2- yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C21 H23N₇O, 389.46; m/z found 390.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.12-7.73 (m, 3H), 7.42 (m, 2H), 7.10 (t, J = 7.2, 0.5H), 6.92 (m, 0.5H), 6.43-6.04 (m, 1 H), 4.75-3.00 (m, 7H), 2.93-1 .76 (m, 9H).

Example 26: (1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(5-methyl-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 5-methyl-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 59) for 2- thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H2₅N₇O, 403.48; m/z found 404.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.00-7.72 (m, 2H), 7.42-6.71 (m, 3H), 6.42-6.04 (m, 1 H), 4.75-3.78 (m, 5H), 3.74-2.65 (m, 3H), 2.48-2.25 (m, 3H), 2.19-1 .72 (m, 8H).

Example 27: (1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(5-methyl-2-pyrimidin-2-yl-phenyl)-methanone.

A mixture of (1 R, 6S)-8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (60 mg, 0.28 mmol), 5-methyl-2-pyrimidin-2-yl-benzoic acid (61 .82 mg, 0.29 mmol), HOAT (56.12 mg, 0.41 mmol), 1 -(3- dimethylanninopropyl)-3-ethylcarbodiinnide HCI (79.1 mg, 0.41 mmol), TEA (83.5 mg, 0.83 mmol) was taken into DMF (5 mL) and stirred at 50 °C for 4 h. The reaction mixture was cooled and diluted with ethyl acetate (50 mL). It was washed with sat. aqueous NaHCO₃ solution (2 x 25 mL) and with water (2 x 60 mL). The ethyl acetate layer was dried over Na2SO₄, filtered and concentrated. The crude product was purified three times on Agilent Basic HPLC system to yield the title compound (24 mg, 21 %). MS (ESI) mass calcd. for C₂₄H₂6N₆O, 414.51 ; m/z found 415.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 9.17-5.47(m, 7H), 4.89-1 .08 (m, 19H).

Example 28: (1 R, 6S)- [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-d

bicyclo[4.2.0]oct-3-yl]-(2-pyrimidin-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-pyrimidin-2-yl-benzoic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C23H₂ N₆O, 400.48; m/z found 401 .2 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 8.90-6.00(m, 8H), 4.84-3.62 (m, 5H), 3.38-1 .50 (m, 1 1 H).

Example 29: (1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- uoro-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2- thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C₂₁ H₂₂FN7O, 407.45; m/z found 408.2

[M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.93-7.70 (m, 2H), 7.58-7.24 (m, 2H), 7.24- 7.04 (m, 0.6H), 6.85 (t, J = 8.3, 0.4H), 6.35-6.0 (m, 1 H), 4.77-4.33 (m, 1 H), 4.23-3.92 (m, 3H), 3.92-3.04 (m, 2H), 2.91 -2.66 (m, 1 H), 2.66-1 .92 (m, 7H), 1 .84-1 .62 (m, 2H).

Example 30: (1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 3-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2- thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C₂i H₂₂FN₇O, 407.45; m/z found 408.2

[M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.89-7.65 (m, 2H), 7.50-7.27 (m, 1 H), 7.18- 6.70 (m, 2H), 6.44-6.07 (m, 1 H), 4.83-4.57 (m, 1 H), 4.39-4.24 (m, 1 H), 4.19- 3.77 (m, 4H), 3.75-3.18 (m, 2H), 3.15-2.70 (m, 2H), 2.40-1 .60 (m, 6H).

Example 31 : (1 R, 6S)-[8-(3,6-Dimethyl-pyrazin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct- 3-yl]-(4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(3,6-dimethyl-pyrazin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate J) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 3-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C21 H22FN₇O, 407.45; m/z found 408.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.89-7.60 (m, 3H), 7.57-7.27 (m, 1 H), 7.20-6.99 (m, 1 H), 6.90-6.55 (m, 1 H), 4.85 (s, br, 0.35H), 4.50-3.12 (m, 7H), 2.97-2.57 (m, 1 .65H), 2.44-2.04 (m, 7H).

Example 32: (1 R, 6S)-(2-Fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-2- trifluoromethyl-pyrimidin-4-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[8-(6-methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 9) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 3-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C2i Hi₉F N₇O, 461 .42; m/z found 462.1 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 7.89-7.60 (m, 3H), 7.57-7.27 (m, 1 H), 7.20-6.99 (m, 1 H), 6.90-6.55 (m, 1 H), 4.85 (s, br, 0.35H), 4.50-3.12 (m, 7H), 2.97-2.57 (m, 1 .65H), 2.44-2.04 (m, 7H). Example 33: (1 R, 6S) (5-Fluoro-2-pyrimidin-2-yl-phenyl)-(8-quinoxalin-2-yl-3,8- diaza-bicyclo[4.2.0]oct-3-yl)-methanone.

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 5-fluoro-2-pyrimidin-2-yl-benzoic acid for 2-thiophen-2- yl-benzoic acid Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C2₅H₂i FN₆O, 440.48; m/z found 441 .2 [M+H]⁺.

Example 34: (1 R, 6S)-(4-Fluoro-2-[1 _>2_>3]triazol-2-yl-phenyl)-[8-(6-methyl-2- trifluoromethyl-pyrimidin-4-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(6-methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 9) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂i Hi₉F₄N₇O, 461 .42; m/z found 462.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.04-5.83 (m, 6H), 4.84-1 .46 (m, 13H). Example 35: (1 R, 6S)-[8-(6-Methyl-2-tnfluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(6-methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 9) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid

(Intermediate 14) for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C21 H20F3N₇O, 443.43; m/z found 444.2 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.16-5.81 (m, 7H), 4.84-1 .60 (m, 13H).

Example 36: (1 R, 6S)-[8-(2-Dimethylamino-6-trifluoromethyl-pyrimidin diaza-bicyclo[4.2.0]oct-3-yl]-(2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-trifluoromethyl- pyrimidin-2-yl]-dimethyl-amine (Intermediate 1 1 ) for (1 R, 6S) 8-(4,6-dimethyl- pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. Additionally, the reaction time was shortened to 30 minutes. MS (ESI) mass calcd. for C22H. 23F3N8O, 472.47; m/z found 473 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.19-6.80 (m, 7H), 4.49-3.78 (m, 5H), 3.75-3.30 (m, 2H), 3.22-3.10 (m, 2H), 3.06-2.74 (m, 5H), 2.24-1 .87 (m, 2H).

Example 37: (1 R, 6S)-[8-(2-Dimethylamino-6-trifluoromethyl-pyrimidin-4-yl)-3,8- diaza-bicyclo[4.2.0]oct-3-yl]-(2-fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-trifluoromethyl- pyrimidin-2-yl]-dimethyl-amine (Intermediate 1 1 ) for (1 R, 6S) 8-(4,6-dimethyl- pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 6-fluoro-2-[1 ,2,3]triazol-2-yl- benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C^H^NsO, 490.46; m/z found 491 .0 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 7.98-7.73 (m, 2H), 7.52-7.28 (m, 2H), 7.19-6.73 (m, 1 H), 5.88- 5.43 (m, 1 H), 4.50-4.24 (m, 1 H), 4.21 -3.85 (m, 5H), 3.82-3.40 (m, 2H), 3.24- 2.77 (m, 6H), 2.31 -1 .91 (m, 2H).

Example 38: (1 R, 6S)-[8-(2-Dimethylamino-6-trifluoromethyl-pyrimidin-4-yl)-3,8- diaza-bicyclo[4.2.0]oct-3-yl]-(4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-trifluoromethyl- pyrimidin-2-yl]-dimethyl-amine (Intermediate 1 1 ) for (1 R, 6S) 8-(4,6-dimethyl- pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl- benzoic acid (Internnediate 16) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C^H^NsO, 490.46; m/z found 491 .0 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 7.91 -7.66 (m, 2H), 7.48-7.26 (m, 1 H), 7.21 -6.71 (m, 2H), 5.87- 5.47 (m, 1 H), 4.50-3.78 (m, 5H), 3.73-3.27 (m, 2H), 3.23-2.47 (m, 7H), 2.29- 1 .90 (m, 2H).

Example 39: (1 R, 6S)-(8-Quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-(2- [1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting substituting (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)- quinoxaline (Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C23H21 N7O, 41 1 .47; m/z found 412.2 [M+H]⁺.

Example 40: (1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- icyclo[4.2.0]oct-3-yl]-(5-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-methyl-pyrimidin-2- yl]-dimethyl-amine (Internnediate 8) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)- 3,8-diaza-bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Internnediate 13) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H2₅FN8O, 436.49; m/z found 437.2 [M+H]⁺. ¹H NMR (400 MHz, CDCI3): 8.14-6.61 (m, 5H), 5.82-5.45 (m, 1 H), 4.75-3.27 (m, 6H), 3.22-2.55 (m, 8H), 2.37-1 .78m (m, 5H).

Example 41 : (1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza- (5-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2- thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C21 H22FN₇O, 407.45; m/z found 408.1 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.12-7.71 (m, 2H), 7.42-6.93 (m, 2H), 6.88-6.04 (m, 2H), 4.76-3.80 (m, 5H), 3.77-2.69 (m, 3H), 2.42-1 .91 m (m, 8H).

Example 42: (1 R, 6S)-(5-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-2- trifluoromethyl-pyrimidin-4-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(6-methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 9) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂i Hi₉F₄N₇O, 461 .422; m/z found 462.0 [M+H]⁺. ¹ H NMR (400 MHz, CDCI₃): 8.09-7.71 (m, 2H), 7.55-6.50 (m, 3H), 6.14 (d, J = 81 .2, 1 H), 4.76-3.62 (m, 6H), 3.50-2.85 (m, 2H), 2.78-1 .92 (m, 5H).

Example 43: (1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-methyl-pyrimidin-2- yl]-dimethyl-amine (Intermediate L) for (1 R, 6S)-2-(3,8-diaza-bicyclo[4.2.0]oct- 8-yl)-quinoxaline and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2- thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂₂H₂₆N₈O, 418.501 ; m/z found 419.1 [M+H]⁺. ¹ H NMR (400 MHz, CDCI3): 8.13-7.73 (m, 2H), 7.65-7.28 (m, 2H), 7.24-6.88 (m, 1 H), 5.51 -5.10 (m, 1 H), 4.66-2.65 (m, 14H), 2.32-1 .85 (m, 5H).

Example 44: (1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-methyl-pyrimidin-2- yl]-dimethyl-amine (Intermediate L) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)- 3,8-diaza-bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H2₅ FN8O, 436.492; m/z found 437.0 [M+H]⁺. ¹H NMR (400 MHz, CDCI3): 8.19-7.72 (m, 2M), 7.55-7.29 (m, 2H), 7.21 -6.81 (m, 1 H), 5.52-5.08 (m, 1 H), 4.70-4.26 (m, 1 H), 4.13-3.44 (m, 5H), 3.23-3.03 (m, 2H), 2.95-2.70 (m, 5H), 2.30-1 .68 (m, 6H).

Example 45: (1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-methyl-pyrimidin-2- yl]-dimethyl-amine (Intermediate L) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)- 3,8-diaza-bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H2₅ FN₈O, 436.492; m/z found 437.0 [M+H]⁺. ¹H NMR (400 MHz, CDCI₃): 7.91 -7.28 (m, 3H), 7.24-6.76 (m, 2H), 5.50-5.12 (m, 1 H), 4.66-4.04 (m, 2H), 4.02-3.74 (m, 3H), 3.71 -3.02 (m, 3H), 3.00-2.70 (m, 6H), 2.34-1 .85 (m, 5H).

Example 46: (1 R, 6S)-[8-(2-Dimethylamino-6-trifluoromethyl-pyrimidin-4-yl)-3,8- diaza-bicyclo[4.2.0]oct-3-yl]-(5-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[4-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)-6-trifluoromethyl- pyrimidin-2-yl]-dimethyl-amine (Intermediate 1 1 ) for (1 R, 6S) 8-(4,6-dimethyl- pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl- benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂2H₂2F₄N₈O, 490.46; m/z found 491 .0 [M+H]⁺. ¹ H NMR (400 MHz, CDCIs): 8.17-7.73 (m, 2H), 7.44-7.09 (m, 2H), 7.07-6.58 (m, 1 H), 5.87- 5.54 (m, 1 H), 4.51 -3.30 (m, 7H), 3.20-2.75 (m, 7H), 2.28-1 .87 (m, 2H).

Example 47: 3-(Biphenyl-2-ylcarbonyl)-6-(4-phenylpyrimidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 19 and 2-chloro-4-phenyl-pyrimidine. MS (ESI) mass calcd. for C₂₈H₂₄N₄O, 432.53; m/z found, 433.3 [M+H]⁺.

Example 48: 2-[3-(Biphenyl-2-ylcarbonyl)-3,6-diazabicyclo[3.2.0]hept-6- yl]quinoxaline.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 19 and 2-chloro-quinoxaline. MS (ESI) mass calcd. for C₂6H₂2N₄O, 406.49; m/z found, 407.2 [M+H]⁺.

Example 49: 2-{3-[(2-Thiophen-2-ylphenyl)carbonyl]-3,6- diazabicyclo[3.2.0]hept-6-yl}quinoxaline.

The compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate T and 2-chloro-quinoxaline. MS (ESI) mass calcd. for C2 H2oN₄OS, 412.52; m/z found, 413.3 [M+H]⁺.

Example 50: 6-(4-Phenylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- diazabicyclo [3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2. Step A, using Intermediate T and 2-chloro-4-phenyl-pyrimidine. MS (ESI) mass calcd. for C₂6H₂2N₄OS, 438.56; m/z found, 439.3 [M+H]⁺. Example 51 : 2-(3-{[5-(2-Fluorophenyl)-2-methyl-1 ,3-thiazol-4-yl]carbonyl}-3,6- diazabicyclo[3.2.0]hept-6-yl)quinoxaline.

The compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 21 and 2-chloro-quinoxaline as staring materials. (ESI) mass calcd. for C₂₄H2oFN₅OS, 445.52; m/z found, 446.3 [M+H]⁺.

Example 52: 3-{[5-(2-Fluorophenyl)-2-methyl-1 ,3-thiazol-4-yl]carbonyl}-6-(4- phenylpyrimidin-2-yl)-3,6-diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 21 and 2-chloro-4-phenyl-pyrimidine. MS (ESI) mass calcd. for C26H22FN₅OS, 471 .56; m/z found, 472.1 [M+H]⁺.

Example 53: 3-[(2-Methoxyphenyl)carbonyl]-6-(4-phenylpyrimidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 22 and 2-chloro-4-phenyl-pyrimidine. MS (ESI) mass calcd. for 0₂₃Η₂2Ν₄Ο, 386.46; m/z found, 387.0 [M+H]⁺.

Example 54: 2-{3-[(2-Methoxyphenyl)carbonyl]-3,6-diazabicyclo[3.2.0]hept-6- yl}quinoxaline.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 22 and 2-chloro-quinoxaline as staring materials. MS (ESI) mass calcd. for C2i H₂oN₄O₂, 360.42; m/z found, 361 .3 [M+H]⁺.

Example 55: 6-(4-Phenylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- diazabic clo [3.2.0]heptane.

The title compound was isolated using chiral SFC. The preparative conditions used were: Chiralpak AS-H 250 x 21 mm (L x I.D.) at 40 Celsius eluting with 8.6ml_/min MeOH with 0.2% isopropylamine 33 mL/min CO₂ BPR: 150 bar Sample Concentration: ~ 10.6 mg/mL in MeOH Injection Volume: ~500μΙ_ Detection: UV 214nm. This was the first eluting peak.

MS (ESI) mass calcd. for C₂6H₂2N₄OS, 438.55; m/z found, 439.2 [M+H]⁺.

Example 56: 6-(4-Phenylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- iazabicyclo [3.2.0]heptane.

The title compound was isolated using chiral SFC. The preparative conditions used were: Chiralpak AS-H 250 x 21 mm (L x I.D.) at 40 Celsius eluting with 8.6ml_/min MeOH with 0.2% isopropylamine 33 mL/min CO₂ BPR: 150 bar Sample Concentration: ~ 10.6 mg/mL in MeOH Injection Volume: ~500μί Detection: UV 214nm. This was the second eluting peak. MS (ESI) mass calcd. for C26H₂2N₄OS, 438.55; m/z found, 439.2 [M+H]⁺.

Example 57: 6-(4,6-Dimethylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]- -diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate T and 2-chloro-4,6-dimethylpyrimidine. MS (ESI) mass calcd. for C₂6H₂2N₄OS, 390.51 ; m/z found, 391 .2 [M+H]⁺. Example 58: 3-[(2-Bromophenyl)carbonyl]-6-(4,6-dimethylpyrimidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 23 and 2-chloro-4,6-dimethylpyrimidine. MS (ESI) mass calcd. for Ci₈Hi₉BrN₄O, 387.28; m/z found, 389.1 [M+H]⁺.

Example 59: (2-Bromo-phenyl)-[6-(4-methyl-pyrimidin-2-yl)-3,6-diaza- yl]-methanone.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 23 and 2-chloro-4-methylpyrimidine. MS (ESI) mass calcd. for Ci₇Hi₇BrN₄O, 373.26; m/z found, 373.1 [M+H]⁺.

Example 60: 6-(4-Methylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate T and 2-chloro-4-methylpyrimidine. MS (ESI) mass calcd. for C₂i H₂oN₄OS, 376.48; m/z found, 377.1 [M+H]⁺.

Example 61 : 3-(Biphenyl-2-ylcarbonyl)-6-(4-methylpyrimidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 19 and 2-chloro-4-methylpyrimidine. MS (ESI) mass calcd. for C₂3H₂2N₄O, 370.46; m/z found, 371 .2 [M+H]⁺.

Example 62: 6-(4-Methoxypyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]- -diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate T and 2-chloro-4-methoxypyrimidine. MS (ESI) mass calcd. for C2i H₂oN₄O₂S, 392.48; m/z found, 393.1 [M+H]⁺.

Example 63: 3-(Biphenyl-2-ylcarbonyl)-6-(4-methoxypyrimidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to for Intermediate 2, Step A, using Intermediate 19 and 2-chloro-4-methoxypyrimidine. MS (ESI) mass calcd. for C₂₃H₂₂N₄O₂, 386.46; m/z found, 387.2 [M+H]⁺.

Example 64: 6-(4,6-Dimethoxypyrimidin-2-yl)-3-[(2-ethoxynaphthalen-1 - yl)carbonyl]-3,6-diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 24 and 2-chloro-4,6-dimethoxypyrimidine. MS (ESI) mass calcd. for C₂₄H₂6N₄O₄, 434.5; m/z found, 435.2 [M+H]⁺.

Example 65: 6-(4,6-Dimethylpyrimidin-2-yl)-3-[(2-ethoxynaphthalen-1 - yl)carbonyl]-3,6-diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 24 and 2-chloro-4,6-dimethylpyrimidine. MS (ESI) mass calcd. for C₂ H26N₄O₂, 402.5; m/z found, 403.2 [M+H]⁺.

Example 66: 6-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,6-diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 25 and 2-chloro-4,6-dimethylpyrimidine. MS (ESI) mass calcd. for C20H21 N7O, 375.44; m/z found, 376.2 [M+H]⁺.

Example 67: 6-(4-Phenylpyrimidin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- l)phenyl]carbonyl}-3,6-diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A,using Intermediate 25 and 2-chloro-4-phenyl-pyrimidine. MS (ESI) mass calcd. for C₂ H₂i N₇O, 423.48; m/z found, 424.2 [M+H]⁺.

Example 68: 6-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,6-diazabicyclo[3.2.0]heptane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 26 and 2-chloro-4,6-dimethylpyrimidine. MS (ESI) mass calcd. for C21 H23N7O, 389.46; m/z found, 390.2 [M+H]⁺.

Example 69: 6-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,6-diazabicyclo[3.2.0]heptane.

The title c compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 25 and 2-chloro-4-phenyl-pyrimidine. MS (ESI) mass calcd. for C25H23N7O, 437.51 ; m/z found, 438.2 [M+H]⁺.

The following prophetic examples (70-86) may be synthesized using the general schemes provided above.

Example 70: [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- -fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C21 H22FN₇O, 407.44.

Example 71 : (2-Fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-pyndin-2-yl)- -diaza-bicyclo[4.2.0]oct-3-yl]-methanone.

MS (ESI) mass calcd. for C₂i H₂i FN₆O, 392.43.

Example 72: [8-(4,6-Dimethoxy-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- (2-fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C21 H22FN7O3, 439.44.

Example 73: [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- -methyl-5-phenyl-thiazol-4-yl)-methanone.

MS (ESI) mass calcd. for C23H2₅N₅OS, 419.54. Example 74: [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- 2-phenyl-2H-pyrazol-3-yl)-methanone.

MS (ESI) mass calcd. for 0₂2Η₂₄Ν₆Ο, 388.47.

Example 75: [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- -phenyl-isoxazol-4-yl)-methanone.

MS (ESI) mass calcd. for C22H23N5O2, 389.45.

Example 76: [6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]- -fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C20H20FN₇O, 393.42. Example 77: [6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]- iazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C₂oH₂oFN₇O, 393.42.

Example 78: [6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]- -fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C₂₀H₂₀FN₇O, 393.42.

Example 79: [6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]- 4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C₂₀H₂₀FN₇O, 393.42. Example 80: [6-(3,6-Dimethyl-pyrazin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(2- l-phenyl)-methanone.

MS (ESI) mass calcd. for C20H20FN₇O, 393.42.

Example 81 : [6-(3,6-Dimethyl-pyrazin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(3- phenyl)-methanone.

MS (ESI) mass calcd. for C20H20FN₇O, 393.42.

Example 82: [6-(4,6-Dimethoxy-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3- -(3-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone.

MS (ESI) mass calcd. for C20H20FN7O3, 3435 Example 83: (3-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[6-(4-methyl-pynmidin-2-yl)- -diaza-bicyclo[3.2.0]hept-3-yl]-methanone.

MS (ESI) mass calcd. for CigHisFN/O, 379.39.

Example 84: (3-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[6-(4-methoxy-pynmidin-2- -3,6-diaza-bicyclo[3.2.0]hept-3-yl]-methanone.

MS (ESI) mass calcd. for C19H18FN7O2, 395.39.

Example 85: [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- '-fluoro-biphenyl-2-yl)-methanone.

MS (ESI) mass calcd. for C^F sFNUO, 416.49. Example 86: [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- 4'-methyl-biphenyl-2-yl)-methanone.

MS (ESI) mass calcd. for C₂6H₂5N₄O, 412.53.

Example 87: (1 R,6S)-8-(6-Chloropyridazin-4-yl)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol- -yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 3,5-dichloropyridazine. MS (ESI) mass calcd. for Ci₉Hi₇CIFN₇O, 413.9; m/z found, 414.1 [M+H]⁺.

Example 88: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[6-methyl-2-(1 H-1 ,2,3- triazol-1 -yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 51 for 2-thiophen-2-yl-benzoic acid. MS (ESI) calcd. For C₂i H₂₄N₈O, 404.50; m/z found 405.1 [M+H]⁺

Example 89: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2- (trifluoromethyl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-(trifluoromethyl)nicotinic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C19H20F3N₅O, 391 .40; m/z found 392.0 [M+H]⁺.

Example 90: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[4-methoxy-2-(2H-1 ,2,3- triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid (Intermediate 49) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C22H25N7O2, 419.49; m/z found 420.2 [M+H]⁺.

Example 91 : (1 R,6S)-3-{[6-Methyl-2-(1 H-1 ,2,3-triazol-1 -yl)pyridin-3- yl]carbonyl}-8-[6-methyl-2-(trifluoromethyl)pyrimidin-4-yl]-3,8- diazabicyclo[4.2.0]octane. c

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[8-(6-methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 9) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 6-methyl-2-(1 H-1 ,2,3-triazol-1 -yl)nicotinic acid (Intermediate 51 ) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C21 H21 F3N8O, 458.45; m/z found 459.0 [M+H]⁺.

Example 92: (1 R,6S)-3-[(2-Fluoro-6-pyrimidin-2-ylphenyl)carbonyl]-8-[6-methyl- -(trifluoromethyl)pyrimidin-4-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-[8-(6-methyl-2-trifluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 9) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-fluoro-6-(pyrimidin-2-yl)benzoic acid (Intermediate 48) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C23H2oF₄N6O, 472.45; m/z found 473.0 [M+H]⁺.

Example 93: (1 R,6S)-3-{[6-Methyl-2-(1 H-1 ,2,3-triazol-1 -yl)pyridin-3- yl]carbonyl}-8-[4-(trifluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(4-(trifluoromethyl)pyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 6-methyl-2-(1 H-1 ,2,3-triazol-1 -yl)nicotinic acid

(Intermediate 51 ) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C20H19F3N8O, 444.42; m/z found 445.0 [M+H]⁺.

Example 94: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -(trifluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(4-(trifluoromethyl)pyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane (Intermediate 27) for (1 R, 6S) 8-(4,6-dimethyl- pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl- benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C₂oHi₇F₄N₇O, 447.40; m/z found 448.0 [M+H]⁺.

Example 95: (1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -(trifluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(4-(trifluoromethyl)pyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane (Intermediate 27) for (1 R, 6S) 8-(4,6-dimethyl- pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl- benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. For C₂oHi7F₄N₇O, 447.40; m/z found 448.0 [M+H]⁺.

Example 96: (1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(3,6-dimethyl-pyrazin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 10) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid

(Intermediate 14) for 2-thiophen-2-yl-benzoic acid and DCM in place of DMF.

DCM was used in place of DMF. MS (ESI) mass calcd. For 0₂ιΗ₂₃Ν₇Ο, 389.46; m/z found 390.1 [M+H]⁺. ¹ H NMR (CDCI₃): 8.03-7.91 (m, 1 H), 7.81 -7.64 (m, 2H), 7.54-7.20 (m, 3H), 6.99-6.87 (m, 1 H), 4.87-3.93 (m, 4H), 3.78-3.48 (m,

2H), 3.29-2.75 (m, 2H), 2.39-2.29 (m, 4H), 2.06-2.02 (m, 4H).

Example 97: (1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(3,6-Dimethyl-pyrazin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 10) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C21 H22FN₇O, 407.45; m/z found 408.2 [M+H]⁺. ¹ H NMR (CD3OD): 8.05-7.84 (m, 2H), 7.66-7.24 (m, 4H), 4.59-3.44 (m, 7H), 3.04-2.31 (m, 6H), 2.09-2.96 (m, 3H).

Example 98: (1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[2-fluoro-6-(2H-1 ,2,3- triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(3,6-Dimethyl-pyrazin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 10) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-Fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C21 H22FN₇O, 407.45; m/z found 408.2 [M+H]⁺. ¹ H NMR (CD3OD): 7.96-7.23 (m, 6H), 4.50-4.44 (m, 1 H), 4.31 -4.19 (m, 2H), 4.1 1 -3.77 (m, 3H), 3.62-3.42 (m, 1 H), 2.86-2.77 (m, 1 H), 2.40-2.36 (m, 3H), 2.31 -2.05 (m, 2H), 2.04-1 .92 (m, 3H).

Example 99: (1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[3-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R, 6S)-8-(3,6-Dimethyl-pyrazin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane (Intermediate 10) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2- yl)-3,8-diaza-bicyclo[4.2.0]octane and 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid (Intermediate 27) for 2-thiophen-2-yl-benzoic acid DCM was used in place of DMF. MS (ESI) mass calcd. For C₂iH₂₂FN₇O, 407.45; m/z found 408.2

[M+H]⁺. ¹H NMR (CDCI₃): 7.87-7.30 (m, 4H), 7.24-6.71 (m, 2H), 4.80-4.02 (m, 4H), 3.84-2.72 (m, 4H), 2.39-2.35 (m, 4H), 2.1 1 -1 .99 (m, 4H).

Example 100: (1 R,6S)-8-(5-Methylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(5-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 29) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH₂i N₇O, 375.44; m/z found 376.0 [M+H]⁺. ¹H NMR (CDCI3): 8.06- 7.78 (m, 3H), 7.72-7.44 (m, 3H), 7.39-7.28 (m, 1 H), 7.16-6.96 (m, 1 H), 4.56- 3.98 (m, 4H), 3.80-2.96 (m, 4H), 2.46-2.03 (m, 5H).

Example 101 : (1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(5-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 29) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Internnediate 15) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.1 [M+H]⁺. ¹H NMR (CDCI3): 7.99-7.69 (m, 3H), 7.58-7.39 (m, 2H), 7.31 (s, 1 H), 7.19-6.84 (m, 1 H), 4.67-4.34 (m, 1 H), 4.15-3.80 (m, 4H), 3.69-3.18 (m, 2H), 2.96 (br s, 1 H), 2.45- 2.05 (m, 5H).

Example 102: (1 R,6S)-3-{[4-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(5-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 29) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.2 [M+H]⁺. ¹H NMR

(CDCI3): 7.99-7.69 (m, 3H), 7.58-7.39 (m, 2H), 7.31 (s, 1 H), 7.19-6.84 (m, 1 H), 4.67-4.34 (m, 1 H), 4.15-3.80 (m, 4H), 3.69-3.18 (m, 2H), 2.96 (br s, 1 H), 2.45- 2.05 (m, 5H).

Example 103: (1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- (5-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(5-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 29) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid

(Intermediate 27) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH₂oFN₇O, 393.43; m/z found 394.1 [M+H]⁺ ¹ H NMR (CDCIs): 7.97-7.77 (m, 2H), 7.73-7.36 (m, 2H), 7.33-6.83 (m, 3H), 4.54-4.32 (m, 1 H), 4.13-3.91 (m, 3H), 3.73-3.06 (m, 3H), 2.95-2.74 (m, 1 H), 2.44-2.40 (m, 3H), 1 .98 (br s, 2H).

Example 104: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(5-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 29) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH₂oFN₇O, 393.43; m/z found 394.1 [M+H]⁺. ¹H NMR (CD₃OD): 8.06-7.72 (m, 4H), 7.61 -7.47 (m, 1 H), 7.41 -6.53 (m, 2H), 4.70-3.75 (m, 5H), 3.58-2.88 (m, 3H), 2.43-1 .93 (m, 5H). Example 105: (1 R,6S)-8-(3-Methylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(3-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 31 ) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH2iN₇O, 375.44; m/z found 376.1 [M+H]⁺. ¹H NMR (CD₃OD): 8.08-8.01 (m, 1 H), 7.98-7.88 (m, 2H), 7.84-7.78 (m, 1 H), 7.70-7.38 (m, 4H), 4.55-3.84 (m, 4H), 3.75-3.1 1 (m, 3H), 2.70-2.29 (m, 4H), 2.22-1 .48 (m, 2H).

Example 106: (1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(3-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 31 ) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH₂oFN₇O, 393.43; m/z found 394.1 [M+H]^{+ 1}H NMR

(CD₃OD): 7.99-7.79 (m, 4H), 7.72-7.59 (m, 2H), 7.38-7.21 (m, 1 H), 4.63-4.01 (m, 4H), 3.82-3.24 (m, 3H), 2.74-2.25 (m, 4H), 2.16-1 .29 (m, 2H). Example 107: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(3-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 31 ) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.1 [M+H]⁺. ¹H NMR

(CD3OD): 8.10-8.01 (m, 1 H), 7.97-7.88 (m, 2H), 7.83-7.74 (m, 1 H), 7.67-7.61 (m, 1 H), 7.47-7.22 (m, 2H), 4.52-4.30 (m, 2H), 4.22-3.83 (m, 2H), 3.75-3.1 1 (m, 3H), 2.72-2.31 (m, 4H), 2.18-1 .50 (m, 2H).

Example 108: (1 R,6S)-3-{[4-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(3-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 31 ) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.1 [M+H]⁺. ¹H NMR (CD3OD): 8.02-7.98 (m, 1 H), 7.92-7.63 (m, 4H), 7.61 -7.41 (m, 1 H), 7.35-7.22 (m, 1 H), 4.53-3.85 (m, 5H), 3.74-3.1 1 (m, 2H), 2.70-2.28 (m, 4H), 2.21 -1 .47 (m, 2H).

Example 109: (1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(3-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 31 ) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid

(Intermediate 27) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.1 [M+H]⁺. ¹ H NMR (CD3OD): 8.02-7.65 (m, 5H), 7.57-7.46 (m, 1 H), 7.35-7.33 (m, 1 H), 4.50-3.95 (m, 4H), 3.74-3.18 (m, 3H), 2.70-2.41 (m, 4H), 1 .99-1 .52 (m, 2H).

Example 1 10: (1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(6-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 30) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid (Intermediate 27) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.2 [M+H]⁺. ¹ H NMR (CDCI3): 7.87-6.76 (m, 7H), 4.61 -3.36 (m, 7H), 3.03-1 .76 (m, 6H).

Example 1 1 1 : (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(6-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 30) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.1 [M+H]⁺. ¹H NMR

(CD3OD): 8.1 1 -7.84 (m, 2H), 7.81 -7.58 (m, 1 H), 7.52-6.40 (m, 4H), 4.70-4.26 (m, 1 H), 4.23-3.67 (m, 4H), 3.67-3.40 (m, 1 H), 3.12-1 .53 (m, 7H).

Example 1 12: (1 R,6S)-8-(6-Methylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(6-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 30) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH2iN₇O, 375.44; m/z found 376.1 [M+H]⁺ _. ¹ H NMR (CD₃OD): 8.08-7.75 (m, 3H), 7.68-7.37 (m, 4H), 7.33-6.82 (m, 1 H), 4.70-3.78 (m, 5H), 3.64-2.97 (m, 3H), 2.43-2.01 (m, 5H).

Example 1 13: (1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(6-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 30) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂oH₂i N₇O, 375.44; m/z found 376.1 [M+H]⁺ _. ¹ H NMR

(CD₃OD): 8.08-7.75 (m, 3H), 7.68-7.37 (m, 4H), 7.33-6.82 (m, 1 H), 4.70-3.78 (m, 5H), 3.64-2.97 (m, 3H), 2.43-2.01 (m, 5H). MS (ESI) mass calcd. For C₂oH₂oFN₇O, 393.43; m/z found 394.1 [M+H]⁺ _. ¹ H NMR (CD₃OD): 7.99-7.75 (m, 3H), 7.68-6.92 (m, 4H), 4.71 -3.35 (m, 7H), 3.16-2.98 (m, 1 H), 2.54-1 .85 (m, 5H).

Example 1 14: (1 R,6S)-3-{[4-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- -methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting (1 R,6S)-8-(6-methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane (Intermediate 30) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C20H20FN₇O, 393.43; m/z found 394.2[M+H]⁺. ¹H NMR

(CD3OD): 7.99 (s, 1 H), 7.84-7.64 (m, 2H), 7.48-7.43 (m, 1 H), 7.39-7.35 (m, 1 H), 7.28-7.23 (m, 1 H), 6.94-6.84 (m, 1 H), 4.73-4.29 (m, 1 H), 4.15-3.77 (m, 4H), 3.62-2.96 (m, 3H), 2.42-1 .70 (m, 5H).

Example 1 15: 2-[(1 R,6S)-3-{[4-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]quinoxaline.

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C23H20FN₇O, 429.46; m/z found 430.1 [M+H]⁺. ¹H NMR

(CD3OD): 8.55-8.19 (m, 1 H), 7.98-7.92 (m, 2H), 7.76-7.60 (m, 2H), 7.55-7.42 (m, 3H), 7.33-6.20 (m, 2H), 4.73-4.27 (m, 3H), 4.13-3.50 (m, 3H), 3.35-3.14 (m, 2H), 2.37-1 .81 (m, 2H).

Example 1 16: 2-[(1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 3,8-diazabicyclo[4.2.0]oct-8-yl]quinoxaline.

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid

(Intermediate 50) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂₃H2oFN₇O, 429.46; m/z found 430.1 [M+H]⁺ ¹ H NMR (CD3OD): 8.27-8.14 (m, 1 H), 8.08-7.58 (m, 5H), 7.48-6.45 (m, 4H), 4.83-4.54 (m, 1 H), 4.25-3.97 (m, 3H), 3.74-3.63 (m, 1 H), 3.43-3.37 (m, 1 H), 3.19-3.06 (m, 2H), 2.27-1 .82 (m, 2H).

Example 1 17: 2-[(1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]quinoxaline.

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂3H₂oFN₇O, 429.46; m/z found 430.2 [M+H]⁺. ¹H NMR

(CD3OD): 8.42-7.97 (m, 2H), 7.88-7.44 (m, 5H), 7.39-6.20 (m, 3H), 5.08-4.67 (m, 1 H), 4.41 -3.44 (m, 6H), 3.25-3.07 (m, 1 H), 2.39-1 .86 (m, 2H). Example 1 18: 2-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]quinoxaline.

(Intermediate 3) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C23H20FN₇O, 429.46; m/z found 430.1 [M+H]⁺. ¹H NMR

(CD3OD): 8.60-8.30 (m, 1 H), 8.04-7.33 (m, 8H), 7.24-6.55 (m, 1 H), 5.15-4.72 (m, 1 H), 4.54-4.43 (m, 2H), 4.32-3.53 (m, 4H), 3.26-3.16 (m, 1 H), 2.36-1 .91 (m, 2H).

Example 1 19: 5-Chloro-2-[(1 R,6S)-3-{[2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-((1 R,6S)-3,8-diazabicyclo[4.2.0]octan-8-yl)-5- chlorobenzo[d]oxazole (Intermediate 32) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin- 2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C22H19CIN6O2, 434.89; m/z found 435.1

[M+H]⁺ _. ¹H NMR (CD3OD): 8.03-7.28 (m, 6H), 7.23-6.88 (m, 3H), 4.72-4.54 (m, 1 H), 4.35-3.96 (m, 3H), 3.90-3.35 (m, 3H), 3.13-1 .71 (m, 3H). Example 120: 5-Chloro-2-[(1 R,6S)-3-{[2-fluoro-6-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-((1 R,6S)-3,8-diazabicyclo[4.2.0]octan-8-yl)-5- chlorobenzo[d]oxazole (Intermediate 32) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin- 2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 15) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂2Hi8CIFN₆O2, 452.88; m/z found 453.0 [M+H]⁺ _. ¹H NMR (CD3OD): 8.04-7.74 (m, 2H), 7.67-7.24 (m, 4H), 7.15-6.64 (m, 2H), 5.04-4.23 (m, 3H), 4.20-3.35 (m, 4H), 3.20 (br s, 1 H), 2.37-1 .88 (m, 2H).

Example 121 : 5-Chloro-2-[(1 R,6S)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-((1 R,6S)-3,8-diazabicyclo[4.2.0]octan-8-yl)-5- chlorobenzo[d]oxazole (Intermediate 32) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin- 2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 5-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 13) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C22H18CIFN6O2, 452.88; m/z found 453.1 [M+H]⁺ _. ¹H NMR (CD3OD): 8.02-7.63 (m, 2H), 7.48-7.24 (m, 3H), 7.21 -6.69 (m, 3H), 4.86-3.35 (m, 7H), 3.15-2.95 (m, 1 H), 2.27-1 .72 (m, 2H). Example 122: 5-Chloro-2-[(1 R,6S)-3-{[4-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-((1 R,6S)-3,8-diazabicyclo[4.2.0]octan-8-yl)-5- chlorobenzo[d]oxazole (Intermediate 32) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin- 2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 4-fluoro-2-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 16) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C₂2Hi8CIFN₆O2, 452.88; m/z found 453.1 [M+H]⁺ _. ¹H NMR (CD3OD): 7.99-7.64 (m, 2H), 7.53-7.46 (m, 1 H), 7.40-7.15 (m, 3H), 7.1 1 -6.60 (m, 2H), 4.74-4.53 (m, 1 H), 4.33-3.97 (m, 3H), 3.90-3.35 (m, 3H), 3.12-3.02 (m, 1 H), 2.33-1 .73 (m, 2H).

Example 123: 5-Chloro-2-[(1 R,6S)-3-{[3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-((1 R,6S)-3,8-diazabicyclo[4.2.0]octan-8-yl)-5- chlorobenzo[d]oxazole (Intermediate 32) for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin- 2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)benzoic acid (Intermediate 50) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C22H18CIFN6O2, 452.88; m/z found 453.1 [M+H]⁺ _. ¹H NMR (CD₃OD): 8.01 -7.35 (m, 5H), 7.25-6.81 (m, 3H), 4.75-4.24 (m, 2H), 4.12-3.03 (m, 6H), 2.25-1 .81 (m, 2H).

Example 124: (1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- (6-meth lpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 40 for (1 R, RS) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 2-fluoro-6-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C2i H₂iFN₆O, 392.4; m/z found, 393.2 [M+H]⁺.

Example 125: (1 R,6S)-8-(6-Methylpyridin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2- yl)phen l]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 124 substituting 2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-fluoro-6-(2H-1 ,2,3-triazol- 2-yl)benzoic acid. MS (ESI) mass calcd. for C₂i H₂2N₆O, 374.5; m/z found, 375.2 [M+H]⁺. ¹ H NMR (500 MHz, CD₃OD): 8.00 - 7.93 (m, 2H), 7.66 - 7.47 (m, 4H), 7.27 - 7.08 (m, 1 H), 6.83 - 6.76 (m, 1 H), 6.56 - 6.49 (m, 1 H), 4.71 - 4.62 (m, 1 H), 4.41 - 4.27 (m, 2H), 4.17 - 4.04 (m, 1 H), 3.99 - 3.84 (m, 1 H), 3.27 - 3.16 (m, 2H), 2.62 - 2.54 (m, 1 H), 2.42 - 2.27 (m, 3H), 2.18 - 1 .99 (m, 2H).

Example 126: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- (6-meth lpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 124 substituting 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-fluoro-6-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C₂i H₂i FN₆O, 392.4; m/z found, 393.2 [M+H]⁺.

Example 127: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- (4-methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 41 for (1 R, RS) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂iH₂iFN₆O, 392.4; m/z found, 393.2 [M+H]⁺. Example 128: (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[5-fluoro-2-(2H-1 ,2,3- triazol-2- l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 43 for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂2H₂3FN₆O, 406.5; m/z found, 408.2 [M+H]⁺.

Example 129: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- 6-(trifluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 45 for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂iHi₈F₄N₆O, 446.4; m/z found, 447.2 [M+H]⁺. ¹H NMR (500 MHz, CDCI₃): 7.91 (dd, J = 9.0, 4.7 Hz, 1 H), 7.79 (s, 2H), 7.63 - 7.54 (m, 1 H), 7.15 - 6.91 (m, 2H), 6.58 - 6.49 (m, 1 H), 6.33 (d, J = 8.4 Hz, 1 H), 4.43 - 4.35 (m, 1 H), 4.18 - 4.07 (m, 1 H), 4.05 - 3.86 (m, 4H), 3.00 - 2.88 (m, 2H), 2.13 - 1 .95 (m, 2H). Example 130: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-4-(tnfluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 44 for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂iHi₈F₄N₆O, 446.4; m/z found, 447.2 [M+H]⁺.

Example 131 : (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- (5-meth lpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 42 for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂iH₂iFN₆O, 392.4; m/z found, 393.2 [M+H]⁺.

Example 132: 4-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]oct-3-yl]carbonyl}-1 ,8-naphthyridine.

The title compound was prepared in a manner analogous to Example 1 substituting 1 ,8-naphthyridine-4-carboxylic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C2i H₂2N₆O, 374.5; m/z found, 375.2 [M+H]⁺.

Example 133: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-2-(1 H- pyrazol-1 - l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 3-methyl-2-(1 H-pyrazol-1 -yl)benzoic acid for 2-thiophene-2-yl- benzoic acid. MS (ESI) mass calcd. for C₂3H26N₆O, 402.5; m/z found, 403.2 [M+H]⁺.

Example 134: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methoxy-2-(2H- -triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophene-2- yl-benzoic acid. MS (ESI) mass calcd. for C22H25N7O2, 419.5; m/z found, 420.2 [M+H]⁺.

Example 135: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-2-(2H-1 ,2,3- triazol-2- l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 37 for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H2₅N₇O, 403.5; m/z found, 404.2 [M+H]⁺. ¹H NMR (500 MHz, CDCI3): 7.80 (s, 1 H), 7.44 - 7.34 (m, 1 H), 7.30 (d, 1 H), 7.22 - 7.07 (m, 1 H), 6.29 (s, 1 H), 4.43 - 4.31 (m, 1 H), 4.13 - 3.85 (m, 4H), 2.86 - 2.76 (m, 1 H), 2.36 - 2.25 (m, 3H), 2.24 - 2.13 (m, 6H), 2.02 - 1 .82 (m, 2H), 1 .70 (s, 3H).

Example 136: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-methoxy-2- methylpyrimidin-4-yl)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methoxy-2-methylpyrimidine-4-carboxylic acid for 2-thiophene-2- yl-benzoic acid. MS (ESI) mass calcd. for Ci9H₂ N₆O2, 368.4; m/z found, 369.2 [M+H]⁺. Example 137: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(3-phenylpyrazin-2- yl)carbon l]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 3-phenylpyrazine-2-carboxylic acid for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C^ ^NeO, 400.5; m/z found, 401 .2 [M+H]⁺. ¹ H NMR (500 MHz, CD₃OD): 8.78 - 8.70 (m, 1 H), 8.63 - 8.46 (m, 1 H), 7.71 - 7.58 (m, 2H), 7.39 - 7.09 (m, 3H), 6.61 - 6.26 (m, 1 H), 4.52 - 4.35 (m, 1 H), 4.10 (t, J = 8.4 Hz, 1 H), 4.05 - 3.93 (m, 2H), 3.72 - 3.51 (m, 1 H), 3.47 - 3.32 (m, 1 H), 2.93 - 2.67 (m, 1 H), 2.38 - 2.30 (m, 2H), 2.21 - 1 .59 (m, 7H).

Example 138: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-2-(1 H-1 ,2,3- triazol-1 - l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 38 for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H2₅N₇O, 403.5; m/z found, 404.2 [M+H]⁺. ¹H NMR (500 MHz, CD3OD): 8.1 1 - 8.05 (m, 1 H), 7.95 - 7.86 (m, 1 H), 7.59 - 7.52 (m, 1 H), 7.48 (d, J = 7.1 Hz, 1 H), 7.30 - 7.18 (m, 1 H), 6.49 (s, 1 H), 4.45 - 4.37 (m, 1 H), 4.07 (t, J = 8.3 Hz, 1 H), 3.99 - 3.90 (m, 2H), 3.23 - 3.1 1 (m, 2H), 2.91 - 2.83 (m, 1 H), 2.81 - 2.76 (m, 1 H), 2.21 (s, 6H), 2.13 - 2.09 (m, 3H), 2.01 - 1 .85 (m, 2H).

Example 139: (1 R,6S)-3-{[5-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -(4-methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 124 substituting 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 5-fluoro-6-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C22H₂₄N₆O2, 404.5; m/z found, 404.2 [M+H]⁺.

Example 140: (1 R,6S)-3-{[5-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 8- 4-(trifluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 2-thiophen-2-yl benzoic acid and Intermediate 44 for (1 R, 6S) 8-(4,6-dimethyl-pyrimidin-2-yl)- 3,8-diaza-bicyclo[4.2.0]octane. MS (ESI) mass calcd. for C22H21 F3N6O2, 458.5 m/z found, 459.2 [M+H]⁺. Example 141 : N,N-Dimethyl-2-[(1 R,6S)-3-{[3-methyl-2-(2H-1 ,2,3-triazol-2- l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]pyridin-4-amine.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 46 for (1 R, RS) 8-(4,6-dimethyl-pyrimidin-2-yl)-3,8- diaza-bicyclo[4.2.0]octane and Intermediate 37 for 2-thiophene-2-yl-benzoic acid. MS (ESI) mass calcd. for C23H2₇N₇O, 417.5; m/z found, 418.2 [M+H]⁺.

Example 142: 2-[(1 R,6S)-3-{[4-Methoxy-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]-N,N-dimethylpyridin-4- amine.

The title compound was prepared in a manner analogous to Example 141 substituting 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for Intermediate 37. MS (ESI) mass calcd. for C23H2₇N₇O2, 433.5; m/z found, 434.2 [M+H]⁺. ¹H NMR (500 MHz, CD3OD): 7.96 (s, 1 H), 7.59 - 7.50 (m, 2H), 7.41 (dd, J = 31 .5, 8.0 Hz, 1 H), 7.25 - 7.04 (m, 1 H), 6.83 - 6.68 (m, 1 H), 6.49 - 6.17 (m, 1 H), 5.15 - 4.99 (m, 1 H), 4.62 - 4.42 (m, 1 H), 4.20 - 4.01 (m, 3H), 3.97 - 3.80 (m, 4H), 3.69 - 3.38 (m, 2H), 3.22 - 3.1 1 (m, 3H), 2.94 (d, J = 13.9 Hz, 4H), 2.34 - 1 .94 (m, 2H). Example 143: 2-{(1 R,6S)-3-[(3-Fluoro-2-pyrimidin-2-ylphenyl)carbonyl]-3,8- dia ,N-dimethylpyridin-4-amine.

The title compound was prepared in a manner analogous to Example 141 substituting 3-fluoro-2-(pyrimidin-2-yl)benzoic acid for Intermediate 37. MS (ESI) mass calcd. for C^F sFNeO, 432.5; m/z found, 433.2 [M+H]⁺.

Example 144: 2-[(1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 3,8-diazabicyclo[4.2.0]oct-8-yl]-N,N-dimethylpyridin-4-amine.

The title compound was prepared in a manner analogous to Example 141 substituting 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for Intermediate 37. MS (ESI) mass calcd. for C₂2H₂ FN₇O, 421 .5; m/z found, 422.2 [M+H]⁺.

Example 145: (1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- [4-(trifluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 5-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C₂i H₁₈F₄N₆O, 446.4; m/z found, 447.2 [M+H]⁺.

Example 146: (1 R,6S)-3-{[4-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 8- 4-(trifluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 5-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C22H21 F3N6O2, 458.5; m/z found, 459.2 [M+H]⁺.

Example 147: (1 R,6S)-3-{[3-Methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- 4-(trifluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting Intermediate 37 for 5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C22H21 F3N6O, 442.5; m/z found, 443.2 [M+H]⁺.

Example 148: (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[3-fluoro-2-(2H-1 ,2,3- triazol-2- l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 5-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C₂2H₂3FN₆O, 406.5; m/z found, 407.2 [M+H]⁺. ¹H NMR (500 MHz, CD₃OD): 8.05 - 7.94 (m, 1 H), 7.71 - 7.44 (m, 3H), 7.42 - 7.26 (m, 1 H), 6.72 - 6.64 (m, 1 H), 6.47 - 6.32 (m, 1 H), 4.82 - 4.62 (m, 1 H), 4.34 - 4.22 (m, 2H), 4.15 - 3.93 (m, 1 H), 3.79 - 3.56 (m, 2H), 3.22 - 3.08 (m, 1 H), 2.55 - 2.28 (m, 6H), 2.21 - 1 .82 (m, 3H).

Example 149: (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[4-methoxy-2-(2H-1 ,2,3- triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 5-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C23H26N6O2, 418.5; m/z found, 419.2 [M+H]⁺. ¹H NMR (500 MHz, CD₃OD): 7.98 (s, 1 H), 7.62 - 7.46 (m, 2H), 7.42 - 6.33 (m, 4H), 4.73 - 4.54 (m, 1 H), 4.36 - 4.20 (m, 2H), 4.17 - 4.07 (m, 1 H), 4.02 - 3.78 (m, 4H), 3.70 - 3.41 (m, 2H), 3.27 - 3.17 (m, 1 H), 2.57 - 2.20 (m, 6H), 2.14 - 2.04 (m, 2H).

Example 150: 2-[(1 R,6S)-3-{[5-Methoxy-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]-N,N-dimethylpyridin-4- amine.

The title compound was prepared in a manner analogous to Example 141 substituting 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for Intermediate 37. MS (ESI) mass calcd. for C23H27N7O2, 433.5; m/z found, 434.2 [M+H]⁺.

Example 151 : (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[5-methoxy-2-(2H-1 ,2,3- triazol-2-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)benzoic acid for 5-fluoro-2-(2H- 1 ,2,3-triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C23H26N6O2, 418.5; m/z found, 419.2 [M+H]⁺. ¹H NMR (500 MHz, CD₃OD): 7.95 - 7.91 (m, 2H), 7.51 (s, 1 H), 7.20 - 7.00 (m, 2H), 6.70 - 6.63 (m, Hz, 1 H), 6.37 - 6.35 (m, 1 H), 4.67 - 4.57 (m, 1 H), 4.34 - 4.21 (m, 2H), 4.16 - 4.07 (m, 1 H), 3.96 - 3.85 (m, 3H), 3.73 - 3.67 (m, 1 H), 3.58 (dd, J = 14.5, 6.1 Hz, 1 H), 3.23 (s, 1 H), 2.52 - 2.37 (m, 3H), 2.28 (s, 3H), 2.17 - 1 .98 (m, 3H).

Example 152: (1 R,6S)-3-[(3-Fluoro-2-pyrimidin-2-ylphenyl)carbonyl]-8-[4- trifluoromethyl)pyridin-2-yl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 3-fluoro-2-(pyrimidin-2-yl)benzoic acid for 5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C₂3Hi₉F₄N₅O, 457.4; m/z found, 458.2 [M+H]⁺.

Example 153: (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-[(3-fluoro-2-pyrimidin-2- ylphen l)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 130 substituting 3-fluoro-2-(pyrimidin-2-yl)benzoic acid for 5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)benzoic acid. MS (ESI) mass calcd. for C2₄H₂₄FN₅O, 417.5; m/z found, 418.2 [M+H]⁺. Example 154: (1 R,6S)-3-[(6-Bromo-2-fluoro-3-methoxyphenyl)carbonyl]-8-(4,6- dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 6-bromo-2-fluoro-3-methoxybenzoic acid for 2-thiophene-2-yl- benzoic acid. MS (ESI) mass calcd. for C₂oH22BrFN₄O₂, 449.3; m/z found, 450.2 [M+H]⁺.

Example 155: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-fluoro-2-(1 H- pyrazol-1 - l)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting Intermediate 33 for 2-thiophene-2-yl-benzoic acid. MS (ESI) calcd. for C22H23FN6O, 406.5; m/z found, 407.2 [M+H]⁺.

Example 156: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(2-fluoro-3-methoxy-6- pyrimidin-2-ylphenyl)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

To a microwave safe vial was added Example 187 (100 mg, 0.22 mmol), 2- tributylstannylpyrimidine (82.3 mg, 0.22 mmol), tetrakis (25.7 mg, 0.022 mmol), copper iodide (4.23 mg, 0.022 mmol) and dioxane (4 mL). The resulting mixture was heated to 150 °C in a microwave reactor. After 2h the crude mixture was concentrated, dissolved in methanol (2 mL), filtered and purified by basic reverse-phase HPLC to yield the title compound (26.3 mg, 26%). MS (ESI) mass calcd. for C₂ H2₅FN₆O2, 448.5; m/z found, 449.2 [M+H]⁺.

Example 157: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5,6-dimethyl- 1 ,2,3-triazol-2- l)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5,6-dimethyl-2-(2H-1 ,2,3-triazol-1 -yl)nicotinic acid for 2-thiophen-2- yl-benzoic acid in the last step. MS (ESI) mass calcd. for C22H26N8O, 418.5; m/z found, 419.2 [M+H]⁺.

Example 158: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5,6-dimethyl-2-(1 H- 1 ,2,3-triazol-1 -yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5,6-dimethyl-2-(1 H-1 ,2,3-triazol-2-yl)nicotinic acid for 2-thiophen-2- yl-benzoic acid in the last MS (ESI) mass calcd. for C22H26N8O, 418.5; m/z found, 419.2 [M+H]⁺.

Example 159: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(1 H-1 ,2,3-triazol-1 - yl)-6- trifluoromethyl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 2-(1 H-1 ,2,3-triazol-1 -yl)-6-(trifluoromethyl)nicotinic acid for 2- thiophen-2-yl-benzoic acid in the last step. MS (ESI) mass calcd. for

C21 H21 F3N8O, 458.5; m/z found, 459.2 [M+H]⁺.

Example 160: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(2H-1 ,2,3- triazol-2-yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methyl-2-(2H-1 ,2,3-triazol-2-yl)nicotinic acid for 2-thiophen-2-yl- benzoic acid in the last step. MS (ESI) mass calcd. for C₂i H₂₄N₈O, 404.5; m/z found, 405.2 [M+H]⁺.

Example 161 : (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(1 H-1 ,2,3- triazol-1 -yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methyl-2-(1 H-1 ,2,3-triazol-1 -yl)nicotinic acid for 2-thiophen-2-yl- benzoic acid in the last step. MS (ESI) mass calcd. for C₂i H₂₄N₈O, 404.5; m/z found, 405.2 [M+H]⁺.

Example 162: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[6-methoxy-2-(2H- -triazol-2-yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 6-methoxy-2-(2H-1 ,2,3-triazol-2-yl)nicotinic acid for 2-thiophen-2-yl- benzoic acid in the last step. MS (ESI) mass calcd. for C₂i H₂₄N₈O₂, 420.5; m/z found, 421 .2 [M+H]⁺. Example 163: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[6-methoxy-2-(1 H- -triazol-1 -yl)pyndin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 6-methoxy-2-(1 H-1 ,2,3-triazol-2-yl)nicotinic acid for 2-thiophen-2-yl- benzoic acid in the last step. MS (ESI) mass calcd. for C₂iH₂₄N₈O₂, 420.5; m/z found, 421 .2 [M+H]⁺.

Example 164: (1 R,6S)-3-[(2-Bromo-5-fluorophenyl)carbonyl]-8-(4,6- dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 2-bromo-5-fluorobenzoic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for Ci₉H₂oBrFN₄O, 419.3; m/z found, 419.1 [M+H]⁺.

Example 165: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-fluoro-2-pyrimidin-5- ylphenyl)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

Example 198 was prepared by the following procedure: (1 R,6S)-3-[(2-bromo-5- fluorophenyl)carbonyl]-8-(4,6-dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0] octane (100 mg, 0.24 mmol), pyrimidine-5-boronic acid (44 mg, 0.36 mmol), Pd(ddpf)CI₂ (19 mg, 0.02 mmol) and K₂CO₃ (98 mg, 0.72 mmol) were

suspended a 1 .2 ml of a mixture of 1 ,4-dioxane and water (5:1 ) in a sealed tube and heated to 150 °C for 2h. The reaction was cooled to 23 °C, and purified directly on 16 g S1O2 with 0-50% ethyl acetate / hexanes to give 24 mg (24% yield). MS (ESI) mass calcd. for C23H23FN6O, 418.5; m/z found, 419.2 [M+H]⁺.

Example 166: 5-(2-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]oct-3-yl]carbonyl}-4-fluorophenyl)-N,N-dimethylpyridin-2- amine.

The title compound was prepared in a manner analogous to Example 165 using (1 R,6S)-3-[(2-bromo-5-fluorophenyl)carbonyl]-8-(4,6-dimethylpyrimidin-2- yl)-3,8-diazabicyclo[4.2.0] and 2-(dimethylamino)pyridine-5-boronic acid hydrate. MS (ESI) mass calcd. for C₂6H₂9FN₆O, 460.6; m/z found, 461 .3

[M+H]⁺. Example 167: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-(9H-fluoren-4- ylcarbonyl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 9H-fluorene-4-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂6H₂6N₄O, 410.5; m/z found, 41 1 .2 [M+H]⁺.

Example 168: 4-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]oct-3-yl]carbonyl}-9H-fluoren-9-one.

The title compound was prepared in a manner analogous to Example 1 substituting 9H-fluorenone-4-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂6H₂ N₄O₂, 424.5; m/z found, 425.2 [M+H]⁺.

Example 169: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(3-methyl-1 ,2,4- oxadiazol-5-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 165 using (1 R,6S)-3-[(2-Bromo-5-fluorophenyl)carbonyl]-8-(4,6-dimethylpyrimidin-2-yl)- 3,8-diazabicyclo[4.2.0] andl -(tetrahydropyran-2-yl)-1 h-pyrazole-5-boronic acid pinacol ester. MS (ESI) mass calcd. for C27H31 FN6O2, 490.6; m/z found, 491 .3 [M+H]⁺.

Example 170: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-({5-fluoro-2-[1 - (tetrahydro-2H-pyran-2-yl)-1 H-pyrazol-5-yl]phenyl}carbonyl)-3,8- diazabic clo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 165 using (1 R,6S)-3-[(2-Bromo-5-fluorophenyl)carbonyl]-8-(4,6-dimethylpyrimidin-2-yl)- 3,8-diazabicyclo[4.2.0] and1 -(tetrahydropyran-2-yl)-1 h-pyrazole-5-boronic acid pinacol ester. MS (ESI) mass calcd. for C27H31 FN6O2, 490.6; m/z found, 491 .3 [M+H]⁺.

Example 171 : (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-fluoro-2-(1 H- pyrazol-5-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-fluoro-2-(1 H-pyrazol-5- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane. (1 R,6S)-8-(4,6- Dimethylpyrimidin-2-yl)-3-({5-fluoro-2-[1 -(tetrahydro-2H-pyran-2-yl)-1 H-pyrazol- 5-yl]phenyl}carbonyl)-3,8-diazabicyclo[4.2.0]octane (8 mg, 0.017 mmol) was combined with 6 M aq. HCI (8.154 mL, 0.05 mmol) in formic acid (2.5 mL, 0.75 mmol) and stirred for 90 min. The reaction mixture was concentrated from MeOH (3 x 12 mL), then the mixture was dissolved in NH₃ MeOH and concentrated to neutralize acid. The residue was dissolved in CHCI3 and purified by FCC to afford the title compound (6.7 mg, 100%). MS (ESI) mass calcd. for C22H23FN6O, 406.5; m/z found, 407.2 [M+H]⁺.

Example 172: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(1 H-1 ,2,4-triazol-5- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 , substituting 2-(1 H-1 ,2,4-triazol-5-yl)benzoic acid for 2-thiophenyl-2-yl benzoic acid. MS (ESI) mass calcd. for C21 H23N₇O, 389.5; m/z found, 390.2 [M+H]⁺.

Example 173: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-(4-fluoroph methyl-1 ,3-thiazol-4-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-(4-fluorophenyl)-2-methylthiazole-4-carboxylic acid. MS (ESI) mass calcd. for C23H₂₄FN₅OS, 437.5; m/z found, 438.2 [M+H]⁺.

Example 174: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-phenyl-1 H-pyrazol- -yl)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-phenyl-1 h-pyrazole-4-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C₂2H₂₄N₆O, 388.5; m/z found, 389.2 [M+H]⁺.

Example 175: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-methyl-3- phenylisoxazol-4-yl)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methyl-3-phenylisoxazole-4-carboxylic acid for 2-thiophen-2-yl- benzoic acid. MS (ESI) mass calcd. for C23H25N5O2, 403.5; m/z found, 404.2 [M+H]⁺.

Example 176: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-phenylisoxazol-4- yl)carbon l]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-phenyl-4-isoxazolecarboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C22H23N5O2, 389.5; m/z found, 390.2 [M+H]⁺.

Example 177: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-(2-fluorophenyl)-1 ,3- oxazol-4- l]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-(2-fluorophenyl)oxazole-4-carboxylic acid for 2-thiophen-2-yl- benzoic acid. MS (ESI) mass calcd. for C22H22FN₅O2, 407.5; m/z found, 408.2 [M+H]⁺. Example 178: (1 R,6S)-3-{[5-(3-Chlorophenyl)-1 ,3-oxazol-4-yl]carbonyl}-8-(4,6- dimeth lpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 5-(3-chlorophenyl)-oxazole-4-carboxylic acid for 2-thiophen-2-yl- benzoic acid. (ESI) mass calcd. for C22H22CIN₅O2, 423.9; m/z found, 424.2 [M+H]⁺.

Example 179: 4'-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]oct-3-yl]carbonyl}-3',5-dimethyl-3,5'-biisoxazole.

The title compound was prepared in a manner analogous to Example 1 substituting 3-methyl-5-(5-methylisoxazol-3-yl)isoxazole-4-carboxylic acid for 2- thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C2i H₂₄N₆O3, 408.5; m/z found, 409.2 [M+H]⁺.

Example 180: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-5-(4-methyl- 1 ,2,3-thiadiazol-5-yl)isoxazol-4-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 3-methyl-5-(4-methyl-1 ,2,3-thiadiazol-5-yl)isoxazole-4-carboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C20H23N₇O2S, 425.5; m/z found, 426.2 [M+H]⁺.

Example 181 : (1 R,6S)-3-[(3-Bromopyridin-2-yl)carbonyl]-8-(4,6- dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 3-bromo-2-pyridinecarboxylic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for Ci₈H₂oBrN₅O, 402.3; m/z found, 402.1 [M+H]⁺.

Example 182: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-(1 H-1 ,2,3-triazoM - yl)pyridin-2- l]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared by treating (1 R,6S)-3-[(3-bromopyridin-2- yl)carbonyl]-8-(4,6-dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane (30 mg, 0.08 mmol), with 1 H-1 ,2,3-triazole (43 uL, 0.75 mmol), Cs₂CO₃ (49 mg, 0.15 mmol), Cul (3.5 mg, 0.02 mmol), and (R,R)-(-)-N,N'-dimethyl-1 ,2- cyclohexanediamine (12 uL, 0.05 mmol) in 1 ,4-dioxane containing 3% water. The misture was heated to 160 °C in a sealed tube. The reaction was purified directly on 16 g SiO₂ with 0-2% NH₃ MeOH / CH₂CI₂ to give partially purified material which was further purified to the individual two isomers, the title compound (2 mg, 4% yield) and Example183 (10 mg, 10 % yield) by reverse phase HPLC. MS (ESI) mass calcd. for C₂₀H₂₂N₈O, 390.5; m/z found, 391 .2 [M+H]⁺.

Example 183: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-(2H-1 ,2,3-triazol-2- yl)pyridin-2- l]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was isolated during the procedure used to prepare Example 182. MS (ESI) mass calcd. for C₂₀H₂₂N₈O, 390.5; m/z found, 391 .2 [M+H]⁺.

Example 184: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-fluoro-2-(1 H- pyrazol-3-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 3-fluoro-2-(1 H-pyrazol-5-yl)benzoic acid. MS (ESI) mass calcd. for C22H23FN6O, 406.5; m/z found, 407.2 [M+H]⁺.

Example 185: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(3-fluoro-2-pyrimidin-2- ylphen l)carbonyl]-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Example 1 substituting 3-fluoro-2-(pyrimidin-2-yl)benzoic acid. MS (ESI) mass calcd. for C23H23FN6O, 418.5; m/z found, 419.2 [M+H]⁺.

Example 186: 4-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]-6-methylpyrimidin-2-amine.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 2-amino-4-chloro-6-methylpyrimidine. MS (ESI) mass calcd. for C₂oH₂i FN₈O, 408.4; m/z found, 409.2 [M+H]⁺.

Example 187: 4-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]-N,6-dimethylpyrimidin-2-amine.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 4-chloro-N,6-dimethyl-2-pyrimidinamine. MS (ESI) mass calcd. for C^ F sFNsO, 422.5; m/z found, 423.2 [M+H]⁺.

Example 188: (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-fluoro-2-(1 -methyl- 1 H-p razol-3-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane.

A solution of the (1 R,6S)-8-(4,6-dimethylpyrimidin-2-yl)-3-{[5-fluoro-2-(1 H- pyrazol-3-yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane (Example 171 ) in DMF was treated with NaH at RT and stirred for 15 minutes until no more gas evolution occurred. The solution was cooled to -5 °C and then treated with Mel. Reaction allowed to stir for 20 min and then worked up by the addition of water followed by multiple extractions with EtOAc. Purified on 12 g S1O2 with 0- 3.5% NH₃ MeOH in CH₂CI₂. MS (ESI) mass calcd. for C^H sFNeO, 420.5; m/z found, 421 .2 [M+H]⁺.

Example 189: 6-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 3,8-diazabicyclo[4.2.0]oct-8-yl]-N,N-dimethylpyrimidin-4-amine.

—

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and (6-chloro-pyrimidin-4-yl)-dimethyl-amine. MS (ESI) mass calcd. for C21 H23FN8O, 422.5; m/z found, 423.2 [M+H]⁺.

Example 190: 6-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]-N-methylpyrimidin-4-amine.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 4-chloro-6-methylaminopyrimidine. MS (ESI) mass calcd. for C₂oH2i FN₈O, 408.4; m/z found, 409.2 [M+H]⁺. Example 191 : 6-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- -diazabicyclo[4.2.0]oct-8-yl]-2-methylpyrimidin-4-amine.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 4-amino-6-chloro-2-methylpyrimidine. MS (ESI) mass calcd. for C₂oH₂i FN₈O, 408.4; m/z found, 409.2 [M+H]⁺.

Example 192: 6-[(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 3 8-diazabicyclo[4.2.0]oct-8-yl]pyrimidine-2,4-diamine.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 4-chloro-2,6-diaminopyrimidine. MS (ESI) mass calcd. for C19H20FN9O, 409.4; m/z found, 410.2 [M+H]⁺.

Example 193: (1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8- (6-methylpyrimidin-4-yl)-3,8-diazabicyclo[4.2.0]octane.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 4-chloro-6-methylpyrimidine. MS (ESI) mass calcd. for C₂₀H₂oFN₇O, 393.4; m/z found, 394.2 [M+H]⁺.

Example 194: N-Cyclopropyl-6-[(1 R,6S)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]oct-8-yl]pyrimidin-4-amine.

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using (1 R,6S)-3,8-diazabicyclo[4.2.0]octan-3-yl(5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl)methanone and 4-chloro-6-(cyclopropylamino)pyrimidine. MS (ESI) mass calcd. for C₂₂H₂₃FN₈O, 434.5; m/z found, 435.2 [M+H]⁺.

Example 195: (5-Methyl-2-(trifluoromethyl)phenyl)((1 R,6S)-8-(2- phenylpyrimidin-4-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

The title compound was prepared in a manner analogous to Example 1 substituting 5-methyl-2-(trifluoromethyl)benzoic acid for 2-thiophen-2-yl-benzoic acid. MS (ESI) mass calcd. for C25H23F3N.A 452.2; m/z found, 453.2 [M+H]⁺.

Example 196: ((1 R,6S)-8-(2-Phenylpyrimidin-4-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(2-(1 ,1 ,2,2-tetrafluoroethoxy)phenyl)methanone.

The title compound was prepared in a manner analogous to Example 1 substituting 2-(1 ,1 ,2,2-tetrafluoroethoxy)benzoic acid for 2-thiophen-2-yl- benzoic acid. MS (ESI) mass calcd. for C2₅H₂2F₄N₄O₂, 486.2; m/z found, 487.2 [M+H]⁺.

Example 197: (5-Methyl-3-phenylisoxazol-4-yl)((1 R,6S)-8-(2-phenylpyrimidin- 4-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone .

The title compound was prepared in a manner analogous to Example 1 substituting 5-methyl-3-phenylisoxazole-4-carboxylic acid for 2-thiophen-2-yl- benzoic acid. MS (ESI) mass calcd. for C27H25N5O2, 451 .2; m/z found, 451 .2 [M+H]⁺.

The following prophetic examples (198-269) may be synthesized using the general schemes provided above. Example 198: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 199: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 200: (2-(2H-1 ,2,3-Triazol-2-yl)phenyl)((1 R,6S)-8-(5,6-dimethylpyrazin- -yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 201 : ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(2-fluoro-6-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 202: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 203: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 204: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 205: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-propoxypyridin-2-yl)methanone.

MS (ESI) mass calcd. For C21 H27N5O2, 381

Example 206: (3-Propoxypyridin-2-yl)((1 R,6S)-8-(5-(trifluoromethyl)pyrimidin-2- -3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C20H22F3N5O2, 421 .17.

Example 207: (3-Propoxypyridin-2-yl)((1 R,6S)-8-(5-(trifluoromethyl)pyridin-2- -3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C^ F sFsN^, 420.18.

Example 208: (3-Propoxypyridin-2-yl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C23H25N5O2, 403.20. Example 209: (2,6-Dimethoxyphenyl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For 0₂3Η₂₄Ν₄Ο₂, 404

Example 210: (2,6-Dimethoxyphenyl)((1 R,6S)-8-(5-(trifluoromethyl)pyrid

-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C21 H22F3N3O3, 421 .16.

Example 21 1 : (2,6-Dimethoxyphenyl)((1 R,6S)-8-(5-(trifluoromethyl)pyrimidin-2- -3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C₂oH2i F₃N₄O3, 422.16.

Example 212: (2,6-Dimethoxyphenyl)((1 R,6S)-8-(4,6-dimethylpyrimidin-2-yl)- 3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C₂i H₂6N₄O3, 382

Example 213: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-methylfuran-2-yl)methanone.

MS (ESI) mass calcd. For Ci₈H₂2N₄O2, 326.17.

Example 214: (3-Methylfuran-2-yl)((1 R,6S)-8-(5-(trifluoromethyl)pyrimidin-2-yl)- -diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For Ci₇Hi7F₃N₄O2, 366

Example 215: (3-Methylfuran-2-yl)((1 R,6S)-8-(5-(trifluoromethyl)pyrid

-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C18H18F3N3O2, 365.14. Example 216: (3-Methylfuran-2-yl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C₂oH2oN₄O₂, 348.16.

Example 217: 2-((1 R_>6S)-3-([1 _>1 '-Biphenyl]-2-ylsulfonyl)-3_>8- diazabicyclo[4.2.0]octan-8-yl)quinoxaline.

MS (ESI) mass calcd. For C26H₂₄N₄O₂S, 456.16.

Example 218: (I R^S^-dLI '-Biphenyll^-ylsulfonylVe-iS- (trifluoromethyl)pyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

MS (ESI) mass calcd. For C₂ H22F3N3O₂S, 473.14.

Example 219: (I R^S^-dLI '-Biphenyll^-ylsulfonylVe-iS- (trifluoromethyl)pyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

MS (ESI) mass calcd. For

474.13.

Example 220: (1 R,6S)-3-([1 ,1 '-Biphenyl]-2-ylsulfonyl)-8-(4,6-dimethylpyrimidin- -yl)-3,8-diazabicyclo[4.2.0]octane.

MS (ESI) mass calcd. For C₂₄H26N₄O₂S, 434.18.

Example 221 : (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-((2- methoxyphenyl)sulfonyl)-3,8-diazabicyclo[4.2.0]octane.

MS (ESI) mass calcd. For Ci9H₂ N₄O₃S, 388.16.

Example 222: (1 R,6S)-3-((2-Methoxyphenyl)sulfonyl)-8-(5- (trifluoromethyl)pyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

MS (ESI) mass calcd. For CisHigFsNUOsS, 428.1 1 .

Example 223: (1 R,6S)-3-((2-Methoxyphenyl)sulfonyl)-8-(5- (trifluoromethyl)pyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

MS (ESI) mass calcd. For C19H20F3N3O3S, 427.12.

Example 224: 2-((1 R,6S)-3-((2-Methoxyphenyl)sulfonyl)-3,8- diazabicyclo[4.2.0]octan-8-yl)quinoxaline.

MS (ESI) mass calcd. For C2iH₂2N₄O₃S, 410.14.

Example 225: (3,6'-Dimethyl-[2,3'-bipyridin]-2'-yl)((1 R,6S)-8-(quinoxalin-2-yl)- -diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C^F eNeOe, 450.22.

Example 226: (S.e'-Dimethyl-^S'-bipyridinl^'-ylXO R,6S)-8-(5- (trifluoromethyl)pyridin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C^sF^FsNsO, 467.19.

Example 227: (S.e'-Dimethyl-p.S'-bipyridinl^'-ylKil R,6S)-8-(5-

(trifluoromethyl)pyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C^F sFsNeO, 468.19.

Example 228: (S^'-Dimethyl-^^'-bipyridinl^'-ylXil R,6S)-8-(4,6- dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. For C^s sNeO, 428.23.

Example 229: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(2-fluoro-6-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. For C21 H22FN₇O, 407.19.

Example 230: ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C21 H22FN₇O, 407.19.

Example 231 : ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-iodophenyl)methanone.

MS (ESI) mass calcd. for Ci₉H₂oFIN₄O, 466.1

Example 232: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(oxazol-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C22H22FN5O2, 407.2.

Example 233: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(pyridin-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C2 H₂₄FN₅O, 417.2.

Example 234: (2-(3-Chloropyridin-2-yl)-3-fluorophenyl)((1 R,6S)-8-(4,6- dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)methanone.

MS (ESI) mass calcd. for C^F sCIFNsO, 451 .2. Example 235: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(3-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .2.

Example 236: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(6-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .2.

Example 237: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .2.

Example 238: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(5-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .2.

Example 239: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(3-fluoropyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C₂₄H23F2N₅O, 435.2.

Example 240: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(6-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 241 : ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 242: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(5-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 243: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(3-fluoropyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C₂ H23F2N₅O, 435.19

Example 244: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(pyridin-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C2 H₂₄FN₅O, 417.20

Example 245: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(5-fluoro-2-(oxazol-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C22H22FN5O2, 407.18;

Example 246: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(6-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 247: (( R.eSJ-S^^-Dimethylpyrimidin^-y -S.S- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 248: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(5-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ; Example 249: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(3-fluoropyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C₂₄H23F2N₅O, 435.19;

Example 250: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2 ]octan-3-yl)(6-fluoro-2-(pyridin-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C2 H₂₄FN₅O, 417.20;

Example 251 : ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(oxazol-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C22H22FN5O2, 407.18;

Example 252: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(6-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 253: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 254: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 255: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(3-fluoropyridin-2- yl)phenyl)methanone.

Example 256: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(pyridin-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C2 H₂₄FN₅O, 417.20;

Example 257: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(oxazol-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C22H22FN5O2, 407.18;

Example 258: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(6-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 259: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 260: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(6-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 261 : ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(3-fluoropyridin-2- yl)phenyl)methanone.

Example 262: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(pyridin-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C2 H₂₄FN₅O, 417.20;

Example 263: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(4-fluoro-2-(oxazol-2-yl)phenyl)methanone.

Example 264: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(6-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 265: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

Example 266: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(4-methylpyridin-2- yl)phenyl)methanone.

MS (ESI) mass calcd. for C2₅H26FN₅O, 431 .21 ;

Example 267: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(3-fluoropyridin-2- yl)phenyl)methanone.

Example 268: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(pyridin-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C₂ H₂₄FN₅O, 417.20;

Example 269: ((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)(3-fluoro-2-(oxazol-2-yl)phenyl)methanone.

MS (ESI) mass calcd. for C22H22FN5O2, 407.18;

Example 270: (1 R,6S)-3-{[2-(2H-1 ,2,3-Triazol-2-yl)phenyl]carbonyl}-8-(4,5,6- trimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane.

Step A: (1 R,6S)-8-(4,5,6-Trimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane. (1 R,6S)-8-(4,5,6-Trimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane was prepared in a manner analogous to Intermediate 40, using Intermediate 66 and Intermediate 39 as starting materials. MS (ESI) mass calcd. for Ci₃H₂₀N₄, 232.17; m/z found, 233.1 [M+H]⁺.

Step B: (1 R,6S)-3-{[2-(2H-1 ,2,3-Triazol-2-yl)phenyl]carbonyl}-8-(4,5,6- trimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octane. (1 R,6S)-3-{[2-(2H-1 ,2,3- Triazol-2-yl)phenyl]carbonyl}-8-(4,5,6-trimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane was made in a manner analogous to Example 1 using Intermediate 14 and the product of Step A as starting materials. MS (ESI): mass calculated for C22H2₅N₇O, 403.21 , m/z found 404.2 [M+1 ]⁺. ¹ H NMR (500 MHz, CDCI3): 8.02 - 7.91 (m, 1 H), 7.81 (s, 1 H), 7.55 - 7.27 (m, 2H), 7.12 - 7.04 (m, 1 H), 7.00 - 6.92 (m, 1 H), 4.68 - 4.50 (m, 1 H), 4.34 - 4.24 (m, 1 H), 4.1 1 - 3.86 (m, 3H), 3.83 - 3.67 (m, 1 H), 2.90 - 2.67 (m, 1 H), 2.40 - 2.32 (m, 2H), 2.25 - 1 .88 (m, 9H), 1 .76 - 1 .54 (m, 1 H). Biological Assays

The in vitro affinity of the compounds for the human orexin-1 and orexin- 2 receptors was determined by competitive radioligand binding using [³H]SB SB674042 (1 -(5-(2-fluoro-phenyl)-2-methyl-thiazol-4-yl)-1 -((S)-2-(5-phenyl- (1 ,3,4)oxadiazol-2-ylmethyl)-pyrrolidin-1 -yl)-methanone) (Langmead et al., British Journal of Pharmacology 2004, 141 :340-346.) and [³H]EMPA (N-ethyl- 2[(6-methoxy-pyridin-3-yl)-(toluene-2-sulfonyl)-amino]-N-pyridin-3-ylmethyl acetamide) (Malherbe et al., British Journal of Pharmacology, 2009, 156(8), 1326-1341 ), respectively.

The in vitro functional antagonism of the compounds on the human orexin-1 and orexin-2 receptors was determined using fluorometric imaging plate reader (FLIPR) based calcium assays.

Human orexin 1 receptor radioligand binding studies

Chinese ovary cells (CHO) stably expressing human orexin 1 receptor (Genebank accession number NM_001526) were grown to confluency in DMEM/F12 (Gibco, Cat #1 1039), 10%FBS, 1X Pen/Strep, 600 μg/mL G418 media on 150 cm² tissue culture plates, washed with 5 mM EDTA in PBS (HyClone Dulbecco's Phoshpate Buffered Saline 1 X with Calcium and Magnesium, Cat # SH30264.01 , hereafter referred to simply as PBS) and scraped into 50 ml tubes. After centrifugation (2K xG, 10 min at 4°C), the supernatant was aspirated and the pellets frozen and stored at -80°C. Cells were resuspended in PBS in the presence of 1 tablet of protease inhibitor cocktail (Roche, Cat. #1 1836145001 ) per 50 mL. Each cell pellet from a 15 cm plate was resuspended in 10 mL, stored on ice, and vortexed for 45 sec prior to addition to the reactions. Competition binding experiments in 96 well polypropylene plates were performed using [³H]-SB674042 (Moravek

Corporation, specific activity = 35.3 Ci/mmol), diluted to a 10 nM concentration in PBS (4 nM final). Compounds were solubilized in 100% DMSO (Acros

Organics, Cat. #61042-1000) and tested over a range of 7 concentrations (from 0.1 nM to 10 μΜ). The final concentration of DMSO in the reactions is equal to or less than 0.1 %. Total and nonspecific binding was determined in the absence and presence of 10 μΜ (1 -(6,8-difluoro-2-methylquinolin-4-yl)-3-[4- (dimethylamino)phenyl]urea, CAS Registry # 288150-92-5). The total volume of each reaction is 200 μΐ (20 μΐ of diluted compounds, 80 μΐ of [³H]- SB674042 diluted in PBS and 100 μΐ of the cell suspension). Reactions were run for 60 min at room temperature and terminated by filtration through GF/C filter plates (PerkinElmer, Cat. #6005174) presoaked in 0.3% polyethylenimine using the cell harvester (PerkinElmer Filtermate). The plates were washed 3 times by aspirating 30 ml PBS through the plates. Plates were dried in 55°C oven for 60 min, scintillation fluid was added, and the radioactivity was counted on a Topcount (Packard).

IC₅o values (i.e. concentration of unlabelled compound required to compete for 50% of specific binding to the radioligand) were calculated using the GraphPad Prism software (GraphPad Prism Software Inc., San Diego, CA) with a fit to a sigmoidal dose-response curve. Apparent K, values were calculated as K, = IC₅o/(1 ⁺C/Kd), where C is concentration of radioligand and K_d = 4 nM.

Human orexin 2 receptor radioligand binding studies

HEK293 stably expressing human orexin-2 receptor (Genebank accession number NM_001526) were grown to confluency in DMEM/F12 (Gibco, Cat #1 1039), in DMEM, 10%FBS, 1 X Pen/Strep, 1 X NaPyruvate, 1X HEPES, 600 ug/ml G418 media on 150 cm² tissue culture plates, washed with 5 mM EDTA in PBS (HyClone Dulbecco's Phoshpate Buffered Saline 1X with Calcium and Magnesium, Cat # SH30264.01 , hereafter referred to simply as PBS) and scraped into 50 ml tubes. After centrifugation (2K xG, 10 min at 4°C), the supernatant was aspirated and the pellets frozen and stored at -80°C. Cells were resuspended in PBS in the presence of 1 tablet of protease inhibitor cocktail (Roche, Cat. #1 1836145001 ) per 50 ml_. Each cell pellet from a 15 cm plate was resuspended in 10 ml_, stored on ice, and vortexed for 45 sec just prior to addition to the reactions. Competition binding experiments in 96 well polypropylene plates were performed using [³H]-EMPA (Moravek Corporation, specific activity = 27 Ci/mmol), diluted to a 20 nM concentration in PBS (5 nM final concentration). Compounds were solubilized in 100% DMSO (Acros Organics, Cat. #61042-1000) and tested over a range of 7 concentrations (from 0.1 nM to 10 μΜ). The final concentration of DMSO in the reactions is equal to or less than 0.1 %. Total and nonspecific binding was determined in the absence and presence of 10 μΜ (N-[2-(3,4-dimethoxyphenyl)ethyl]-N- methylnaphthalene-1 -carboxamide, CAS Registry # 1089563-88-1 ). The total volume of each reaction is 200 μΙ_ (20 μΙ_ of diluted compounds, 80 μΙ_ of [³H]- EMPA diluted in PBS and 100 μΙ_ of the cell suspension). Reactions were run for 60 min at room temperature and terminated by filtration through GF/C filter plates (PerkinElmer, Cat. #6005174) presoaked in 0.3% polyethyleninnine using the cell harvester (PerkinElmer Filtermate). The plates were washed 3 times by aspirating 30 ml PBS through the plates. Plates were dried in 55°C oven for 60 min, scintillation fluid was added, and the radioactivity was counted on a Topcount (Packard). IC₅₀ values (i.e. concentration of unlabelled compound required to compete for 50% of specific binding to the radioligand) were calculated using the GraphPad Prism software (GraphPad Prism Software Inc., San Diego, CA) with a fit to a sigmoidal dose-response curve. Apparent K, values were calculated as K, = IC₅o/(1 +C/K_d), where C is concentration of radioligand and K_d = 2 nM.

Human orexin 1 receptor Ca²⁺ mobilization assay

CHO cells stably transfected with the human orexin-1 receptor

(Genebank accession number NM_001526) were grown to confluency in DMEM/F12, 10% FBS, 1 X Na Pyruvate, 1 X pen-strep, 400 μς/ιτιΙ G418. Cells were seeded on to 96-well Packard viewplates at a density of 50,000 cells/well and incubated overnight at 37°C, 5% CO2. The cells were dye-loaded with 4 μΜ Ca²⁺ dye Fluo-3AM in serum-free DMEM/F-12 with 2.5 mM probenecid and incubated at 37°C, 5% CO2 for one hour. Cells were pre-incubated with compounds (diluted in DMEM/F-12) for 30 minutes before agonist (orexin A, 10 nM) stimulation. Ligand-induced Ca²⁺ release was measured using a

Fluorometric Imaging Plate Reader (FLIPR, Molecular Devices, Sunnyvale, CA). Functional responses were measured as peak fluorescence intensity minus basal. The concentration of agonist that produced a half-maximal response is represented by the EC₅0 value. Antagonistic potency values were converted to apparent pK_B values using a modified Cheng-Prusoff correction. Apparent pK_B = - log IC₅o/1 +[conc agonist/EC₅o] - Data are expressed as mean ± S.E.M.

Human orexin 2 receptor Ca²⁺ mobilization assay

PFSK cells endogenously expressing the human orexin 2 receptor were grown to confluency in RPMI1640, 10% FBS, 1X pen-strep. Cells were seeded on to 96-well Packard viewplates at a density of 50,000 cells/well and incubated overnight at 37°C, 5% CO₂. The cells were dye-loaded with 4 μΜ Ca²⁺ dye Fluo-3AM in serum-free DMEM/F-12 with 2.5 mM probenecid and incubated at 37°C, 5% CO2 for one hour. Cells were pre-incubated with compounds (diluted in DMEM/F-12) for 30 minutes before agonist (orexin B, 100 nM) stimulation. Ligand-induced Ca²⁺ release was measured using a Fluorometric Imaging Plate Reader (FLIPR, Molecular Devices, Sunnyvale, CA). Functional responses were measured as peak fluorescence intensity minus basal. The concentration of agonist that produced a half-maximal response is represented by the EC50 value. Antagonistic potency values were converted to apparent pK_B values using a modified Cheng-Prusoff correction. Apparent pK_B = - log IC₅o/1 +[conc agonist/EC₅o] - Data are expressed as mean ± S.E.M, the designation of NT means not tested.

OR-2 K; OR-2 OR-1 K; OR-2 K; OR-2 OR-1 K;

Ex # Ex #

(nM) Kb (nM) (nM) Kb (nM)

1 4 4 64 109 10000 NT 10000

2 4 2 61 110 220 NT 10000

3 8 7 169 111 176 NT 5000

4 7 3 8 112 115 9 1960

5 10 11 8 113 161 NT 8999

6 20 8 18 114 494 NT 10000

7 15 6 371 115 60 20 177

8 24 35 24 116 28 7 23

9 33 11 22 117 18 6 23

10 44 10 18 118 40 9 33

11 140 145 143 119 17 11 32

12 209 78 659 120 26 12 43

13 144 NT 78 121 75 23 91

14 114 NT 96 122 59 26 128

15 257 112 237 123 45 11 95

16 284 62 460 124 92 NT 4148

17 542 251 305 125 73 NT 3298

18 763 NT 3833 126 149 NT 5468

19 1066 NT 254 127 210 NT 10000

20 2112 NT 379 128 26 3 1013

21 3780 NT 1208 129 36 13 265

22 29 11 473 130 31 10 1715

23 20 8 619 131 250 NT 1600

24 6 5 44 132 10000 NT 10000

25 15 4 416 133 36 9 550

26 13 4 52 134 16 4 277

27 28 16 143 135 15 3 135

28 21 5 330 136 10000 NT 10000

29 11 5 325 137 275 NT 10000

30 13 8 978 138 70 19 1649

31 81 50 10000 139 208 NT 6500

32 13 3 134 140 70 14 1072

33 51 25 47 141 734 NT 8999

34 50 13 1043 142 8999 NT 10000

35 24 6 117 143 8999 NT 10000

36 5 3 11 144 2811 NT 10000

37 10 5 19 145 110 14 3299

38 16 8 77 146 299 NT 8999

39 20 8 32 147 91 15 793

40 91 8 1210 148 36 3 845

41 12 3 441 149 190 NT 10000

42 34 6 400 150 532 NT 10000 OR-2 K; OR-2 OR-1 K; OR-2 K; OR-2 OR-1 K;

Ex # Ex #

(nM) Kb (nM) (nM) Kb (nM)

43 90 5 475 151 17 2 341

44 73 7 480 152 223 NT 1852

45 119 10 697 153 82 6 687

46 15 8 47 154 140 NT 1200

47 132 100 206 155 57 4 1530

48 179 126 258 156 185 NT 860

49 77 40 114 157 230 NT 3900

50 94 63 39 158 170 NT 3200

51 501 NT 432 159 540 NT 10000

52 137 126 104 160 370 NT 5999

53 1812 NT 3703 161 280 NT 4500

54 2417 NT 3447 162 380 NT 10000

55 92 63 274 163 700 NT 10000

56 129 NT 55 164 190 NT 3900

57 29 16 3566 165 550 NT 10000

58 1051 NT 9654 166 72 NT 3841

59 9322 NT 10000 167 55 13 219

60 188 NT 10000 168 740 NT 7300

61 980 NT 10000 169 59 7 1589

62 123 50 5000 170 0 NT 0

63 392 NT 10000 171 15 3 392

64 109 40 808 172 48 8 1249

65 42 20 1066 173 62 20 2149

66 163 NT 9654 174 5999 NT 10000

67 156 NT 225 175 488 NT 10000

68 192 NT 5000 176 1300 NT 10000

69 61 40 128 177 340 NT 2400

87 1400 NT 10000 178 126 16 7000

88 234 NT 8200 179 1100 NT 10000

89 220 NT 10000 180 6500 NT 10000

90 150 NT 10000 181 1300 NT 10000

91 520 NT 5400 182 1500 NT 10000

92 84 NT 220 183 200 NT 10000

93 230 NT 3700 184 9 2 156

94 370 NT 10000 185 56 10 600

95 23 NT 625 186 680 NT 10000

96 258 8 5843 187 310 NT 10000

97 1289 NT 5019 188 35 9 1300

98 274 3 4916 189 110 NT 4100

99 96 13 4135 190 1100 NT 10000

100 200 NT 8700 191 230 NT 10000

101 190 NT 6599 192 1400 NT 10000 OR-2 Ki OR-2 OR-1 Ki OR-2 Ki OR-2 OR-1 Ki

Ex # Ex #

(nM) Kb (nM) (nM) Kb (nM)

102 420 NT 10000 193 780 NT 10000

103 360 NT 10000 194 650 NT 10000

104 342 NT 3536 195 28 8 16

105 10000 NT 10000 196 14 5 14

106 10000 NT 10000 197 3100 NT 2600

107 10000 NT 10000 270 11 2.5 16

108 10000 NT 10000

Claims

What is claimed is:

1 . A chemical entity that is a compound of Formula (I):

wherein:

n is 0-1 ;

R¹ is a member selected from the group consisting of:

R^a is independently selected from the group consisting of: halo, -Ci- alkyl, and -Ci- alkoxy, wherein two adjacent R^a members may come together to form a six membered aromatic ring;

R^b is a member selected from the group consisting of:

a) halo, -Ci_-4alkoxy, -CF₃, or -CF₂CHF₂;

b) 5-membered heteroaryl ring containing one oxygen or one sulfur members;

c) 5-6 membered heteroaryl ring containing one to three nitrogen members, optionally containing one oxygen member, substituted or unsubstituted with halo, -Ci- alkyl,

tetrahydropyran-2-yl, or -N(CH₃)2; and

d) phenyl substituted or unsubstituted with -F, or -CH₃;

R^c is a member independently selected from the group consisting of:

-Ci_-4alkyl, -CF₃, and -Ci_-4alkoxy;

R^d is a member selected from the group consisting of:

a) 5-6 membered heteroaryl ring selected from the group

consisting of: 1 H-1 ,2,3-triazol-1 -yl, 2H-1 ,2,3-triazol-2-yl, 1 H- pyrazol-3-yl, and 6-methyl-pyridin-2-yl; and

b) -CF₃, -Br, or -Ci_-4alkoxy; C) 6-membered heteroaryl ring selected from the group consisting of: pyrimidin-yl or pyrazin-yl, substituted or unsubstituted with a member independently selected from -CH₃, -OCH₃, or phenyl;

E) 3-methylfuran-2-yl, 9H-fluorene, 9H-fluoren-9-one, 3,5'-biisoxazole,

[3-methyl-5-(4-methyl-1 ,2,3-thiadiazol-5-yl)isoxazol-4-yl], or naphthyridine;

R² is a member selected from the group consisting of:

A) 6-membered heteroaryl ring containing two nitrogen members

substituted or unsubstituted with one or more members independently selected from the group consisting of: halo, -Ci_-4alkyl, -Ci_-4alkoxy, -CF₃, -NH₂, -NHCH3, -N(Ci_-4alkyl)i_-2, -NHcyclopropyl, and phenyl;

B) pyridine substituted or unsubstituted with one or two members

C) quinoxalin-2-yl, benzooxazol-2-yl, or 5-chloro-1 ,3-benzoxazole;

and pharmaceutically acceptable salts of compounds of Formula (I).

2. A chemical entity selected from compounds of Formula (II):

wherein

R³ is phenyl substituted or unsubstituted with a member independently

selected from the group consisting of -Ci- alkyl, -Ci- alkoxy, and phenyl; R⁴ is a member selected from the group consisting of (5-trifluoromethyl)-pyridin

2-yl, (5-trifluoromethyl)-pyrimidin-2-yl, 4,6-dimethylpyrimidin-2-yl, 4- phenylpyrimidin-2-yl, and quinoxalin-2-yl; and pharmaceutically acceptable salts of compounds of Formula (II).

3. A chemical entity defined in claim 1 , wherein n is 0. 4. A chemical entity defined in claim 1 , wherein n is 1 .

5. A chemical entity defined in claim 1 , wherein R¹ is phenyl, where R^a is a member selected from the group consisting of -F, -OCH₃, and -CH₃. 6. A chemical entity defined in claim 1 , wherein R^b is a member selected from the group consisting of -Br, -I, -OCH₃, -CF₂CHF₂ and -CF₃.

7. A chemical entity defined in claim 1 , wherein R^b is a member selected from the group consisting of 2-pyrrol-1 -yl, pyridin-2-yl, 3-chloropyridin-2-yl, 3- fluoropyridin-2-yl, 3-methylpyridin-2-yl, 4-methylpyridin-2-yl, 5-methylpyridin-2- yl, 6-methylpyridin-2-yl, pyridin-3-yl, N,N-dimethylpyridin-2-amine, pyrimidin-2- yl, pyrimidin-5-yl, 2H-1 ,2,3-triazol-2-yl, 1 H-1 ,2,3-triazol-1 -yl, 1 H-1 ,2,4-triazol-5- yl, 1 H-pyrazol-1 -yl, 1 H-pyrazol-3-yl, 1 -methyl-1 H-pyrazol-3-yl, 1 -(tetrahydro-2H- pyran-2-yl)-1 H-pyrazol-5-yl, 1 H-pyrazol-5-yl, 3-methyl-1 ,2,4-oxadiazol-5-yl, oxazol-2-yl, 2-thiophen-2-yl and 2-furan-2-yl.

8. A chemical entity defined in claim 1 , wherein R^b is a member selected from the group consisting of phenyl, 3-fluorophenyl or 4-methylphenyl. 9. A chemical entity defined in claim 1 , wherein R¹ is pyridine, where R^c is a member independently selected from the group consisting of -CH₃, -OCH₃, and -CF₃, and R^d is a member selected from the group consisting of -Br, - OCH₂CH₂CH₃, -CF₃, 1 H-1 ,2,3-triazol-1 -yl, 2H-1 ,2,3-triazol-2-yl, and 3- methylpyridin-2-yl.

10. A chemical entity defined in claim 1 , wherein R¹ is 2-ethoxy-naphthalen-1 - yl, 4-phenyl-pyrimidin-2-yl, 5-(2-fluorophenyl)-2-methyl-1 ,3-thiazol-4-yl, 2- phenyl-2H-pyrazol-3-yl, 5-phenyl-isoxazol-4-yl, 5-methoxy-2-methylpyrimidin-4- yl, 3-phenylpyrazin-2-yl, 5-phenyl-1 H-pyrazol-4-yl, 5-methyl-3-phenylisoxazol-4- yl, 5-phenylisoxazol-4-yl, 5-(2-fluorophenyl)-1 ,3-oxazol-4-yl, 5-(3-chlorophenyl)-

I , 3-oxazol-4-yl, 3',5-dinnethyl-3,5'-biisoxazole, 3-methyl-5-(4-methyl-1 ,2,3- thiadiazol-5-yl)isoxazol-4-yl, 5-methyl-3-phenylisoxazol-4-yl,and 3-methylfuran- 2-yl.

I I . A chemical entity defined in claim 1 , wherein R¹ phenyl and R^b is a member selected from the group consisting of pyrimidin-2-yl, 2H-1 ,2,3-triazol-2-yl, 1 H- pyrazol-3-yl, and 2-thiophen-2-yl.

12. A chemical entity defined in claim 1 , wherein R¹ is 2-(2H-1 ,2,3-triazol-2- yl)phenyl, 2-fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl, 3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl, 3-methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 4-fluoro-2-(2H-1 ,2,3-triazol- 2-yl)phenyl, 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl, 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 3-fluoro-2-(1 H- pyrazol-3-yl)phenyl, 5-fluoro-2-(1 -methyl-1 H-pyrazol-3-yl, or 2-thiophen-2-yl- phenyl.

13. A chemical entity defined in claim 1 , wherein R² is pyrimidine, pyrazine or pyridazine substituted or unsubstituted with one or more members

independently selected from the group consisting of -Ci_-4alkyl, -OCH₃, -CF₃, - CI, -N(CH₃)₂, -NH₂, -NHCHs, and phenyl.

14. A chemical entity defined in claim 1 , wherein R² is 2-dimethylamino-6- methyl-pyrimidin-4-yl, 2-dimethylamino-6-trifluoromethyl-pyrimidin-4-yl, 2-fluoro- 6-pyrimidin-2-yl-phenyl, 2-methylpyrimidin-4-amine, 2-phenylpyrimidin-4-yl, 4,6- dimethoxypyrimidin-2-yl, 4,6-dimethylpyrimidin-2-yl, 4-methoxypyrimidin-2-yl, 4- methylpyrimidin-2-yl, 4-(trifluoromethyl)pyrimidin-2-yl, 4-phenylpyrimidin-2-yl, 5- (trifluoromethyl)pyrimidin-2-yl, 6-methyl-2-trifluoromethyl-pyrimidin-4-yl, 6- methylpyrimidin-4-yl, 6-methylpyrimidin-2-amine, N,6-dimethylpyrimidin-2- amine, N,N-dimethylpyrimidin-4-amine, N-cyclopropyl-pyrimidin-4-amine, N- methylpyrimidin-4-amine, pyrimidine-2,4-diamine, 3,6-dimethylpyrazin-2-yl, 3- methylpyrazin-2-yl, 5-methylpyrazin-2-yl, 5,6-dimethylpyrazin-2-yl, 6- methylpyrazin-2-yl, or 6-chloropyridazin-4-yl.

15. A chemical entity defined in claim 1 , wherein R² is pyridine substituted or unsubstituted with one or more members independently selected from the group consisting of -CH₃, -CF₃, and -N(CH₃)2-

16. A chemical entity defined in claim 1 , wherein R² is 4-methylpyridin-2-yl, 4- (trifluoromethyl)pyridin-2-yl, 4,6-dimethylpyridin-2-yl, 5-(trifluoromethyl)pyridin- 2-yl, 5-methylpyridin-2-yl, 6-methylpyridin-2-yl, 6-(trifluoromethyl)pyridin-2-yl, or N,N-dimethylpyridin-4-amine.

17. A chemical entity defined in claim 1 , wherein R² is 2-dimethylamino-6- trifluoromethyl-pyrimidin-4-yl, 4,6-dimethylpyrimidin-2-yl, or 4- (trifluoromethyl)pyrimidin-2-yl.

18. A chemical entity defined in claim 1 , wherein R¹ is 2-(2H-1 ,2,3-triazol-2- yl)phenyl, 2-fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl, 3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl, 3-methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 4-fluoro-2-(2H-1 ,2,3-triazol- 2-yl)phenyl, 4-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 5-fluoro-2-(2H-1 ,2,3- triazol-2-yl)phenyl, 5-methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl, 3-fluoro-2-(1 H- pyrazol-3-yl)phenyl, 5-fluoro-2-(1 -methyl-1 H-pyrazol-3-yl, or 2-thiophen-2-yl- phenyl and R² is 2-dimethylamino-6-trifluoromethyl-pyrimidin-4-yl, 4,6- dimethylpyrimidin-2-yl, or 4-(trifluoromethyl)pyrimidin-2-yl.

19. A chemical entity defined in claim 2, wherein R³ is 2,5-dimethylphenyl, 2,4- dimethylphenyl, biphenyl or 2-methoxyphenyl and R⁴ is 4-phenylpyrimidin-2-yl, 4,6-dimethylpyrimidin-2-yl, (5-trifluoromethyl)-pyridin-2-yl, (5-trifluoromethyl)- pyrimidin-2-yl, or quinoxalin-2-yl.

20. A chemical entity selected from the group consisting of:

(1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- thiophen-2-yl-phenyl)-methanone; (1 R, 6S) [8-(4,6-Dimethyl-pynmidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- furan-2-yl-phenyl)-methanone;

(1 R, 6S)-Biphenyl-2-yl -[8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-methanone;

(1 R, 6S) (8-Quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-(2-thiophen-2-yl- phenyl)-methanone;

(1 R, 6S) Biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)- methanone;

(1 R, 6S) (2-Furan-2-yl-phenyl)-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3- yl)-methanone;

(1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- pyrrol-1 -yl-phenyl)-methanone;

Biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-nnethanone; Biphenyl-2-yl-[8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]- methanone;

(1 R, 6S) (4'-Methyl-biphenyl-2-yl)-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct- 3-yl)-methanone;

(8-Benzooxazol-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-biphenyl-2-yl-methanone; (2,6-Dimethoxy-phenyl)-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)- methanone;

(1 R, 6S) (2-Bromo-phenyl)-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)- methanone;

(1 R, 6S) (2-Pyridin-3-yl-phenyl)-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3- yl)-methanone;

(2,6-Dimethoxy-phenyl)-[8-(4-phenyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct- 3-yl]-methanone;

(8-Benzooxazol-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-(2,6-dinnethoxy-phenyl)- methanone;

(1 S, 6R) Biphenyl-2-yl-(8-quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)- methanone;

(1 S, 6R) Biphenyl-2-yl-[8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-methanone; 3-(2,5-Dimethyl-benzenesulfonyl)-8-(4-phenyl-pynmidin-2-yl)-3,8-diaza- bicyclo[4.2.0]octane;

(1 R, 6S) 2-[3-(2,4-Dimethyl-benzenesulfonyl)-3,8-diaza-bicyclo[4.2.0]oct-8-yl]- quinoxaline;

2-[3-(2,5-Dimethyl-benzenesulfonyl)-3,8-diaza-bicyclo[4.2.0]oct-8-yl]- quinoxaline;

(1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- fluoro-6-pyrinnidin-2-yl-phenyl)-nnethanone;

(1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(5- fluoro-2-pyrinnidin-2-yl-phenyl)-nnethanone;

(1 R, 6S) [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- ethoxy-naphthalen-1 -yl)-methanone;

(1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- [1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

(1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(5- methyl-2-[1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

(1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(5- methyl-2-pyrinnidin-2-yl-phenyl)-nnethanone;

(1 R, 6S)- [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- pyrinnidin-2-yl-phenyl)-nnethanone;

(1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2- fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

(1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(4- fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(3,6-Dimethyl-pyrazin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(4- fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

(1 R, 6S)-(2-Fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-2-tnfluoromethyl- pyrinnidin-4-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-nnethanone;

(1 R, 6S) (5-Fluoro-2-pyrinnidin-2-yl-phenyl)-(8-quinoxalin-2-yl-3,8-diaza- bicyclo[4.2.0]oct-3-yl)-methanone;

(1 R, 6S)-(4-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-2-tnfluoromethyl- pyrinnidin-4-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-nnethanone; (1 R, 6S)-[8-(6-Methyl-2-tnfluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-tnfluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-tnfluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-tnfluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-(8-Quinoxalin-2-yl-3,8-diaza-bicyclo[4.2.0]oct-3-yl)-(2-[1 ,2,3]triazol-2- yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(5-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(5- fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

(1 R, 6S)-(5-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-2-tnfluoromethyl- pyrinnidin-4-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-nnethanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(2-fluor o-6-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-methyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(4-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

(1 R, 6S)-[8-(2-Dimethylamino-6-tnfluoromethyl-pyrimidin-4-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-(5-fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-methanone;

3-(Biphenyl-2-ylcarbonyl)-6-(4-phenylpyrinnidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane;

2-[3-(Biphenyl-2-ylcarbonyl)-3,6-diazabicyclo[3.2.0]hept-6-yl]quinoxaline;

2-{3-[(2-Thiophen-2-ylphenyl)carbonyl]-3,6-diazabicyclo[3.2.0]hept-6- yl}quinoxaline;

6-(4-Phenylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6-diazabicyc [3.2.0]heptane;

2-(3-{[5-(2-Fluorophenyl)-2-methyl-1 ,3-thiazol-4-yl]carbonyl}-3,6- diazabicyclo[3.2.0]hept-6-yl)quinoxaline; 3-{[5-(2-Fluorophenyl)-2-methyl-1 ,3-thiazol-4-yl]carbonyl}-6-(4-phenylpyrimidin-

2- yl)-3,6-diazabicyclo[3.2.0]heptane;

3- [(2-Methoxyphenyl)carbonyl]-6-(4-phenylpyrinnidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane;

2-{3-[(2-Methoxyphenyl)carbonyl]-3,6-diazabicyclo[3.2.0]hept-6-yl}quinoxaline; 6-(4-Phenylpyrimidin-2-yl)-3-[(2-thioph^

[3.2.0]heptane;

6-(4-Phenylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6-diazabicycl^ [3.2.0]heptane;

6-(4,6-Dimethylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- diazabicyclo[3.2.0]heptane;

3-[(2-Bromophenyl)carbonyl]-6-(4,6-dimethylpynmidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane;

(2-Bromo-phenyl)-[6-(4-methyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]- methanone;

6-(4-Methylpyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- diazabicyclo[3.2.0]heptane;

3-(Biphenyl-2-ylcarbonyl)-6-(4-methylpyrinnidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane;

6-(4-Methoxypyrimidin-2-yl)-3-[(2-thiophen-2-ylphenyl)carbonyl]-3,6- diazabicyclo[3.2.0]heptane;

3-(Biphenyl-2-ylcarbonyl)-6-(4-methoxypyrinnidin-2-yl)-3,6- diazabicyclo[3.2.0]heptane;

6-(4,6-Dimethoxypyrimidin-2-yl)-3-[(2-ethoxynaphthalen-1 -yl)carbonyl]-3,6- diazabicyclo[3.2.0]heptane;

6-(4,6-Dimethylpyrimidin-2-yl)-3-[(2-ethoxynaphthalen-1 -yl)carbonyl]-3,6- diazabicyclo[3.2.0]heptane;

6-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(2H-1 ,2,3-tnazol-2-yl)phenyl]carbonyl}-3,6- diazabicyclo[3.2.0]heptane;

6-(4-Phenylpyrimidin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-3,6- diazabicyclo[3.2.0]heptane;

6-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(2H-1 ,2,3-tnazol-2- yl)phenyl]carbonyl}-3,6-diazabicyclo[3.2.0]heptane; 6-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(2H-1 ,2,3-tnazol-2- yl)phenyl]carbonyl}-3,6-diazabicyclo[3.2.0]heptane;

[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(3-fluoro-2- [1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

(2-Fluoro-6-[1 ,2,3]triazol-2-yl-phenyl)-[8-(6-methyl-pyndin-2-yl)-3,8-diaza- bicyclo[4.2.0]oct-3-yl]-methanone;

[8-(4,6-Dimethoxy-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2-fluoro-6- [1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2-methyl-5- phenyl-thiazol-4-yl)-methanone;

[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(2-phenyl-2H- pyrazol-3-yl)-methanone;

[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(5-phenyl- isoxazol-4-yl)-methanone;

[6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(5-fluoro-2- [1 ,2,3]triazol-2-yl-phenyl)-methanone;

[6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(3-fluoro-2- [1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

[6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(2-fluoro-6- [1 ,2,3]triazol-2-yl-phenyl)-methanone;

[6-(4,6-Dimethyl-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(4-fluoro-2- [1 ,2,3]triazol-2-yl-phenyl)-methanone;

[6-(3,6-Dimethyl-pyrazin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(2-fluoro-6- [1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

[6-(3,6-Dimethyl-pyrazin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(3-fluoro-2- [1 ,2,3]triazol-2-yl-phenyl)-nnethanone;

[6-(4,6-Dimethoxy-pyrimidin-2-yl)-3,6-diaza-bicyclo[3.2.0]hept-3-yl]-(3-fluoro-2- [1 ,2,3]triazol-2-yl-phenyl)-methanone;

(3-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[6-(4-methyl-pynmidin-2-yl)-3,6-diaza- bicyclo[3.2.0]hept-3-yl]-methanone;

(3-Fluoro-2-[1 ,2,3]triazol-2-yl-phenyl)-[6-(4-methoxy-pynmidin-2-yl)-3,6-diaza- bicyclo[3.2.0]hept-3-yl]-methanone; [8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]oct-3-yl]-(3'-fluoro- biphenyl-2-yl)-methanone;

[8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4 .0]oct-3-yl]-(4'-methyl- biphenyl-2-yl)-methanone;

(1 R,6S)-8-(6-Chloropyridazin-4-yl)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[6-methyl-2-(1 H-1 ,2,3-triazol-1 - yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(tnfluoromethyl)pyndin-^^ yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[4-methoxy-2-(2H-1 ,2,3-tnazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[6-Methyl-2-(1 H-1 ,2,3-triazol-1 -yl)pyridin-3-yl]carbonyl}-8-[6-methyl-

2-(tnfluoromethyl)pyrimidin-4-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-[(2-Fluoro-6-pyrimidin-2-ylphenyl)carbonyl]-8-[6-methyl-2-

(tnfluoromethyl)pyrimidin-4-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[6-Methyl-2-(1 H-1 ,2,3-triazol-1 -yl)pyridin-3-yl]carbonyl}-8-[4-

(tnfluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(I R^SJ-S-itS-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-S-K- (tnfluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(I R^SJ-S-i^-Fluoro-e^H-l ^^-triazol^-y phenyllcarbonylJ-S-K-

(tnfluoromethyl)pyrimidin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[2-fluoro-6-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(3,6-Dimethylpyrazin-2-yl)-3-{[3-fluoro-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(5-Methylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-

3,8-diazabicyclo[4.2.0]octane; (I R^SVS-tP-Fluoro-e^H-l ^^-triazol^-y phenyllcarbonylJ-e-iS- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(I R^SVS-tK-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-e-iS- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[3-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(5- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(5- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(3-Methylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 3,8-diazabicyclo[4.2.0]octane;

(I R^SVa-tP-Fluoro-e^H-l ^^-triazol^-y phenyllcarbonylJ-e-iS- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(I R^SVa-dS-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-e-iS- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[4-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(3- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(I R^SVa-tP-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-e-ia- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(I R^SVa-tP-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-e-ie- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(I R^SVS-dS-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-e-ie- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(6-Methylpyrazin-2-yl)-3-{[2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-

3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(6- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(I R^SVS-tK-Fluoro^^H-l ^^-triazol^-y phenyllcarbonylJ-e-ie- methylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

2-[(1 R_>6S)-3-{[4-Fluoro-2-(2H-1 _>2_>3-triazol-2-yl)phenyl]carbonyl}-3_>8- diazabicyclo[4.2.0]oct-8-yl]quinoxaline;

2-[(1 R_>6S)-3-{[3-Fluoro-2-(2H-1 _>2_>3-triazol-2-yl)phenyl]carbonyl}-3_>8- diazabicyclo[4.2.0]oct-8-yl]quinoxaline; 2-[(1 R_>6S)-3-{[2-Fluoro-6-(2H-1 _>2_J3-triazol-2-yl)phenyl]carbonyl}-3_>8- diazabicyclo[4.2.0]oct-8-yl]quinoxaline;

2-[(1 R_>6S)-3-{[5-Fluoro-2-(2H-1 _>2_>3-triazol-2-yl)phenyl]carbonyl}-3_>8- diazabicyclo[4.2.0]oct-8-yl]quinoxaline;

5-Chloro-2-[(1 R,6S)-3-{[2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-3,8- diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole;

5-Chloro-2-[(1 R,6S)-3-{[2-fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-3,8- diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole;

5-Chloro-2-[(1 R,6S)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-3,8- diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole;

5-Chloro-2-[(1 R_>6S)-3-{[4-fluoro-2-(2H-1 _>2_>3-triazol-2-yl)phenyl]carbonyl}-3_>8- diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole;

5-Chloro-2-[(1 R,6S)-3-{[3-fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-3,8- diazabicyclo[4.2.0]oct-8-yl]-1 ,3-benzoxazole;

(1 R,6S)-3-{[2-Fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(6- methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(6-Methylpyridin-2-yl)-3-{[2-(2H-1 ,2,3-thazol-2-yl)phenyl]carbonyl}- 3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(6- methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(4- methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[5-fluoro-2-(2H-1 ,2,3-thazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-[6-

(thfluoromethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-[4-

(thfluoromethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(5- methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

4-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]oct-3- yl]carbonyl}-1 ,8-naphthyridine; (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-2-(1 H-pyrazol-1 - yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methoxy-2-(2H-1 ,2,3-tnazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-methoxy-2-methylpynmidin-4- yl)carbonyl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(3-phenylpyrazin-2-yl)carbonyl]-3,8- diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-2-(1 H-1 ,2,3-triazol-1 - yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(4- methylpyridin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-[4-

(trifluoronnethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

N,N-Dimethyl-2-[(1 R,6S)-3-{[3-methyl-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-

3,8-diazabicyclo[4.2.0]oct-8-yl]pyridin-4-annine;

2-[(^,65)-3-{[4-Μθίήοχν-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03^οηνΙ}-3,8- diazabicyclo[4.2.0]oct-8-yl]-N,N-dinnethylpyndin-4-annine;

2-{(1 R,6S)-3-[(3-Fluoro-2-pyrimidin-2-ylphenyl)carbonyl]-3,8- diazabicyclo[4.2.0]oct-8-yl}-N,N-dinnethylpyndin-4-annine;

2-[(^,65)-3-{[3-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2.0]oct-8-yl]-N,N-dinnethylpyndin-4-annine;

(1 R,6S)-3-{[3-Fluoro-2-(2H-1 ^.S-triazol^-y phenyllcarbonylJ-S-K-

(trifluoronnethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[4-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-[4-

(trifluoronnethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-8-[4- (trifluoronnethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[3-fluoro-2-(2H-1 ,2,3-tnazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane; (1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[4-methoxy-2-(2H-1 ,2,3-tnazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

2-[(1 R,6S)-3-{[5-Methoxy-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-3,8- diazabicyclo[4.2.0]oct-8-yl]-N,N-dinnethylpyndin-4-annine;

(1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-{[5-methoxy-2-(2H-1 ,2,3-triazol-2- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-[(3-Fluoro-2-pyrimidin-2-ylphenyl)carbonyl]-8-[4-

(trifluoronnethyl)pyndin-2-yl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyridin-2-yl)-3-[(3-fluoro-2-pynmidin-2- ylphenyl)carbonyl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-[(6-Bromo-2-fluoro-3-methoxyphenyl)carbonyl]-8-(4,6- dimethylpyrinnidin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-fluoro-2-(1 H-pyrazol-1 - yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(2-fluoro-3-methoxy-6-pynmidin-2- ylphenyl)carbonyl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5,6-dimethyl-2-(2H-1 ,2,3-tnazol-2- yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5,6-dimethyl-2-(1 H-1 ,2,3-triazol-1 - yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(1 H-1 ,2,3-triazol-1 -yl)-6-

(trifluoronnethyl)pyndin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(2H-1 ,2,3-tnazol-2- yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-methyl-2-(1 H-1 ,2,3-triazol-1 - yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[6-methoxy-2-(2H-1 ,2,3-tnazol-2- yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[6-methoxy-2-(1 H-1 ,2,3-triazol-1 - yl)pyridin-3-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-[(2-Bromo-5-fluorophenyl)carbonyl]-8-(4,6-dimethylpyrimidin-2-yl)-

3,8-diazabicyclo[4.2.0]octane; (1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-fluoro-2-pynmidin-5- ylphenyl)carbonyl]-3,8-diazabicyclo[4.2.0]octane;

5-(2-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]oct-3- yl]carbonyl}-4-fluorophenyl)-N,N-dinnethylpyndin-2-annine;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-(9H-fluoren-4-ylcarbonyl)-3,8- diazabicyclo[4.2.0]octane;

4-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]oct-3- yl]carbonyl}-9H-fluoren-9-one;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(3-methyl-1 ,2,4-oxadiazol-5- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-({5-fluoro-2-[1 -(tetrahydro-2H-pyran-2- yl)-1 H-pyrazol-5-yl]phenyl}carbonyl)-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-fluoro-2-(1 H-pyrazol-5- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[2-(1 H-1 ,2,4-triazol-5- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-(4-fluorophenyl)-2-methyl-1 ,3- thiazol-4-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-phenyl-1 H-pyrazol-4-yl)carbonyl]- 3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-methyl-3-phenylisoxazol-4- yl)carbonyl]-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(5-phenylisoxazol-4-yl)carbonyl]-3,8- diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-(2-fluorophenyl)-1 ,3-oxazol-4- yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-3-{[5-(3-Chlorophenyl)-1 ,3-oxazol-4-yl]carbonyl}-8-(4,6- dimethylpyrinnidin-2-yl)-3,8-diazabicyclo[4.2.0]octane;

4'-{[(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]oct-3- yl]carbonyl}-3',5-dinnethyl-3,5'-biisoxazole;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-methyl-5-(4-methyl-1 ,2,3- thiadiazol-5-yl)isoxazol-4-yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane; (1 R,6S)-3-[(3-Bromopyridin-2-yl)carbonyl]-8-(4,6-dimethylpynmidin-2-yl)-3,8- diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-(1 H-1 ,2,3-triazol-1 -yl)pyridin-2- yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-(2H-1 ,2,3-triazol-2-yl)pyridin-2- yl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[3-fluoro-2-(1 H-pyrazol-3- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-[(3-fluoro-2-pynmidin-2- ylphenyl)carbonyl]-3,8-diazabicyclo[4.2.0]octane;

4-[(^,65)-3-{[5-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2.0]oct-8-yl]-6-methylpyrinnidin-2-annine;

4-[(^,65)-3-{[5-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2 ]oct-8-yl]-N,6-dimethylpynmidin-2-amine;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-{[5-fluoro-2-(1 -methyl-1 H-pyrazol-3- yl)phenyl]carbonyl}-3,8-diazabicyclo[4.2.0]octane;

6-[(^,65)-3-{[5-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2 ]oct-8-yl]-N,N-dimethylpynmidin-4-amine;

6-[(^,65)-3-{[5-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2.0]oct-8-yl]-N-methylpyrinnidin-4-annine;

6-[(^,65)-3-{[5-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2.0]oct-8-yl]-2-methylpyrinnidin-4-annine;

6-[(^,65)-3-{[5-ΡΙυθΓθ-2-(2Η-1 ,2,3-ίπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-3,8- diazabicyclo[4.2.0]oct-8-yl]pyrinnidine-2,4-diannine;

(1 R,6S)-3-{[5-Fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}-8-(6- methylpyrinnidin-4-yl)-3,8-diazabicyclo[4.2.0]octane;

N-Cyclopropyl-6-[(1 R,6S)-3-{[5-fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl]carbonyl}- 3,8-diazabicyclo[4.2.0]oct-8-yl]pyrinnidin-4-annine;

(5-methyl-2-(trifluoromethyl)phenyl)((1 R,6S)-8-(2-phenylpyrimidin-4-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

((1 R,6S)-8-(2-phenylpyrimidin-4-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(2- (1 ,1 ,2,2-tetrafluoroethoxy)phenyl)nnethanone; (5-methyl-3-phenylisoxazol-4-yl)((1 R,6S)-8-(2-phenylpyrimidin-4-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl)nnethanone;

(2-(2H-1 ,2,3-triazol-2-yl)phenyl)((1 R,6S)-8-(5,6-dimethylpyrazin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

((1 R,6S)-8-(5,6-dimethylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(2- fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl)methanone;

((1 R,6S)-8-(5,6-dimethylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(2H-1 ,2,3-triazol-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- propoxypyridin-2-yl)nnethanone;

(3-propoxypyridin-2-yl)((1 R,6S)-8-(5-(tnfluoromethyl)pynmidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(3-propoxypyridin-2-yl)((1 R,6S)-8-(5-(tnfluoromethyl)pyndin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(3-Propoxypyridin-2-yl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(2,6-dimethoxyphenyl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8-diazabicyclo[4.2.0]octan-

3-yl)methanone;

(2,6-Dimethoxyphenyl)((1 R,6S)-8-(5-(trifluoromethyl)pyndin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(2,6-Dimethoxyphenyl)((1 R,6S)-8-(5-(trifluoromethyl)pynmidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(2,6-Dimethoxyphenyl)((1 R,6S)-8-(4,6-dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone; ((1 R,6S)-8-(4,6-Dimethylpynmidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- methylfuran-2-yl)methanone;

(3-Methylfuran-2-yl)((1 R,6S)-8-(5-(trifluoromethyl)pynmidin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(3-Methylfuran-2-yl)((1 R,6S)-8-(5-(trifluoromethyl)pyndin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(3-Methylfuran-2-yl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3- yl)methanone;

2-((1 R,6S)-3-([1 ,1 '-Biphenyl]-2-ylsulfonyl)-3,8-diazabicyclo[4.2.0]octan-8- yl)quinoxaline;

(1 R,6S)-3-([1 ,1 '-Biphenyl]-2-ylsulfonyl)-8-(5-(trifluoromethyl)pyndin-2-yl)-3,8- diazabicyclo[4.2.0]octane;

(1 R,6S)-3-([1 ,1 '-Biphenyl]-2-ylsulfonyl)-8-(5-(trifluoromethyl)pynmidin-2-yl)-^ diazabicyclo[4.2.0]octane;

(1 R,6S)-3-([1 ,1 '-Biphenyl]-2-ylsulfonyl)-8-(4,6-dimethylpyrimidin-2-yl)-3,8- diazabicyclo[4.2.0]octane;

(1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3-((2-methoxyphenyl)sulfonyl)-3,8- diazabicyclo[4.2.0]octane;

(1 R,6S)-3-((2-Methoxyphenyl)sulfonyl)-8-(5-(trifluoromethyl)pynmidin-2-yl)^^ diazabicyclo[4.2.0]octane;

(1 R,6S)-3-((2-Methoxyphenyl)sulfonyl)-8-(5-(trifluoromethyl)pyridin-2-yl)-3 diazabicyclo[4.2.0]octane;

2-((1 R,6S)-3-((2-Methoxyphenyl)sulfonyl)-3,8-diazabicyclo[4.2.0]octan-8- yl)quinoxaline;

(3,6'-Dimethyl-[2,3'-bipyridin]-2'-yl)((1 R,6S)-8-(quinoxalin-2-yl)-3,8- diazabicyclo[4.2.0]octan-3-yl)methanone;

(3,6'-Dimethyl-[2,3'-bipyridin]-2'-yl)^

3,8-diazabicyclo[4.2.0]octan-3-yl)nnethanone;

(3,6'-Dimethyl-[2,3'-bipyridin]-2'-yl)((1 R,6S)-8-(5-(tnfluoromethyl)pynmidin 3,8-diazabicyclo[4.2.0]octan-3-yl)methanone;

(3,6'-Dimethyl-[2,3'-bipyridin]-2'-yl)((1 R,6S)-8-(4,6-dimethylpynmidin-2-yl)-3,8 diazabicyclo[4.2.0]octan-3-yl)methanone; ((1 R,6S)-8-(5,6-Dimethylpyrazin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(2- fluoro-6-(2H-1 ,2,3-triazol-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-iodophenyl)methanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(oxazol-2-yl)phenyl)methanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(pyridin-2-yl)phenyl)nnethanone;

(2-(3-Chloropyridin-2-yl)-3-fluorophenyl)((1 R,6S)-8-(4,6-dimethylpyrimidin-2-y 3,8-diazabicyclo[4.2.0]octan-3-yl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(3-methylpyridin-2-yl)phenyl)methanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(6-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(4-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(5-methylpyridin-2-yl)phenyl)nnethanone;

((1 R₎6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(3-fluoropyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(6-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(4-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(5-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(3-fluoropyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(pyridin-2-yl)phenyl)nnethanone; ((1 R,6S)-8-(4,6-Dimethylpynmidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(5- fluoro-2-(oxazol-2-yl)phenyl)methanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(6-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(4-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(5-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(3-fluoropyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(pyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(oxazol-2-yl)phenyl)methanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(6-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(4-methylpyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(3-fluoropyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(pyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(oxazol-2-yl)phenyl)methanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(6- fluoro-2-(4-methylpyridin-2-yl)phenyl)nnethanone; ((1 R,6S)-8-(4,6-Dimethylpynmidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(4- fluoro-2-(3-fluoropyridin-2-yl)phenyl)nnethanone;

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(3-fluoropyridin-2-yl)phenyl)nnethanone;

(^,65)-3-{[2-(2Η-1 ,2,3-Τπ3ζοΙ-2-νΙ)ρήθηνΙ]03 οηνΙ}-8-(4,5,6- trinnethylpynnnidin-2-yl)-3,8-diazabicyclo[4.2.0]octane ; and

((1 R,6S)-8-(4,6-Dimethylpyrimidin-2-yl)-3,8-diazabicyclo[4.2.0]octan-3-yl)(3- fluoro-2-(oxazol-2-yl)phenyl)methanone.

21 . A pharmaceutical composition for treating a disease, disorder or medical condition mediated by orexin activity comprising:

(a) an effective amount of at least one chemical entity selected from compounds of Formula (I):

wherein:

n is 0-1 ;

R is a member selected from the group consisting of:

A) phenyl substituted or unsubstituted with one or two R^a members

,b.

and substituted in the ortho position with R R^a is independently selected from the group consisting of: halo, -Ci- 4alkyl, and -Ci_-4alkoxy, wherein two adjacent R^a members may come together to form a six membered aromatic ring;

R^b is a member selected from the group consisting of:

a) halo, -Ci_-4alkoxy, -CF₃, or -CF₂CHF₂;

b) 5-membered heteroaryl ring containing one oxygen or one sulfur members;

tetrahydropyran-2-yl, or -N(CH₃)₂; and

d) phenyl substituted or unsubstituted with -F, or -CH₃;

R^c is a member independently selected from the group consisting of:

-Ci_-4alkyl, -CF₃, and -Ci_-4alkoxy,

R^d is a member selected from the group consisting of:

a) 5-6 membered heteroaryl ring selected from the group

b) -CF₃, -Br, or -Ci_-4alkoxy;

C) 6-membered heteroaryl ring selected from the group consisting of: pyrimidin-yl and pyrazin-yl, substituted or unsubstituted with a member independently selected from -CH₃, -OCH₃, or phenyl;

E) 3-methylfuran-2-yl, 9H-fluorene, 9H-fluoren-9-one, 3,5'-biisoxazole,

[3-methyl-5-(4-methyl-1 ,2,3-thiadiazol-5-yl)isoxazol-4-yl], or naphthyridine;

member selected from the group consisting of: A) 6-membered heteroaryl ring containing two nitrogen members substituted or unsubstituted with one or more members

independently selected from the group consisting of: halo, -Ci- alkyl, -Ci_-4alkoxy, -CF₃, -NH₂, -NHCH₃, -N(Ci_-4alkyl)i_-2, -NHcyclopropyl, and phenyl;

B) pyridine substituted or unsubstituted with one or two members

independently selected from the group consisting of: -Ci- alkyl, -N(d. 4alkyl)₂, and -CF₃; and

C) quinoxalin-2-yl, benzooxazol-2-yl, or 5-chloro-1 ,3-benzoxazole;

and pharmaceutically acceptable salts of compounds of Formula (I); and

(b) at least one pharmaceutically acceptable excipient.

22. A pharmaceutical composition comprising and effective amount of at least one chemical entity of claim 20, and at least one pharmaceutically acceptable excipient.

23. A method of treating a subject suffering from or diagnosed with a disease, disorder, or medical condition mediated by orexin receptor activity, comprising administering to a subject in need of such treatment an effective amount of at least one chemical entity selected from compounds of Formula (I)

wherein:

n is 0-1 ;

R¹ is a member selected from the group consisting of:

R^b is a member selected from the group consisting of: a) halo, -Ci_-4alkoxy, -CF₃, or -CF₂CHF₂;

b) 5-nnennbered heteroaryl ring containing one oxygen or one sulfur members;

tetrahydropyran-2-yl, or -N(CH₃)₂; and

d) phenyl substituted or unsubstituted with -F, or -CH₃;

B) pyridine substituted or unsubstituted with one or two R^c members and substituted with R^d, wherein R^d is positioned adjacent to the point of attachment by R¹;

R^c is a member independently selected from the group

consisting of: -Ci_-4alkyl, -CF₃, and -Ci_-4alkoxy,

R^d is a member selected from the group consisting of:

a) 5-6 membered heteroaryl ring selected from the group

b) -CF₃, -Br, or -Ci_-4alkoxy;

D) 5-membered heteroaryl ring selected from the group consisting of:

2-methyl-1 ,3-thiazol-yl, 5-methyl-isoxazol-4-yl, 2H-pyrazol-3-yl, 1 H- pyrazol-4-yl, isoxazolyl, and 1 ,3-oxazol-4-yl, each substituted with phenyl substituted or unsubstituted with -F or -CI; and

E) 3-methylfuran-2-yl, 9H-fluorene, 9H-fluoren-9-one, 3,5'-biisoxazole,

[3-methyl-5-(4-methyl-1 ,2,3-thiadiazol-5-yl)isoxazol-4-yl], or naphthyridine;

member selected from the group consisting of:

A) 6-membered heteroaryl ring containing two nitrogen members

substituted or unsubstituted with one or more members

independently selected from the group consisting of: halo, -Ci_-4alkyl, -Ci_-4alkoxy, -CF₃, -NH₂, -NHCH₃, -N(Ci_-4alkyl)i_-2, -NHcyclopropyl, and phenyl;

B) pyridine substituted or unsubstituted with one or two members

independently selected from the group consisting of -Ci_-4alkyl, - N(Ci_-4alkyl)₂, or -CF₃; and

C) quinoxalin-2-yl, benzooxazol-2-yl, or 5-chloro-1 ,3-benzoxazole;

and pharmaceutically acceptable salts of compounds of Formula (I), and at least one pharmaceutically acceptable excipient. 24. A method according to Claim 23, wherein the disease, disorder, or medical condition is selected from the group consisting of: disorders of the sleep-wake cycle, insomnia, restless legs syndrome, jet-lag, disturbed sleep, sleep disorders secondary to neurological disorders, manias, depressions, manic depression, schizophrenia, pain syndromes, fibromyalgia, neuropathic pain , catatonia, Parkinson's disease, Tourette's syndrome, anxiety, delirium, dementias, overweight or obesity and conditions related to overweight or obesity, insulin resistance, type II diabetes, hyperlipidemia, gallstones, angina, hypertension, breathlessness, tachycardia, infertility, sleep apnea, back and joint pain, varicose veins, osteoarthritis, hypertension, tachycardia, arrhythmias, angina pectoris, acute heart failure, ulcers, irritable bowel syndrome, diarrhea and gastroesophageal reflux.

25. A method according to Claim 23, wherein the disease, disorder, or medical condition is insomnia.