NZ615014B2 - Morpholine-spirocyclic piperidine amides as modulators of ion channels - Google Patents

Abstract

Disclosed are 1'-benzoyl-spiro[morpholine-2,4'-piperidine] derivatives and analogues as represented by the general formula (I) wherein the substituents are as defined herein. Representative compounds include 1'-(4-(3-hydroxypentan-3-yl)-3-methylbenzoyl)-4-(pyrimidin-2-yl)-6-ethyl-spiro[morpholine-2,4'-piperidine], 1'-(4-isopropoxy-3-methylbenzoyl)-4-(benzyl)-6-hydroxyethyl-spiro[morpholine-2,4'-piperidine], 1'-(4-(cyclopropyl(hydroxy)methyl)-benzoyl)-4-(2,2,2-trifluoroethyl)-6-phenyl-spiro[morpholine-2,4'-piperidine], 1'-(4-(isopropoxy)-3-methylbenzoyl)-4-(2-butyn-1-yl)-6-(2-fluoroethyl)-spiro[morpholine-2,4'-piperidine]. Also disclosed is a pharmaceutical composition comprising a compound as defined above and a pharmaceutically acceptable carrier, for inhibiting a voltage gated sodium ion channel, and for treating or lessening the severity of a condition selected from acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, herpatic neuralgia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, psychiatric disorders, anxiety, depression, dipolar disorder, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, cancer pain, stroke, cerebral ischemia, traumatic brain injury, amyotrophic lateral sclerosis, stress- or exercise induced angina, palpitations, hypertension, migraine, and abnormal gastro-intestinal motility. ,4'-piperidine], 1'-(4-isopropoxy-3-methylbenzoyl)-4-(benzyl)-6-hydroxyethyl-spiro[morpholine-2,4'-piperidine], 1'-(4-(cyclopropyl(hydroxy)methyl)-benzoyl)-4-(2,2,2-trifluoroethyl)-6-phenyl-spiro[morpholine-2,4'-piperidine], 1'-(4-(isopropoxy)-3-methylbenzoyl)-4-(2-butyn-1-yl)-6-(2-fluoroethyl)-spiro[morpholine-2,4'-piperidine]. Also disclosed is a pharmaceutical composition comprising a compound as defined above and a pharmaceutically acceptable carrier, for inhibiting a voltage gated sodium ion channel, and for treating or lessening the severity of a condition selected from acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, herpatic neuralgia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, psychiatric disorders, anxiety, depression, dipolar disorder, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, cancer pain, stroke, cerebral ischemia, traumatic brain injury, amyotrophic lateral sclerosis, stress- or exercise induced angina, palpitations, hypertension, migraine, and abnormal gastro-intestinal motility.

Description

MORPHOLINE-SPIROCYCLIC PIPERIDINE AMIDES AS MODULATORS OF ION CHANNELS CROSS REFERENCE TO RELATED ATIONS This application claims priority to United States provisional patent application serial numbers 61/452,538, filed March 14, 2011, and 61/567,809, filed er 7, 2011, the entire ts of all applications are incorporated herein by reference.

TECHNICAL FIELD OF THE INVENTION The ion relates to compounds useful as inhibitors of ion channels.

The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders.

BACKGROUND OF THE INVENTION Pain is a protective ism that allows healthy animals to avoid tissue damage and to prevent further damage to injured tissue. Nonetheless there are many conditions where pain persists beyond its usefulness, or where patients would benefit from inhibition of pain. Voltage-gated sodium channels are believed to play a critical role in pain signaling. This belief is based on the known roles of these channels in normal physiology, pathological states g from mutations in sodium channel genes, nical work in animal models of disease, and the clinical usefulness of known sodium channel modulating agents (Cummins, T. R., Sheets, P.

L., and Waxman, S. G., The roles of sodium channels in nociception: Implications for mechanisms of pain. Pain 131 (3), 243 ; England, 8., Voltage-gated sodium channels: the search for subtype-selective sics. Expert Opin Investig Drugs 17 (12), 1849 (2008); Krafte, D. S. and Bannon, A. W., Sodium channels and nociception: recent concepts and therapeutic opportunities. Curr Opin col 8 (1), 50 (2008)).

Voltage-gated sodium channels (NaV’s) are key biological mediators of electrical ing. NaV’s are the primary mediators of the rapid upstroke of the action potential ofmany excitable cell types (6.g. neurons, skeletal myocytes, cardiac 2012/028882 myocytes), and thus are critical for the initiation of signaling in those cells (Hille, , Ion Channels ofExcitable Membranes, Third ed. (Sinauer ates, Inc., Sunderland, MA, 2001)). Because of the role NaV’s play in the initiation and propagation of neuronal signals, antagonists that reduce NaV currents can prevent or reduce neural signaling. Thus NaV channels are considered likely targets in pathologic states where reduced excitability is predicted to alleviate the clinical symptoms, such as pain, epilepsy, and some cardiac hmias (Chahine, M., Chatelier, A., Babich, 0., and Krupp, J. 1., Voltage—gated sodium channels in neurological disorders. CNS Neural Dl'sora’ Drug Targets 7 (2), 144 (2008)).

[005] The NaV’s form a subfamily of the voltage-gated ion Channel super— family and comprises 9 ms, designated NaV 1.1 — NaV 1.9. The tissue localizations of the nine isoforms vary greatly. NaV 1.4 is the primary sodium channel of skeletal muscle, and NaV 1.5 is primary sodium channel of cardiac myocytes. NaV’s 1.7, 1.8 and 1.9 are primarily localized to the peripheral nervous system, while NaV’s 1.1, 1.2, 1.3, and 1.6 are al channels found in both the central and peripheral nervous systems. The onal behaviors of the nine isoforms are r but distinct in the specifics of their voltage—dependent and kinetic behavior (Catterall, W. A., Goldin, A. L., and Waxman, S. G., International Union of Pharmacology. XLVII.

Nomenclature and structure—function relationships of voltage-gated sodium channels. col Rev 57 (4), 397 ).

NaV channels have been identified as the primary target for some ally useful pharmaceutical agents that reduce pain (Cummins, T. R., Sheets, P. L., and Waxman, S. G., The roles of sodium channels in nociception: Implications for mechanisms of pain. Pain 131 (3), 243 (2007)). The local anesthetic drugs such as lidocaine block pain by inhibiting NaV channels. These nds provide excellent local pain reduction but suffer the drawback of abolishing normal acute pain and sensory inputs. Systemic administration of these compounds results in dose limiting side effects that are generally ascribed to block of neural channels in the CNS (nausea, sedation, confusion, ataxia). Cardiac side effects can also occur, and indeed these compounds are also used as class 1 anti-arrhythmics, ably due to block of NaV1.5 channels in the heart. Other nds that have proven effective at reducing pain have also been suggested to act by sodium channel blockade ing carbamazepine, lamotragine, and tricyclic antidepressants palm, B., Anticonvulsants: aspects of their mechanisms of action. Eur J Pain 6 Suppl A, 3 (2002); Wang, G. K., Mitchell, J ., and Wang, S. Y., Block of persistent late NaJr currents by antidepressant sertraline and paroxetine. JMembr Biol 222 (2), 79 (2008)).

These compounds are likewise dose limited by adverse effects similar to those seen with the local anesthetics. Antagonists that specifically block only the m(s) critical for nocioception are expected to have increased efficacy since the reduction of adverse s caused by block of off-target channels should enable higher dosing and thus more complete block of target ls isoforms.

Four NaV isoforms, NaV 1.3, 1.7, 1.8, and 1.9, have been specifically indicated as likely pain targets. NaV 1.3 is normally found in the pain sensing neurons of the dorsal root ganglia (DRG) only early in pment and is lost soon after birth both in humans and in s. Nonetheless, nerve damaging injuries have been found to result in a return of the NaV 1.3 channels to DRG neurons and this may contribute to the abnormal pain signaling in various chronic pain conditions resulting from nerve damage (neuropathic pain). These data have led to the suggestion that pharmaceutical block of NaV 1.3 could be an effective treatment for neuropathic pain. In opposition to this idea, global genetic knockout of NaV 1.3 in mice does not t the development of allodynia in mouse models of neuropathic pain (Nassar, M. A. et al., Nerve injury induces robust allodynia and ectopic discharges in NaV 1.3 null mutant mice. M01 Pain 2, 33 (2006)). It remains unknown whether compensatory changes in other channels allow for normal neuropathic pain in NaV 1.3 knockout mice, though it has been reported that knockout of NaV 1.1 results in drastic upregulation ofNaV 1.3.

The converse effect in NaV 1.3 knockouts might explain these results.

NaV 1.7, 1.8, and 1.9 are highly expressed in DRG neurons, including the neurons whose axons make up the C—fibers and A8 nerve fibers that are believed to carry most pain s from the nocioceptive terminals to the central nervous. Like NaV 1.3, NaV 1.7 expression increases after nerve injury and may contribute to neuropathic pain states. The zation of NaV 1.7, 1.8, and 1.9 in nocioceptors led to the hypothesis that reducing the sodium currents through these channels might ate pain. Indeed, specific interventions that reduce the levels of these channels have proven effective in animal models of pain.

Specific reduction ofNaV 1.7 in rodents by multiple different techniques has resulted in the reduction of observable pain behaviors in model animals.

Injection of a viral antisense NaV 1.7 cDNA construct greatly reduces normal pain responses due to inflammation or mechanical injury (Yeomans, D. C. et al., Decrease in inflammatory hyperalgesia by herpes —mediated knockdown of.NaV 1.7 sodium channels in primary afferents. Hum Gene Ther 16 (2), 271 (2005)). Likewise, a genetic knockout ofNaV 1.7 in a subset of ptor neurons reduced acute and inflammatory pain in mouse models (Nassar, M. A. et al., Nociceptor—specific gene deletion reveals a major role for NaV 1.7 (PNl) in acute and inflammatory pain. Proc Natl Acad Sci USA 101 (34), 12706 (2004)). Global knockouts ofNaV 1.7 in mice lead to animals that die on the first day after birth. These mice fail to feed and this is the presumed cause of death.

[0010] Treatments that specifically reduce NaV 1.8 channels in rodent models effectively reduce pain sensitivity. Knockdown ofNaV 1.8 in rats by intrathecal injection of antisense oligodeoxynucleotides reduces neuropathic pain behaviors, while leaving acute pain sensation intact (Lai, J. et al., Inhibition of athic pain by decreased expression of the tetrodotoxin—resistant sodium channel, NaV1.8. Pain 95 (1-2), 143 (2002); Porreca, F. et al., A comparison of the ial role of the tetrodotoxin-insensitive sodium channels, PN3/SNS and NaN/SNS2, in rat models of chronic pain. Proc Natl Acad Sci U S A 96 (14), 7640 (1999)). Global genetic knockout ofNaV 1.8 in mice or specific destruction of NaV 1.8 expressing neurons greatly reduces perception of acute mechanical, inflammatory, and visceral pain (Akopian, A. N. et al., The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways. Nat ci 2 (6), 541 ; Abrahamsen, B. et al., The cell and molecular basis of ical, cold, and inflammatory pain.

Science 321 (5889), 702 (2008); Laird, J. M., Souslova, V., Wood, I. N., and o, F., Deficits in visceral pain and ed hyperalgesia in NaV 1.8 (SNS/PN3)-null mice.

J Neurosci 22 (19), 8352 ). In contrast to the antisense experiments in rats, genetic knockout mice appear to develop neuropathic pain behaviors normally after nerve injury (Lai, J. et a1., Inhibition of neuropathic pain by decreased expression of the tetrodotoxin-resistant sodium channel, NaVl .8. Pain 95 (1-2), 143 (2002); Akopian, A. N. et al., The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways. Nat Neurosci 2 (6), 541 ; Abrahamsen, B. et a1., The cell and molecular basis of mechanical, cold, and inflammatory pain. Science 321 (5889), 702 (2008); Laird, J. M., Souslova, V., Wood, J. N., and Cervero, F., s in visceral pain and ed hyperalgesia in NaV 1.8 (SNS/PN3)—nu11 mice. J Neurosci 22 (19), 8352 (2002)).

NaV 1.9 global knock out mice have sed sensitivity to inflammation d pain, despite normal acute, and neuropathic pain behaviors (Amaya, F. et al., The voltage-gated sodium channel .9 is an effector of peripheral inflammatory pain hypersensitivity. J ci 26 (50), 12852 (2006); Priest, B. T. et a1., Contribution of the tetrodotoxin-resistant voltage-gated sodium channel NaV1.9 to sensory transmission and nociceptive behavior. Proc Natl Acad Sci USA 102 (26), 9382 (2005)). Spinal knockdown ofNaV 1.9 had no apparent effect on pain behavior in rats (Porreca, F. et al., A comparison of the potential role of the tetrodotoxin-insensitive sodium channels, PN3/SNS and NaN/SNSZ, in rat models of chronic pain. Proc Natl Acad Sci US A 96 (14), 7640 (1999)).

The understanding of the role of NaV channels in human physiology and pathology has been greatly advanced by the discovery and analysis of naturally occurring human mutations. NaV 1.1 and NaV 1.2 mutations result in various forms of epilepsy (Fujiwara, T., Clinical spectrum of mutations in SCNlA gene: severe nic sy in infancy and related epilepsies. Epilepsy Res 70 Suppl 1, S223 (2006); George, A. L., Jr., Inherited disorders of voltage-gated sodium channels. J Clin Invest 115 (8), 1990 ; Misra, S. N., , K. M., and George, A. L., Jr., Impaired NaV1.2 function and d cell surface expression in benign familial neonatal-infantile es. Epilepsia 49 (9), 1535 (2008)). Mutations of the NaV 1.4 cause muscular disorders like paramyotonia congenital (Vicart, S., Sternberg, D., Fontaine, B., and Meola, G., Human skeletal muscle sodium channelopathies. Neurol Sci 26 (4), 194 (2005)). NaV 1.5 mutations result in cardiac abnormalities like Brugada Syndrome and long QT syndrome (Bennett, P. B., Yazawa, K., Makita, N., and George, A. L., Jr., Molecular mechanism for an inherited cardiac arrhythmia.

Nature 376 , 683 (1995); Darbar, D. et al., Cardiac sodium channel (SCNSA) ts associated with atrial ation. Circulation 117 (15), 1927 (2008); Wang, Q. et al., SCNSA mutations associated with an inherited cardiac hmia, long QT syndrome. Cell 80 (5), 805 (1995)).

Recent discoveries have demonstrated that mutations in the gene that encodes the NaV 1.7 channel (SCN9A) can cause both ed and reduced pain syndromes. Work by Waxman’s group and others have identified at least 15 mutations that result in enhanced current through NaV 1.7 and are linked to dominant congenital pain syndromes. Mutations that lower the threshold for NaV 1.7 tion cause inherited erythromelalgia (IEM). lEM patients exhibit abnormal burning pain in their extremities. Mutations that interfere with the normal inactivation properties ofNaV 1.7 lead to prolonged sodium currents and cause paroxysmal extreme pain er (PEPD). PEPD patients exhibit periocular, perimandibular, and rectal pain symptoms that progresses throughout life (Drenth, J. P. et al., SCN9A mutations define primary erytherrnalgia as a neuropathic disorder of voltage gated sodium channels. J Invest Dermatol 124 (6), 1333 (2005); Estacion, M. et al., NaV 1.7 gain-of—function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder ons and produces symptoms of both disorders. JNeurosci 28 (43), 11079 (2008)).

NaV 1.7 null ons in human patients were recently described by several groups (Ahmad, S. et al., A stop codon mutation in SCN9A causes lack of pain ion. Hum Mol Genet 16 (17), 2114 (2007); Cox, J. J. et al., An SCN9A channelopathy causes congenital inability to ence pain. Nature 444 (7121), 894 (2006); Goldberg, Y. P. et al., f—function mutations in the NaV 1.7 gene underlie congenital erence to pain in multiple human populations. Clin Genet 71 (4), 311 (2007)). In all cases patients exhibit congenital indifference to pain. These patients report no pain under any circumstances. Many of these patients suffer dire injuries early in childhood since they do not have the protective, normal pain that helps to prevent tissue damage and develop appropriate protective behaviors. Aside from the striking loss of pain sensation and reduced or absent of smell (Goldberg, Y. P. et al., Loss-of—function mutations in the NaV 1.7 gene underlie congenital indifference to pain in multiple human populations. Clin Genet 71 (4), 311 (2007)), these patients appear completely normal. Despite the normally high expression ofNaV 1.7 in sympathetic neurons (Toledo-Aral, J. J. et al., Identification of PNl, a predominant voltage-dependent sodium channel expressed pally in peripheral neurons. Proc Natl Acad Sci U S A 94 (4), 1527 (1997)) and adrenal chromatin cells (Klugbauer, N., Lacinova, L., Flockerzi, V., and Hofmann, F., Structure and functional expression of a new member of the tetrodotoxin-sensitive voltage—activated sodium channel family from human neuroendocrine cells. EMBO J 14 (6), 1.084 (1995)), these NaV 1.7-null patients show no sign of neuroendocrine or sympathetic nervous dysfunction.

The gain of NaV 1.7 function ons that cause pain, coupled with the loss of NaV 1.7 function mutations that abolish pain, provide strong evidence that NaV 1.7 plays an important role in human pain signaling. The relative good health of NaV 1.7-null patients indicates that ablation of NaV 1.7 is well tolerated in these patients. unately, the efficacy of currently used sodium l blockers for the disease states described above has been to a large extent limited by a number of side effects. These side effects e various CNS disturbances such as blurred vision, dizziness, nausea, and on as well more potentially life threatening cardiac arrhythmias and cardiac failure. Accordingly, there remains a need to develop additional Na l nists, ably those with higher potency and fewer side effects, SUMMARY OF THE INVENTION It has now been found that compounds of this invention, and pharmaceutically able compositions thereof, are useful as inhibitors of voltage— gated sodium channels. These compounds have the general formula I: 2012/028882 (R1 >n 2 /\ /R p N —(R3)o or a pharmaceutically acceptable salt thereof.

These compounds and ceutically acceptable compositions are useful for treating or lessening the severity of a variety of diseases, disorders, or ions, including, but not limited to, acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, inal neuralgia, herpetic gia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, psychiatric disorders such as anxiety and depression, myotonia, hmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, or cancer pain.

DETAILED DESCRIPTION OF THE INVENTION In one aspect, the ion provides compounds of formula I: (“N/R2 —(R3)o or a pharmaceutically acceptable salt f, wherein, independently for each ence: R1 is C1-C6 alkyl, C1-C6 fluoroalkyl, C3-C8 cycloalkyl, halo, CN, NR8802R8, $02118, SR8, SOR8, NRSCOR“, NRSCOst, CON(R8)2, SOzN(R8)2, CF3, optionally substituted heterocycloalkyl, phenyl, heteroaryl, or a straight chain, branched, or cyclic (Cl -C8)-R9 wherein up to two CH2 units may be ed with O, CO, S, SO, 802, N, CR, or NR8, or two R1 taken er form an oxo group; R2 is H, C1-C6 alkyl, Cl-C6 fluoroalkyl, CF3, optionally substituted cycloalkyl, aryl, heteroaryl or cycloalkyl, COR8, COzRS, CON(R8)2, CF3, CHFZ, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, 802, N, CR, or NR8; R3 is Cl-C6 alkyl or halo; R8 is H, Cl-C6 alkyl, or C3-C8 cycloalkyl, a straight chain, branched, or cyclic (C1- C8)-R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, 80;, N, CF2, or NR, or 2 R8 taken together with the atoms to which they are attached form a ring; R9 is H, CF3, CHFZ, CHZF, COZR, OH, optionally substituted aryl, heteroaryl, C3-C8 cycloalkyl, heterocycloalkyl, N(R)2, NRCOR, CON(R)2, CN, or SOzR; R is H, C1-C6 alkyl, ally substituted aryl, heteroaryl, C3-C8 cycloalkyl, or heterocycloalkyl; A is an optionally substituted aryl, heteroaryl or heterocyclic; n is an integer from 0 to 4 ive; and o is an r from 0 to 4 inclusive.

In a further embodiment, R1 is C1-C6 alkyl, C1-C6 fluoroalkyl, C3-C8 cycloalkyl, CN, CON(R8)2, SO2N(R 8) 2, CF3, optionally substituted heterocycloalkyl, phenyl, heteroaryl, or a straight chain, ed, or cyclic (C1-C8)-R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8, or two R1 taken together form an oxo group.

For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75th Ed. Additionally, general ples of organic chemistry are described in "Organic Chemistry", Thomas Sorrell, University Science Books, Sausalito: 1999, and "March’s Advanced Organic Chemistry", 5th Ed., Ed.: Smith, M.B. and March, J., John Wiley & Sons, New York: 2001, the entire contents of which are hereby incorporated by nce.

As described , compounds of the invention can optionally be substituted with one or more substituents, such as are illustrated generally above, or as exemplified by ular classes, subclasses, and species of the invention. The phrase “optionally substituted” is used interchangeably with the phrase “substituted or unsubstituted.” As described herein, the variables R1-R9 in formula I ass specific groups, such as, for example, alkyl and aryl. Unless ise noted, each of the specific groups for the les R, R1-R9 can be optionally substituted with one or more substituents of halo, cyano, oxoalkoxy, hydroxy, amino, nitro, aryl, haloalkyl, and alkyl. For instance, an alkyl group can be optionally substituted with one or more of halo, cyano, oxoalkoxy, hydroxy, amino, nitro, aryl, haloalkyl, and alkyl. As an additional example, an aryl group can be optionally substituted with one or more of halo, cyano, alkoxy, hydroxy, nitro, haloalkyl, and alkyl. As one of ordinary skill in the art will recognize, combinations of substituents envisioned by this invention are those 2012/028882 combinations that result in the ion of stable or chemically feasible compounds.

The term e", as used , refers to compounds that are not substantially altered when subjected to conditions to allow for their production, detection, and preferably their recovery, purification, and use for one or more of the purposes disclosed herein.

In some embodiments, a stable compound or chemically le nd is one that is not substantially altered when kept at a temperature of40°C or less, in the absence of moisture or other chemically ve conditions, for at least a week. When two alkoxy groups are bound to the same atom or adjacent atoms, the two alkoxy groups can form a ring together with the atom(s) to which they are bound.

[0023] In general, the term “substituted,” whether preceded by the term “optionally” or not, refers to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent. Specific substituents are described above in the definitions and below in the description of compounds and examples thereof Unless otherwise indicated, an optionally substituted group can have a substituent at each tutable position of the group, and when more than one position in any given structure can be substituted with more than one substituent selected from a specified group, the substituent can be either the same or different at every position. A ring tuent, such as a heterocycloalkyl, can be bound to another ring, such as a cycloalkyl, to form a spiro—bicyclic ring system, e. g., both rings share one common atom. As one of ordinary skill in the art will recognize, combinations of substituents envisioned by this invention are those combinations that result in the formation of stable or chemically feasible compounds.

The phrase "up to", as used herein, refers to zero or any integer number that is equal or less than the number ing the phrase. For example, "up to 3" means any one of 0, l, 2, and 3.The term "aliphatic", "aliphatic group" or "alkyl" as used herein, means a straight-chain (i.e., unbranched) or branched, substituted or unsubstituted hydrocarbon chain that is completely saturated or that contains one or more units of unsaturation. Unless otherwise ed, aliphatic groups contain 1-20 aliphatic carbon atoms. In some embodiments, aliphatic groups contain 1-10 aliphatic carbon atoms. In other embodiments, aliphatic groups contain 1-8 aliphatic carbon atoms. In still other embodiments, aliphatic groups contain 1—6 aliphatic carbon atoms, -11_ and in yet other embodi ments aliphatic groups contain 1-4 aliphatic carbon atoms.

Suitable aliphatic groups include, but are not limited to, linear or branched, substituted or unsubstituted alkyl, alkenyl, alkynyl groups. The term "cycloaliphatic" or “cycloalky ” mean a monocyclic hydrocarbon, bicyclic, or tricyclic arbon that is completely saturated or that ns one or more units of unsaturation, but which is not aromatic and has a single point of attachment to the rest of the molecule. In some embodiments, "cycloaliphatic" refers to a monocyclic C3-C3 hydrocarbon or bicyclic C8-C12 hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not ic, that has a single point of ment to the rest of the molecule wherein any individual ring in said ic ring system has 3—7 members.

The term “electron withdrawing group”, as used herein means an atom or a group that is electronegative relative to hydrogen. See, e.g., “Advanced Organic Chemistry: Reactions, Mechanisms, and Structure,” Jerry March, 4th Ed., John Wiley & Sons (1992), e.g., pp. 14-16, 18-19, etc. Exemplary such substituents include halo such as Cl, Br, or F, CN, COOH, CF3, etc.

Unless ise specified, the term "heterocycle", "heterocyclyl", "heterocycloaliphatic", "heterocycloalkyl" or "heterocyclic" as used herein means non- aromatic, monocyclic, bicyclic, or lic ring s in which one or more ring atoms in one or more ring members is an independently selected heteroatom.

Heterocyclic ring can be saturated or can contain one or more unsaturated bonds. In some embodiments, the "heterocycle", "heterocyclyl", "heterocycloaliphatic", "heterocycloalkyl"or ocyclic" group has three to fourteen ring members in which one or more ring members is a heteroatom independently selected from oxygen, sulfur, nitrogen, or phosphorus, and each ring in the ring system contains 3 to 7 ring members.

The term "heteroatom" means oxygen, sulfur, nitrogen, phosphorus, or silicon (including, any oxidized form of nitrogen, sulfur, phosphorus, or silicon; the nized form of any basic nitrogen or; a substitutable nitrogen of a heterocyclic ring, for example N (as in 3,4-dihydro-2H—pyrrolyl), NH (as in pyrrolidinyl) or NR+ (as in tituted pyrrolidinyl)).

The term "unsaturated", as used herein, means that a moiety has one or more units of unsaturation but is not aromatic.

The term "alkoxy", or "thioalkyl", as used herein, refers to an alkyl group, as usly defined, attached to the principal carbon chain h an oxygen ("alkoxy") or sulfur ("thioalkyl") atom.

[0030] The term "ary " used alone or as part of a larger moiety as in "aralkyl", "aralkoxy", or "aryloxyalky ”, refers to monocyclic, bicyclic,'and tricyclic ring systems having a total of five to en ring carbon atoms, wherein at least one ring in the system is aromatic and wherein each ring in the system contains 3 to 7 ring carbon atoms. The term "ary " may be used interchangeably with the term "aryl ring". The term "heteroaryl", used alone or as part of a larger moiety as in "heteroaralkyl" or "heteroarylalkoxy", refers to monocyclic, bicyclic, and tricyclic ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is aromatic, at least one ring in the system contains one or more heteroatoms, and wherein each ring in the system contains 3 to 7 ring members. The term "heteroaryl" may be used interchangeably with the term ”heteroaryl. ring" or the term oaromatic".

The term idene chain" refers to a straight or branched carbon chain that may be fully saturated or have one or more units of unsaturation and has two points of attachment to the rest of the molecule.

Unless otheiwise stated, structures ed herein are also meant to e all isomeric (e.g., enantiomeric, diastereomeric, and geometric (or conformational)) forms of the structure; for example, the R and S configurations for each asymmetric center, (Z) and (E) double bond s, and (Z) and (E) conformational isomers. Therefore, single stereochemical isomers as well as enantiomeric, diastereomeric, and geometric (or conformational) mixtures of the present compounds are within the scope of the ion.

Unless otherwise stated, all tautomeric forms of the compounds of the invention are within the scope of the invention. Thus, included within the scope of the invention are tautomers of compounds of formula I.

Additionally, unless otherwise stated, structures depicted herein are also meant to include nds that differ only in the presence of one or more isotopically enriched atoms. For example, compounds of a I, wherein one or more hydrogen atoms are replaced deuterium or tritium, or one or more carbon atoms are replaced by a 13C- or 14C-enriched carbon are within the scope of this invention. Such compounds are useful, for example, as ical tools, probes in biological assays, or sodium channel blockers with improved therapeutic profile.

In the formulas and drawings, a line transversing a ring and bonded to an R group such as in means that the R group can be bonded to any carbon, or if applicable, atom such as N, of that ring as valency allows.

Within a definition of a term as, for e, R1, R2, RS, R4, R5, or R6 when a CH2 unit or, interchangeably, ene unit may be replaced by O, CO, S, SO, S02 or NR8, it is meant to include any CH2 unit, including a CH2 within a terminal methyl group. For example, 2CH2SH is within the definition of Cl —C6 alkyl wherein up to two CH2 units may be replaced by S because the CH2 unit of the al methyl group has been ed by S.

In another embodiment, the invention features a compound of formula I and the attendant definitions, wherein R1 is halo or optionally substituted aryl, heteroaryl, Cl-C6 alkyl, Cl-C6 fluoroalkyl, a straight chain, branched, or cyclic (C1- C8)-R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, SO2, N, or NR8, or 2 R1 taken together form an oxo group. In another embodiment, R1 is F or optionally substituted phenyl, pyridyl, oxazole, thiazole, pyrazole, oxadiazole, CH2OCH3, CH2F, CH2OCH(CH3)2, CH2OCHF2, CH3, CH2CH3, CH2OH, C(CH3)2OH, N1 Z/(j 2 CHZCHQOH CHZOCHZCHg, CH(CH2)2, 2A3 fl 24:1Q “”1; ,fl ZA“; ZAon In another embodiment, the invention features a compound of formula I and the attendant definitions, wherein R2 is H, C1-C6 alkyl, C1—C6 fluoroalkyl, CF3, an ally substituted cycloalkyl, aryl, heterocycloalkyl, aryl, or a straight chain, branched, or cyclic (C1-C8)—R9 wherein up to two CH2 units may be replaced with O, CO, 3, so, 302, N, or NR8. In another embodiment, R2 is H, CHZCHFZ, , CH(CH3)CH2F, CH2CH(CH3)2, CH3, CHZCH3, tBu, CHzCN, )2, CH3)2, CH2C(CH3)20H, CH2CH2CH(CH3)2, CHZCH20H, C(O)CH3, C(O)CH2CH3, C(O)CH(CH3)2, CHZCFZCH3, CH2CCCH3, CH2C(O)tBu, CH2CH20CH3, CH20CH3, CH2C(O)CH3, CH2C(O)OCH3, CH2CH20CH2CH2CH3, CHzCCCHzCHg, CHZCHZOCHZCHg, CHZCHZSCHg, CHzCHzCHZOCHg, ‘1’ fl m\ \ \ N 55 O N CH2CH(CH2CH3)2, n-butyl, n-propyl, W 55 , , \ \ \ \ /o ,F30 6, o 55, 55, 55 //\O / / r? N/ grqgma, “Ck CkCk Qk MJCk El é—Q,Q55,Q\é,\“‘&é,@{fléfi<>, H fiéfl, @530; fvfl,é%,é—CO,ZAO,©§2£:I, woo mg 2%; / twice In another embodiment, the invention features a compound of formula I and the attendant definitions, wherein n is O, 1, 2, or 3. In another embodiment, n is 1 or 2. In another ment, n is 1.

[0040] In another ment, the invention features a compound of formula I and the attendant definitions, wherein o is 0 or 1. In r embodiment, o is 0.

In another embodiment, the invention features a compound of formu1a I and the attendant definitions, wherein A is wherein: R4 is H, C1-C6 alkyl, C3-C8 cycloa1ky1, C1-C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, NRSSOZRS, sozRS, SORg, SR8, COZRB, NR8COR8, R8, CON(R8)2, SO2N(R8)2, CHF2, CF3, 001:3, OCHF2,R9,heterocycloalky1, cycloalkoxy, aryl, heteroaryl, or a ht chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be ed with O, CO, S, SO, s02, N, CF2, 0r NR8; R5 is H, C1-C6 alkyl, C3-C8 cycloalkyl, Cl-C6 alkoxy, C3—C8 cycloalkoxy, halo, CN, OH, 0R8, N(R8)2, NR8802R8, SO2R8, SORS, SR8, CO2R8, g, NR8C02R8, CON(R8)2, SO2N(R8)2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a ht chain, branched, or cyclic (C1~C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8; R6 is H, Cl-C6 alkyl, C3-C8 cycloalkyl, C1—C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, R8, sozRg, SORS, SR8, CO2R8, NR8C0R8,NR8CO2R8, CON(R8)2, SO2N(R8)2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; or two occurrences of R4 and R5, or R5 and R6 together with the carbons to which they are attached form an optionally substituted ring comprising up to 2 heteroatoms.

In another embodiment, R4 is H, Cl-C6 alkyl, C1 -C6 alkoxy, halo, OCF3, OCHF2, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, SO2, N, or NR7. In another embodiment, R4 is H, F, CH3, OCH3, OCF3, or OCHF2.

In another embodiment, R5 is H, C1-C6 alkyl, Cl-C6 alkoxy, halo, CF3, CN, or a straight chain, branched, or cyclic (Cl-C8)-R9 n up to three CH2 units may be replaced with O, CO, S, SO, SO2, N, or NR8. In another ment, R5 is H, CH3, OCH3, OCH2CH3, OCH(CH3)2, F, C1, CN, CF3, or CH2OH.

In another embodiment, R6 is H, Cl-C6 alkyl, Cl—C6 alkoxy, SO2R8, SO2N(R8)2, R9, or a straight chain, branched, or cyclic (Cl-C8)-R9, wherein up to three CH2 units may be replaced with O, S, SO, SO2, N, or NR8. In another embodiment, R6 is H, CH2OH, OCH3, OCH2CH3, OCH2CH2CH3, OCH2CH2CH(CH3)2, OtBu, tBu, 3)2, OCH2C(CH3)ZOCH3, CH(OH)CH(CH3)2, C(OH)(CH2CH3)2, CH3)ZOH, H, OCHZCHZOCHg, OCHZCHZOH, OCH2CH2CHZOH, CCCHZOCHg, SOZCH3, SOZCHZCH(CH3)2, SOZCH(CH3)2, SOZCHZCHg, SOZC(CH3)3, CON(CH2CH3)2,C(CH3)2COZCH3,EMmMEX EQOE0&0 a'8oNvés:‘Naf‘gflfifi 190,4}TO9 SHQO55 :—S—q é—S—<:: ,OI' H0><>O.

In another embodiment, the invention features a compound of formula I R5 R4 R6 and the attendant definitions, wherein R5 is selected from: :Ex(Em Qk fix 105%7%U 33; SSQN:QOLj:OOM\ WO 25613 OH 55 55 0\ m0 U0OMe Q 55 CI +, F em 0 e as o ,,s" 0 O CO, @583, HO 1:3’8\ 55 55 s5 55 s5 F m: “3% Ue JG D 8\ F HO OMe FXF , ,FXF o” /O CN , , , , 550 550 0’9 (I) HO>O, 0”st 55mgH0 ,or In another embodiment, the invention es a compound of a I and the attendant definitions, wherein A is heteroaryl or heterocyclic. In another embodiment, A is a monocyclic heteroaryl comprising 1 to 3 heteroatoms independently selected from N, O, or S. In another embodiment, A is selected from a bicyclic heteroaryl sing from 1 to 3 heteoratoms independently selected from N, O, or S.

In another embodiment, A is 6“ 1N\ R5 5 95‘ N / / R4 R6 R4 R6 R4 R6 R5 R5 ,or R5 wherein: R4 is H, Cl-C6 alkyl, C3-C8 lkyl, C1-C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, NRSSOZRS, SOzRg, SORS, SR8, COzRg, NR8COR8, NRgCOzRS, CON(R8)2, SOZN(R8)2, CHFZ, (31:3, OCF3, OCHFZ, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain, branched, or cyclic )—R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CFZ, or NR8; R5 is H, C1-C6 alkyl, C3-C8 cycloalkyl, Cl-C6 alkoxy, C3-C8 cycloalkoxy, halo, CN, OH, 0R8, N(R8)2, RS, sozRg, SORS, SR8, (:0st, NRBCORS, NRSCOZRg, CON(R8)2, SOZN(R8)2, CF3, OCF3, OCHFZ,R9,heterocycloa1ky1, heterocycloalkoxy, aryl, heteroaryl, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, S0, 802, N, CFz, or NR8; R6 is H, c1-co alkyl, C3-C8 cycloalkyl, Cl-C6 alkoxy, halo, CN, 0H, 0R8, N(R8)2, NRSSOZRg, SOst, SORS, SR8, COZRB, NRSCORS, NR8C02R8, CON(R8)2, SOZN(R8)2, CF3, 001:3, OCHFg, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8; or two occurrences of R4 and R5, or R5 and R6 er with the s to Which they are attached form an optionally substituted ring comprising up to 2 heteroatoms.

In another embodiment, R4 is H or C1-C6 alkyl. In another embodiment, R4 is H.

In r embodiment, R5 is H, Cl-C6 alkyl, or Cl-C6 alkoxy. In another embodiment, R5 is H, CH3, or OCH3.

In another embodiment, R6 is H, CN, Cl-C6 alkoxy, or CF3. In another embodiment, R6 is H, CN, OCH3, or CF3.

In another ment, the invention features a compound of formula I and the attendant definitions, wherein A is selected from the ing: N”* 9T; 55D U° , t9Y3 55U EU U\ I”) OMe, or MeO

[0052] In another embodiment, the invention es the compounds of formula I and the attendant definitions, wherein the compound has formula IA: (R7) —/p | \ /\ ,R2 i/ N wherein: R2 is H, C1-C6 alkyl, Cl-C6 fluoroalkyl, an ally substituted cycloalkyl, aryl, heteroaryl, or heterocycloalkyl, or a straight chain, branched, or cyclic (Cl - C8)—R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, S02, N, CF2, or NR8; R5 is H, Cl-C6 alkyl, Cl—C6 alkoxy, Cl—C6 fluoroalkyl, halo, CF3, OCF3, OCHF2, or a straight chain, branched, or cyclic )—R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, S02, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 alkoxy, CN, SO2R8, CON(R8)2, SO2N(R8)2, heterocycloalkyl, or a straight chain, branched, or cyclic (Cl-C8)—R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8; R7 is C1—C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from 0 to 3 ive.

In another embodiment, R2 is selected from Cl-C6 alkyl, C1-C6 fluoroalkyl, lkyl, aryl, heterocycloalkyl, heteroaryl, or a straight chain, branched, or cyclic (Cl-C8)—R9 wherein up to two CH2 units may be ed with O, CO, S, SO, 802, N, CF2, or NR8. In another embodiment, R2 is CH3, CH2CH3, CH(CH3)2, CH2CH(CH3)2, CH2CHF2, CH2CF3, CH(CH3)CH2F, CH2CN, CH2CH2OH, H3)2OH, COCH2CH3, or COCH(CH3)2.

In another embodiment, R5 is selected from H, Cl-C6 alkyl, Cl-C6 alkoxy, C1-C6 fluroroalkyl, halo, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, S02, N, CF2, or NR8. In another embodiment, R5 is H, CH3, OCH3, OCH2CH3, CF3, C1, F, or CH2OH.

In another embodiment, R6 is selected from H, C1-C6 alkoxy, or a straight chain, branched, or cyclic )-R9 wherein up to three CH2 units may be replaced with O, CO, S, S0, 802, N, CF2, or NR8. In another ment, R6 is H, CH2OH, OCH2CH3, OtBu, 3)2, OCH2C(CH3)2OCH3, CH(OH)CH(CH3)2, OCH2C(CH3)2OH, C(CH3)2OH, OCH2CH2OCH3, OCH2CH2OH, OCH2CH2CH2OH, CCCH2OCH3, SO2CH3, SO2CH2CH(CH3)2, SO2CH(CH3)2, SO2CH2CH3, SO2C(CH3)3, :5 OH 3 é ‘CO, E—O£0, CON(CH2CH3)2, C(CH3)2CO2CH3, N\__/O, X , In another embodiment, R7 is halo. In another embodiment, R7 is F. 35QR,

[0057] In another embodiment, the R5 moiety is selected from: 2012/028882 kaxfilxfiu \Qfiam o \\ SS CI 7 7 9 ; U .35 55 OMe 07:0 s' 8’ , , 55 3 In another embodiment, the ion es a compound of a I and the attendant definitions of the above embodiments, wherein the compound has formula IB: (R7)p—\ I wherein: R2 is H, C1-C6 alkyl, Cl~C6 fluoroalkyl, an optionally substituted cycloalkyl, aryl, heteroaryl, or heterocycloalkyl, or a straight chain, branched, or cyclic (Cl- C8)-R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, 802, N, CFz, or NR8; R5 is H, Cl-C6 alkyl, Cl-C6 alkoxy, Cl—C6 fluoroalkyl, halo, CF3, OCF3, OCHFz, or a straight chain, branched, or cyclic (C1-C8)—R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 alkoxy, CN, 302113, CON(R8)2, SO2N(R8)2, heterocycloalkyl, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be ed with O, CO, S, SO, 802, N, CF2, or NR8; R7 is C1-C6 alkyl, C3-C8 lkyl, C1-C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from O to 3 inclusive.

In another embodiment, R2 is selected from Cl—C6 alkyl, Cl-C6 fluoroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, or a straight chain, branched, or cyclic (Cl 9 wherein up to two CH2 units may be replaced with O, CO, S, S0, 802, N, CF2, or NR8. In another embodiment, R2 is CH3, CH2CH3, CH(CH3)2, CH2CH(CH3)2, CH2CHF2, CH2CF3, CH(CH3)CH2F, CH2CN, CH2CH2OH, CH2C(CH3)2OH, COCH2CH3, or COCH(CH3)2.

In another embodiment, R5 is selected from H, C1-C6 alkyl, Cl-C6 alkoxy, Cl-C6 fluroroalkyl, halo, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, S02, N, CF2, or NR8. In another embodiment, R5 is H, CH3, OCH3, OCH2CH3, CF3, C1, F, or CH2OH.

In another ment, R6 is selected from H, C1—C6 alkoxy, or a straight chain, branched, or cyclic (Cl—C8)-R9 n up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8. In another embodiment, R6 is H, CH2OH, OCH2CH3, OtBu, OCH(CH3)2, OCH2C(CH3)2OCH3, CH(OH)CH(CH3)2, OCH2C(CH3)2OH, C(CH3)2OH, OCH2CH2OCH3, OCH2CH2OH, OCH2CH2CH2OH, CCCH2OCH3, SO2CH3, SO2CH2CH(CH3)2, SO2CS:4[(CH3)2, SO2CH2CH3, H3)3, CON(CHz(3H3)2,C(CH3)2C02CH3,a Lil"—NO/—\ é—CO é—0%:0 go:3;NH iEEG ><jo ,01‘ H0 In another embodiment, R7 is halo. In r embodiment, R7 is F.

WO 25613 In another embodiment, the R5 moiety is selected from: 55 55 § 6 o/l\ ; ‘OJ\ ; ‘O/k :; \OJ\ F OMe m , , 55 5‘ 9‘ f ‘\I::Ij 00 OH O§(OH, COST, U) 01 OH, 0 OMe , , 6 9 \I::1\4p 9 § 65 NH \W:::[%¢oF A \W:;:L /«\/»\ \7:::L7< N O OH, OH, F 7 WO 25613 OH, OH , , m0OMe 55\E:[o\ 0 \\ OMe, SSUCI , Ox , U e s‘ We 0 0,,8 [IO [’0 O 98 \ 08 \ HO O 9 7 3 9 HO or , .

[0064] In another embodiment, the invention features a compound of formula I and the attendant ions, wherein the compound has formula IC: /\ ,R2 r N wherein, the Het ring is a mono or bicyclic optionally substituted heterocyclic or heteroaryl ring; -28~ R2 is H, C1-C6 alkyl, Cl-C6 fluoroalkyl, an optionally tuted aryl, heteroaryl, or heterocycloalkyl, or a straight chain, branched, or cyclic (Cl —C8)—R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8; R5 is H, Cl-C6 alkyl, Cl-C6 alkoxy, halo, CF3, OCF3, OCHF2, or a straight chain, branched, or cyclic (Cl-C8)—R9 wherein up to three CH2 units may be replaced with o, co, 8, so, soz, N, CF2, or NR8; R6 is H, C1-C6 alkyl, Cl-C6 , CN, SO2R8, )2, SO2N(R8)2, heterocycloalkyl, or a straight chain, branched, or cyclic (Cl ~C8)—R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8 R7 is C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, 01:3, OCF3, or OCHF2; and p is an integer from O to 3 inclusive.

In another embodiment, the Het ring is an optionally substituted thiazole, pyridine, pyrazole, oxazole, or oxadiazole.

In another embodiment, p is 0 or 1.

In another embodiment, R7 is Cl-C6 alkyl.

In r embodiment, R7 is CH3, CH2CH3, CH(CH3)2, or tBu.

In another ment, the Het ring is gum,m, h: pg,/N \N \ (7N fl I :N (”(55 HNgl/ \ (N4/ o Q93/ 0 go i0 Nékég Nékr; )0 \ \ \ _ \_ /N‘o N/J\ge Fulfil); bile; N95; or \<N/J\;; In another embodiment, R2 is selected from C1-C6 alkyl or a straight chain, ed, or cyclic (C1-C8)-R9 wherein up to two CH2 units may be replaced with o, co, 3, so, soz, N, CF2, or NR8. In another embodiment, R2 is CH2CH3, tBu, CH2CHF2, CH2CF3, 01' -o@.

In another embodiment, R5 is selected from H, C1-C6 alkyl, Cl-C6 alkoxy, or halo. In r embodiment, R5 is H, CH3, OCH3, F, or C1.

In another embodiment, R6 is H, Cl-C6 alkoxy, or a straight chain, branched, or cyclic (C1-C8)-R9 wherein up to three CH2 units may be replaced with O, co, 8, so, 802, N, 01:2, or NR8. In another embodiment, R6 is OCH(CH3)2, O 0 He; E—fi-NC/ C(CH3)20H, OCHZCHZOH, OCHzCHzCHzOH, O 01‘ O In another embodiment, the invention features a compound of formula I and the attendant definitions, wherein the compound has a ID: (MPGHetWR2 wherein, the Het ring is a mono or bicyclic ally substituted heterocyclic or heteroaryl ring; R2 is H, C1-C6 alkyl, C1-C6 lkyl, an optionally substituted aryl, heteroaryl, or heterocycloalkyl, or a ht chain, branched, or cyclic (Cl—C8)-R.9 wherein up to two CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or NR8; R5 is H, C1-C6 alkyl, Cl-C6 alkoxy, halo, CF3, OCF3, OCHF2, or a ht chain, branched, or cyclic (C1-C8)-R9 wherein up to three CH2 units may be replaced with o, co, s, so, 802, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 alkoxy, CN, SO2R8, CON(R8)2, SO2N(R8)2, heterocycloalkyl, or a straight chain, branched, or cyclic (C1-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CF2, or R7 is C1—C6 alkyl, C3—C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, 0R8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from 0 to 3 inclusive.

In another ment, the Het ring is an ally substituted thiazole, pyridine, pyrazole, oxazole, or oxadiazole.

In another ment, p is 0 or 1.

In another embodiment, R7 is C1—C6 alkyl.

[0077] In another embodiment, R7 is CH3, CH2CH3, CH(CHg)2, or tBu.

In another embodiment, the Het ring is //{k9}, CK?) ma},N \N \ fl?! l \/N / /N)\$5’ $6, “(#155,\ HN/i f0 (\0 go i0 ?/\O N/ N;/\ N/J\$:e Nék; Néksre N/J\£ Hid, l, ”RNA/x,\ \ \ _ /N‘O

[0079] In another embodiment, R2 is selected from Cl-C6 alkyl or a straight chain, branched, or cyclic (C1—C8)—R9 wherein up to two CH2 units may be replaced with O, CO, S, SO, 80;, N, CFz, or NR8. In another embodiment, R2 is CH2CH3, tBu, CI‘12CHF2, CH2CF3, 01‘ -o@.

In another embodiment, R5 is selected from H, C1—C6 alkyl, Cl-C6 alkoxy, or halo. In another embodiment, R5 is H, CH3, OCH3, F, or Cl.

In another embodiment, R6 is H, Cl-C6 alkoxy, or a straight chain, branched, or cyclic (Cl-C8)-R9 wherein up to three CH2 units may be replaced with O, CO, S, SO, 802, N, CFZ, or NR8. In another ment, R6 is OCH(CH3)2, C(CH3)ZOH, OCH2CH20H, O 0 He; :—§-@ OCHZCHzCHZOH, O or O In another embodiment, the ion features a nd of formula I and the attendant definitions, wherein the compound is selected from the following table: Table 1 _32_ WO 25613 WO 25613 2012/028882 WO 25613 WO 25613 WO 25613 -38— WO 25613 WO 25613 WO 25613 -41_ WO 25613 '1 '10 ’1 19 WO 25613 WO 25613 WO 25613 WO 25613 -46— WO 25613 WO 25613 ~48- WO 25613 WO 25613 WO 25613 WO 25613 WO 25613 WO 25613 0Q”A9 WO 25613 2’67 WO 25613 WO 25613 In another aspect, the invention features a pharmaceutical ition comprising a compound of the invention and a pharmaceutically acceptable carrier.

[0083] In another aspect, the invention features a method of inhibiting a e-gated sodium ion channel in: a patient; or a biological sample; WO 25613 comprising administering to the patient, or contacting the biological , with a compound or composition of the invention. In another embodiment, the voltage-gated sodium ion channel is NaV 1.7.

In another aspect, the invention es a method of treating or lessening the ty in a subject of acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, herpatic neuralgia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, atric disorders, anxiety, depression, dipolar disorder, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, , multiple sclerosis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, rgical pain, cancer pain, stroke, cerebral ischemia, traumatic brain injury, amyotrophic lateral sclerosis, stress- Or exercise induced angina, palpitations, hypertension, migraine, or abormal gastro- intestinal motility, comprising administering an effective amount of a compound or composition of the invention.

In another ment, the method is used for treating or lessening the severity of femur cancer pain; non-malignant chronic bone pain; rheumatoid arthritis; osteoarthritis; spinal is; neuropathic low back pain; neuropathic low back pain; myofascial pain me; fibromyalgia; temporomandibular joint pain; chronic visceral pain, abdominal pain; pancreatic; IBS pain; chronic and acute headache pain; migraine; tension headache, including, cluster hes; chronic and acute neuropathic pain, post-herpatic neuralgia; diabetic neuropathy; HIV—associated neuropathy; trigeminal neuralgia; Charcot~Marie Tooth neuropathy; hereditary sensory neuropathies; peripheral nerve injury; painful neuromas; ectopic al and distal discharges; radiculopathy; chemotherapy induced neuropathic pain; radiotherapy— induced neuropathic pain; post-mastectomy pain; central pain; spinal cord injury pain; troke pain; thalamic pain; complex al pain syndrome; phantom pain; intractable pain; acute pain, acute perative pain; acute musculoskeletal pain; joint pain; mechanical low back pain; neck pain; tendonitis; injury/exercise pain; acute al pain, abdominal pain; ephritis; appendicitis; cholecystitis; intestinal ction; hernias; chest pain, cardiac pain; pelvic pain, renal colic pain, acute obstetric pain, labor pain; cesarean section pain; acute inflammatory, burn and trauma pain; acute intermittent pain, endometriosis; acute herpes zoster pain; sickle cell anemia; acute pancreatitis; breakthrough pain; orofacial pain including sinusitis pain, dental pain; multiple sclerosis (MS) pain; pain in sion; leprosy pain; Behcet's disease pain; adiposis dolorosa; phlebitic pain; Guillain-Barre pain; painful legs and moving toes; Haglund syndrome; erythromelalgia pain; Fabry's disease pain; bladder and urogenital disease, including, urinary incontinence; hyperactivity r; painful bladder syndrome; interstitial cyctitis (IC); prostatitis; complex regional pain syndrome (CRPS), type I and type II; Widespread pain, paroxysmal extreme pain, pruritis, tinnitis, or angina-induced pain.

The compounds of the ion may be prepared readily using the ing methods. Illustrated below in Scheme 1 h Scheme 21 are methods for preparing the compounds of the invention.

[0087] Scheme 1 emf (Rafi his») 0 5%», __a)_. O NH Nm/Q) a) Acid, ng reagent (e. g. EDCI or HATU), base (6.g. triethylamine or diisopropylethylamine); solvent (e.g. DMF or CH2C12) Scheme 2 (R3)o c)¢\PG1 '\ - PGz or N-PG2 RzorPG1 N NH2 o¢\R2 R1 R" N —> \J HOWW a) HO\>LN,PG10rR2 b) HogRr OH (R3)o R1 H R1 82 R1' :3 R1 (R3)o f) (R330 —-—-—> RAE O q O ’1 N\ NH 0) or F361 R1' H R1 3 N N N 1 1 (Foo R1 R (Foo R d) 5R3)0 —_, / __..

N\ N\ e) N\ 2 2 PG2 [33 PG R1‘ R1' H R RLEN N N (R3)o Rli R1 (R3)o 0 /W /W R1 = alkyl or aryl; R11 = H or alkyl; PG1 = acid-stable protecting group (e.g. PMB, benzyl); PG2 = abile protecting group (e.g. Boc); R2 = alkyl or aryl a) reducing agent (e.g.NaBH4 or NaCNBH3), solvent (e.g. MeOH); b) solvent (e.g.

EtOH), reflux; 0) Hr: protic acid (e.g.methanesulfonic anhydride), base (6.g. iPerEt), solvent (e.g. THF); (1) For PG1 as PMB or Bn: catalyst (e. g. Pd/C or Pd(OH)2/C), en source (e.g. H2 or ammonium formate), solvent (e.g. MeOH, EtOH or iPrOH,); e) RZX (X: halo, OTs): base (e. g. NaHCO3 or NaH, diisopropylethylamine ), solvent (6.g. DMF or CH2C12) or RZX (X: CHO): ng agent (e.g. NaCNBH3 or -61— NaBH4), solvent (e.g. EtOH) f) PG2 as acid labile protecting group: H+ (e. g. HCl or TFA), solvent (6.g. CHzClz or dioxane).

Scheme 3 R1 OH C) 1 \E PG or R2 / R 1 O $3” KCEHWN or N‘PGZ P61 PG1 , c) le:NJCWM11H _... , ___, O 1 d) R LNJC R3)oO NxPGZ e) H r F? R1rso ao R1316% —_»o R 0 f) g) N‘PGZ N‘PGZ mossNH RI =optionally tuted phenyl; PG1 = acid-stable protecting group (6. g. PMB, benzyl); PG2 = acid-labile protecting group (6.g. Boc); a) reducing agent (e.g. NaBH4 BHg); solvent (e.g. MeOH); b) solvent (e. g.

EtOH), reflux; 0) Hr: protic acid (e.g. HBr); d) for PG1 = Boc: BoczO, base (e.g.

Et3N), solvent (e.g. DCM); e) for PG2 = benzyl: catalyst (e.g. Pd/C or Pd(OH)2/C), hydrogen source (e.g. H2 or ammonium formate), t (e.g. MeOH, EtOH or iPrOH); t) RZX (X: halo, OTs): base (e.g. NaHC03 or NaH, diisopropylethylamine ), solvent (e. g. DMF or CHZClz) or RZX (X: CHO): reducing agent (6. g. NaCNBH; or NaBH4), solvent (6.g. EtOH) g) when PG2 = Boc; H+ (e.g. HCl or TFA), solvent (e.g. dioxane or CHZClz). -62— Scheme 4 PG1NH2 (RifiN’PGZ VBr (Raw NfiPG R NH2 0 PG1 or R2 PG1 or RZNR1JWO(Rikki PG2 _, LN SR3)0 c) R1OjCfi‘lx:,G2 or d) H R11:3d.

R1 = optionally substituted 2—pyridyl; PG1 = acid-stable protecting group (e. g. benzyl); PG2 = acid-labile protecting group (e.g. Boc) a) base (e.g. iPerEt), solvent (e.g. DMF); b) base (e.g. iPerEt), solvent (e.g. DMF); c) H+ (e.g. p-toluenesulfonic acid), 80 0C; (1) when PGl = benzyl; catalyst (e.g. Pd/C or Pd(OH)2/C), hydrogen source (e.g. H2 or ammonium formate), solvent (6.g. MeOH, EtOH or iPrOH,) e) RZX (X: halo, OTs): base (e.g. NaHCO3 or NaH, ropylethylamine ), solvent (e.g. DMF or ) or RZX (X: CHO): reducing agent (e.g. NaCNBH3 or NaBH4), solvent (e.g. EtOH) f) when PG2 = Boc; HJr (e.g.

HCl or TFA), solvent (e.g. e or CHgClz) Scheme 5 FI’G1 or R2 PG1 or R2 (730 _. HN R3)o (R3)o NPG ’ 2 a) HO P62 P26 PGI = acid-stable protecting group (e.g. ); PG2 = acid—labile protecting group (e. g. B00) a) Amine (e.g. benzylamine), solvent (e.g. methanol, ethanol, isopropanol); b) catalyst (e. g. Pd(PPh3) 4), ligand (e.g. PPh3), (Z)-but-2—ene—1,4-diyl diacetate, base (e.g. triethylamine, diisopropylethylamine), solvent (e.g. THF, diethyl ether, dioxane).

Scheme 6 IIDG1 or R2 E’Gl or R2 {to —> \ /j —> o a),b) o 0) N‘PGZ £163”NTK® PG1 or R2)0/ REZ/OJ >069 HOm: 3}; :]_/® :lN R2 \ :69 E’ \/E $R3)O d”) J: O f), g), h) ori) l¥® HO WW/ HO —’ O /j —> R0 g)orh) Nm/ WY o o PG1 = acid-stable protecting group (e. g. benzyl); PG2 = abile protecting group (e. g. B00) a) deprotection conditions for PGZ: H+ (e.g. HCl or TFA); b) A—COZH, coupling agent (e. g. I—IATU or EDCI), base (e.g. Et3N or iPrZNEt), solvent (e.g. DMF, CH3CN or CHZClz); c) ozone, reductive workup (e. g. NaBH4), solvent (e. g. methanol, ethanol, isopropanol); d) R-X (X = leaving group: halo, OTs, OTf), base (6. g. NaH, KOtBu, NaOtBu), solvent (e.g. THF, DMF, CH3CN); 6) when PGl = ; catalyst (e.g.

Pd/C or Pd(OH)2/C), en source (e.g. H2 or ammonium formate), solvent (6.g.

MeOH, EtOH or iPrOH,); f) RZ-X (X = leaving group: halo, OTs, OTf), base (e. g.

K2C03, NaHCO3, Et3N), solvent (e.g. THF, DCM, EtOH, CH3CN, DMF); g) ive amination conditions, e.g. NaBH(OAc)3, DCE, AcOH, TEA, appropriate ketone or aldehyde; h) nucelophilic aromatic substitution conditions, 6.g. aryl halide, DMSO, K2C03, heat; i) iated amine arylation ions: catalyst (e. g.

Pd2(dba)3 or Pd(OAc)2), ligand (e.g. rac-BINAP or DPPF), base (NaOtBu or KOH), solvent (6. g. toluene or dioxane).

Scheme 7 PG1 or R2 dbéWUO MUG—fig1: Mr / HO O an/A O 2012/028882 PG1 = acid-stable protecting group (e.g. benzyl) a) catecholborane, st (e. g. Rh(PPh3) 3C1), solvent (e.g. THF, diethyl ether, dioxane; basic oxidative workup (e.g aq. HzOz/NaOH); b) when PG1 = benzyl; catalyst (e. g. Pd/C or Pd(OH)2/C), en source (e.g. H2 or ammonium formate), solvent (e. g. MeOH, EtOH or iPrOH,); c) Rz-X (X = leaving group: halo, OTs, OTt), base (e.g. K2CO3, NaHCO3, Eth), solvent (e.g. THF, DCM, EtOH, CH3CN, DMF).

Scheme 8 dEGJCf: ifd:or R2 fiGl or R2 l l O \ R2 or R2 N $5 H 3 N (R )0 f,——»”) JOEL ®,h . 0 5?” N ® Y r O ml Tb) Q::HJCSLZM"—’Ffi\):)ori) :ijlz a) Johio PG1 = acid—stable protecting group (e. g. benzyl); PG2 = acid-labile protecting group (e. g. B00) a) deprotection conditions for PGZ: H+ (e.g. HCl or TFA); b) A—COzH, coupling agent (6. g. HATU or EDCI), base (e.g. Et3N or iPerEt), solvent (e.g. DMF, CH3CN or CH2C12); 0) when PG1 = benzyl; st (e.g. Pd/C or Pd(OH)2/C), hydrogen source (6. g. ammonium formate), solvent (e.g. MeOH, EtOH or ); f) RZ-X (X = leaving group: halo, OTs, OTf), base (e.g. K2CO3, NaHC03, Eth), solvent (e. g. THF, DCM, EtOH, CH3CN, DMF); g) reductive amination conditions, 6. g. NaBH(OAc)3, DCE, AcOH, TEA, appropriate ketone or de; h) nucelophilic substitution conditions, e.g. aryl halide, DMSO, heat; i) Pd-mediated amine arylation conditions: catalyst (e.g. Pd2(dba)3 or Pd(OAc)2), ligand (e.g. rac-BINAP or DPPF), base (NaOtBu or KOH), solvent (e. g. toluene or dioxane).

Scheme 9 PG1 or R2 E’G 1 2 or R or R2 VE: N R3” 5R3” (R3)0 ”(®b) C)——> HO O W”UYCE10569 O Y® HOXi:H: f) 9) {33:® HOg:by PG1 = acid-stable protecting group (e.g. benzyl); R1 = alkyl. a) Oxidant (e. g. OsO4, NMO), solvent (e.g. acetone/water); b) Oxidant (e.g. NaIO4), solvent (e.g. THF/water); c) Oxidant (e. g. NaClOz), solvent (6. g. tBuOH/water); d) alkylating agent (e.g. MeI, dimethyl sulfate), base (e.g. K2C03, NaHC03, Eth), solvent (e.g. THF, DMF); e) Grignard reagent or alkyllithium (e.g. methylmagnesium halide or methyllithium), solvent (e.g. THF, diethyl ether, dioxane); l) deprotection ions e.g. when PGl = : catalyst (e. g. Pd/C or Pd(OH)2/C), hydrogen source (6.g. H2 or um formate), solvent (e.g. MeOH, EtOH or ); g) R2- X (X = leaving group: halo, OTs, OTf), base (e. g. K2CO3, NaHCOg, Eth), t (e.g. THF, DCM, EtOH, CH3CN, DMF).

Scheme 10 R1 PG1 R1 PG1 1 §R3)O | PG NH [{I § R3 0 fl )° , (R3)o N\PG2 a) HO W N‘PG2 N N ————> ———> (R3)o ——> R3)0 ), 1 O fl h) 1 R O NPG3 N \PGB NH PG1 = acid—stable protecting group (e. g. benzyl); PG2 = acid—labile protecting group (e.g. Boc); PG3 = base-labile protecting group (e.g. trifluoroacetate). a) Protected amine (e.g. N—benzyl—Z-methylprop-Z-en-l-amine), solvent (e. g. methanol, ethanol, isopropanol); b) 12, solvent (e.g. H20, DCM, MTBE, diethyl ether, THF), base (e.g. NaHC03, K2C03, Eth); c) Reductant (e.g. NaBH4 or LiAlH4), solvent (e.g. DMSO or THF); d) PG2 = Boc; H+ (e. g. HCl or TFA); e) m3 = roacetate; trifluoracetic anhydride or ethyl trifluoroacetate, base (e.g. pyridine or Et3N); f) PG1 = benzyl; catalyst (e.g. Pd/C or Pd(OH)2/C), hydrogen source (e.g. H2 or ammonium formate), solvent (e.g. MeOH, EtOH or iPrOH,); g) Rz—X (X = leaving solvent (e. g. THF, DCM, group: halo, OTs, OTt), base (6.g. K2CO3, NaHC03, Et3N), EtOH, CH3CN, DMF); h) Base (e.g. NaOH, K2C03, Na2C03), solvent (e.g. MeOH, EtOH, H20).

Scheme 11 W30 —» HN (R3)o __.+ Rlfi/lLNPG CI Raw NPG2 3” HO /W HO ‘PGZ NP62, Fl’G 1 O N j (R3>o ———+ (R3)o W d)'e) o :ii N‘PG2 EEC/(W 0 K1 (R3)o ___. ojCll @5R3)o g) R1 PGl = table protecting group (e. g. para-methoxybenzyl); PG2 = acid—labile protecting group (6.g. Boc); R1 = optionally substituted phenyl. a) Amine (e.g. p—methoxybenzylamine), solvent (6.g. methanol, ethanol, isopropanol); b) 2—haloarylacetyl de, base (e.g. Eth, i-PrNEtz, pyridine), solvent (e. g. THF, DCM, CH3CN); c) Base (e.g. NaH, , NaOt—Bu), solvent (e. g. THF, DMF, CH3CN, DMSO, t—BuOI—I); (1) PG1 = PMB; oxidant (e.g. CAN or DDQ), solvent (e.g.

HzO/CH3CN or DCM, DMF, dioxane); 6) PG2 = Boc; H+ (e.g. HCl or TFA); f) A- COZH, coupling agent (e. g. HATU or EDCI), base (e.g. Et3N or iPerEt), solvent (e.g.

DMF, CH3CN or CH2Clz); g) Rz-X (X = leaving group: halo, OTs, OTf), base (e.g.

K2CO3, , Et3N), solvent (e.g. THF, DCM, EtOH, CH3CN, DMF). -69— WO 25613 Scheme 12 R3)o R R HO ),b) c)d) PG R3)o N O N ———> (R3) ————> R3)O e) f) C' / g) / N N o 0 PG1 = base-labile protecting group (e.g. trifluoroacetate); PG2 = acid-stable protecting group (6.g. benzyl); R = optionally substituted phenyl. a) Aldehyde (e. g. 3-methylbutanal), reductant (e.g. NaBH4, NaBH(OAc)3, NaBHgCN), solvent (e. g. methanol, THF, DCM, DCE); b) PGl = trifluoroacetate; trifluoracetic anhydride or ethyl trifluoroacetate, base (e.g. pyridine or Eth); c) PG2 = ; catalyst (e. g. Pd/C or Pd(OH)2/C), hydrogen source (e.g. H2 or ammonium formate), solvent (e. g. MeOH, EtOH or iPrOH,); d) A—COZH, coupling agent (e.g. HATU or EDCI), base (e.g. Et3N or iPerEt), t (e.g. DMF, CH3CN or CHZCIZ); 6) Base (e. g. NaOH, K2C03, Na2C03), solvent (6.g. MeOH, EtOH, H20); f) 2-halo arylacetyl de, base (6.g. Eth, i-PrNEtz, pyridine), solvent (e. g. THF, DCM, CH3CN); g) Base (e. g. NaH, KOt—Bu, NaOI—Bu), solvent (6. g. THF, DMF, CH3CN, DMSO, t-BuOH).

Scheme 13 '32 F32 F32 N \ N N (R3)o —> (I) (R3)o —» R7 \ (R3)o /O N \ R o /W a) / o /W b) o /W N N N 0 ‘PG 0 ‘PG 0 \PG R12 F52 R|2 N N N —> SR3” ————+ /R3)o + /R3)o C) \ O 11 d) /l O \ O R7 \ \ R7 N \ R7 \ N \ N/NH PG N/N PG N/N\R7 PG F32 F52 N N (Rho (R3)o ___, /to veto+ 7 701/ \ N N’N‘RY 71/ R7 o PG = acid-labile protecting group (6.g. Boc). a) N,O-dimethylhydroxylamine, base (6.g. LiHMDS, NaHMDS, LDA), solvent (6.g.

THF, diethyl ether); b) alkynylmagnesium halide, solvent (6.g. THF, diethyl ether); c) hydrazine, solvent (e.g. MeOH, EtOH, i-PrOH); d) R7-X (X = leaving group: halo, OTs, OTf), base (6. g. NaH, KOt-Bu, NaOt—Bu), solvent (6. g. THF, DMF, CH3CN, DMSO, t—BuOH); 6) PG = Boc; H+ (e.g. HCl or TFA); t) A-COZH, coupling agent (eg. HATU or EDCI), base (e.g. Et3N or iPerEt), t (6. g. DMF, CH3CN or CH2C12).

Scheme 14 R2 R2 l R2 I l | \ N N /N N 9 Q§%o ~_____. (Rho ______. | N / / o a) R7 o /W b) R7 o N N 0 ‘PG 0 ‘PG 0 R2 R2 | | N N 7 7 ____+ R /ww ____+ R fifi” c) \ o d). e) \ 0 N 1H N/NH ‘PG NzNH PG1 = acid-labile protecting group (e.g. Boo); R7 = alkyl. a) Alkylmagnesium halide, solvent (e. g. THF, l ether); b) DMF-DMA; c) hydrazine, t (e.g. MeOH, EtOH, i—PrOH); (1) PG1 = Boc; HJr (e.g. HCl or TFA).

Scheme 15 Jk*_wikukw w%@e%@o PG1 = table protecting group (e.g. benzyl); PG2 = acid-labile ting group (e.g. Boc) a) when PG1 = Boo; H+ (e.g. HCl or TFA), solvent (e.g. l'PrOH, EtOH, dioxane or CH2C12); b) A-COzH; coupling agent (e.g. HATU or EDCI), base (e.g. Et3N or iPerEt), solvent (e.g. DMF, CHgCN or CI‘IzClg) c) i. Oxidant (e.g. OsO4, NMO), solvent (e.g. acetone/water); ii. Oxidant (e.g. NaIO4), solvent (e.g. THF/water); iii. 2012/028882 Oxidant (e. g. NaClOz), solvent (e. g. tBuOH/water); (1) base (e. g. LiOH or NaOH), solvent (6. g. THF or e or MeOH), water.

Scheme 16 F32 F52 Mo HO / N N O R30 ”OH, N\ R30) ) 0 PG1 / / R7/A \ _.—> 7 R K7 Nj/[O R _ NxPG1 \<\Nj/[O\ NH O b) NH2 a) O N’ N’ PG1 = acid-labile protecting group (e. g. Boo) a) Activating/ dehydrating reagent (e.g. T3P, HATU, EDCI), base (e. g. Eth), t (e. g. 2-methy1tetrahydrofuran, DMF); b) when PG1 = Boc; H+ (e. g. HCl or TFA), solvent (e.g. l'PrOH, EtOH, dioxane or CH2C12)

[00103] Scheme 17 “O Qmi:16: N/OH ___—0, R7\<NNj/[EjCR3: _—.

NH2 3) % (Rap N /j ———————> 7 NYE:1C?) R74 \ O R {N N (A) N ’ O \H/ C) 7f® PG1 = acid-stable protecting group (e.g. benzyl) a) Activating/dehydrating reagent (e.g. T3P, HATU, EDCI), base (6.g. Eth), solvent (e. g. 2-methyltetrahydorfuran, DMF); b) when PG1 = benzyl; i. l-chloroethyl formate, solvent (e.g. DCE); ii. MeOH; c) RZ-X (X = leaving group: halo, OTs, on), base (e. g. K2C03, Ncho3, Eth), solvent (e.g. EtOH, CHgCN).

Scheme 18 R2 R2 t t: WNWgCH (R3)o H q —> (R )o3 Ne b) HJK/NW/[OO N, // 0 PG2 0 PG2 F52 d) SR3)0 0 WP O 22 O F’GKL‘NHZOJJVNO <R3>o §Rs>o R7 N\ )or d) O a) /N ‘CPG2 xx 1] \PGZ i e) §\/x \% 36%” O PG1 = abile protecting group (6.g. Boc) a) Coupling agent (e.g. T3P, HATU, EDCI), base (e.g. Et3N or DIEA), solvent (e. g. 2— rnethyltetrahydorfiiran, DMF or CH3CN); b) i. Oxidant (e. g. OsO4, NMO), solvent (e.g. acetone/water); ii. Oxidant (e.g. NaIO4), solvent (e.g. THF/water); c) X = S, (e.g. lO Lawesson’s reagent or P285), solvent (e.g. THF or e); d) X = O, dehydrating reagent (6.g. POClg, Iz/Pth or Burgess salt), base (e.g. Eth), solvent (6.g. toluene, DCM, THF); e) PGl = Boc; HJr (e.g. HCl or TFA), solvent (e.g. iPrOH, EtOH, dioxane or CH2C12) WO 25613 Scheme 19 ii/ WK/NHZO ‘0) 0rd) * R3 0 > Win“,1 NW) o @ih}®R3 ox o R7 0 ' H N N R3)o (R3)o N\ / O 4—« N\ O w XX N 0 xx NY R7 O R7 0 PG = acid—stable protecting group (e.g. benzyl); a) Coupling agent (e.g. T3P, HATU, EDCI), base (e.g. Et3N or DIEA), solvent (e. g. 2- tetrahydrofuran, DMF or CH3CN); b) i. Oxidant (e.g. 0504, NMO), solvent (e.g. acetone/water); ii. Oxidant (e.g. NalO4), solvent (e.g. THF/Water); c) X = S, (e. g.

Lawesson’s reagent or P285), solvent (6.g. THF or toluene); d) X = O, dehydrating reagent (e.g. POC13, Iz/Pth or Burgess salt), base (e.g. Et3N), solvent (e.g. toluene, DCM, THF); 6) PG = benzyl; (e.g. Pd/C, or Pd(OH)2/C, H2 or ammonium e) solvent (e. g. iPrOH, EtOH or CH3CN); i) Rz-X (X = leaving group: halo, OTs, OTf), base (e.g. K2C03, NaHC03, Et3N), solvent (e.g. EtOH, CH3CN).

Scheme 20 I'DGl fi’Gl \/[N N (R3)O SR3” \ W G) __ , o o o a Q) RM.”$536(97’ «YUCYCDTR7\\/N PG1 = stable protecting group (e.g. benzyl) a) i. Oxidant (e.g. 0504, NMO), solvent (e. g. acetone/water); ii. Oxidant (e.g. NaIO4), solvent (e.g. ter); b) ammonium hydroxide, aldehyde/acyl equivalents (e. g. substituted/unsubstituted glyoxal, tuted 2-aeetoxy ketones, alpha—bromo ketones), solvent (e.g. MeOH); c) NaH, Mel, DMF/THF; (1) PG1 = benzyl; (e.g. Pd/C, or Pd(OH)2/C, H2 or ammonium formate), solvent (e.g. iPrOH, EtOH or CH3CN); e) RZ-X (X = leaving group: halo, OTs, OTf), base (e. g. K2C03, NaHCOg, Et3N), solvent (e.g. EtOH, CH3CN).

WO 25613 Scheme 21 PG1 or R2 $2 Haj: (R3)0 R7 (R3)o R7 0 W N\H/® PG1 = acid-stable protecting group (e.g. benzyl); PG2 = acid-labile protecting group (e.g. Boc) a) when PG‘ = benzyl; catalyst (e.g. Pd/C or Pd(OH)2/C), hydrogen source (e.g. H; or ammonium formate), solvent (e.g. MeOH, EtOH or iPrOH,); b) RZ-X (X = leaving group: halo, OTs, OTt), base (eg. K2C03, , Eth), solvent (eg. THF, DCM, EtOH, CH3CN, DMF); c) X (X = leaving group: MsCl, TsCl), base (eg. Eth), solvent (e.g. THF, DMF); d) R7-NH-R7 (R7, R7 = alkyl, cycloalkyl or heterocycle, base (e.g. NaH), solvent ( e. g. DCM, THF, DMF). {00108} Scheme 22 PG = acid-labile protecting group (eg. Boc). a) ethyl 2-halo—2,2-disubstituted acetate, solvent (e.g. F, DCM, ; b) base (6.g. KOtBu), solvent (6.g. THF); c) reductant (e.g. borane-dirnethylsulfide), solvent (e.g. THF); d) Rz—X (X = leaving group: halo, OTs, OTt), base (e.g. K2C03, , Eth), t (e.g. THF, DCM, EtOH, CH3CN, DMF); e) reductive amination conditions, e.g. NaBH(OAc)3, DCE, AcOH, TEA, appropriate ketone or aldehyde; f) nucelophilic substitution conditions, 6. g. aryl halide, DMSO, heat; g) deprotection conditions for PG: H+ (e.g. HCl or TFA); h) A-COZH, coupling agent (6. g. HATU or EDCI), base (e.g. Et3N or iPerEt), solvent (e.g. DMF, CH3CN or CHZClz).

[00109] Scheme 23 E2 F361 E2 3 (R3)0 J 02% W a Ho w F Ho ’W a). b) o c) o /1 o N\ N, MPG, PG2 2 R2 F52 ,1] N VE (R330 _. %_. FVE 5R3)o d) o 11 e) o/ 11 (9 \PG2 dl/ PG1 = acid—stable protecting group (e. g. benzyl); PG2 = acid-labile protecting group (6. g. B00) a) when PG1 = benzyl; catalyst (e.g. Pd/C or Pd(OH)2/C), hydrogen source (e.g. ammonium formate), solvent (e. g. MeOH, EtOH or iPrOH,); b) Rz-X (X = g group: halo, OTS, OTf), base (e. g. K2C03, NaHC03, Eth), solvent (e.g. THF, DCM, EtOH, CH3CN, DMF); c) laminosulfur trifluoride, DCM, d) deprotection conditions for PGZ: H+ (e.g. HCl or TFA); e) A—COZH, coupling agent (e.g. HATU or EDCI), base (e.g. Eth or iPerEt), solvent (e.g. DMF, CH3CN or CHzClz).

Uses Formulation and Administration Pharmaceutically acceptable compositions As discussed above, the invention provides compounds that are ~78- inhibitors of voltage-gated sodium ion channels, and thus the present compounds are useful for the treatment of diseases, disorders, and conditions ing, but not limited to acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal gia, herpetic neuralgia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, psychiatric disorders such as anxiety and depression, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, and incontinence. Accordingly, in another aspect of the invention, pharmaceutically acceptable compositions are provided, wherein these compositions comprise any of the compounds as described herein, and optionally comprise a pharmaceutically acceptable carrier, adjuvant or vehicle. In certain embodiments, these compositions optionally further comprise one or more additional therapeutic .

] It will also be appreciated that n of the compounds of invention can exist in free form for treatment, or where appropriate, as a pharmaceutically acceptable derivative f. According to the invention, a pharmaceutically acceptable derivative includes, but is not limited to, pharmaceutically acceptable salts, , salts of such , or any other adduct or derivative which upon administration to a subject in need is capable of providing, directly or ctly, a compound as otherwise described herein, or a metabolite or residue thereof.

] As used herein, the term “pharmaceutically acceptable salt” refers to those salts which are, within the scope of sound medical judgement, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, tion, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. A “pharmaceutically acceptable salt” means any non—toxic salt or salt of an ester of a nd of this invention that, upon administration to a ent, is capable of providing, either directly or indirectly, a compound of this invention or an inhibitorily active metabolite or residue thereof. As used herein, the term “inhibitorily active metabolite or residue thereof ’ means that a metabolite or e thereof is also an inhibitor of a voltage-gated sodium ion channel.

[00113] Pharrnaceutically acceptable salts are well known in the art. For example, S. M. Berge, et al. describe pharmaceutically acceptable salts in detail in J.

Pharmaceutical Sciences, 1977, 66, 1-19, incorporated herein by reference.

Pharmaceutically able salts of the compounds of this invention include those derived from suitable inorganic and organic acids and bases. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and oric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, ic acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange, Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, ate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, lsulfate, ethanesulfonate, e, fumarate, glucoheptonate, ophosphate, gluconate, hemisulfate, heptanoate, ate, hydroiodide, 2-hydroxy-ethanesulfonate, ionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, , oxalate, palmitate, pamoate, pectinate, persulfate, 3- phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p~toluenesulfonate, undecanoate, valerate salts, and the like. Salts derived from appropriate bases e alkali metal, alkaline earth metal, ammonium and N+(C1_4alkyl)4 salts. This invention also envisions the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil—soluble or dispersable products may be obtained by such quaternization. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary um, and amine cations formed using rions such as halide, hydroxide, carboxylate, sulfate, phosphate, e, loweralkyl sulfonate and aryl sulfonate.

As described above, the pharmaceutically acceptable compositions of the ion additionally comprise a ceutically acceptable carrier, adjuvant, or vehicle, which, as used herein, includes any and all solvents, diluents, or other liquid vehicle, dispersion or suspension aids, surface active agents, isotonic agents, thickening or emulsifying agents, preservatives, solid binders, lubricants and the like, as suited to the particular dosage form desired. Remington’s Pharmaceutical Sciences, Sixteenth n, E. W. Martin (Mack Publishing Co., Easton, Pa., 1980) discloses various carriers used in ating pharmaceutically acceptable compositions and known techniques for the preparation thereof. Except insofar as any conventional carrier medium is atible with the compounds of the invention, such as by producing any undesirable biological effect or otherwise interacting in a deleterious manner with any other component(s) of the pharmaceutically acceptable composition, its use is contemplated to be within the scope of this invention. Some examples of materials which can serve as pharmaceutically acceptable rs include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, or potassium e, l glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal , magnesium trisilicate, polyvinyl pyrrolidone, polyacrylates, waxes, polyethylene- polyoxypropylene—block polymers, wool fat, sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols; such a ene glycol or polyethylene glycol; esters such as ethyl oleate and ethyl laurate; agar; ing agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer’s solution; ethyl alcohol, and phosphate buffer solutions, as well as other xic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming , preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.

Uses ofCompounds and Pharmaceutically Acceptable Compositions ] In yet another aspect, a method for the treatment or lessening the severity of acute, c, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, ic neuralgia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, psychiatric disorders such as anxiety and depression, dipolar disorder, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, or cancer pain is provided comprising administering an ive amount of a, compound, or a pharmaceutically acceptable composition comprising a compound to a subject in need f.

] In certain embodiments, a method of treatment or ing the severity of stroke, cerebral ischemia, traumatic brain injury, ophic lateral sclerosis, stress- or se induced angina, palpitations, hypertension, migraine, or abormal gastro-intestinal motility is provided sing administering an ive amount of a compound, or a ceutically acceptable composition comprising a compound to a subject in need thereof.

] In n embodiments, a method for the treatment or lessening the ty of acute, chronic, neuropathic, or inflammatory pain is provided comprising administering an effective amount of a compound or a ceutically acceptable composition to a subject in need thereof. In certain other embodiments, a method for the treatment or lessening the severity of radicular pain, sciatica, back pain, head pain, or neck pain is provided comprising administering an effective amount of a compound or a pharmaceutically acceptable composition to a subject in need thereof. In still other embodiments, a method for the treatment or lessening the severity of severe or intractable pain, acute pain, postsurgical pain, back pain, tinnitis or cancer pain is provided comprising administering an effective amount of a compound or a pharmaceutically acceptable composition to a subject in need thereof.

In certain embodiments, a method for the treatment or lessening the severity of femur cancer pain; non-malignant chronic bone pain; rheumatoid arthritis; osteoarthritis; spinal is; neuropathic low back pain; neuropathic low back pain; myofascial pain syndrome; fibromyalgia; temporomandibular joint pain; chronic visceral pain, including, abdominal; pancreatic; IBS pain; chronic and acute he pain; migraine; tension headache, including, r headaches; chronic and acute -82— neuropathic pain, including, post-herpetic neuralgia; diabetic neuropathy; HlV- associated neuropathy; trigeminal neuralgia; Charcot-Marie Tooth neuropathy; hereditary sensory neuropathies; peripheral nerve ; l neuromas; ectopic proximal and distal discharges; radiculopathy; chemotherapy induced neuropathic pain; radiotherapy-induced neuropathic pain; post-mastectomy pain; central pain; spinal cord injury pain; post-stroke pain; thalamic pain; complex regional pain syndrome; phantom pain; intractable pain; acute pain, acute post-operative pain; acute musculoskeletal pain; joint pain; mechanical low back pain; neck pain; tendonitis; injury/exercise pain; acute visceral pain, including, abdominal pain; pyelonephritis; icitis; cholecystitis; intestinal obstruction; hernias; etc; chest pain, including, cardiac Pain; pelvic pain, renal colic pain, acute ric pain, including, labor pain; cesarean section pain; acute inflammatory, burn and trauma pain; acute intermittent pain, including, triosis; acute herpes zoster pain; sickle cell anemia; acute pancreatitis; hrough pain; orofacial pain including sinusitis pain, dental pain; multiple sclerosis (MS) pain; pain in depression; leprosy pain; behcet’s disease pain; adiposis dolorosa; phlebitic pain; Guillain-Barre pain; painful legs and moving toes; Haglund syndrome; erythromelalgia pain; Fabry’s disease pain; bladder and urogenital disease, including, urinary incontinence; ctivity bladder; l r syndrome; interstitial cyctitis (1C); or prostatitis; complex regional pain syndrome (CRPS), type I and type II; angina-induced pain is provided, comprising administering an effective amount of a compound or a pharmaceutically acceptable composition to a subject in need thereof.

In certain embodiments of the invention an “effective amount” of the compound or ceutically acceptable composition is that amount ive for treating or lessening the severity of one or more of acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster hes, inal neuralgia, ic gia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, atric disorders such as anxiety and depression, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sclerosis, irritable bowel syndrome, incontinence, Visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, tinnitis or cancer pain.

The compounds and compositions, according to the method of the invention, may be administered using any amount and any route of administration effective for treating or ing the severity of one or more of acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, herpetic neuralgia, general neuralgias, epilepsy or epilepsy conditions, neurodegenerative disorders, psychiatric disorders such as anxiety and depression, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, le sclerosis, irritable bowel syndrome, incontinence, al pain, osteoarthritis pain, postherpetic neuralgia, diabetic neuropathy, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, nociceptive pain, breakthrough pain, postsurgical pain, tinnitis or cancer pain. The exact amount required will vary from subject to subject, depending on the species, age, and general condition of the subject, the severity of the infection, the particular agent, its mode of administration, and the like.

The compounds of the invention are ably formulated in dosage unit form for ease of administration and uniformity of . The expression “dosage unit form” as used herein refers to a physically discrete unit of agent appropriate for the subject to be treated. It will be understood, however, that the total daily usage of the compounds and itions of the invention will be decided by the attending physician within the scope of sound medical judgment. The specific effective dose level for any particular subject or organism will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition ed; the age, body weight, general health, sex and diet of the subject; the time of administration, route of stration, and rate of excretion of the specific compound employed; the duration of the ent; drugs used in ation or coincidental with the specific compound ed, and like factors well known in the medical arts. The term “subject” or “patient”, as used herein, means an animal, preferably a mammal, and most ably a human.

The pharmaceutically able compositions of this invention can be administered to humans and other animals , rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by s, ointments, or drops), —84- y, as an oral or nasal spray, or the like, depending on the severity of the infection being treated. In certain embodiments, the compounds of the invention may be administered orally or parenterally at dosage levels of about 0.01 mg/kg to about 50 mg/kg and preferably from about 1 mg/kg to about 25 mg/kg, of subject body weight per day, one or more times a day, to obtain the desired therapeutic effect.

Liquid dosage forms for oraladministration include, but are not limited to, ceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may n inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and fiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3- ne glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of an, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and ding agents, ning, flavoring, and perfuming agents.

Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic erally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.

Among the acceptable vehicles and solvents that may be employed are water, ’s solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending . For this purpose any bland fixed oil can be employed including tic mono— or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of inj ectables.

The injectable formulations can be sterilized, for example, by ion h a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in e water or other sterile injectable medium prior to use.

In order to prolong the effect of a compound of the invention, it is often desirable to slow the absorption of the compound from aneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous al with poor water solubility. The rate of absorption of the compound then depends upon its rate of dissolution that, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered compound form is lished by dissolving or suspending the compound in an oil vehicle. able depot forms are made by forming microencapsule matrices of the compound in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of compound to polymer and the nature of the particular polymer employed, the rate of compound release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also ed by entrapping the compound in liposomes or microemulsions that are compatible with body tissues. ] itions for rectal or vaginal administration are preferably suppositories which can be prepared by mixing the compounds of this invention with le non—irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at t temperature but liquid at body ature and therefore melt in the rectum or vaginal cavity and release the active compound.

[00127] Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharrnaceutically able excipient or carrier such as sodium citrate or dicalcium phosphate and/or a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, (1) disintegrating agents such as agar--agar, m carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and ol earate, h) absorbents such as kaolin and bentonite clay, and i) ants such as talc, calcium stearate, magnesium stearate, solid polyethylene ~86- glycols, sodium lauryl sulfate, and es thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like. The solid dosage forms of tablets, s, capsules, pills, and granules can be prepared with coatings and shells such as c coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed . Examples of ing compositions that can be used include polymeric substances and waxes. Solid itions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polethylene s and the like.

[00129] The active compounds can also be in microencapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings, release lling coatings and other coatings well known in the pharmaceutical formulating art. In such solid dosage forms the active compound may be admixed with at least one inert diluent such as e, lactose or starch. Such dosage forms may also comprise, as is normal practice, additional substances other than inert diluents, e. g., tableting lubricants and other tableting aids such a magnesium stearate and microcrystalline ose. In the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. They may optionally contain opacifying agents and can also be of a composition that they e the active ingredient(s) only, or preferentially, in a certain part of the inal tract, ally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes.

Dosage forms for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions WO 25613 with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulation, eardrops, and eye drops are also contemplated as being within the scope of this invention. Additionally, the invention contemplates the use of ermal patches, which have the added advantage of providing controlled delivery of a compound to the body. Such dosage forms are prepared by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel. , [00131] As described generally above, the nds of the invention are useful as inhibitors of e—gated sodium ion channels. In one embodiment, the compounds and compositions of the invention are inhibitors of one or more of NaVl.l, NaVl.2, NaV1.3, NaV1.4, NaVl.5, NaVl.6, NaVl.7,NaV1.8, or NaV1.9, and thus, without wishing to be bound by any particular theory, the compounds and compositions are particularly useful for treating or lessening the severity of a disease, condition, or disorder where activation or hyperactivity of one or more ofNaVl .1, NaVl.2, NaVl .3, NaV1.4, NaVl.5, NaVl.6, NaVl.7, NaVl.8, or NaVl .9 is implicated in the disease, condition, or disorder. When activation or hyperactivity ofNaVl .l, NaVl .2, NaV1.3, NaV1.4, NaV1.5,NaV1.6, NaVl.7, NaVl .8, or NaV1.9 is implicated in a particular disease, condition, or disorder, the disease, condition, or disorder may also be referred to as a l, NaVl .2, NaVl .3, NaVl .4, NaVl.5, NaVl.6, NaVl .7, NaV1.8 or NaVl .9-mediated disease, condition or disorder”. ingly, in r aspect, the invention provides a method for treating or lessening the severity of a disease, condition, or disorder where activation or hyperactivity of one or more of NaVl.l,NaV1.2,NaV1.3, NaV1.4,NaV1.5, NaVl.6,NaV1.7,NaVl.8, or NaV1.9 is implicated in the disease state.

The activity of a compound utilized in this ion as an inhibitor of NaVl.l,NaV1.2, NaV1.3, NaV1.4, , NaVl.6,NaV1.7,NaV1.8, or NaV1.9 may be assayed according to s described generally in the es , or according to methods available to one of ordinary skill in the art.

In certain exemplary embodiments, nds of the invention are usefiJl as inhibitors of NaVl .7 and/or NaVl .8.

It will also be appreciated that the compounds and pharmaceutically acceptable compositions of the invention can be employed in combination therapies, that is, the compounds and pharmaceutically able compositions can be administered concurrently with, prior to, or subsequent to, one or more other desired therapeutics or medical procedures. The particular combination of therapies (therapeutics or procedures) to employ in a ation regimen will take into account ibility of the desired eutics and/or procedures and the desired therapeutic effect to be achieved. It will also be appreciated that the therapies ed may achieve a d effect for the same disorder (for example, an ive compound may be administered concurrently with another agent used to treat the same disorder), or they may achieve different effects (e.g., control of any adverse s). As used herein, additional therapeutic agents that are normally administered to treat or prevent a particular disease, or condition, are known as “appropriate for the disease, or condition, being treated”. For example, exemplary additional therapeutic agents include, but are not limited to: nonopioid analgesics (indoles such as Etodolac, Indomethacin, Sulindac, Tolmetin; naphthylalkanones such sa Nabumetone; oxicams such as Piroxicam; para-aminophenol derivatives, such as Acetaminophen; propionic acids such as Fenoprofen, Flurbiprofen, Ibuprofen, Ketoprofen, Naproxen, Naproxen sodium, Oxaprozin; salicylates such as Asprin, Choline magnesium trisalicylate, Diflunisal; tes such as meclofenamic acid, Mefenamic acid; and pyrazoles such as Phenylbutazone); or opioid (narcotic) agonists (such as Codeine, Fentanyl, Hydromorphone, Levorphanol, Meperidine, Methadone, Morphine, Oxycodone, Oxymorphone, Propoxyphene, Buprenorphine, Butorphanol, ne, Nalbuphine, and Pentazocine). Additionally, nondrug analgesic ches may be utilized in conjunction with administration of one or more compounds of the ion. For example, anesthesiologic (intraspinal infusion, neural blocade), neurosurgical (neurolysis of CNS pathways), neurostimulatory (transcutaneous ical nerve stimulation, dorsal column stimulation), physiatric (physical therapy, orthotic devices, diathermy), or psychologic tive methods-hypnosis, biofeedback, or behavioral methods) ches may also be utilized. Additional appropriate therapeutic agents or approaches are described generally in The Merck Manual, Seventeenth Edition, Ed.

Mark H. Beers and Robert , Merck Research Laboratories, 1999, and the Food and Drug Administration website, www.fda.go_v, the entire contents of which are hereby incorporated by reference.

In another embodiment, additional appropriate therapeutic agents are selected from the following: (1) an opioid analgesic, e. g. morphine, , hydromorphone, oxymorphone, levorphanol, levallorphan, methadone, dine, fentanyl, cocaine, codeine, dihydrocodeine, oxycodone, hydrocodone, propoxyphene, ene, nalorphine, naloxone, naltrexone, buprenorphine, butorphanol, nalbuphine or pentazocine; (2) a nonsteroidal antiinflammatory drug ), e.g. aspirin, diclofenac, diflusinal, etodolac, fenbufen, fenoprofen, flufenisal, flurbiprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, meclofenamic acid, mefenamic acid, meloxicam, nabumetone, naproxen, nimesulide, nitroflurbiprofen, olsalazine, oxaprozin, phenylbutazone, piroxicam, alazine, sulindac, tolmetin 0r rac; (3) a barbiturate sedative, e.g. amobarbital, aprobarbital, butabarbital, butabital, mephobarbital, metharbital, methohexital, arbital, phenobartital, secobarbital, talbutal, theamylal or thiopental; (4) a benzodiazepine having a sedative action, e. g. iazepoxide, clorazepate, diazepam, flurazepam, lorazepam, oxazepam, temazepam or triazolam; (5) an Hi antagonist having a sedative action, e.g. diphenhydramine, mine, promethazine, chlorpheniramine or chlorcyclizine; (6) a ve such as glutethimide, meprobamate, methaqualone or dichloralphenazone;

[00142] (7) a skeletal muscle relaxant, e. g. baclofen, prodol, oxazone, cyclobenzaprine, methocarbamol or orphrenadine; (8) an NMDA receptor antagonist, e.g. dextromethorphan ((+) hydroxy—N— methylmorphinan) or its lite dextrorphan ((+)-3—hydroxy—N- methylmorphinan), ketamine, memantine, pyrroloquinoline quinine, cis—4- WO 25613 (phosphonomethyl) piperidinecarboxylic acid, budipine, EN—323l (MorphiDex(R), a combination. formulation of morphine and dextromethorphan), topiramate, neramexane or perzinfotel including an NR2B antagonist, e.g. ifenprodil, traxoprodil or (-)-(R) {2-[4-(3-fluorophenyl)hydroxy-l- piperidinyl]—1-hyd'roxyethy1-3 ,4-dihydro- 2(1H)—quinolinone; (9) an alphwadrenergic, e.g. doxazosin, tamsulosin, clonidine, guanfacine, dexmetatomidine, modafinil, or 4-amino—6,7-dimethoxy(5~methane- sulfonamidO-l, 2,3,4- tetrahydroisoquinol—Z-yl)(2-pyridyl) quinazoline; ] (10) a tricyclic antidepressant, e.g. desipramine, imipramine, ptyline or nortriptyline; (11) an anticonvulsant, e. g. carbamazepine, lamotrigine, topiratmate or ate; (12) a inin (NK) antagonist, particularly an NK-3, NK-2 or NK-I antagonist, e.g. ([alpha]R,9R)—7~[3,5-bis(trifluoromethyl)benzyl]~8,9, 10,11 - ydromethyl(4- methylphenyl)—7H—[1 ,4]diazocino[2,l-g] [l,7]-naphthyridine— 6dione (TAK-637), 5— [[(2R,3 S)—2-[(lR)—1—[3,5-bis(trifluor0methyl)phenyl]ethoxy— 3-(4-fluorophenyl)morpholinyl]-methyl]-l,2-dihydro-3H—l,2,4-triazol0ne (MK- 869), aprepitant, lanepitant, dapitant or 3-[[2—meth0xy—5—(trifluoromethoxy)phenyl]- methylamino] phenylpiperidine (ZS ,3 S); ] (13) a muscarinic nist, e.g oxybutynin, tolterodine, erine, tropsium chloride, darifenacin, solifenacin, temiverine and ipratropium; (14) a COX-2 selective inhibitor, e.g. celecoxib, xib, parecoxib, valdecoxib, deracoxib, etoricoxib, or lumiracoxib; (15) a coal-tar analgesic, in particular paracetamol;

[00151] (1.6) a neuroleptic such as droperidol, chlorpromazine, haloperidol, perphenazine, thioridazine, mesoridazine, trifluoperazine, fluphenazine, clozapine, olanzapine, Iisperidone, ziprasidone, pine, sertindole, razole, sonepiprazole, blonanserin, iloperidone, perospirone, raclopride, zotepine, bifeprunox, asenapine, lurasidone, amisulpride, balaperidone, palindore, eplivanserin, osanetant, 3O rimonabant, meclinertant, Miraxion(R) or sarizotan; (17) a 'vanilloid receptor t (e. g. resinferatoxin) or antagonist (e. g. epine); (18) a beta-adrenergic such as propranolol; (19) a local anaesthetic such as mexiletine;

[00155] (20) a corticosteroid such as dexamethasone; (21) a 5-HT receptor agonist or antagonist, particularly a 5—HTi B/l D agonist such as eletriptan, sumatriptan, naratriptan, zolrnitriptan or rizatriptan; (22) a 5-HT2A receptor antagonist such as lpha-(2,3-dirnethoxy- phenyl)—l-[2-(4- fluorophenylethyl)]piperidinemethanol (MDL— 100907);

[00158] (23) a cholinergic inic) analgesic, such as ispronicline (TC- 1734), (E)-N—rnethyl (3-pyridinyl)-3—buten—l -amine (RJR—2403), (R)—5-(2— azetidinylmethoxy)—2~chloropyridine (ABT-594) or ne; (24) Tramadol®; (25) a PDEV inhibitor, such as 5-[2-ethoxy—5-(4-methyl-l-piperaziny1- 1 5 sulphonyl)phenyl]- l-methyl-3 -n-propyl—l,6—dihydro-7H—pyrazolo[4,3-d]pyrimidin—7- one (sildenafil), (6R,12aR)— 2,3,6,7,12,12a-hexahydrornethyl-6—(3,4— methylenedioxyphenyl)-pyrazino[2',l':6,1]- pyrido[3,4—b]indole-l,4-dione (lC-35 l or tadalafil), 2—[2-ethoxy—5-(4-ethyl-piperazin-l-yl-l- sulphonyl)—phenyl]methyl propyl-3H—imidazo[5,l-t][1,2,4]triazinone (vardenafil), 5— (5—acetylbutoxyu3- pyridinyl)—3-ethyl—2-(l—ethyl-3—azetidinyl)-2,6-dihydro-7H—pyrazolo[4,3—d]pyrirnidin one, 5—(5—acetyl—2-propoxy—3-pyridinyl)—3-ethyl—2-(l-isopropyl- 3—azetidinyl)—2,6- dihydro—7H—pyrazolo[4,3-<i]pvrirnidm-7—one, thoxy—5—(4-ethylpiperazin-l_ ylsulphony1)pyridinyl]ethy1[2-methoxyethy1]—2,6-dihydro—7H— lo[4,3- d]pyrimidinone, 4-[(3 omethoxybenzy1)amino]—2-[(2S)—2- (hydroxymethyl)pyrrolidin-l -yl]-N—(pyrimidin—2—y11nethy1)pyrirnidinecarboxamide, 3-(1 — methyloxo-3~propyl-6,7—dihydro-lH—pyrazolo[4,3—d]pyrimidin—5-yl)-N-[2-(l- methylpyrrolidiny1)ethyl]-4—propoxybenzenesulfonarnide; (2) an alphadelta ligand such as gabapentin, alin, 3 -methyl gabapentin, (l[alpha],3 [alpha] ,5 [alpha])(3-amino-methyl-bicyclo[3 .2.0]hept-3 -yl)-acetic acid, (3 S,5R)-3—aminomethyl- 5—methyl—heptanoic acid, (3S,5R)-3—aminomethyl— heptanoic acid, (3S,5R)—3-amino- 5-methyl-octanoic acid, (28,4S)(3- chlorophenoxy)proline, )(3—fluorobenzy1)- proline, [(lR,5R,6S)-6— (aminomethyl)bicyclo[3.2.0]hepty1]acetic acid, 3-(l—aminomethyl- cyclohexylmethyl)—4H-[ 1 ,2,4]oxadiazol—5-one, C-[ 1 -(I H—tetrazol-S-ylmethyl)- cycloheptyl]- methylamine, (3 S,4S)—(l—aminomethyl-3,4-dimethyl-cyclopentyl)—acetic acid, (3 S, 5R)— 3-aminomethy1methyl-octanoic acid, (3S,5R)—3-amino—5-methyl- nonanoic acid, (3S,5R)— 3-amino~5—methyl-octanoic acid, (3R,4R,5R)—3-amino—4,5- dimethyl-heptanoic acid and (3R,4R,5R)—3-amino-4,5-dimethy1-octanoic acid; (26) a cannabinoid;

[00162] (27) metabotropic glutamate subtype 1 receptor (mGluR1) antagonist; (28) a serotonin reuptake inhibitor such as sertraline, line lite demethylsertraline, ine, norfluoxetine (fluoxetine desmethyl metabolite), fluvoxamine, paroxetine, citalopram, citalopram metabolite desmethylcitalopram, escitalopram, d,l- fenfluramine, femoxetine, ifoxetine, cyanodothiepin, litoxetine, dapoxetine, nefazodone, cericlamine and trazodone; (29) a noradrenaline (norepinephrine) reuptake inhibitor, such as maprotiline, lofepramine, mirtazepine, oxaprotiline, fezolamine, tomoxetine, mianserin, buproprion, buproprion metabolite ybuproprion, nomifensine and Viloxazine (Vivalan(R)), especially a selective noradrenaline reuptake inhibitor such as reboxetine, in particular (S,S)—reboxetine; (30) a dual serotonin-noradrenaline reuptake inhibitor, such as venlafaxine, venlafaxine metabolite O-desmethylvenlafaxine, clomipramine, clomipramine metabolite hylclomipramine, duloxetine, ipran and imipramine;

[00166] (31) an inducible nitric oxide se (iNOS) inhibitor such as S-[2- [(l— iminoethyl)amino] ethyl]~L—homocysteine, S— [2- inoethyl)-amino] ethyl] ~4,4- dioiro-L- cysteine, S-[2-[(l-iminoethy1)amino]ethyl]—2-methyl-L-cysteine, (2S,5Z) amino—2—methyl- 7-[(l—iminoethyl)amino]heptenoic acid, R,3S)—3-amino hydroxy- 1—(5-thiazoly1)-butlethioJ-S-chloro—S-pyridinecarbonitrile; 2-[[(1R,3 S)—3- 4-hydroxy—l-(5- thiazolyl)butyl]thio]chlorobenzonitrile, (2S,4R)amino—4- [[2-chloro-5— (trifluoromethyl)phenyl]thio]thiazolebutanol, 2-[[(1R,3S)amino hydroxy—l-(S-thiazolyl) butyl]thio](trifluoromethy1)—3 pyridinecarbonitrile, 2— [[(1R,3 S)—3- 4-hydroxy— 1 -(5-thiazolyl)buty1]thio] chlorobenzonitrile, N—[4- [2~(3-ch10robenzy1amino)ethyl]pheny1]thiophene—Z-carboxamidine, or guanidinoethyldisulfide; (32) an cholinesterase inhibitor such as donepezil; (33) a prostaglandin E2 subtype 4 (EP4) nist such as N-[({2-[4- (2—ethy1—4,6- dimethyl—lH-imidazo[4,5-c]pyridin-l-yl)phenyl]ethyl} amino)-carb0ny1]-4— methylbenzenesulfonamide or 4—[(1 5)—1-( loro-2—(3-fluorophenoxy)pyridin y1]carbonyl} ethy1]benzoic acid; (34) a leukotriene B4 antagonist; such as 1-(3-biphenyl-4—ylrnethy1 hydroxy—chroman-7— yl)-cyclopentanecarboxylic acid (CP- 105696), 5—[2—(2- Carboxyethyl)[6-(4- methoxyphenyl)—5E- hexenyl]oxyphenoxy]-valeric acid (ONO- 4057) or DPC-11870, ] (35) a 5-lipoxygenase inhibitor, such as Zileuton, 6-[(3-fluoro[4— methoxy—3 ,4,5,6- tetrahydro-2H—pyrany1])phenoxy—methyl]methy1quinolone (ZD-2138), or 2,3,5— hyl~6—(3—pyridylmethyl),1 ,4-benzoquinone (CV-6504); (36) a sodium channel blocker, such as lidocaine; (37) a 5—HT3 antagonist, such as ondansetron; and the pharmaceutically acceptable salts and solvates thereof.

The amount of additional therapeutic agent present in the compositions of this invention will be no more than the amount that would normally be administered in a composition comprising that therapeutic agent as the only active agent. Preferably the amount of additional eutic agent in the presently disclosed compositions will range from about 50% to 100% of the amount normally present in a composition comprising that agent as the only therapeutically active agent.

The compounds of this invention or pharmaceutically acceptable compositions thereof may also be incorporated into compositions for coating an implantable l device, such as prostheses, artificial valves, vascular grafts, stents 3O and catheters. ingly, the ion, in another aspect, includes a composition WO 25613 for coating an implantable device comprising a compound of the ion as described generally above, and in classes and subclasses herein, and a carrier suitable for coating said implantable device. In still r aspect, the invention includes an implantable device coated with a composition comprising a compound of the invention as described lly above, and in classes and sses herein, and a carrier le for coating said implantable device. Suitable coatings and the general preparation of coated implantable devices are described in US Patents 6,099,562; 5,886,026; and 5,304,121.

The coatings are typically biocompatible polymeric materials such as a hydrogel polymer, polymethyldisiloxane, polycaprolactone, polyethylene glycol, polylactic acid, ethylene Vinyl acetate, and mixtures thereof. The coatings may ally be further covered by a suitable topcoat of fluorosilicone, polysaccarides, polyethylene glycol, phospholipids or combinations thereof to impart controlled e characteristics in the composition. r aspect of the invention relates to inhibiting one or more of NaVl.l, NaVl .2, NaVl.3, NaVl.4, NaV1.5, NaV1.6, NaVl.7, NaVl .8, or NaV1.9, activity in a biological sample or a subject, which method comprises administering to the subject, or contacting said biological sample with a compound of formula 1 or a composition sing said compound. The term gical sample”, as used herein, includes, without limitation, cell cultures or extracts thereof; biopsied material obtained from a mammal or extracts thereof; and blood, , urine, feces, semen, tears, or other body fluids or extracts thereof.

Inhibition of one or more ofNaVl .1, NaVl .2, NaVl.3, NaVl.4, NaVl .5, , NaVl .7, NaVl .8, or NaVl .9, activity in a biological sample is useful for a variety of purposes that are known to one of skill in the art. Examples of such purposes e, but are not limited to, the study of sodium ion channels in biological and pathological phenomena; and the comparative tion of new sodium ion channel inhibitors.

EXAMPLES General methods. 1H NMR (400 MHz or 300 MHz) and ”C NMR (100 MHZ) spectra were obtained as solutions in deuterioacetonitrile (CD3CN), chloroform-d (CDC13), deuteromethanol (MeOD—d4), or dimethyl sulfoxide-D6 (DMSO). Mass spectra (MS) were obtained using an Applied Biosystems API EX LC/MS system equipped with a enex 50 x 4.60 mm luna-Su C18 column. The LC/MS eluting system was 1-99% or 10-99% acetonitrile in H20 with 0.035% V/v trifluoroacetic acid, 0.035% v/v formic acid, 5 mM HCl or 5 mM ammonium formate using a 3 or 15 minute linear gradient and a flow rate of 12 mL/minute. Silica gel chromatography was performed using silica gel-60 with a le size of 23 0—400 mesh. Pyridine, dichloromethane (CH2C12), tetrahydrofuran (THF), ylformamide (DMF), acetonitrile (ACN), methanol , and 1,4-dioxane were from Aldrich Sure-Seal bottles kept under dry nitrogen. All reactions were stirred magnetically unless otherwise noted.

Preparation of 10-phenyl—8—(2,2,2-trifluoroethyl)—11-oxa—3,8- diazaspiro[5.5] undecane @1010...

] Step 1:

[00180] To a solution of 2-amino—l-phenyl-ethanol (12.0 g, 87.48 mmol) in methanol (60 mL) was added benzaldehyde (9.3 g, 8.9 mL, 87.48 mmol) and the reaction mixture was stirred for 1 hour at room temperature. The reaction mixture was then cooled to 0 °C and sodium borohydride (3.3 g, 87.48 mmol) was added. The reaction mixture was gradually allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated in vacuo, diluted with water, and filtered. The residue was rinsed with cold isopropanol (3x), then dried in vacuo to give zylamino)-l-phenylethanol as white ls (14.0 g, 70 %). ESI-MS m/z calc. 227.1, found 228.2 (M+l)+; Retention time:0.8 minutes (3 min run). 1H NMR (400 MHz, MeOD) 6 7.37 — 7.27 (m, 8H), 7.27 - 7.19 (m, 2H), 4.78 (dd, J = 8.5, 4.5 Hz, 1H), 3.77 (q, J = 13.0 Hz, 2H), 2.82 - 2.68 (m, 2H).

Step 2: -96— A solution of 2-(benzylamino)—l-phenylethanol (5.3 g, 23.44 mmol) and tert~butyl 6-azaspiro[2.5]octane-6—carboxylate (5.0 g, 23.44 mmol) in ethanol (30 mL) was heated overnight at 75 OC. The solvent was evaporated and the crude material was used in the next step without further purification. ESl-MS m/z calc. 440.2, found 441.7 (M+1)+; Retention time:1.41 minutes (3 min run).

Step 3: To tert—butyl 4—[[benzyl—(2—hydroxy—2“phenyl-ethyl)amino]methyl] hydroxy~piperidinecarboxylate (6.2 g, 14.07 mmol) was added HBr (60 mL of 48 %w/w, ) and the reaction mixture was stirred at 55 0C for 10 hours. The reaction e was evaporated in vacuo, basified the aqueous with 50% aq. NaOH to le3, then ted with DCM (3 x 75 mL). The combined organics were dried over MgSO4, d and concentrated in vacuo to give 4—benzyl—2-phenyl-1—oxa-4,9- diazaspiro[5.5]undecane (4.4 g, 97 %) as a yellow oil, which was used directly without r purification. ESl—MS m/z calc. 322.2, found 323.7 (M+1)+; Retention time: 1.72 minutes (3 min run).

Step 4: To crude 4-benzy1phenyloxa—4,9-diazaspiro[5.5]undecane (4.1 g, 12.72 mmol) in DCM (15 mL) was added BoczO (2.8 g, 2.9 mL, 12.72 mmol) and the reaction mixture was stirred for 2 hours. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography using 0-60% EtOAc/hexane as eluent to give tert—butyl 10-benzylpheny1-7—oxa-3,10—diazaspiro[5.5]undecane carboxylate as a white foam (3.6 g, 66 %) found 423.7 . ESI-MS m/z calc. 422.3, (M+1)+; Retention time: 1.71 minutes (3 min run). 1H NMR (400 MHZ, CDC13) 5 7.38 = 13.3 Hz, 1H), 3.39 (d, J - 7.25 (m, 10H), 4.88 - 4.78 (m, 1H), 3.69 (s, 2H), 3.57 (d, J = 13.3 Hz,1H), 3.35 - 2.91 (m,1H), 2.67 - - 3.26 (m, 1H), 3.18 - 3.06 (m, 1H), 3.00 2.60 (m, 1H), 2.59 - 2.49 (m, 1H), 2.05 - 1.46 - 1.89 (m, 2H), 1.64 — 1.57 (m, 1H), 1.53 (m, 2H), 1.43 (s, 9H).

] Step 5: To tert-butyl 10-benzyl-8—phenyloxa—3,10-diazaspiro[5.5]undecane- 3-carboxylate (1.58 g, 3.74 mmol) and Pd(OH)2 (280 mg, 0.40 mmol) in ethanol (16 mL) was added ammonium formate (1.10 g, 17.39 mmol) and the reaction mixture was heated to 60°C for 40 min. The reaction mixture was cooled, filtered, concentrated to % of original , d with ethyl acetate and washed with sat. aq. NaHC03 (pH 10)/brine. The aqueous was extracted further with ethyl acetate and the combined cs were dried over , filtered and concentrated in vacuo to give utyl 8-pheny1oxa-3,10—diazaspiro[5.5]undecane-3—carboxylate (1.15 g, 93 %) as a white solid. ESI-MS m/z calc. 332.2, found 333.3 (M+1)+; Retention time: 1.13 minutes (3 min run). 1H NMR (400 MHz, CDC13)5 7.40 - 7.23 (m, 5H), 4.69 (dd, J = 10.7, 2.7 Hz, 1H), 3.76 (br. s, 2H), 3.31 (t, J = 10.7 Hz, 1H), 3.17 = - 3.02 (m, 2H), 2.75 (dd, J 355,124 Hz, 2H), 2.63 (dd, J = 12.3, 10.8 Hz,1H), 2.49 (d, J = 12.5 Hz, 1H), 1.69 — 1.57 (m, J = 12.6 Hz,1H),1.57 - 1.39 (m, 11H).

Step 6: To tert—butyl 10-phenyl-1 1—oxa-3,8-diazaspiro[5.5]undecane—3- carboxylate (0.98 g, 2.93 mmol) and NaHCO3 (0.99 g, 11.73 mmol) in ethanol at room temperature was added 2,2,2-trifluoroethyl trifluoromethanesulfonate (0.82 g, 545 uL, 3.52 mmol) and the reaction mixture was heated at 80 °C for 6 hours. The reaction mixture was cooled, the solid precipitate was removed by filtration and the solvent was removed in vacuo. The residue was taken up in DCM and washed sequentially with 1:1 NaOH(1N): NaHCO3 and then brine. The organics were separated, dried over sodium sulfate and concentrated in vacuo to give tert—butyl 10—phenyl-8—(2,2,2-trifluoroethyl)— 11-oxa-3,8-diazaspiro[5.5]undecanecarboxylate (1.15 g, 95 %). ESI—MS m/z calc. 414.2, found 415.3 (M+l)+; Retention time: 2.46 minutes (3 min run). 1H NMR (400 MHZ, CDC13) 6 7.44 — 7.26 (m, 5H), 4.81 (dd, J: 10.5, 2.6 Hz, 1H), 3.73 (s,2H), 3.31 (s, 1H), 3.09 (s,1H), 2.98 (m, 3H), 2.74 (dd, J=11.0, 1.5 Hz, 1H), 2.51 (d, J=14.1 Hz, 1H), 2.40 — 2.29 (m,2H), 1.58 (s, 3H), 1.44 (s, 9H).

Step 7: To tert—butyl nyl(2,2,2-trifluoroethyl)oxa-3,8— diazaspiro[5.5]undecane—3—carboxylate (779 mg, 1.86 mmol) in dichloromethane (5 mL) was added 2,2,2-trifluoroacetic acid (5 mL, 64.90 mmol) at room temperature.

The reaction mixture was stirred for 40 minutes, then d with dichloromethane (75 mL) and the organic solution was washed with saturated sodium onate (twice) and then brine. The organic layer was dried over sodium sulfate, filtered and the solvent was removed in vacuo to give ny1(2,2,2-trifluoroethyl)-1l-oxa-3,8— diazaspiro[5.5]undecane as an amber oil (585 mg, 99%). ESI—MS m/z calc. 314.2, found 315.3 (M+1)+; Retention time: 1.29 minutes (3 min run). 1H NMR (400 MHz, CD3CN) 5 7.44 - 7.25 (m, 5H), 4.82 (dd, J = 10.6, 2.8 Hz, 1H), 3.74 (br s, 1H), 3.06 (q, J = 9.8 Hz, 2H), 3.02 = 11.2, 1.5 Hz, 1H), 2.85 - 2.74 (m, — 2.91 (m, 2H), 2.88 (dd, J 3H), 2.34 (d, J = 14.8 Hz, 1H), 2.28 (dt, J = 10.9, 5.3 Hz, 2H), 1.76 = 16.0, - 1.64 (m, J 8.7, 5.3 Hz,1H),1.64 - 1.52 (m, 2H).

Preparation of 4-(2,2-difluoroethyl)—2-phenyloxa—4,9- diazaspiro [5.5]undecane This compound was prepared using the procedure as described above, using 2-difluoroethyl trifluoromethanesulfonate as the alkylation reagent in step 6.

Preparation of -difluoroethyl)—2—(4-fluorophenyl)—1-oxa-4,9- diazaspiro[5.5]undecane 010m This compound was prepared using the ure as bed above, starting with 2—amino(4-fluorophenyl)ethanol in step 1 and using 2-difluoroethyl trifluoromethanesulfonate as the alkylation reagent in step 6. ESI-MS m/z calc. 314.2, found 315.2 (M+1)+; Retention time: 1.08 minutes (3 min run). ation of 4-(2,2-difluoroethyl)—2-(4-fluorophenyl)—1-0xa—4,9- diazaspiro [5.5] undecane This compound was prepared using the procedure as described above, starting with 2-amino(2-fluoropheny1)ethan01 in step 1 and using 2-difluoroethy1 trifluoromethanesulfonate as the alkylation reagent in step 6. ESI-MS m/z caic. 058, found 315.3 (M+1)+; Retention time: 1.32 minutes (3 min run).

Preparation of 2-(2-phenyl—1-0xa—4,9-diazaspiro[5.5]undecan y1)acetonitrile ///N ] This nd was prepared using the procedure as described above, using 2—ch10roacetonitri1e as the alkylation reagent in step 6. ESI-MS m/z calc. 307.8, found 309.4 ; Retention time: 0.89 minutes (3 min run).

Preparation of 4-benzyl—2-(4-chlorophenyl)—l-oxa-4,9- diazaspir0[5.5] undecane Cl This compound was prepared using the steps 1-4 and 7 in the procedure as described above, starting with 2—amino—1-(4-chloropheny1)ethanol in step —100- 1. ESI-MS m/z calc. 356.9, found 357.3 (M+1)+; Retention time: 1.17 s (3 min run) .

Preparation of 4-benzyl—2-(p-tolyl)0xa—4,9- diazaspiro [5.5] undecane This compound was prepared using the steps 1—3 in the procedure as described above, starting with o(p-toly1)ethanol in step 1. ESI-MS m/z calc. 336.5, found 337.3 (M+1)+; Retention time: 0.65 minutes (3 min run).

Preparation of 8-ethylphenyl—11-oxa—3,8— diazaspiro[5.5]undecane @1010...

] Step 1: To a solution of tert-butyl 8-phenyloxa—3,10— diazaspiro[5.5]undecanecarboxylate (735 mg, 2.21 mmol) in methanol (10 mL) was added acetaldehyde (107 mg, 136 uL, 2.43 mmol), then sodium cyanoborohydride (195 mg, 1.5 mL, 3.10 mmol) and the reaction mixture was stirred for 2 hours. The reaction mixture was concentrated in vacuo, diluted with DCM (50 mL), washed with 1:1 aq. sat. NaHCO3 /25 % NaOH (10 mL), and the aqueous layer was extracted with DCM (2 x 25 mL). The combined cs were dried (MgSO4), concentrated in vacuo and purified by silica gel column chromatography using (0-75% EtOAc/DCM) as eluent to give tert—butyl 8—ethyl—10-phenyl—l 1-oxa—3 ,8-diazaspiro[5.5]undecane-3 -carboxylate 2012/028882 (540 mg, 68 %) as a Viscous yellow oil. ESI-MS m/z calc. 360.5, found 361.7 (M+1)+; Retention time: 1.15 minutes (3 min run).

Step 2: To tert—butyl 8-ethylpheny1-l1-oxa-3,8-diazaspiro[5.5]undecane carboxylate (540 mg, 1.50 mmol) in DCM (1.5 mL) was added 2,2,2—trifluoroacetic acid (1 mL, 12.98 mmol) and the on was d for 30 minutes. The reaction mixture was concentrated in vacuo, diluted with DCM (50 mL), washed with 1:1 sat. aq. /NaHCO3 (10 ml) and the aqueous was extracted further with DCM (2 X 25 mL). The combined organics were dried (MgSO4) and evaporated to give 8-ethyl phenyl-l 1-oxa-3,8-diazaspiro[5.5]undecane (390 mg, 100 %) as a pale yellow solid, which was used without further purification. ESI—MS m/z calc. 260.4, found 261.3 (M+1)+; Retention time: 0.3 minutes (3 min run).

Preparation of 8-is0butyl—10-phenyl—1l-oxa-3,8— diazaspiro[5.5] undecane gag.

This compound was prepared following the above procedure, using 2— methylpropanal in step 1. ESI—MS m/z calc. 288.2, found 289.3 (M+l)+; Retention time: 0.79 s (3 min run).

] Preparation of 4-ethyl(4-flu0r0phenyl)—1-0xa—4,9- diazaspiro[5.5]undecane This compound was prepared following the above procedure, using tert-butyl 2-(4-fluorophenyl)oxa—4,9-diazaspiro[5.5]undecanecarboxylate in step 1. ESI-MS m/z calc. 278.2, found 279.3 (M+1)+; Retention time: 0.20 minutes (3 min run).

Preparation of 4-ethyl-2,2-dimethyl—1—0xa-4,9- diazaspir0[5.5]undecane 40h.

] Step 1: A mixture of N—benzyl—2—methyl—prop—2—enamine (0.57 g, 3.52 mmol) and tert—butyl 1-oxaazaspiro[2.5]octanecarboxylate (0.75 g, 3.52 mmol) in ethanol (4 mL) was heated at 80 °C in a sealed vial for 16 hours. The reaction mixture was cooled and trated in vacuo to give tert—butyl 4-[[benzyl(2- methylallyl)amino]methy1]—4-hydroxy-piperidinecarboxylate (1.32 g, 100 %) as a colorless oil. ESI—MS m/z calc. 374.5, found 375.7 (M+1)+; Retention time: 1.24 minutes (3 min run).

Step 2:

[00218] To a solution of tert—butyl 4-[[benzy1(2-methylallyl)amino]methyl] hydroxy—piperidine-l—carboxylate (1.2 g, 3.20 mmol) in 2—methoxy—2-methy1-propane (11 mL) was added aq. NaHC03 (4.3 mL ofl M, 4.30 mmol) then iodine (0.9 g, 181 uL, 3.52 mmol) and the reaction mixture was rapidly d for 16 hours. The reaction mixture was diluted with ethyl acetate (25 mL), quenched with 5 mL 1 M Na28203 aq., shaken vigorously and separated. The organic layer was washed with 1:1 sat. aq. / 1 M Na28203 aq. (10 mL), dried over MgSO4 and concentrated in vacuo to give the iodide intermediate as a colorless oil. The oil was dissolved in DMSO (4 mL), and NaBH4 (0.1 g, 3.81 mmol) was added and the reaction mixture was heated at 100 °C for 2 hours. A further t of NaBH4 (0.05 g, 1.32 mmol) was added and the reaction mixture was heated at 100 °C for 2 hours. After cooling, the on was quenched with 5 M aq. HCl (5 mL), stirred for 15 s, then added 5 M aq. NaOH (5 mL) and 1M aq. Na28203 (5 mL). The reaction mixture was vigorously stirred for 16 hours, then extracted with ethyl acetate (3 x 5 mL), dried over MgSO4 then purified by silica gel column tography using 0-100% EtOAc/hexane as eluent to give tert- butyl 2-benzy1-4,4—dimethyl—5-oxa-2,9-diazaspiro[5.5]undecane—9-carboxylate (0.5 g, 42 %) as a colorless oil. ESI-MS m/z calc. 374.5, found 375.7 (M+1)+; Retention time: 1.24 minutes (3 min run).

Step 3: To tert—butyl 2—benzyl-4,4—dimethyloxa-2,9— diazaspiro[5.5]undecanecarboxylate (560 mg, 1.50 mmol) was added hydrogen chloride (7.5 mL of 4 M in dioxane, 29.90 mmol), followed by ethanol (2 mL) and the reaction mixture was d for 30 minutes. The reaction mixture was trated in vacuo, dissolved in water (5 mL), washed with methyl tert—butyl ether (5 mL), basified with solid NaHCO; then adjusted to pH 13-14 with 50% aq. NaOH. The s layer was extracted with ethyl acetate (3 x 25 mL), dried over MgSO4 and concentrated to give 2-benzyl-4,4-dimethyloxa-2,9-diazaspiro[5.5]undecane (400 mg, 98 %) as a yellow oil, which was used directly without further purification. ESI-MS m/z calc. 274.4, found 275.5 (M+1)+; Retention time: 0.75 s (3 min run).

Step 4: To yl-4,4-dimethy1oxa—2,9-diazaspiro[5.5]undecane (170 mg, 0.62 mmol) and pyridine (98 mg, 100 uL, 1.24 mmol) in DCM (2 mL) at -78 °C was added dropwise trifluoroacetic anhydride (130 mg, 86 uL, 0.62 mmol) and the on mixture was allowed to warm to room temperature over 16 hours. The reaction mixture was then concentrated in vacuo and purified by silica gel column chromatography using 0-100% EtOAc/DCM as eluent to give 1-(8-benzyl-10,10-dimethyl—11-oxa-3,8- diazaspiro[5.5]undecanyl)-2,2,2-trifluoro-ethanone (160 mg, 70 %)as a colorless oil.

ESI-MS m/z calc. 370.4, found 371.1 (M+1)+; Retention time: 1.48 minutes (3 min run).

Step 5: A mixture of acetic acid (100 uL, 1.76 mmol), Pd(OH)2 (11 mg, 0.02 mmol), 1-(8-benzyl-10,10—dimethyl-1 1-oxa—3 zaspiro[5 . 5]undecan-3 -yl)—2,2,2- trifluoro-ethanone (80 mg, 0.22 mmol), HCl (108 uL of4 M in dioxane, 0.43 mmol) and ethanol (2 mL) was treated to an atmosphere of hydrogen at 85 psi. for 3 days. The —104- WO 25613 reaction mixture was filtered and the catalyst was washed with ol, then concentrated in vacuo to give 1-(10,10-dimethyl-11—oxa-3,8-diazaspiro[5.5]undecan yl)-2,2,2-trifluoro-ethanone acetic acid salt as a yellow solid. ESI-MS m/z calc. 280.1, found 281.5 (M+1)+; Retention time: 0.91 minutes (3 min run).

Step 6: To 1-(10,10-dimethy1—1 1—oxa-3,8-diazaspiro[5.5]undecanyl)—2,2,2- trifluoro-ethanone acetic acid salt (90 mg, 0.26 mmol) in ethanol (1.4 mL) was added NaHCO3 (89 mg, 1.06 mmol) then iodoethane (42 uL, 0.53 mmol). The reaction mixture was heated at 60 0C for 5 hours, then at room temperature for 72 hours, then microfiltered and purified by prep LCMS (1-99% ACN/Water, 5 mM HCl modifier) to give 1-(8-ethyl—lO,10—dimethyl-l 1-oxa—3,8—diazaspiro[5.5]undecan-3—yl)—2,2,2- trifluoro-ethanone hydrochloride salt (47 mg, 52 %) as a white solid. ESI—MS m/z calc. 308.2, found 309.7 (M+1)+; Retention time: 0.90 minutes (3 min run).

] Step 7’:

[00228] To 1~(8-ethyl—10,10-dimethyloxa—3,8-diazaspiro[5.5]undecan—3- yl)-2,2,2-trifluoro-ethanone hydrochloride salt (47 mg, 0.14 mmol) and lithium ide (10 mg, 0.42 mmol) was added water (0.15 mL) and THF (0.6 mL) and the reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated in vacuo, partitioned between DCM (10 mL) / 1:1 brinezNH4OH (2 mL), ted with DCM (5 x 10 mL), dried over MgSO4 and concentrated in vacuo to give 4-ethyl-2,2-dimethyl-l—oxa—4,9—diazaspiro[5.5]undecane (24 mg, 81 %). ESl-MS m/z calc. 212.2, found 213.5 (M+1)+; ion time: 0.19 minutes (3 min run).

Preparation of 9-(tert—butoxycarbonyl)—4-(2,2,2-trifluoroethyl)—1- oxa-4,9-diazaspiro[5.5] undecane-Z-carboxylic acid o:60 y NTgo The synthesis of tert-butyl 4-[(benzylamino)methyl]hydroxy— piperidine-l-carboxylate was carried out as described above. -105— Step 1: To tetrakis(tripheny1phosphine)palladium(0) (487 mg, 0.42 mmol) and triphenylphosphine (442 mg, 1.69 mmol) in degassed THF (75 mL) was added triethylamine (2.35 mL, 16.85 mmol) . The reaction mixture was stirred for 1 hour under an atmosphere of nitrogen. A solution of tert-butyl 4-[(benzylamino)methyl]—4- hydroxy—piperidine-l-carboxylate (2.7 g, 8.43 mmol) in degassed THF (10 mL) was added Via cannula, ed by the addition of [(Z)—4-acetoxybutenyl] acetate (1.35 mL, 8.47 mmol) and the reaction e was d in a sealed re flask at 45 °C for 16 hours. The reaction mixture was concentrated in vacuo, diluted with ethyl acetate, chilled to -15 0C, and the solid was removed by filtration over Celite®. The filtrate was trated in vacuo and the residue was purified by silica gel column chromatography using 0-60% EtOAc/hexane as eluent to give tert—butyl 10-benzyl-8— vinyl—7-oxa—3,10-diazaspir0[5.5]undecanecarboxylate (2.9 g, 92 %) as a pale yellow oil. 1H NMR (400 MHz, CDC13 ) 5 7.38 — 7.19 (m, 5H), 5.77 (ddd, J = 17.3, 10.6, 5.5 Hz, 1H), 5.36 — 5.23 (m, 1H), 5.13 (dt, J =10.6, 1.4 Hz, 1H), 4.25 (s, 1H), 3.64 (s, 2H), 3.53 (d, J = 13.3 Hz,1H), 3.37 (d, J =13.3 Hz, 1H), 3.29 (s, 1H), 3.10 (s, 1H), 2.84 — 2.72 (m, 1H), 2.55 (dd, J =11.1,1.4 Hz, 1H), 2.41 (d, J = 13.7 , 1.95 — 1.75 (m, 2H), 1.50 — 1.34 (m, 11H).

Step 2:

[00234] To tert—butyl 10-benzy1viny1oxa—3,10-diazaspiro[5.5]undecane-3— carboxylate (2.07 g, 5.56 mmol) and 4-methy1morpholine 4-oxide (725 mg, 6.19 mmol) in acetone (19 mL) and water (2 mL) was added osmium tetroxide in water (704 “L of 2.5 %w/w, 0.06 mmol) dropwise and the solution was stirred for 2 hours. The on mixture was quenched with 1M sodium lfate (50 mL) and stirred for 5 minutes, then extracted with EtOAc (4 x 50 mL), washed with sat. aq. NaHC03 (30 mL), and dried over MgSO4, filtered and concentrated in vacuo to give the diol intermediate. The diol was diluted with DCM (20 mL), filtered over a plug of neutral alumina, washing extensively with 20% MeOH/DCM (> 1 L). The filtrate was concentrated in vacuo to give tert—butyl 8-benzyl(1,2-dihydroxyethyl)oxa—3,8- diazaspiro[5.5]undecanecarboxylate (2.10 g, 93 %) as a white foam. ESI-MS m/z calc. 406.5, found 407.7 (M+1)+; Retention time: 1.13 (3 min run) 1H NMR (400 -106— MHz, DMSO) 5 7.36 - 7.27 (m, 4H), 7.27 — 7.21 (m, 1H), 4.62 (d, J = 5.9 Hz, 1H), 4.34 (t, J = 5.6 Hz, 1H), 3.74 = 7.6 Hz, 2H), 3.42 — 3.33 (m, 2H), - 3.49 (m, 4H), 3.45 (d, J 3.23 (tt, J = 5.7, 2.7 Hz, 1H), 2.94 (d, J = 10.6 Hz, 2H), 2.59 (ddd, J = 11.7, 8.5, 2.3 Hz, 1H), 2.35 (ddd, J = 89,52, 1.8 Hz, 1H), 1.81 — 1.67 (m, 2H), 1.38 (s,9H), 1.34 (dd, J = 6.7, 3.0 Hz, 2H), 1.29 - 1.18 (m, 1H).

Step 3: To tert—butyl yl—10—(l,2-dihydroxyethyl)-11—oxa-3,8- diazaspiro[5.5]undecanecarboxylate (1.5 g, 3.69 mmol) in THF (35 mL) was added NaIO4 (2 g, 9.4 mmol) followed by the on of H20 (13 mL). The reaction mixture was stirred at room temp for 2.5 hours. The reaction mixture was filtered, then concentrated in vacuo and the residue was partitioned between sat. aq. sodium onate (50 mL) and ethyl acetate (50 mL). The aqueous layer was extracted further with ethyl acetate (2 x 50 mL). The organic layers were ed, dried over MgSO4, filtered and concentrated in vacuo. To the ediate aldehyde (~1.4 g) was added ’BuOH (17 mL) and 2-methylbutene (10.5 mL, 99.04 mmol) and the reaction mixture was cooled to 0 0C. A solution of NaClOz (1.1 g, 9.65 mmol) and NaHzPO4 (1.33 g, 9.67 mmol) in water (17 mL) was added dropwise over 5 minutes, and the reaction mixture was stirred for 30 minutes at 0 °C. The reaction mixture was warmed to room temperature, then extracted with ethyl acetate (4 x 50 mL) and the combined organics were dried over MgSO4, filtered and trated in vacuo to give the crude acid as a yellow oil. The oil was dissolved in toluene (2.5 mL) and methanol (2.5 mL), then diazomethyl(trimethyl)silane (1.85 mL of 2 M in hexanes, 3.69 mmol) was added dropwise until faint yellow color persisted . Acetic acid was added to make solution colorless (2 drops). The reaction mixture was concentrated in vacuo then purified by silica gel column chromatography using 0-70% EtOAc/hexane as eluent to give 9—tert- butyl 2—methyl 4—benzyloxa-4,9—diazaspiro[5.5]undecane—2,9—dicarboxy1ate (1 g, 67%) as a colorless oil. 1H NMR (400 MHz, CDCl}) 5 7.37 - 7.20 (m, 5H), 4.43 (dd, J = 10.5, 2.1 Hz, 1H), 3.74 (s, 3H), 3.57 (d, J = 13.3 Hz, 3H), 3.45 - 3.29 (m, 2H), 3.14 (t, J = 10.9 Hz, 1H), 3.08 = 11.3, 0.9 Hz, 1H), 2.30 (dd, J = - 3.01 (m, 1H), 2.56 (dd, J 8.7, 5.7 Hz,1H), 2.13 (dd, J = 19.9, 8.9 Hz, 1H), 1.91 (d, J = 11.3 Hz, 1H), 1.69 - 1.46 -107~ (m, 3H), 1.43 (s, 9H). ESI—MS m/z calc. 404.5, found 405.7 (M+1)+; Retention time: 1.62 (3 min run).

Step 4: A mixture of 9-tert—butyl 2-methyl 4-benzyloxa—4,9- diazaspiro[5.5]undecane-2,9-dicarboxylate (670 mg, 1.66 mmol), ammonium formate (623 mg, 9.936 mmol) and palladium, 10 wt.% on ted carbon (353 mg, 3.31 mmol) in EtOH (5 mL) was heated at 65 °C for 50 s . The reaction mixture was cooled to room temperature, filtered and partitioned between EtOAc/ 1M aq. NaOH.

The layers were separated and the organic layer was dried over Na2804, d and concentrated in vacuo to yield 9-tert—buty1 2-methyl 1—oxa—4,9— diazaspiro[5.5]undecane-2,9-dicarboxylate as a foam (386 mg, 74 %) . ESI-MS m/z calc. 314.2, found 315.5 (M+1) + ; Retention time: 0.99 minutes (3 min run).

Step 5: 2,2,2—Trifluoroethyl trifluoromethanesulfonate (164 uL, 1.06 mmol) was added to a solution of 9-tert—butyl 2-methyl 1-oxa-4,9-diazaspiro[5.5]undecane- 2,9—dicarboxylate (222 mg, 0.71 mmol) and NaHC03 (237 mg, 2.83 mmol) in anhydrous EtOH (6 mL) at room temperature. The reaction mixture was purged with argon, sealed with a cap and heated at 70 °C for 12 hours. The reaction mixture was cooled to room temperature, d and concentrated in vacuo. The crude material was purified by silica gel column tography using 0 to 30 % EtOAc in DCM as eluent to yield 9-tert—butyl yl. 4-(2,2,2-trifluoroethyl)-l-oxa-4,9- diazaspiro[5.5]undecane—2,9-dicarboxylate (197 mg, 68 %). ESI-MS m/z calc. 410.4, found 411.5 (M+1)+; Retention time: 2.08 minutes (3 min run).

Step 6:

[00242] 9-Tert—butyl 2-methyl 4-(2,2,2-trifluoroethyl)oxa—4,9- diazaspiro[5.5]undecane—2,9—dicarboxylate (197 mg, 0.48 mmol) was dissolved in MeOH (1 mL) / H20 (1 mL), followed by the addition of LiOH (46 mg, 1.92 mmol) and the reaction mixture was stirred for 2 hours at room temperature. The solvent was removed in vacuo and the residue was dissolved in water (2 mL) and cooled to 0 °C, then acetic acid (115 mg, 109 ML, 1.92 mmol) was added dropwise (pH = 5). The product was partitioned between EtOAc / water, the layers were separated and the aqueous layer was ted once more with EtOAc . The organics were dried over Na2804, filtered and concentrated in vacuo to yield an oil. The oil was co-evaporated twice with toluene and dried under high vacuum to yield 9-(tert—butoxycarbony1)—4- (2,2,2-trifluoroethyl)oxa—4,9-diazaspiro[5.5]undecane—2—carboxylic acid (142 mg, 77 %) as a white foam . ESI—MS m/z calc. 382.4, found 383.5(M+1)+; Retention time: 1.58 minutes (3 min run).

Preparation of 9-(tert—butoxycarbonyl)—4—(2,2-difluor0ethyl)—1-oxa- 4,9—diazaspiro[5.5]undecane-Z-carboxylic acid We?OH This compound was ed using the chemistry as described above using 2,2—difluoroethy1 trifluoromethanesulfonate as the alkylating agent in step 5. 1H NMR (400 MHZ, DMSO) 8 6.28 (t, J = 4.1 Hz, 1H), 6.14 (t, J = 4.0 Hz, 1H), 6.00 (t, J = 4.1‘Hz, 1H), 4.20 (d, J = 8.8 Hz, 1H), 3.49 (d, J = 9.0 Hz, 2H), 3.22 (s, 1H), 3.04 (d, J = 10.3 Hz, 2H), 2.72 (ddd, J = 14.4, 13.7, 7.8 Hz, 3H), 2.23 - 1.94 (m, 3H), 1.58 - 1.28 (m, 11H); ESl—MS m/z calc. 364.4, found 365.3 (M+1)+; Retention time: 1.36 minutes (3 min run).

Preparation of 9-(tert-but0xycarbonyl)(tert—butyl)—1-0xa—4,9- diazaspiro[5.5]undecane-Z-carboxylic acid Ofiio W NTgO This nd was prepared using steps 1-3 and 6 in the chemistry described above using tert—butyl rt—butylamino)methyl)hydroxypiperidine—1— carboxylate in step 1. 1H NMR (400 MHZ, CDCl}) 8 4.32 (d, J = 10.6 Hz, 1H), 4.21 - 2012/028882 4.16 (m, 1H), 3.84 - 3.50 (m, 3H), 3.33 (t, J = 20.1 Hz, 2H), 3.14 (d, J = 10.9 Hz, 1H), 2.78 (d, J = 11.4 Hz, 1H), 2.23 (s, 1H), 2.09 (dt, J = 24.2, 13.0 Hz, 4H), 1.59 (dd, J = 49.3, 11.8 Hz, 3H), 1.42 (d, J = 29.3 Hz, 12H), 1.00 (d, J = 36.2 Hz, 10H); ESI-MS m/z calc. 356.2, found 357.5 (M+1)+; Retention time: 0.66 minutes (3 min run).

[00247] Preparation of 9-(tert—butoxycarbonyl)—4—ethyloxa-4,9- diazaspiro[5.5]undecane-Z-carboxylic acid (3%th4 This compound was ed using steps 1-3 and 6 in the chemistry described above using tert—butyl 4-((ethylamino)methy1)hydroxypiperidinej1— carboxylate in step 1. ESI-MS m/z calc. 328.5, found 329.5 (M+1)+; Retention time: 1.44 s (3 min run).

Preparation of 4-(2,2-difluoroethyl)(5-ethyloxazol—2-yl)—1-oxa- 4,9—diazaspiro[5.5] undecane

[00250] Step 1: To 9-(tert—butoxycarbonyl)-4—(2,2-difluoroethyl)-l-oxa—4,9- diazaspiro[5.5]undecanecarboxylic acid (418 mg, 1.15 mmol), l-aminobutan-Z-one (156 mg, 1.26 mmol) and propane phosphonic acid anhydride (T3P) (1.095 g, 1.0 mL of 50 %w/w, 1.72 mmol) in 2—methyltetrahydrofuran (3.1 mL) was added triethylamine (640 uL, 4.59 mmol) at room temperature . The reaction e was then heated at 40 0C for 5 hours. The reaction mixture was cooled ed with sat. aq. NaHCO3 and extracted with ethyl acetate. The combined organics were dried over NaZSO4, filtered and concentrated in vacuo, then purified by silica gel column chromatography using 0— —110— 50% EtOAc in DCM to yield tert—butyl 4-(2,2-difluoroethyl)—2-((2- oxobutyl)carbamoyl)-1—oxa—4,9—diazaspiro[5.5]undecanecarboxylate (300 mg, 60 %).1H NMR (400 MHz, CDC13) 5 7.40 - 5.64 (m, 1H), 4.31 (dd, J - 7.30 (m, 1H), 6.09 = 11.0, 3.0 Hz, 1H), 4.21 = 10.9, 7.5, 6.3 Hz, 2H), 3.39 - - 4.05 (m, 2H), 3.77 (ddt, J 3.17 (m, 2H), 3.14 - 2.95 (m, 1H), 2.80 = 7.3 Hz, 2H), 2.41 - - 2.63 (m, 3H), 2.50 (q, J 2.27 (m, 1H), 2.25 - 2.11 (m, 2H), 1.67 - 1.51 (m, 3H), 1.46 (s, 9H), 1.13 (t, J = 7.4 Hz, 3H). ESI—MS m/z calc. 433.2, found 434.5 (M+1)+; Retention time: 1.78 minutes (3 min run).

] Step 2:

[00253] To tert—butyl 4-(2,2-difluoroethyl)—2-((2-oxobutyl)carbamoyl)oxa— 4,9-diazaspiro[5.5]undecanecarboxylate (200 mg, 0.46 mmol) in THF (2 mL) was added Burgess' salt (275 mg, 1.15 mmol) and the reaction mixture was heated at 75° C under a nitrogen here for 2 hours. The reaction mixture was cooled to room temperature, and partitioned between EtOAc and saturated aq. NaHCO3. The layers were separated and the aqueous layer was extracted once more with EtOAc. The combined organics were dried over NaZSO4, filtered and concentrated in vacuo to give an orange oil. The residue was d by silica gel column chromatography using 0- % EtOAc in DCM as eluent to yield tert—butyl 4-(2,2-difluoroethyl)—2-(5- ethyloxazolyl)—1-oxa-4,9-diazaspiro[5.5]undecanecarboxylate (160 mg, 84 %) as a colorless oil. ESI—MS m/z calc. 415.2, found 416.5 (M+1)+; Retention time: 2.06 minutes (3 min run); 1H NMR (400 MHz, CDC13) 8 6.69 (s, 1H), 6.06 - 5.68 (m, 1H), 4.89 (dd, J = 10.7, 2.5 Hz, 1H), 3.85 - 3.01 (m, 3H), 2.87 - 2.59 - 3.58 (m, 2H), 3.37 (m, 6H), 2.45 (d, J = 13.6 Hz, 1H), 2.30 (d, J = 11.3 Hz, 1H), 1.65 - 1.48 (m, 3H), 1.45 (s, 9H), 1.25 (t, J = 7.6 Hz, 3H).

[00254] Step 3: ] To a solution of tert—butyl 4-(2,2-difluoroethyl)—2-(5-ethyloxazolyl)— 4,9—diazaspiro[5.5]undecane—9-carboxylate (154 mg, 0.37 mmol) in DCM (0.4 mL) was added HCl (464 uL of 4 M solution in e, 1.85 mmol) and the reaction mixture was stirred at room temperature for 1 hour. The solvent and excess HCl were 3O removed under reduced pressure and the residue was triturated with Et20 to yield 4— (2,2-difluoroethyl)—2-(5-ethyloxazolyl)—1—oxa—4,9—diazaspiro[5.5]undecane -lll— hydrochloride salt (138 mg, 96 %) as a white solid. ESI-MS m/z calc. 3152, found 316.3 (M+1)+; Retention time: 1.07 s (3 min run).

Preparation of 4-(2,2-diflu0roethyl)—2-(5-isopropyloxazol—Z-yl) oxa-4,9-diazaspiro[5.5]undecane This compound was ed using the method described above using 1—aminomethy1-butan-2—one in step 1. ESI-MS m/z calc. 329.2, found 330.3 (M+1)+; Retention time: 1.12 minutes (3 min run). ation of 2-(5-(tert—butyl)oxazoly1)(2,2-difluoroethyl) oxa-4,9-diazaspiro[5.5]undecane This compound was prepared using the method described above using 1-amino-3,3-dimethy1-butanone in step 1. ESI-MS m/z calc. 343.20, found 344.1 (M+1)+; Retention time: 1.23 minutes (3 min run).

[00260] Preparation of 8-tert—butyl—10-(5-methyloxazol—2-yl)—1l-oxa—3,8- piro [5.5] undecane «rich.

This compound was prepared using the method described above using 9-(tert—butoxycarbony1)-4—(lert—butyl)-1—oxa-4,9-diazaspiro[5.5]undecane—2-carboxy1ic —112- acid and l-aminopropan-Z-one in step 1. ESl-MS m/z calc. 293.4, found 294.3 ; Retention time: 0.39 minutes (3 min run).

Preparation of 4-(2,2-difluoroethyl)(0xazol—2-yl)—1-0xa—4,9- pir0[5.5] undecane Step 1: To t—butoxycarbonyl)~4—(2,2-difluoroethyl)- l -oxa—4,9— diazaspiro[5.5]undecanecarboxylic acid (520 mg, 1.43 mmol) , propenamine (118 ML, 1.57 mmol) and T3P (2.12 mL of 50 %w/w, 3.59 mmol) in 2- methyltetrahydrofuran (4 mL) was added triethylamine (597 uL, 4.28 mmol) at room temperature and the on mixture was d for 2 hours. The reaction mixture was then quenched with saturated NaHC03 solution (3 mL) and stirred for an additional 10 minutes, then diluted with EtOAc and the layers were separated. The aqueous layer was extracted once more with EtOAc, and the combined organics were dried over Na2S04, filtered and concentrated in vacuo to an oil. The residue was purified by silica gel column chromatography using 0-50% EtOAc in hexanes to yield tert—butyl 2- (allylcarbamoyl)—4—(2,2-difluoroethyl)oxa-4,9-diazaspiro[5.5]undecane carboxylate (480 mg, 83 %) . ESI-MS m/z calc. 403.2, found 404.5 (M+1)+; Retention time: 1.78 minutes (3 min run) .

[00265] Step 2: To tert—butyl 2-(allylcarbamoyl)(2,2-difluoroethyl)—1-oxa—4,9- diazaspiro[5.5]undecanecarboxylate (480 mg, 1.19 mmol) and 4-methylmorpholine 4-0xide (153 mg, 1.31 mmol) in acetone (4.5 mL) and water (480 uL) was added osmium tetroxide in water (75.63 uL of 4 %w/w, 0.01 mmol) dropwise and the solution was stirred for 2.5 hours at room temperature. The reaction e was quenched with 1M sodium thiosulfate (12 mL) and stirred for 5 minutes, then extracted with EtOAc, washed with sat. aq. NaHC03, brine, dried over MgSO4, filtered and concentrated in vacuo to give tert—butyl 4-(2,2-difluoroethyl)((2,3- dihydroxypropyl)carbamoyl)-1—oxa—4,9-diazaspiro[5.5]undecanecarboxylate (520 mg, 99 %) which was used t further purification. ESI-MS m/z calc. 437.2, found 438.5 (M+1)+; Retention time: 1.54 minutes (3 min run).

Step 3: To tert-butyl 4-(2,2-difluoroethyl)—2-((2,3— dihydroxypropyl)carbamoyl)- l -oxa-4,9—diazaspiro[5.5]undecane—9-carboxylate (422 mg, 0.96 mmol) in THF (10 mL) was added NaIO4 (522 mg, 2.44 mmol) followed by H20 (4 mL) the on mixture was stirred at room temperature for 2 hours . The reaction mixture was filtered and ioned between sat. aq. sodium bicarbonate/ethyl acetate. The aqueous layer was extracted further with ethyl acetate (3 x 50 mL). The organics were combined, washed with sat. aq. sodium onate (50 mL), dried over MgSO4, and concentrated in vacuo to yield utyl 4-(2,2-difluoroethyl)((2- oxoethy1)carbamoyl)-l-oxa—4,9—diazaspiro[5.5]undecanecarboxylate (377 mg, 96 %) as a white solid, which was taken onto the next step without purification. EST—MS m/z calc. 405.2, found 406.5 (M+1)+; Retention time: 1.32 minutes (3 min run) Step 4: To tert—butyl 4-(2,2~difluoroethy1)((2-oxoethyl)carbamoyl)oxa— azaspiro[5.5]undecane-9—carboxylate (331 mg, 0.82 mmol) in THF (3 mL) was added Burgess' Salt (486 mg, 2.04 mmol). The reaction mixture was heated at 70° C for 20 minutes under an atmosphere of nitrogen. The reaction mixture was cooled to room temperature, partitioned between EtOAc and ted aq. NaHC03, the layers separated and the aqueous layer was extracted once more with EtOAc. The combined cs were dried over NaZSO4, filtered and concentrated in vacuo to give an orange oil. The residue was purified by silica gel column chromatography using 0-30% EtOAc in DCM as eluent to yield tert—butyl 4—(2,2-difluoroethyl)-2—(oxazolyl)oxa—4,9- diazaspiro[5.5]undecane—9~carboxylate (121 mg, 38 %) as an off white foam. ESI—MS m/z calc. 387.2, found 388.3 (M+l)+; Retention time: 1.81 minutes (3 min run) Step 5: —114- HCl (781 ML of 4 M in dioxane, 3.12 mmol) was added to a on of tert-butyl 4—(2,2—difluoroethyl)(oxazoly1)—1-0xa-4,9-diazaspiro[5.5]undecane carboxylate (121 mg, 0.31 mmol) in DCM (0.7 mL) and the reaction mixture was stirred for 1 hour at room temperature. The solvent and excess HCl was removed under reduced pressure and the resulting solid was dissolved in methanol (3 mL) and purified by Waters mass directed LC/MS: (1-99% ACN/ H20 (SmM HCl)). The desired fractions were combined and concentrated in vacuo to yield -difluoroethyl)—2- (oxazol—2-yl)-l-oxa-4,9-diazaspiro[5.5]undecane hydrochloride salt (95 mg, 94 %) as a white solid. ESI—MS m/z calc. 287.1, found 288.3 (M+1)+; Retention time: 0.96 minutes (3 min run); 1H NMR (400 MHZ, DMSO) 5 8.15 (d, J = 0.8 Hz, 1H), 7.23 (d, J = 0.8 Hz, 1H), 6.22 (tt, J = 55.1, 4.0 Hz,1H), 4.94 (dd, J = 10.8, 2.6 Hz, 1H), 3.19 - 2.79 (m, 8H), 2.65 = 11.9, 1.5 Hz, 1H), 1.83 - 1.70 (m, 2H), - 2.54 (m, 2H), 2.25 (dd, J 1.65 (dd, J = 15.1, 3.9 Hz,1H).

Preparation of methylthiazolyl)(2,2,2-triflu0roethyl)— 1 1-0xa-3,8-diazaspiro[5.5]undecane Step 1: T3P (591 mg, 553 uL of'50 %w/w, 0.93 mmol) was added to a mixture of 9-(tert-butoxycarbonyl)-4—(2,2,2-trifluoroethyl)oxa—4,9-diazaspiro[5.5]undecane- 2-carboxylic acid (142 mg, 0.37 mmol), l-aminopropan—Z—one hydrochloride salt (41 mg, 0.37 mmol) and Et3N (188 mg, 259 uL, 1.86 mmol) in yltetrahydrofuran (706 ML). The reaction mixture was then heated at 45°C for 2 hours. The reaction mixture was cooled to room temperature and partitioned between EtOAc/saturated aq.

NaHC03. The layers were ted and the aqueous layer was extracted with EtOAC (2 x). The combined organics were dried over NaZSO4, filtered and concentrated in vacuo to a dark foam. The crude product was purified by silica gel column tography using 0-50% EtOAC in DCM as eluent to afford tert—butyl 10- (acetonylcarbamoyl)—8-(2,2,2-trifluoroethy1)-1 1-oxa-3,8-diazaspiro[5.5]undecane~3- carboxylate (80 mg, 49 %) as a yellow solid. ESI—MS m/z calc. 437.5, found 438.7 (M+1)+; Retention time: 1.01 s (3 min run).

Step 2: Tert—butyl 10—(acetony1carbamoy1)—8-(2,2,2-trifluoroethy1)—1l-oxa-3,8- diazaspiro[5.5]undecane—3-carboxylate (80 mg, 0.18 mmol) was dissolved in anhydrous THF (1.5 mL) followed by the addition of Lawesson's reagent (114 mg, 0.27 mmol) and the reaction mixture was heated at 70 °C for 1 hour under an atmosphere of nitrogen. The on mixture was cooled to room temperature and the solvent was removed under reduced re. The e was purified by silica gel column chromatography using 0-10% EtOAc in DCM as eluent to yield tert-butyl 10~ (5-methy1thiazolyl)(2,2,2-trifluoroethyl)—1 1-oxa—3,8-diazaspiro[5.5]undecane—3- carboxylate (95 mg, 100 %). ESl-MS m/z calc. 435.5, found 436.5 (M+1)+; Retention time: 1.67 minutes (3 min run); 1H NMR (400 MHZ, CDCl3) 5 7.54 (s, 1H), 5.20 (dd, J = 9.4, 0.8 Hz,1H), 3.82 = 10.1 Hz, 1H), 3.31 - 3.21 (m, - 3.76 (m, 2H), 3.43 (d, J 1H), 3.09 = 11.4, 0.5 Hz, 1H), 2.50 (s, 1H), 2.46 (s, 3H), - 2.94 (m, 3H), 2.72 (dd, J 2.45 = 11.2, 4.8 - 2.38 (m, 2H), 1.79 - 1.67 (m, 1H), 1.65 - 1.57 (m, 1H), 1.53 (dd, J Hz, 1H), 1.45 (s, 9H).

Step 3: 2O [00279] Hydrogen chloride (229 uL of 4 M solution in dioxane, 0.9160 mmol) was added to tert—butyl 10—(5—methy1thiazol—2—yl)—8-(2,2,2-trifluoroethy1)—11—oxa—3,8- diazaspiro[5.5]undecane—3-carboxy1ate (95 mg, 0.18 mmol) in anhydrous dichloromethane (1 mL) and the reaction mixture was stirred for 2 hours at room temperature. The excess HCl and solvent were removed under reduced re to yield 1 0-(5-methy1thiazolyl)—8-(2,2,2-trifluoroethyl)-1 1—oxa—3 ,8- diazaspiro[5.5]undecane hloride salt (74 mg, 99 %) as a light yellow solid. ESI— MS m/z calc. 335.1, found 336.5 (M+1)+; Retention time: 0.91 s (3 min run).

Preparation of 8—ethyl(5-methylthiazolyl)oxa-3,8— diazaspiro[5.5] undecane This compound was prepared using the procedure as bed above starting from 9—(tert—butoxycarbonyl)ethyl— 1 -oxa-4,9—diazaspiro[5.5]undecane carboxylic acid. ESl-MS m/z calc. 281.4, found 282.5 (M+1)+; Retention time: 0.20 minutes (3 min run).

] Preparation of 8-(2,2-diflu0r0ethyl)—10-(4-methyl—lH-pyrazol-S— yl)-11—0xa-3,8-diazaspir0[5.5]undecane N'\ O I NH Step 1: To 3-tert-butyl OlO-methyl 8-(2,2-difluoroethyl)—l l-oxa-3,8- piro[5.5]undecane-3,10-dicarboxylate (1.50 g, 3.96 mmol) and powdered (N, 0)- dimethylhydroxylamine hydrochloride salt (654 mg, 6.71 mmol) in THF (25 mL) at -78 0C was added lithium bis(trimethylsi1yl)amine (12.6 mL of 1 M, 12.6 mmol) over a period of 5 minutes. The mixture was stirred at the same temperature for 15 minutes, it was then warmed to 0 °C and stirred for an additional 30 minutes. The on mixture was quenched with sat. aq. NH4C1 (30 mL), ted with ether (3 x 50 mL), and the combined organics were dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by silica gel column tography (0-100% ethyl acetate/dichloromethane) to give tert—butyl 8-(2,2-difluoroethyl)-10— [methoxy(methyl)carbamoy1]-1 1—oxa—3 ,8-diazaspiro[5.5]undecane—3-carboxylate (1.3 8 g, 85%) as a colorless oil. ESI—MS m/z calc. 407.2, found 408.5 (M+1)+; Retention time: 1.59 minutes (3 min run). 1H NMR (400 MHz, CDC13) 5 5.93 - 5.61 (m, 1H), -1l7— 2012/028882 4.66 — 4.58 (m, 1H), 3.72 (s, 3H), 3.65 - 3.46 (m, 2H), 3.33 - 3.22 (m, 1H), 3.14 (s, 3H), 2.83 - 2.77 (m, 1H), 2.70 - 2.57 (m, 3H), 2.47 — 2.40 (m, 1H), 2.28 - 2.12 (m, 2H), 1.61 - 1.48 (m, 3H), 1.46 — 1.35 (m, 10H).

Step 2: To tert-butyl 8-(2,2-difluoroethy1)[methoxy(methyl)carbamoyl]- l 1-oxa-3,8-diazaspiro[5.5]undecanecarboxylate (295 mg, 0.72 mmol) in THF (3 mL) at -78 °C under an atmosphere of nitrogen, was added ethylmagnesium bromide (1.7 mL of 1 M in THF, 1.7 mmol) dropwise. The reaction mixture was stirred at the same temperature for 0.5 hours, then at 0 °C for 1 hour. The reaction mixture was ed with ethyl acetate (20 mL) and sat. aq. NaHC03 (10 mL). The s layer was further extracted with EtOAc (2 x 20 mL), and the combined cs were dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by silica gel column chromatography (0-100% ethyl acetate/hexane) to give utyl 8- ifluoroethy1)—10-propanoyl-1 1-oxa—3,8—diazaspir0[5.5]undecane-3 ~carboxylate (227 mg, 83%) as a colorless oil. ESI-MS m/z calc. 376.2, found 377.3 (M+1)+; Retention time: 1.76 minutes. 1H NMR (400 MHz, CDC13) 5 6.01 - 5.70 (m, 1H), 4.21 - 4.15 (m, 1H), 3.91 - 3.75 (m, 2H), 3.33 - 3.22 (m, 1H), 3.15 - 2.98 (m, 2H), 2.79 - 2.57 (m, 5H), 2.43 — 2.35 (m, 1H), 2.19 - 2.06 (m, 2H), 1.61 — 1.39 (m, 12H), 1.06 (t, J = 7.3 Hz, 3H).

[00287] Step 3: tert-Butyl 8-(2,2—difluoroethyl)—10-propanoyl-l 1 -oxa—3,8- diazaspiro[5.5]undecanecarboxylate (225 mg, 0.598 mmol) and DMF-DMA (1.0 mL, 7.53 mmol) were heated in a sealed Vial at 105 °C overnight. The reaction mixture was concentrated and then diluted with methanol (1 mL). Hydrazine (60 uL, 1.9 mmol) was added in 3 aliquots every hour over 3 hours and then the reaction mixture was stirred for an additional 1 hour. The reaction mixture was diluted with methanol, microfiltered and purified by preparative LCMS (IO-99% ACN/Water, HCl modifier) to give utyl 8-(2,2-difluoroethyl)-l0—(4-methyl-1H-pyrazol—5-yl)—1l-oxa—3,8— diazaspiro[5.5]undecane—3-carboxylate (80 mg, 0.2 mmol, 33.42%) as a yellow oil.

EST-MS m/z calc. 400.2, found 401.5 (M+1)+; Retention time: 1.36 minutes (3 min run). ~118— Step 4: To tert—butyl 8-(2,2-difluoroethyl)(4-methyl-1H-pyrazolyl)-1 1— oxa—3,8-diazaspiro[5.5]undecanecarboxylate (80 mg, 0.20 mmol) in ethanol (0.2 mL) was added HCl (500 uL of 4 M in dioxane, 2.00 mmol) and the on mixture was stirred for lhour. The reaction mixture was concentrated in vacuo to give, 8-(2,2— difluoroethyl)—1 0-(4—methy1-1H-pyrazoly1)—1 1-oxa—3 ,8—diazaspiro[5.5]undecane hydrochloride salt as a yellow solid. ESI-MS m/z calc. 300.2, found 301.3 ; Retention time: 0.48 minutes (3 min run). 1H NMR (400 MHZ, DMSO) 5 8.74 (s, 2H), 7.45 (s, 1H), 6.49-6.08 (m, 1H), 5.76 (s, 1H), 4.88 (d, J = 9.6 Hz, 1H), 3.21 - 2.57 (m, 10H), 2.06 (s, 3H), 1.81 - 1.56 (m, 4H).

Preparation of 8-(2,2-difluoroethyl)—10-(2-pyridyl)oxa-3,8- diazaspiro[5.5] ne ] Step 1;

[00293] To utyl 4-[(benzylamino)methy1]-4—hydroxy—piperidine-l - carboxylate (3.0 g, 9.36 mmol) in DMF (19 mL) at 0 °C was added diisopropyl ethylamine (3.4 mL, 19.66 mmol) followed by the addition of 2-bromo—1-(2- pyridy1)ethanone hydrobromide salt (2.6 g, 9.36 mmol)and reaction mixture was stirred for 2 hours warming from 0 °C to 10 OC. The reaction mixture was diluted with ethyl acetate and washed with sat. NaHC03 solution and then brine. The organics were separated, dried over Na2804, filtered and concentrated in vacuo to give a residue, which was purified using silica gel column chromatography using MeOH/DCM (1-15 %) as eluent to give tert—butyl 4-[[benzyl—[2-oxo(2-pyridyl)ethyl]amino]methyl] hydroxy—piperidine-l-carboxylate (3.8, 92 %). ESI-MS m/z calc. 439.2, found 440.0 (M+1)+; Retention time: 1.12 minutes (3 min run).

Step 2: -1l9- 2012/028882 To tert-butyl 4—[[benzyl-[2-oxo(2—pyridyl)ethyl]amino]methy1] hydroxy—piperidine-l-carboxylate (190 mg, 0.43 mmol) in benzene (11 mL) was added 4—methylbenzenesulfonic acid (99 mg, 0.52 mmol) and reaction mixture was heated at 80 °C for 30 minutes. The reaction e was cooled, d with ethyl acetate and washed tially with sat. NaHC03 and brine solution. The organic layer was separated, dried over Na2S04, filtered and trated in vacuo to give residue, which was purified using silica gel column chromatography using EtOAc/DCM (10-100 %) as eluent to give tert—butyl yl(2-pyridyl)-1l-oxa—3,8-diazaspiro[5.5]undec ene—3-carboxylate (86 mg, 45 %). ESI—MS m/z calc. 421.5, found 422.2 (M+1)+; Retention time: 1.42 minutes (3 min run). 1H NMR (400 MHZ, CDC13 ) 8 8.40 ~ 8.34 (m, 1H), 7.56 (dd, J = 4.0, 3.5 Hz, 1H), 7.37 ~ 7.27 (m, 6H), 7.07 (s, 1H), 6.92 (d, J = 1.5 Hz, 1H), 4.22 (s, 2H), 3.99 — 3.76 (m, 2H), 3.17 (t, J = 11.8 Hz, 2H), 2.78 (s, 2H), 1.83 (s, 2H), 1.44 (s, 9H), 1.40 (d, J = 4.4 Hz, 2H).

Step 3:

[00297] To tert—butyl 8-benzyl-10—(2-pyridyl)-1l-oxa—3,8— diazaspiro[5.5]undecene—3-carboxylate (80 mg, 0.19 mmol) in methanol (13 mL) was added Pd(OH)2 (50 mg, 0.36 mmol) and ammonium formate (180 mg, 2.85 mmol) and the reaction mixture was heated at 70 °C for 1 hour. The reaction mixture was cooled, diluted with ethyl acetate and filtered through Celite®. The organic layer was washed with 1:1 NaOHzNaHC03 solution, dried over , d and concentrated in vacuo to yield tert—butyl 10-(2-pyridyl)-l l-oxa-3,8- diazaspir0[5.5]undecane—3—carboxylate (63 mg, 100 %) as an oil which was used in the next step without further purification. ESI—MS m/z calc. 333.4, found 334.4 (M+1)+; Retention time: 1.00 minutes (3 min run).

[00298] Step 4: To tert—butyl pyridyl)-l1-oxa-3,8—diazaspiro[5.5]undecane carboxylate (63 mg, 0.19 mmol) in ethanol was added sodium hydrogen carbonate (64 mg, 0.76 mmol) followed by the addition of 2,2-difluoroethyl trifluoromethanesulfonate (49 mg, 0.23 mmol) and reaction mixture was heated at 80 °C for 40 minutes. The reaction mixture was cooled to room temperature and diluted with DCM and the organic layer was washed with 1:1 NaOHzNaHC03 solution. The -120— organics were separated, dried over NaZSO4, filtered and trated in vacuo to give tert—butyl 8-(2,2-difluoroethy1)-1 0-(2—pyridy1)—1 1-oxa-3 ,8-diazaspiro[5.5]undecane—3 - carboxylate as an oil. To the oil was added HCl (237.5 ML of 4 M in dioxane, 0.95 mmol) at room temperature under an here of nitrogen and the reaction e was stirred for 30 minutes. The solvent was removed in vacuo and the residue was triturated with ether to give 8-(2,2—difluoroethy1)(2-pyridy1)oxa-3,8- diazaspiro[5.5]undecane (45 mg, 79 %). ESI-MS m/z calc. 297.3, found 298.4 (M+1)+'u Retention time: 0.35 minutes (3 min run).

Preparation of 4-(2,2—difluoroethyD—2-(6-methylpyridinyl)—1- 0xa-4,9-diazaspir0[5.5]undecane This nd was prepared using the chemistry as described above using 2-bromo(6-methy1pyridy1)ethanone in step 1. EST—MS m/z calc. 311.2, found 312.1 (M+1)+; Retention time: 0.3 minutes (3 min run).

[00302] Preparation of 4-(2,2-diflu0roethyl)—2-(3-methylpyridinyl)—1- oxa-4,9-diazaspiro[5.5]undecane F N X NH {\ / This compound was ed using the chemistry as described above using 2—bromo—1-(3-methy1pyridin—2—y1)ethanone in step 1. ESI-MS m/z calc. 311.4, found 312.0 (M+1)+; ion time: 0.23 minutes (3 min run).

Preparation of 8-(2,2-difluor0ethyl)—10-(1H-pyrazol—3-yl)—1l-oxa— 3,8-diazaspiro [5.5] undecane (NTNH:/ 030NH Step 1: To a mixture of 3-z‘ert—butoxycarbonyl-8—(2,2-difluoroethyl)-1 l-oxa- 3,8-diazaspiro[5.5]undecane—10-carboxylic acid (100 mg, 0.27 mmol), N,0— dimethylhydroxylamine hydrochloride salt (29 mg, 0.30 mmol) and T3P (245 ML of 50 %w/w, 0.41 mmol) in 2-methyltetrahydrofuran (1 mL) was added triethylamine (153 uL, 1.10 mmol). The reaction mixture was d overnight, then diluted with ethyl acetate (5 mL), washed with sat. aq. NaHCO3 (5 mL), dried over MgSO4 and concentrated in vacuo to give the Weinreb amide intermediate. The ediate was ved in THF (1 mL) and cooled to 0 0C under an atmosphere of nitrogen, and chloro(ethynyl)magnesium (1 mL of 0.6 M in THF, 0.60 mmol) was added dropwise.

The reaction mixture was stirred at 0 °C for 2 h, then at room temperature for 1 hour.

The reaction mixture was quenched with sat. aq. NH4C1, extracted with ethyl acetate, dried over MgSO4 and purified by silica gel column chromatography using 0-100% EtOAc/hexanes eluent to give tert-butyl 8-(2,2-difluoroethyl)-10—prop—2-ynoy1-1 1-oxa— 3,8-diazaspiro[5.5]undecane-3—carboxy1ate (25 mg, 24 %) as a colorless oil. ESl-MS m/z calc. 372.4, found 373.1 (M+1)+; Retention time: 1.82 (3 min run; 1H NMR (400 MHz, CDC13) 5 5.84 (tt, J = 55.8, 4.2 Hz, 1H), 4.30 (d, J = 8.6 Hz, 1H), 3.78 (s, 2H), 3.38 (s, 1H), 3.34 (d, J = 10.2 Hz, 1H), 3.13 (dd, J = 308,113 Hz, 2H), 2.86 — 2.56 (m, 3H), 2.35 (d, J = 14.6 Hz, 1H), 2.22 (dd, J = 22.1, 11.2 Hz, 2H), 1.70 - 1.36 (m, 1211).

Step 2: A solution of utyl 8-(2,2—difluoroethyl)propynoyl-11—oxa— 3,8-diazaspiro[5.5]undecane-3—carboxy1ate (25 mg, 0.07 mmol), hydrazine (42 uL, 1.34 mmol) and l (0.5 mL) was d for 1 hour at room temperature. The solution was concentrated in vacuo to give the crude pyrazole as a yellow oil. HCl (400 uL of 4 M in dioxane, 1.60 mmol) followed by ethanol (0.2 mL) was added and the on mixture was stirred for 15 minutes at room temperature. The reaction. mixture was concentrated in vacuo to give 8-(2,2-difluoroethyl)(1H-pyrazol~3—yl)oxa— —122- 2012/028882 3,8—diazaspiro[5.5]undecane as a gummy yellow solid. ESI-MS m/z calc. 286.2, found 287.1 (M+1)+; Retention time: 0.32 minutes (3 min run).

Preparation 0f2-(1H-pyraz01-3—yl)(2,2,2-trifluoroethyl)—1-oxa- 4,9-diazaspiro[5.5]undecane HN—dM010NH 5 This compound was prepared using the chemistry as bed above starting from 9—(tert-butoxycarbonyl)—4-(2,2,2-trifluoroethy1)—1-oxa—4,9- diazaspiro[5.5]undecane—2-carboxylic acid. ESI-MS m/z calc. 304.2, found 305.3 (M+1)+; Retention time: 0.76 minutes (3 min run).

[00311] Preparation of 2-(5-methyl—1H-pyrazol—3-yl)—4-(2,2,2- trifluoroethyl)—1-0xa—4,9-diazaspir0 [5.5] undecane This compound was prepared using the chemistry as described above starting from t-butoxycarbonyl)(2,2,2—trifluoroethy1)-1—oxa—4,9- diazaspiro[5.5]undecane—2-carboxylic acid and using bromo-prop-l-yny1—magnesium.

ESI-MS m/z calc. 318.2, found 319.1 (M+1)+; Retention time: 0.85 minutes . (3 min run) .

Preparation of 8-ethyl—9—phenyl—11—0xa-3,8- diazaspiro [5.5] ne Qiis.

Step 1: -123— A solution of tert—butyloxaazaspiro[2.5]octanecarboxylate (0.7 g, 3.42 mmol) and 2—[(4-methoxyphenyl)methylamino]phenyl-ethanol (800 mg, 3.109 mmol) in ethanol (5 mL) was stirred at 60 °C for 72 hours. The on mixture was concentrated in vacuo and purified by silica gel column chromatography using 0 to % MeOH in DCM as eluent to yield tert—butyl 4-hydroxy—4-[[(2-hydroxyphenyl- ethyl)-[(4—methoxypheny1)methyl]amino]methyl]piperidinecarboxylate (1.2 g, 82 %). ESLMS m/z calc. 470.6, found 471.5 (M+1)+; Retention time: 1.45 minutes (3 min run).

Step 2:

[00317] To a solution of tert—butyl 4—hydroxy—4—[[(2—hydroxypheny1-ethyl)- [(4-methoxypheny1)methyl]amino]methyl]piperidinecarboxylate (1.0 g, 2.13 mmol) in THF (10mL) was added DIEA (1.1 mL, 6.38 mmol) followed by an addition of a solution of methylsulfonyl methanesulfonate (1.1 g, 6.38 mmol) in THF (2 mL) under an atmosphere of en at 0 OC. The reaction mixture was warmed to room temperature and then heated at 40 °C for 16 hours. The reaction mixture was ed with water and the s layer was extracted with DCM. The organic layer was washed with a sat. solution of NaHCOg, followed by washing with water. The organic layer was dried over MgSO4 and trated in vacuo. The residue was purified by silica gel column chromatography using 0 to 100% DCM in hexanes as eluent to obtain tert—butyl 8- [(4-methoxyphenyl)methyl] ny1- 1 1 -oxa—3 zaspiro [5 5]undecane— oxylate (0.5 g, 51 %). ESI-MS m/z calc. 452.6, found 453.5 (M+1)+; Retention time: 1.62 minutes (3 min run).

Step 3: To tert-butyl 8-[(4-methoxyphenyl)methyl]pheny1oxa—3,8- diazaspiro[5.5]undecanecarboxylate (500 mg, 1.11 mmol) Pd (500 mg, 4.70 mmol) and ammonium formate (697 mg, 11.05 mmol) was added methanol. The reaction mixture was then heated at 70 0C for 16 hours. The reaction mixture was filtered through a plug of celite and the solvent was concentrated in vacuo to obtain tert-butyl 9-pheny1-11—oxa-3,8-diazaspiro[5.5]undecane—3—carboxylate (340 mg, 93 %) as an oil.

ESl-MS m/z calc. 332.4, found 333.5 (M+1)+; Retention time: 1.21 minutes (3 min run) . —l24- WO 25613 Step 4: To a on of utyl 9-pheny1-1 l—oxa-3,8- diazaspiro[5.5]undecanecarboxy1ate (336 mg, 1.01 mmol) in ethanol (3 mL) was added acetaldehyde (62 uL, 1.11 mmol) then sodium orohydride (89 mg, 1.42 mmol) and the reaction mixture was stirred for 2 hours. The reaction mixture was concentrated in vacuo, partitioned between DCM (50 mL) and 1:1 aq. sat. NaHCO3/25 % NaOH (10 mL), and the aqueous layer was further extracted with DCM (2 x 25 mL).

The combined organics were dried with MgSO4 and concentrated in vacuo to give tert- butyl 8-ethy1phenyloxa-3,8-diazaspiro[5.5]undecanecarboxylate (298 mg, 82 %). ESl-MS m/z calc. 360.5, found 361.7 (M+l)+; Retention time: 1.30 minutes (3 min run).

Step 5: To a solution of tert—butyl 8-ethylphenyl-l l-oxa—3,8— diazaspiro[5.5]undecanecarboxylate (295 mg, 0.82 mmol) in DCM (3 mL) was added en chloride (2 mL of 4 M dioxane, 8.18 mmol). The reaction e was stirred for 1 hour. The solvent was decanted and the residue was triturated with methanol and hexanes. The solvent was concentrated in vacuo to obtain 8-ethy1 phenyl-l1-oxa—3,8-diazaspiro[5.5]undecane hydrochloride salt (230 mg, 95 %) as a fluffy solid. ESI-MS m/z calc. 260.2, found 261.1 (M+1)+; Retention time: 0.2 minutes (3 min run).

Preparation of tert—butyl l0xa—3,8- diazaspiro[5.5] undecane—3-carboxylate This compound was prepared using the chemistry as described above starting from tert—butyl 6-azaspiro[2.5]octane—6—carboxylate. ESI—MS m/z calc. 212.2, found 213.5 (M+1)+; Retention time: 0.21 minutes (3 min run).

Preparation of 2-(methoxymethyl)—4-(pyrimidin-Z-yl)—1-oxa-4,9- diazaspiro [5.5] undecane . N N / N H Step 1: A mixture of tert—butyl 8-benzyl-10—(hydroxymethyl)-11—0xa-3,8- diazaspiro[5.5]undecane-3—carboxy1ate (4.10 g, 10.9 mmol), ammonium formate (6.87 g, 109 mmol) and Pd(OH)2 (1.53 g, 10.9 mmol) was heated at 60 °C for 1 h. The on mixture was cooled, filtered, and concentrated in vacuo to provide tert—butyl droxymethy1)—11-oxa-3,8-diazaspiro[5.5]undecanecarboxylate (3.10 g, 10.8 mmol, 99%) . ESI—MS m/z calc. 286.2, found 287.2 (M+1)+; Retention time: 0.75 minutes (3 min run).

[00329] Step 2: A solution of tert—butyl 10-(hydroxymethyl)—11-oxa-3,8—diazaspiro[5.5] undecane—3-carboxylate (3.10 g, 10.8 mmol), ropyrimidine (1.86 g, 16.2 mmol) and sodium carbonate (2.30 g, 21.7 mmol) in DMSO (15 mL) was heated at 110 °C for 1 h. The reaction mixture was diluted with ethyl acetate (200 mL), washed with water (4 X 100 mL), dried over NaZSO4, and concentrated in vacuo. Silica gel column chromatography (0—60% ethyl acetate/hexane) provided tert—butyl 10-(hydroxymethyl)— midin-2—yl—11-oxa-3,8-diazaspiro[5.5]undecanecarboxylate (3.18 g, 8.73 mmol, 80%). ESI-MS m/z calc. 364.2, found 365.3 (M+1)+; Retention time: 1.21 minutes (3 min run). 1H NMR (400 MHz, CDC13) 8 8.29 (d, J = 4.7 Hz, 2H), 6.50 (t, J = 4.7 Hz, 1H), 4.64 (ddd, J = 16.0, 8.5, 1.5 Hz, 2H), 3.90 — 3.80 (m, 1H), 3.79 - 3.56 (m, 4H), 3.44 — 3.22 (m, 1H), 3.13 (t, J = 10.6 Hz, 1H), 2.90 ~ 2.71 (m, 2H), 2.19 (d, J = 8.9 Hz, 1H), 1.98 (dd, J = 10.6, 3.6 Hz, 1H), 1.69 — 1.58 (m, 2H), 1.45 (s, 9H).

Step 3: ] To a solution of tert—butyl l0-(hydroxymethyl)pyrimidin—2—yl-1 1- oxa—3,8-diazaspiro[5.5]undecane—3-carboxylate (1.45 g, 3.98 mmol) in dichloromethane (15 mL) was added triethylamine (1.66 mL, 11.9 mmol) and 4- (dimethylamino)—pyridine (195 mg, 1.59 mmol) at 0 OC. Tosyl chloride (910 mg, 4.78 mmol) was then added in one portion. The reaction mixture was allowed to warm to room temperature and stirred for 16 h. The reaction mixture was quenched with water and the layers were separated. The aqueous layer was ted with dichloromethane, and the combined c layers washed with saturated sodium bicarbonate solution and brine. The organic layer was dried over NaZSO4, filtered and trated in vacuo. Silica gel column chromatography (0—80% ethyl acetate/hexanes) provided tert- butyl imidinyl)—2-(tosyloxymethyl)oxa-4,9-diazaspiro[5.5] undecane—9- carboxylate (1.83 g, 3.53 mmol, 89%). ESI—MS m/z calc. 518.2, found 519.3 (M+1)+; Retention time: 1.83 minutes (3 min run). 1H NMR (400 MHz, MeOD) 6 8.31 (d, J = 4.8 Hz, 2H), 7.82 (d, J = 8.3 Hz, 2H), 7.45 (d, J = 8.2 Hz, 2H), 6.60 (t, J = 4.8 Hz, 1H), 4.67 — 4.48 (m, 2H), 4.12 (d, J = 4.6 Hz, 2H), 3.89 (ddd, J = 12.0, 7.5, 4.6 Hz, 1H), 3.71 — 3.56 (m, 2H), 3.05 (ddd, J = 20.6, 17.0, 8.8 Hz, 2H), 2.80 <~ 2.65 (m, 2H), 2.46 (s, 3H), 1.88 (d, J = 14.1 Hz, 1H), 1.50 (dt, J = 7.9, 4.0 Hz, 2H), 1.45 (s, 9H), 1.38 — 1.27 (m, 1H).

[00333] Step 4: Tert—butyl 4-(pyrimidin—2-yl)(tosyloxymethyl)-l ,9— diazaspiro[5.5] necarboxylate (1.83 g, 3.53 mmol) was dissolved in a solution of sodium methoxide (71 mL of 0.5 M in methanol, 35 mmol) and refluxed for 18 h. The solvent was evaporated to dryness and the residue dissolved in dichloromethane (200 mL). The solution was washed with water and brine, dried over NaZSO4, filtered and concentrated in vacuo. Silica gel chromatography (5—80% ethyl acetate/hexanes) provided tert—butyl 10-(methoxymethy1)pyrimidiny1—11—oxa-3,8- diazaspiro[5.5]undecane-3—carboxylate as colorless oil. ESl—MS m/z calc. 378.2, found 379.3 (M+1)+; Retention time: 1.54 minutes (3 min run). 1H NMR (400 MHZ, MeOD) 8 8.31 (d, J = 4.8 Hz, 2H), 6.58 (t, J = 4.8 Hz, 1H), 4.72 — 4.52 (m, 2H), 3.91 (ddd, J = 10.9, 7.9, 4.9 Hz, 1H), 3.76 — 3.59 (m, 2H), 3.56 — 3.44 (m, 2H), 3.40 (s, 3H), 3.13 (t, J = 11.1 Hz, 1H), 2.85 — 2.65 (m, 2H), 1.98 (d, J = 14.6 Hz, 2H), 1.59 (dd, J = 8.7, 4.5 Hz, 2H), 1.45 (s, 9H), 1.44 ~— 1.37 (m, 1H).

] Step 5:

[00336] Tert—butyl 1 0-(methoxymethy1)pyrimidinyl-1 1-oxa-3 ,8- diazaspiro[5.5]undecane-3—carboxylate (1.18 g, 3.12 mmol) was dissolved in 2012/028882 romethane (2 mL) and treated with a solution ofHCl (1.6 mL of 4 M in dioxane, 6.2 mmol). The mixture was allowed to stir for 2 h. The reaction mixture was evaporated to dryness to provide 2-(methoxymethyl)—4-(pyrimidinyl)oxa-4,9- diazaspiro[S .5] undecane hydrochloride. ESI-MS m/z calc.278.2, found 279.2 M+1)+; Retention time: 0.68 min (3 min run). 1H NMR (400 MHz, MeOD) 8 8.59 (d, J = 5.2 Hz, 2H), 6.99 (t, J = 5.2 Hz, 1H), 4.52 (ddd, J = 44.3, 13.4, 1.7 Hz, 2H), 4.12 — 3.97 (m, 1H), 3.56 (ddd, J = 26.1, 10.3, 4.9 Hz, 2H), 3.42 (s, 3H), 3.34 (dd, J = 10.9, 5.0 Hz, 2H), 3.27 — 3.19 (m, 2H), 3.13 (dd, J =13.2,11.1Hz,2H), 2.42 (d, J = 15.2 Hz,1H), 1.94 (dd, J = 10.7, 4.3 Hz, 2H), 1.74 (ddd, J =15.3, 12.8, 4.4 Hz, 1H).

[00337] Preparation of 2-ethyl(pyridinyl)oxa-4,9- diazaspiro[5.5] undecane Step 1: To a solution of tert—butyl 10—benzylvinyl-7—oxa—3,l0-diazaspiro[5.5]undecane carboxylate (3.10 g, 8.32 mmol) in methanol (60 mL) was added Pd(OH)2 (1.40 g, 9.99 mmol) and ammonium formate (10.5 g, 166 mmol) and the mixture heated at 55 0C for 20 min. The reaction mixture was filtered, concentrated to ~10 mL, then d with dichloromethane and saturated sodium bicarbonate solution. The organic layer was separated and the aqueous layer extracted with dichloromethane (5 X 20 mL). The combined organic layers were dried over NaZSO4, d, and concentrated in vacuo to provide utyl 4-ethyloxa—2,9-diazaspiro[5.5]undecane-9— carboxylate (2.27 g, 7.99 mmol, 96%). ESI-MS m/z calc. 284.21, found 285.1 (M+1)+; Retention time: 1.09 minutes (3 min. run).

Step 2: A solution of rac-BINAP (43.8 mg, 0.070 mmol) and Pd2(dba)3 (32.2 mg, 0.0352 mmol) in e (1 mL) was stirred under nitrogen here in a sealed vial at 90 0C for 10 min, then cooled to 40 OC and cannulated into a stirring solution of tert— butyl 4-ethy1oxa-2,9-diazaspiro[5.5]undecanecarboxylate (500 mg, 1.76 mmol) and 2-chloropyridine (200 mg, 165 uL, 1.76 mmol) in toluene (6 mL). The solution was treated with sodium tert—butoxide (275 mg, 2.87 mmol), flushed with nitrogen and stirred for 3 h at 90 OC. The reaction mixture was cooled, diluted with ethyl acetate (100 mL), filtered through Celite and concentrated in vacuo. Silica gel chromatography (120 g silica, 10-70% ethyl acetate/hexane) provided tert-butyl 10- ethyl(2-pyridyl)-1 1-oxa-3,8-diazaspiro[5.5]undecanecarboxylate (486 mg, 1.34 mmol, 76%) as an orange-colored oil. ESl-MS m/z calc. 361.2, found 362.3 (M+1)+; Retention time: 1.25 minutes ( 3 min run). 1H NMR (400 MHz, DMSO-dg) 5 8.08 (dd, J = 49,14 Hz,1H), 7.51 (ddd, J = 8.8, 7.1, 2.0 Hz, 1H), 6.85 (d, J = 8.7 , 6.61 (dd, J = 6.7, 4.9 Hz, 1H), 4.24 (d, J = 12.0 Hz, 1H), 4.11 (d, J = 12.9 Hz, 1H), 3.75 = 13.0 Hz,1H), 2.40 - 3.51 (m, 3H), 3.15 (br s, 1H), 2.91 (br s,1H), 2.59 (d, J (dd, J = 12.6, 10.9 Hz, 1H), 2.02 (d, J = 13.3 Hz,1H), 1.60 - 1.42 (m, 4H), 1.39 (s, 9H), 1.36 - 1.26 (m, 1H), 0.95 (t, J = 7.5 Hz, 3H).

[00340] Step 3: Tert—butyl lO-ethyl(2-pyridyl)—1 l—oxa-3,8—diazaspiro[5.5]undecanecarboxylate (480 mg, 1.33 mmol) was dissolved in dichloromethane (5 mL) at 0 0C and treated dropwise with HCl in dioxane (2.65 mL of 4 M, 10.6 mmol). The reaction was then allowed to warm to room ature and stirred for 1 h. The reaction mixture was diluted with romethane (50 mL) and saturated sodium onate on.

The organic layer was separated and the aqueous layer extracted with dichloromethane (3 X 20 mL). The aqueous layer was further diluted with 25 mL of 1 N NaOH and extracted with dichloromethane (3 X 20 mL). The combined organic extracts were dried over , filtered, and concentrated to e 10-ethyl-8—(2-pyridyl)-1 1- oxa—3,8-diazaspiro[5.5]undecane (345 mg, 1.32 mmol, 99%) an orange—colored oil.

ESl-MS m/z calc. 261.2, found 2623 (M+1)+; Retention time: 0.3 minutes (3 min run). 1H NMR (400 MHz, DMSO-d6) 8 8.08 (dd, J = 4.9, 1.4 Hz, 1H), 7.50 (ddd, J = 8.8, 7.1, 2.0 Hz, 1H), 6.84 (d, J = 8.6 Hz, 1H), 6.60 (dd, J = 6.6, 5.0 Hz, 1H), 4.17 (t, J = 11.3 Hz, 2H), 3.58 - 3.54 (m, 2H), 2.96 - 2.84 (m, 1H), 2.81 - 2.71 (m, 1H), 2.71 - 2.65 (m, 2H), 2.55 (d, J = 12.9 Hz, 1H), 2.40 (dd, J = 12.6, 11.0 Hz, 1H), 1.93 (d, J = 13.9 Hz,1H), 1.59 - 1.38 (m, 5H), 0.96 (t, J = 7.5 Hz, 3H). —129- Preparation of 4-(but—2—ynyl)—2-(fluoromethyl)0xa-4,9— diazaspiro[5.5]undecane Step 1: To a solution of utyl 8-benzyl(hydroxyrnethyl)-l l-oxa-3,8- diazaspiro[5.5]undecane—3—carboxylate (2.00 g, 5.31 mmol) in ol (38 mL) was added Pd(OH)2 (671 mg, 4.78 mmol) and ammonium formate (4.02 g, 63.7 mmol) and the mixture heated at 50 CC for 1 h. Additional catalyst (2.6 mmol) and ammmonium formate (25 mmol) were added and the reaction heated for an additional 2 h. The reaction mixture was d and concentrated to ~ 10 mL volume. The concentrate was diluted with dichloromethane and saturated sodium bicarbonate solution. The organic layer was separated and the aqueous layer washed with dichloromethane (5 X 50 mL). The ed organics were dried over NaZSO4, filtered, and concentrated to provide tert—butyl lO-(hydroxymethyl)—l 1-oxa—3,8-diazaspiro[5.5]undecane—3- carboxylate (1.37 g, 4.77 mmol, 90%) a s an colored glass. ESI—MS m/z calc. 286.2, found 287.3 (M+l)+ ; Retention time: 0.65 s (3 min run).

Step 2: ] Tert—butyl lO-(hydroxymethyl)-11—oxa-3,8—diazaspiro[5.5]undecane carboxylate (1.35 g, 4.71 mmol), K2COg (3.26 g, 23.6 mmol) and l-bromobut—2-yne 2O (495 uL, 5.66 mmol) were combined in N,N—dimethylformamide (15 mL) and heated for 48 h at 45 °C under nitrogen. The reaction mixture was diluted with ethyl acetate (150 mL) and filtered. The filtrate was washed with water, 50% saturated sodium bicarbonate solution, and brine. The c layer was dried over NaZSO4, filtered, and concentrated in vacuo. The desired fractions obtained from silica gel chromatography (5-20% methanol/ dichloromethane) were combined and concentrated, then brought up in ethyl acetate, filtered and concentrated in vacuo to provide tert—butyl-S-but—2—ynyl- lO—(hydroxymethyl)-l l—oxa-3 ,8-diazaspiro[5 . 5]undecane—3—carboxyl.ate (l .12 g, 3 .3 l ~130- mmol, 70%). ESI-MS m/z calc. 338.2, found 339.3 (M+l)+; Retention time: 0.86 minutes (3 min run).

Step 3: To a solution of laminosulfiir trifluoride (19.5 uL, 0.148 mmol) in dichloromethane (1.0 mL) at -7 8 0C was added dropwise a solution of tert-butyl 8- but-2—ynyl-10—(hydroxymethyl)-1 1-oxa-3 ,8-diazaspiro[5.5]undecane—3-carboxylate (50.0 mg, 0.148 mmol) in dichloromethane (1 mL). The reaction was stirred for 10 min at -78 °C then d to warm to room temperature and stirred for 16 h. Silica gel chromatography (4 g silica, 0-15% methanol/dichloromethane) provided tert—butyl 8—butynyl(fluoromethyl)-1 1-oxa-3,8-diazaspiro[5 .5]undecanecarboxylate (23.0 mg, 46%). ESI—MS m/z calc. 340.2, found 341.3 (M+1)+; ion time: 1.16 minutes (3 min run). 1H NMR (400 MHz, CDC13) 8 4.52 - 4.40 (m, 1H), 4.39 - 4.28 (m,1H), 4.06 - 3.91 (m,1H), 3.71 (br s, 2H), 3.35 - 3.14 (m, 3H), 3.08 (t, J = 11.4 Hz, 1H), 2.78 (d, J = 10.3 Hz,1H), 2.58 (d, J =11.1Hz,1H), 2.31 (d, J = 13.5 Hz,1H), 2.06 (t, J = 12.5 Hz, 2H),1,84(t, J = 2.3 Hz, 3H), 1.57 - 1.44 (m, 12H).

Step 4: Tert—butyl 8-but—2-ynyl—l0-(fluoromethyl)—1 3,8- diazaspiro[5.5]undecanecarboxylate (23.0 mg, 0.0676 mmol) was dissolved in dichloromethane (2 mL) and treated with HCl in dioxane (1.69 mL of 4 M, 6.76 mmol). The reaction mixture was stirred for 2 h, then diluted with romethane (10 mL) and 1 :1 saturated sodium bicarbonate/1 M NaOH (10 mL). The organic layer was separated, dried over Na2SO4, and concentrated to yield 8-butyny1—10- (fluoromethyl)-1l-oxa-3,8-diazaspiro[5.5]undecane hloride (16.0 mg, 0.0666 mmol, 98%). ESI—MS m/z calc. 240.2, found 241.5 (M+1)+; Retention time: 0.22 minutes (3 min run).

Preparation of 4-(butynyl)-2,2-difluor0-l—oxa-4,9- diazaspiro[5.5] undecane Step 1: To a solution of utyl 4—(aminomethyl)hydroxy—piperidinecarboxy1ate (3.00 g, 13.0 mmol) in N,N—dimethylformamide (30 mL) was added ethyl 2-bromo-2,2- ,difluoro-acetate (2.65 g, 13.0 mmol) and the reaction mixture stirred for l h under nitrogen. The reaction mixture was mixture diluted with ethyl acetate and water (25 mL) and brine (25 mL). The organic layer was dried over Na2S04, filtered and trated to provide tert—butyl 4—[[(2-bromo-2,2-difluoro-acetyl)amino]methyl] hydroxy—piperidine—l-carboxylate (4.98 g, 12.9 mmol, 99%). 1H NMR (400 MHz, DMSO-dg) 8 9.04 (t, J = 5.9 Hz, 1H), 4.66 (s, 1H), 3.65 (d, J = 12.7 Hz, 2H), 3.16 (d, J = 6.1 Hz, 2H), 3.02 (s, 2H), 1.38 (m, 13H).

Step 2: To a stirring solution of potassium tert—butoxide (7.23 mL of 1 M, 7.23 mmol) in tetrahydrofuran (20 mL) at 70 °C was added a solution of tert-butyl 4-[[(2- bromo-2,2-difluoro-acetyl)amino]methyl]hydroxy—piperidinecarboxylate (1.4 g, 3.62 mmol) in tetrahydrofuran (20 mL) over 15 min. After 20 min the on mixture was diluted with 1:1 brine/saturated NH4C1 and ethyl e. The organic layer was separated, washed with brine, dried over Na2804, filtered and concentrated in vacuo.

Silica gel chromatography (40 g , 30-100% ethyl acetate/hexane, product visualized by TLC with ninhydrin staining + heat ) provided tert-butyl 4,4-difluoro 9—diazaspiro[5.5]undecanecarboxylate (340 mg, 1.11 mmol, 31%) as a white solid. ESl—MS m/z calc: 306.1, found 307.5 (M+1)+; Retention time: 1.32 minutes (3 min run). 1H NMR (400 MHZ, DMSO-dg) 8 9.00 (s, 1H), 3.75 (d, J = 13.3 Hz, 2H), 3.45 (d, J = 3.2 Hz, 2H), 3.07 (br s, 2H), 1.79 (d, J = 13.6 Hz, 2H), 1.72 - 1.60 (m, 2H), 1.41 (s, 9H).

[00354] Step 3: Borane dimethylsulfide (36.3 uL, 0.408 mmol) was added dropwise to a on of tert—butyl 10,10-difluorooxo-l1—oxa-3,8-diazaspiro[5.5]undecane—3- carboxylate (125 mg, 0.408 mmol) in tetrahydrofuran (3 mL). The reaction mixture was heated at 55 °C for 2 h then cooled to room temperature. The mixture was quenched with the careful dropwise addition of methanol (~2 mL). N,N'— dimethylethane—l ,2-diamine (33.3 uL, 0.313 mmol) was then added and the mixture —132- heated at 70 °C for 40 min. The reaction was concentrated, and silica gel chromatography (4 g , 1% triethylamine /4% methanol/dichloromethane)) provided tert-butyl 8-but-2—yny1-10,l O-difluoro—l 1 -oxa-3 ,8 -diazaspiro [ 5 - . 5]undecane-3 carboxylate which was taken ly to the next reaction.

Step 4: To a mixture of crude tert—butyl 10,10-difluoro0xa—3,8- piro[5.5]undecane—3-carboxylate (65.0 mg, 0.222 mmol) and K2CO3 (61.5 mg, 0.445 mmol) in MN—dimethylformamide (1.0 mL) was added obut—2-yne (29.2 uL, 0.334 mmol) and the reaction heated at 45 °C for 48 h. The reaction was diluted with ethyl acetate and filtered. The filtrate was dried over NaZSO4, filtered and concentrated. Silica gel chromatography (4 g silica, 1-100% ethyl acetate/hexane) provided tert—butyl 2—ynyl—10,10-difluoro-l1-oxa-3,8-diazaspiro[5.5]undecane—3— ylate (50.0 mg, 65%) as a colorless oil. ESI-MS m/z calc. 344.2, found 345.3 (M+1)+; Retention time: 1.91 minutes (3 min run). 1H NMR (400 MHZ, CDC13) 5 3.80 (br s, 2H), 3.35 (q, J = 2.2 Hz, 2H), 3.23 (t, J = 12.1 Hz, 2H), 2.80 (t, J = 8.5 Hz, 2H), 2.48 (s, 2H), 2.02 (d, J : 13.2 Hz, 2H), 1.84 (t, J = 2.3 Hz, 3H), 1.54 — 1.48 (m, 2H), 1.46 (s, 9H).

Step 5: Tert—butyl 8-butynyl-10,10—difluoro-1 l-oxa-3,8- diazaspiro[5.5]undecane~3—carboxylate (50.0 mg, 0.145 mmol) was ved in dichloromethane (1 mL) and treated with HCl in dioxane (1.3 mL of 4 M, 5.1 mmol).

The reaction mixture was stirred for 1 h then concentrated in vacuo several times with acetonitrile to yield a white solid. The solid was dissolved in 1:1 DCM/acetonitrile and stirred with solid K2C03 for 1 h. The mixture was filtered and concentrated to provide 8—butynyl-10,10-difluoro-l1-oxa-3,8-diazaspiro[5.5]undecane (34 mg, 96%). ESI- MS m/z calc. 244.1, found 245.3 (M+l)+; Retention time: 0.79 minutes (3 min run).

Preparation of 4-tert-butyl—2-ethyl—1-0xa-4,9— diazaspir0[5.5] undecane 2012/028882 Step 1: To is(triphenylphosphine)palladium (0) (1.03 g, 0.891 mmol) and triphenylphosphine (934 mg, 3 .56 mmol) in degassed tetrahydrofuran (150 mL) in a re flask was added triethylamine (5.0 mL, 36 mmol). The mixture was stirred for 1 h under nitrogen atmosphere. A solution of tert-butyl 4-[(tert— butylamino)methyl]hydroxy—piperidinecarboxylate (5.10 g, 17.8 mmol) in ed tetrahydrofuran (20 mL) was added Via cannula, followed by [(Z) ybutenyl] acetate (2.85 mL, 17.9 mmol) and the mixture was stirred at 45 0C for 16 h. Silica gel chromatography (0-40% ethyl acetate/hexane, ninhydrin stain on TLC to Visualize) ed tert—butyl —butylVinyloxa-4,9- diazaspiro[5.5]undecanecarboxylate (5.1 g, 15 mmol, 85%) as a pale yellow oil. 1H NMR (400 MHz, CDC13) d 5.97 - 5.65 (m, 1H), 5.29 (dt, J =17.3, 1.6 Hz, 1H), 5.17 - .07 (m, 1H), 4.13 (s, 1H), 3.64 (s, 2H), 3.32 (t, J = 10.3 Hz,1H), 3.12 (t, J = 11.1 Hz, 1H), 2.85 (dt, J = 11.0, 2.5 Hz,1H), 2.68 (dd, J = 11.1, 2.2 Hz,1H), 2.33 (d, J = 14.2 Hz, 1H), 2.00 — 1.73 (m, 2H), 1.66 — 1.49 (m, 3H), 1.51 - 1.35 (m, 11H), 1.09 - 0.91 (m, 9H).

Step 2: To a solution of tert—butyl 4-tert—butylVinyl—l—oxa-4,9- diazaspiro[5.5]undecane-9—carboxy1ate (550 mg, 1.62 mmol) in methanol (10 mL) was added. Pd(OH)2 (447 mg, 3.18 mmol) and ammonium formate (2.19 g, 34.7 mmol) and the reaction mixture heated at 55 0C for 20 min. The reaction mixture was filtered, concentrated to ~10 mL and then diluted with dichloromethane and 1:1 saturated NaHCO; solution/1M NaOH. The dichloromethane layer was separated and the aqueous layer extracted with dichloromethane (5 X 20 mL). The combined organic layers were dried over Na2804, filtered and concentrated in vacuo to provide tert—butyl 8-tert—butyl—10-ethyl-1l-oxa-3,8-diazaspiro[5.5]undecanecarboxylate (530 mg, 1.56 mmol, 96%) as a colorless oil. ESI-MS m/z calc. 340.3, found 341.3 (M+1)+; 434— Retention time: 1.16 minutes (3 min run). 1H NMR (400 MHz, DMSO-dg) 8 3.59 (t, J = 11.7 Hz, 2H), 3.48 = 10.7 — 3.36 (m, 1H), 3.11 (br s,1H), 2.91 (br s, 1H), 2.80 (d, J Hz, 1H), 2.71 (dd, J =11.1, 1.7 Hz, 1H), 2.23 (d, J = 14.0 Hz, 1H), 1.81 (d, J =11.1 HZ, 1H), 1.71 (t, J = 10.6 Hz, 1H), 1.39 (s, 9H), 1.38 — 1.22 (m, 5H), 0.96 (s, 9H), 0.89 (t, J = 7.4 Hz, 3H).

Step 3: Tert—butyl 8-tert-butyl-lO-ethyl-l1-oxa—3,8-diazaspiro[5.5]undecane—3- carboxylate (530 mg, 1.56 mmol) was dissolved in dichloromethane and treated with a solution of HCl in dioxane (8.0 mL of 4 M, 33 mmol) and stirred for 15 min. The reaction mixture was diluted with romethane and washed with 1:1 saturated NaHC03/1 M NaOH. The organic layer was dried over Na2S04, filtered and concentrated to provide 8-tert—butyl-lO-ethyloxa—3,8-diazaspiro[5.5]undecane (390 mg, 99%) as an oily solid. ESI-MS m/z calc. 240.2, found 241.3 (M+l)+; Retention time: 0.21 minutes (3 min run).

[00367] Preparation of 4-tert-butyl(methoxymethyl)—1-0xa-4,9- diazaspir0[5.5] undecane .600.

Step 1: To tert-butyl 4-tert-butylVinyloxa-4,9-diazaspiro[5.5]undecane—9- carboxylate (1.00 g, 2.95 mmol) and 4-methylmorpholine 4-oxide (381 mg, 3.25 mmol) in acetone (9.0 mL) and water (1.0 mL) was added a solution of osmium ide in 2—methylpropanol (370 uL of 2.5 %w/w, 0.0295 mmol) and the on d 2 h. The reaction quenched with 300 mL of l M sodium bisulfite and stirred for min. The mixture was extracted with ethyl acetate (2 X 200 mL). The combined organic layers were washed with brine, dried over NaZSO4, filtered and concentrated in vacuo to e utyl 8-tert—butyl(l,2-dihydroxyethyl)-11—oxa—3,8- diazaspiro[5.5]undecane—3-carboxy1ate as a white foamy solid. The crude material was taken ly to the next step. ESl—MS m/z calc. 372.3, found 373.3 (M+l)+; Retention time: 0.83 minutes (3 min run).

Step 2: ] To a solution of tert—butyl 8-tert—buty1(l,2-dihydroxyethyl)-l l-oxa— 3,8-diazaspiro[5.5]undecane—3-carboxy1ate (1.10 g, 2.95 mmol) in tetrahydrofuran (22 mL) was added sodium periodate (1.58 g, 7.38 mmol) and water (8.0 mL), resulting in a thick white precipitate. The reaction mixture was heated at 40 °C for 3 h, then additional sodium periodate added (2.95 mmol) and the mixture stirred for 16 h. The reaction mixture was filtered through Celite and rinsed with tetrahydrofuran (30 mL).

The filtrate solution was cooled to 0 °C and treated portion-wise with sodium dride (223 mg, 5.91 mmol) over 5 min. The reaction mixture was stirred for 30 min then diluted with brine (400 mL) and ethyl acetate (400 mL). The organic phase was separated and the aqueous phase extracted with ethyl acetate (3 X 100 mL). The combined organic layers were dried over NaZSO4, filtered and concentrated in vacuo.

Silica gel chromatography (80 g silica, 1-10% methanol/dichloromethane) provided tert—butyl 8-tert—butyl- l roxymethy1)-l 3 zaspiro[5.5]undecane—3— carboxylate (720 mg, 2.10 mmol, 71%) as colorless oil. ESI-MS m/z calc. 342.3, found 343.5 (M+l)+; Retention time: 0.89 minutes (3 min run).

] Step 3:

[00373] To a solution of tert-butyl 8-ter't-butyl-lO-(hydroxymethyl)-l 3,8- diazaspiro[5.5]undecanecarboxylate (720 mg, 2.10 mmol) in MN- dimethylformamide (7.0 mL) was added sodium hydride (588 mg, 14.7 mmol) and the reaction stirred for 10 min. Methyl iodide (916 uL, 14.7 mmol) was added and the reaction mixture stirred for 20 min. The reaction was quenched with saturated aqueous NH4C1 and extracted with ethyl acetate (2 X 25 mL). The combined organic layers were dried over NaZSO4, filtered and trated to provide tert—butyl 8-tert—butyl—10- (methoxymethyl)-11—oxa-3,8-diazaspiro[5.5]undecane-3—carboxylate (732 mg, 2.05 mmol, 98%). ESl—MS m/z calc. 356.3, found 357.3 (M+1)+; Retention time: 0.97 minutes (3 min run).

[00374] Step 4: -l36- Tert—butyl 8-tert—butyl— l 0-(methoxymethyl)—1 l-oxa-3,8- diazaspiro[5.5]undecane-3—carboxylate (732 mg, 2.05 mmol) was dissolved in dichloromethane (10 mL) and treated dropwise with a on of HCl in dioxane (12.8 mL of 4 M, 51.3 mmol). The reaction was stirred for 1.5 h and then diluted with dichloromethane. The organic phase was washed with 1:1 saturated NaHCO3/ l M NaOH, dried over NaZSO4 and concentrated to provide 8-terl’-butyl (methoxymethyl)—11-oxa-3,8-diazaspiro[5.5]undecane (526 mg, 2.05 mmol, 99%) as a viscous amber colored oil. ESI—MS m/z calc. 256.2, found 257.3 (M+1)+; Retention time: 0.2 minutes (3 min run). 1H NMR (400 MHz, CDClg) 5 3.88 — 3.71 (m, 1H), 3.43 — 3.38 (m, 1H), 3.37 (d, J = 2.5 Hz, 3H), 3.35 — 3.30 (m, 1H), 3.24 (td, J = 12.2, 3.4 Hz,1H), 3.15 — 3.07 (m, 1H), 3.02 (td, J =12.2, 3.0 , 2.93 — 2.84 (m, 1H), 2.78 4 2.68 (m, 1H), 2.58 (d, J = 8.9 Hz, 2H), 2.48 — 2.19 (m, 1H), 1.97 (d, J = 11.4 Hz, 1H), 1.92 (ddd, J 12.2, 9.6 Hz, 2H), 1.84 — 1.74 (m, 1H), 1.70 — 1.55 (m, 2H), 1.00 (s, 9H).

[00376] Preparation of 4-(2,2-difluoropropyl)—2—(methoxymethyl)—l-oxa- 4,9-diazaspiro[5.5]undecane Step 1: To a mixture of tert—butyl lO-(methoxymethyl)-1l-oxa—3,8- diazaspiro[5.5]undecane-3—carboxylate and K2CO3 (115 mg, 0.832 mmol) in acetonitrile (1.4 mL) was added 1-bromopropanone (304 mg, 2.00 mmol). The reaction e was heated under argon in a sealed tube for 16 h. The mixture was cooled, d with dichloromethane and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to provide utyl 2— (methoxymethyl)—4-(2-oxopropyl)oxa—4,9-diazaspiro[5.5]undecanecarboxylate.

ESI-MS m/z calc. 356.2, found 357.3 (M+l)+; Retention time: 0.98 minutes (3 min run). —137— Step 2: To a on of tert—butyl 2-(methoxymethyl)-4—(2-oxopropyl)oxa- 4,9-diazaspiro[5.5]undecane—9-carboxylate in dichloromethane (1 mL) was added and MN—diethylaminosulfur trifluoride (195 uL, 1.47 mmol). Cesium fluoride (9.0 mg, 0.059 mmol) was then added in two portions followed by trifluoroacetic acid (5 uL, 0.06 mmol). The reaction was stirred for 15 min then cooled to 0 0C and quenched with 5 mL of saturated aqueous NaHCO3. The reaction was diluted with romethane (5 mL) and the layers separated. The organic layer was washed with water, dried over NaZSO4, filtered and concentrated in vacuo to provide tert—butyl 8- (2,2-difluoropropyl)—10—(methoxymethyl)-1 1-oxa—3 , 8-diazaspiro [5.5]undecane—3 - carboxylate as yellow oil. ESI-MS m/z calc. 378.2, found 379.3 (M+1)+; Retention time: 1.53 minutes (3 min run).

Step 3: Tert—butyl 8-(2,2-difluoropropyl)—l 0-(methoxymethyl)-1 1-oxa—3,8- diazaspiro[5.5]undecane-3—carboxylate (77.0 mg, 0.204 mmol) was treated with HCl in dioxane (509 uL of 4 M, 2.04 mmol) and stirred for 2 h. The solvent was ated to provide -difluoropropy1)(methoxymethyl)-1—oxa—4,9- diazaspiro[5.5]undecane hydrochloride as yellow solid (64 mg, 0.20 mmol, 99%). ESI- MS m/z calc. 278.2, found 279.3 (M+1)+; ion time: 0.79 minutes (3 min run).

] Preparation of 5-Isopropoxy—6-methylpicolinic acid HO«(fr\ Step 1: 2-Methylpyridinol (8.3 g, 76.1 mmol) was suspended in acetonitrile (125 mL). A solution ofNBS (27.7 g, 155.6 mmol) in acetonitrile (275 mL) was added to the suspension dropwise over 1 hour. The on e was heated at reflux for 1.5 hours. The reaction mixture was concentrated in vacuo and the residue was purified by silica gel column chromatography using dichloromethane as eluent to give 4,6- dibromomethylpyridinol (15.8 g, 78 %) as a yellow solid. 1H NMR (300 MHz, DMSO) 2.41 (s, 3H), 7.70 (s, 1H), 9.98 (s, 1H).

Step 2: 4,6~Dibromomethylpyridin01 (15.8 g, 59.4 mmol) was dissolved in THF (200 mL). The solution was cooled to -78 0C and n-BuLi (50 mL, 125 mmol, 2.5 M in hexane) was added dropwise keeping the temperature below -78 °C. The reaction e was allowed to stir at that temperature for 2 hours. The reaction e was quenched with water (50 mL) and was neutralized with 2 N HCl. The aqueous e was extracted with dichloromethane (2 times). The ed organic layers were dried (NaZSO4) and concentrated in vacuo to give 6-bromo methylpyridin—3-ol (10.5 g, 95 %) as a yellow oil. 1H-NMR (300 MHZ, DMSO) 2.29 (s, 3H), 7.08 (d, 1H), 7.26 (d, 1H), 10.08 (s, 1H).

] Step 3: 6-Bromo—2—methylpyridin—3-ol (10.5 g, 55.9 mmol) was dissolved in DMF (100 mL). K2C03 (19.3 g, 139.6 mmol) and 2—bromopr0pane (13.1 ml, 139.6 mmol) were added to the solution and the reaction mixture was heated at 100 °C overnight. The reaction mixture was poured onto a mixture of water and EtOAc (200 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2x).

The combined organic layers were dried (NaZSO4) and concentrated in vacuo. The crude oil was purified by silica gel column chromatography (0-20% ethyl acetate/heptanes) to give 6-bromoisopropoxy—2-methylpyridine (10.9 g, 85 %) as a yellow oil. 1H-NMR (300 MHz, CDC13) 1.42 (d, 6H), 2.48 (s, 3H), 4.65 (m, 1H), 7.20 (d, 1H), 8.04 (d, 1H).

] Step 4:

[00391] 6—Bromo-3—isopropoxy—2-methylpyridine (2.00 g, 8.70 mmol), PdC12(PPh3)2 (0.18 g, 0.26 mmol) and Et3N (1.8 m1, 13.04 mmol) were added to MeOH (5.2 mL) and acetonitrile (20 mL) in a Berghoff reactor. The reactor was charged with 10 bar CO (g) and was heated at 60 °C overnight. The reaction e was concentrated in vacuo and the residue was partitioned between DCM and water.

The layers were separated and the organic layer was washed with brine and dried ~139— (NazSO4). The mixture was concentrated in vacuo and purified by silica gel column chromatography to give methyl 5-isopropoxy—6-methylpicolinate (1.3 g, 71 %) as a yellow oil. 1H-NMR (300 MHz, CDClg) 1.40 (d, 6H), 2.53 (s, 3H), 3.98 (s, 3H), 4.62 (m, 1H), 7.12 (d, 1H), 7.98 (d, 1H).

Step 5: 5—Isopropoxy—6-methylpicolinate (1.3 g, 6.22 mmol) was dissolved in THF/water 2:1 (9 mL). LiOH *H20 (0.26 g, 6.22 mmol) was added and the reaction mixture was stirred at room temperature overnight. The mixture was poured into a mixture of water and EtOAc and the layers were separated. The aqueous layer was acidified to pH 4 with 2 N HCl and was ted with EtOAc (2x). The combined organics were dried (Na2804) and trated in vacuo to give 5-isopropoxy—6- ,methylpicolinic acid (860 mg, 74 %) as a beige solid. 1H-NMR (300 MHz, DMSO) 1.31 (d, 6H), 4.73 (m, 1H), 7.44 (d, 1H), 7.86 (d, 1H).

Preparation of ydroxy—1-methyl-ethyl)—3-methyl-benzoic acid 4-Bromo-3—methylbenzoic acid (3.96 g, 18.4 mmol) was dissolved in tetrahydrofuran (100 mL) and the solution was cooled to —78 °C. n-Butyllithium in hexanes (16.2 mL of 2.5 M, 41 mmol) was added dropwise over 20 s. The reaction mixture was allowed to stir for 30 minutes at -78 °C and then acetone (1.35 mL, 18.4 mmol) was added in a dropwise manner. The reaction mixture was allowed to stir for 30 minutes at —78 oC, and then allowed to warm to room temperature. The reaction mixture was then diluted with lM aqueous sodium hydroxide (100 mL). The organic layer was discarded and then the aqueous layer was acidified with 4M aqueous hydrochloric acid. The aqueous layer was then extracted 3 times with ethyl acetate.

The ed extracts were dried over sodium sulfate and then concentrated in vacuo.

The crude material was purified by silica gel column chromatography using a gradient of 0-10% ol in dichloromethane to give 4-(1~hydroxy—1—methyl-ethyl)methyl- —l40— benzoic acid (1.51 g, 42%). 1H NMR (400 MHz, DMSO) 8 12.74 (s, 1H), 7.68 (dd, J = 3.9, 2.5 Hz, 2H), 7.55 (d, J = 8.7 Hz, 1H), 5.06 (s, 1H), 2.56 (s, 3H), 1.51 (s, 6H).

Preparation of 4-(2-Methoxyethoxy)methylbenzoic acid

[00397] To a solution of 4-hydroxy—3-methy1-benzoic acid (2.0 g, 13 mmol) in THF (24 mL) was added tetrabutylphosphonium hydroxide (18 mL of 40 %w/v, 26 mmol). The reaction mixture was cooled to 0 oC and then 1-bromomethoxy—ethane (1.8 g, 1.2 mL, 13 mmol) was added. The reaction mixture was allowed to warm to room temperature overnight. The reaction mixture was acidified using 1M HCl and the aqueous layer was extracted with ethyl acetate. The organics were dried over sodium sulfate and trated in vacuo to yield 4-(2—methoxyethoxy)-3—methylbenzoic acid (182 mg, 6 %). ESI-MS m/z calc. 210.2, found 209.2 (M-H)‘; Retention time: 0.96 minutes (3 min run).

] The following compound was sized using the ures described above: 4-(3-methoxypropoxy)-3—methy1benzoic acid.

Preparation of 4-tert—Butoxy-S-methoxybenzoic acid Step 1: 4—Hydroxy—3-methoxy—benzaldehyde (500 mg, 3 .29 mmol), BocZO (1.74 g, 7.97 mmol), and Sc(OTf)3 (80 mg, 0.16 mmol) were ed in dichloromethane (5 mL). The reaction mixture was allowed to stir at room temperature for 24 hours. Water (5 mL) and dichloromethane (5 mL) were added and the two phases were separated. The aqueous layer was extracted with dichloromethane (3 x 5 -141— mL) and the combined cs were d with 10% aqueous potassium hydroxide until all remaining starting material was not observed in the organic phase (TLC, 40% ethyl acetate in hexanes). The two phases were separated and the dichloromethane layer was then washed twice with a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and concentrated in vacuo to give 4-tert—butoxy—3- methoxybenzaldehyde (130 mg, 19%) as a yellow oil. ESI—MS m/z calc. 208.1, found 209.2 (M+1)+. Retention time: 0.96 s (6 min run).

Step 2: 4-tert-Butoxymethoxybenzaldehyde (130 mg, 0.62 mmol) was suspended in a mixture of e (520 uL) and potassium hydroxide (6.5 mL of 0.20 M, 1.3 mmol). KMnO4 (150 mg, 0.93 mmol) was added and the reaction was d vigorously for 16 hours. The reaction mixture was filtered and then concentrated in vacuo to 3 mL. Hydrochloric acid (1M, 4 mL) was added and the resulting precipitate was filtered and washed with 1M HCl and a small amount of water to yield 4-tert— butoxy—3-methoxy—benzoic acid (68 mg, 49 %) as a white solid. ESl-MS m/z calc. 224.1, found 225.2 (M+1)+. Retention time: 1.66 minutes (3 min run). 1H NMR (400 MHz, DMSO) 8 12.80 (s, 1H), 7.66 — 7.41 (m, 2H), 7.09 (d, J: 8.8 Hz, 1H), 3.78 (s, 3H), 1.32 (s, 9H).

Preparation of 3-Methoxy—4-(2-meth0xymethylpropoxy)benzoic acid Step 1: To a d solution of methyl 4-hydroxy—3-methoxy-benzoate (2 g, .98 mmol), 2-methylprop-2—enol (871.0 mg, 1.0 mL, 12.1 mmol) and nylphosphine (3.17 g, 2.8 mL, 12.1 mmol) in THF (63.28 mL) at 0 °C was added DIAD (2.44 g, 2.34 mL, 12.1 mmol). The ice bath was removed and the reaction was stirred at 55 °C for 16 hours. The reaction mixture was diluted with EtOAc and washed sequentially with NaHCO3 (2 x 20 mL) and brine (2 x 20 mL) solutions. The -l42- organic layer was separated, dried over Na2S04, filtered and the solvent was evaporated under reduced pressure. The crude product was purified with silica gel using (0—30% ) ethyl acetate- hexanes to yield methyl 3-methoxy(2- methylallyloxy)benzoate (1.94 g, 75%) as a viscous liquid. ESl—MS m/z calc. 236.1, found 237.1 (M+1)+. Retention time: 1.63 s (3 min run). 1H NMR (400 MHz, DMSO) 5 7.56 (dd, J = 8.4, 2.0 Hz, 1H), 7.47 (d, J = 1.9 Hz, 1H), 7.06 (d, J = 8.5 Hz, 1H), 5.07 (br s, 1H), 4.97 (br s, 1H), 4.55 (s, 2H), 3.83 (s, 3H), 3.82 (s, 3H), 1.78 (s, 3H).

Step 2: ] To methyl oxy—4-(2-methy1ally10xy)benzoate (313 mg, 1.33 mmol) in MeOH (2.5 mL) was added H2804 (71 uL, 1.3 mmol) and the reaction mixture was heated in a microwave vial at 100 0C for 15.5 hours. The reaction mixture was trated in vacuo and the crude product was purified by silica gel column chromatography using 0-30% ethyl acetate in hexane as eluent to yield methyl 3— methoxy—4-(2-methoxy—2-methy1—propoxy)benzoate (208 mg, 59 %). ESI—MS m/z calc. 268.1, found 269.5 (M+1)+; Retention time: 1.46 s (3 min run). 1H NMR (400 MHz, DMSO) 5 7.57 (dd, J: 8.4, 2.0 Hz, 1H), 7.45 (d, J: 1.9 Hz, 1H), 7.10 (d, J: 8.5 Hz, 1H), 3.90 (s, 2H), 3.83 (s, 3H), 3.82 (s, 3H), 3.17 (s, 3H), 1.22 (s, 6H).

Step 3:

[00410] Methyl 3-methoxy(2-methoxy—2—methyl-propoxy)benzoate (177 mg, 0.66 mmol), dioxane (1.9 mL) and NaOH (1.8 mL of 1 M, 1.80 mmol) were combined and the reaction mixture was heated at 80 °C for 15 minutes. The reaction mixture was concentrated in vacuo and the crude mixture was dissolved in water. The mixture was washed with EtOAc (3x). The aqueous layer was acidified with 1N HCl then washed with EtOAc (3x). The combined organic layers was dried over Na2S04, filtered and the solvent was evaporated under reduced pressure to yield oxy(2-methoxy-2— methyl-propoxy)benzoic acid (130 mg, 77 %). ESI-MS m/z calc. 254.1, found 255.5 (M+1)+; Retention time: 1.14 minutes (3 min run). 1H NMR (400 MHZ, DMSO) 5 12.61 (s, 1H), 7.54 (dd, J: 8419 Hz, 1H), 7.45 (d, J: 1.8 Hz, 1H), 7.07 (d, J: 8.5 Hz, 1H), 3.89 (s, 2H), 3.81 (s, 3H), 3.17 (s, 3H), 1.22 (s, 6H). ation of 4-(2-Hydr0xypropan-2—yl)meth0xybenzoic acid —143— 2012/028882 HO \ 4-Bromomethoxy-benzoic acid (2.00 g, 8.67 mmol) was dissolved in THF (50 mL) and the solution was cooled to -7 8 OC. n—BuLi in hexanes (7.6 mL of 2.5 M, 19 mmol) was added dropwise over 15 minutes. The reaction mixture was allowed to stir for 30 minutes at -78 °C and then acetone (640 uL, 8.9 mmol) was added in a dropwise . The reaction mixture was allowed to stir for 30 minutes at -78 °C, and then it was allowed to warm to room temperature. The reaction mixture was then diluted with 100 mL of 1M aqueous sodium hydroxide (100 mL). The organic layer was discarded and the aqueous layer was made acidic with 4M aqueous hloric acid. The aqueous layer was then extracted 3 times with ethyl acetate. The combined extracts were dried over sodium sulfate and then evaporated to dryness. The crude material was purified by column tography using 0-5% ol in dichloromethane as eluent to give 4-(2-hydroxypropan-2—yl)methoxybenzoic acid (618 mg, 34%). ESI-MS m/z calc. 210.1, found 209.1 (M-l)"; Retention time: 0.68 minutes (3 min run).

Preparation of 4-(Is0propylsulfonyl)—3-methylbenzoic acid A OH /, \\ Step 1: ] Butyllithium (16 mL of 1.6 M, 25.6 mmol) was added dropwise to a mixture of 4-bromo—3-methyl-benzoic acid (2.5 g, 11.6 mmol) and THF (63 mL) at -78 OC. The reaction mixture was d to stir at —78 °C for 30 minutes before a solution of 2-isopropyldisulfanylpropane (1.7 g, 11.6 mmol) in THF (2 mL) was added dropwise. The mixture was allowed to stir at -78 0C for 30 minutes, then 30 minutes at room temperature. The reaction mixture was then diluted with 1M aqueous sodium hydroxide (100 mL). The organic layer was discarded and the aqueous layer was acidified with 4M aqueous hydrochloric acid. The aqueous layer was then extracted 3 —144— times with ethyl acetate. The combined ts were dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography using a gradient of 0-5% MeOH in dichloromethane to give 4- (isopropylthio)methylbenzoic acid (873 mg, 18 %). MS m/z calc. 210.3, found 211.2 (M+1)+. Retention time: 2.32 minutes (3 min run).

] Step 2: 3-Chlorobenzenecarboperoxoic acid (933 mg, 4.2 mmol) was added to a mixture of 4—(isopropy1thio)methy1benzoic acid (250 mg, 1.2 mmol) and dichloromethane (5 mL) at 25 OC. The reaction mixture was allowed to stir at 25 °C for 2 hours, then concentrated in vacuo. The white solid material was taken up in dichloromethane and was subjected to silica gel column chromatography (0-2% MeOH/dichloromethane) to give 4-isopropy1sulfony1methy1-benzoic acid (90 mg, 31%) as a white solid. ESI-MS m/z calc. 242.3, found 243.2 (M+l)+. ion time: 1.57 minutes (3 min run). IH NMR. (400 MHZ, DMSO) 5 13.50 (s, 1H), 8.50 — 7.66 (m, 3H), 3.50 -3.47 (m, 1H), 2.67 (s, 3H), 1.19 (d, J: 1.16 Hz, 6H).

Preparation of 3-Chloroisopropoxybenzoic acid 1” OH / 0 Step 1: To a solution of 3-chlorohydroxy—benzoic acid (1.0 g, 5.8 mmol) in methanol (30 mL) was added ic acid (3 mL, 56.3 mmol) and the e was stirred at 60 °C for 12 hours. The reaction e was cooled to room temperature and the methanol was removed in vacuo. The residue was partitioned between a saturated solution of K2CO3 and ethyl acetate (3 x 30 mL), dried, filtered and concentrated in vacuo to yield methyl 3-chloro—4-hydroxy—benzoate (0.9 g, 83 %) as a white solid. ESI- MS m/z calc 186.5, found 187.5 (M+1)+; Retention time: 1.17 minutes (3 min run). 1H NMR (400.0 MHz, CDC13) 8 8.05 (d, J = 2.2 Hz, 1H), 7.90 - 7.87 (dd, J: 8.8, 2.2 H, 1H), 7.06 (d, J = 8.8 Hz, 1H) and 3.90 (s, 3H).

Step 2: 2012/028882 To methyl 3-chlorohydroxy—benzoate (3.0 g, 16.1 mmol) in DMF (19 mL) was added potassium carbonate (8.9 g, 64.3 mmol) ed by 2-iodopr0pane (5.5 g, 3.2 mL, 32.2 mmol). The reaction mixture was heated at 60 °C for 1.5 hours.

The reaction mixture was cooled, filtered and diluted with EtOAc and the solvent was concentrated in vacuo. The al was dissolved in EtOAc and washed with water (3 x 10 mL) and brine (1 x 10 mL). The organic layer was dried over NaZSO4, filtered and the solvent was removed in vacuo to give methyl 3-chlorois0propoxybenzoate.

To the ester was added e (47 mL) and sodium hydroxide (42.7 mL of 1 M, 42.7 mmol) and the reaction was heated at 80 °C for 15 minutes. The reaction was cooled and solvent was removed in vacuo. The resulting residue was dissolved in water and washed with EtOAc (3 x 10 mL) and the layers were separated. The aqueous layer was acidified to pH 1 and was extracted with EtOAc (3 x 10 mL). The organic layer was separated and dried over Na2804, filtered and the solvent was removed in vacuo to yield 3-chloro—4—isopropoxy—benzoic acid (2.86 g, 83%) as a white solid. ESI-MS m/z calc. 213.6, found 215.3 (M+l)+; Retention time: 1.51 minutes (3 min run). 1H NMR (400.0 MHz, CDC13) 8 8.05 (d, J = 2.2 Hz, 1H), 7.90 - 7.87 (dd, J: 8.8, 2.2 H, 1H), 7.06 (d, J = 8.8 Hz, 1H) and 3.90 (s, 3H) ppm.

Preparation of 4-isopr0poxymethyl-benzoic acid “OKCKx0

[00424] Step 1: To a solution of oxy—3-methylbenzoic acid (10.0 g, 65.7 mmol) and DMF (100 uL) in methanol (35 mL) was added dropwise thionyl chloride (7.8 g, 4.8 mL, 65.7 mmol). The reaction mixture was d to stir at room temperature for 2 hours. The reaction mixture was quenched with the addition of aqueous saturated sodium bicarbonate solution (50 mL) and methanol was removed in vacuo. The aqueous layer was then extracted with EtOAc (3X 50 mL). The organic layers were dried over sodium sulfate, filtered and trated in vacuo to e methyl 4- hydroxy—3-methyl-benzoate (10.5 g, 96 %) as a light brown solid. EST-MS m/z calc. 166.4, found 167.4 (M+l)+; Retention time: 1.09 minutes (3 min run). —146— Step 2: To methyl 4—hydroxy—3-methyl—benzoate (1.0 g, 59.8 mmol) in dry DMF (62 mL) was added finely ground potassium carbonate (33.1 g, 239.3 mmol) followed by 2-iodopropane (20.3 g, 12.0 mL, 119.6 mmol). The reaction mixture was heated at 60 °C for 2 hours. The reaction mixture was cooled and d with ether (350 mL), and filtered over . The filtrate was washed with water (3 x 100 mL) and brine (100 mL) solution. The layers were separated and organics were dried over MgSO4. The t was evaporated and resulting residue was purified by silica gel using 0-30% hexanes mixtures as eluent to give methyl 4-isopropoxy methylbenzoate as a colorless oil (11.2 g, 89 %). ESI—MS m/z calc. 208.25, found 209.2 (M+1)+; Retention time: 1.93 minutes (3 min run). Lithium hydroxide (4.4 g, 181.6 mmol) was added to a solution of methyl 4-isopropoxy—3-methylbenzoate (11.2 g, 53.8 mmol) in tetrahydrofuran (31 mL) and water (31 mL). The mixture was rapidly stirred and heated at 65 0C for 6 hours. The reaction mixture was , diluted with water (75 mL) and extracted with ether (2 x 50 mL). The aqueous layer was acidified to pH 2 with 6N aq. HCl and extracted with ethyl acetate (4 x 75 mL). The combined organics were washed with water (75 mL) and brine on (75 mL) and layers were separated.

The organics were dried over MgSO4 and concentrated in vacuo to give 4-isopropoxy- 3-methy1-benzoic acid (9.5 g, 82 %) as colorless crystals. ESI-MS m/z calc. 194.2, found 195.3 (M+1)+; ion time: 1.53 minutes (3 min run). 1H NMR (400 MHz, DMSO) 6 7.78 = 8.6 Hz, 1H), 4.70 (dt, J = 12.1, 6.0 Hz, 1H), - 7.71 (m, 2H), 7.02 (d, J 2.15 (s, 3H), 1.30 (d, J = 6.0 Hz, 6H).

Preparation of 4-(2-Methoxy-Z-methyl-propoxy)benzoic acid (3)40

[00429] Step 1: A mixture of 1-chloromethy1—propanol (10 mL), 4- hydroxybenzonitrile (2.0 g, 16.8 mmol), potassium carbonate (9.3 g, 67.3 mmol), water (6 mL) and ethanol (60 mL) was heated at 80 °C overnight. The reaction mixture -147— was cooled, concentrated in vacuo and residue was d with ether (200 mL) and filtered. The filtrate was washed with water (50 mL) and brine on (50 mL). The cs were separated and dried over MgSO4 and purified by silica gel column chromatography using 0-100% EtOAc/DCM as eluent to give 4-(2-hydroxy—2-methyl- propoxy)benzonitrile (3.0 g, 94 %) as a yellow solid. ESl—MS m/z calc. 191.1, found 192.3 (M+1)+; Retention time: 1.05 minutes (3 min run).

Step 2: To 4-(2-hydroxymethyl-propoxy)benzonitrile (l g, 5.2 mmol) in DMF (10 mL) was added sodium hydride (220 mg, 5.5 mmol) and the reaction e was stirred for 20 minutes. Iodomethane (816 mg, 358 uL, 5.8 mmol) was added and the reaction mixture was stirred. for 1 hour at room temperature and 1 hour at 50 0C.

The reaction mixture was cooled and diluted with ether (250 mL) and washed with water (3 x 50 mL) and brine (50 mL) solution. The organics were separated and dried over MgSO4 and concentrated in vacuo to give 4-(2—hydroxy—2- methylpropoxy)benzonitrile. ESl-MS m/z calc. 205.2, found 206.3 (M+1)+; Retention time: 1.38 minutes (3 min run). To 4-(2—hydroxy—2-methylpropoxy)benzonitrile in ethanol (15 mL) was added sodium hydroxide (5.3 mL of 5 M, 26.1 mmol) and reaction was heated at 85 °C for 2 hours. The reaction mixture was cooled and concentrated in vacuo, then diluted with ethyl acetate (50 mL) and 3N HCl solution was added to adjust to pH 2 and the layers were separated. The aqueous layer was extracted with ethyl acetate (3 x 50 mL). The ed organics were washed with brine solution (2 x 50 mL), dried over MgSO4 and concentrated in vacuo to give 4-(2- y—2—methyl—propoxy)benzoic acid (0.9 g, 77 %) as a white solid. ESl-MS m/z calc. 224.2, found 225.3 (M+l)+; Retention time: 1.15 minutes (3 min run). 1H NMR (400 MHz, DMSO) 5 7.98 = 8.4 Hz, - 7.73 (m, 2H), 7.10 — 6.90 (m, 2H), 3.90 (d, J 2H), 3.15 (d, J = 3.8 Hz, 3H), 1.19 (d, J = 15.0 Hz, 6H).

Preparation of 4-(2-Hydr0xymethyl—propoxy)methyl—benzoic acid A mixture of 1-chloromethyl-propanol (10 mL), oxy—3- methyl-benzoic acid (2.0 g, 13.15 mmol), potassium carbonate (7.3 g, 52.71 mmol), water (6 mL) and ethanol (60 mL) was heated at 80 °C for 16 hours. The reaction mixture was cooled to room temperature and partitioned between 1N NaOH and EtOAc and the layers were ted. The organic layer was washed with 1N NaOH (2 x 10 mL) and the combined aqueous layers were washed with EtOAc. The combined organic layers were dried and concentrated in vacuo to give ethyl 4-(2-hydroxy methyl-propoxy)—3-methyl—benzoate. The ester was dissolved in ethanol (15 mL) and water (2 mL), sodium hydroxide (1.1 g, 26.30 mmol) was added and the reaction mixture was stirred at 40 °C for 4 hours. The on mixture was poured into 1N NaOH solution and extracted with ether (2 x 10 mL). The aqueous layer was acidified to pH 2—3 using 6N HCl solution and extracted with EtOAc (3 x 10 mL). The organics were ted and washed with brine solution. The organic layer was dried (NaQSO4 ) and concentrated in vacuo and the resulting material was triturated with ether to give 4- (2-hydroxy-2—methyl-propoxy)—3—methyl-benzoic acid (2.2 g, 75 %) as a white solid.

ESI—MS m/z calc. 224.1, found 225.5 (M+l) ; Retention time: 1.06 s (3 min run) 1H NMR (400 MHZ, DMSO) 5 7.75 (dd, J = 8.5, 2.0 Hz, 1H), 7.73 - 7.70 (m, 1H), 6.96 (d, J = 8.6 Hz, 1H), 4.67 (s, 1H, OH), 3.76 (s, 2H), 2.20 (s, 3H), 1.22 (s, 6H).

Preparation of 5-Isopropoxypyridine-Z-carboxylic acid O OH ] Step 1: To a solution of 5-hydroxypyridine-2—carboxylic acid (1.0 g, 7.2 mmol) in methanol (15 mL) was added sulfuric acid (881 uL, 16.53 mmol) dropwise and the reaction mixture was stirred at room temperature overnight. The on mixture was concentrated in vacuo, diluted with DCM (100 mL), washed with sat. aq NaHCO3 solution. The organic layer was separated and dried with sodium sulfate, filtered and concentrated in vacuo to give methyl 5-hydroxypyridine—2-carboxylate, which was used without further purification. ESI-MS m/z calc. 150.1, found 154.1 (M+l)+; Retention time: 0.33 minutes (3 min run).

Step 2: To methyl 5~hydroxypyridine—2—carboxylate (0.6 g, 3.92 mmol) in DMF (3.6 mL) was added potassium carbonate (2.2 g, 15.7 mmol) followed by 2— ropane (736 uL, 7.8 mmol) The reaction mixture was heated at 60 °C for 1.5 hours. The reaction mixture was cooled and d using EtOAc and the solvent was evaporated under reduced re. The residue was dissolved in EtOAc and washed with water (3 x 10 mL) and brine solution (10 mL). The organics were ted and dried over NaZSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography using 0-50% EtOAc: hexanes as eluent to give methyl 5-isopropoxypyridine—Z-carboxylate (555 mg, 73 %) as a colorless oil. ESI—MS m/z calc. 195.1, found 196.3 (M+l)+; Retention time: 1.09 minutes (3 min run).

Lithium hydroxide (5.7 mL of 2 M, 11.37 mmol) was added to a solution of methyl 5- isopropoxypyridinecarboxylate (555 mg, 2.84 mmol) in dioxane (4 mL) and stirred at 55 0C for 2 hours. The on mixture was diluted with ethyl acetate and washed with water and layers were separated. The aqueous layer was acidified with 1N HCl solution and extracted with ethyl acetate. The organics were separated and dried over sodium sulfate, filtered and concentrated in vacuo to give5-isopropoxypyridine-2— carboxylic acid (150 mg, 29 %). ESI-MS m/z calc. 182.1, found 182.3 (M+1)+; Retention time: 0.33 s (3 min run).

Preparation of 2-Fluoro-4—isopropoxy—benzoic acid Step 1 : ] To a solution of 2-fluoro—4—hydroxy—benzoic acid (5.32 g, 34.1 mmol) in methanol (21 mL) was added thionyl chloride (4.86 g, 3 mL, 40.9 mmol) dropwise and the reaction mixture was stirred at 40 °C for 3 hours. The reaction mixture was concentrated in vacuo and diluted with DCM (100 mL) and washed with aqueous saturated NaHC03 (2 x 50 mL) solution. The organics were separated and dried with MgSO4, filtered and concentrated in vacuo to give methyl 2-fluorohydroxy—benzoate (2.3 g, 40 %). ESl-MS m/z calc. 170.1, found 171.3 ; Retention time: 0.84 minutes (3 min run).

Step 2 : To a mixture of methyl 2-fluorohydroxy—benzoate (2.1 g, 12.4 mmol), potassium carbonate (6.8 g, 49.5 mmol) in dry DMF (13 mL) was added 2- iodopropane (2.5 mL, 24.8 mmol) and the reaction e was heated at 60 °C for 2 hours. The reaction was cooled and diluted with ether (50 mL) and filtered over Celite®. The filtrate was washed sequentially with water (3 x 25 mL) and brine solution (25 mL). The organic layer was separated and dried over MgSO4 and solvent was concentrated in vacuo to give a residue which was purified by silica gel column chromatography using 5-45% EtOAc/hexanes to give methyl 2-fluoro poxybenzoate as a colorless oil (2.2 g, 83 %). To a solution of methyl 2-fluoro-4— isopropoxybenzoate (2.2 g, 10.3 mmol) in THF (5.5 mL) was added a sion of m hydroxide (0.9 g, 37.1 mmol) in water (5.5 mL). The reaction e was stirred at 70 °C for 2 hours. The reaction mixture was cooled to room temperature and the excess LiOH was removed by filtration. The e was diluted with water (9 ml), and washed with ether (2 x 5 mL). The aqueous layer was separated and cooled to 0 °C and the pH was adjusted to pH 2 by addition of 6 M HCl solution. The aqueous layer was extracted with EtOAc (3 x 30 mL). The organics were separated and washed sequentially with water and brine. The organic layer was separated, dried and concentrated in vacuo to give 2-fluoro—4-isopropoxy—benzoic acid (2.45 g, 67%) as a white solid. 1H NMR (400 MHz, CDC13) 5 7.98 (t, J = 8.8 Hz, 1H), 6.69 (ddd, J = 15.1, .9, 2.0 Hz, 2H), 4.63 (dt, J = 12.1, 6.0 Hz, 1H), 1.39 (d, J = 6.1 Hz, 6H). ation of 3-Methyl(oxetanyloxy)benzoic acid Step 1: To a solution of 4-hydroxy—3-methylbenzoic acid (10.00 g, 65.7 mmol) and DMF (100 uL) in MeOH (35 mL) was added dropwise thionyl chloride (4.8 mL, 65.7 mmol) at room temperature. The reaction mixture was stirred at room temperature for 2 hours. The reaction e was ed with the addition of aqueous saturated sodium bicarbonate solution (50 mL), and methanol was removed under reduced pressure. The residue was extracted with EtOAc (3 X 50 mL) and dried over sodium. sulfate, filtered and concentrated in vacuo to e methyl 4-hydroxy—3- methyl-benzoate (10.53 g, 96 %) as a light brown solid. ESl-MS m/z calc. 166.0, found 167.1 (M+1)+; Retention time: 1.09 minutes (3 min run).

Step 2: To methyl 4-hydroxy—3—methyl-benzoate (498 mg, 3 mmol) was added DMF (3 mL) and sodium hydride (240 mg, 6.0 mmol) followed by oxetanol (445 mg, 6 mmol) and the reaction mixture was heated at 80 0C for 4 hours. The reaction was cooled and quenched with brine solution and extracted with EtOAc (3 x 10 mL).

The organic layer was separated and dried over sodium sulfate and evaporated to give methyl 3-methyl(oxetanyloxy)benzoate. To methyl 3-methyl—4—(oxetan-3— yloxy)benzoate was added sodium ide (3 mL of 1 M NaOH, 3 mmol) solution and the reaction mixture was d for 1 hour. The reaction was acidified with l M HCl solution to pH 3 and extracted with EtOAc. The organics were separated and dried and concentrated in vacuo to give yl(oxetan-3—yloxy)benzoic acid. ESI-MS m/z calc. 208.1, found 209.3 (M+l)+; Retention time: 1.04 minutes (3 min run). -152— ] ation of 4-Ethylsulfonyl—3-methyl—benzoic acid Step 1: To a solution of 4-fluoromethyl-benzoic acid (27.4 g, 178.0 mmol) in methanol (200 mL) was slowly added thionyl chloride (17.8 mL, 243.3 mmol). The solution was stirred at 35 °C for 7 hours. The solution was allowed to cool to room temperature and concentrated in vacuo to an oil. This oil was dissolved in EtOAc (75 mL) and washed sequentially with saturated aqueous sodium bicarbonate solution (2X 75 mL) and brine solution (1 X 75 mL). The organic layer was separated and dried over sodium sulfate, d and concentrated in vacuo to provide methyl o—3— methyl-benzoate (25.4 g, 85 %) as a red oil. ESI—MS m/z calc. 168.0, found 169.2 (M+1)+; ion time: 1.48 minutes (3 min run). 1H NMR (400 MHz, CDC13) 8 7.92 = 8.9 Hz, 1H), 3.90 (s, 3H), 2.31 (d, J = ~ 7.88 (m, 1H), 7.88 — 7.83 (m, 1H), 7.04 (t, J 2.0 Hz, 3H). ' [00453] Step 2: To methyl 4—fluoromethyl—benzoate (8.0 g, 47.6 mmol) in DMF (64 mL) was added ethylsulfanylsodium (10.0 g, 118.9 mmol) and the reaction was heated for 16 hours at 55 OC. The reaction mixture was cooled to room temperature and ed with brine solution and stirred for 20 minutes. The reaction mixture was extracted with EtOAc (3 x 10 mL). The aqueous layer was treated with Clorox® bleach solution (150 mL) and the reaction mixture immediately turned colorless. The reaction mixture was stirred for 10 minutes. The reaction was treated with 1N HCl solution to pH 1 and extracted with EtOAc (3 x 10 mL). The organics were separated and washed with brine solution (3 x 10 mL). The organic layer was dried over sodium sulfate and the solvent was removed in vacuo to e 4-ethylsulfonyl—3-methyl- benzoic acid (9.4 g, 86 %) as a white solid. 1H NMR (400 MHZ, CDC13) 5 8.13 (dd, J = 13.8, 8.3 Hz, 3H), 3.22 (q, J = 7.4 Hz, 2H), 2.79 (s, 3H), 1.31 (t, J = 7.4 Hz, 3H). -153— Preparation of 4-Tert—butylsulfonylbenzoic acid Step 1: Ethyl 4—fluorobenzoate (1.5 g, 8.9 mmol) and tert—butylsulfanylsodium (2.0 g, 17.8 mmol) were ed in ethylformamide (10 mL). The reaction mixture was heated to 80 0C for 2 hours. After this time, a precipitate formed and MN- dimethylformamide (15 mL) was added and the reaction mixture was stirred for an additional 20 hours at 80 OC. The reaction mixture was partitioned between ethyl e (100 mL) and water (100 mL). The aqueous layer was acidified with 4M hydrochloric acid, extracted with ethyl acetate (2 x). The combined extracts were dried over sodium sulfate, filtered, and concentrated in vacuo to yield 4-(tert- butylthio)benzoic acid as a colorless oil. The oil was dissolved in acetic acid (10 mL) and hydrogen peroxide (5 mL of 30 %w/w, 52.0 mmol) was added to the reaction mixture. The resulting mixture was heated to 80 °C for 2 hours. The on mixture was then allowed to cool to room temperature, and diluted with water (50 mL) and ethyl acetate (100 mL). The aqueous layer was extracted with ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulfate, filtered, and concentrated in vacuo to yield 4-tert—butylsulfonylbenzoic acid (2.2 g, 92 %) as a white solid. ‘H NMR (400 MHz, DMSO) 6 13.59 (s, 1H), 8.18 (d, J = 8.0 Hz, 2H), 7.94 (d, J = 7.6 Hz, 2H), 1.25 (s, 9H); ESI-MS m/z calc. 242.1, found 241.3 (M-l)‘; Retention time: 1.33 minutes (3 min run).

Preparation of 3-Fluor0isopropoxy—5-methoxy-benzoic acid F O\ -154— 2012/028882 A solution of 3-fluorohydroxy—5—rnethoxy—benzaldehyde (250 mg, 1.5 mmol) in DMF (2.5 mL) was treated with potassium carbonate (812 mg, 5.9 mmol) and stirred for 30 minutes. 2-lodopropane (500 mg, 2.9 mmol) was added over 10 minutes and reaction mixture was stirred for 20 hours. The reaction e was partitioned between EtOAc and saturated aqueous sodium chloride solution. The organic layer was washed with saturated sodium bicarbonate solution. The organic layer was ted and dried over sodium sulfate, filtered and concentrated in vacuo to give 3—fluoroisopropoxy—5-methoxybenzaldehyde. To the aldehyde was added tert- butanol (6.7 mL) and 2-methylbutene (4 mL, 38.2 mmol) and the reaction mixture was cooled to 0 °C. A solution of chlorite (345 mg, 3.8 mmol) and sodium dihydrogen phosphate hydrate (527 mg, 3.8 mmol) in water (6.7 mL) was added dropwise over 5 minutes, and the reaction mixture was stirred 30 minutes. The on mixture was warmed to room temperature and stirred for 12 hours. The reaction mixture was basified with 1 N NaOH solution and extracted with ethyl acetate (2 x 50 mL). The aqueous layer was acidified with 1 N HCl solution and extracted with EtOAc (4 X 50 mL). The combined cs were dried (NaZSO4), filtered, and concentrated in vacuo to afford 3—fluoroisopropoxy—5-methoxy—benzoic acid (190 mg, 56 %) as a white solid. ESl-MS m/z calc. 228.0, found 229.3 (M—l)+; Retention time: 1.57 s (3 min run).

[00460] Preparation of lopropylsulfamoyl)benzoic acid HO O O=§—NH To 4-chlorosulfonylbenzoic acid (10.0 g, 45.3 mmol) in dichloromethane (350 mL) at 0 0C was added cyclopropanamine (15.5 g, 19 mL, 271.9 mmol). The reaction mixture was allowed to warm to room temperature over 16 hours.

The solvent was evaporated under reduced pressure. The residue was ved in water (150 mL) and acidified using hloric acid. The aqueous layer was extracted with EtOAc (2 x 200 mL). The organic layer was dried over sodium sulfate, filtered and trated in vacuo to give 4—(cyclopropylsulfamoyl)benzoic acid (10.0 g, 92 %) as a white solid. ESI-MS m/z calc. 241.0, found 242.5 ; Retention time: 0.84 minutes (3 min run); 1H NMR (400 MHz, DMSO) 5 13.27 (s, 1H), 7.97 (d, J = 8.3 Hz, 2H), 7.91 (d, J = 2.5 Hz, 1H), 7.75 (d, J = 8.3 Hz, 2H), 2.03 — 1.90 (m, 1H), 0.38 — 0.28 (m, 2H), 0.23 — 0.15 (m, 2H).

Preparation of 4-(3-Hydroxypropoxy)—3-methyl-benzoic acid Step 1: To a solution of methyl 4-hydroxy—3-methyl-benzoate (3.03 g, 18.2 mmol) in DMF (9 mL) was added 3-bromopropan-1~ol (3.80 g, 2.4 mL, 27.4 mmol) and cesium carbonate (17.8 g, 54.7 mmol) and the reaction mixture was heated at 60 °C for 16 hours. The reaction mixture was cooled to room temperature and then ioned between water (250 mL) and ethyl acetate (2 x 100 ml). The organic layers were combined, washed with brine solution (50 mL), dried over NaZSO4, filtered and concentrated in vacuo to yield a crude oil that was purified by silica gel column chromatography eluting with EtOAc/hexanes (1 0-100 %) to give methyl 4-(3- hydroxypropoxy)—3—methyl—benzoate (1.87 g, 46 %) as a white solid. ESI-MS m/z calc. 224.0, found 225.0 (M+1)+; Retention time: 1.27 minutes (3 min run); 1H NMR (400 MHz, CDC13) 6 7.94 — 7.77 (m, 2H), 6.85 (d, J = 8.5 Hz, 1H), 4.18 (t, J = 5.9 Hz, 2H), 398— 3.82 (m, 5H), 2.24 (s, 3H), 2.10 (p, J = 5.9 Hz, 2H).

Step 2: To a solution of methyl 4-(3-hydroxypropoxy)-3 -methyl-benzoate (0.9 g, 4.01 mmol) in dioxane (8 mL) was added 1N NaOH (5mL) and the reaction mixture was heated at 70 °C for 22 hours. The solvent was trated in vacuo and the crude residue was ved in water (20 mL) and extracted with ethyl acetate (1 x 20 mL).

The aqueous layer was acidified with 1 M HCl solution and extracted with ethyl e (2 x 20 mL). The organics were separated, dried with NaZSO4 and concentrated in vacuo to give 4—(3—hydroxypropoxy)methyl-benzoic acid (0.7 g, 87 %) as a white solid. ESI—MS m/z calc. 210.0, found 211.0 (M+1)+; Retention time: 0.95 minutes (3 min run); 1H NMR (400 MHz, DMSO) 8 12.5 (bs, 1H), 7.97 — 7.60 (m, 2H), 7.01 (d, J = 8.6 Hz, 1H), 4.57 (s, 1H), 4.11 (t, J = 6.2 Hz, 2H), 3.59 (t, J = 5.5 Hz, 2H), 2.19 (s, 3H), 1.89 (p, J = 6.2 Hz, 2H).

Preparation of 3-Fluoro(1—hydr0xymethy1—ethyl)benzoic acid 0 OH

[00468] Step 1: 4-Bromo—3-fluoro-benzoic acid (5.0 g, 22.8 mmol) was dissolved THF (60 mL) and the solution was cooled to -78 0C. n-Butyllithium (20 mL of 2.5 M in hexanes, 50.2 mmol) was added dropwise and the mixture was allowed to stir for 1 minute at -78 °C, then e (3.7 mL, 50.2 mmol) was added dropwise. The reaction mixture was allowed to warm to room temperature and stirred for 16 hours. The reaction mixture was quenched with sat. NH4Cl on, diluted with saturated citric acid solution and the aqueous layer was ted with EtOAc (3x 20 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The desired compound was contaminated with 3-fluoro-4— hydroxybenzoic acid and the mixture was taken forward without any purification. ESI- MS m/z calc. 198.2, found 197 (M-l)+; Retention time: 2.13 minutes (15 min run).

Step 2: To a solution of 3—fluoro(1—hydroxymethyl-ethyl)benzoic acid (9.1 g, 45.7 mmol) in DMF (40 mL) was added cesium carbonate (22.3 g, 68.5 mmol) followed by benzyl bromide (11.7 g, 8.1 mL, 68.5 mmol) and on e was stirred at room temperature for 16 hours. The on mixture was partitioned between EtOAc and H20. The aqueous layer was extracted with EtOAc (3x 20 mL). The ed organic layers were washed sequentially with H20 (3x 10 mL), brine solution. The organics were separated and dried over MgSO4, filtered and concentrated in vacuo. The resulting residue was purified by silica gel column chromatography eluting with 10-20% EtOAc-hexanes to provide benzyl 3—flu0ro-4—(1-hydroxy—1— -ethyl)benzoate (2.8 g, 21 %) ESI-MS m/z calc. 288.2, found 289.3 (M+'l)+; Retention time: 1.79 min (3 min run). To a solution of benzyl 3-fluoro—4-(1-hydroxy—1- methyl-ethyl)benzoate (2.8 g, 9.71 mmol) in MeOH (50 mL) was added palladium on carbon (100 mg, 0.09 mmol) and the reaction mixture was subjected to an atmosphere of hydrogen for 16 hours. The catalyst was d via filtration over Celite® and the t removed in vacuo to e 3-fluoro-4—(l-hydroxymethyl-ethyl)benzoic acid (1.8 g, 96 %) as a white solid. ESI-MS m/z calc. 198.2, found 199.9 (M+1)+; Retention time: 0.91 minutes (3 min run).

Preparation of 4-(2-Hydr0xy-2—methyl—propyl)benzoic acid Step 1: HOmy). 0 A solution of methyl)magnesium in diethyl ether (25 mL of 3 M, 74.5 mmol) in THF (8 mL) and toluene (25 mL) was added to a solution of ethyl 2- (4—br0mophenyl)acetate (8.23 g, 33.9 mmol) in EtzO (165 mL) and the reaction mixture was stirred at 40 °C for 1 hour. The reaction mixture was quenched by the addition of saturated aqueous ammonium chloride (200mL) and the phases were ted. The organics were dried over sodium sulfate, filtered and concentrated in vacuo. The resulting residue was purified by silica gel column chromatography g with 0-30% EtOAc—hexanes to give 1-(4-br0mophenyl)-2—methyl-propan—2-ol (5.68 g, 73 %), as a clear oil. ESI-MS m/z calc. 228.1, found 229.5 (M+1)+; Retention time: 1.45 minutes (3 min run).

Step 2: 1-(4-bromophenyl)methyl—pr0panol (2.77 g, 12.1 mmol) was dissolved in dry THF (30 mL) and the solution was cooled to -78 OC . Tert—butyllithium -158— in e (15 mL of 1.7 M, 25.4 mmol) was added dropwise over 10 minutes and the reaction mixture was stirred at -78 °C for 2 hours. The reaction mixture was added via cannula to crushed solid C02 (53.2 g, 1.21 mol) in Et20 under a flow of nitrogen gas.

The reaction mixture was allowed to warm to room temperature, diluted with EtOAc and washed with water. The aqueous phase was acidified (pH 2) with 1N HCl on and the aqueous layer was extracted with EtOAc. The organics were dried over sodium sulfate, filtered and concentrated in vacuo to give 4-(2-hydroxy—2-methyl- propyl)benzoic acid (620 mg, 26 %) as a white solid. ESI-MS m/z calc. 194.0, found 195.3 (M+l)+; Retention time: 0.93 minutes (3 min run).

[00477] Preparation of 3-Methyl—4-(oxetanyl)benzoic acid Step 1: To (4-cyano—2—methyl—phenyl)boronic acid (1.75 g, 10.90 mmol), nickel iodide (0.10 g, 0.33 mmol), (lS,2S)—2-aminocyclohexan-l-ol (0.05 g, 0.33 mmol) and NaHMDS (2.01 g, 10.90 mmol) in isopropanol (10 mL) under an atmosphere of nitrogen was added 3-iodooxetane (1.00 g, 5.40 mmol) in isopropanol (1 mL) via cannula. The reaction mixture was heated at 90 °C for 2 hours, then cooled, diluted with ethanol (20 mL) and filtered over Celite®. The filtrate was concentrated in vacuo, then the residue was purified by silica gel column chromatography using 0-60% EtOAc/hexane as eluant to give hyl(oxetanyl)benzonitri1e (0.62 g, 65 %) as a white solid . ESI-MS m/z calc. 173.], found 174.3 (M+l)+; ion time: 1.09 minutes (3 min run).

] Step 2: To 3-methyl(oxetanyl)benzonitrile (500 mg, 2.89 mmol) in ethanol (7.5 mL) was added NaOH (3 mL of 5 M, 15.00 mmol) and the reaction mixture was heated at 85 0C for 1 hour. The on e was cooled to room temperature, concentrated in vacuo and diluted with ethyl acetate (20 mL). 6N HCl solution (~3 mL) was added until pH 6 was reached, then the aqueous layer was -159— extracted with ethyl acetate (2 x 20 mL), and the ed organics were washed with brine solution (10 mL). The organics were separated, dried over MgSO4 and concentrated in vacuo to give a white solid, which was triturated with ether to give a mixture (2:3 by NMR) of acid and amide. ESI-MS m/z (acid) calc. 192.1, found 193.3 (M+1)+; Retention time: 0.88 minutes (3 min run). ESI-MS m/z (amide) calc. 191.1, found 192.3 (M+1) +; Retention time: 0.47 min (3 min run).

Preparation of 2-(Difluoromethoxy)—3—fluoro-benzoic acid ] Step 1:

[00484] To a solution of 3-fluorohydroxy-benzoic acid (5.0 g, 32 mmol) in methanol (20 mL) was added thionyl chloride (5.0 g, 42 mmol) dropwise and the reaction mixture was stirred at 40 °C for 3 hours, then heated at 50 0C for 16 hours.

The on mixture was cooled and concentrated in vacuo and ing residue was purified by silica gel column chromatography using 0—50% ethyl. acetate/hexanes mixtures as eluant to give methyl 3-fluorohydroxy—benzoate (5.1 g, 94 %) as white crystals. ESI-MS m/z calc. 170.0, found 170.9 (M+1)+; Retention time: 1.33 minutes (3 min run) .

Step 2: A e of methyl 3—fluorohydroxy—benzoate (1.5 g, 8.8 mmol), 2~chloro—2,2-difluoro-acetic acid (1.62 g, 1.05 mL, 10.6 mmol) and potassium carbonate (1.46 g, 10.6 mmol) were heated in DMF (5 mL) at 120 0C for 5 hours. The on mixture was diluted with water (20 mL) and extracted with ether (2 x 10 mL).

The organics were separated and washed sequentially with water (5 mL) and brine solution (5 mL). The organics were dried (MgSO4) and concentrated in vacuo to give residue which was d by silica gel column chromatography using 0-30% EtOAc/hexanes as eluent to give methyl 2-(difluoromethoxy)fluorobenzoate (0.8 g, 39 %). To methyl 2—(difluoromethoxy)fluorobenzoate (0.8 g, 3.64 mmol) was was added 12% aq. NaOH (3 mL) and the reaction mixture was heated at 50 °C for 1 hour. >160- 2012/028882 The aqueous layer was extracted with 1 :1 ether/hexane (2 X 5 mL). The aqueous layer was acidified to pH 1 with 6 N HCl solution to give a suspension. The solid was filtered and washed with water, then dried in vacuo to give uoromethoxy)—3— fluoro-benzoic acid (555 mg, 31 %) as an off-white solid. 1H NMR (400 MHZ, CDCl3) 6 7.83 (d, J: 7.8 Hz, 1H), 7.43 (dd, J: 13.1, 4.8 Hz,1H), 7.35 (td, J: 8.1, 4.9 Hz, 1H), 6.68 (t, J: 74.4 Hz, 1H).

Preparation of 4-(1-Hydroxymethyl-ethyl)benzoic acid 4-Isopropylbenzoic acid (5.0 g, 30.5 mmol) was dissolved in a on of potassium hydroxide (4.1 g, 2 mL, 73.1 mmol) in water (125 mL). To the reaction mixture was added a solution of potassium permanganate (9.6 g, 60.9 mmol) in water (125 mL). The combined mixture was allowed to stir at 60 °C for 2 hours. The on mixture was cooled to 0 °C and treated with ethylene glycol (100 uL) and cooled to 0 °C. The solid were removed by filtration and the fitrate was acidified to pH l by addition of 6 N HCl on. The solid was removed by filtration, and the fitrate was extracted with l ether (3>< 200 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to provide 4-(1 -hydroxy- l-methyl-ethyl)benzoic acid (5.1 g, 93 %) as a white solid. ESl-MS m/z calc. 180.1, found 181.2 (M+1)+ ; Retention time: 0.6 minutes (3 min run). 1H NMR (400 MHz, MeOD) 8 8.00 — 7.95 (m, 2H), 7.61 — 7.56 (m, 2H), 2.64 (s, 1H), 1.54 (s, 6H).

Preparation of 4-(Diethylcarbamoyl)—3-fluoro-benzoic acid 0 OH /\NO To 4-cyano—2—fluoro—benzoic acid (2.0 g, 12.1 mmol) in DMF (18 mL) at room temperature was added N-ethylethanamine (1.5 g, 2.1 mL, 13.3 mmol) -l6l- followed by O-(7-azabenzotriazol— 1 —yl)-N,N,N',N'—tetramethyluronium hexafluorophosphate (4.6 g, 12.1 mmol) and ropylethylamine (3.9 g, 5.3 mL, .3 mmol) and the reaction mixture was stirred for 3 hours. The reaction e was diluted with EtOAc and washed with brine solution. The organics were separated, dried and concentrated in vacuo. The residue was purified by silica gel column chromatography using EtOAc-DCM (10-100%) as eluent to give 4-cyano-N,N—diethy1— 2-fluoro-benzamide (2.0 g, 75 %). 1H NMR (400 MHz, CDCl3) 8 7.51 (dd, J = 7.8, 1.3 Hz, 1H), 7.47 — 7.37 (m, 2H), 3.56 (q, J = 7.0 Hz, 2H), 3.16 (q, J = 7.1 Hz, 2H), 1.24 (td, J :- 7.1, 2.0 Hz, 4H). To 4—cyano-N,N-diethylfluoro-benzamide (1.75 g, 7.9 mmol) was added a 2:1 e ofTHFzMeOH (15 mL), followed by 4 N NaOH on (10 mL, 39.6 mmol) and the reaction mixture was heated at 65 °C for 2.5 hours. The reaction mixture was cooled, diluted with EtOAc and washed with 2 M HCl solution. The organics were separated, dried and trated in vacuo to give 4— (diethylcarbamoyl)—3-flu0ro—benzoic acid (1.91 g, 66 %) as a solid. ESI-MS m/z calc. 239.24, found 240.2 (M+1) + ; Retention time: 0.99 minutes (3 min run).

Preparation of 5-Tert—butoxypyridinecarboxylic acid To NaOtBu (1.57 g, 16.4 mmol) in HMPA (6 mL) was added DMF (6 mL), ed by 5—fluoropyridinecarbonitrile (l g, 8.19 mmol) and the reaction mixture was stirred for 16 hours under an atmosphere of nitrogen. The reaction mixture was diluted with water (100 mL) and extracted with DCM (3 x 50 mL) and layers were separated. The organics were washed sequentially with water (50 mL) and sat. aq.

NaHC03 solution (50 mL) and the organic layer was separated, dried over MgSO4 and trated in vacuo. The residue was purified by silica gel column chromatography eluting with 0—50% EtOAc/hexanes to give 5~tert—butoxypyridine—2—carb0nitrile (0.90 g, 62 %) as a yellow solid. ESI—MS m/z calc. 176.0, found 177.5 (M+1)+; Retention time: 1.3 minutes (3 min run). 1H NMR (400 MHZ, CDC13) 5 8.38 (dd, J = 2.7, 0.5 Hz, 1H), 7.67 - 7.56 (m, 1H), 7.41 — 7.31 (m, 1H), 1.52 — 1.38 (m, 10H). To 5—z‘ert- butoxypyridine-Z-carbonitrile (0.75 g, 4.26 mmol) in ethanol (10 mL) was added NaOH (4.3 mL of 5 M, 21.3 mmol) and the reaction mixture was heated at 85 °C for 1 —162- hour. The reaction mixture was cooled, concentrated in vacuo and diluted with ethyl acetate (50 mL). The organic layer was washed with mixture of brine solution (10 mL) and 6N HCl (3 mL). The organic layer was separated, dried over MgSO4 and concentrated in vacuo to give 5-tert—butoxypyridinecarboxylic acid (0.82 g, 99 %) as a yellow solid. ESI—MS m/z calc. 195.1, found 196.1 (M+1)+; Retention time: 0.62 minutes (3 min run).

] Preparation of 3-Flu0ro—4-(2-hydroxy—2-methyl—propyl)benzoic acid

[00494] Step 1: Trimethylsilyl diazomethane (11.6 mL of 2 M in toluene, 23.2 mmol) was added dropwise to a solution of 2-(4-bromofluoro—phenyl)acetic acid (4.5 g, 19.3 mmol) in a mixture of toluene (7.65 mL)/ methanol (7.65 mL) under a nitrogen atmosphere at room temperature. The on mixture was then quenched with a few drops of acetic acid and the solvents were trated in vacuo. The residue was purified by silica gel column chromatography using 0-10% EtOAc-hexanes as eluent to yield methyl 2-(4—bromo—2~fluoro—phenyl)acetate (4.3 g, 91 %) . 1H NMR (400 MHz, CDC13) 8 7,28 - 7.22 (m, 2H), 7.15 (t, J = 8.0 Hz, 1H), 3.71 (s, 3H), 3.63 (d, J = 1.0 Hz, 2H).

[00496] Step 2: A solution of methyl romo-2—fluoro-phenyl)acetate (4.0 g, 16.2 mmol) in THF (56 mL) was cooled to 0 0C under a nitrogen atmosphere and to this on was added methylmagnesium bromide on (16.2 mL of 3 M in diethyl ether, 48.6 mmol) over 30 minutes. The reaction mixture was stirred for 2 hours, then quenched with saturated s ammonium chloride solution and extracted with EtOAc. The aqueous layer was extracted once more with EtOAc, and the combined organics were dried over NaZSO4, filtered and trated in vacuo. The resulting residue was purified by silica gel column chromatography using 0-15% EtOAc- hexanes as eluent to yield romofluoro-phenyl)-2—methy1—propanol (3.0 g, 75 %) as a colorless oil. ESl—MS m/z calc. 246.0, found 231.1 (M—17)+; Retention time: 1.53 minutes (3 min run); 1H NMR (400 MHz, CDC13) 5 7.26 - 7.21 (m, 2H), 7.14 (t, J = 8.1 Hz, 1H), 2.78 (d, J = 1.4 Hz, 2H), 1.24 (d, J = 0.8 Hz, 6H).

Step 3 : A reaction vessel charged withl -(4—bromofluoro-phenyl)methy1- propan—2-ol (2.35 g, 9.51 mmol), palladium acetate (214 mg, 0.95 mmol), 3- diphenylphosphanylpropyl-diphenyl-phosphane (404 mg, 0.95 mmol) and triethylamine (4.24 mL, 30.4 mmol) in DMF (26 mL) was added MeOH (20 mL). The reaction vessel was charged to 50 psi with CO gas and heated at 80 °C for 15 hours.

The reaction mixture was allowed to cool, partitioned between EtOAc and brine solution. The layers were separated and the aqueous layer was extracted once more with EtOAc. The combined organics were washed with brine (2 x 10 mL), dried over Na2S04, filtered and concentrated in vacuo to an orange oil. The residue was purified by silica gel column chromatography using 0—30% EtOAc-hexanes as eluent to yield methyl 3-fluoro—4-(2—hydroxy—2-methyl—propyl)benzoate (1.83 g, 85 %). ESI—MS m/z calc. 226.1, found 227.5 (M+l)+; Retention time: 1.29 minutes ( 3 min run); 1H NMR (400 MHz, CDC13) 5 7.78 (dd, J = 7.9, 1.7 Hz, 1H), 7.71 (dd, J = 10.3, 1.6 Hz, 1H), 7.34 (t, J = 7.6 Hz, 1H), 3.92 (s, 3H), 2.88 (d, J = 1.3 Hz, 2H), 1.26 (s, 6H).

Step 4 : Methyl 3-fluoro(2—hydroxy—2-methy1-propyl)benzoate (1.59 g, 7.03 mmol) was dissolved in a mixture ofTHF (40 mL)/ water (20 mL)/ MeOH (20 mL) and LiOH (1.01 g, 42.2 mmol) was added. The reaction mixture was heated at 55 °C for 30 minutes. The reaction mixture was cooled to room temperature and the concentrated in vacuo. The residue was ved in water and cooled to 0 °C and d with l M HCl solution (to pH 3). The resulting precipitate was filtered, washed with water and dried under high vacuum to yield 3-fluoro(2-hydroxymethy1- propyl)benzoic acid (999 mg, 67 %) as a white solid. ESI-MS m/z calc. 212.1, found 211.1 (M—1)+; ion time: 0.98 minutes (3 min run); 1H NMR (400 MHz, CDC13) 8 7.84 (dd, J = 79,16 Hz, 1H), 7.77 (dd, J = 10.1, 1.6 Hz, 1H), 7.39 (d, J = 15.1 Hz, 1H), 2.91 (s, 2H), 1.28 (s, 6H).

Preparation of 4-(2-Hydroxyeth0xy)methyl-benzoic acid ] Step 1: To a solution of methyl 4-hydroxy—3-methyl—benzoate (5.77 g, 34.7 mmol) in DMF (17 mL) was added 2—bromoethanol (6.51 g, 3.7 mL, 52.1 mmol) and cesium carbonate (33.95 g, 104.2 mmol) and the reaction mixture was heated at 60°C for 16 hours. The reaction mixture was cooled to room ature and then partioned between water (250 mL) and ethyl acetate (2 X 100 ml). The organic layers were combined, dried over NaZSO4, filtered and concentrated in vacuo to yield a crude oil that was purified by silica gel column chromatography using EtOAc/hexanes (10 to 100 %) as eluent to give methyl 4-(2-hydroxyethoxy)—3-methyl~benzoate (1.87 g, 26 %) as a white solid. ESI—MS m/z calc. 210.1, found 211.1 (M+1) +; Retention time: 1.08 minutes (3 min run); 1H NMR (400 MHZ, CDC13) 5 7.94 - 7.79 (m, 2H), 6.84 (d, J = 8.5 Hz, 1H), 4.23 — 4.08 (m, 2H), 4.08 — 3.96 (m, 2H), 3.88 (s, 3H), 2.34 — 2.18 (m, 3H).

Step 2 : To a solution of methyl 4-(2-hydroxyethoxy)methy1—benzoate (1.87 g, 8.9 mmol) in dioxane (16 mL) was added 1N NaOH (5 mL) and the reaction mixture was heated at 70 0C for 18 hours. 5M NaOH (0.5 ml) was added and the reaction was d at 70°C for 22 hours. The reaction mixture was cooled and solvent was concentrated in vacuo and the crude residue was dissolved in water (20 mL) and extracted with ethyl acetate (2 x 20 mL). The aqueous layer was acidified with 1 M HCl on and extracted with ethyl e (2 x 20 mL). The organics were separated, dried with Na2804 and concentrated in vacuo to give 4—(2-hydroxyethoxy)— -165— 3-methyl-benzoic acid (0.77 g, 44 %) as a white solid. ESl—MS m/z calc. 196.1, found 197.0 (M+1)+; Retention time: 0.72 minutes (3 min run). 1H NMR (400 MHZ, DMSO) 12.51 (s, 1H), 7.96 — 7.49 (m, 2H), 7.00 (d, J = 8.6 Hz, 1H), 4.87 (t, J = 5.4 Hz, 1H), 4.06 (t, J = 5.0 Hz, 2H), 3.75 (q, J = 5.1 Hz, 2H), 2.17 (d, J = 20.3 Hz, 3H).

[00507] Preparation of 4-Pyrrolidin-l-ylsulfonylbenzoic acid Ozézo O OH ] To a solution of 4-chlorosulfonylbenzoic acid (2 g, 9.07 mmol) in dichloromethane (10 mL) was added a solution of pyrrolidine (1.29 g, 1.51 mL, 18.1 mmol) in dichloromethane (10 mL) and the reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was filtered and the White solid ed was washed with water (50 ml) and diethyl ether (10 ml) and dried under vacuum to give 4-pyrrolidin—1—ylsulfonylbenzoic acid (700 mg, 30 %). ESI-MS m/z calc. 255.0, found 256.3 (M+1)+; Retention time: 1.18 minutes (3 min run); 1H NMR (400 MHZ, DMSO) 6 13.49 (s, 1H), 8.15 (d, J = 8.5 Hz, 2H), 7.92 (d, J = 8.5 Hz, 2H), 3.17 (t, J = 6.7 Hz, 4H), 1.65 (t, J = 6.7 Hz, 4H). ] ation of 3—Flu0r0(3—meth0xypropynyl)benzoic acid Step 1 : To a mixture of methyl 4-bromo—3—fluoro-benzoate (2.5 g, 10.7 mmol) and copper (I) iodide (204 mg, 1.07 mmol) and palladium dichlorobis(triphenylphosphine) complex (753 mg, 1.07 mmol) under an atmosphere of argon was added DMF (21 mL) and the reaction mixture was cooled to 0 °C. -l66- 2012/028882 Triethylamine (1.95 mL, 13.9 mmol) was added followed by 3-methoxypropyne (997 uL, 11.8 mmol) and the on mixture was stirred at 60 °C for 70 minutes. The on mixture was cooled, diluted with EtOAc and filtered over Celite®. The filtrate was washed sequentially with 1 M HCl, 10% NH4OH and brine. The organic layer was separated, dried and concentrated in vacuo and the resulting residue was purified by silica gel column chromatography using EtOAc-hexanes (10—100%) as eluent to give methyl 3-fluoro-4—(3—methoxyprop-l-ynyl)benzoate (1.45 g, 61 %). ESI—MS m/z calc. 222.2, found 223.2 (M+1)+; Retention time: 1.53 s (3 min run); IH NMR (400 MHz, CDCl3) 8 7.75 (ddd, J = 11.2, 8.8, 1.5 Hz, 2H), 7.50 (dd, J = 7.9, 7.0 Hz, 1H), 4.37 (s, 2H), 3.92 (s, 3H), 3.47 (s, 3H).

Step 2 : To methyl 3-fluoro(3-methoxypropynyl)benzoate (1.4 g, 6.3 mmol) in 2:1 mixture of THF: MeOH (15 mL) at room temperature was added 4 M sodium hydroxide solution (1.9 mL, 7.56 mmol) and reaction mixture was d for 1 hour. The solvent was removed in vacuo and the reaction mixture was extracted with ethyl ether, and layers were separated. The aqueous layer was acidified with 1M HCl solution and extracted with ethyl ether. The organics were separated, dried and concentrated in vacuo to give 4—(3-hydroxypropoxy)—3-methyl-benzoic acid (1.1 g, 85 %) as a white solid. ESI—MS m/z calc. 208.2, found 209.2 (M+1)+; ion time: 1.22 minutes (3 min run); 1H NMR (400 MHz, CDCl3) 5 7.85 (dd, J = 8.0, 1.4 Hz, 1H), 7.80 (dd, J = 9.5, 1.3 Hz, 1H), 7.59 — 7.49 (m, 1H), 4.39 (s, 2H), 3.48 (s, 3H).

Preparation of 4-(3-Hydroxyoxetanyl)benzoic acid To 4-bromobenzoic acid (434 mg, 2.16 mmol) in THF (9 mL) at -78 °C was added dropwise n—butyllithium (2.84 mL of 1.6 M in s, 4.54 mmol). The reaction mixture was stirred for 30 minutes, then oxetan-3—one (218 mg, 3.03 mmol) in THF (1 mL) was added dropwise. The reaction mixture was stirred for 30 minutes at - 78 °C and allowed to warm to room ature over 30 minutes. The reaction mixture —167- was d with ethyl acetate (15 mL) and acidified to pH 2 with 2 N HCl. The layers were separated and the aqueous was re-extracted with ethyl acetate (15 mL). The combined organics were washed with brine solution (10 mL), dried over MgSO4 and concentrated in vacuo to give a white solid as a 1:1 mixture of 4-(3 -hydroxyoxetan yl)benzoic acid /benzoic acid (380 mg, 91 %).

Preparation of 4-Tetrahydrofuranylsulf0nylbenzoic acid Step 1: To a suspension of methyl 4-sulfanylbenzoate (0.85 g, 5.05 mmol), ium carbonate (1.39 g, 10.1 mmol) in DMF (10 mL) at room temperature was addded 3-iodotetrahydrofuran (1.00 g, 5.05 mmol). The resulting suspension was stirred for 16 hours. The reaction mixture was diluted with DCM (25 mL), filtered and the solvent was evaporated under reduced pressure. The residue was dissolved in DCM (25 mL) and washed with water (3 x 15 mL) and saturated aqueous brine solution (1 x 15 mL). The organic layer was dried over sodium sulfate, filtered and trated in vacuo to yield methyl 4-tetrahydrofuran—3-ylsulfanylbenzoate (1.03 g, 86 %) as a yellow solid. ESI-MS m/z calc. 238.1, found 239.3 ; ion time: 1.47 minutes (3 min run); 1H NMR (400 MHZ, DMSO) 5 7.91 — 7.83 (m, 2H), 7.48 — 7.39 (m, 2H), 4.16 — 4.08 (m, 2H), 3.91 — 3.72 (m, 5H), 3.55 (q, J = 7.6 Hz, 1H), 2.49 — 2.35 (m, 1H), 1.86 w 1.74 (m, 1H).

Step 2: Methyl ahydrofuran-3—ylsulfanylbenzoate (1.01 g, 4.24 mmol) was dissolved in methanol (25 mL), followed by the addition of water (2.5 mL), and Oxone (2.61 g, 4.24 mmol). The reaction mixture was stirred at room ature for 24 hours. An additional 0.1 eq of Oxone (0.26 g) was added and the reaction mixture was stirred for 2 hours, then filtered and the solvent was concentrated in vacuo. The resulting residue was dissolved in dichloromethane (30 mL) and washed with water (2 x 25 mL). The organic layer was dried over sodium e, filtered and concentrated in vacuo to yield methyl 4-tetrahydrofuranylsulfonylbenzoate (1.07 g, 93 %) as a yellow solid. ESI-MS m/z calc. 270.1, found 271.3 (M+1) +; Retention time: 1.02 minutes (3 min run).

] Step 3: To methyl 4-tetrahydrofuranylsu1fonylbenzoate (1.07 g, 3.96 mmol) in dioxane (11 mL) was added 1 M sodium hydroxide (10.5 mL, 10.5 mmol) and the reaction was heated at 80 °C for 10 minutes. The solvent was evaporated under reduced pressure. The residue was dissolved in water (30 mL) and washed with ethyl acetate (3 x 25 mL). The aqueous layer was acidified with hydrochloric acid. The aqueous layer was extracted with ethyl acetate (2 x 30 mL). The organic layer was dried over sodium sulfate, d and concentrated in vacuo to yield 4- tetrahydrofuran-3—ylsulfonylbenzoic acid (0.86 g, 85 %) as a white solid. EST-MS m/z calc. 256.0, found 257.3 (M+1)+; ion time: 0.69 minutes (3 min run); 1H NMR (400 MHz, DMSO) 5 13.59 (s, 1H), 8.19 (d, J = 8.3 Hz, 2H), 8.05 (d, J = 8.3 Hz, 2H), 4.38 — 4.15 (m, 1H), 4.06 — 3.97 (m, 1H), 3.87 — 3.71 (m, 2H), 3.72 — 3.54 (m, 1H), 2.20 — 2.06 (m, 2H).

Preparation of 3-Methyl—4-methylsulfonyl—benzoic acid 0 OH

[00524] Step 1 : ] Thionyl chloride (5.8 g, 3.5 mL, 48.7 mmol) was added dropwise to a solution of 4-fluoro-3—methyl—benzoic acid (5.0 g, 32.4 mmol) in methanol (40 mL).

The reaction mixture was stirred at 35 °C for 16 hours. The reaction mixture was concentrated in vacuo and the resulting methyl 4-fluoromethylbenzoate was used in the next step t further purification. ESI-MS m/z calc. 167.1, found 168.2 (M+1)+; Retention time: 1.57 minutes (3 min run). The crude ester was dissolved in DMF (20 mL) and powdered sodium thiomethoxide (2.3 g, 32.4 mmol) was added and -1. 69- 2012/028882 the reaction mixture was stirred at room temperature for 1 hour and at 80 °C for 1 hour.

The reaction mixture was concentrated in vacuo, the residue was partitioned between 1M HCl solution and ethyl acetate. The layers were separated and the organic was washed with 1M hydrochloric acid solution. The ethyl acetate layer was then dried over magnesium sulfate, filtered, and concentrated in vacuo to give methyl 3-methyl—4- (methylthio)benzoate. ESI-MS m/z calc. 182.2, found 183.1 (M+1)+; Retention time: 1.48 s (3 min run). Methyl 3-methyl(methylthio)benzoate (32.4 mmol) was heated in a mixture of acetic acid (80 mL) and hydrogen peroxide (40 mL of 30 %w/w, ) at 80 °C for 30 minutes. The reaction mixture was cooled, concentrated in vacuo and then partitioned between water and ethyl acetate. The layers were separated and the c was washed sequentially with water (1 x 20 mL), sat. NaHC03 (1x 20 mL) and brine (1x 20 mL), then dried over MgSO4 and concentrated in vacuo. The residue was triturated with ethyl ether to give methyl 3—methyl-4~methylsulfonyl—benzoate (5.8 g) as a white solid. The mother liquor was concentrated in vacuo then triturated with hexanes (3x) to give a second crop (1.2 g) ned yield 95 %). ESI-MS m/z calc. 2283, found 229.5 (M+1)+; ion time: 1.04 minutes (3 min run); 1H NMR (400 MHz, CDC13) 5 8.20 - 8.09 (m, 1H), 8.04-8.00 (m, 2H), 3.96 (s, 3H), 3.10 (s, 3H), 2.77 (s, 3H).

Step 2 :

[00527] To a mixture of methyl ylmethylsulfonyl-benzoate (5.8 g, .4 mmol) in dioxane (25 mL) was added NaOH (20 g, 125.0 mmol) (aq. 25%) and the reaction mixture was heated at 75 °C for 1 hour. The reaction mixture was cooled and was concentrated in vacuo to half the volume and adjusted to pH 2 with 6N HCl solution. The aqueous layer was extracted with ethyl acetate (3 x 100 mL). The cs were washed with brine solution (50 mL), dried over MgSO4 and concentrated in vacuo to give 3-methylmethylsulfonyl-benzoic acid (5.3 g, 97 %) as a white solid.

ESI-MS m/z calc. 214.5, found 215.5 (M-|~1)+; Retention time: 0.67 minutes (3 min run); 1H NMR (400 MHz, DMSO) 8 13.48 (s, 1H), 8.13 - 7.81 (m, 3H), 3.33 (s, 3H), 2.70 (s, 3H). —170— Preparation of 4-Ethoxy—3-(hydroxymethyl)benzoic acid HO O Step 1: A suspension of methyl ylhydroxy—benzoate (3.0 g, 16.7 mmol), bromoethane (2.7 g, 1.85 mL, 24.9 mmol) and powdered K2CO3 (6.9 g, 49.9 mmol) in DMF (15 mL) was heated at 40 °C for 16 hours. After 16 hours, a further aliquot of bromoethane (1 mL) was added and the reaction mixture was heated for a further 2 hours. The reaction mixture was diluted with DCM (50 mL), filtered and concentrated in vacuo to give a yellow solid, which was diluted with ether (200 mL), washed sequentially with water (50 mL), sat. aq. NaHCO3 (50 mL) and brine solution (50 mL). The organics were ted, dried over MgSO4 and concentrated in vacuo to give methyl xyformylbenzoate (3.52 g, 100 %) as a white solid. ESI—MS m/z calc. 208.0, found 209.3 (M+1)+; Retention time: 1.34 minutes (3 min run). Methyl 4— ethoxy—3—formylbenzoate (1.73 g, 8.91 mmol) was dissolved in THF (20 mL) and cooled to 0 °C. LiBH4 (100 mg, 4.59 mmol) was added and the reaction mixture was stirred for 1 hour, then slowly quenched with dropwise addition of acetic acid. The reaction mixture was concentrated in vacuo, d with ethyl e (50 mL), washed sequentially with sat. aq. NaHCO3 (20 mL) and brine (20 mL). The organics were separated, dried over MgSO4 and purified by silica gel column chromatography using 0-100% EtOAc/DCM as eluent to give methyl 4-ethoxy(hydroxymethyl)benzoate (1.6 g, 46 %) as a white solid. ESI-MS m/z calc. 210.0, found 211.3 (M+1)+; Retention time: 1.11 s (3 min run); 1H NMR (400 MHz, CDC13) 6 8.05 - 7.86 (m, 2H), 6.99 - 6.79 (m, 1H), 4.72 (s, 2H), 4.16 (q, J = 7.0 Hz, 2H), 3.89 (s, 3H), 1.64 (d, J = 7.0 HZ, 2H), 1.47 (t, J = 7.0 Hz, 3H).

[00531] Step 2: To a solution of methyl 4-ethoxy-3—(hydroxymethy1)benzoate (1.6 g, 7.61 mmol) in dioxane (10 mL) was added NaOH (6.0 g, 37.5 mmol) and the reaction -l71— mixture was heated at 50 °C for 2 hours. The on mixture was concentrated in vacuo to half—volume, acidified to pH 2 with aq. 6N HCl solution. The resulting suspension was filtered, the solid rinsed with water and acetonitrile, then dried in vacuo to give 4-ethoxy(hydroxymethyl)benzoic acid (740 mg, 50 %) as a white solid. lH NMR (400 MHZ, DMSO) 8 12.51 (s, 1H), 8.00 (s, 1H), 7.81 (dd, J = 8.5, 2.2 Hz, 1H), 7.01 (d, J = 8.6 Hz, 1H), 5.13 (t, J = 5.7 Hz,1H), 4.50 (d, J = 5.2 Hz, 2H), 4.11 (q, J = 7.0 Hz, 2H), 1.34 (t, J = 7.0 Hz, 3H).

Preparation of yl—4-methylsulfonyl—benzoic acid 0 OH

[00534] Thionyl chloride (2 mL, 27.4 mmol) was added dropwise to a solution of 4-fluoro—2-methy1-benzoic acid (1.25 g, 8.11 mmol) in methanol (10 mL). The reaction mixture was stirred at 60 °C for 2 hours. The reaction mixture was concentrated in vacuo and methyl 4-fluoro—2-methylbenzoate was used in the next step without further purification. Methyl 4-fluoromethylbenzoate was dissolved in DMF (5 mL) and sodium thiomethoxide (1.1 g, 15.7 mmol) was added and the reaction e was heated to 80 °C for 2 hours. The reaction mixture was then partitioned between 1M hydrochloric acid and ethyl e. The layers were separated and the organic layer was washed with 1M hloric acid, dried over magnesium sulfate, filtered, and concentrated in vacuo to give 2—methyl-4—(methylthio)benzoic acid which was carried to the next step without further purification. 2-Methyl—4— (methylthio)benzoic acid was suspended in acetic acid (10 mL) and hydrogen peroxide (5 mL of 30 %w/w) was added and the reaction mixture was heated to 80 °C for 2 hours. The on mixture was concentrated in vacuo, then partitioned between 0.2 M HCl (25 mL) and ethyl e (50 mL). The layers were separated and the aqueous extracted with ethyl acetate (50 mL). The combined organics washed with brine (20 mL), dried over MgSO4 and trated in vacuo. The resulting solid was rinsed with ether (2 x 10 mL) and dried in vacuo to give 2—methyl-4—methylsulfonyl-benzoic acid (0.87 g, 50 %) as a white solid. ESI-MS m/z calc. 214.0, found 215.5 (M+l)+; -l 72- 2012/028882 Retention time: 0.48 minutes (3 min run); 1H NMR (400 MHz, DMSO) 5 7.99 (d, J = 8.1 Hz, 1H), 7.87 (s, 1H), 7.82 (d, J = 8.0 Hz, 1H), 3.25 (s, 3H), 2.59 (s, 3H).

] Preparation of 3-Meth0xymethylsulfonyl—benzoic acid 0 | ,,S\ To 3—fluoromethylsulfonyl-benzoic acid (490 mg, 2.25 mmol), sodium hydride (270 mg, 6.74 mmol), methanol (1.55 g, 2.0 mL, 48.3 mmol) was added DMF (5 mL) and reaction mixture was heated at 100 0C for 1 hour. The reaction e was cooled and d with EtOAc and acidified using 1 M HCl solution. The organic layer was separated, washed with saturated aqueous brine solution (3x), dried over sodium sulfate and concentrated in vacuo to give 3—methoxy— 4-methylsulfonyl-benzoic acid (496 mg, 95 %). ESI—MS m/z calc. 230.0, found 231.3 (M+1)+; Retention time: 0.49 minutes (3 min run).

] Preparation of 4-[Cyclopropyl(hydroxy)methyl]benzoic acid Ho, 0 V Step 1 : (4-Ethoxycarbonylphenyl)-iodo-zinc (20 mL of 0.5 M in THF, 10.0 mmol) was added over 10 min to dichloro-bis(triphenylphosphoranyl)palladium (211 mg, 0.3 mmol) in THF (20 mL) under an atmosphere of nitrogen at 0 °C. The reaction mixture was stirred for 15 minutes, cyclopropanecarbonyl chloride (941 mg, 817 uL, 9.0 mmol) was added dropwise at 0 °C and stirred for 2 hours. The reaction mixture was quenched with 1M HCl (20 mL), extracted with ethyl acetate (2 x 50 mL). The organic layer was washed sequentially with sat. aq. NaHC03 (5 mL) and brine solution (50 mL), dried over MgSO4 and purified by silica gel column chromatography using 0- -l73- % EtOAc/hexanes as eluent to give ethyl 4-(cyclopropanecarbonyl)benzoate (1.54 g, 71 %) as a pale yellow oil. ESI—MS m/z calc. 218.0, found 219.3 (M+1)+; ion time: 1.57 minutes (3 min run).

Step 2 : To ethyl 4-(cyclopropanecarbonyl)benzoate (400 mg, 1.83 mmol) in ethanol (10 mL) was added at room temperature NaBH4 (69 mg, 1.83 mmol) and the reaction mixture was stirred for 1 hour. The reaction mixture was then concentrated in vacuo and NaOH (1.5 g, 9.38 mmol) and dioxane (1.5 mL) were added and the on mixture was heated at 80 °C for 3 hours. The reaction mixture was concentrated in vacuo to half the volume and pH was adjusted to 2 with 3 N HCI. The aqueous layer was extracted with ethyl acetate (3 x 10 mL), and the combined organics were washed with brine solution (5 mL), dried over MgSO4 and concentrated in vacuo to give 4- propyl(hydroxy)methy1]benzoic acid (300 mg, 85 %). ESl-MS m/z calc. 192.2, found 193.5 (M+1)+; Retention time: 0.78 minutes (3 min run); 1H NMR (400 MHz, DMSO) 8 7.89 (d, J = 8.1 Hz, 2H), 7.49 (d, J = 8.1 Hz, 2H), 5.33 (d, J = 4.4 Hz, 1H), 4.04 (dd, J = 7.3, 4.3 Hz, 1H), 1.12 - 0.87 (m, 1H), 0.54 - 0.20 (m, 4H). ation of r0isopr0poxy-benzoic acid A0Fj:j/LKOH Step 1 :

[00544] To methyl 3-fluorohydroxy—benzoate (2.0 g, 11.8 mmol) in DMF (12 mL) was added K2CO3 (6.50 g, 47.04 mmol) followed by 2-iodopropane (2.35 mL, 23.5 mmol). The reaction mixture was heated at 60 °C for 1.5 hours. The reaction mixture was cooled and diluted with EtOAc, filtered and the solvent was evaporated in vacuo. The resulting residue was dissolved in EtOAc and washed sequentially with water (3 x 10 mL) and brine solution (1 x 10 mL). The organics were ted and dried over NaZSO4, filtered and concentrated in vacuo to give the desired ester. ESI-MS m/z calc. 212.2, found 213.3 (M+1)+; Retention time: 1.7 minutes (3 min run). 1H NMR (400 MHz, DMSO) 6 7.76 (ddd, J = 8.6, 2.1, 1.2 Hz, 1H), 7.69 (dd, J =11.9, 2.1 —174— Hz, 1H), 7.31 (t, J = 8.6 Hz, 1H), 4.79 (dt, J = 12.1, 6.0 Hz, 1H), 3.82 (s, 3H), 1.32 (d, J = 6.5 Hz, 6H).

Step 2 : ] To the ester from above was added dioxane (31 mL) and NaOH solution (31.2 mL of 1 M, 31.2 mmol) and the reaction was heated at 80 °C for 20 minutes, then concentrated in vacuo. The crude mixture was dissolved in water and washed with EtOAc (3 x 10 mL). The layers were separated and the aqueous layer was acidified using 1 M HCl solution. The aqueous layer was extracted with EtOAc (3 x mL). The organic layer was dried over NaZSO4, filtered and concentrated in vacuo to yield 3-fluoroisopropoxy—benzoic acid (1.7 g, 72 %) as a white solid. ESI-MS m/z calc. 198.1, found 199.1 (M+1)+; Retention time: 1.7 minutes (3 min run). 1H NMR (400 MHZ, DMSO) 8 12.90 (br s, 1H), 7.73 (ddd, J = 8.6, 2.0, 1.1 Hz, 1H), 7.65 (dd, J = 11.9, 2.1 Hz, 1H), 7.28 (t, J = 8.6 Hz, 1H), 4.77 (hept, J = 6.1 Hz,1H), 1.32 (d, J = 6.0 Hz, 6H).

] Preparation of ropoxymethoxy-benzoic acid I O A0OflLOH Step 1 : 2-Bromopropane (3.39 mL, 36.2 mmol) was added to a suspension of 4-bromomethoxy—phenol (5 g, 24.1 mmol), K2C03 (6.67 g, 48.3 mmol) and DMSO (71 mL) at room temperature. The heterogeneous mixture was stirred at 55 °C for 2 hours, then cooled to room temperature and diluted with water. The reaction mixture was extracted with EtZO and the t was washed successively with 10% aq. NaOH solution, water, then brine solution. The organics were separated and dried over sodium sulfate, filtered and concentrated in vacuo to give 4-bromoisopropoxy—2- methoxy-benzene (5.83 g, 94 %) as a pale yellow oil. ESI-MS m/z calc. 244.0, found 245.0 (M+1)+; ion time: 1.93 minutes (3 min run). 1H NMR (400 MHZ, CDClg) 7.03 - 6.95 (m, 2H), 6.76 (dd, J = 7.7, 1.1 Hz, 1H), 4.47 (dt, J = 12.2, 6.1 Hz, 1H), 3.84 (s, 3H), 1.35 (d, J = 6.1 Hz, 6H). -175— Step 2 : Under an atmosphere of nitrogen mL of 1.6 M , tert-butyllithium (2.14 in toluene, 3.42 mmol) was added dropwise to a solution of 4-bromo—1—isopropoxy—2- methoxy—benzene (400 mg, 1.63 mmol) in THF (6 mL) at -78 °C. The reaction mixture was d to stir for 1 hour at -78°C, then added dropwise to a flask containing C02 (1.8 g, 40.8 mmol) , dry ice) in THF (2 mL). The reaction mixture was allowed to stir for 30 s warming to room temperature. Water (20 mL) was added to the reaction mixture and the volatiles were removed in vacuo. The resultant aqueous layer was acidified with 1N HCl solution to pH 1 and was extracted with ethyl acetate (3 x 15 mL). The organics were separated and the combined organics were washed with brine solution, dried over sodium sulfate, filtered and trated in vacuo to give 4-isopropoxy—3-methoxy—benzoic acid (310 mg, 85 %) as a white solid. ESI—MS m/z calc. 210.1, found 211.1 (M+1)+; Retention time: 1.23 minutes (3 min run). 1H NMR (400 MHZ, DMSO) 8 12.63 (s, 1H), 7.53 (dd, J = 8.4, 2.0 , 7.44 (d, J = 2.0 Hz, 1H), 7.04 (d, J = 8.7 Hz, 1H), 4.67 (dt, J = 12.1, 6.0 Hz, 1H), 3.78 (s, 3H), 1.28 (d, J = 6.0 Hz, 6H).

Preparation of 4-Isobutylsulfonylbenzoic acid Step 1 :

[00554] Potassium carbonate (1.2 g, 8.9 mmol) was added to a mixture of methyl 4-sulfanylbenzoate (1.0 g, 6.0 mmol), l-bromomethyl-propane (1.2 g, 970 uL, 8.9 mmol), and DMF (10 mL) at room temperature. The reaction mixture was allowed to stir for 4 hours and the ing solid was removed by filtration. The filtrate were partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the organic layer was washed with brine solution, then dried over sodium sulfate, filtered and trated in vacuo to give methyl 4~isobutylsulfanylbenzoate (1.1 g, 83 %) as a clear oil. ESI—MS m/z calc. 242.0, found 243.2 (M+1)+; Retention time: 1.73 minutes (3 min run). 1H NMR (400 MHz, CDC13) 5 8.30 (d, J = 8.3 Hz, 2H), 8.05 (d, J = 8.3 Hz, 2H), 3.03 (d, J = 6.5 Hz, 2H), 2.27 (dt, J = 13.3, 6.6 Hz, 1H), 1.08 (d, J = 6.7 Hz, 6H).

Step 2 : 3-Chlorobenzenecarboperoxoic acid (3.6 g, 15.6 mmol) was added to a on of methyl 4-isobuty1sulfanylbenzoate (1.0 g, 4.5 mmol) in DCM (20 mL) at room temperature. The reaction mixture was allowed to stir for 2 hours, then concentrated in vacuo. The resulting residue was d by silica gel column chromatography using (0-100%) ethyl acetate/hexanes as eluent to give methyl 4- isobutylsulfonylbenzoate. ESI-MS m/z calc. 256.1, found 2572 (M+1)+; Retention time: 1.96 minutes (3 min run). 1H NMR (400 MHZ, CDC13) 5 8.23 (d, J = 8.4 Hz, 2H), 8.00 (d, J = 8.3 Hz, 2H), 3.98 (s, 3H), 3.02 (d, J = 6.5 Hz, 2H), 2.25 (dp, J = 13.3, 6.6 Hz, 1H), 1.07 (d, J = 6.7 Hz, 6H).

Step 3 : A mixture of methyl 4-isobutylsulfonylbenzoate (1.0 g, 3.9 mmol), NaOH solution (10 mL of 1 M, 10.00 mmol), and dioxane (10 mL) was heated at 80 °C for 1.5 hours. The reaction mixture was cooled to room temperature, then concentrated in vacuo. The solid residue was dissolved in water and washed with ethyl acetate (1 x mL). The aqueous layer was acidified with 1N HCl on and was extracted with ethyl e (2 x 10 mL) and layers were separated. The combined organics were 2O washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography using (0-100%) ethyl e/hexanes as eluent to give 4—isobutylsulfonylbenzoic acid (1.0 g, 98 %). ESI—MS m/z calc. 242.1, found 243.2 (M+1)+; Retention time: 1.73 minutes (3 min run). 1H NMR (400 MHz, CDC13)5 8.30 (d, J = 8.3 Hz, 2H), 8.05 (d, J = 8.3 Hz, 2H), 3.03 (d, J = 6.7 Hz, 6H). = 6.5 Hz, 2H), 2.27 (dt, J = 13.3, 6.6 Hz, 1H), 1.08 (d, J Preparation of 4-(2-Hydroxy-Z—methyl-propoxy)benzoic acid Step 1 : -l77— WO 25613 A mixture of 1-chloromethyl—propanol (10 mL ), 4- hydroxybenzonitrile (2 g, 16.8 mmol), K2C03 (9.3 g, 67.3 mmol) in water (6 mL) and ethanol (60 mL) was heated at 80 °C for 16 hours. The reaction mixture was cooled and the solvent was concentrated in vacuo. The residue was diluted with ether (200 mL) and filtered and the filtrate was washed sequentially with water (50 mL) and brine solution (50 mL). The organics were separated and dried over MgSO4 and solvent was removed in vacuo to give a residue which was purified by silica gel column chromatography using (0-100%) EtOAc/DCM as eluent to give 4-(2-hydroxy methyl-propoxy)benzonitrile (3.0 g, 94 %) as a yellow solid. ESI-MS m/z calc. 191.1, found 192.3 (M+1)+; Retention time: 1.05 minutes (3 min run).

Step 2 : To 4-(2-hydroxy—2-methyl-propoxy)benzonitrile (1.0 g, 5.2 mmol) in ethanol (15 mL) was added NaOH solution (5 mL of 5 M, 25 mmol) and the reaction mixture was heated at 85 0C for 1 hour, concentrated in vacuo and diluted with ethyl e (50 mL). To the organic layer was added a mixture of brine on (10 mL) and 6N HCl (3 mL, to adjust to pH 6), The organic layer was ted, dried over MgSO4 and concentrated in vacuo to give a yellow solid, which was triturated twice with diethyl ether to give 4-(2-hydroxy—2-methyl-propoxy)benzoic acid (0.8 g, 76 %) as a white solid. ESI-MS m/z calc. 195.1, found 196.1 (M+1)+; Retention time: 0.62 minutes (3 min run). 1H NMR (400 MHZ, DMSO) 6 12.59 (s, 1H), 7.98 - 7.66 (m, 2H), 7.09 — 6.81 (m, 2H), 4.66 (d, J = 9.3 Hz, 1H), 3.77 (d, J = 7.9 Hz, 2H), 1.30 - 1.00 (s, 6H).

Preparation of 3—(Hydr0xymethyl)—4-isopropoxy-benzoic acid OH O 4..EG/MOH ] Step 1 : ] To a mixture of methyl 3-formyl—4-hydroxy—benzoate (10.0 g, 55.5 mmol), potassium carbonate (30.7 g, 222.0 mmol) and NN—dimethylformamide (62.5 mL) was added 2—iodopropane (18.9 g, 11.1 mL, 111.0 mmol) and the reaction mixture -178— WO 25613 was heated at 60 °C for 18 hours. The reaction mixture was filtered, the filtrate was concentrated in vacuo to give a residue which was dissolved in ethyl e (150 mL) and washed sequentially with water (3 x 75 mL) and brine solution (1 x 75 mL). The layers were separated and the organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to yield methyl 3-formylisopropoxy—benzoate (12.2 g, 99 %) as a yellow viscous liquid. ESI-MS m/z calc. 222.2, found 223.3 (M+1)+; Retention time: 1.51 minutes ( 3 min run). 1H NMR (400 MHz, DMSO) 8 10.35 (s, 1H), 8.23 (d, J = 2.3 Hz,1H), 8.17 (dd, J = 8.8, 2.3 Hz, 1H), 7.39 (d, J = 8.9 Hz, 1H), 4.98 — 4.83 (m, 1H), 3.85 (s, 3H), 1.38 (d, J = 6.0 Hz, 6H).

[00567] Step 2 : Methyl 3-formyl—4-isopropoxy—benzoate (180 mg, 0.8 mmol) was dissolved in tetrahydrofuran (5 mL) and lithium borohydride (35 mg, 1.6 mmol) was added. The reaction mixture was stirred at room temperature for 30 minutes, then quenched with methanol (3 mL). The reaction mixture was neutralized by the addition of a saturated aqueous solution of sodium bicarbonate (3 mL) and extracted with ethyl acetate (3 x 10 mL). The organic layers were washed with brine on (1 x 10 mL), dried over sodium sulfate, filtered and concentrated in vacuo to yield methyl 3- (hydroxymethyl)isopropoxy—benzoate (180 mg, 99 %) as a viscous liquid. ESI-MS m/z calc. 224.3, found 225.3 (M+l)+; Retention time: 1.26 minutes ( 3 min run); 1H NMR (400 MHz, DMSO) 8 8.09 (s, 1H), 7.89 (d, J = 8.6 Hz, 1H), 7.13 (d, J = 8.6 Hz, 1H), 5.25 (t, J = 5.6 Hz, 1H), 4.86 — 4.68 (m, 1H), 4.54 (d, J = 5.6 Hz, 2H), 3.87 (s, 3H), 1.35 (d, J = 6.0 Hz, 6H).

Step 3 : To methyl 3-(hydroxymethyl)-4—isopropoxy—benzoate (180 mg, 0.8 mmol) in dioxane (2 mL) was added sodium ide (2.1 mL of 1 M, 2.1 mmol) and the reaction mixture was heated at 80 °C for 50 minutes. The solvent was evaporated under reduced pressure. The residue was dissolved in water (10 mL) and washed with ethyl acetate (3 x 10 mL). The layers were separated and s layer was acidified with hloric acid. The aqueous layer was extracted with ethyl aceatate (3 x 10 mL). The organic layer was separated, dried over sodium sulfate, d and concentrated in vacuo to yield 3-(hydroxymethyl)-4—isopropoxy—benzoic acid (150 mg, —l79— 2012/028882 89 %) as a white solid. ESI—MS m/z calc. 210.2, found 211.3 (M-t1)+; Retention time: 1.01 minutes ( 3 min run).

Preparation of 3-Methoxy—4-(2-methoxy-1,1-dimethyl0xo— ethyl)benzoic acid Step 1 : ] To MgSO4 (4.8 g, 1.8 mL, 40 mmol) in DCM (40 mL) was added HZSO4 (1.0 g, 533 uL, 10 mmol) at 0 OC and the reaction mixture was allowed to stir for 30 minutes. 4-Bromomethoxy-benzoic acid (2.3 g, 10 mmol) was added followed by 2-methylpropanol (3.7 g, 4.8 mL, 50 mmol). The reaction mixture was d to stir at room temperature for 16 hours. MgSO4 was removed by ion and 1N NaOH solution was added until pH 9, was achieved. The layers were separated and the organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to yield tert—butyl 4-bromomethoxy—benzoate (0.4 g, 14 %).

[00574] Step 2 : To difluorozinc (36 mg, 0.35 mmol) and Pd (tBU3P)2 (7 mg, 0.01 mmol) under an atmosphere of nitrogen was added tert—butyl 4—bromomethoxy— benzoate (200 mg, 0.69 mmol) dissolved in DMF (2.5 mL), followed by (lumethoxy methyl-prop-l-enoxy)-trimethylsilane (182 mg, 1.05 mmol). The reaction mixture was heated at 80°C for 16 hours. The reaction mixture was cooled, filtered and partitioned n EtOAc and brine solution. The organics were separated, dried over sodium sulfate and concentrated in vacuo. The resulting residue was dissolved in DCM (1 mL) and d with TFA (794 mg, 537 uL, 6.97 mmol). The reaction mixture was allowed to stir for 2 hours and the solvent was concentrated in vacuo, the e was dissolved in DMF, filtered and purified by HPLC using MeOHszO mixture (1 -99%) with HCl modifier (5 mM) to give 3-methoxy—4-(2-methoxy~1,1-dimethy1oxo-ethyl)benzoic acid (55 mg, 31 %). ESl-MS m/z calc. 252.0, found 253.2 (M+1)+; Retention time: 2.46 minutes ( 3 min run).

Preparation of 4-ethoxy-3—methylbenzoic acid HojflO\/ Step 1 : To a on of oxy—3-methyl-benzoic acid (1.00 g, 6.57 mmol) in NN—dimethylformamide (10 mL) was added potassium carbonate (2.73 g, 19.7 mmol) and bromoethane (3 .58 g, 2.44 mL, 32.9 mmol). The reaction mixture heated at 45 0C for 48 h in a sealed tube. The reaction mixture allowed to cool then d with water and ether. The ether layer was washed with 50% saturated NaHC03 (50 mL) and brine (50 mL), dried over Na2804, and concentrated in vacuo to provide ethyl 4- ethoxy—3-methy1benzoate as an -colored oil. The crude product was taken directly to the next step. EST-MS m/z calc. 208.10994, found 209.3 r ; Retention time: 1.78 minutes (3 min run).

Step 2 : The crude ethyl 4-ethoxy—3--methy1-benzoate was suspended in a solution of NaOH. (10.5 g, 263 mmol) in water (50 mL) and methanol (25 mL). The reaction mixture was refluxed for 1 h. The reaction mixture was cooled to 0 °C, acidified with 12 M HCl (24.7 mL, 296 mmol) and the resulting solid filtered. The solid was slurried with acetonitrile and filtered to e 4-ethoxy-3—methyl-benzoic acid (760 mg, 4.22 mmol, 64%) as a light pink solid. EST-MS m/z calc. 180.07864, found 181.3 (M+1)+; Retention time: 1.31 minutes (3 min run). 1H NMR (400 MHz, DMSO-d6)512.50(3, 1H), 7.77 (dd, J = 8.5, 2.2 Hz, 1H), 7.73 (d, J = 1.5 Hz, 1H), 7.00 (d, J = 8.6 Hz, 1H), 4.11 (q, J = 7.0 Hz, 2H), 2.17 (s, 3H), 1.36 (t, J = 7.0 Hz, 3H).

Preparation of 3-methyl—4-propoxybenzoic acid .OYCLO\/\

[00582] Step 1 : To a solution of 4-hydroxy—3-methy1-benzoic acid (3.00 g, 19.7 mmol) -181— in NN—dimethylformamide (30 mL) was added and 1-iodopropane (16.8 g, 9.62 mL, 98.6 mmol). The reaction e was stirred at 60 °C for 3 h. The reaction mixture was allowed to cool then diluted with water and ether. The ether layer was washed with water (50 mL) and brine (50 mL), dried over , and trated. Silica gel chromatography (5-30% ethyl acetate/hexane) ed propyl 3-methy1 propoxybenzoate as an orange—colored oil that was taken directly to the next step.

Step 2 : The crude propyl 3—methylpropoxybenzoate was dissolved in methanol (25 mL) and water (50 mL) and treated with solid sodium hydroxide (31.6 g, 789 mmol). The reaction mixture was refluxed for 1 h. The reaction mixture cooled to 0 °C and ed with 12 M HCl (74 mL, 890 mmol). The resulting solid filtered to provide 3«methylpropoxy—benzoic acid (3.22 g, 16.6 mmol, 84%) as a light pink solid. ESI-MS m/z calc. 194.0943, found 195.3 r ; Retention time: 1.41 minutes (3 min run). 1H NMR (400 MHz, DMSO—d6) 5 12.50 (s, 1H), 7.77 (dd, J ——= 8.5, 2.2 Hz, 1H), 7.73 (d, J = 1.4 Hz, 1H), 6.99 (d, J = 8.6 Hz, 1H), 4.01 (t, J = 6.4 Hz, 2H), 2.18 (s, 3H), 1.82 — 1.69 (m, 2H), 1.01 (t, J = 7.4 Hz, 3H).

] Preparation of 4-(1-hydr0xycyclobutyl)methylbenz0ic acid To a solution of 4-bromo—3 -methy1-benzoic acid (2.95 g, 13.7 mmol) in tetrahydrofuran (53 mL) at -78 °C was added n-butyllithium (17.6 mL of 1.6 M in hexanes, 28 mmol) dropwise while maintaining the internal temperature below -65°C resulting in a thin, light yellow slurry. The mixture was stirred at -78°C for 30 min.

Cyclobutanone (962 mg, 1.03 mL, 13.7 mmol) was added dropwise to the above slurry while maintaining the internal temperature below —65°C. The mixture was stirred at - 78°C for 10 min, warmed to room temperature and stirred for 2 h. The reaction mixture was quenched with saturated NH4C1 (50 mL) and 1N HCl (25 mL) then extracted with ethyl acetate (3 X 100 mL). The combined organics were dried over Na2S04, filtered and concentrated in vacuo. Silica gel chromatography (0—10% —182— methanol/dichloromethane) provided the product as an off-white solid. The solid was slurried with hexanes, filtered, and dried to provide 4-(1-hydroxycyclobutyl)—3—methyl- benzoic acid (1.30 g, 6.30 mmol, 46%) as a white solid. ESI-MS m/z calc. 189.09155, found 189.5 (M-OH)Jr ; Retention time: 1.0 minute (3 min run). 1H NMR (400 MHz, DMSO-dg) 8 12.76 (s, 1H), 7.77 — 7.66 (m, 2H), 7.36 (d, J: 7.8 Hz, 1H), 5.38 (s, 1H), 2.56 — 2.51 (m, 2H), 2.38 (s, 3H), 2.32 - 2.23 (m, 2H), 2.06 -— 1.90 (m, 1H), 1.61 — 1.51 (m, 1H). ation of 4-(1-hydr0xycyclopentyl)-3—methylbenzoic acid

[00589] 4-Bromomethyl-benzoic acid (4.00 g, 18.6 mmol) was dissolved in tetrahydrofuran (80 mL) and the solution was cooled to -78 0C. n-Butyllithium (16.4 mL of 2.5 M in hexanes, 40.9 mmol) was added dropwise over 20 min while maintaining the internal ature below -65 °C resulting in a thin, light yellow slurry. The reaction mixture was allowed to stir for 30 min at —78 0C. Cyclopentanone (1.57 g, 1.65 mL, 18.6 mmol) was then added in a dropwise manner. The mixture was d at -78 °C for 30 min, warmed to room temperature and stirred for 2 h. The on mixture was then diluted with 1 M NaOH (100 mL) and washed with diethyl ether. The organic layer was discarded and the aqueous layer was acidified with 4 M HCl to <pH 3. The aqueous layer was extracted with ethyl acetate (3 X 50 mL). The combined extracts were dried over NaZSO4 and concentrated in vacuo. The crude product was filtered through silica gel eluting with 0-1 0% methanol/dichloromethane, and all product containing fraction concentrated in vacuo. The resulting solid was slurried in romethane and d to provide 4-(1-hydroxycyclopentyl) methylbenzoic acid (1.10 g, 26%) as a White solid. ESI-MS m/Z calc. 220.10994, found 221.5 (M+1)+ ; ion time: 1.16 minutes (3 min run). 1H NMR (400 MHz, DMSO-dg) 8 12.74 (s, 1H), 7.70 (d, J = 1.4 Hz, 1H), 7.67 (dd, J = 8.1, 1.7 Hz, 1H), 7.51 (d, J = 8.2 Hz, 1H), 4.77 (s, 1H), 2.54 (s, 3H), 2.07 - 1.98 (m, 2H), 1.98 - 1.89 (m, 2H), 1.87 - 1.77 (m, 2H), 1.72 - 1.59 (m, 2H).

] Preparation of 3-fluoro—4-(1-hydroxycyclopentyl)benzoic acid 4-Bromofluoro-benzoic acid (3.00 g, 13.7 mmol) was dissolved in tetrahydrofuran (60 mL) and the solution was cooled to -78 0C. n—Butyllithium (18.8 mL of 1.6 M in hexanes, 30 mmol) was added dropwise over 20 min while maintaining the internal temperature under -70 °C. The reaction mixture was allowed to stir for 30 min at -78 °C and then cyclopentanone (1.21 mL, 13.7 mmol) was added in a dropwise while maintaining the al temperature below -70 °C. The mixture was stirred at - 78 °C for 30 min the allowed to warm to room temperature. The reaction mixture was diluted with saturated NH4Cl (50 mL) and 1 M HCl (25 mL) and extracted with dichloromethane (3 X 50 mL). The combined extracts were dried over NaZSO4 and concentrated in vacuo. Silica gel chromatography (0—5% methanol/dichloromethane) provided 3-fluoro(1-hydroxycyclopentyl)benzoic acid (400 mg, 13%) as a white solid. ESI-MS m/z calc. 224.1, found 225.3 (MH)+ ; ion time: 1.16 minutes (3 min run). 1H NMR (400 MHZ, DMSO-d6) 5 13.12 (s, 1H), 7.80 - 7.70 (m, 2H), 7.60 - 7.51 (m, 1H), 5.13 (s, 1H), 2.08 - 1.95 (m, 2H),1.95 - 1.81 (m, 4H), 1.81 — 1.67 (m, 2H).

Preparation of 4-(1-hydroxycyclopentyl)benzoic acid

[00593] A on of 4-bromobenzoic acid (4.02 g, 20.0 mmol) in tetrahydrofuran (100 mL) was purged with argon for 5 min. llithium (16.0 mL of 2.5 M in hexanes, 40 mmol) was added se at —78 °C, resulting in a yellow thick syrup. The mixture was stirred at -78 0C for 30 min. Cyclopentanone (3.89 mL, 44.0 mmol) was added dropwise. The reaction was quenched immediately with saturated NH4C1 and allowed to warm to room temperature. The mixture was acidified ~184- with 1 N HCl to pH ~3 and extracted with ethyl e (3 X 50 mL). The combined organic layers were washed with brine, dried over MgSO4 and concentrated in 'vacuo.

The solid residue was suspended in hexanes, filtered, and the solid washed with additional hexanes. The solid was re-suspended in dichloromethane followed by hexanes. The resulting precipitate was filtered, washed with hexane and air dried to yield 4-(1-hydroxycyclopentyl)benzoic acid (1.25 g, 30%) as a white solid. 1H NMR (400 MHz, DMSO-d6) 5 12.78 (s, 1H), 7.88 (d, J: 8.5 Hz, 2H), 7.58 (d, J: 8.5 Hz, 2H), 4.93 (s, 1H), 1.93 — 1.71 (m, 8H).

Preparation of 4-(1-hydr0xycyclohexyl)benzoic acid 0 To a solution of 4-br0mobenzoic acid (3.00 g, 14.9 mmol) in tetrahydrofuran (54 mL) at —78 0C was added n-butyllithium (19.1 mL of 1.6 M in hexanes, 30.6 mmol) dropwise while maintaing the internal temperature below -65 °C.

The mixture was stirred at —78 0C for 30 min. Cyclohexanone (1.55 mL, 14.9 mmol) was added dropwise while maintaining the reaction temperature below -65 °C. The e was d at —78 0C for 10 min then allowed to warm to room temperature and stirred for 2 h. The reaction e was quenched with saturated NH4Cl (50 mL) and 1N HCl (25 mL). The mixture was extracted with ethyl e (3 X 100 mL). The ed organics were dried over Na2804, filtered and concentrated in vacuo. The residue was stirred with 1:1 dichloromethane/hexane (20 mL) to provide a white solid, which was d and discarded. The filtrate was concentrated in vacuo and purified by silica gel chromatography (0-5% methanol/dichloromethane) to provide an off— white solid. The solid was stirred with hexane, filtered, and dried to e 4-(1- hydroxycyclohexyl)benzoic acid (375 mg, 11%). ESI-MS m/z calc. 220.1, found 221.3 (M+1)+ ; Retention time: 1.18 minutes (3 min run). 1H NMR (400 MHZ, DMSO—dg) 5 12.77 (s, 1H), 7.88 (d, J = 8.3 Hz, 2H), 7.60 (d, J = 8.5 Hz, 2H), 4.84 (s, 1H), 1.81 - 1.46 (m, 9H), 1.35 — 1.17 (m, 1H). —185— WO 25613 Preparation of 4-(3-hydr0xypentanyl)methylbenzoic acid ] 4-Bromo-3—mcthyl—benzoic acid (3.00 g, 14.0 mmol) was dissolved in tetrahydrofuran (60 mL) and cooled to -78 °C. n-Butyllithium (19.2 mL of 1.6 M in hexanes, 31 mmol) was added dropwise over 20 min while maintaining the internal temperature below -70 0C, resulting in the ion of a yellow precipitate. The mixture was stirred for 30 min at -78 0C. Pentanone (1.48 mL, 14.0 mmol) was added dropwise while ining the internal temperature below -70 0C. The reaction mixture was allowed to stir for 30 min at -78 °C then allowed to warm to room temperature. The reaction mixture was quenched with saturated NH4Cl (50 mL), stirred for 10 min, then further diluted with l N HCl until pH <3. The mixture was then extracted with ethyl acetate (3 X 100 mL). The combined extracts were dried over NaZSO4 and trated in vacuo. Silica gel chromatography (0—5% methanel/dichloromethane) provided the product as an off-white solid, which was slurried in 1:1 dichloromethane/hexanes and filtered to provide 4-(1-ethylhydroxy— propyl)—3-methyl-benzoic acid (1.56 g, 50%) as a white solid. ESI-MS m/z calc. 222.1, found 223.3 (M+1)Jr ; ion time: 1.22 minutes (3 min run). 1H NMR (400 MHz, DMSO—d6) 8 12.70 (s, 1H), 7.71 = 8.1 Hz, 1H), 4.59 (s, 1H), - 7.64 (m, 2H), 7.58 (d, J 2.47 (s, 3H), 2.02 = 7.4 Hz, 6H). - 1.87 (m, 2H), 1.81 - 1.66 (m, 2H), 0.64 (t, J

[00598] Preparation of 4-(3-hydroxypentan—3-yl)benzoic acid Step 1 : To a solution of methyl 4—sulfanylbenzoate (2.00 g, 11.9 mmol) in N,N-dimethylformamide (13 mL) was added potassium carbonate (6.57 g, 47.6 mmol) and 1-br0m0chloro—propane (2.35 mL, 23.8 mmol). The mixture was heated at 60 -186— 0C for 16 h. The on mixture was filtered and the solvent removed in vacuo. The material was dissolved in dichloromethane (10 mL) and washed with water (3 X 10 mL) and a saturated aqueous NH4C1 (10 mL). The organic layer was dried over Na2804, d and the t removed in vacuo. Silica gel chromatography (0- 100% dichloromethane/hexane) provided methyl 4-(3-chloropropylsulfanyl)benzoate (1.87 g, 64%) as a ess viscous liquid. ESI-MS m/z calc. 244.0, found 245.1 (M+1)+; Retention time: 1.83 minutes (3 min run). 1H NMR (400 MHz, DMSO-d6) 5 7.88 (d, J = 8.5 Hz, 2H), 7.43 (d, J = 8.2 Hz, 2H), 3.84 (s, 3H), 3.79 — 3.61 (m, 2H), 3.18 (t, J = 7.2 Hz, 2H), 2.20 — 1.97 (m, 2H).

[00601] Step 2 : Methyl 4-(3-chloropropylsulfanyl)benzoate (1.84 g, 7.52 mmol) was dissolved in methanol (46 mL), followed by the addition of water (4.6 mL) and Oxone (4.62 g, 7.52 mmol). The reaction mixture was stirred at room temperature for 14 h.

The reaction e was filtered and the t removed in vacuo. The resulting solid was dissolved in dichloromethane and washed with water (2 X 10 mL). The organic layer was dried over , filtered and the t removed in vacuo to yield methyl 4-(3-chloropropylsulfonyl)benzoate (1.89 g, 9.1%) as a viscous liquid. ESI-MS m/z calc. 276.0, found 277.1 (M+1)+; Retention time: 1.36 minutes (3 min run). 1H NMR (400 MHz, DMSO—d6) 8 8.21 (d, J = 8.3 Hz, 2H), 8.07 (d, J = 8.3 Hz, 2H), 3.92 (s, 3H), 3.73 — 3.46 (m, 4H), 2.21 — 1.79 (m, 2H).

Step 3 : To a solution of methyl 4-(3~chloropropylsulfonyl)benzoate (1.89 g, 6.83 mmol) in 2—methylpropanol (20 mL) was added potassium tert—butoxide (1.53 g, 13.7 mmol) and the slurry heated at 80 °C for 10 min. Additional 2—methylpropan- 2-01 (20 mL) was added to facilitate stirring and the heating continued for 25 min. The on mixture was diluted with water (100 mL) and washed with ethyl acetate (3 X 100 mL). The aqueous layer was acidified with 1N HCl and extracted with ethyl acetate (3 X 100 mL). The combined organics were dried over NaZSO4, filtered and the solvent removed in Vacuo to provide 4—cyclopropylsulfonylbenzoic acid (1.22 g, 79%) as a beige solid. ESl-MS m/z calc. 2260, found 227.3 (M+1)+; Retention time: 0.86 minutes (3 min run).

Preparation of (4-isopr0poxy—3-methyl-phenyl)—[10-phenyl—8— (2,2,2-trifluoroethyl)—11-0xa-3,8-diazaspir0[5.5]undecanyl]methanone ;(FF dob. 0 ] To l0-phenyl(2,2,2-trifluor0ethyl)-1 l-oxa—3,8— piro[5.5]undecane (hydrochloride salt) (150 mg, 0.39 mmol) and 4-isopropoxy— 3-methyl-benzoic acid (75 mg, 0.39 mmol) in DMF (1 mL) was added at room temperature O-(7-azabenzotriazol-l —yl)-N,N,N',N'—tetramethyluronium hexafluorophosphate ( 162 mg, 0.43 mmol) and diisopropylethylamine (337 uL, 1.94 mmol) and reaction mixture was stirred at room temperature for 30 minutes. The reaction was diluted with ethyl acetate and washed with 1M NaOH and then brine solution. The organic layer was separated, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography using 10-60% EtOAc/hexane to give the desired compound as a white foam (147 mg, 73 %) ESI-MS m/z calc. 490.2, found 491.4 (M+l)+; Retention time: 2.42 minutes (3 min run).

] The following nds were made using Method A as described above: Names Acid names Amine Names (3 -chloro—4-isopropoxy— pheny1)-[10-phenyl lO—phenyl-S—(2,2,2- (2,2,2-trifluoroethyl)—1 1— 3 -chloroisopropoxy— trifluoroethyl)-l 1 —oxa- oxa—3,8~ benzoic acid 3 ,8— diazaspiro[5 . 5 ]undecan- diazaspiro[5 eeane 3-yl]methanone (4-isopr0poxy—3—methy1- pheny1)-[10-phcny1 10-pheny1(2,2,2— (2,2,2-triflu0rocthy1)-1 1- 4-is0propoxy—3-methy1- trifluorocthyl)-1 1-0xa— oxa-3,8- benzoic acid 3,8— diazaspiro [ 5 .5]undecan- diazaspir0[5.5]undecane 3—yl]mcthanonc (3 -flu0rois0prop0xy— phcny1)-[ 1 y1 10-pheny1—8—(2,2,2— (2,2,2—triflu0rocthy1)—l 14-is0prop0xy— trifluoroethyl)-1 1 -oxa- oxa—3,8— c acid 3 ,8— diazaspiro[5.5]undccan- diazaspiro[5.5]undccane 3 -y1]methanone [4-(2—methoxymethy1- y)pheny1]—[10- -phcny1-8—(2,2,2- phenyl-S-(2,2,2— 4-(2—methoxy~2—mcthy1— trifluoroethy1)-1 l—oxa— trifluoroethyl)- 1 1-0xa— propoxy)bcnzoic acid 3,8- 3 ,8- diazaspiro[5.5]undecane diazaspiro [ 5 . 5]undecan— 3-yl]mcthanone (4-isopropoxy-3 - methoxy-phcny1)—[ 1 0- —pheny1—8—(2,2,2— phenyl—8—(2,2,2- 4-isoprop0xy-3—methoxy— trifluoroethyl)oxatrifluoroethy1 )—1 1 -oxa— benzoic acid 3,8- 3 ,8- diazaspir0[5 ecane diazaspiro [ 5 . 5]undccan— 3-y1]methan0ne (5-isopr0poxy-6—methyl- -phenyl-8—(2,2,2- 2-pyridy1)-[ 1 0—pheny1-8— 5—isopr0p0xy-6~methy1- trifluoroethyl)-1 1 —oxa— (2,2,2-trifluoroethy1)—1 1- pyridine-Z—carboxylic 3 ,8- oxa-3 ,8- acid diazaspiro[5 . 5]undccanc diazaspiro[5.5]undecan- 2012/028882 3-y1]methan0ne isobutylsulfonylpheny1)- -pheny1~8-(2,2,2- [10-pheny1—8-(2,2,2- 4-isobuty1sulfonylbcnzoic trifluoroethyl)- 1 1 -0xatrifluoroethyl )—1 1 -oxa— acid 3,8- 3,8- diazaspiro[5.5]undecane pir0[5.5]undecan— 3-y1]methan0ne [4-(2-hydr0xy—2-methyl— propoxy)methy1- -pheny1-8~(2,2,2- pheny1]—[1 0—phenyl 4-(2-hydroxy—2—methy1- trifluoroethyl)-1 1-0xa— (2,2,2-trifluoroethy1)-1 1- propoxy)—3-methy1- 3 ,8- oxa-3,8- benzoic acid diazaspiro[5 . 5]undecane diazaspir0[5 . 5]undecan- 3-y1]methan0ne (4-isopropylsulfony1—3- methyl-pheny1)-[10- -pheny1-8—(2,2,2- phenyl-S-(2,2,2— 4—isopropylsulfony1 roethyl)- 1 1 -0xa— trifluoroethyl)- 1 1 -0xa— methyl-benzoic acid 3,8- 3 ,8- diazaspiro[5.5]undecane diazaspiro[5.5]undecany1]methanone (3 -methylmorph01in0- phenyl)-[10—pheny1-8— 10-pheny1—8—(2,2,2- (2,2,2-triflu0roethy1)-1 1- y1m0rpholino- trifluoroethy1)-1 1—0xa— oxa-3,8- benzoic acid 3,8- diazaspiro[5.5]undecan- diazaspiro [5.5]undecane 3-y1]methanone ~190— 2012/028882 (5-isopropoxy—2-pyridy1)- [lO-pheny1—8 —(2,2,2- 10-phcny1(2,2,2- trifluoroethyl)—1 1 -0xa— 5-isopropoxypyridine roethyl)-1 1-oxa- 3,8- carboxylic acid 3 ,8- diazaspir0[5 . 5]undccan- diazaspiro[5.5]undecane 3-y1]methanone (2-fluoroisopr0p0xy— pheny1)—[1 O-pheny1 10-pheny1-8—(2,2,2- -triflu0roethy1)-1 1— 2-flu0r0isopr0poxy- trifluoroethyl)-1 1-oxa— oxa-3,8- benzoic acid 3,8- pir0[5 .5]undecan- diazaspir0[5.5]undecane 3-y1]methan0ne [3—methy1—4-(oxetan-3 - yloxy)pheny1]—[10- -phcny1(2,2,2— pheny1(2,2,2- 3-methy1(oxetan-3— roethyl)-1 l-oxa- trifluoroethyl)-1 1 -0xa— yloxy)benzoic acid 3 ,8- 3,8- diazaspiro[5.5]undccane diazaspir0[5 . 5]undecan- 3-y1]methan0ne [3-meth0xy—4-(2- methoxyethoxy)pheny1] - —pheny1(2,2,2- [10-pheny1—8-(2,2,2- 3-methoxy(2- trifluoroethyl)-1 1 -oxa— trifluoroethyl)—1 1 -0xa- methoxyethoxy)benzoic 3 ,8- 3 ,8- acid diazaspir0[5.5]undecane diazaspiro[5 . can- 3-y1]methan0ne [3-(hydr0xymcthy1)-4_ -pheny1—8—(2,2,2- iSOPmpoxy-phenyl]-[10. 3—(hydroxymethy1) trifluoroethyl)-1 1-oxa— phenyl-S-(2,2,2- isopropoxy—benzoic acid 3,8— trifluoroethyl)— 1 1 -0xa— diazaspiro[5.5]undecane 3 ,8- -191— diazaspir0[5.5]undecan- 3-y1]mcthanone (4-isopr0p0xypheny1)~ [10-pheny1-8—(2,2,2- . -pheny1-8—(2,2,2- trifluoroethyl)-1 l-oxa- trifluoroethyl)-1 1 -oxa- r0p0xybenzoic ac1d_ 3 8 3,8— diazaspiro[5.5]undecan- diazaspir0[5 .5]undecane 3-yl]methan0ne (4—ethylsulfony1-3 - methyl-pheny1)-[10- -pheny1—8-(2,2,2— pheny1~8-(2,2,2- 4-ethylsu1fony1-3 -methy1— trifluoroethyl)—1 1 -oxa— trifluoroethy1)-1 1—oxa- benzoic acid 3 ,8- 3,8— diazaspiro[5.5]undecane diazaspiro[5.5]undecan- 3-y1]mcthanone (4-tert- ulfonylphenyl)-[ 1 0- —pheny1(2,2,2— pheny1-8—(2,2,2- 4-tert- trifluoroethyl)-1 l—oxa- trifluoroethyl)- 1 l-oxa- butylsulfonylbenzoic acid 3 ,8- 3,8— piro[5.5]undecanc diazaspiro[5 . 5 ]undecan— 3-y1]methanone [4-(1 -hydroxy-1—methyl— ethy1)-3 -methy1-pheny1]— -pheny1(2,2,2— [10—pheny1—8—(2,2,2— ydr0xy-1—methy1— roethyl)-1 1-oxa- trifluorocthyl)—1 1 -0xa— ethy1)methy1-benzoic 3,8- 3,8- acid diazaspiro[5.5]undecane diazaspiro[5 . 5]undecan— 3-y1]methanonc t-butoxy-3 - methoxy—phenyl)-[ 1 0— —pheny1(2,2,2- -S—(2,2,2— 4-tert—but0xy—3-meth0xy— trifluoroethyl)-1 l—oxa- trifluoroethyl)-1 1 -0xa— benzoic acid 3,8— 3 ,8- diazaspir0[5.5]undecane diazaspir0[5 . can- 3-yl]methan0ne (3 -fluor0isopropoxy— -meth0xy-pheny1)—[10- -pheny1—8-(232,2— phenyl-S—(2,2,2— 3 -flu0roisopropoxy—5- trifluoroethyl)-1 1 -oxa— trifluoroethyl)-1 1 -0xa— methoxy—benzoic acid 3,8- 3,8- diazaspir0[5.5]undecane diazaspiro[5 . 5 ]undecan- 3-y1]methan0ne N—cyclopropy1[10- phenyl«8—(2,2,2— trifluoroethyl)—1 1 -0xa-— ny1—8—(2,2,2- 3 ,8- trifluoroethyl)-1 l-oxa- (cyclopropylsulfamoy1)be diazaspiro[5 . 5]undecane- 3 ,8- nzoic acid 3 _ diazaspiro [ 5 . 5 ]undecane carbonyl]benzenesu1fona mide [4-(2-hydr0xy—2-methy1- propy1)phcny1]-[10- nyl(2,2,2— pheny1(2,2,2- 4—(2-hydr0xy—2-methy1— trifluoroethyl)-1 1 -oxa- trifluoroethyl)-1 l—oxapropy1 )benzoic acid 3,8- 3 ,8- diazaspir0[5.5]undecane diazaspiro[5 . 5]undecany1]methan0ne —193- (3 -methy1 sulfonyl-phcny1)- -pheny1—8-(2,2,2- eny1—8—(2,2,2- 3—methy1—4- trifluorocthyl)-1 l-oxatrifluoroethyl )-1 1 -oxa— methylsulfonyl-benzoic 3,8- 3 8 — acid diazaspiro[5.5]undccane diazaspir0[5.5]undccan— 3-y1]methanone [3—methy1—4-(0xctan yl)phcny1]—[10-pheny1 ny1-8—(2,2,2- (2,2,2—trifluoroethy1)-1 1methy1—4-(oxetan tn'fluoroethy1)-1 1-oxa— oxa-3 ,8- y1)benzoic acid 3 ,8- diazaspir0[5 .5]undecan- diazaspiro[5.5]undecane 3-y1]mcthan0ne (2-mcthy1-1,3 - benzoxazol—7—y1)—[1 O- -phcny1—8-(2,2,2— phenyl—S-(2,2,2- 2-methy1-1,3- trifluoroethyl)-1 1-0xa- trifluoroethyl)-1 1-0xa- 'benzoxazolecarboxylic 3,8- 3,8— acid diazaspiro [ 5 .5]undccane diazaspir0[5 . 5]undecan- 3-y1]methanone [4-(1—hydr0xy—1—mcthy1— ethyl)pheny1]—[ 1 0-pheny1- 10-pheny1-8—(2,2,2— 8—(2,2,2—trifluoroethyl)- 4-(1 -hydroxy— 1 -methyl— roethyl)-1 1-0xa- 1 1 -oxa-3 ,8- ethy1)bcnzoic acid 3 ,8- diazaspiro[5.5]undecan- diazaspiro[5 .5]undccane 3~y1]methan0ne [3 -flu0r0( 1 -hydroxy— -pheny1(2,2,2— 1 -methyl-ethyl)pheny1] - 3-flu0r0(1—hydroxy—1 — trifluoroethyl)-1 1-oxa- [l 0-pheny1(2,2,2- -ethy1)benzoic acid 3,8- roethyl)-1 1 -0xa— diazaspiro [5 .5]undccanc 3 8 - -194— WO 25613 diazaspir0[5.5]undecan- 3-y1]methanonc N,N—dicthy1-2—fluoro-4— [10-pheny1é8-(2,2,2- 10-phcny1(2,2,2— roethyl)—1 1 -oxa- 4-(diethylcarbam0y1)-3 - trifluorocthyl)- 1 1 —0xa— 3 ,8- fluoro-bcnzoic acid 3 ,8- diazaspir0[5.5]undecane— diazaspiro[5.5]undecane 3-carbony1]benzamide (5-tert-but0xypyridyl)- [lO—phcnyl-S-(2,2,2- 10-phcny1-8—(2,2,2- trifluoroethyl)-1 1 -oxa- -butoxypyridinc-Z- trifluoroethyl)-1 1 -oxa— 3,8— carboxylic acid 3 ,8- diazaspir0[5 .5]undecan- diazaspir0[5 .5]undccane 3-y1]methan0ne hydr0xy—2-mcthy1— y)pheny1]—[10- -pheny1-8—(2,2,2- phenyl(2,2,2— 4—(2'-hydroxymethy1- trifluorocthyl)-1 1 -oxatrifluoroethyl )- 1 1 -0xa— propoxy)bcnzoic acid 3,8— diazaspir0[5.5]undccanc diazaspiro[5 .5]undecan— 3-y1]methan0nc [3-fluoro-4—(2-hydr0xy— 2-methy1-propy1)pheny1]— -phcny1—8-(2,2,2- [1 0-pheny1(2,2,2- 3 —flu0ro(2-hyd1‘0xy trifluoroethyl)-1 1 -oxa— tn'fluorocthyl)-1 l—oxa- methyl-propyl)benzoic 3,8— acid diazaspiro[5.5]undecane_ diazaspiro[5 .5]undccan- 3-y1]methan0nc -195— WO 25613 2012/028882 methyl 2-[2-mcth0xy-4— eny1(2,2,2- -pheny1(2,2,2— trifluoroethyl)-1 1 -0xa— 3-meth0xy—4—(2—meth0xy— trifluoroethy1)-1 1 -oxa— 3,8- 1,1-dimethy10xo— 3,8- diazaspir0[5.5]undccane- cthy1)bcnzoic acid diazaspiro[5.5]undccanc 3-carbony1]phcnyl] methyl-propanoatc [3-fluoro(3 - yprop—l - -phcny1-8—(2,2,2- yny1)phcny1] -[ 1 0-phcny1— 3-fluor0(3— trifluoroethy1)-1 1 —oxa- 8-(2,2,2-triflu0roethyl)- methoxyprop 3,8- 1 1-0xa-3 ,8- ynyl)benzoic acid diazaspiro[5.5]undccanc diazaspiro[5.5]undecan- 3-y1]methanone (3-ch10r0pheny1)~[10- phenyl-S-(2,2,2- 10-pheny1-8—(2,2,2— trifluorocthyl)-1 l-oxa— trifluorocthy1)-1 1 -oxa— 3-ch10r0benzoic acid 3 ,8- 3 ,8— diazaspir0[5 . 5]undecan- diazaspiro [5 . 5]undccanc 3—y1]mcthan0ne [4-(3 xyoxetan-3 - y1)pheny1]-[10-pheny1 10-pheny1-8—(2,2,2- (2,2,2—t1iflu0roethyl)- 1 1- 4-(3 -hydroxy0xetan-3~ trifluorocthyl)— 1 l-oxa- oxa-3 ,8— y1)benzoic acid 3,8- diazaspiro [ 5 .5]undccan- diazaspir0[5.5]undecanc 3—y1]methanonc (2-mcthy1-4— -pheny1—8—(2,2,2- methylsulfonyl-phcnyl)- 2-methy1 trifluoroethyl)-1 l—oxa— [10-phcny1(2,2,2— methylsulfonyl-bcnzoic 3,8— trifluorocthyl)— 1 1—0xa- acid diazaspiro[5.5]undccanc 3 ,8 - —196- diazaspiro[5.5]undecan- 3-y1]methanone 2-methy1—6-[ 1 0—pheny1 (2,2,2-triflu0roethy1)-1 1- 10—pheny1—8—(2,2,2- -cyan0methy1- 0xa—3 ,8— trifluoroethyl)—1 l—oxa- pyridine-Z—carboxylic diazaspiro[5 . 5]undecane— 3 ,8- acid 3-carbony1]pyridine diazaspiro[5 . 5]undecane carbonitrile (3-methoxy methylsulfonyl—pheny1)- ny1(2,2,2— eny1—8-(2,2,2- 3-meth0xy—4- trifluoroethyl)-1 1-0xa- trifluoroethyl)—1 l—oxa- methylsulfonyl-benzoic 3,8- 3 8 - , acid diazaspir0[5.5]undecane diazaspiro[5.5]undecan- 3-y1]mcthan0ne (3-flu0rometh0xy— pheny1)-[10-pheny1—8— 10-phenyl(2,2,2- (2,2,2—trifluoroethyl)—1 1- 3-flu0r0-5—methoxy- trifluoroethyl)-1 1-0xa— oxa-3 ,8- benzoic acid 3,8- piro[5.5]undecan- diazaspiro[5.5]undecane 3—y1]mcthanone (difluoromethoxy)pheny1 —pheny1-8—(2,2,2— ]—[10—pheny1(2,2,2- 2- trifluoroethyI)—1 l-oxa- trifluoroethyl)—1 l-oxa- (difluoromethoxy)benzoic 3 ,8- 3 8 - acid diazaspiro[5,5]undecane diazaspiro[5 . 5]undecan- 3-yl]methanone [2-(diflu0romcth0xy) fluoro-phenylH 1 0- 1 0-pheny1—8-(2,2,2- pheny1(2,2,2- 2—(diflu0romethoxy) trifluoroethy1)-1 1 -oxa— trifluoroethyl)-1 1-oxa- fluoro-benzoic acid 3 ,8- 3 ,8- diazaspiro[5.5]undccane diazaspiro[5.5]undecan- ethan0ne (3 ,5-dich10r0pheny1)-[ 1 0— pheny1(2,2,2- 10-pheny1—8-(2,2,2— trifluoroethyl)-1 1 -oxa- roethyl)—1 l-oxa- 3,5—dichlorobenzoic acid 3 ,8- 3 ,8- diazaspir0[5.5]undecan— diazaspiro[5.5]undecane 3 than0ne (3—ch10r0isoprop0xy- pheny1)—[8—(2,2— 8—(2,2-diflu0roethy1)-10~ difluoroethy1)-1 O—phenyl- 3—chlor0isopr0poxy— phenyl-l l—oxa-3,8- 1 1-0xa-3,8— benzoic acid diazaspiro[5.5]undecane diazaspir0[5 . 5]undccan- nethanone [8-(2,2-diflu0roethy1)—l 0— phenyl-l 1-0xa—3 ,8- 8-(2,2-diflu0roethy1) diazaSpiro[5 . 5 ]undecan— 3 -flu0r0isopr0p0xy- phenyl-l 1-0xa—3,8— 3—yl]-(3-fluor0 benzoic acid diazaspir0[5 ecane isopropoxy— pheny1)methan0ne [8-(2,2—diflu0roethy1) phenyl-l 1-0xa—3 ,8- -diflu0roethy1) 4—is0propoxy—3-methy1- diazaspir0[5 . 5]undecan- phenyl-l 1-0xa-3 ,8- benzoic acid 3-y1] -(4-isopropoxy—3 - diazaspiro[5.5]undecane methyl— phenyl)methanone [8-(2,2-diflu0roethy1)- 1 0- phenyl-l 1-0xa—3,8— -isoprop0xymethy1- 8—(2,2-diflu0roethy1)—10- piro[5.5]undecan- pyridine-Z-carboxylic phenyl-l l-oxa-3 ,8— 3 -yl]—(5-isopropoxy-6— acid diazaspiro[5.5]undecane methyl pyridyl)mcthanone 2-diflu0roethy1)—10- phenyl-l 1-0xa—3 ,8- 8-(2,2~diflu0roethy1)—1 0- diazaspir0[5 . 5]undecan— 4-isoprop0xymeth0xy- phenyl-l 1-0xa—3 ,8y1] -(4-isopr0p0xy—3 - benzoic acid diazaspiro[5.5]undecane methoxy— pheny1)methanone [8-(2,2—difluorocthy1)—10— phenyl-l 1-0xa—3 ,8- 4-(1-hydroxy—1-methy1- 8-(2,2-diflu0roethy1) diazaspir0[5 . 5]undccan— ethy1)methoxy—benzoic phenyl—l l—oxa-3 ,8y1]—[4-(1-hydr0xy—1- acid diazaspiro[5 .5]undecane methyl-ethy1)-3 -meth0xy— pheny1]methanone 2—diflu0roethy1)- 1 0- phenyl-l 1-0xa-3 ,8- 4-(1 -hyd.r0xy—1 -methy1- 8—(2,2-difluoroethy1) diazaspiro [5 . 5]undecan— ethy1)methy1-benzoic phenyl-l l-oxa-3,8y1]-[4—(1—hydroxy—1- acid diazaspiro[5.5]undecane methyl-ethyl)—3 -methy1- phenyl]methanone [8-(2,2-difluoroethy1)-10— —difluoroethy1)-10— (2-pyridy1)—1 1-0xa—3,8- 4-pyrr01idin— 1 — (2-‘pyridy1)-1 3 ,8— pir0[5 ylsulfonylbenzoic acid . 5]undecan- diazaspiro [ 5 . 5 ]undecane 3 -y1]-(4-pyrr01idin -199— ylsulfonylphenyl} methanone [8-(2,2-diflu0roethy1) phenyl~11~oxa—3 ,8- 8—(2,2-diflu0roethy1)-1 0- diazaspiro[5 . 5] undecan— 4-(1-hydr0xy—1-methy1- phenyl—l 3 ,8- 3-y1]-[4—(1—hydr0xy—1 — ethy1)benzoic acid ' diazaspiro[5.5]undecane methyl- ethyl)pheny1]methan0ne [3 -eth0xy—4- (hydroxymethy1)phenyl] ethoxy-4— 8 —10—phenyl-1 1— (8—ethy1pheny1-1 1- (hydroxymethy1)benzoic 0xa—3 ,8- oxa-3,8- acid diazaspiro[5.5]undecane diazaspir0[5 . 5]undecan— ethanone [8 -(2,2-difluoroethyl) phenyl—l 1-oxa-3 ,8- 8-(2,2-difluoroethy1) 6—methoxypyn'dine diazaspiro[5 . 5]undecan- phenyl-l 3,8— carboxylic acid 3-y1] -(6-meth0xy—2- diazaspiro[5 . 5]undecane pyridyl)methanone [8—(2,2—diflu0roethy1)- 1 0— (2-pyridyl)-1 1—0xa—3,8- diazaspiro[5 . 5]undecan— 8-(2,2—diflu0roethy1)—10— 4-isopropylsu1f0ny1—3y1]-(4- (2—pyridy1)—1 l-oxa-3 ,8- —benzoic acid isopropylsulfonyl diazaspir0[5.5]undecane methyl- pheny1)methanonc [8-(2,2-difluoroethy1) - —difluoroethy1) phenyl-l l-oxa-3,8- (trifluoromethyl)pyridine- phenyl-l 1-0xa-3,8— diazaspir0[5 . 5]undecan— 2-carboxy1ic acid diazaspir0[5.5]undecane 3-y1]-[5— (trifluoromethyl) pyridyl]methanone 6-[8-(2,2—difluoroethy1)- -phcny1—1 1-oxa-3,8— 5-cyano—6-methy1- 8-(2,2—diflu0roethy1)—10- diazaspir0[5.5]undecane- pyridine-Z-carboxylic phenyl—l 1-0xa—3,8— 3-carbony1]-2—methy1- acid pir0[5.5]undecane pyridinecarb0nitrile [8-(2,2-diflu0roethyl) (2-pyridy1)—1 1-0xa—3 ,8- -difluoroethy1) diazaspiro[5 . 5]undecan- 4—isopr0poxy—3 -methy1- (2-pyridy1)—1 1-0xa-3 ,8- 3-y1]—(4-isopropoxy—3- benzoic acid diazaspiro[5 . 5]undecane pheny1)methan0ne [8-(2,2-difluoroethyl)— 1 0- (2-pyridy1)—1 1-0xa-3,8- —diflu0roethy1) diazaspiro[5.5]undccan- 3—flu0roisoprop0xy— (2—pyridy1)—1 1—0xa—3 ,8- 3-y1]—(3-fluor0 benzoic acid diazaspir0[5.5]undecane poxy— pheny1)methan0ne (3 -chloro—4-isoprop0xy- pheny1)-[8-(2,2- 8-(2,2-diflu0roethy1)-10— difluoroethy1)(2- 3-ch10r0isoprop0xy— (2-pyridyl)-1 1-oxa—3 ,8- pyridyl)-1 1-0xa-3,8— benzoic acid diazaspiro[5.5]undecane diazaspir0[5 .5]undecan- 3—yl]methanone [8-(2,2-difluoroethy1)—1 0- (2—pyr1dy1)-1 1-0xa-3 ,8- 8-(2,2—diflu0roethyl)-1 0- r0p0xy—3—meth0Xy- p1ro[5.5]undecan- (2-pyridy1)0xa—3 ,8— benzoic acid 3—y1]—(4-isopr0p0xy—3— diazaspiro[5.5]undecane methoxy— pheny1)methanone [8—(2,2-diflu0roethy1) idy1)-1 1—0xa—3 ,8- 8-(2,2-diflu0roethy1) diazaspiro[5 . 5]undecanflu0r0isopropoxy (2-pyridyl)—1 1-0xa-3,8- 3-yl]-(3-fluor0 methoxy-benzoic acid diazaspiro[5 . 5]undecane isopropoxy-S-methoxy— phenyl)methanone [8-(2,2-diflu0roethy1)—1 0— idy1)-1 l—oxa-3,8- 8-(2,2-difluorocthy1) diazaspiro[5.5]undecanflu0ro(1 -hydr0xy— 1 - (2-pyridy1)-1 1-0xa-3 ,8y1]—[3 -flu0ro(1 — methyl-ethy1)benzoic acid diazaspir0[5.5]undccane hydroxymethyl- ethy1)phenyl]methanone [8-(2,2-diflu0roethy1)—10- (2-pyridyl)-1 1-0xa-3,8- diazaspiro[5 . 5]undecan- 8-(2,2-difluoroethyl) ydroxyethoxy)—3— 3—y1]—[4-(2- (2-pyridy1)-1 1-0xa—3,8- methyl-benzoic acid hydroxyethoxy) diazaspiro[5.5]undecane methyl- ]methan0ne 2—difluoroethy1)—10— (1H-pyrazol~3 -y1)-1 1— 8-(2,2—diflu0roethy1)—10- oxa—3,8— 3-fluor0isopr0p0xy— (1H—pyrazol-3 -y1) diazaspiro[5 . 5]undecan- benzoic acid 0xa-3 ,8- 3-y1]—(3 -flu0ro—4- diazaspiro[5.5]Lmdecane isopropoxypheny1 )methan0ne [8-(2,2-difluoroethy1) (1 -mcthy1pyrazoly1)- 8-(2,2-diflu0roethyl) 1 l-oxa-3,8- 4-isopr0p0xy—3—methy1- (1 -methy1pyrazol—3 -y1)— diazaspiro[5.5]undecan- benzoic acid 1 1—0xa-3 ,8y1]-(4-isopr0poxy diazaspiro[5.5]undecane phenyl )methan0ne [8-(2,2-diflu0roethy1)-1 O- (2-methy1pyrazol-3 —y1)— -diflu0roethy1) 1 1 -oxa-3 ,8— 4—is0pr0poxymcthy1- (2-methylpyrazol-3 -y1)- diazaspir0[5 . 5 ]undecan- benzoic acid 1 1—0xa—3 ,8y1] oprop0xy—3- diazaspiro[5.5]undccane methylphenyl )methan0ne [8-(2,2-diflu0roethy1) (1H-pyrazol-3—y1)-1 1— 8-(2,2—difluoroethyl)-10— oxa—3 ,8- 4-isopr0poxymethy1- (1H-pyrazol—3 -y1)—1 1— diazaspir0[5 . 5 ]undecan— benzoic acid 8- 3 4-isopropoxy diazaspir0[5.5]undecane methyl— pheny1)methan0ne (4-isoprop0xy-3—methy1— pheny1)-[10-(1H-pyrazol- -(1H-pyrazoly1)-8— 3-y1)(2,2,2— 4-is0prop0xy—3-methy1- (2,2,2—trifluoroethy1)—1 1- trifluoroethy1)-1 l—oxa- benzoic acid 0xa—3,8- 3 ,8- diazaspir0[5.5]undecane piro[5 . 5]undecan- 3-y1]methan0ne (3-chlor0-4—isopropoxy- 10-(1H—pyrazol-3 -y1)—8- 3-ch10r0-4—isopr0poxypheny1 )-[10-(1H-pyrazol- (2,2,2-trifluoroethy1)-1 1- benzoic acid 3—y1)—8—(2,2,2- oxa-3,8— ~203- WO 25613 roethyl)-1 l-oxa- diazaspiro[5.5]undecane 3 ,8- diazaspir0[5 . 5]undecan- 3-yl]methanone [8—(2,2-difluoroethy1) (l-ethylpyrazoly )1 8-(2,2-difluoroethy1)—1 O- oxa—3,8- 4-isopr0p0xy-3 -methyl- (1 —ethy1pyrazoly1)-1 1- diazaspir0[5.5]undecan- ‘ benzoic acid 0xa-3,8- 3 1] (4 . —y - -1s0pr0poxy—3— diazaspir0[5.5]undecane methyl- pheny1)methanone [8-(2,2-difluoroethy1) ( 1H-pyrazol—3-Y)1 8-(2,2—difluoroethy1)—10- oxa-3,8— 4-isopr0poxy—3-methoxy- (1H-pyrazoly1)-1 1- pir0[5.5]undecan- benzoic acid oxa-3,8yl] (4- -isopto 0xp y-3— diazaspiro[5.5]undecanc methoxy- pheny1)methan0ne [1 0-(5-tert-butyloxazol— 8-(2,2— difluoroethyl)- 1 1-0xa— 10-(5—tert-buty10xazol 3,8— ' 4-isopropoxymethy1- y1)(2,2—diflu0roethy1)- piro[5.5]undecan- benzoic acid 1 1-0xa—3,8— 3—y1]-(4-isopr0poxy—3 - diazaspiro[5.5]undccane methyl— pheny1)methan0ne [1 0-(5-tert-butyloxazol- -(5-tert-butyloxazol—2- 2-y1)(2,2fluoroisopropoxy— y1)-8—(2,2—diflu0roethy1)- difluoroethy1)-1 1-oxa- benzoic acid 11-oxa—3,8- 3,8- diazaspir0[5.5]undecanc diazaspiro[5.5]undecan- (3 -fluor0 isopropoxy— pheny1)methanone [8-(2,2-diflu0roethy1) (4-fluor0pheny1)-1 1-oxa- 8-(2,2-difluoroethy1)—10- 3 ,8- 4—isopr0p0xy-3 —meth0xy— (4-fluor0pheny1)-1 1 -oxa- diazaspiro[5 . 5]undecan- benzoic acid 3 ,8y1]-(4—is0pr0poxy—3 - diazaspir0[5 . 5]undecane methoxy— phenyl)methanone [8-(2,2-diflu0roethyl) (4-fluoropheny1)-1 l-oxa— 8-(2,2-diflu0roethy1)- 1 0- 3,8- 4—isopr0poxy—3—methy1- (4-flu0ropheny1)—1 1 -oxa— piro[5 . 5]undecan- benzoic acid 3 ,8— 3-yl]—(4-isopr0poxy—3- " , diazaspiro[5.5]undecane methylpheny1 )methan0ne (3 -ch10r0isopropoxy— pheny1)-[8-(2,2— -diflu0roethy1)—1 O- difluoroethy1)-10—(4_ 3 -ch10ro—4-isopropoxy- (4-flu0r0pheny1)-1 l-oxa- fluoropheny1)-1 I-oxa- c acid 3 ,8- 3,8- diazaspiro[5.5]undecane piro[5.5]undecan— 3-y1]methan0ne [8-(2,2—diflu0roethy1) (4—flu0ropheny1)—1 1-oxa- 8-(2,2-difluoroethy1)—1 0- 3 ,8- 3-flu0ro—4-isoprop0xy— (4—flu0ropheny1)-1 1—0xa— diazaspir0[5.5]undecan- benzoic acid 3,8- 3—y1]-(3-fluor0 diazaspiro[5.5]undecane isopropoxy- WO 25613 pheny1)mcthanone [8-(2,2—diflu0roethy1)-10— (4-flu0rophcny1)—1 1-oxa- 8-(2,2-diflu0roethy1)-1 0- 3 ,8- 3—fluoro(1 —hydr0xy-1 - (4—fluor0pheny1)—1 1 -oxa- diazaspiro[5 . 5]undecanmethyl-ethy1 )benzoic acid 3 ,8y1] - [3 —flu0r0(1 - diazaspiro[5.5]undecane hydroxy- 1 l— ethy1)pheny1]mcthanone [8-(2,2-diflu0roethyl) (4-flu0ropheny1)—1 lmoxa- 3 ,8- 8-(2,2-difluoroethy1) 4-(2-hydr0xy-2—methyl- diazaspir0[5 . 5]'undecan- ropheny1)—1 1 -0xa— propoxy)-3~methy1y1] —[4-(2-hydr0xy-2— 3 ,8- benzoic acid —propoxy) diazaspiro[5.5]undecane methyl- phenyl]mcthanonc [8-(2,2-diflu0roethy1) (4-flu0r0phcny1)-1 1 -oxa— -diflu0roethy1) 3,8— 4—isobutylsulfonylbenzoic (4-flu0r0pheny1)-1 1 -oxa— diazaspir0[5.5]undecan- acid 3 ,8— 3-y11-(4- diazaspiro[5.5]undecane isobutylsulfonylphcnyl)- methanone (4-tert- butylsulfonylphenyl)- [8 — 8—(2,2-diflu0roethy1) (2,2—diflu0rocthy1)(4_ 4-tert- (4-fluor0pheny1)—1 1 -oxafluoropheny1 )-1 l-oxa_ butylsulfonylbenzoic acid 3,8- 3 ,8- diazaspir0[5.5]undecane diazflaspiro[5 . 5 ]undccan- —206- 3—y1]methan0ne (4-tert—butoxy—3 - methoxy-phenyl)—[8—(2,2- 8—(2,2—difluoroethy1)—1 0- difluoroethy1)— 1 O-(4- 4-tert-but0xy—3-meth0xy— (4-fluoropheny1)-1 1 -oxa- fluorophenyl)-1 1 -oxa— benzoic acid 3,8- 3 8 — diazaspir0[5.5]undecane diazaspiro[5 . 5]undecan- 3-yl]methan0nc N—cyclopropyl[8—(2,2- difluoroethyl)(4- 8—(2,2-diflu0roethy1) heny1)-1 1 ~0xa- 4- r0pheny1)-1 1 -0xa- 3 ,8— (cyclopropylsulfam0y1)be 3 ,8- diazaspir0[5 . 5]undecane— nzoic acid diazaspiro[5 .5]undecane 3 -carb0ny1]bcnzene- sulfonamide [8-(2,2—diflu0roethy1)—10- r0pheny1)- 1 1 -0xa- 8—(2,2-diflu0roethy1) 3 8 - 4-tetrahydrofuran—3— (4-fluoropheny1)—1 l-oxadiazaspiro [5 . 5]undecan— ylsulfonylbenzoic acid 3,8y1]-(4-tetrahydr0fi1ran- diazaspir0[5 .5]undecane 3 -ylsu1f0nylpheny1)- methanone [8-(2,2—diflu0roethy1) (4-fluor0pheny1)—1 1 -oxa— 8-(2,2—diflu0roethy1)-10— 3 ,8- 3-(hydroxymethy1) r0pheny1)—1 1—oxa- diazaspir0[5 . 5]undecan- isopropoxy—benzoic acid 3 ,8y1] -[3 - diazaspiro[5.5]undecane (hydroxymethy1)-4— isopropoxy- phenyl]methan0ne [8—(2,2—diflu0roethy1)- l 0- (4-fluor0pheny1)—1 1 -oxa- 8-(2,2-diflu0roethy1)-1 0— 3 ,8methy1 (4-fluoropheny1)—1 1 azaspir0 [5.5]undecan- sulfonyl-benzoic 3,8- 3-y1]—(3 -methy1 acid diazaspiro[5.5]undecane methylsulfonyl— pheny1)mcthanone [8-(2,2-diflu0roethy1)— 1 O- (4-fluor0pheny1)-1 1 -oxa— 3,8- 8-(2,2-difluoroethy1)~10— diazaspiro[5 . 5]undecan— 4-(3-hydr0xypr0poxy)—3- r0pheny1)- 1 l-oxa- 3-y1]-[4-(3- methyl-benzoic acid 3 ,8— hydroxypropoxy)-3 - diazaspiro[5.5]undecane methylphenyl ]methan0ne [8-(2,2-diflu0roethyl)-10— (1 -methylpyrazol-3 -y1)- 8-(2,2-diflu0roethy1) 1 1 -oxa-3 ,8flu0r0isopr0poxy- (1 -mcthy1pyrazol-3 -y1)— diazaspiro[5.5]undccan— benzoic acid 1 1 —oxa-3 ,8- 3—y1]-(3-fluoro—4- diazaspir0[5°5]undecane isopropoxy— phenyl)methanone (3-flu0r0—4-isopr0poxy- -(5-methy1-1H- pheny1)-[10-(5-methy1— pyrazoly1)(2,2,2— 1H-pyrazol—3-y1)-8— 3—fluor0—4-isoprop0xy- trifluoroethyl)—11-oxa— —triflu0roethy1)-1 1- benzoic acid 3,8— 0xa-3 ,8- diazaspiro[5 . 5 ane diazaspiro[5.5]undccan- 3-y1]mcthan0ne (4-is0pr0poxy-3—methyl- phenyl)—[ 1 0-(5-methy1- 10-(5-methy1-1H- 1H-pyrazol-3 - pyrazol—3 -y1)(2,2,2- 4-isopr0poxy-3—methy1— (2,2,2—trifluoroethy1)-1 1- trifluoroethyl)— 1 l—oxa- benzoic acid 0xa-3,8— 3,8- diazaspiro[5 . 5]undecan— diazaspir0[5.5]undecane ethanone (3-flu0roisopr0p0xy— pheny1)-[10-(1H-pyrazol- —(1H—pyrazol-3—y1)-8— 3—y1)(2,2,2- 3-flu0r0isopropoxy- (2,2,2-trifluorocthy1)-1 1- trifluoroethyl)- 1 1 -oxa— benzoic acid oxa—3,8— 3,8- diazaspir0[5.5]undecane diazaspir0[5.5]undecan- 3-y1]methanone (8-isobuty1- 1 O-phenyl— 1 l-oxa-3 ,8— 8-isobuty1pheny1-1 1- diazaspiro [ 5 . 5]undecan— 4-isopr0p0xy—3-methy1— oxa-3 ,8- 3—y1)-(4-isoprop0xy—3 - benzoic acid diazaspiro[5.5]undccane methyl— pheny1)methanone y1pheny1—1 1- oxa—3 ,8— 8—ethy1-1 O-phenyl-l 1- 6-isopropoxypyridine—3- piro[5 . 5]undecan- oxa—3,8— carboxylic acid 3 6-isoprop0xy diazaspir0[5 .5]undecane pyridy1)methanone (8—ethy1—10-phcny1-1 1— 4-(1 -hydroxy— 1 -methyl- 1phenyl—1 1- 0xa-3 ,8- cthyl)bcnzoic acid oxa-3,8- diazaspiro[5.5]undecan— 3 -y1)-[4-(1-hydroxy diazaspiro[5.5]undecane methyl- ethy1)pheny1]methanone [4-cthoxy—3- (hydroxymethy1)pheny1] - 4-eth0xy-3 - 8—ethy1- 1 O-phenyl-l 1 - (8-ethy1phcny1—1 1- (hydroxymethy1)bcnzoic oxa-3 ,8- 0xa-3 8 - acid diazaspir0[5.5]undecane diazaspiro[5.5]undccan- 3-y1)methan0nc (8—ethylphcny1-1 1- oxa-3,8- 8-ethy1phcnyl-1 1- diazaspir0[5 . 5]undecan- 4-is0pr0p0xy—3-methy1- oxa-3 ,8y1)—(4—is0pr0p0xy—3 - benzoic acid diazaspir0[5 .5]undccane methyl- phenyl)methanone (8-ethy1phenyl—1 1— oxa-3 ,8- 8-ethy1—10-pheny1—1 1— piro[5 . 5]undccan- 4—isoprop0xymethoxy— 0xa—3 ,8- 3-y1)-(4-isopropoxy—3 - benzoic acid diazaspiro[5.5]undecane methoxy— phenyl)methanonc (8-ethylphenyl-1 1- 1pheny1-1 1- diazaspiro[5 . 5]undccan- 3—fluor0isopr0p0xy- oxa—3 ,8- 3-y1)-(3-flu0r0-4— c acid diazaspiro [ 5 .5]undecane isopropoxy- pheny1)methan0nc y1pheny1-1 1- 8—cthy1-1 O-phcnyl-l 1 - 3-(hydr0xymcthy1) 0xa-3,8- oxa—3,8- isopropoxy-benzoic acid diazaspiro[5.5]undecan- diazaspiro[5.5]undccane -210— 3 -y1)- [3 — xymethyl) isopropoxy— pheny1]methanone N-cyclopropy1(8- ethyl-1 O-phenyl-l 1 -0xa- 4- 8—cthy1-1 0—pheny1—1 1- 3,8- (cyclopropylsulfamoyl)be oxa-3 ,8— diazaspiro[5.5]undecane- _ nzo1c acid diazaspiro[5.5]undecane 3-carbony1)benzene- sulfonamide [8-(2,2-difluoroethy1) 0xazoly1—1 1—0xa—3 ,8— 8-(2,2-diflu0roethy1)—1 0- piro[5 . 5]undecan— 4-isopropoxy—3 -methy1- oxazol—Z-yl—l 1-0xa-3 ,8- 3-y1]-(4-isopr0p0xy benzoic acid diazaspiro[5.5]undecane methyl- phenyl)methanone [8-(2,2—difluoroethy1) (6-methylpyridy1)-1 1- 8-(2,2-diflu0roethyl) oxa—3 ,8flu0r0(1 -hydr0xy- '1 - (6—methylpyridyl)—1 1- diazaspiro[5.5]undecan- methyl-ethyl)benzoic ac1d_ oxa—3 ,8— [3 -fl‘uoro(1 - diazaspiro[5.5]undecane hydroxy—l -methy1— ethy1)pheny1]methan0ne [8—(2,2-difluoroethy1) hy1pyridyl)-1 1- -difluorocthy1) oxa—3 ,8- 4-isopr0poxy—3 -methy1- (6-methy1pyridy1)—1 1- diazaspiro [ 5 . 5 ] undecan- benzoic acid 0xa-3 ,8- 3-y1]-(4-isopr0p0xy diazaspir0[5 . 5]undecane methylpheny1 )methanone —211- (3-ch10rois0pr0p0xy- :pheny1)-[8-(2,2- 8-(2,2-diflu0roethyl)-10— difluoroethyl)(6— 3 —ch10ro—4-isopropoxy- (6—methy1-2—pyridy1)— 1 1— methylpyridy1)— 1 1 - benzoic acid oxa-3 ,8- oxa—3 ,8- diazaspiro[5.5]undecane diazaspiro [5 . 5]undecan- ethan0nc [8-(2,2-diflu0roethy1) (6-methy1-2—pyridy1)—1 1- 8-(2,2-diflu0roethy1) 3-fluoroisopr0p0xy— (6-methy1—2—pyridy1)-1 1 - diazaspiro [ 5 . 5]undecan- benzoic acid oxa—3 ,8- 3 —y1]-(3-fluoro—4- diazaspir0[5.5]undecane poxy— pheny1)methanone [8—(2,2-diflu0roethyl)- 1 0- (6—rncthy1—2-pyridy1)-1 1 - 8—(2,2-difluoroethy1)—10- 0xa-3,8— 4-isopr0p0xy—3 -methoxy— (6-methyl-2—pyridy1)-1 1- diazaspiro [ 5 . 5 ]undecan- benzmc ac1d_ _ oxa—3 ,8y1] -(4-isoprop0xy—3 - diazaspir0[5.5]undecane pheny1)methan0ne [8-(2,2~difluoroethy1)-10— (6-methy1-2—pyridy1)—1 1- 0xa—3 ,8- 8-(2,2-difluoroethy1)-1 0- diazaspir0[5 . 5 ]undecan- 4-isopr0pylsu1fonyl-3 - (6-methy1—2-pyridyl)-1 1— 3—y1]—(4- methyl-benzoic acid oxa—3 ,8- isopropylsulfonyl pir0[5 .5]undecane methyl— phenyl)methanone 2-difluoroethy1)~10— (6-methy1-2—pyridyl)—1 1— 8-(2,2-diflu0roethy1) 0xa-3 ,8flu0roisopr0poxy—5- (6—methy1-2—pyridy1)-1 1- diazaspiro[5 . 5]undecan- methoxy-benzoic acid oxa-3 ,8y1]—(3 -flu0r0 diazaspiro [ 5 .5]undecane isopropoxy—S-methoxy— pheny1)methan0ne 2-[3-[4-(1-hydroxy—1 - methyl-ethy1)benzoyl] - 2-(10—phcny10xa-3 ,8- 4—( 1 —hydr0xymethyl- -pheny1—1 1-0xa—3,8- diazaspir0[5.5]undecan— ethy1)bcnzoic acid diazaspir0[5 . 5]undecan- 8—y1)acet0nitrile cet0nitrile [4-(3-hydroxypr0p0xy)methy1-pheny1]—[10- ny1(2,2,2- phcny1(2,2,2- 4-(3-hydroxypr0poxy) trifluoroethyl)-1 1-0xa— trifluoroethyl)-1 1 —oxa- methyl-benzoic acid 3,8- 3 ,8- diazaspiro[5.5]undecane diazaspiro[5 . 5]undecan- 3—yl]mcthanone 2-[3-(5-isoprop0xy methyl-pyridine-Z- -isopr0poxy—6-Inethy1- 2—(10-phcny1—11—0xa—3 ,8- yl)-10—pheny1-1 1- pyridinecarboxylic pir0[5 . 5]undecan- oxa-3 ,8- acid 8-y1)acetonitrilc diazaspiro [ 5 . 5]undecan- cctonitrilc [4‘(2-hydroxyethoxy)-3 - methyl-phenylH 1 0- 1 0-pheny1-8—(2,2,2- phenyl(2,2,2- 4-(2-hydroxyeth0xy) trifluoroethyl)-1 1 —oxa— trifluoroethyl)-1 1 -0xa- methyl-benzoic acid 3 ,8- 3 ,8- diazaspiro[5.5]undecane diazaspir0[5 5]undecan- -213— 3-y1]methanone 2-[3-[4-(1 -hydr0xy-1 - methyl-ethy1)methoxy- 4-(1 —hydr0xy—1 -methy1— 2-(10—pheny1-1 1-0xa—3,8— benzoy1]-1 0—phenyl-1 1- ethy1)meth0xy—benzoic piro[5.5]undecan- 0xa—3 ,8- acid 8-y1)acctonitrile diazaspiro [ 5 . 5]undecan- 8-y1]acet0nitrile 2-[3-[4-(1-hydroxy~1— methyl-ethy1)—3-methy1- 4-(1 -hydr0xy-1 —methy1— 2—(10-pheny10xa—3 ,8- benzoy1]—10-phenyl—1 1- -3 -methyl—benzoic diazaspiro[5 . 5 ] undecan- oxa—3 ,8- acid 8-y1)acetonitrile diazaspiro[5 . 5 ]undecan- 8-y1]acetonitrile 2-[3-(4—isopropoxy—3— methyl-benzoy1)- 1. 0- 2-(10-pheny1—11-oXa—3,8— 4-isopropoxymethy1- phenyl-l 1-oxa-3,8- diazaspir0[5.5]undecan- benzoic acid diazaspir0[5.5]undecan- 8-y1)acetonitrile 8-y1]acetonitrile 2—[3 opr0p0xy—3 - methoxy—bcnzoy1) 2-(10-phcny1-1 3,8— 4-isopropoxy—3-mcth0xy— phenyl-l 1-oxa—3 ,8— diazaspiro[5.5]undecan- benzoic acid diazaspir0[5 . can- 8-y1)acctonitrile 8-y1]acetonitrile [8-(2,2—diflu0roethyl)- 1 0— (5-isopr0py10xazoly1)- 8—(2,2-diflu0roethyl)-1 0- 1 1 ,8— 4-isopr0poxy-3—methy1— (5-isopr0py10xazol—2-yl)- diazaspiro[5.5]undecan- benzoic acid 1 1-0xa-3 ,8y1] -(4-isopr0pcxy-3— diazaspiro[5.5]undecane methyl- —214- pheny1)methanone [8-ethy1—10-(4- fluoropheny1)-1 1 —oxa- 8-ethy1—10-(4- 3,8- 3-flu0ro—4-isopropoxy— fluoropheny1)-1 1 -0xadiazaspiro [5.5]undecan- benzoic acid 3,8— 3 —y1]-(3 -flu0ro diazaspiro[5.5]undecane isopropoxy— pheny1)methanonc t-buty1(5- methyloxazol—Z-y1)—1 1- 8-tert-buty1-10—(5- oxa-3,8- 4-isopr0p0xy—3-methy1- methyloxazol-Z-y1)—1 1— diazaspir0[5.5]undecan- benzoic acid oxa-3 ,8y1] -(4-isopr0p0xy—3- diazaspir0[5.5]undecane methyl- pheny1)methan0ne [8-tert-buty1—10-(5— 1nethy10xazoly1)—1 1- 8-tert-buty1-1 0-(5- 0xa-3 ,8- 3—flu0r0—4-isopr0p0xy- oxazol-Z-y1)—1 1- diazaspir0[5 .5]undecan- benzoic acid 0xa—3 ,8- —(3-flu0ro-4— diazaspiro[5 . 5 ]undecanc isopropoxy— pheny1)methanone (8-ethy1pheny1-1 1- 0xa-3 ,8- 8-cthy1-9—pheny1—1 1-oxa- pir0[5 . 5]undecan- r0p0xy—3-methy1— 3 ,8- 3-y1)-(4-isoprop0xy—3- benzoic acid diazaspir0[5.5]undecane methyl- pheny1)methanone -215— (8—ethy1—9-pheny1-1 1 — oxa—3 ,8- 8-ethy1-9—pheny1—1 l-oxa— diazaspir0[5.5]undecan- 4-is0propoxymethoxy— 3,8- 3-y1)-(4-is0pr0poxy—3- benzoic acid diazaspiro[5.5]undecane methoxy— phenyl)methanone [8-ethy1(5- methylthiazol-Z-y1)-1 1- 8-ethy1-10—(5— oxa—3 ,8- 4-isop1f0p0xy—3-methyl- methylthiazol-Z-y1)-1 1 - diazaspiro[5 . 5]undecan- benzoic acid 0xa-3 ,8y1] -(4-isopropoxy—3~ pir0[5 .5]undecane methyl— pheny1)methan0ne [8—ethy1(5- methylthiazol—Z-yl)-1 1— 8-ethy1-10—(5- 0xa-3 ,8— r0p0xy—3-meth0xy- methylthiazol-Z-y1)-1 1- diazaspiro[5 . 5]undccan- benzoic acid oxa—3 ,8y1] -(4-isopr0p0xy—3- diazaspiro[5.5]undecane methoxy— pheny1)methan0ne [8-(2,2—difluoroethy1) (5—ethy10xazoly1)-1 1- 8—(2,2-difluoroethy1)—10- 4-isopropoxy-3—methy1- (5-cthyloxazoly1)—1 1- diazaspiro[5 . 5]undecan- benzoic acid oxa—3 ,8- 3—y1]—(4—isopr0p0xy—3- diazaspir0[5.5]undecane methyl- pheny1)methanonc 4-isoprop0xy—3— heny1-1—oxa-4,9- methyl-benzoy1) 4-isoprop0xy—3 - diazaspiro[5.5]undecan— phenyl-l 1-0xa-3 ,8- methylbenzoic acid 4-y1)pr0pan-1 -0ne diazaspiro[5.5]undecan- —216- 8—y1]pr0pan-1—0ne [8-(2,2-difluoroethy1)- 1 O— propy10xazol—2-y1)— 8-(2,2-diflu0rocthy1)— 1 O— 1 1—oxa-3,8- 3-fluor0isopropoxy— (5-is0propyloxazol-2—y1)- diazaspiro[5 . 5 ] undecan- benzoic acid 1 1-0xa—3,8— 3-y1]-(3 —4- diazaspir0[5 . 5]undecane isopropoxy— pheny1)methan0ne (8-ethy1-10,10-dimethy1- 1 1 -oxa-3 ,8- 8-ethy1- 10,1 0—dimethy1- piro[5. 5]undecan- 4-isopropoxy—3-methy1- 11-0xa-3,8- 3-y1)-(4-isoprop0xy—3 - benzoic acid diazaspir0[5 .5]undccane methylpheny1 )methanone (8,9-diethy1oxa—3,8- diazaspir0[5 . 5]undecan- 4-isopr0poxymethy1- 8,9-diethy1—11-0xa—3 ,8— 3 -y1)-(4-isopr0p0xy—3- benzoic acid diazaspiro[5.5]undecane methyl- pheny1)methanonc (4-isopr0poxymethy1- )—[10—(5- 1 0-(5-methylthiazol methylthiazol-Z-yl) y1)—8—(2,2,2- 4-isopr0p0xy—3-methyl- —trifluoroethy1)-1 1— trifluorocthy1)-1 l-oxa- benzoic acid 0xa-3 ,8- 3 ,8- diazaspiro[5 . 5 ]undccan— diazaspiro[5.5]undecane 3-y1]methanone (4-isoprop0xy—3— 10—(5-methy1thiazol 4-isopr0poxy—3-mcth0xy- y—phcny1)-[ 1 0—(5— y1)'8_(27272' benzoic acid methylthiazol-Z—yl)—8— trifluoroethyl)—1 1 -oxa- —217— (2,2,2-triflu0roethyl)- 1 1— 3,8- oxa-3 8 - , diazaspir0[5.5]undecane diazaspiro[5.5]undecan— 3 -y1]methan0ne [8—(2,2—diflu0roethy1)-1 O- (2-fluoropheny1)—1 1 -oxa- -difluoroethy1)-2_ 3,8- 4—isopropoxy—3— (Z-fluoropheny1)-1 -oxa— piro[5 . 5 ]undecan- methylbenzoic acid 4,9— 3—y1]—(3—flu0r0—4- diazaspiro[5.5]undecane isopropoxy- phenyl)methan0ne [8—(2,2—difluoroethy1)-1 O- r0pheny1)-1 1 -oxa- 4-(2,2-diflu0roethy1)-2_ 3,8- 3-fluoro (2-flu0r0phenyl)0xa- diazaspir0[5 . 5]undecan— isopropoxybenzmc a01d. _ 4,9y1]-(4-isopropoxy—3 - diazaspiro[5.5]undecane methyl- phenyl)methanone [8-(2,2-diflu0roethy1)-10— oxazol-Z-yl-l 1-0xa-3,8— 4-(2,2-difluoroethy1)-2_ diazaspir0[5 . 5]undecan4- (oxazol-Z—y1)—1-0xa-4,9- 3—y1]—(3-fluoro isopropoxybenzoic acid diazaspiro [ 5 . 5]undecane isopropoxy— phenyl)methan0ne [8-(2,2-diflu0roethy1)—10— (3 -methy1-2—pyridy1)-1 1 _ 4-(2,2—difluoroethy1)-2_ OX3-3,8— 3-fluor0 (3 1pyridin-2—y1)-1 - diazaspiro[5 . 5]undecan- isopropoxybenzoic acid oxa—4,9— 3—y1]~(3—flu0r0 diazaspir0[5.5]undecane isopropoxy- pheny1)methanone 2—diflu0roethy1)—10- (4—methy1-1H-pyrazol-5 - 4-(2,2-diflu0roethy1) y1)-11—0xa—3,8- 4-isoprop0xy-3 - (4-methy1-1H-pyrazol diazaspiro[5.5]undecan- methylbenzoic acid y1)0xa—4,9y1]-(4-is0pr0p0xy—3— diazaspir0[5 . cane methylpheny1 )methanone [8-(2,2—difluoroethy1)—10— hy1—1H-pyrazol 4-(2,2-difluorocthy1)-2_ y1)-1 1-oxa-3,8— 3-flu0r0 hy1—1H-pyrazol—5- diazaspir0[5.5]undecan- isopropoxybenzoic acid y1)-1—oxa-4,9- 3-y1] -(3 -fluor0 diazaspir0[5.5]undecane isopropoxy- pheny1)methanonc [8-tcrt-buty1—10- (methoxymethy1)—1 1 -oxa— 8-tert—buty1 3 ,8— 4-isopr0p0xy—3-methyl- (methoxymethy1)-1 1- diazaspiro[5.5]undccan- benzoic acid oxa-3,8- 3 —y1] (4 . — -1sopr0p0xy-3 - diazasp1r0[5. .5]undecane methyl- pheny1)mcthan0ne (8-tert-butyl-1 0-ethy1—1 1— 0xa-3,8- 8-tert-buty1—10-ethy1-1 1— diazaspiro[5.5]undccan~ 4-isopr0poxymcthy1Y)(1 - 4-isopr0 oxp y—3 - benzoic acid diazaspir0[5.5]undecane methyl- pheny1)methan0ne (8—but-2—yny1-10—cthy1— 1 1 -oxa-3 8- 4-mcthoxy—3- 8-butyny1-10—ethy1- piro[5.5]undecan- oromcthyl)bcnzoic 1 1—0xa-3,8— 3—y1)-[4—methcxy—3- acid diazaspiro[5.5]undecane (trifluoromethy1)pheny1] methanonc (8-but—2-yny1ethy1- 1 1 -0xa-3 ,8- -isopr0p0xymethy1- 8-butyny1-10—ethy1- diazaspiro[5 .5]undccan- pyridine-Z-carboxylic 1 1 -oxa—3,8- 3-y1)—(5-isoprop0xy—6- acid diazaspir0[5.5]undecane pyridy1)mcthanonc -(8—butyny1cthyl- 1 1-0xa—3,8- 8-but-2—ynylcthy1cyan0-4—isopr0p0xy- diazaspiro[5 . 5]undecane- 1 1-oxa-3 ,8- benzoic acid 3 —carbony1)—2- pir0[5.5]undccane isopropoxy—benzonitrile (8—but-2—yny1- 1 O-ethyl- 1 1-0xa—3 ,8- 8-butyny1ethy1- diazaspiro[5 . 5]undecan- 3-chlor0isopr0p0xy— 1 1-oxa-3,8- (3 -ch10r0 benzoic acid diazaspiro[5.5]undecane iscpropcxy— pheny1)methan0ne (8-butyny1—10—ethy1— 1 1-0xa—3 ,8- 8-but—2-yny1-10—ethy1- diazaspiro[5.5]undccan- o—4—is0propoxy- 1 1-oxa—3,8~ 3-y1)—(3 -flu0r0 benzoic acid diazaspir0[5 .5]undecane isopropoxy- pheny1)methanone (4-tcrt-buty1—3-mcth0xy- pheny1)-(8-but-2—yny1- 1 0- 8-but—2-yny1—10—ethy1- 4—tert-buty1—3-methoxy— ethyl-l 1-0xa-3 ,8- 1 1-0xa—3 ,8- benzoic acid diazaspir0[5 . 5]undecan- pir0[5.5]undecane ethanone [4-( 1 - hydroxycyclobuty1)phcny 1 0-(methoxymethy1) 1] —[ 1 0—(mcth0xymethy1)- 4—(1 - [3 [ 3 - hydroxycyclobuty1)benzoi (trifluorcmethy1)phenyl] - (trifluoromcthyl)phcny1]- c acid 1 1-0xa—3,8— 1 1 -oxa-3 8- diazaspir0[5.5]undccanc diazaspir0[5 . 5]undecan— 3-y1]mcthan0ne [4-(2—hydroxy—2-methy1— propoxy)methy1— 1 0-(methoxymcthy1)-8 - pheny1]-[10- 4-(2-hydroxy—2-mcthy1- [3- xymethy1)[3 - propoxy)-3—methy1— (trifluoromcthyl)phenyl]— oromcthy1)phcnyl] - benzoic acid 1 1-0xa—3 ,8- 1 1 -0xa-3 8- diazaspiro[5.5]undecane diazaspiro[5 . 5]undccan— 3—y1]methanone (1 0-ethy1pyrimidin y1—11—0xa—3,8— piro[5.5]undccan- 10-cthy1pyrimidin 4-(1 -hydroxycyclobuty1)— 3-y1)-[4-(1- y1~11-0xa-3,8— 3-mcthyl-benzoic acid hydroxycyclobuty1) diazaspiro [5 . 5]undccane methyl- pheny1]mcthan0ne [10-ethy1(2-pyridy1)- 1 1 -oxa—3 ,8- diazaspir0[5.5]undecan— 10—ethy1-8—(2-pyridy1)- 4- 1-h drox( y y yc clobuty)1 - [4-(1 - 11-0xa—3,8- 3-methy1-benzoic acid hydroxycyclobuty1) diazaspiro[5.5]undccane methyl— phenyl]methan0ne [4-( 1 - ycyclobuty1)—3 - methyl-pheny1]—[ 1 0- 10—(meth0xymcthy1) (methoxymethy1) 4-(1 -hydroxycyclobuty1)- pyrimidin-Z-yl-l 1 -0xa- pyrimidin—Z-yl- 1 1-0xa- 3-methy1—benzoic acid 3 ,8- 3 ,8 - pir0[5.5]undecanc diazaspiro[5 . 5 ]undecan- 3-y1]methan0ne [1 O-ethy1(2-pyridy1)— 1 1 —oxa—3,8— 4-(1— 10-ethy1(2-pyridy1)- piro[5 . 5]undecan- hydroxycyclohexy1)benzo 1 3,8- 3—y1]—[4—( 1 - ic acid diazaspir0[5.5]undccanc hydroxycyclohcxy1)- pheny1]methanone (1 O-ethy1pyrimidin y10xa—3 ,8- 4-(1- 10—cthy1pyrimidin diazaspiro[5 . 5]undecan— hydroxycyclohexyl)benzo y1-1 1—oxa-3 ,8— 3 -y1)-[4-(1- ic acid diazaspiro[5.5]undccanc hydroxycyclohexyl} phenyl]rnethanone [4-(1 — 4'(1 ' 1 0-(methoxymethy1)—8- hydroxycyclohexy1)- hydroxycyclohexy1)benzo pyfimidin_2_y1_1 1—0xa- pheny1]-[10~ ic acid 3,8- (methoxymethyl)—8- —222— pyrimidin-Z-yl-l 1-oxa- diazaspiro[5 . 5]undecane 3 ,8— diazaspir0[5 . 5]undecan- 3-y1]methan0ne [10-6thyl(2-pyridy1)- 1 1 -oxa—3,8- 4-(1 - 10—ethy1—8-(2-pyridy1)- diazaspiro[5 . 5]undecan- hydroxycyclopcnty1)benz 11-0xa—3,8— 3-y1]-[4-(1- oic acid diazaspiro[5.5]undccane hydroxycyclopenty1)phcn yl]mcthanone [1 O—ethyl-S—(Z-pyridyl)- 1 1-oxa-3,8- 3-flu0r0(1 - lO-ethy1(2—pyridyl)- diazaspir0[5 . can- hydroxycyclopenty1)benz 1 1-oxa—3,8— 3-y1]-[3-flu0r0-4—(1 - oic acid diazaspir0[5 . cane hydroxycyclopenty1)- pheny1]rncthanonc [IO-ethyl-S—(Z—pyridyl)- 1 1 -0xa-3,8- diazaspiro[5.5]undecan- 4-(1 - 10-ethy1(2-pyridyl)— 3-y1]—[4-( 1 — hydroxycyclopenty1)-3 - 1 l-oxa-3,8- hydroxycyclopentyl)—3 - methyl-benzoic acid diazaspiro[5.5]undecane methyl— phenyl]methanone [10-ethyl(2-pyridy1)- 1 1 -oxa—3 ,8— -ethy1(2-pyridy1)- diazaspiro [ 5 . 5 ]undccan- 0-4—(1 xy-1 - 11-oxa-3,8yl] -[3 -fluor0—4~(1 — methyl-cthy1)benzoic acid diazaspir0[5.5]undecane hydroxy—l -methy1- cthyl)pheny1]methanone [1 O-ethy1(2-pyridy1)- 1 l —oxa-3,8- 4-(1 -hydr0xy— 1 -methyl- 10-ethy1(2-pyridy1)- diazaspiro[5 . 5]undecan- ethy1)methy1-benzoic 11—0xa—3,8— 3-y1]-[4-(1-hydr0xy-1— acid pir0[5 . cane methyl-ethy1)-3 -methy1— pheny1]methanone (1 O-ethyl-S-pyrimidin-Z- y1-1 l—oxa-3,8- diazaspir0[5.5]undecan— 10—ethy1-8—pyrimidin ropy1sulf0ny1—3- 3—y1)-(4- yl-l 1-0xa-3 ,8— methyl-benzoic acid isopropylsulfony1—3— diazaspiro[5.5]undecane methyl— pheny1)mcthanone (1 O—ethylpyrimidin-2— yl-l l—oxa—3,8- 3—flu0ro(1 - IO-ethy1pyrimidin piro[5.5]undecan- hydroxycyclopentyl)benz yl—l 1-oxa-3 ,8- 3-y1)-[3-flu0ro(1 — oic acid piro[5.5]undecane hydroxycyclopentyl)- phenyl]methan0ne [4-(1 -ethy1— 1 -hydr0xy— propy1)—3-methy1- pheny1]-( 1 O—ethyl-S- 4-(1-ethy1hydroxy- 10-cthy1-8—pyrimidin-2— pyrimidin-Z—yl-l l-oxa- propy1)methy1-bcnzoic yl-l 1-0xa-3 ,8- 3 ,8- acid diazaspiro[5 .5]undecane diazaspir0[5.5]undecan— 3 -y1)methanone (1 O-cthy1—8-pyrimidin yl-l l-oxa-3 ,8— 4-( 1 - 10-ethy1-8—pyrimidin diazaspiro[5.5]undccan- hydroxycyclopenty1)-3 - y1—1 1-oxa-3 ,8- 3—y1)-[4-(1 - methyl—benzoic acid diazaspir0[5.5]undecane hydroxycyclopentyD-3 - —224- methyl- pheny1]methanone [4-(1 - hydroxycyclopenty1)-3 - methyl-phenyl] - [1 0- 10-(rnethoxymethy1) 4-( 1 - (methoxymethy1)—8- pyrimidin-Z-yl-l 1—oxa- hydroxycyclopcnty1)-3 - pyrimidin-Z-yl-l l-oxa- 3 ,8- methyl-benzoic acid 3 8 - , diazaspiro[5.5]undecane diazaspiro[5.5]undecan— 3—y1]methanone [4-(1- hydroxycyclopenty1)— pheny1]-[10- 10-(methoxymcthy1)—8- 4-(1 - (methoxymethy1) pyrimidin-Z-yl-l 1-0xa- hydroxycyclopentyl)benz pyrimidin-Z-yI-l l-oxa- 3 ,8- oic acid 3 ,8- piro[5.5]undecane pir0[5.5]undecan- ethanone [4—(1- hydroxycyclobutyl)- pheny1]-[10- 1 0-(meth0xymethy1) 4-(1 - (methoxymethy1)—8- pyrimidin-Z-yl-l 1 -oxa— hydroxycyclobutyl)benzoi pyrimidin—Z-yl-l l—oxa- 3,8- c acid 3 8 — diazaspir0[5 . 5]undecane , diazaspiro[5 . 5 ]undecan- 3—y1]methan0ne [4-(2-hydr0xymethyl- 4-(2—hydroxy—2-methy1- thoxymethyl)-8— propoxy)methy1— propoxy)methyl- pyrimidin-Z—yl-l 1-0xa— pheny1]-[10- benzoic acid 3 ,8- —225- (methoxymethyl)-8— diazaspir0[5 . 5]undecane pyrimidin-Z—yl-l l-oxa- 3,8- diazaspir0[5.5]undecan- 3-y1]methan0ne 2-isoprop0xy-5—[10- (methoxy1nethy1)—8— 10-(meth0xymethy1)—8- pyrimidin-Z-yl-l 1-oxa- 0is0pr0poxy- pyrimidin-Z-yl-l 1-0xa- 3,8— benzoic acid 3 ,8— diazaspiro [5 . 5]undecane- diazaspir0[5.5]undecane 3-carbony1]benzonitrile (4-tert-buty1—3 -meth0xy— pheny1)-[10- 1 0-(methoxymethy1) xymethy1) 4-tert-buty1methoxy— pyrimidin—2~y1-1 l—oxa— pyrimidin-Z-yl-l 1-oxa- benzoic acid 3,8- 3 ,8 — diazaspiro[5 . cane diazaspiro [5 . 5]undecan- 3-y1]methanone [3-methoxy—4-(2— methoxyethoxy)phenyl] — -(methoxymethy1)—8— [1 0—(methoxymethy1)-8— oxy—4-(2— pyrimidin-Z-yl—l 1—0xa— pyrimidin-Z—yl-l 1-0xa— methoxyethoxy)benzoic 3 ,8— 3 8- acid diazaspiro[5.5]undecane diazaspir0[5 . 5 ]undecan- 3-y1]methan0ne (5-isopropoxymethy1- 2-pyridy1)—[10- 1 0-(methoxymethy1) r0p0xymethy1- (methoxymethyl) pyrimidin-Z-yl-l l-oxa- pyridine—Z-carboxylic pyrimidin-Z-yI-l l-oxa- 3,8- acid 3 ,8— diazaspir0[5 .5]undecane diazaspiro[5 . 5]undecan- 3-y1]methanone (3 yphenyl)—[10— (methoxymcthy1) 10-(meth0xymcthy1) pyrimidin-Z—yl-l l-oxa- pyrimidin-Z-yl-l 1-0xa- 3-ethoxybenzoic acid 3,8— 3 ,8- pir0[5 . 5]undecan— diazaspiro [ 5 . 5]undecane ethanone (4-isopr0poxypheny1)— [10-(meth0xymethy1) 10-(meth0xymethy1)—8— pyrimidin-Z-yl-l 1-0xa— pyrimidin-Z-yl-l l-oxa- rop0xybenzoic acid 3,8- 3 ,8— diazaspiro[5 . 5]undecan- diazaspiro [ 5 . 5]undecane 3—y1]methanone cyclopr0pylsulfonyp1 hen -(meth0xymethyl) y1)-[1 O-(methoxymethy1)— 4- pyrimidin-Z-yl-l 1-oxa- 8-pyrimidin—2-y1—1 1 -0xa— cyclopropylsulfonylbenzo 3 ,8— 3,8— ic acid diazaspiro[5.5]undecane diazaspiro[5.5]undccan- 3-y1]methan0ne [4-(1 -hydr0xy—1 -methyl- ethyl)-3 -methy1—phenyl] - -(meth0xymethy1) [1 0-(meth0xymethyI) 4-(1 -hydroxy—1 -methy1- pyrimidin-Z—yl-l l—oxa— pyrimidin—2—y1-1 l-oxa— ethy1)methy1-benzoic 3,8- acid diazaspir0[5 .5]undecane diazaspiro[5 . 5 an- 3-y1]methanone WO 25613 [4-(1 -hydroxy-1 -methy1- ethy1)pheny1]-[10- -(meth0xymethyl)—8- (methoxymethy1)—8 — 4-(1-hydr0xymethy1- din-Z-yl—l l—oxa- pyrimidin-Z-yl-l 1 -0xa-' ethy1)benzoic acid 3,8- diazaspiro[5.5]undecane d1azaspir0[5.5]undecan-. ethan0ne [3 -flu0ro-4—(1—hydroxy— 1 -methy1—ethyl)pheny1]— -(meth0xymethy1)-8— [10-(methoxymethy1) 3 -flu0ro—4-(1-hydroxy—1- pyrimidin-Z-yl—l l-oxa- pyrimidin-Z-yl-‘l 1 -0xa— methyl-ethy1)bcnzoic acid 3 ,8- diazaspiro[5 .5]undecane diazaspir0[5 . 5]undecan- 3-y1]methan0nc (3 -flu0r0isopropoxy— pheny1)-[10- -(methoxyrnethy1)-8— (methoxymethyl)-8— 3 -fluor0-4—isopropoxy- pyrimidin-Z-yl-l 1-oxa- pyrimidin-Z-yl-l l-oxa— c acid 3,8- 3,8— diazaspir0[5.5]undccane diazaspir0[5.5]undecan- 3-y1]methanone (4-isopentyloxy-3— methoxy p- heny )1 - 10-[ -(1neth0xymethy1) (methoxymcthy1) 4-isopentyloxy—3- pyrimidin—2~y1~1 l—oxa— pyrimidin-Z-yl—l 1 -oxa— methoxy—benzoic acid 3,8- pir0[5.5]undecane diazaspir0[5 .5]undecan- 3-y1]methanone [4-(1-hydr0xy—2-methy1- propyl)pheny1]—[10- -(methoxymethy1)-8— (methoxymethyl) 4-( 1 xy—2-methy1- pyrimidin-Z—yl-l 1—oxa- pyrimidin-Z-yl—l l-oxa- )benzoic acid 3 ,8- 3 ,8 - diazaspiro[5.5]undecane piro[5 . 5]undecan— 3-y1]methan0ne [2-(diflu0r0methoxy)— pheny1]—[10- -(meth0xymethy1)—8- (methoxymethy1) 2- pyrimidin—Z-yl—l 1-oxa- pyrimidin—Z—yl-l 1-oxa- (difluoromethoxy)benzoic 3,8- 3 ,8- acid diazaspiro[5 . 5]undccane diazaspir0[5 . 5]undecan- 3-y1]methanonc [4-(2—hydr0xymethy1— propy1)pheny1] -[ 1 0- -(methoxymethy1)—8- (methoxymethy1)—8— 4-(2-hydr0xy—2-methy1- pyrimidin-2~y1-1 l-oxa- pyrimidin-Z—yl—l l—oxa— propyl)benzoic acid 3 ,8— 3 ,8 - diazaspiro[5.5]undecane diazaspir0[5 .5]undecan— 3-y1]methanone (difluoromethylsulfonyl) pheny1]-[10- 10-(methoxymethy1)-8_ (methoxymethy1)-8— din-Z-yl-l 1 -oxa— (difluoromethylsulfonyl)b pyrimidin-Z-yl-l '1 -oxa- 3 ,8— enzoic acid 3 ,8 - diazaspir0[5.5]undecane diazaspir0[5.5]undecan- 3-yl]methan0ne [10—(methoxymethy1)—8- pyrimidin-Z-yl-l l-oxa— —(meth0xymethy1) 3 8- , 4-meth0xy—3- pyrimidin-Z—yl-l l-oxa— diazaspiro [5 . can— (trifluoromethyl)benzoic 3,8— 3 -y1]-[4-methoxy—3 - acid diazaspir0[5.5]undecane (trifluoromethyl)pheny1] methanone [3 -(hydroxymethy1)_4- iSOPTOpoxy-phenyl].[1 0- -(mcthoxymethy1) (methoxymethyl)-8_ 3 -(hydroxymethy1) pyrimidin—Z-yl-l 1-oxa- pYrimidin-Z-yl-l 1-0xa— isopropoxy—benzoic acid 3 ,8- 3 ,8- diazaspir0[5 . cane diazaspir0[5 . can- 3-y1]methan0ne pr0poxy methoxy—pheny1)-[10- -(methoxymethy1)-8— (mcthoxymethy1) 4-is0pr0poxy-3—methoxy- pyrimidin-Z-yl-l 1-oxa- pyrimidin-2~y1—1 l-oxa- benzoic acid 3,8- 3,8- diazaspiro[5 . 5]undecane diazaspir0[5 . 5]undecan- 3-y1]methancne N-cyclopropyl-4—[ 1 0— (methoxymethy1) -(meth0xymethy1)-8— pyrimidin-Z-yl-l l—oxa- 4- pyrimidin-Z-yl-l 1-0xa- 3 ,8- (cyclopropylsulfamoyl)be 3 ,8- diazaspiro[5.5]undecane— nzoic acid diazaspir0[5 . 5]undecane 3—carb0ny1]benzene- sulfonamide (8-butyny1— 1 0-ethy1— 1 1 -0xa—3,8- 8-butyny1ethy1— diazaspiro[5.5]undccan— 3-methy1-4—pr0 0xp y- ll-oxa-3,8y1)-(3-methyl-4— benzoic acid d1azasp1r0[5' _ .5]undecane propoxy— pheny1)methanonc (8-but—2-ynylcthy1- 1 1—0xa—3 ,8- 8—butynyl- 1 l- x mcthy y1- diazaspiro[5.5]undecan— 11-0xa-3,8- benzcic acid (4-eth0xy—3-methy1- d1azasp1ro[5.5]undecane_ ‘ phenyl)mcthanone (8-but—2-yny1ethy1- 1 1 -0xa—3 ,8- 8-butynylethy1- diazaspir0[5 . 5]undecan- 4-meth0xymethy1- 1 1 -oxa-3 ,8— 3 -y1)-(4-meth0xy—3- benzoic acid d1azasp1r0[5_ . .5]undecane methyl— pheny1)methanone [3 —flu0r0( 1 -hydr0xy— 1 -methyl-ethy1)pheny1] - -(methoxymethyl)-8— [1 O—(mcthoxymcthy1) [3 - [3fluor0-4—(1 -hydr0xy— 1 - oromethyl)phenyl] — orcmethyl)pheny1]— methyl-ethy1)benzoic acid 1 1-oxa-3,8- 1 1 -0xa-3 8- diazaspiro[5.5]undecane diazaspiro[5.5]undecan- 3-y1]methan0ne (8-butynyl-10,10- difluoro-l 1-0xa—3 ,8— 8-but—2-yny1—10,10— 4-is0pr0 ox mctp y hy1- diazaspiro[5 . 5]undecan- difluoro-ll-oxa—3,8— benzoic acid d1azasp1ro[5.5]undccanc_ ' (4-isopropoxy—3— methyl— )methan0ne [8-butyny1-10— (fluoromethy1)-1 1-oxa- 8-butyny1—10- 3,8- 4-isoprop0xy-3—methy1- (fluoromethy1)-1 1 -oxa- d1azaspiro[5.5]undecan-_ c acid 3,8y1] (4- —1soprop0xy—3—_ diazaspir0[5.5]undecane methyl- pheny1)methan0ne [8—(2,2-difluoropr0py1)- -(methoxymethy1)-1 1— 8-(2,2-difluor0propy1)— oxa-3 ,8- 4-is0pr0p0xy—3-methyl— 10—(meth0xymethy1)-1 1- diazaspiro[5_ . 5]undecan— benzoic acid 0xa—3 ,8— 3-y1] -(4-isopr0p0xy—3- diazaspir0[5.5]undecane methyl— pheny1)methanone Preparation of (4-is0propoxymethyl-phenyl)—(10-phenyl-1l-oxa— azaspiro [5.5]undecanyl)methanone dbQTN 0 Step 1: A mixture nzyl—2-pheny10xa-4,9—diazaspiro[5.5]undecane (222 mg, 0.69 mmol), 4—isopr0poxy—3-methy1~benzoic acid (140 mg, 0.72 mmol) and HATU (262 mg, 0.69 mmol) was stirred in a mixture ofDCM (1 mL) and DMF (1 mL) for 5 minutes. Triethylamine (192 uL, 1.38 mmol) was added and the reaction mixture was stirred for 16 hours, then concentrated in vacuo, diluted with sat. aq. NaHCOg, ted with ethyl acetate (3 x 2 mL), dried over MgSO4, filtered and trated in vacuo and purified by silica gel column chromatography using 0-60% EtOAc/DCM as eluent to give (10-benzylpheny1-7—oxa—3,10-diazaspiro[5.5]undecan-3—y1)—(4- isopropoxy—3-methyl-phenyl)methanone (343 mg, 100%) as a yellow oil. ESI-MS m/z calc. 406.5, found 407.7 ; Retention time: 1.13 minutes (3 min run).

Step 2: To (1 ylphenyloxa—3,10—diazaspiro[5.5]undecany1)-(4- isopropoxymethyl-phenyl)methanone (264 mg, 0.53 mmol), ammonium formate (167 mg, 2.65 mmol), ium (30 mg, 0.03 mmol) (10% on carbon) was added methanol (5 mL) and the reaction mixture was stirred at 75 °C for 40 minutes. The reaction mixture was cooled, filtered over celite and concentrated in vacuo. The residue was partitioned between ethyl acetate and 1:1 sat. aq. NaHC03/25% aq. NaOH, dried over MgSO4, filtered and trated in vacuo to give (4—isopropoxy—3-methyl- phenyl)-(8-phenyl—7-oxa—3,10-diazaspiro[5.5]undecanyl)methanone (170 mg, 79 %), which was used directly without further purification in the next step. ESI—MS m/z calc. 408.5, found 409.7 (M+1)+; Retention time: 1.24 minutes (3 min run) Preparation of (4-isopropoxymethyl-phenyl)—(8-methyl—10- -l1-0xa—3,8—diazaspiro[5.5]undecanyl)methan0ne @1230,55% To (4-isopropoxy—3 -methyl-phenyl)—(8-phenyloxa—3 , 1 0- diazaspiro[5.5]undecanyl)methanone (22 mg, 0.05 mmol) in DCM (0.3 mL) was added iodomethane (15 mg, 7 ML, 0.11 mmol) followed by the addition of triethylamine (15 uL, 0.11 mmol) and the reaction mixture was stirred for 16 hours at room temperature. The reaction mixture was concentrated in vacuo, diluted with methanol, filtered and purified by prep LCMS (1-99% ACN/HZO, 5 mM HCl modifier) —233- WO 25613 to give (4-isopropoxy—3-methyl-phenyl)-(l0-methylpheny1-7—oxa—3, 1 0- diazaspiro[5.5]undecanyl)methanone hydrochloride salt as a glassy solid (13 mg, 54 %). ESI—MS m/z calc. 422.3, found 423.5 ; Retention time: 1.31 minutes (3 min run).

Preparation of (4-isoprop0xy—3-methyl—phenyl)—(8-is0pr0pyl—10- —l1-oxa-3,8-diazaspir0[5.5]undecanyl)methanone To (4-isopropoxymethy1—pheny1)-(8-phenyloxa—3,10- diazaspiro[5.5]undecan—3-yl)methanone (30 mg, 0.07 mmol) and acetone (130 uL, 1.77 mmol) in DCE (0.5 mL) was added sodium triacetoxyborohydride (50 mg, 0.24 mmol) and the reaction mixture was stirred for 5 hours. The reaction mixture was concentrated in vacuo, diluted with methanol, microfiltered and purified by preparative LCMS (1— 99% ACN/HZO, 5 mM HCl modifier) to give (4—isopropoxy—3-methyl—phenyl)—(10- isopropylphenyloxa—3 ,10—diazaspiro[5.5]undecan-3 -y1)methanone hloride salt (13 mg, 36 %) as a glassy solid. ESI-MS m/z calc. 450.2, found 451.5 (M+1)+; Retention time: 1.38 minutes (3 min run).

Preparation of [8-(2-hydroxy—2-methyl—propyl)—10-phenyl—1l-oxa- 3,8—diazaspiro[5.5]undecanyl]-(4-isopropoxy—3-methyl—phenyl)methanone - 606.6% [0061 8] (4-Isopropoxy—3-methyl-phenyl)—(8-pheny1oxa—3 ,10- diazaspiro[5.5]undecany1)methanone (21 mg, 0.05 mmol) and 2,2—dimethyloxirane (11 mg, 14 uL, 0.15 mmol) were stirred in ethanol (0.3 mL) at 40 °C for 16 hours. The —234— reaction mixture was diluted with methanol, microfiltered, and purified by prep LCMS (10—99% ACN/Water, 5 mM HCl modifier) to give [10-(2—hydroxymethyl-propyl)- yloxa-3 , 1 0-diazaspiro[5 . 5]undecanyl]—(4-isopropoxy—3 -methy1- phenyl)methanone hydrochloride salt (12 mg, 46 %) as a glassy solid. ESl-MS m/Z calc. 480.3, found 481.7 (M+1)+; ion time: 1.49 miutes (3 min run).

Preparation of [8-(2-hydr0xyethyl)—10-phenyl—11—0xa—3,8- diazaspiro[5.5]undecanyl]-(4-isopropoxymethyl-phenyl)methanone (4-lsopropoxy-3 -methyl-phenyl)-(8-phenyloxa-3 ,10- diazaspiro[5.5]undecanyl)methanone (21 mg, 0.05 mmol), 2-(2- bromoethoxy)tetrahydropyran (13 mg, 9 uL, 0.06 mmol) and K2C03 (21 mg, 0.15 mmol) were combined in DMF (0.3 mL) and stirred at 40 °C for 16 hours. The reaction mixture was d with ether (3 mL), microfiltered and evaporated to give the THP— ether intermediate, which was dissolved in methanol (0.5 mL), then HCl (0.5 mL of 4 M in dioxane, 2.00 mmol) was added and the reaction mixture was stirred for 30 minutes. The reaction mixture was concentrated in vacuo, diluted with methanol, ltered and purified by prep LCMS (10—99% ACN/Water, 5 mM HCl modifier) to give l0-(2-hydroxyethy1)pheny1—7-oxa—3,10-diazaspiro[5.5]undecanyl-(4- isopropoxy—3-methyl-phenyl)methanone hydrochloride salt (10 mg, 40 %) as a glassy solid. ESI-MS m/z calc. 452.3, found 453.2 (M+l)+; Retention time: 1.08 minutes (3 min run).

} Preparation of (2-(4-chlorophenyl)(2,2-difluoroethyl)—1-0xa—4,9- diazaspir0[5.5]undecanyl)(4-isopropoxy-S-methylphenyl)methanone C. 030087” Step 1: To a solution of 8-benzyl(4-chlorophenyl)—11-0xa—3,8- diazaspiro[5.5]undecane (100 mg, 0.28 mmol) and 4-isopropoxy—3-methyl—benzoic acid (54 mg, 0.28 mmol) in DMF (1 mL) was added DIEA (98 uL, 0.56 mmol) followed by the addition of HATU (128 mg, 0.34 mmol). The reaction mixture was stirred for 10 minutes, then ed with water and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with water (twice). The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography using 0 to 50% EtOAc/hexanes as el‘uent to obtain [8-benzyl(4-chlorophenyl)oxa-3,8—diazaspiro[5.5]undecan yl]-(4-isopropoxy—3-methy1-pheny1)methanone (44 mg, 29 %). ESI-MS m/z calc. 532.2, found 533.3 (M+1)+; Retention time: 2.17 minutes (3 min run).

Step 2:

[00625] l-Chloroethyl carbonochloridate (142mg, 108 uL, 0.99 mmol) was added to a on of [8-benzyl—10-(4-chlorophenyl)—11-oxa—3,8- piro[5.5]undecany1]-(4-isopropoxy—3-methy1-phenyl)methanone (44 mg, 0.08 mmol) in DOE (508 uL) at room ature and then the reaction mixture was heated at reflux for 1 hour. The excess solvent was removed in vacuo and the carbamate intermediate was dissolved in MeOH (2 mL) and heated at reflux for 20 minutes. The reaction mixture was cooled to room temperature, filtered and purified by Waters mass directed LC/MS-HPLC: (1-99% ACN/ H20 (5mM HCl)). The desired fractions were concentrated to dryness, ved in EtOAc and washed with 1M NaOH. The combined organics were dried over Na2S04, filtered and concentrated in vacuo to yield -chloropheny1)—1 1—oxa—3 ,8—diazaspiro[5.5]undecanyl] -(4-isopropoxy—3 - methyl—phenyl)methanone (22 mg, 60 %) . ESI-MS m/z calc. 442.2, found 443.5 (M+l)+; Retention time: 1.51 minutes (3 min run) ] Step 3: 2,2-difluoroethyl trifluoromethanesulfonate (17 mg, 0.08 mmol) was added to a solution of [10-(4-chlorophenyl)oxa~3,8-diazaspiro[5.5]undecany1]- (4-isopropoxy-3—methyl-phenyl)methanone (22 mg, 0.05 mmol) and NaHC03 (13 mg, 0.15 mmol) in anhydrous ethanol (0.3 mL) at room temperature. The reaction mixture was purged with argon, sealed with a cap and heated at 70 0C for 40 minutes. The reaction mixture was cooled to room temperature, diluted with MeOH to 1 mL, microfiltered and purified by Waters mass ed LC/MS: (IO-99% ACN/ H20 (5mM HCl)) to yield [10-(4-chlorophenyl)(2,2—difluoroethyl)-1l-oxa-3,8- diazaspiro[5.5]undecan-3—yl]—(4-isopropoxy—3-methyl-phenyl)methanone (27 mg, 100 %). ESI-MS m/z calc. 478, found 507.2 (M+1)+; Retention time: 2.17 minutes (3 min run).

[00628] Preparation of (2-(2-chlorophenyl)—4-(2,2-difluor0ethyl)—1-0xa-4,9- diazaspiro[5.5]undecan-9—yl)(3-flu0r0isopropoxyphenyl)methan0ne O 06O N F yo CI This compound was ed following the above procedure, using 8- benzyl-l0-(2—chlorophenyl)—11—oxa—3,8-diazaspiro[5.5]undecane in step 1 and using 3- fluoroisopropoxy—benzoic acid as the acid reagent in step 3. ESI-MS m/z calc. 510.2, found 511.5 (M+1)+; Retention time: 2.25 minutes. 1H NMR (400 MHz, DMSO) 5 7.61 (dd, J = 7.8, 1.2 Hz, 1H), 7.50 - 7.31 (m, 3H), 7.30 - 7.12 (m, 3H), 6.36 - 6.00 (m, 1H), 5.08 (d, J = 13.4 Hz,1H), 4.74 - 4.64 (m, 1H), 4.12 - 3.91 (m, 1H), 3.73 — 3.59 (m, 2H), 3.32 (dd, J = 32.0, 10.6 Hz,1H), 3.06 (dd, J = 11.0, 3.1 Hz, 1H), 2.91 (dd, J = 11.6, 2.6 Hz, 1H), 2.86 = 9.6 Hz, 1H), - 2.65 (m, 2H), 2.44 - 2.30 (m, 1H), 2.19 (d, J 2.13 = 6.0 Hz, 6H). - 1.99 (m, 1H), 1.70 - 1.55 (m, 3H), 1.30 (d, J -237— ation of (4-(2,2-difluoroethyl)(p-tolyl)-1—oxa-4,9— diazaspiro[5.5]undecanyl)(4-isopropoxy—3—methylphenyl)methanone ©1013yfiiror Step 1:

[00632] A mixture of yl(p-toly1)-l l-oxa—3,8- diazaspiro[5.5]undecane (100 mg, 0.30 mmol), 4—isopropoxy—3—methy1-benzoic acid (61 mg, 0.31 mmol) and HATU (119 mg, 0.31 mmol) was stirred in DCM (450 uL) and DMF (450 uL) for 5 minutes. Triethylamine (83 uL, 0.59 mmol) was added and the reaction mixture was stirred overnight. The reaction mixture was diluted with sat. aq. NaHC03 (5 mL) and ted with DCM (3 x 5 mL), dried over MgSO4, filtered, trated in vacuo and purified by silica gel column chromatography (0-100% EtOAc/hexane) to give [8-benzyl(p-tolyl)—l l—0xa—3,8-diazaspiro[5.5]undecan yl]-(4-isopropoxy—3-methyl-phenyl)methanone as a ess oil (120 mg, 79 %). ESIMS m/z calc. 512.3, found 513.3 (M+1)+; ion time: 1.86 minutes (3 min run).

[00633] Step 2: To [8-benzyl(p-toly1)-l 3,8-diazaspiro[5.5]undecanyl]-(4- isopropoxy—3-methy1-phenyl)methanone (120 mg, 0.23 mmol) in ethanol (1.2 mL) was added ammonium formate (69 mg, 1.09 mmol) and Pd(OH)2 (18 mg, 0.025 mmol) and the on mixture was heated at 75 °C for 60 minutes. The reaction mixture was cooled, filtered, concentrated in vacuo and the residue was dissolved with ethyl acetate (10 mL) and washed with sat. aq. NaHCO3 (5 mL). The aqueous layer was extracted further with ethyl acetate (2 x 10 mL). The combined organics were dried over MgSO4, filtered and concentrated in vacuo to give the amine intermediate. The amine intermediate was dissolved in ethanol (600 uL) and NaHCO3 (79 mg, 0.94 mmol) and 2,2—difluoroethyl trifluoromethanesulfonate (74 mg, 0.35 mmol) were added . The reaction mixture was heated at 40 0C overnight, filtered and then purified by preparative LCMS (10-99% ACN/water, HCl modifier as modifier) to give [8-(2,2- difluoroethyl)- 1 0-(p-toly1)—1 1-oxa-3 ,8-diazaspiro[5.5]undecan-3—yl]-(4-isopropoxy-3 - methyl-pheny1)methanone. ESI-MS m/z calc. 486.3, found 487.3 (M+1)+; Retention time: 2.39 minutes (3 min run).

Preparation of (4-benzyl—2-(5-methyloxazol—Z-yl)0xa-4,9- diazaspiro[5.5]undecanyl)(4-isoprop0xymethylphenyl)methanone .93 Y Step 1: To tert—butyl 8-benzylVinyloxa—3,8-diazaspiro[5.5]undecane— 3-carboxylate (600 mg, 1.61 mmol) in l (1 mL) was added HCl (4 mL of 4 M in dioxane, 16.11 mmol) and the mixture was stirred for 30 minutes. The reaction mixture was concentrated in vacuo, then DMF (4 mL), 4-isopropoxy—3-methy1-benzoic acid (313 mg, 1.61 mmol) and ylamino(triazolo[4,5-b]pyridin-3— yloxy)methylene]~dimethy1—ammonium hexafluorophosphate (613 mg, 1.61 mmol) were added and the reaction mixture was d for 10 minutes. ylamine (898 ML, 6.44 mmol) was added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was trated in vacuo, diluted with DCM (5 mL), washed with 1 N aq. NaOH (2 mL) and brine (2 mL), dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography using 0-100% EtOAc/hexane as eluent to give (8-benzy1—10-vinyl0xa—3,8- diazaspiro[5.5]undecan-3—yl)—(4-isopropoxy—3—methy1-pheny1)methanone as a pale yellow oil (715 mg, 99 %). 1H NMR (400 MHz, CDC13) 8 7.35 - 7.22 (m, 5H), 7.20 - 7.14 (m, 2H), 6.79 (d, J = 8.2 Hz, 1H), 5.83 - 5.74 (m, 1H), 5.34 - 5.26 (m, 1H), 5.15 (d, J = 10.6 Hz, 1H), 4.59 - 4.50 (m, 1H), 4.33 - 4.14 (m, 2H), 3.59 - 3.14 (1n, 7H), 2.79 (d, J = 11.0 Hz,1H), 2.56 (d, J =11.1Hz,1H), 2.19 (s, 3H), 1.91 — 1.80 (m, 2H),1.69 - 1.39 (m, 2H), 1.34 (d, J = 6.0 Hz, 6H); ESI-MS m/z calc. 448.6, found 449.5 (M+1)+; Retention time: 1.54 minutes (3 min run). 2012/028882 Step 2: To (8-benzy1Vinyloxa-3,8-diazaspiro[5.5]undecanyl)-(4- isopropoxy—3-methy1-phenyl)methanone (2.4 g, 5.6 mmol) and 4-methylmorpholine 4- oxide (698 mg, 5.96 mmol) in e (22 mL) and water (2.5 mL) was added osmium tetroxide (677 uL of 2.5 %w/w, 0.05 mmol) dropwise and the reaction mixture was d for 2 hours. The reaction mixture was quenched with 1M sodium thiosulfate (100 mL) and stirred for 5 minutes, then extracted with EtOAc (4 x 100 mL), washed with sat. aq. sodium bicarbonate (100 mL) and dried over MgSO4 and concentrated in vacuo to give the diol intermediate (~2.5 g). The reaction mixture was purified by basic alumina column chromatography using 0-20% MeOH/DCM as eluent to obtain [8-benzy1—10—(1,2-dihydroxyethyl)-l 1-oxa—3,8-diazaspiro[5.5]undecan-3 -y1]- (4—isopropoxymethyl-phenyl)methanone (2.18 g, 84 %). ESI-MS m/z calc. 482.6, found 483.7 (M+l)+; Retention time: 1.10 minutes (3 min run).

Step 3:

[00641] To [8-benzy1-l 0-(1 ,2—dihydroxyethyl)—l 3 ,8- diazaspiro[5.5]undecanyl]-(4-isopropoxy—3-methyl-pheny1)methanone (1.53 g, 3.17 mmol) in THF (28 mL) was added NaIO4 (1.36 g, 6.34 mmol) followed by the addition of water (10 mL). The reaction mixture was stirred at room temperature for 2 hours, then filtered through celite, and concentrated in vacuo. The residue was partitioned between sat. aq. sodium bicarbonate (50 mL) and ethyl acetate (50 mL) and the aqueous layer was ted further with ethyl acetate (3 x 50 mL). The organics were ed, washed with sat. aq. sodium onate (50 mL), dried over MgSO4, and concentrated in vacuo. To the intermediate aldehyde (~1 .4 g) was added 2- methylpropan-Z—ol (17 mL) and 2-methylbut—2-ene (9 mL, 8508 mmol) and the reaction e was cooled to 0 °C. A solution of NaClOz (938 mg, 8.29 mmol) and NaHgPO4 (1.15 g, 8.31 mmol) in water (17 mL) was added dropwise over 5 minutes, and the reaction mixture was stirred for 30 minutes. The reaction mixture was warmed to room temperature, then extracted with ethyl acetate (4 x 50 mL) and the combined organic layer was washed with brine (15 mL), dried over MgSO4, filtered and concentrated in vacuo to give 8-benzyl(4-isopropoxy—3-methy1-benzoy1)-l l-oxa- -240— 3,8-diazaspiro[5.5]undecanecarboxylic acid as a white foam (1.48 g, 100 %). ESI- MS m/z calc. 466.6, found 467.5 (M+1)+; Retention time: 1.27 minutes (3 min run).

Step 4: To 8-benzy1(4-isopropoxy—3-methyl-benzoyl)-l l-oxa—3,8- diazaspiro[5.5]undecane-l0-carboxy1ic acid (201 mg, 0.43 mmol), 1-aminopropan one (47 mg, 0.43 mmol) and T3P (641 uL of 50 %w/w, 1.08 mmol) was added 2— methyltetrahydrofiiran (1 mL) and the reaction mixture was then heated at 75°C for 2 hours. The reaction mixture was cooled to room temperature and partitioned n saturated aq. NaHC03. The layers were separated and the aqueous layer was extracted with EtOAc (2x). The combined organics were dried over , filtered and concentrated in vacuo to a dark foam. The crude product was purified by silica gel column chromatography using 20-70% EtOAC in DCM as eluent to afford onyl— 8-benzyl-3 -(4-isopropoxy—3 -methyl—benzoyl)— 1 1-oxa-3 ,8-diazaspiro[5.5]undecane carboxamide (92 mg, 41 %) as a yellow solid. ESI—MS m/z calc. 521.6, found 522.5 ; Retention time: 1.48 minutes (3 min run).

Step 5: To N—acetonylbenzyl—3-(4-isopropoxy—3-methyl—benzoy1)—1 1—oxa- 3,8-diazaspiro[5.5]undecane—10-carboxamide (136 mg, 0.26 mmol) in THF (3 mL) was added Burgess' Salt (155 mg, 0.65 mmol) and the reaction mixture was heated at 75 °C in a sealed vial for 2 hours. The solvents were removed under reduced pressure, and the residue was ved in DMF (1 mL), filtered and purified by Waters preparative LC/MS (1-99% ACN/ H20 (5mM HCl)). The desired fractions were concentrated in vacuo and the residue ioned between EtOAc/ saturated aqueous NaHC03 solution. The layers were separated and the s layer was extracted with EtOAc (2x). The combined organics were dried over Na2804, filtered and concentrated in vacuo to yield 8-benzyl(5-methyloxazol-2—yl)-1l-oxa—3,8—diazaspiro[5.5]undecan- 3-yl]-(4—isopropoxy—3-methyl-pheny1)methanone (76 mg, 58 %) as a foam. ESI-MS m/z calc. 503.6, found 504.5 (M+1)+; Retention time: 1.74 minutes (3 min run).

Preparation of (4-isopropoxy-3—methylphenyl)(2-(5-methyloxazol— 2-yl)(2,2,2—triflu0r0ethyl)—1-0xa—4,9-diazaspiro[5.5] undecanyl)methanone K? Y

[00647] Step 1: A mixture of 8—benzyl—10—(5-methyloxazoly1)0xa—3,8- diazaspiro[5.5]undecany1-(4-is0propoxy—3-methy1—pheny1)methanone (46 mg, 0.09 mmol), palladium, 10 wt.% on activated carbon (19 mg, 0.18 mmol) and ammonium formate (35 mg, 0.55 mmol) in EtOH (750 uL) was heated to 65 °C for 50 s.

The reaction mixture was cooled to room temperature, microfiltered and 80% of the solvent was removed in vacuo and then diluted with DMF (1 mL) and purified by Waters prep LC/MS (1—99% ACN/ H20 (5mM HCl)) to yield (4-isopropoxy—3-methyl- pheny1)-[10-(5—methyloxazol-2—yl)-1 3 ,8-diazaspiro[5.5]undecan-3 -y1]methanone hydrochloride salt (32 mg, 78 %). ESI—MS m/z calc. 4132, found 414.7 ; Retention time: 0.99 s (3 min run).

Step 2: A mixture of (4-isoprOpoxy—3-methy1—pheny1)—[10-(5—methyloxazol yl)-1l-oxa-3,8-diazaspiro[5.5]undecan~3—yl]methan0ne hydrochloride salt (32 mg, 0.07 mmol), 2,2,2-trifluoroethyl trifluoromethanesulfonate (17 uL, 0.11 mmol) and NaHC03 (24 mg, 0.28 mmol) in ous EtOH (800 uL) was heated at 80 0C in a sealed vial for 18 hours. The reaction mixture was allowed to cool to room temperature, microfiltered and purified by Waters mass directed LC/MS: (10-99% ACN/ H20 (5mM HC1)) and concentrated in vacuo to yield (4-isopropoxymethy1- pheny1)-[10—(5—methyloxazol—2-yl)(2,2,2-trifluoroethy1)—l 1-oxa-3 ,8- diazaspiro[5.5]undecanyl]methanone (3 mg, 9 %) as a white solid. ESI—MS m/z calc. 495.5, found 496.7 (M+1)+; Retention time: 1.99 minutes (3 min run); 1H NMR (400 MHz, DMSO) 5 7.27 — 7.13 (m, 2H), 6.96 (d, J = 9.0 Hz, 1H), 6.82 (d, J = 1.2 Hz, -242— 1H), 4.86 (dd, J = 12.0, 4.7 Hz, 1H), 4.71 - 4.54 (m, 1H), 3.32 — 3.14 (m, 5H), 3.07 (dd, J = 11.5, 2.6 Hz, 1H), 2.90 = 18.3, 7.2 Hz, 1H), 2.41 - 2.83 (m, 1H), 2.70 (dd, J - 2.23 (m, 6H), 2.13 (s, 3H), 1.64 - 1.39 (m, 3H), 1.29 (d, J = 6.0 Hz, 6H). ation of [8-(2,2-diflu0roethyl)—10-(1—methylimidazolyl)— -3,8-diazaspir0[5.5]undecanyl]-(4-isopropoxymethyl— phenyl)methanone Step 1: ] To a solution of [8-benzyl(1,2-dihydroxyethyl)-l1—oxa-3,8- diazaspiro[5.5]undecanyl]-(4-isopropoxy—3—methyl-phenyl)methanone (417 mg, 0.86 mmol) in THF (10 mL) was added NaIO4 (468 mg, 2.19 mmol) and H20 (4 mL).

The reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was filtered and partitioned between sat. aq. sodium bicarbonate/ethyl acetate. The aqueous layer was extracted further with ethyl acetate (3 x 50 mL). The organics were combined, washed with sat. aq. sodium bicarbonate (50 mL), dried over MgSO4, filtered and concentrated in vacuo to yield yl(4-isopropoxymethyl- benzoyl)oxa—3,8-diazaspiro[5.5]undecanecarbaldehyde (3 84 mg, 99 %) as a White solid . ESI-MS m/z calc. 450.3, found 451.3 (M+1)+; Retention time: 1.33 minutes (3 min run).

[00654] Step 2: Oxaldehyde (543.1 ML of 40 %w/w, 4.75 mmol) was added to a solution of 8-benzyl—3-(4-isopr0poxy—3-methyl-benzoyl)—11—0xa—3,8- diazaspiro[5.5]undecane—10-carbaldehyde (306 mg, 0.68 mmol) and ammonium hydroxide (881.4 uL of 30 %w/w, 6.79 mmol) in MeOH (3 mL) and the reaction —243— mixture was stirred at room temperature. After 3 hours, an additional 0.5 eq of oxaldehyde and 1.0 eq. of ammonium hydroxide were added and the reaction mixture was d for an additional 14 hours. The reaction mixture was partitioned between EtOAc and saturated aqueous NaHCOg, the layers were separated and the aqueous layer was extracted once more with EtOAc. The combined organics were dried over NaZSO4, filtered and concentrated in vacuo to give a dark oil. The residue was purified by silica gel column chromatography using 0—5% MeOH in DCM to yield [8-benzyl- lO-(lH-imidazol-Z—yl)—1 1-oxa—3,8—diazaspiro[5.5]undecan—3-yl]-(4-isopropoxy—3— methyl-phenyl)methanone (236 mg, 71 %) as a yellow solid. ESI-MS m/z calc. 488.3, found 489.5 (M+1)+ ; Retention time: 1.45 s (3 min run).

Step 3: [8-Benzyl-l 0-(1 H-imidazol-Z-y1)-l 1-oxa-3,8-diazaspiro[5.5]undecan- 3-y1]—(4-isopropoxy—3-methyl—phenyl)methanone (233 mg, 0.48 mmol) was suspended in a mixture of anhydrous DMF (1.5 mL) / THF (0.1 mL) under an atmosphere of nitrogen at 0 OC. NaH (19 mg, 0.48 mmol) was added and the on mixture was stirred for 30 minutes, then Mel (68 mg, 30 uL, 0.48 mmol) was added and the reaction mixture was d for 10 s. The reaction mixture was quenched with water and diluted with EtOAc, the layers were separated and the aqueous layer was extracted once more with EtOAc. The combined cs were washed with brine solution (2 x 5 mL), dried over NaZSO4, filtered and concentrated in vacuo to an oil. The residue was purified by silica gel column chromatography using 0—5% MeOH in DCM to yield [8- benzyl—l0-(1-methylimidazolyl)—l 1—oxa—3,8-diazaspiro[5.5]undecan—3 -yl]-(4- isopropoxy—3-methyl-phenyl)methanone (205 mg, 86 %) as a white foam. ESl-MS m/z calc. 502.3, found 503.1 (M+1)Jr ; Retention time: 1.51 minutes (3 min run); 1H NMR (400 MHz, DMSO) 5 7.38 = 8.4, 5.9, 2.2 Hz, 1H), 7.19 (d, - 7.30 (m, 4H), 7.25 (ddd, J J = 7.0 Hz, 2H), 7.10 (d, J =1.1Hz,1H), 6.96 (t, J = 5.9 Hz,1H), 6.75 (d, J =1.1Hz, 1H), 4.96 (ddd, J = 9.9, 6.7, 2.4 Hz, 1H), 4.68 = — 4.59 (m, 1H), 3.70 (s, 3H), 3.53 (td, J 13.6, 9.0 Hz, 3H), 3.30 - 3.15 (m, 2H), 2.93 (dd, J =11.1, 0.7 Hz,1H), 2.74 - 2.69 (m, 1H), 2.66 - 2.52 (m, 2H), 2.13 (s, 3H), 1.95 — 1.86 (m, 1H), 1.61 — 1.33 (m, 4H), 1.28 (d, J = 6.9 Hz, 6H).

Step 4: To a solution of [8-benzy1—10-(l-methylimidazolyl)—11-oxa-3,8— diazaspiro[5.5]undecan—3-yl]-(4-isopropoxy—3-methyl-phenyl)methanone (50 mg, 0.10 mmol) in EtOH (500 uL) was added Pd(OH)2 (6.98 mg, 0.01 mmol) and ammonium formate (29 mg, 0.46 mmol) and the reaction mixture was heated at 65°C for 1.5 hours.

The reaction mixture was cooled to room temperature, diluted with ethyl acetate, filtered and washed with sat. aq. NaHC03 (pH 10)/brine. The aqueous was extracted further with ethyl acetate. The combined cs were dried over Na2804, d and trated in vacuo to give (4-isopropoxy—3-methyl-phenyl)-[10-(1—methy1imidazol- 11—oxa-3,8-diazaspiro[5.5]undecan—3-yl]methanone (38 mg, 94 %) as a clear colorless oil. ESI-MS m/z calc. 412.2, found 413.3 (M+1)+ ; Retention time: 1.16 minutes (3 min run).

Step 5: 2,2-Difluoroethyl trifluoromethanesulfonate (24 mg, 0.11 mmol) was added to a mixture of (4-isopropoxy—3-methyl-phenyl)—[10-(1-methylimidazol—2-yl)— 11-oxa-3,8-diazaspiro[5.5]undecan-3—yl]methanone (38 mg, 0.09 mmol) and NaHC03 (23 mg, 0.28 mmol) in EtOH (0.3 mL). The reaction e was purged with argon, sealed and heated at 50 °C for 1 hour. The reaction mixture was cooled to room temperature, diluted with DMF (1 mL), and microfiltered. The residue was purified by Waters mass directed LC/MS: (1-99% ACN/ H20 (SmM HCl)) to yield [8-(2,2- difluoroethyl)—10-(1-methy1imidazolyl)—1 1-oxa-3 ,8—diazaspiro[5 . 5]undecan—3-yl]-(4- isopropoxy—3-methyl—phenyl)methanone hydrochloride salt (28 mg, 58 %). ESl-MS m/z calc. 476.3, found 477.3 (M+1)+; Retention time: 1.5 s (3 min run); 1H NMR (400 MHz, DMSO) 8 7.74 (d, J = 1.9 Hz, 1H), 7.69 (d, J = 1.9 Hz, 1H), 7.18 (dd, J = 6.0, 2.0 Hz, 2H), 7.04 - 6.90 (m, 1H), 6.20 (tt, J = 55.5, 4.0 Hz, 1H), 5.34 - 5.28 (m, 1H), 4.69 - 4.57 (m, 1H), 3.91 (s, 3H), 3.69 - 3.41 (m, 1H), 3.37 - 3.09 (m, 3H), 2.87 (ddd, J = 19.6, 18.4, 7.9 Hz, 3H), 2.57 = - 2.51 (m, 2H), 2.46 - 2.31 (m, 1H), 2.26 (d, J 11.6 Hz, 1H), 2.13 (s, 3H), 1.70 - 1.52 (m, 3H), 1.29 (d, J = 6.0 Hz, 6H).

Preparation of 8-(2,2-difluor0ethyl)—10-(1-ethylpyrazolyl) oxa-3,8-diazaspiro[5.5]undecanyl]-(4-isopropoxymethyl—phenyl)methanone 2012/028882 and 8-(2,2-difluoroethyl)—10-(2—ethylpyrazolyl)oxa-3,8- diazaspiro [5.5] undecan—3-yl]-(4-isopr0poxy—3-methyl-phenyl)methanone F F W N” K O

[00663] To 8-(2,2-difluoroethyl)-l0-(lH-pyrazol-3—yl)-l l-oxa-3,8- diazaspiro[5.5]undecane (193 mg, 0.54 mmol), 4-isopropoxy—3-methy1-benzoic acid (110 mg, 0.56 mmol) and HATU (215 mg, 0.56 mmol) was added N,N— dimethylformamide (1.3 mL). The reaction mixture was stirred for 5 minutes at room temperature, then diisopropylethylamine (3 74 “L, 2.15 mmol) was added and the reaction mixture was stirred overnight. The reaction mixture was then diluted with sat.

NaHC03 (5 mL) and the aqueous layer was extracted with ethyl acetate (2 x 10 mL).

The combined organic layer was washed with water (5 mL), dried over MgSO4, filtered and concentrated in vacuo. The residue was passed h a silica gel plug, eluting with 30% EtOAc/DCM. The solvent was concentrated in vacuo and the residue was dissolved in N,N-dimethy1formamide (1.3 mL) under an atmosphere of nitrogen, cooled to 0 °C, then treated with NaH (21 mg, 0.54 mmol). The reaction mixture was stirred at 0 °C for 10 minutes, then at room ature for 5 minutes, then iodoethane (50 uL, 0.63 mmol) was added and the reaction mixture stirred for 1 hour. The reaction mixture was diluted with methanol, microfiltered and purified by preparative LCMS (10-99% ter, 5 mM HCl modifier) to give 8-(2,2-difluoroethyl)-l0-(1- ethylpyrazolyl)-1 1—oxa-3 ,8—diazaspiro[5 . 5]undecanyl]—(4-isopropoxy—3 -methy1- phenyl)methanone (26 mg, 14 %) and 8-(2,2-difluoroethyl)-l0~(2-ethy1pyrazoly1)- 1 l -oxa—3 , 8~diazaspiro[5 . 5 an—3 -yl] -(4-isopropoxymethy1-phenyl)methanone (24 mg, 13 %).

] Data for 8—(2,2-difluoroethyl)-l 0-(1 pyrazol—3-y1)-1 l-oxa—3,8— diazaspiro[5.5]undecanyl-(4-isopropoxy—3-methyl-phenyl)methanone: ESl—MS m/z calc. 490.3, found 491.3 (M+1) + ; Retention time: 1.89 minutes (3 min run); 1H NMR 2012/028882 (400 MHz, CD3CN) 5 7.54 (d, J = 2.3 Hz, 1H), 7.20 - 7.17 (m, 2H), 7.00-6.71 (m, 1H), 6.92 (d, J = 9.0 Hz, 1H), 6.34 (d, J = 2.3 Hz, 1H), 5.26 (d, J = 10.2 Hz, 1H), 4.66 — 4.60 (m, 1H), 4.14 (q, J z 7.3 Hz, 2H), 3.63 = - 3.13 (m, 3H), 3.08 (d, J — 3.35 (m, 5H), 3.37 13.2 Hz, 1H), 2.95 (d, J = 12.6 Hz, 1H), 2.18 (s, 3H), 1.75 - 1.55 (m,4H), 1.41 (t, J = 8 Hz, 3H), 1.32 (d, J = 6.0 Hz, 6H).

Data for 8-(2,2—difluoroethyl)-l0-(2—ethy1pyrazol—3—yl)—1 1-oxa—3,8- diazaspiro[5 ESI—MS m/z . 5 ] undecan-3 -yl-(4~isopropoxy—3 -methyl-phenyl)methanone: calc. 490.3, found 491.5 (M+l)+; Retention time: 1.82 minutes (3 min run); 1H NMR (400 MHz, CD3CN) 8 7.45 (s, 1H), 7.22 - 7.20 (m, 2H), 6.94 (d, J = 8 Hz, 1H), 6.63 — 6.34 (m, 1H), 6.34 (s, 1H), 6.29 (s, 1H), 5.29 (d, J = 8.6 Hz, 1H), 4.74 - 4.54 (m, 1H), 4.24 (q, J = 7.0 Hz, 2H), 3.40 - 3.09 (m, 6H), 3.05 - - 2.59 (m, 3H), 2.20 (s, 3H), 1.89 1.50 (m, 4H), 1.43 (t, J = 8 Hz, 3H), 1.34 (d, J = 6 Hz, 6H).

Preparation of tert—butyl 8-(2,2-difluor0ethyl)—10-(1- methylpyrazol—3-yl)—11-0xa—3,8—diazaspiro[5.5]undecane—S-carboxylate and tert- butyl 8-(2,2-diflu0r0ethyl)—10-(2-methylpyrazolyl)-1l-oxa-3,8- diazaspiro[5.5] undecane—B-carboxylate F F KKF H\F N N Mob Mob /N’|N NECK \N’N\ NEE/OK A solution tert—butyl 8-(2,2—difluoroethyl)—10-propynoyl-1l-oxa—3,8— diazaspiro[5.5]undecane—3-carboxylate (40 mg, 0.11 mmol), hydrazine (69 mg, 67 uL, 2.15 mmol) and ethanol (800 11L) was stirred for one hour at room temperature. The reaction e was concentrated in vacuo, diluted with 1:1 of 1M aq. NaOH/ sat. aq.

NaHCO3 (2 mL), and extracted with DCM (3 x 3 mL). The combined cs were dried over MgSO4, filtered and trated in vacuo to give the pyrazole ediate, which was dissolved in MN—dimethylformamide (0.5 mL) and NaH (8 mg, 0.20 mmol) was added. The reaction mixture was stirred for 20 minutes at room temperature, then iodomethane (30 mg, 13 11L, 0.21 mmol) was added and the reaction mixture was stirred for 2 hours. The reaction mixture was concentrated in vacuo and the residue was —247- purified by silica gel column chromatography using 0-100% EtOAc/DCM as eluent to give tert-butyl 8-(2,2-difluoroethyl)(1-methylpyrazol-3—yl)—11-oxa—3,8- diazaspiro[5.5]undecane—3—carboxylate and tert—butyl 8—(2,2-difluoroethyl)(2- pyrazol—3-yl)—11—oxa—3,8-diazaspiro[5.5]undecanecarboxylate as a colorless foam in a 1:1 mixture (36 mg, 84 %). ESI—MS m/z calc. 400.2, found 401.5 (M+1)+ ; Retention time: 1.63 and 1.71 minutes (3 min run); 1H NMR (400 MHz, CDC13) 5 7.34 - 4.78 (m, 1H), 3.89 - - 7.21 (m, 1H), 6.17 - 6.10 (m, 1H), 5.95 - 5.64 (m, 1H), 4.85 3.79 (m, 3H), 3.74 - 3.48 (m, 2H), 3.28 — 2.60 - 3.04 (m, 2H), 2.99 - 2.94 (m, 1H), 2.75 (m, 3H), 2.50 - 1.37 (m, 9 H). - 2.32 (m, 2H), 1.60 - 1.41 (m, 4 H), 1.39

[00668] Preparation of 8-(2,2-diflu0roethyl)—10-(1-methylpyrazol—3-yl)—11- oxa-3,8-diazaspiro[5.5]undecanyl]-(4-isopropoxymethyl-phenyl)methan0ne and 8-(2,2-diflu0r0ethyl)—10-(2-methylpyrazol—3-yl)—11-0xa-3,8- piro[5.5]undecan-3—yl]—(4-isopropoxy-3—methyl-phen‘meethanone The mixture of regioisomeric pyrazoles, utyl - difluoroethyl)—10-(2—methylpyrazol-3—yl)-l 1-oxa-3 ,8-diazaspiro[5 .5]undecane—3- carboxylate and tert—butyl 8—(2,2-difluoroethyl)(2-methylpyrazolyl)~11-oxa—3,8- diazaspiro[5.5]undecanecarboxylate (31 mg, 0.08 mmol) was dissolved in ethanol (100 uL) and HCl (193.5 uL of 4 M in dioxane, 0.77 mmol) was added. The reaction mixture was stirred for 2 hours at room temperature, and then concentrated in vacuo. 4- Isopropoxy—3-methyl—benzoic acid (15.04 mg, 0.08 mmol), HATU (29 mg, 0.08 mmol) and N,N—dimethylformamide (484 uL) were added, followed by the addition of diisopropylethylamine (54 uL, 0.31 mmol). The reaction mixture was stirred for 2 hours at room temperature, then diluted with methanol, microfiltered and purified by preparative LCMS (IO-99% ACN/Water, 5 mM HCl modifier) to give the title compounds as white solids.

Data for 8-(2,2-difluoroethyl)—10-(1-methylpyrazolyl)—11-0xa—3,8- piro[5.5]undecanyl-(4-isoprop0xymethyl—phenyl)methanone: ESI—MS m/z calc. 476.3, found 477.3 (M+1)+; Retention time: 1.77 minutes (3 min run); 1H NMR (400 MHZ, CD3CN) 8 7.50 (d, J = 2.3 Hz, 1H), 7.21 - - 7.17 (m, 2H), 7.00 6.69 (m, 1H), 6.92 (d, J = 9.1 Hz, 1H), 6.35 (d, J = 2.3 Hz, 1H), 5.26 (d, J = 9.6 Hz, 1H), 4.66 - 4.60 (m, 1H), 3.85 (s, 3H), 3.67 - 3.37 (m, 5H), 3.36 = 12.7 - 3.01 (m, 4H), 2.95 (d, J Hz, 1H), 2.18 (s, 3H), 1.81 = 5.4 Hz, 6H). - 1.51 (m, 4H), 1.32 (t, J

[00671] Data for 8-(2,2—difluoroethyl)—10-(2—methy1pyrazol—3-yl)—l l-oxa—3,8- diazaspiro[5.5]undecan-3—yl-(4-isopr0poxymethyl-phenyl)methanone: 1H NMR (400 MHz, CD3CN) 5 7.39 (d, J = 1.9 Hz, 1H), 7.24 - 7.19 (m, 2H), 6.92 (d, J = 9.0 Hz, 1H), 6.72 — 4.61 - 5.26 (m, 1H), 4.70 - 6.39 (m, 1H), 6.28 (d, J :19 Hz, 1H), 5.32 (m, 1H), 3.90 (s, 3H), 3.49 - 2.69 (m, 4H), 2.21 — 3.19 (1n, 6H), 3.05 (s, 3H), 1.85 - 1.54 (m, 4H), 1.30 (t, J = 10.1 Hz, 6H); ESI-MS m/z calc. 476.3, found 477.4 (M+1) ; Retention time: 6.04 minutes (15 min run). (4-(2,2-Difluoroethyl)(1-methyl-1H-pyrazol—3 -yl)—1-oxa—4,9- piro[5.5]undecan-9—yl)(3-fluoro~4-isopropoxyphenyl)methanone was prepared using the procedure as described above, using 3-fluoroisopropoxy—benzoic acid as the acid reagent.

Preparation of 8-(2,2-difluoroethyl)—9-phenyl—11-0xa—3,8- diazaspiro[5.5]undecanyl]-(4-isopropoxymeth0xy-phenyl)methanone ] Step 1:

[00675] To a solution of tert—butyl 8-[(4-methoxyphenyl)methyl]—9-pheny1—1 1- oxa-3,8-diazaspiro[5.5]undecanecarboxylate (500 mg, 1.11 mmol) in DCM (1 mL) —249- WO 25613 was added HCl (3 mL of 4 M in dioxane, 11.05 mmol) se. The reaction mixture was stirred overnight at room temperature. The solvent was concentrated in vacuo and the residue was dissolved in the minimum amount of DCM and precipitated with ether.

The solvent was decanted and the residue was again washed with ether and dried to give 8—[(4—methoxypheny1)methyl]phenyl- 1 1-oxa—3 ,8—diazaspiro[5.5]undecane (400 mg, 93 %). ESI-MS m/z calc. 352.2, found 353.7 (M+1)+; Retention time: 0.99 minutes (3 min run).

] Step 2: To a solution of 8-[(4-methoxyphenyl)methyl]—9-phenyloxa—3,8- diazaspiro[5.5]undecane (400 mg, 1.03 mmol) in DMF (2 mL) was added DIEA (266 mg, 358 uL, 2.06 mmol) followed by the addition of 4-isopropoxymethoxy—benzoic acid (238 mg, 1.13 mmol) and HATU (469 mg, 1.23 mmol). The reaction e was stirred for 10 minutes at room temperature. The reaction mixture was quenched with water and the s layer was extracted with ethyl acetate. The organic layer was washed with water (3 x 10 mL), dried over MgSO4, filtered and concentrated in vacuo.

The crude material was purified by silica gel column chromatography using 0 to 60% EtOAc in hexanes as eluent to obtain (4-isopropoxy-3—methoxy-phenyl)—[8—(4- methoxyphenyl)methyl]phenyl-1 1 -oxa—3 ,8-diazaspiro[5 . 5 ]undecan-3 -ylmethanone (300 mg, 54 %). 1H NMR (400 MHz, CDC13) 8 7.40 — 7.18 (m, 7H), 6.97 — 6.78 (m, 5H), 4.94 — 4.71 (m, 1H), 4.59 — 4.50 (m, 1H), 4.33 — 4.17 (m, 1H), 3.83 (d, J = 13.0 Hz, 6H), 3.69 — 3.39 (m, 3H), 3.32 (d, J =13.0 Hz, 1H), 3.02 — 2.89 (m, 1H), 2.80 (s, 2H), 2.69 — 2.48 (m, 2H), 2.09 — 1.85 (m, 2H), 1.37 (d, J = 6.1 Hz, 6H), 1.29 — 1.14 (m, 1H), 0.95 — 0.79 (1n, 1H); ESI-MS m/z calc. 544.7, found 545.3 (M+1)+; Retention time: 1.58 minutes (3 min run).

[00678] Step 3: To (4—isopropoxy—3-methoxy—phenyl)—[8—[(4-methoxyphenyl)methyl]- 9-phenyloxa-3,8-diazaspiro[5.5]undecanyl]methanone (175 mg, 0.32 mmol), Pd(OH)2 (129 mg, 0.9186 mmol) and ammonium e (405 mg, 6.43 mmol) was added ethanol. The reaction mixture was then heated at 65 °C for 16 hours. The reaction mixture was d, the solvent evaporated and the residue was purified by silica gel column chromatography using 0 to 60% EtOAc in hexanes as eluent to give (4-isopropoxy—3 -methoxy—phenyl)—(9-phenyl—1 1-oxa-3 ,8-diazaspiro[5 .5]undecan-3 - yl)methanone. ESI—MS m/z calc. 424.5, found 425.5 (M+1)+; Retention time: 1.28 minutes (3 min run).

Step 4: To a solution of (4-isopropoxymethoxy-phenyl)—(9-phenyl-l l-oxa— 3,8-diazaspiro[5.5]undecanyl)methanone (15 mg, 0.04 mmol) in ethanol (375 uL) was added NaHCO3 (12 mg, 0.14 mmol), followed by the addition of 2,2-difluoroethyl romethanesulfonate (11 mg, 0.05 mmol). The reaction mixture was heated at 80° C for 16 hours. The reaction mixture was filtered and purified by Waters mass directed LC/MS: (1-99% ACN/ HZO (SmM HCl) to obtain [8—(2,2—difluoroethyl)phenyl-1 1- 8-diazaspiro[5.5]undecan-3~y1]-(4—isopropoxy—3-methoxy-phenyl)methanone (5 mg, 29 %). 1H NMR (400 MHz, CDC13) 5 7.45 - 7.36 (m, 5H), 6.98 - 6.83 (m, 3H), .25 (d, J = 10.4 Hz, 1H), 4.57 (dt, J = 12.2, 6.1 Hz, 1H), 3.85 (s, 3H), 3.60 (d, J = 10.9 Hz, 1H), 3.47 — 3.12 (m, 6H), 2.86 - 2.60 (m, 3H), 1.88 = 6.1 - 1.50 (m, 5H), 1.38 (d, J Hz, 6H); ESI-MS m/z calc. 488.5, found 489.7 (M+1)+; Retention time: 2.17 minutes (3 min run). (4—Isopropoxy—3—methoxy-phenyl)-[9-phenyl—8—(2,2,2-trifluoroethyl)— 1 l-oxa—3,8-diazaspiro[5.5]undecan-3—yl]methanone was prepared using the chemistry described above using 2,2,2—trifluoroethyl trifluoromethanesulfonate in step 4. ESI-MS m/z calc. 506.6, found 507.5 (M+1)+; ion time: 2.27 minutes (3 min run).

Preparation of [10-ethyl—8-(2,2,2-triflu0r0ethyl)—11-0xa—3,8- diazaspiro[5.5]undecanyl]-(4-isopr0poxy—3-methyl-phenyl)methanone $03»,ng Step 1:

[00685] To utyl 8-benzylViny1-l 1~oxa-3 ,8-diazaspiro[5 .5]undecane—3 - carboxylate (600 mg, 1.61 mmol) in ethanol (1 mL) was added HCl (4.028 mL of 4 M in dioxane, 16.11 mmol) and the on mixture was stirred for 30 minutes. The -251— reaction mixture was concentrated in vacuo, then DMF (4 mL), ropoxy—3— methyl-benzoic acid (313 mg, 1.61 mmol) and HATU (613 mg, 1.61 mmol) were added and the reaction mixture was stirred for 10 minutes. Triethylamine (898 uL, 6.44 mmol) was added and the reaction mixture was stirred for 16 hours, The reaction e was concentrated in vacuo, diluted with DCM (5 mL), washed with 1 N aq.

NaOH (2 mL) and brine (2 mL), dried over MgSO4, filtered and concentrated in vacuo. column chromatography using 0-100% . The crude material was purified by silica gel EtOAc/hexanes eluent to give (8-benzy1-10—viny1oxa-3,8-diazaspiro[5.5]undecan- 3-y1)-(4-isopropoxymethy1-phenyl)methanone (715 mg, 99 %) as a pale yellow oil. 1H NMR (400 MHz, CDC13) 8 7.35 = 8.2 - 7.22 (m, 5H), 7.20 - 7.14 (m, 2H), 6.79 (d, J Hz, 1H), 5.83 = 10.6 Hz, 1H), 4.59 - - 5.74 (m, 1H), 5.34 - 5.26 (m, 1H), 5.15 (d, J 4.50 (m, 1H), 4.33 = 11.0 Hz,1H), 2.56 - 4.14 (m, 2H), 3.59 - 3.14 (m, 7H), 2.79 (d, J (d, J =11.1Hz,1H), 2.19(s,3H), 1.91 —1.80(m,2H), 1.69 = - 1.39 (m, 2H), 1.34 (d, J 6.0 Hz, 6H); EST-MS m/z calc. 448.6, found 449.5 (M+1)+; Retention time: 1.48 minutes (3 min run).

Step 2: To (8-benzylvinyl-1 1-oxa—3,8-diazaspiro[5.5]undecanyl)—(4- isopropoxy—3-methyl-pheny1)methanone (150 mg, 0.33 mmol), ammonium formate (74 mg, 1.17 mmol) and Pd (17 mg, 0.02 mmol) (10% on activated carbon) was added methanol (2 mL) and the reaction mixture was heated at 75 0C for 30 minutes. The reaction mixture was , microfiltered and concentrated in vacuo, then diluted with DCM (20 mL), washed with aq. 1M NaOH (10 mL), extracted with DCM (120 mL), washed with brine (10 mL), dried over MgSO4 and concentrated in vacuo to give (10- ethyl-l l—oxa-3 ,8-diazaspiro[5.5]undecan—3-y1)-(4-isopropoxy—3—methy1— )methanone (100 mg, 83 %) as a colorless oil. ESI-MS m/z calc. 360.5, found 361.3 (M+1)+; Retention time: 1.25 s (3 min run).

Step 3: To hy1-11—oxa-3,8-diazaspiro[5.5]undecany1)-(4-isopropoxy— 3-methy1-pheny1)methanone (33 mg, 0.09 mmol) in ethanol (0.5 mL) was added NaHC03 (15mg, 0.18 mmol) then iodoethane (21 mg, 11 uL, 0.14 mmol). The on mixture was heated at 50 °C for 16 hours, then microfiltered and purified by prep -252— LCMS (1-99%‘ACN/Water, 5 mM HCl modifier) to give (8,10-diethyl-l1—oxa—3,8- diazaspiro[5.5]undecan-3—yl)-(4-isopropoxy—3-methy1—phenyl)methanone hydrochloride salt (39 mg, 100 %); ESI—MS m/z calc. 388.3, found 389.7 (M+l)+; Retention time: 1.36 (3 min run). [l0-ethyl—8-(2,2,2-trifluoroethyl)-1 l -oxa-3,8-diazaspiro[5.5]undecan- (4-isopropoxy—3-methyl-phenyl)methanone was also prepared using the procedure above using 2,2,2—trifluoroethyl trifluoromethanesulfonate in step 3. ESI-MS m/z calc. 442.2, found 443.7 ; Retention time: 2.33 (3 min run).

Preparation of (8-benzyl—10-ethyl—11-0xa—3,8— diazaspiro[5.5]undecanyl)—(4-isopropoxymethyl-phenyl)methanone Joby? ] A mixture of(8-benzyl-10~Vinyl—11-oxa-3,8—diazaspiro[5.5]undecan yl)-(4-isopropoxy—3—methyl-pheny1)methanone (50 mg, 0.11 mmol) and Pd (4 mg, 0.003 mmol) (10 % on activated carbon) in methanol (1 mL) was stirred under an atmosphere of en for 2 hours. The reaction mixture was microfiltered and purified by prep LCMS (10-99% ACN/Water, 5 mM HCl modifier) to give (8-benzyl- -ethy1—1 1-oxa-3,8—diazaspiro[5.5]undecan-3 -y1)-(4—isopropoxy—3-methy1— phenyl)methanone hydrochloride salt (8 mg, 15 %) as a white solid. ESl—MS m/z calc. 450.3, found 451.5 (M+1)+; ion time: 1.36 minutes ( 3 min run).

[00693] Preparation of [8-benzyl—10-(hydr0xymethyl)—1l-oxa—3,8— diazaspiro[5.5]undecan-S-yl]-(4-is0propoxy—3-methyl—phenyl)methanone N23 \ HOVEOJO‘m/Ejof -253— To (8-benzyl—10-vinyl-1 1-oxa—3,8-diazaspiro[5.5]undecanyl)-(4- isopropoxy—3-methyl-phenyl)methanone (135 mg, 0.30 mmol) in DCM (4 mL) and methanol (1 mL) at —78 °C was bubbled ozone until the solution turned faint blue.

NaBH4 (91 mg, 2.41 mmol) and methanol (~2 mL) was added under an atmosphere of nitrogen and the reaction e was stirred at —78 °C for 30 minutes, then at 0 °C for 1 hour. The reaction mixture was concentrated in vacuo, quenched with 4N HCl/ dioxane, concentrated in vacuo, then diluted with methanol—water (1 :1), microfiltered and purified by prep LCMS (1-99% ACN/Water, 5 mM HCl modifier) to give [8- benzyl-l 0-(hydroxymethyl)-l 1-oxa—3 ,8-diazaspiro[5.5]undecan-3—yl]—(4-isopropoxy—3- methyl-phenyl)methanone (50 mg, 34 %). ESI—MS m/z calc. 452.6, found 453.5 (M+1)+; Retention time: 1.18 minutes ( 3 min run). ] ation of [10-(eth0xymethyl)ethyl—11—0xa-3,8- diazaspiro[5.5]undecanyl]-(4-isopropoxy—3-methyl—phenyl)methanone coiibfior

[00696] Step 1: ] To [8-benzyl(hydroxymethyl)—1 1-oxa-3 ,8-diazaspiro[5.5]undecan- 3-yl]-(4—isopropoxy—3—methyl-phenyl)methanone hydrochloride salt (43 mg, 0.09 mmol) in DMF (0.5 mL) was added sodium e (11 mg, 0.30 mmol) and the on mixture was stirred for 20 minutes. Iodoethane (30 uL, 0.38 mmol) was added and the reaction mixture was stirred for 3 hours, then diluted with EtOAc, filtered, concentrated in vacuo. The residue was purified by silica gel column tography usinglO-IOO EtOAc/hexanes eluent to give the ether intermediate as pale yellow oil.

The oil was dissolved in methanol (0.6 mL), and Pd (5 mg, 0.004 mmol) and ammonium formate (27 mg, 0.44 mmol) were added and the reaction mixture was heated at 75 0C for 40 minutes. The reaction mixture was filtered, concentrated in vacuo, diluted with ethyl acetate, washed with 1:1 3M NaOH/sat. aq. NaHCO3, dried over MgSO4, d and concentrated in vacuo to give [lO-(ethoxymethyl)-l1-oxa- 3,8-diazaspiro[5.5]undecan—3—yl]-(4-isopropoxy—3—methy1-phenyl)methanone (25 mg, —254— 2012/028882 74 %) as a pale yellow oil found 391.3 (M+l)+; Retention . ESI-MS m/z calc. 390.5, time: 1.17 minutes ( 3 min run).

Step 2: To [lO-(ethoxymethyl)-1 3,8-diazaspiro[5.5]undecany1]-(4- isopropoxy—3-methyl-phenyl)methanone (25 mg, 0.06 mmol) and NaHC03 (16 mg, 0.19 mmol) in ethanol (0.5 mL) was added iodoethane (15 mg, 8 ML, 0.10 mmol) and the reaction mixture was heated in a sealed vial at 70 °C for 24 hours. The reaction mixture was microfiltered and purified by prep LCMS (1-99% ter, 5 mM HCl modifier) to give [10-(ethoxymethyl)-8—ethyloxa—3,8-diazaspiro[5.5]undecanyl]- (4-isopropoxy—3—methyl-phenyl)methanone hydrochloride salt (19 mg, 66 %) as a colorless oil. ESI-MS m/z calc. 418.3, found 419.7 (M+1)+; Retention time: 1.20 minutes (3 min run). ation of [8-benzyl—10-(1-hydr0xy-1—methyl-ethyl)—1l—oxa- 3,8—diazaspiro[5.5]undecanyl]-(4-is0propoxymethyl-phenyl)methanone Step 1: 8—Benzyl-3 -(4—isopropoxy—3-methyl-benzoyl)—1 1-oxa—3,8- diazaspiro[5.5]undecanecarboxylic acid (10 mg, 0.02 mmol), K2C03 (12 mg, 0.09 mmol) and iodomethane (2 uL, 0.03 mmol) in DMF (0.1 mL) was stirred for 1 hour.

The mixture was diluted with ethyl acetate (5 mL), washed with water (2 mL) and brine (2 mL), dried over magnesium sulfate, filtered and evaporated to give methyl 8- benzyl(4-isopropoxy—3—methyl—benzoyl)—1 l -oxa—3 ,8-diazaspiro[5.5]undecane-1 0- carboxylate (10mg, 100 %). ESI-MS m/z calc. 480.6, found 481.5 (M+l)+; ion time: 1.82 minutes ( 3 min run). -255— Step 2: To methyl 8-benzyl(4-isopropoxy—3-methyl—benzoyl)-l l-oxa—3,8~ diazaspiro[5.5]undecane—10—carboxylate (100 mg, 0.21 mmol) in THF (0.5 mL) at -78 °C was added chloro(methy1)magnesium (150 [LL of 3 M in THF, 0.45 mmol) and the reaction mixture was stirred for 2 hours then allowed to warm to room temperature.

The reaction mixture was diluted with water, extracted with ethyl acetate and dried over MgSO4, then purified by silica gel column tography using 0-100% EtOAc/DCM as eluent to give [8—benzyl(1-hydroxy-l -methyl—ethyl)-l 3,8- piro[5.5]undecany1]-(4-isopropoxy—3-methy1-phenyl)methanone (81 mg, 80 %) as a white foam. ESl-MS m/z calc. 480.6, found 481.7 (M+l)+; Retention time: 1.22 minutes ( 3 min run).

Preparation of [10-(1-hydr0xy—1-methyl-ethyl)—8—(2,2,2- trifluoroethyl)—11-0xa-3,8-diazaspiro[5.5]undecanyl]-(4-isoprop0xy—3-methyl— phenyl)methan0ne %bYfij rN O 0 Step 1: [8-Benzy1—10-(1 -hydroxy—l-methyl-ethyl)-1 1-oxa-3,8- diazaspiro[5.5]undecanyl]-(4-isopropoxy—3-methy1-pheny1)methanone (75 mg, 0.16 mmol) was dissolved in ethanol (3 mL) and Pd (8 mg, 0.008 mmol) and ammonium formate (50 mg, 0.80 mmol) were added and the reaction mixture was heated at 75 °C for 30 minutes. The reaction mixture was filtered, concentrated in vacuo, diluted with ethyl acetate, washed with 3M NaOH, dried over MgSO4, d and concentrated in vacuo to give (2-(2-hydroxypropanyl)oxa-4,9-diazaspiro[5.5]undecan-9—yl)(4- isopropoxy—3-methylphenyl)methanone (60 mg, 94 %). ESI—MS m/z calc. 390.3, found 391.5 (M+1)+; ion time: 1.27 minutes ( 3 min run). —256- Step 2: (2-(2-Hydroxypropanyl)oxa—4,9-diazaspiro[5.5]undecanyl)(4- isopropoxy—3-methylphenyl)methanone (25 mg, 0.06 mmol) was dissolved in dry ethanol (300 uL) and NaHC03 (50 mg, 0.60 mmol) and 2,2,2-trifluoroethyl trifluoromethanesulfonate (20 uL, 0.13 mmol) were added and the reaction mixture was heated at 80 0C for 16 hours. The reaction mixture was filtered, concentrated in vacuo and purified by silica gel column chromatography using 0-100% EtOAc/hexanes as eluent to give -hydroxy—1-methyl-ethy1)(2,2,2-trifluoroethyl)—1 1-oxa-3,8- diazaspiro[5.5]undecanyl]-(4-isopropoxy—3-methyl-phenyl)methanone (15 mg, 53 %) as a colorless oil. ESI-MS m/z calc. 472.5, found 473.5 (M+1)+; Retention time: 1.93 minutes ( 3 min run).

Preparation of [8-benzyl—10-(2-hydr0xyethyl)—11-0xa-3,8- diazaspiro[5.5]undecan-3—yl]-(4-isopr0poxy—3-methyl-phenyl)methanone

[00711] To (8—benzylvinyl-l 1-oxa—3,8-diazaspiro[5.5]undecan—3-yl)—(4- poxy—3—methyl-phenyl)methanone (95 mg, 0.21 mmol) and chloro— tris(triphenylphosphoranyl)rhodium (6 mg, 0.006 mmol) in THF (1 mL) was added catecholborane (635 ML of 1 M in THF, 0.64 mmol) at 0 °C and the reaction mixture was d at room temperature for 1 hour. Sodium ide (0.3 mL of 3 M, 0.90 mmol) was added slowly, followed by the addition of H202 (0.3 mL of 30 %w/w, 2.94 mmol) and the reaction mixture was stirred for 15 minutes. The reaction e was extracted three times with ethyl acetate and the ed organics were concentrated in vacuo and purified by prep LCMS (1-99% ACN/Water, 5 mM HCl modifier) to give [8—benzyl—10—(2—hydroxyethyl)-1 1 -oxa-3 ,8—diazaspiro[5 . 5]undecan-3 -yl] -(4- isopropoxy—3-methyl-pheny1)methanone hydrochloride salt (55 mg, 50 %) as a pale yellow solid. ESI—MS m/z calc. 466.3, found 467.3 (M+1)+; Retention time: 1.01 minutes ( 3 min run).

Preparation of [10-(2-hydroxyethyl)—8—(2,2,2-trifluoroethyl)—1 1- oxa—3,8-diazaspiro[5.5]undecanyl]-(4-isopr0poxy—3-methyl-phenyl)methanone Step 1: To a on of [8—benzyl(2-hydroxyethyl)—11-oxa-3,8— diazaspiro [5 . 5]undecan-3 -y1] -(4—isopropoxy—3 -methy1-phenyl)methanone hydrochloride salt (40 mg, 0.08 mmol) in methanol (750 ML) was added Pd (4 mg, 0.004 mmol) and ammonium formate (25 mg, 0.39 mmol), and the reaction mixture was heated at 75 0C for 1 hour. The reaction mixture was microfiltered and purified by prep LCMS (1-99% ACN/Water, 5 mM HCl modifier) to give [10-(2—hydroxyethyl)- 1 3 ,8-diazaspiro[5.5]undecanyl]-(4—isopropoxy—3 -methyl-phenyl)methanone hydrochloride salt (20 mg, 62 %). ESI-MS m/z calc. 376.2, found 377.3 (M+1)+; Retention time: 1.01 minutes (3 min run).

Step 2: ] To [10-(2-hydroxyethyl)-1 3,8-diazaspiro[5.5]undecany1]-(4— isopropoxy—3-methy1—phenyl)methanone hydrochloride salt (20 mg, 0.05 mmol) and NaHCO3 (16 mg, 0.19 mmol) in ethanol (0.5 mL) was added 2,2,2-trifluoroethyl trifluoromcthanesulfonate (11 uL, 0.07 mmol) and the reaction mixture heated in a sealed Vial at 80 °C for 5 hours. The reaction e was ltered and purified by prep LCMS (10—99% ACN/Water, 5 mM HCl modifier) to give [10-(2-hydroxyethyl)- 8—(2,2,2-trifluoroethyl)-1 1—oxa—3,8-diazaspiro[5.5]undecan-3—yl]-(4-isopropoxy—3- methyl-phenyl)methanone (16 mg, 87 %) as a colorless oil ESI—MS m/z calc. 458.2, found 459.7(M+1)+; Retention time: 1.78 minutes (3 min run).

Preparation of (4-isopropoxy—3-methyl-phenyl)—[10-(5- methyloxazol—Z-yl)—8-(2,2,2-trifluoroethyl)—11-oxa-3,8—diazaspiro[5.5]undecan yl]methanone Fa}F NW): )0\ fiN’O o N o

[00718] Step 1: T3P (546 mg, 510 uL of 50 %w/w, 0.86 mmol) was added to a solution- of 8—benzyl-3—(4-isopropoxy—3 -methyl-benzoyl)—1 3 ,8-diazaspiro[5 .5]undecane— -carboxylic acid (160 mg, 0.34 mmol), roxyacetamidine (25 mg, 0.34 mmol) and triethylamine (173 mg, 239 ML, 1.71 mmol) in 2-methyltetrahydrofuran (800 uL) and the reaction mixture was heated at 75 °C for 2 hours. The reaction mixture was cooled to room temperature and ioned between EtOAc/saturated aq. NaHCO3.

The layers were separated and the aqueous layer was extracted with EtOAc (2 x). The combined organics were dried over Na2804, filtered and concentrated in vacuo to a dark foam. The crude t was purified by silica gel column chromatography using 0—30% EtOAc in DCM as eluent to afford [8-benzyl-l0-(3-methyl-l,2,4-oxadiazol y1)-1 3,8-diazaspiro[5.5]undecan-3 -yl]—(4-isopropoxy-3 -methyl- phenyl)methanone (67 mg, 39 %) as a white solid . ESI—MS m/z calc. 504.6, found 505.3 (M+1)+; Retention time: 1.63 minutes (3 min run).

Step 2:

[00721] A solution of l-chloroethyl chloroformate (89 uL, 0.80 mmol) in DCE (0.1 mL) was added to a stirred solution of [8-benzyl—10-(3-methyl—1,2,4-oxadiazol y1)-l l-oxa—3 ,8—diazaspiro[5 . 5]undecan-3 -yl] -(4-isopropoxy-3 l- )methanone (67 mg, 0.13 mmol) in DCE (488 uL) under an atmosphere of nitrogen and the reaction mixture was heated to reflux. After 1 hour, an additional aliquot of 1—chloroethyl chloroformate (89 uL, 0.80 mmol) was added and the reaction WO 25613 2012/028882 mixture was heated to reflux for a further 8 hours. After 8 hours, an additional 1- chloroethyl chloroformate (89 uL, 0.80 mmol) was added and the reaction e was heated to reflux for a further 15 hours. The excess solvent was removed under reduced re and the carbamate intermediate was dissolved in MeOH (2 mL) and heated at reflux for 1 hour. The reaction mixture was cooled to room temperature, filtered and purified by Waters mass directed LC/MS-HPLC: (lo-99% ACN/ H20 (SmM HCl)) to afford (4-isopropoxy—3-methy1-phenyl)—[10-(3-methy1-1,2,4-oxadiazolyl)-1 1-oxa— 3,8—diazaspiro[5.5]undecany1]methanone hydrochloride salt (28 mg, 47 %). ESI-MS m/z calc. 414.2, found 415.7 (M+1)+; Retention time: 1.54 s (3 min run).

[00722] Step 3: A mixture of (4-isopropoxymethyl-phenyl)-[1 0-(3-methyl-1 ,2,4- oxadiazol—S-y1)-1 l-oxa—3,8—diazaspiro[5 .5]undecanyl]methanone hydrochloride salt (28 mg, 0.06 mmol), 2,2,2-tn'fluoroethy1 trifluoromethanesulfonate (14 uL, 0.09 mmol) and NaHCO3 (21 mg, 0.23 mmol) was heated at 80°C in a sealed vial for 18 hours. The reaction e was allowed to cool to room temperature, microflltered and purified by Waters mass directed LC/MS: (lo-99% ACN/ H 2 O (SmM HC1)) and concentrated to yield (4-isopropoxy—3-methy1-pheny1)—[10-(5-methyloxazoly1)(2,2,2- trifluoroethyl)—l1-oxa—3,8-diazaspiro[5.5]undecan~3-y1]methanone (3 mg, 10 %) as a white solid. ESI-MS m/z calc. 496.5, found 497.7 (M+1)+; Retention time: 1.99 minutes (3 min run); 1H NMR (400 MHz, DMSO) 8 7.27 ; 7.06 (m, 2H), 6.96 (d, J = 9.1 Hz, 1H), 5.17 (dd, J = 13.6, 4.2 Hz,1H), 4.63 (dt, J = 12.1, 6.2 Hz, 1H), 3.31 - 3.19 (m, 5H), 2.92 — 2.81 (m, 1H), 2.67 (dd, J = 12.0, 10.1 Hz, 1H), 2.43 - 2.27 (m, 6H), 2.15 (s, 3H), 1.70 = 6.0 Hz, 6H). - 1.40 (m, 4H), 1.29 (d, J Preparation of 8—ethyl—3-(4-isopropoxymethyl-benzoyl) phenyl-l 1—0xa—3,8-diazaspir0[5.5] undecanone o N6 @1030, Q 0 o )\ WO 25613 Step 1: To a mixture of tert—butyl 4-hydroxy—4-[[(4- methoxyphenyl)methylamino]methyl]piperidinecarboxylate (1.06 g, 3.01 mmol) and diisopropylethylamine (1 mL, 5.74 mmol) in DCM (15 mL) at 0 °C was added 2- chloro—2-phenyl-acetyl chloride (654 mg, 3.46 mmol) and the reaction mixture was stirred at room ature for 16 hours. The reaction mixture was concentrated in vacuo and the residue was d by silica gel column tography using 0-100% EtOAc/DCM as eluent to give tert—butyl 4—[[(2-chlorophenyl-acetyl)-[(4— methoxyphenyl)methyl]amino]methyl]-4—hydroxy—piperidine-l-carboxylate (1.11 g, 73 %) as a pale yellow oil. ESI-MS m/z calc. 502.2, found 503.5 (M+1)+; Retention time: 1.90 minutes (3 min run).

] Step 2: To a suspension of tert—butyl 4-[[(2-chloro-2—phenyl-acetyl)-[(4- methoxyphenyl)methyl]amino]methyl]hydroxy—piperidine- l -carboxylate (322 mg, 0.64 mmol) in DMF (3 mL) at 0 °C was added NaH (27 mg, 0.67 mmol). The reaction mixture was allowed to warm to room temperature overnight, then diluted with water (10 mL) and extracted with ethyl acetate (3 x 15 mL). The combined organic layers were washed with water (10 mL) and brine (10 mL), dried over MgSO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel column chromatography using 0-40% EtOAc/DCM to give tert—butyl 10-[(4- methoxyphenyl)methyl]oxophenyl—7-oxa-3,10—diazaspiro[5.5]undecane carboxylate (215 mg, 72 %) as a colorless oil. ESI—MS m/z calc. 502.2, found 503.5 (M+1)+; Retention time: 1.90 minutes (3 min run).

] Step 3:

[00730] To tert—butyl 10-[(4-methoxyphenyl)methyl]-9—oxo-8—phenyloxa- iazaspiro[5.5]undecane—3-carboxy1ate (215 mg, 0.46 mmol) in acetonitrile (2.5 mL) was added water (2.5 mL) followed by the addition of ceric ammonium nitrate (500 mg, 0.91 mmol). The reaction mixture was stirred for 2 hours. After this time, a further aliquot of ceric ammonium nitrate (250 mg, 0.46 mmol) was added and the reaction mixture was stirred for an additional 45 s, it was then diluted with 1M aq. HCl, extracted with ethyl acetate (2 x 25 mL), dried over MgSO4 and concentrated —26l— in vacuo. The residue was ved in ol (1 mL) and HCl (1 mL of 4 M in dioxane, 4.00 mmol) was added. The reaction mixture was stirred for 1 hour, then concentrated in vacuo. to give 10-phenyl0xa-3,8-diazaspiro[5.5]undecan-9—one hloride salt (130 mg, 100%). ESI-MS m/z calc. 246.1, found 247.5 (M+1)+; Retention time: 0.46 minutes (3 min run).

Step 4: To ropoxy—3-methyl-benzoic acid (114 mg, 0.59 mmol), 4- phenyl-5—oxa-2,9-diazaspiro[5.5]undecan—3-one hydrochloride salt (166 mg, 0.59 mmol) and HATU (223 mg, 0.59 mmol) in DMF (0.5 mL) was added diisopropylethylamine (228 mg, 307 uL, 1.76 mmol) and the reaction mixture was d for 16 hours. The reaction mixture was concentrated in vacuo, diluted with methanol and purified by prep LCMS (1-99% ACN/HZO, 5 mM HCl modifier) to give 3-(4-isopropoxymethyl-benzoyl)—8-phenyl—7-oxa—3,10-diazaspiro[5.5]undecanone (100 mg, 40 %) as a yellow foam. ESI—MS m/z calc. 422.2, found 423.5 (M+1)+; Retention time: 1.61 minutes (3 min run).

Step 5: To a solution of 3-(4-isopropoxy-3—methyl-benzoyl)phenyl-7—oxa— 3,10—diazaspiro[5.5]undeean-9—one (65 mg, 0.15 mmol) in THF (1 mL) at 0 0C was added NaH (6 mg, 0.15 mmol) and the reaction e was stirred for 30 minutes.

Bromoethane (34 mg, 23 uL, 0.31 mmol) was added and the reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was concentrated in vacuo and purified by silica gel column chromatography using 0-100% EtOAc/DCM as eluent to give 2-ethyl—9-(4-is0propoxy-3~methyl-benzoyl)phenyloxa-2,9— diazaspiro[5.5]undecan—3-one as a viscous oil. 1H NMR (400 MHZ, CDClg) 8 7.48 - 7.43 (m, 2H), 7.39 — 7.29 (m, 3H), 7.23 - 7.17 (m, 2H), 6.81 (d, J = 8.2 Hz, 1H), 5.11 (s, 1H), 4.56 (dt, J = 12.1, 6.0 Hz, 1H), 3.63 (d, J = 12.4 Hz, 1H), 3.59 - 3.19 (m, 5H), 3.09 (d, J = 12.4 Hz, 1H), 2.92 (d, J = 28.7 Hz, 1H), 2.22 (s, 1H), 2.23 ~ 2.16 (m, 3H), 1.59 (s, 3H), 1.35 (d, J = 6.0 Hz, 6H), 1.14 (t, J = 7.2 Hz, 3H). ESI-MS m/z calc. 450.3, found 451.1 (M+1)+; Retention time: 1.76 minutes (3 min run). —262- WO 25613 Preparation of 2-isopentyl—9-[4-meth0xy (trifluoromethyl)benzoyl]phenyloxa—2,9-diazaspir0[5.5]undecanone oiohofiéi: Step 1:

[00737] NaBH4 (66 mg, 1.75 mmol) was added portionwise to a d solution of 4-(aminomethyl)-l -benzyl-piperidin—4-ol (167 mg, 0.76 mmol) and 3-methylbutanal (74 uL, 0.68 mmol) in MeOH (7.5 mL) and acetic acid (350 uL). The reaction mixture was stirred for 16 hours at room temperature, then quenched with H20 (5 mL). The aqueous layer was extracted with EtOAc (3 x 50 mL). The combined organics were dried over , filtered and concentrated in vacuo to provide an oil. To the oil was added pyridine (1 mL) followed by dropwise addition of (2,2,2-trifluoroacetyl) 2,2,2— trifluoroacetate (105 uL, 0.76 mmol) at room temperature. The reaction mixture was stirred vigorously for 30 minutes. The reaction mixture was ed with water and aqueous layer was extracted with EtOAc (3 x 100 mL), dried over NaZSO4, filtered and trated in vacuo. The residue was purified by silica gel column chromatography using 0-100% hexanes/EtOAc to provide N—[(l-benzylhydroxypiperidyl)methyl]- 2,2,2-trifluoro-N-isopentyl~acetamide (112 mg, 38 %) as a pale tan oil.

Step 2: Palladium (50.8 mg, 0.48 mmol) 10% on ted carbon and N—[(l— benzyl-4—hydroxy—4-piperidyl)methyl]-2,2,2-trifluoro-N—isopentyl-acetamide (112 mg, 0.29 mmol) in propanol (3 mL) was stirred under an atmosphere of hydrogen for 18 hours. The catalyst was filtered h celite® and washed with MeOH. The organics were concentrated in vacuo to provide a clear oil. To the oil was added DMF (2 mL) and triethylamine (40 [LL 0.29 mmol) and this solution was added dropwise to a solution 4-methoxy(trifluoromethyl)benzoic acid (64 mg, 0.29 mmol) and HATU (110 mg, 0.29 mmol) in DMF (1 mL). The reaction mixture was stirred for 16 hours.

The solution was ioned between water and EtOAc and the layers were separated.

The aqueous layer was extracted with EtOAc (3 x 100 mL). The combined organics were dried over , filtered, and trated in vacuo. The residue was taken up in MeOH and d by reverse phase HPLC ( Gilson 20-99% water/MeOH) to give 2,2,2—trifluoro-N—[[4—hydroxy—l-[4-methoxy—3-(trifluoromethyl)benzoyl] dyl]methyl]-N—isopentyl-acetamide (82 mg, 56 %). ESl-MS m/z calc. 498.5, found 499.5 (M+1)+; Retention time: 1.86 minutes (3 min run).

Step 3: Sodium hydroxide (1.4 mL of 0.2 M, 0.29 mmol) was added to a solution of 2,2,2-trifluoro-N—[[4-hydroxy—1-[4-methoxy—3-(trifluoromethyl)benzoyl] piperidyl]methyl]-N—isopentyl—acetamide (72 mg, 0.14 mmol) in MeOH (722 uL) and the reaction e was heated to 65 °C for 16 hours. The solution was partitioned between water (5 mL) and EtOAc (5 mL) and the aqueous layer was extracted with EtOAc (3x 5 mL). The combined organics were dried over NaZSO4, filtered, and concentrated in vacuo to e the crude amine as a clear oil (54 mg, 92%). ESI-MS m/z calc. 402.4, found 403.7 (M+1)+; Retention time: 1.34 minutes (3 min run). The residue was taken up in THF (480 uL) and added dropwise to a solution of potassium tert—butoxide (36 mg, 0.32 mmol) in tert—butanol (480 uL) and the reaction mixture was heated at 83 °C for 20 minutes. The solution was neutralized with AcOH, and partitioned between water (2 mL) and EtOAc (2 mL), the aqueous layer was extracted with EtOAc (3 x 2 mL). The combined organics were dried over Na2SO4, filtered, and concentrated in vacuo. The residue was dissolved in MeOH (3 mL) and purified by reverse phase HPLC (Gilson) 20-99% water/MeOH to provide 2-isopentyl—9—[4- methoxy(trifluoromethyl)benzoyl]phenyl—5-oxa-2,9—diazaspiro[5.5]undecan one (39 mg, 45 %) as a white foam. ESI—MS m/z calc. 518.6, found 519.5 (M+l)+; Retention time: 2.03 minutes (3 min run).

Preparation of imethyl—1-oxa—4,9-diazaspiro[5.5]undecan yl)(4-isopropoxymethylphenyl)methanone {JOYCE}r ~264- Step 1: 2—(Benzylamino)-2~methyl-propanol hydrochloride (539 mg, 2.50 mmol) was treated with aqueous sodium ide (50 mL of 2 M, 100 mmol), then diethyl ether (50 mL) was added to the solution and stirred for 3 min. The organic layer was separated, washed with brine, dried over NaZSO4, filtered and concentrated in vacuo to provide the 2-(benzylamino)methyl-propan-1—ol free base as a white powder. The 2-(benzy1amino)methy1-propan-l-ol (2.50 mmol) and tert—butyl 1-oxa- 6—azaspiro[2.5]octanecarboxylate (500 mg, 2.344 mmol) were ved in ethanol (2 mL) and the reaction mixture was heated in a sealed tube at 100 °C for 48 h. The ethanol was evaporated and the crude material purified by silica gel column chromatography (1 -100% ethyl acetate/hexanes) to e tert—butyl 4-((benzyl(1- hydroxymethylpr0pan—2-yl)amino)methyl)hydroxypiperidine—1 -carboxylate as white powder (551 mg, 60%). ESl-MS m/z calc. 392.5, found 373.3 (M+1)+; Retention time: 1.14 minutes (3 min run). 1H NMR (400 MHz, DMSO-dg) 5 7.43 (d, J = 7.4 Hz, 2H), 7.24 (t, J = 7.6 Hz, 2H), 7.13 (t, J = 7.3 Hz, 1H), 4.66 (t, J = 5.1 Hz, 1H), 4.43 (s, 1H), 3.91 (s, 2H), 3.62 (s, 2H), 3.22 (d, J = 4.8 Hz, 2H), 2.97 (s, 2H), 2.58 (s, 2H), 1.44 — 1.27 (m, 13H), 0.88 (s, 6H).

Step 2: To a solution of tert—butyl 4—[[benzyl—(2-hydroxy-1,1-dimethyl-ethyl) amino]methy1]hydroxy—piperidinecarb0xylate (330 mg, 0.841 mmol) in tetrahydrofuran was added N,N—diisopropylethylamine (439 uL, 2.52 mmol) and methanesulfonic anhydride (439 mg, 2.52 mmol) under a nitrogen atmosphere. The reaction mixture was heated at 65 °C for 18 h. The reaction e was diluted with ethyl acetate, washed with saturated sodium bicarbonate (2 X 50 mL) and brine (50 mL), dried over , d and concentrated in vacuo. The crude material was purified by silica gel chromatography (0-80% of ethyl acetate/hexanes) to provide tert— butyl 8-benzyl-9,9-dimethyloxa~=3,8-diazaspiro[5.5] undecanecarboxylate (89 mg, 28%) as white solid. ESI—MS m/z calc. 374.5, found 375.3 (M+1)+; Retention time: 1.30 minutes (3 min run).

WO 25613 2012/028882 Step 3: Tert—butyl 8-benzyl-9,9-dimethyloxa-3,8-diazaspiro[5.5]undecane- 3-carboxylate (89 mg, 0.24 mmol) was treated with hydrogen chloride solution in dioxane (240 uL of 4 M, 0.95 mmol). The reaction mixture was stirred for 18 h. The reaction mixture was concentrated in vacuo to provide 8-benzyl-9,9—dimethyloxa— 3,8-diazaspiro[5.5]undecane hydrochloride (56 mg, 86%). ESI-MS m/z calc. 274.4, found 275.5 ; Retention time: 0.80 minutes (3 min run).

Step 4: A solution of ropoxy—3-methylbenzoic acid (31.0 mg, 0.161 mmol) and O-(7—azabenzotriazolyl)—N,N,N,N‘-tetramethyluroniurn hexafluorophosphate (61.3 mg, 0.161 mmol) in acetonitrile was treated with triethylamine (67 uL, 0.48 mmol) and stirred for 5 min. 8-Benzyl-9,9-dimethyl oxa-3,8—diazaspiro[5.5] undecane hydrochloride (56.0 mg, 0.161 mmol) was added and the reaction mixture stirred for 3 h. The reaction mixture was filtered and concentrated in vacuo. The crude material was purified by chromatography (0-80% of ethyl e/hexanes) to provide (8-benzy1—9,9-dimethyl-l1—oxa—3,8— diazaspiro[5.5]undecany1)-(4-isoprop0xy—3-methy1-phenyl)methanone (51.0 mg, 70%) as colorless oil. ESI—MS m/z calc. 450.6, found 451.3 (M+1)+; Retention time: 1.54 minutes (3 min run).

[00751] Step 5: ] To a solution of (8—benzyl-9,9-dimethyl—1 1-oxa—3,8~diazaspiro[5.5] undecany1)—(4-isopropoxyu3-methy1-phenyl)methanone (51 mg, 0.11 mmol) in ethanol (2 mL) was added Pd(OH)2 (16 mg, 0.11 mmol) ed by ammonium formate (29 mg, 0.45 mmol). The reaction mixture was stirred at 40 0C for 18 h, then filtered and concentrated in vacuo to afford (9,9-dimethyloxa—3,8- diazaspiro[5 .5]undecan-3 4-isopropoxy—3 -methyl-phenyl)methanone (40 mg, 98%). ESI-MS m/z calc. 360.5, found 361.3 (M+1)+; Retention time: 1.29 minutes (3 min run). -266— Preparation of (8-but—2-ynyl—9,9—dimethyl—1l-oxa-3,8- piro[5.5]undecanyl)—(4-isopr0poxymethyl-phenyl)methanone TQQWCLOY To a mixture of imethy1-1 1-oxa—3,8-diazaspiro[5.5]undecany1)—(4-isopropoxy— 3—methy1-pheny1)methanone (20.1 mg, 0.0557 mmol) and potassium carbonate (15 mg, 0.11 mmol) in N,N—dimethylformamide (310 uL) was added l-bromobut-Z-yne (8.1 mg, 0.061 mmol) and reaction mixture was heated at 45 °C for 1 h. The reaction mixture was filtered and crude material was purified by HPLC (15—75% CH3CN/5 mM HCl) to provide (8-but-2—ynyl-9,9—dimethyl-11—oxa—3,8-diazaspiro[5.5]undecan—3-y1)- (4-isopropoxy—3-methyl-phenyl)methanone hydrochloride (11 mg, 41%). ESI—MS m/z calc. 412.3, found 413.3 (M+1)+ ; ion time: 1.43 minutes (3 min run). ation of (3,3-dimethyl—4-(pyrimidin-Z-yl)—1-0xa-4,9- diazaspiro[5.5]undecanyl)(4-isoprop0xymethylphenyl)methanone 0 Wonor

[00755] A solution of (9,9-dimethy1-l 1-oxa-3,8-diazaspiro[5.5]undecanyl)- (4-isopropoxymethyl—pheny1)methanone (11.0 mg, 0.0305 mmol), potassium carbonate (4.2 mg, 0.031 mmol) and 2-chloropyrimidine (3.7 mg, 0.031 mmol) in DMSO (90 uL) was heated at 90 °C for 2 h. The reaction was d and purified by HPLC (1-99% CH3CN/5 mM HCl) to provide (3,3-dimethyl(pyrimidin-Z-yl)—l-oxa— 4,9-diazaspiro[5.5]undecan—9-yl)(4—isopropoxy—3-methy1pheny1)methanone hydrochloride (6.0 mg, 0.012 mmol, 38%). ESl-MS m/z calc. 438.3, found 439.3 (M+1)+ ; Retention time: 1.92 minutes (3 min run). -267— Preparation of (4-isopropoxy—3-methylphenyl)(2-(methoxymethyl)— 4-(4-(trifluoromethyl)phenyl)—1-0xa-4,9-diazaspir0[5.5]undecanyl)methanone /OV[:3©Y©C’Y To a Vial charged with (4-isopropoxy—3-methyl-phenyl)-[10-(methoxymethy1)oxa- 3,8-diazaspiro[5.5]undecany1]methanone (30.0 mg, 0.08 mmol), 1—bromo-4— (trifluoromethy1)benzene (19.7 mg, 0.088 mmol), Pd2(dba)3 (23 mg, 0.04 mmol), rac- BINAP (24.8 mg, 0.04 mmol) and sodium utoxide (9.8 mg, 0.088 mmol) were added N—methyl—2-pyrrolidone (0.2 mL) and toluene (1.0 mL). The reaction e was heated at 100 °C under nitrogen 18 h. The reaction mixture was cooled to room temperature, filtered and purified Via HPLC (1-90% CH3CN/5 mM HCl) to provide (4-isopropoxymethy1pheny1)(2-(methoxymethy1)—4-(4-(trifluoromethyl)pheny1)-1 - oxa-4,9-diazaspiro[5.5]undecany1)methanone (5.0 mg, 0.0077 mmol, 10%). ESI— 1.5 MS m/z calc. 520.2549, found 521.3 (M+1)+ ; Retention time: 2.21 minutes (3 min run).

Preparation of lobutyl(meth0xymethyl)—1-0xa—4,9- diazaspiro[5.5]undecanyl)(4-is0propoxy—3-methylphenyl)methanone 690.60% Step 1: A solution of (4-isopropoxy—3-methyl-phenyl)-[lO-(methoxymethyl)— 1l-oxa—3,8-diazaspiro[5.5]undecanyl]methanone (343 mg, 0.912 mmol) and cyclobutanone (96.0 mg, 1.36 mmol) in dichloroethane (3 mL) was treated with acetic acid (78 uL, 1.4 mmol) and stirred for 30 min. AC)3 (387 mg, 1.82 mmol) was added and the reaction mixture stirred for 16 h. The reaction mixture was d with MTBE and washed with 1N NaOH (100 mL). The organic layer was separated and washed with brine, dried over Na2804, filtered and concentrated in vacuo. Silica gel chromatography (5-80% ethyl acetate/hexane) provided (4-cyclobutyl—2— (methoxymethyl)— 1 -oxa—4,9—diazaspiro[5.5] undecanyl)(4-isopropoxy—3 - methylphenyl)methanone (330 mg, 84%). ESI-MS m/z calc. 430.3, found 431.3 ; Retention time: 1.24 minutes (3 min run). 1H NMR (400 MHZ, CDC13) 5 7.19 (d, J = 8.4 Hz, 2H), 6.80 (d, J = 8.1 Hz, 1H), 4.55 (hept, J = 6.2 Hz, 1H), 4.30 - 4.10 (m, 1H), 3.94 - 3.75 (m, 1H), 3.62 - 3.46 (m, 1H), 3.48 - 3.33 (m, 6H), 3.30 — 3.16 (m, 1H), 2.75 (d, J = 10.8 Hz, 1H), 2.67 = 11.1 Hz, 1H), 2.47 - - 2.57 (m, 1H), 2.55 (d, J 2.27 (m, 1H), 2.20 (s, 3H), 1.98 (d, J = 7.3 Hz, 2H), 1.91 - 1.76 (m, 1H), 1.76 - 1.61 (m, 4H), 1.57 = 6.0 Hz, 6H). - 1.39 (m, 3H), 1.34 (d, J Table 2 below recites the analytical data for the compounds of Table 1.

Table 2. —269- WO 25613 1 467.50 1.63 2 467.30 1.01 3 490.20 1.22 4 507.14 1.87 473.39 1.42 6 411.50 1.90 7 423.50 1.31 8 497.23 2.41 1H NMR (400 MHz, 00013) 6 7.48 - 7.43 (m, 2H), 7.39 — 7.29 (m, 3H), 7.23 - 7.17 (m, 2H), 6.81 (d, J = 8.2 Hz, 1H), 5.11 (s, 1H), 4.56 (dt, J = 12.1, 6.0 Hz, 1H), 3.63 (d, J = 12.4 Hz, 1H), 3.59 - 3.19 (m, 9 451'” 1'76 5H), 3.09 (d, J = 12.4 Hz, 1H), 2.92 (d, J = 28.7 Hz, 1H), 2.22 (s, 1H), 2.23 - 2.16 (m, 3H), 1.59 (s, 4H), 1.35 (d, J = 6.0 Hz, 6H), 1.14 (t, J = 7.2 Hz, 3H). 437.70 1.43 1H NMR (400 MHz, CD3CN) 6 7.93 ( J = 1.9 Hz, 1H), 7.26 — 7.10 (m, 2H), 6.92 (d, J = 9.0 Hz 1H), 6.54 (t, J = 52.5 Hz, 1H), 6.28 (d, J = 1.9 Hz, 1H), 5.28 (d, J = 9.5 Hz, 1H), 4.63(tt,J = 12.1, 11 47740 6'04 6.0 Hz, 1H), 3.90 (s, 4H), 3.42 (d, J = 1 1 Hz, H), 3.24 (d, J = 12.4 Hz, 6H), 2.92 (d, J = 27.2 Hz, 3H), 2.74 (s, 2H), 2.51 -2.01 (m, 33H), 1 87 — 1.46 (m, 5H), 1.30 (t, J = 10.1 Hz, 7H). 12 539.29 1.97 13 492.30 2.26 14 468.19 2.37 471.29 2.33 16 468.30 1.51 17 468.50 1.25 18 417.30 1.43 19 459.29 2.78 -270— WO 25613 1H NMR (400 MHz, CD3CN) 6 7.45 (d, J 1.7 Hz, 1H), 7.23 - 7.16 (m, 2H), 7.13 (t, J = 3.8 Hz, 1H), 6.98 - 6.88 (m, 1H), 6.63 (s, 1H), 6.50 (s, 1H), 6.34 (s, 1H), 6.29 (d, J = 1.7 Hz, 1H), 5.29 (d, J = 8.6 Hz, 1H), 4.74 — 4.54 (m, 1H), 4.24 (9, J = 49150 1'82 7.0 Hz, 2H), 3.50 - 3.09 (m, 6H), 3.05 — 2.59 (m, 3H), 2.46 — 2.03 (m, 6H), 1.69 - 1.75 (m, 2H), 1.75 — 1.50 (m, 2H), 1.49 — 1.39 (m, 3H), 1.34 (dd, J = 6.0, 5.1 Hz, 6H), 1.29 (s, 1H), 1.17 (d, J = 6.1 Hz, 2H). 1H NMR (400 MHz, MeOD) 8 7.70 (d, J = 2.3 Hz, 1H), 7.30 = 8.7 Hz, 1H), — 7.16 (m, 2H), 6.96 (d, J 6.43 (d, J = 2.3 Hz, 1H), 6.27 (s, 1H), 6.14 (s, 1H), 6.00 (s, 1H), 5.01 (d, J = 43.6 Hz, 1H), 4.66 (dt, J 21 46330 1'71 = 12.0, 6.0 Hz, 1H), 4.30 (s, 1H), 3.49 (ddd, J = 49.9, 49.0, 23.7 Hz, 3H), 3.19 — 2.96 (m, 3H), 2.60 (dd, J = 42.6, 23.4 Hz, 3H), 2.19 (s, 3H), 1.68 (s, 3H), 1.34 (d, J = 6.0 Hz, 6H). 22 437.70 1.36 23 416.29 1.62 24 481.70 1.49 453.20 1.08 26 495.50 7.63 27 491.25 2.17 28 389.70 1.03 29 465.70 1.72 439.10 1.38 31 454.30 1.29 32 391.30 1.20 33 474.50 1.61 34 389.70 1.36 —271- WO 25613 1H NMR (400 MHz, DMSO) 8 7.74 (d, J 1.9 Hz, 1H), 7.69 (d, J = 1.9 Hz, 1H), 7.18 (dd, J = 6.0, 2.0 Hz, 2H), 7.04 - 6.90 (m, 1H), 6.20 (tt, J = 55.5, 4.0 Hz, 1H), 5.34 - 5.28 (m, 1H), 4.69 — 4.57 (m, 477.30 1.50 1H), 3.91 (s, 3H), 3.69 - 3.41 (m, 1H), 3.37 — 3.09 (m, 3H), 2.87 (ddd, J = 19.6, 18.4, 7.9 Hz, 3H), 2.57 — 2.51 (m, 2H), 2.46 — 2.31 (m, 1H), 2.26 (d, J = 11.6 Hz, 1H), 2.13 (s, 3H), 1.70 — 1.52 (m, 3H), 1.29 (d, J = 6.0 Hz, 6H). 36 499.30 1.76 37 488.40 1.50 38 485.50 7.23 39 509.50 1.97 40 389.70 1.33 41 442.50 1.12 42 492.20 2.17 43 453.50 1.24 1H NMR (400 MHz, 00013) 8 7.53 (t, J = 6.9 Hz, 1H), 7.33 - 7.27 (m, 1H), 7.20 — 7.09 (m, 3H), 7.07 - 7.01 (m, 1H), 6.96 (t, J = 8.2 Hz, 1H), 6.14 - 5.75 (m, 1H), 5.25 - 5.07 (m, 1H), 4.66 — 4.52 (m, 1H), 44 49130 2'27 4.45 - 4.21 (m, 1H), 3.73 - 3.31 (m, 2H), 3.08 (d, J = 10.8 Hz, 1H), 2.85 - 2.61 (m, 4H), 2.39 - 2.17 (m, 2H), 1.66 — 1.45 (m, 3H), 1.37 (d, J = 6.1 Hz, 6H). 1H NMR (400 MHz, 00013) 8 7.53 (t, J = 6.9 Hz, 1H), 7.33 - 7.27 (m, 1H), 7.20 — 7.09 (m, 3H), 7.07 - 7.01 (m, 1H), 6.96 (t, J = 8.2 Hz, 1H), 6.14 — 5.75 (m, 1H), 5.25 — 5.07 (m, 1H), 4.66 - 4.52 (m, 1H), 45 49550 2'14 4.45 —4.21 (m, 1H), 3.73 - 3.31 (m, 2H), 3.08 (d, J = 10.8 Hz, 1H), 2.85 - 2.61 (m, 4H), 2.39 - 2.17 (m, 2H), 1.66 — 1.45 (m, 3H), 1.37 (d, J = 6.1 Hz, 6H). . _ . 46 415.50 1.41 47 445.37 1.33 48 447.33 1.34 49 470.30 1.38 50 465.50 1.64 -272— WO 25613 52 433.11 1.47 53 459.29 2.18 54 464.50 1.29 55 449.34 1.32 56 505.40 2.16 57 478.20 1.06 58 525.29 1.81 59 489.28 1.85 60 521.50 2.15 61 535.20 3.25 62 525.00 2.00 63 487.30 2.39 64 458.18 2.22 65 522.40 1.13 66 503.15 2.65 1H NMR (400 MHz, DMSO) 6 8.35 (d, J = 4.4 Hz, 2H), 7.52 (d, J = 7.8 Hz, 2H), 7.33 (d, J = 7.2 Hz, 2H), 6.62 (s, 1H), 4.75 (s, 1H), 4.65 - 4.48 (m, 67 465.50 1.60 2H), 4.10 (br s, 1H), 3.56 (br s, 1H), 3.39 (br s, 1H), 3.03 (br s, 1H), 2.75 (d, J = 13.3 Hz, 1H), 2.60 — 2.52 (m, 1H), 1.99 (br s, 1H), 1.81 - 1.17 (m, 16H), 0.96 (t, J = 7.3 Hz, 3H). 68 448.24 1.64 69 469.20 2.17 70 478.30 1.94 71 467.10 2.10 72 427.29 2.52 WO 25613 73 419.31 1.28 74 483.30 2.03 75 468.30 1.14 76 474.50 1.07 77 477.30 2.15 78 518.38 2.05 79 484.30 1.59 80 492.50 1.16 1H NMR (400 MHz, MeOD) 8 7.47 (dd, J = 8.7, .4 Hz, 2H), 7.23 (dd, J = 11.7, 3.5 Hz, 2H), 7.12 (t, J = 8.8 Hz, 2H), 6.96 (d, J = 8.3 Hz, 1H), 6.24 (t, J = 54.0 Hz, 81 50700 1'86 1H), 4.95 (s, 1H), 4.33 (s, 1H), 4.13 (t, J = 6.2 Hz, 2H), 3.77 (t, J = 6.3 Hz, 2H), 3.73 — 3.61 (m, 1H), 2.73 (s, 2H), 2.61 — 2.46 (m, 1H), 2.22 (s, 3H), 2.11 - 1.96 (m, 2H), 1.75 (s, 3H). 82 453.50 1.19 83 504.50 1.70 84 481.50 1.62 85 534.40 1.15 86 493.40 2.13 1H NMR (400 MHz, 00013) 8 7.15 (dd, J = 15.8, .3 Hz, 2H), 7.06 - 6.86 (m, 1H), 6.17 (s, 1H), .01 (s, 1H), 4.58 (dt, J = 12.2, 6.1 Hz, 1H), 4.30 (s, 1H), 3.60 (s, 3H), 3.15 (d, J = 11.6 Hz, 1H), 87 499.30 7.16 3.01 (q, J = 9.3 Hz, 2H), 2.74 (d, J =11.1 Hz, 1H), 2.59 (dd, J = 20.7, 9.9 Hz, 2H), 2.47 (d, J = 11.4 Hz, 1H), 2.44 (s, 3H), 2.02 (d, J = 6.7 Hz, 1H), 1.78 (d, J = 45.0 Hz, 1H), 1.53 (d, J = 6.1 Hz, 2H), 1.44 - 1.23 (m, 6H). 88 506.30 2.09 89 443.36 1.42 90 485.12 2.07 91 451.30 1.55 —274- WO 25613 1H NMR (400 MHz, CDCI3) 8 8.40 (s, 2H), 7.20 (d, J = 9.0 Hz, 2H), 8.80 (d, J = 8.0 Hz, 1H), 8.85 (s, 1H), 4.80 (dd, J = 22.7, 12.7 Hz, 2H), 4.55 (dt, J = 12.0, 8.0 Hz, 1H), 3.92 (dt, J = 7.4, 8.8 Hz, 92 441"” 1'55 1H), 3.83 - 3.84 (m, 3H), 3.59 - 3.42 (m, 1H), 3.28 (s, 1H), 3.08 - 2.88 (m, 2H), 2.19 (s, 3H), 2.11 - 1.87 (m, 2H), 1.80 — 1.52 (m, 3H), 1.34 (d, J = 8.0 Hz, 6H). 93 487.50 1.29 94 495.40 2.27 95 488.32 2.40 96 553.12 1.75 97 438.50 1.11 98 491.30 2.12 99 538.28 1.91 1H NMR (400 MHz, 00013) 8 7.45 - 7.38 (m, 5H), 8.98 - 8.83 (m, 3H), 5.25 (d, J = 10.4 Hz, 1H), 4.57 12.2, 8.1 Hz, 1H), 3.85 (s, 3H), 3.80 100 48970 2'17 (dt, J = (d, J = 10.9 Hz, 1H), 3.47 - 3.12 (m, 8H), 2.88 - 2.80 (m, 3H), 1.88 - 1.50 (m, 5H), 1.38 (d, J = 8.1 Hz, 8H). 101 433.35 1.34 102 485.18 2.85 103 484.50 1.25 104 507.50 2.28 105 477.30 2.05 106 459.20 1.91 107 483.38 1.40 108 511.28 1.85 109 539.15 1.95 110 501.30 7.88 111 433.35 1.29 —275— WO 25613 112 461.36 1.42 113 433.29 1.19 114 483.50 1.89 115 464.24 1.59 116 474.30 2.08 117 507.00 1.94 118 487.05 2.28 119 477.32 2.14 1H NMR (400 MHz, 00013) 8 8.45 (d, J = 4.5 Hz, 2H), 7.23 — 7.17 (m, 2H), 8.80 (d, J = 8.1 Hz, 1H), 6.71 (s, 1H), 4.97 (m, 2H), 4.55 (dt, J = — 4.76 12.1, 6.0 Hz, 1H), 4.36 — 4.08 (m, 1H), 4.03 - 3.84 120 45530 1'86 (m, 1H), 3.81 - 3.50 (m, 3H), - 3.61 (m, 1H), 3.81 3.42 (s, 3H), 3.35 - 3.21 (m, 1H), 3.07 - 2.91 (m, 2H), 2.19 (s, 3H), 2.07 - 1.93 (m, 1H), 1.84 — 1.52 (m, 3H), 1.34 (d, J = 6.0 Hz, 6H). 121 502.35 1.17 122 507.20 2.17 1H NMR (501 MHz, DMSO) 8 7.38 - 7.26 (m, 5H), 7.15 (s, 2H), 6.92 (d, J = 8.5 Hz, 1H), 4.59 (dt, J = 11.1, 5.4 Hz, 1H), 4.29 (s, 1H), 3.52 - 3.44 (m, 123 505.30 2.50 2H), 3.24 - 2.98 (m, 3H), 2.91 (d, J = 11.6 Hz, 1H), 2.71 — 2.27 (m, 1H), 2.10 — 2.47 (m, 3H), 2.46 (s, 3H), 1.67 - 1.38 (m, 3H), 1.26 (d, J = 5.8 Hz, 6H), 0.79 (d, J = 5.1 Hz, 3H). 124 521.30 2.22 125 487.29 2.14 126 484.30 1.40 127 473.50 1.94 128 521.34 2.16 129 427.50 1.61 130 451.50 2.03 131 477.29 1.30 -276— WO 25613 132 472.18 2.48 1H NMR (400 MHz, CDCI3) 8 7.43 - 7.30 (m, 8H), 7.26 (s, 1H), 4.86 (s, 1H), 4.47 - 4.27 (m, 1H), 3.66 - 3.12 (m, 3H), 3.04 (dd, J = 18.6, 9.3 Hz, 133 49130 2'09 3H), 2.84 (s, 2H), 2.81 (s, 2H), 2.73 - 2.54 (m, 1H), 2.52 - 1.74 (m, 2H), 1.26 _ 2.37 (m, 2H), 1.86 (5, 6H). _ . fl 134 475.34 1.23 135 495.13 2.22 136 441.29 2.70 137 524.10 2.22 138 521.30 2.04 139 417.30 1.37 140 454.30 0.28 141 385.30 1.22 142 451.50 1.35 143 523.29 1.89 144 432.18 1.87 145 439.70 1.26 146 459.70 1.78 147 447.33 1.42 148 505.30 1.63 1H NMR (400 MHz, DMSO) 6 7.27 - 7.06 (m, 2H), 6.96 (d, J = 9.1 Hz, 1H), 5.17 (dd, J = 13.6, 4.2 Hz, 1H), 4.63 (dt, J = 12.1, 6.2 Hz, 1H), 3.31 — 149 49770 1‘99 3.19 (m, 5H), 2.92 - 2.81 (m, 1H), 2.67 (dd, J = 12.0, 10.1 Hz, 1H), 2.43 - 2.27 (m, 6H), 2.15 (s, 3H), 1.70 — 1.40 (m, 4H), 1.29 (d, J = 6.0 Hz, 6H). 150 477.30 1.59 151 491.14 1.72 152 528.50 1.92 —277- 153 473.26 2.23 1H NMR (400 MHz, CDCI3) 8 7.25 - 7.16 (m, 2H), 6.81 (d, J = 8.2 Hz, 1H), 4.56 (dt, J =12.1,6.0 Hz, 1H), 3.85 — 3.57 (m, 2H), 3.41 (br s, 2H), 3.36 (d, 154 421.30 2.00 J = 2.3 Hz, 2H), 2.88 — 2.76 (m, 2H), 2.51 (s, 2H), 2.20 (s, 3H), 2.09 (d, J = 14.2 Hz, 2H), 1.85 (t, J = 2.3 Hz, 3H), 1.54 (br s, 2H), 1.34 (d, J = 6.0 Hz, 6H). 155 453.10 2.13 156 511.16 2.14 157 441.20 1.82 158 423.70 0.93 159 510.30 1.98 160 433.50 1.25 161 441.29 2.00 162 522.60 1.43 1H NMR (400 MHz, MeOD) 8 .32 (m, 5H), 7.24—7.16 (m, 2H), 6.98—6.90 (m, 1H), 5.08-4.96 (m, 1H), 4.70—4.60 (m, 1H), 4.48—4.28 (m, 1H), 163 40950 1'32 3.86—3.62 (m, 1H), 3.60—3.32 (m, 3H), 3.21 - 2.91 (m, 3H), 2.69—2.43 (m, 1H), 2.19 (s, 3H), 1.96 - 1.55 (m, 3H), 1.34 (d, J = 6.0 Hz, 6H). 164 449.24 2.42 165 539.29 2.02 166 453.50 1.08 167 484.70 0.99 168 473.26 1.83 1 1H NMR (400 MHz, DMSO) 8 7.36 - 7.27 (m, 4H), 7.24 (t, J = 6.7 Hz, 1H), 7.20 - 7.12 (m, 2H), 6.94 (d, J = 8.8 Hz, 1H), 4.63 (dt, J = 12.1, 6.0 Hz, 1H), 3.95 - 3.78 (m, 1H), 3.44 (dd, J = 30.4, 13.6 Hz, 169 467.30 1.21 3H), 3.34 (d, J = 5.5 Hz, 2H), 3.29 - 3.19 (m, 5H), 3.18 - 3.01 (m, 1H), 2.73 (d, J = 10.3 Hz, 1H), 2.69 - 2.56 (m, 1H), 2.33 (d, J = 1.9 Hz, 1H), 2.12 (s, 3H), 1.75 (t, J = 11.0 Hz, 2H), 1.53 - 1.34 (m, 3H), 1.28 (d, J = 6.0 Hz, 6H). _ _ -278— WO 25613 1H NMR (400 MHz, MeOD) 8 7.48 (dd, J = 8.7, .4 Hz, 2H), 7.32 — 7.19 (m, 2H), 7.13 (dd, J = 12.2, 5.4 Hz, 2H), 6.93 (d, J = 8.1 Hz, 1H), 6.22 170 521.00 1.93 (d, J = 55.6 Hz, 1H), 4.95 (s, 1H), 4.36 (s, 1H), 3.82 (s, 2H), 3.75 - 3.36 (m, - 3.64 (m, 1H), 3.57 4H), 2.84 (d, J = 9.5 Hz, 2H), 2.65 (s, 1H), 2.27 (s, 3H), 1.76 (s, 3H), 1.35 (s, 6H). 1H NMR (400 MHz, 00013) 8 8.30 (d, J = 4.8 Hz, 2H), 7.24 = 8.1 - 7.15 (m, 2H), 6.80 (d, J Hz, 1H), 6.53 (t, J = 4.7 Hz, 1H), 6.29 (t, J = 74.3 Hz, 1H), 4.75 (d, J = 13.0 Hz, 1H), 4.65 (d, J = 13.3 Hz, 171 49150 1'86 1H), 4.55 (dt, J = 12.1, 6.1 Hz, 1H), 3.93 (m, 3H), 3.52 (br s, 2H), 3.37 — 3.17 (m, 1H), 2.88 - 2.73 (m, 2H), 2.19 (s, 3H), 2.03 (br s, 1H), 1.71 —1,53 (m, 3H), 1.34 (d, J = 6.1 Hz, 6H). 172 527.26 1.82 173 471.29 2.50 174 484.30 1.39 175 449.34 1.28 176 450.50 1.17 1H NMR (400 MHz, 00013) 8 8.23 (d, J = 2.7 Hz, 1H), 7.63 (d, J = 8.7 Hz, 1H), 7.43 - 7.30 (m, 5H), 7.28 — 7.25 (m, 1H), 4.85 (dd, J = 33.8, 8.9 Hz, 1H), 4.64 (dq, J = 12.0, 6.0 Hz, 1H), 4.40 (d, J = 177 47840 2'21 13.0 Hz, 1H), 3.88 - 3.14 (m, - 3.77 (m, 1H), 3.70 2H), 3.07 — 2.91 (m, 3H), 2.82 — 2.55 (m, 2H), 2.40 (dd, J = 22.0, 10.9 Hz, 2H), 1.76 - 1.60 (m, 3H), 1.40 (d, J = 6.0 Hz, 6H). 178 441.30 1.48 179 481.70 1.24 180 460.30 1.40 181 495.70 1.95 182 463.57 1.82 183 483.30 1.95 184 451.29 1.32 185 413.36 1.43 186 519.50 2.03 ~279- WO 25613 187 473.30 1.91 188 435.30 1.24 189 511.26 1.87 1H NMR (400 MHz, DMSO) 8 7.61 (dd, J = 7.8, 1.2 Hz, 1H), 7.50 — 7.31 (m, 3H), 7.30 — 7.12 (m, 3H), 6.36 - 6.00 (m, 1H), 5.08 (d, J = 13.4 Hz, 1H), 4.74 - 4.64 (m, 1H), 4.12 — 3.91 (m, 1H), 3.73 190 511.50 2.25 - 3.59 (m, 2H), 3.32 (dd, J = 32.0, 10.6 Hz, 1H), 3.06 (dd, J = 11.0, 3.1 Hz, 1H), 2.91 (dd, J = 11.6, 2.6 Hz, 1H), 2.86 - 2.65 (m, 2H), 2.44 — 2.30 (m, 1H), 2.19 (d, J = 9.6 Hz, 1H), 2.13 - 1.99 (m, 1H), 1.70 .- 155 (m, 3H), 1.30 (d, J = 6.0 Hz, 6H). 191 469.33 3.47 192 453.50 1.10 193 475.30 1.38 194 507.29 1.94 195 492.20 1.31 1H NMR (400 MHz, 00013) 8 7.47 (s, 1H), 7.20 (d, J = 8.8 Hz, 2H), 6.81 (d, J = 8.1 Hz, 1H), 5.20 (dd, J = 9311 Hz, 1H), 4.62 - 4.52 (m, 1H), 3.76 (ddd, J = 36.3, 29.5, 14.8 Hz, 1H), 3.50 (dd, J = 196 512'70 2'17 .4, 1.0 Hz, 2H), 3.33 - 3.13 (m, 1H), 3.05 (9, J = 9.3 Hz, 2H), 2.77 (d, J = 11.3 Hz, 1H), 2.60 — 2.42 (m, 6H), 2.20 (s, 3H), 1.79 - 1.46 (m, 4H), 1.35 (d, J = 6.0 Hz, 6H). 197 455.29 2.34 1.98 502.27 2.21 199 493.00 1.87 200 539.00 2.06 201 473.39 1.40 202 511.16 1.80 203 439.70 1.21 204 459.30 1.44 205 419.31 1.26 -280— WO 25613 206 473.39 1.44 207 481.50 1.43 208 487.22 2.12 1H NMR (400 MHz, CDCI3) 8 7.74 (d, J = 0.7 Hz, 1H), 7.22 — 7.17 (m, 2H), 7.16 (6, J = 0.7 Hz, 1H), 7.04 - 6.70 (m, 2H), 5.44 (dd, J = 10.9, 1.9 Hz, 1H), 4.64 - 4.52 (m, 1H), 4.41 — 4.22 (m, 1H), 4.17 209 46430 1'77 — 3.98 (m, 1H), 3.93 - 3.80 (m, 1H), 3.47 - 3.27 (m, 6H), 3.23 (6, J = 15.1 Hz, 1H), 2.81 (6, J = 12.3 Hz, 1H), 2.20 (s, 3H), 1.82 — 1.62 (m, 3H), 1.36 (d, J = 6.0 Hz, 6H). 210 479.20 1.10 1H NMR (400 MHz, CDCI3) 6 7.65(d, J = 2.1 Hz, 1H), 7.,19(6 J= 8.6Hz, 2H) 6.6,80( J=8.1 Hz 1H) 637 (s 1H), 5.,06(s 1H), 4.55(6t, J=12. , 6.1 Hz 1H) 341 (6 J: 73.7Hz, 4H) 3.1( J 211 481.30 7.73 10.6 Hz, 1H), 3.01 (q, J = 9.3 Hz, 2H), 2. 77 (6, J—— 11.4 Hz, 1H), 2.59 (66, J = 19.2, 8.3 Hz, 2H), 2.47 (6, J = 11.3 Hz, 1H), 2.15 (d, J = 37.6 Hz, 3H), 2.01 (s, 1H), 1.64 (6, J = 48.9 Hz, 3H), 1.34 (6, J :60 Hz, 6H). 212 449.20 1.83 213 511.70 2.48 214 492.30 2.00 215 449.34 1.27 216 485.50 1.32 217 413.50 1.50 218 429.33 1.08 219 489.22 2.00 220 495.30 1.36 221 478.50 1.47 222 494.20 1.49 223 519.30 1.78 224 489.23 1.83 225 551.50 1.87 226 467.30 1.57 227 441.70 1.23 228 478.31 1.83 1H NMR (400 MHz, CD3CN) 6 7.54 (d, J = 2.3 Hz, 1H), 7.18 (dd, J = 8.2, 1.2 Hz, 2H), 6.98 (t, J = 4.1 HZ, 1H), 6.92 (d, J = 9.0 Hz, 1H), 6.78 (dt, J = 539,41 Hz,1H) J==23 Hz,1H) 526 (d, J = 10.2 Hz, 1H), 4.63 (dt, J = 12.1, 6.0 Hz, 229 491.30 1.89 1H), 4.14 (q, J = 7.3 Hz, 2H), 3.63 - 3.35 (m, 5H), 337-—313 0n,3H) 308(d,J = 132 Hz,1H) 2.95 (d, J = 12.6 Hz, 1H), 2.64 — 2.02 (m, 11H), 1.73 (ddd, J = 26.1, 9.6, 3.2 Hz, 2H), 1.58 (d, J = 14.5 Hz, 1H), 1.48 - 1.36 (m, 3H), 1.32 (d, J = 6.0 Hz,6H). J 230 520.30 2.34 231 424.15 1.35 232 47333 142 233 443.70 2.33 234 52500 228 1H NMR (400 MHZ, CDCI3) 5 8.40 (d, J = 4.5 Hz, 2H), 7.20 (d, J = 8.8 Hz, 2H), 6.80 (d, J = 8.1 Hz, 1H), 6.64 (s, 1H), 4.85 (d, J = 12.9 Hz, 1H), 4.76 (d, J = 13.1 Hz, 1H), 4.55 (dt, J = 12.1, 6.1 Hz, 235 469.50 1.77 1H), 4.16 (s, 1H), 3.94 (s, 1H), 3.64 — 3.44 (m, 5H), 3.28 (t, J = 11.5 HZ, 1H), 3.28 (t, J =11.5 Hz, 1H), 2.92 (dd, J = 267,125 Hz, 2H), 2.19 (s, 3H), 2.03 (s, 2H), 1.65 (d, J = 47.5 Hz, 4H), 1.34 (d, J = 6.1 Hz, 5H), 1.22 (t, J = 7.0 Hz, 3H). 1H NMR (400 MHz, CDCI3) 6 8.44 (d, J = 4.8 Hz, 2H), 7.21 (d, J = 8.8 Hz, 2H), 6.80 (d, J = 8.1 Hz, 1H), 6.69 (s, 1H), 4.86 (d, J = 13.3 Hz, 1H), 4.77 w,J =124-Hz,1H) 455(dLJ =123,61 H; 236 439.50 1.87 1H), 3.66 (br s, 1H), 3.47 (br s, 1H), 3.17 (br S, 1H), 2.97 (d, J = 13.4 HZ, 1H), 2.81 (t, J = 12.2 Hz, 1H), 2.20 (S, 3H), 2.03 (br S, 1H), 1.78 - 1.52 (m, 6H), 1.34 (d, J = 6.1 Hz, 6H), 1.05 (t, J = 7.5 Hz, 3H). 237 48150 143 238 487.50 1.48 239 417.15 1.38 240 455.29 2.13 241 45923 175 242 39930 137 WO 25613 243 468.50 1 .61 244 495.20 2.07 245 505.28 1 .98 246 474.24 2.03 247 521.20 2.12 248 413.30 1.47 249- 459.35 1.26 250 458.70 1 .28 251 489.50 2.00 252 474.28 1.38 253 504.40 1 .29 254 405.28 1.24 255 433.29 1 .28 256 484.30 1 .94 —283- WO 25613 257 495.50 2.12 258 521.30 2.26 259 459.30 1.17 260 459.30 1.94 261 492.20 1.32 262 459.50 1.51 263 481.10 1.66 264 453.50 1.23 265 536.70 1.23 266 465.50 1.93 267 455.29 2.20 268 474.30 1.33 269 539.15 1.90 270 461.30 1.21 271 469.50 1.54 272 419.70 1.20 273 507.30 1.96 274 507.20 1.93 275 434.20 1.55 276 499.33 3.20 277 414.18 1.20 278 507.40 2.15 279 508.40 1.44 280 538.17 1.83 WO 25613 281 451.50 1.38 282 456.31 2.33 283 448.20 2.01 284 481.24 2.79 285 431.34 1.25 286 453.30 1.98 287 431.33 1.03 288 450.50 1.17 289 479.40 1.98 290 470.15 1.98 291 454.20 1.32 292 549.50 2.28 293 536.40 1.95 294 455.37 1.57 1H NMR (400 MHz, c0013) 8 8.21 (d, J = 5.7 Hz, 1H), 7.86 (t, J = 7.7 Hz, 1H), 7.25 — 7.19 (m, 2H), 6.92 (d, J = 9.2 Hz, 1H), 6.88 (t, J = 6.6 Hz, 1H), 6.80 (d, J = 8.2 Hz, 1H), 4.55 (dt, J = 12.1, 6.1 Hz, 1H), 4.48 (d, J = 13.6 Hz, 1H), 4.35 (d, J = 12.5 295 43870 1'39 Hz, 1H), 3.77 (br s, 1H), 3.43 (br s, 1H), 3.20 (d, J = 13.4 Hz, 1H), 3.12 (br s, 1H), 3.04 — 2.91 (m, 1H), 2.20 (s, 3H), 2.09 (br s, 1H), 1.72 — 1.59 (m, 6H), 1.34 (d, J = 5.9 Hz, 6H), 1.07 (t, J = 7.4 Hz, 3H). 296 476.20 0.96 297 508.70 1.51 1H NMR (400 MHz, DMSO) 6 7.48 (s, 1H), 7.35 - 7.13 (m, 3H), 6.60 - 4.91 - 6.25 (m, 1H), 5.06 (m, 298 481.30 1.48 1H), 4.75 — 3.99 (m, 1H), 3.58 - 4.64 (m, 1H), 4.27 — 2.55 (m, 9H), 2.07 (s, 3H), 1.67 - 1.39 (m, 4H), 1.30 (d, J = 6.0 Hz, 6H). 299 503.26 2.07 300 467.50 1.29 301 491.50 2.33 302 445.31 1.30 303 466.29 2.67 304 501.41 1.58 305 490.20 1.11 1H NMR (400 MHz, CD3CN) 8 7.50 (d, J = 2.3 Hz, 1H), 7.24 — 7.14 (m, 2H), 6.98 (s, 1H), 6.92 (d, J = 9.1 Hz, 1H), 6.81 (dd, J = 31.0, 26.9 Hz, 1H), 6.35 (d, J = 2.3 Hz, 1H), 5.26 (d, J = 9.6 Hz, 1H), 306 477.30 1.77 4.63 (dt, J = 12.0, 6.0 Hz, 1H), 3.85 (s, 4H), 3.67 — 3.37 (m, 5H), 3.36 — 3.14 (m, 3H), 3.08 (d, J = 13.9 Hz, 1H), 2.95 (d, J = 12.7 Hz, 1H), 2.70 — 2.03 (m, 14H), 1.97 (s, 1H), 1.81 - 1.51 (m, 4H), 1.32 (t, J = 5.4 Hz, 7H). 307 495.10 1.88 308 424.50 1.14 1H NMR (400 MHz, DMSO) 8 7.27 — 7.13 (m, 2H), 6.96 (d, J = 9.0 Hz, 1H), 6.82 (d, J = 1.2 Hz, 1H), 4.86 (dd, J = 12.0, 4.7 Hz, 1H), 4.71 — 4.54 (m, 309 496.70 1.99 1H), 3.32 - 3.14 (m, 5H), 3.07 (dd, J = 11.5, 2.6 Hz, 1H), 2.90 - 2.83 (m, 1H), 2.70 (dd, J = 18.3, 7.2 Hz, 1H), 2.41 - 2.23 (m, 6H), 2.13 (s, 3H), 1.64 - 1.39 (m, 3H), 1.29 (d, J = 6.0 Hz, 6H).

ASSAYS FOR DETECTING AND ING Na VINHIBITIONPROPERTIES OF COMPOUND E-VIPR optical membrane potential assay method with electrical stimulation

[00761] Sodium channels are voltage-dependent proteins that can be activated by inducing membrane voltage changes by applying electric fields. The electrical stimulation instrument and methods of use are bed in Ion Channel Assay Methods PCT/USOl/21652, herein incorporated by reference and are referred to as E- VIPR. The instrument ses a microtiter plate handler, an optical system for exciting the coumarin dye while simultaneously recording the coumarin and oxonol emissions, a waveform generator, a current- or voltage-controlled er, and a device for ing electrodes in well. Under integrated computer control, this -286— instrument passes rogrammed ical stimulus protocols to cells within the wells of the microtiter plate. 24 hours before the assay on E-VIPR, HEK cells expressing human NaV subtype, like NaV 1.7, are seeded in 384-well poly-lysine coated plates at 15,000- ,000 cells per well. Other subtypes are performed in an analogous mode in a cell line expressing the NaV of interest. HEK cells are grown in media (exact composition is specific to each cell type and NaV subtype) supplemented with 10% FBS (Fetal Bovine Serum, qualified; GibcoBRL #16140-071) and 1% Pen-Strep (Penicillin- Streptomycin; GibcoBRL #15140-122). Cells are grown in vented cap flasks, in 90% humidity and 10% C02, to 100% confluence. They are usually split by trypsinization 1:10 or 1:20, depending on scheduling needs, and grown for 2-3 days before the next split.

Reagents and Solutions: 100 mg/mL Pluronic F-127 (Sigma #P2443), in dry DMSO

[00764] Compound Plates: ll round bottom plate, e. g. Corning 384-well Polypropylene Round Bottom #3656 Cell Plates: 384-well tissue culture treated plate, e.g. Greiner #781 091 - 1 B 10 mM DiSBAC6(3) (Aurora 0-010) in dry DMSO

[00767] 10 mM CC2-DMPE (Aurora 0—008) in dry DMSO 200 mM ABSCl in H20 Bathl buffer. Glucose 10mM (1.8g/L), Magnesium Chloride (Anhydrous), lmM (0.095g/L), Calcium de, 2mM g/L), HEPES 10mM (2.3 8g/L), Potassium Chloride, 4.5mM (0.335g/L), Sodium Chloride l60mM (9.35 g/L).

] Hexyl Dye Solution: Bathl Buffer + 0.5% B-cyclodextrin (make this prior to use, Sigma #C4767), 8 uM CC2-DMPE + 2.5 uM DiSBAC6(3). To make the solution Add volume of 10% Pluronic F127 stock equal to volumes of CC2-DMPE + DiSBAC6(3). The order of ation is first mix Pluronic and CC2-DMPE, then add DiSBAC6(3) while vortexing, then add Bathl + B-Cyclodextrin.

Assay Protocol: ] 1) Pre-spot compounds (in neat DMSO) into compound plates.

Vehicle control (neat DMSO), the positive control (20mM DMSO stock tetracaine, 125 uM final in assay) and test compounds are added to each well at 160x desired final concentration in neat DMSO. Final compound plate volume will be 80 uL (80-fold intermediate dilution from 1 HL DMSO spot; 160-fold final dilution after transfer to cell plate). Final DMSO concentration for all wells in assay is 0.625%. 2) e Hexyl Dye Solution.

[00773] 3) Prepare cell plates. On the day of the assay, medium is aspirated and cells are washed three times with 100 uL of Bathl Solution, ining 25 [,LL residual volume in each well. 4) se 25 uL per well of Hexyl Dye Solution into cell plates.

Incubate for 20-35 minutes at room temp or ambient conditions. ] 5) Dispense 80 uL per well of Bathl into compound plates. Acid Yellow-17 (1 mM) is added and Potassium Chloride can be altered from 4.5 to 20 mM depending on the NaV subtype and assay sensitivity. 6) Wash cell plates three times with 100 uL per well of Bathl, leaving ML of residual volume. Then transfer 25uL per well from Compound Plates to Cell . Incubate for 20-35 minutes at room temp/ambient condition 7) Read Plate on E—VIPR. Use the current-controlled amplifier to deliver stimulation wave pulses for typically 9 s and a scan rate of 400Hz. A pre—stimulus recording is performed for 0.5seconds to obtain the un—stimulated ities baseline. The stimulatory rm is applied for 9 seconds followed by 0.5 seconds of post-stimulation recording to examine the relaxation to the resting state.

The stimulatory waveform of the electrical stimulation is specific for each cell type and can vary the magnitude, duration and frequency of the applied current to provide an l assay signal.

Data Analysis -288— Data are ed and reported as ized ratios of background- subtracted emission intensities measured in the 460 nm and 580 nm channels.

Background intensities are then subtracted from each assay channel. ound intensities are obtained by measuring the emission intensities during the same time periods from identically treated assay wells in which there are no cells. The response as a function of time is then reported as the ratios obtained using the following formula: (intensity 460 nm - background 460 nm) R(t) = --------------------------------------- (intensity 580 nm - background 530 mm) ] The data is further reduced by calculating the initial (R) and final (Rf) ratios. These are the average ratio values during part or all of the pre-stimulation period, and during sample points during the stimulation period. The response to the stimulus R: Rf/Ri is then calculated and reported as a function of time.

[00780] Control responses are obtained by performing assays in the presence of a compound with the desired properties (positive control), such as tetracaine, and in the absence of pharmacological agents (negative control). Responses to the negative (N) and positive (P) controls are ated as above. The compound antagonist activity A is defined as: R _ P A: * 100 N “ P where R is the ratio response of the test compound ELECTROPHYSIOLOGYASSAYS FOR Na VACTIVITYAND INHIBITION OF TEST COMPOUNDS Patch clamp electrophysiology was used to assess the efficacy and selectivity of sodium l blockers in dorsal root ganglion neurons. Rat neurons were isolated from the dorsal root ons and maintained in e for 2 to 10 days in the presence of NGF (50 ng/ml) (culture media consisted of NeurobasalA supplemented with B27, glutamine and otics). Small diameter neurons eptors, 8-12 am in diameter) have been visually identified and probed with fine tip glass electrodes connected to an amplifier (Axon Instruments). The “voltage clamp’ mode has been used to assess the compound’s ICSO holding the cells at »— 60 mV. In -289— addition, the “current clamp” mode has been ed to test the efficacy of the compounds in blocking action potential tion in response to t injections.

The results of these experiments have contributed to the definition of the efficacy profile of the compounds.

IonWorks assays.

Sodium currents were recorded using the automated patch clamp system, IonWorks (Molecular Devices Corporation, Inc.). Cells expressing Nav subtypes are ted from tissue culture and placed in suspension at 0.5-4 million cells per mL Bathl. The IonWorks instrument measures changes in sodium currents in response to applied voltage clamp similarly to the traditional patch clamp assay, except in a 384—well format. Using the IonWorks, dose-response relationships were determined in voltage clamp mode by depolarizing the cell from the experiment specific holding potential to a test potential of about 0 mV before and following on of the test compound. The ce of the compound on currents are measured at the test ial. azepin-Z-one binding assay The sodium channel ting properties of the compounds of the invention can also be determined by assay methods described in Williams, B. S. et al., “Characterization of a New Class of Potent Inhibitors of the Voltage—Gated Sodium Channel NaV 1.7,” Biochemistry, 2007, 46, 14693-14703, the entire contents of which are incorporated herein by reference.

The exemplified compounds of Table 1 herein are active against one or more sodium channels as measured using the assays described herein above as presented in Table 3.

Table 3. —290- WO 25613 1 ++ 2 + 3 +++ 41 +++ 4 ++ 42 +++ +++ 43 ++ 6 ++ 44 +++ 7 +++ 45 +++ 8 ++ 46 +++ 9 ++ 47 +++ +++ 48 +++ 11 +++ 49 +++ 12 +++ 50 +++ 13 +++ 51 + 14 + 52 +++ + 53 ++ 16 +++ 54 +++ 17 +++ 55 +++ 18 +++ 56 ++ 19 +++ 57 ++ +++ 58 +++ 21 +++ 59 +++ 22 +++ 6O +++ 23 + 61 +++ 24 +++ 62 +++ ++ 63 ++ 26 ++ 64 + 27 +++ 65 + 28 + 66 +++ 29 +++ 67 +++ + 68 ++ 31 + 69 + 32 + 70 +++ 33 +++ 71 + 34 + 72 + 73 +++ 36 ‘74 +++ 37 +++ 75 +++ 38 ++ 76 ++ —291— WO 25613 77 +++ 115 ++ 78 +++ 116 +++ 79 +++ 117 +++ 80 + 118 + 81 + 119 +++ 82 ++ 120 +++ 83 +++ 121 + 84 + 122 + 85 ++ 123 ++ 86 +++ 124 +++ 87 ++ 125 + 88 +++ 126 +++ 89 +++ 127 ++ 90 + 128 +++ 91 +++ 129 +++ 92 + 130 + 93 +++ 131 +++ 94 +++ 132 ++ 95 + 133 +++ 96 + 134 + 97 +++ 135 +++ 98 +++ 136 ++ 99 +++ 137 +++ 100 +++ 138 +++ 101 +++ 139 + 102 +++ 140 +++ 103 +++ 141 + 104 +++ 142 + 105 +++ 143 +++ 106 + 144 ++ 107 +++ 145 + 108 + 146 ++ 109 ++ 147 +++ 110 +++ 148 ++ 111 +++ 149 ++ 112 +++ 150 +++ 113 + 151 + 114 +++ 152 +++ —292- 12/125613 153 +++ 191 +++ 154 + 192 +++ 155 + 193 +++ 156 +++ 194 +++ 157 195 +++ 158 196 +++ 159 197 ++ 160 ++ 198 + 161 199 ++ 162 200 +++ 163 201 +++ 164 202 + 165 +++ :32 166 H 205 3: 167 + 206 +++ 168 207 +++ 169 +++ ‘ 383 170 +++ 21o TL 171 +++ 211 +++ 172 + 212 +++ 213 +++ 173 ++ 214 H 174 +++ 215 ++ 175 +++ 216 ++ 176 +++ 217 +++ _ 218 +++ 177 +++ 178 +++ 28 ::++ 179 + 221 +++ 180 +++ 222 +++ 181 + 223 +++ 224 +++ 182 +++ 183 +++ 3:2 2:1 184 +++ 227 +++ 185 + 228 +++ 229 ++ 186 +++ 187 33? T 188 ++ 232 +++ 189 +++ 233 +++ 234 +++ 190 +++ 235 +++ 12/125613 236 +++» 283 +++ 237 +++ 284 +++ 238 ++ 285 +++ 239 + 286 +++ 240 + 287 +++ 241 ++ 288 +++ 242 ++ 289 ++ 243 +++ 290 + 244 +++ 291 +++ 245 +++ 292 ++ 246 +++ 293 +++ 247 ++ 294 +++ 248 +++ 295 +++ 24g ++ 296 + 250 +++ 297 +++ 251 +++ 298 +++ 252 ++ 299 + 253 ++ 300 +++ 254 ++ 301 +++ 255 + 302 +++ 256 +++ 303 +++ 257 +++ 304 +++ 258 +++ 305 ++ 259 +++ 306 +++ 260 +++ 307 +++ 261 +++ 308 + 262 +++ 309 +++ 263 +++ 264 + 265 ++ 266 ++ 267 ++ 268 ++ 269 ++ 270 ++ 271 +++ 272 + 273 ++ 274 +++ 275 + 276 +++ 277 ++ 278 +++ 279 +++ 280 ++ 281 +++ 282 +++ -294— WO 25613 Many modifications and variations of the embodiments described herein may be made without departing from the scope, as is apparent to those skilled in the art.

The specific embodiments described herein are offered by way of example only. —295- WE

Claims (84)

CLAIM

1. A compound of formula I: (R1)n (R3)o or a pharmaceutically acceptable salt f, wherein, independently for each occurrence: R1 is C1-C6 alkyl, C1-C6 fluoroalkyl, C3-C8 cycloalkyl, halo, NR8SO2R8, SO2R8, SR8, SOR8, 8, NR8CO2R8, CN, CON(R8)2, SO2N(R8)2, CF3, optionally substituted heterocycloalkyl, optionally substituted phenyl, optionally substituted heteroaryl, or an optionally substituted straight chain (C1-C8)-R9, optionally substituted branched (C1-C8)-R9, optionally substituted cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3- C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R2 is H, C1-C6 alkyl, C1-C6 fluoroalkyl, an optionally tuted cycloalkyl, optionally substituted aryl, optionally tuted heteroaryl, optionally substituted heterocycloalkyl, COR8, CO2R8, CON(R8)2, CF3, CHF2, or a straight chain (C1- C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic )-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R3 is C1-C6 alkyl or halo; R8 is H, C1-C6 alkyl, or C3-C8 cycloalkyl, a straight chain (C1-C8)-R9, branched (C1-C8)- R9, or cyclic )-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, ed (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO 8 taken together with the atoms to which they are attached form 2, N, CF2, or NR, or 2 R a ring; R9 is H, CF3, CHF2, CH2F, CO2R, OH, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted C3-C8 cycloalkyl, optionally substituted heterocycloalkyl, N(R)2, NRCOR, CON(R)2, CN, or SO2R; R is H, C1-C6 alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted C3-C8 cycloalkyl, or optionally substituted heterocycloalkyl; A is an aryl, heteroaryl or heterocyclic in which each is ally tuted with C1-C6 alkyl, C3-C8 cycloalkyl, C3-C8 cycloalkoxy, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, NR 8SO 8, SO 8, SOR8, SR8, CO 8, NR8COR 8, NR8CO 8, CON(R8) 8) 2R 2R 2R 2R 2, SO2N(R 2, CHF 9, heterocycloalkyl, heterocycloalkoxy, aryl, aryl, or a 2, CF3, OCF3, OCHF2, R straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH 9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be 2 units of the straight (C1-C8)-R replaced with O, CO, S, SO, SO2, NH, CF2, or NR8; n is an integer from 0 to 4 inclusive; and o is an integer from 0 to 4 inclusive; wherein the alkyl and alkoxy groups include a straight, branched, substituted or unsubstituted hydrocarbon moiety that may be completely saturated, or may include one or more units of unsaturation; wherein the cycloalkyl group includes a non-aromatic, monocyclic, ic, or tricyclic, substituted or unsubstituted hydrocarbon moiety that may be completely saturated, or may e one or more units of unsaturation; wherein the heterocycloalkyl group includes a non-aromatic, monocyclic, bicyclic, or tricyclic, substituted or unsubstituted hydrocarbon moiety that may be completely ted, or may e one or more units of ration, and in which one or more ring carbon atoms in one or more ring members is an independently ed heteroatom; and wherein optional substituents are selected from halo, cyano, oxoalkoxy, hydroxy, amino, nitro, aryl, haloalkyl, and alkyl; with the proviso that the following compounds are excluded: , , wherein x = an integer from 1 to 3 inclusive.

2. The compound of claim 1, wherein R1 is optionally substituted aryl, optionally substituted aryl, C1-C6 alkyl, C1-C6 fluoroalkyl, an optionally substituted straight chain (C1-C8)-R9, optionally substituted branched (C1-C8)-R9, or optionally substituted cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight )-R9, branched (C1- C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, or NR8.

3. The compound of claim 1, wherein R1 is F; or any one of the following groups which may be optionally tuted: phenyl, pyridyl, oxazole, thiazole, pyrazole, oxadiazole, CH2OCH3, CH2F, CH2OCH(CH3)2, CH2OCHF2, CH3, CH2CH3, CH2OH, 2OH, CH2CH2OH, CH2OCH2CH3, CH(CH2)2, S , N , N N N HN N N N , O , , , N , O , O N N NH O F Cl , N , , , , F , N N Cl , N N O , N , , , , N N O , N N , , and N .

4. The compound of claim 1, wherein R2 is H, C1-C6 alkyl, C1-C6 alkyl, CF3, cycloalkyl, aryl, heterocycloalkyl, heteroaryl, or a straight chain (C1-C8)-R9, branched (C1- C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight, branched or cyclic (C3-C8)-R9 units may be replaced with O, CO, S, SO, SO2, N, or NR8.

5. The compound of claim 1, wherein R2 is H, 2, CH2CF3, CH(CH3)CH2F, CH2CH(CH3)2, CH3, CH2CH3, tBu, CH2CN, CH(CH3)2, CH2C(CH3)2OH, CH2CH2CH(CH3)2, CH2CH2OH, C(O)CH2CH3, C(O)CH(CH3)2, CH(CH3)CH2F, CH2CH(CH3)2, CH(CH2CH3)2, CH2C(CH3)2OH, CH2CH2CH(CH3)2, OH, C(O)CH3, C(O)CH2CH3, C(O)CH(CH3)2, CH2CF2CH3, CH2CCCH3, CH2C(O)tBu, CH2CH2OCH3, CH2OCH3, CH2C(O)CH3, CH2C(O)OCH3, CH2CH2OCH2CH2CH3, CH2CCCH2CH3, CH2CH2OCH2CH3, CH2CH2SCH3, CH2OCH3, CH2CH(CH2CH3)2, l, n-propyl, , N , O N , N N N N O , F3C , O , , , , O O N N S N F3C F F NC , N , , , , , , N N N F3C NC F N , , , CF3 , , , , O N , , O , , , , O S , , , , , , , , F , , , , , , N , O , , O , N N N , or N .

6. The compound of claim 1, wherein n is 0, 1, 2, or 3.

7. The compound of claim1, wherein n is 1 or 2.

8. The compound of claim 1, wherein n is 1.

9. The compound of claim 1, wherein o is 0 or 1.

10. The compound of claim 1, wherein o is 0.

11. The compound of claim 1, wherein A is R4 R6 wherein: R4 is H, C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, NR8SO2R8, SO2R8, SOR8, SR8, CO2R8, 8, NR8CO2R8, CON(R8)2, SO2N(R8)2, CHF2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain )-R9, ed (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched )-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R5 is H, C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, C3-C8 cycloalkoxy, halo, CN, OH, OR8, N(R8)2, NR8SO2R8, SO2R8, SOR8, SR8, CO2R8, NR8COR8, NR8CO2R8, CON(R8)2, SO2N(R8)2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, aryl, or a straight chain (C1-C8)-R9, branched (C1- C8)-R9, or cyclic )-R9 wherein up to three CH2 units of the straight (C1- C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, NR8SO2R8, SO2R8, SOR8, SR8, CO2R8, NR8COR8, NR8CO2R8, CON(R8)2, SO2N(R8)2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain (C1-C8)-R9, branched )-R9, or cyclic )- R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic )-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; or two ences of R4 and R5, or R5 and R6 er with the carbons to which they are attached form an optionally substituted ring comprising up to 2 heteroatoms.

12. The compound of claim 11, n R4 is H, C1-C6 alkyl, halo, or OCHF2.

13. The compound of claim 11, wherein R4 is H, F, CH3, or OCHF2.

14. The compound of claim 11, wherein R5 is H, C1-C6 alkyl, C1-C6 alkoxy, halo, CF3, CN, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, or NR8.

15. The compound of claim 11, n R5 is H, CH3, OCH3, OCH2CH3, OCH(CH3)2, F, Cl, CF3, CN, or CH2OH.

16. The compound of claim 11, wherein R6 is H, C1-C6 alkyl, C1-C6 alkoxy, SO2R8, SO2N(R8)2, R9, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)- R9, wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, S, SO, SO2, N, or NR8.

17. The compound of claim 11, n R6 is H, CH2OH, OCH3, OCH2CH3, OCH2CH2CH3, OCH2CH2CH(CH3)2, OtBu, tBu, OCH(CH3)2, OCH2C(CH3)2OCH3, CH(OH)CH(CH3)2, C(OH)(CH2CH3)2, OCH2C(CH3)2OH, C(CH3)2OH, OCH2CH2OCH3, OCH2CH2OH, OCH2CH2CH2OH, CCCH2OCH3, SO2CH3, SO2CH2CH(CH3)2, SO2CH(CH3)2, SO2CH2CH3, SO2C(CH3)3, CON(CH2CH3)2, C(CH3)2CO2CH3, OH O S NH N O O O O , , , , O , O , O O O O F S S S , , OH , F O HO , HO , O , O , or HO . R4 R6

18. The nd of claim 11, wherein R5 is: O O O O , F , OMe , Cl , O O OH S O O , , , , O OH S N OH , O , O , , F O O OH O O , O , , OMe , O O S S HO , , O , OH , OH S F , OH , O , O , O O O O OH OMe , F , , , OH , , OMe , OH, OH O S O O OH , , , , OMe O O O Cl OMe , , O , , O S O O O O S S HO , , O , O , OMe F O O O O S F O , HO , OMe , F F , F F , Cl OCF3 Cl , CF3 , , , , HO , , O , HO , , OH O O S HO , , , O , O O O CN , , HO , , O F S F O HO , F , HO , or .

19. The compound of claim 1, wherein A is heteroaryl or heterocyclic.

20. The compound of claim 19, wherein A is a monocyclic heteroaryl comprising 1 to 3 heteroatoms, wherein said heteroatoms are independently N, O, or S.

21. The compound of claim 19, wherein A is a bicyclic heteroaryl comprising from 1 to 3 atoms, wherein said heteroatoms are independently N, O, or S.

22. The compound of claim 19, wherein A is R4 O N R5 N R4 R6 R4 R6 R4 R6 R5 , R5 , or R5 wherein: R4 is H, C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, NR8SO2R8, SO2R8, SOR8, SR8, CO2R8, 8, NR8CO2R8, CON(R8)2, SO2N(R8)2, CHF2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain )-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R5 is H, C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, C3-C8 cycloalkoxy, halo, CN, OH, OR8, N(R8)2, NR8SO2R8, SO2R8, SOR8, SR8, CO2R8, NR8COR8, NR8CO2R8, CON(R8)2, SO2N(R8)2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain (C1-C8)-R9, branched (C1- C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the ht (C1- C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C3-C8 lkyl, C1-C6 , halo, CN, OH, OR8, N(R8)2, NR8SO2R8, SO2R8, SOR8, SR8, CO2R8, NR8COR8, NR8CO2R8, CON(R8)2, SO2N(R8)2, CF3, OCF3, OCHF2, R9, heterocycloalkyl, heterocycloalkoxy, aryl, heteroaryl, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)- R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; or two occurrences of R4 and R5, or R5 and R6 together with the carbons to which they are attached form an optionally substituted ring comprising up to 2 atoms.

23. The compound of claim 22, n R4 is H or C1-C6 alkyl.

24. The compound of claim 22, wherein R4 is H.

25. The compound of claim 22, wherein R5 is H, C1-C6 alkyl, or C1-C6 alkoxy.

26. The compound of claim 22, n R5 is H, CH3, or OCH3.

27. The compound of claim 22, wherein R6 is H, CN, C1-C6 alkoxy, or CF3.

28. The compound of claim 22, wherein R6 is H, CN, OCH3, or CF3.

29. The compound of claim 22, wherein A is : N O O O N O N , , , , OMe, N N N N N O CF3, , , OMe , or MeO .

30. The compound of claim 1, n the compound has formula IA: wherein: R2 is H, C1-C6 alkyl, C1-C6 fluoroalkyl, an optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heterocycloalkyl, or a straight chain (C1-C8)-R9, ed (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1- C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R5 is H, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 fluoroalkyl , halo, CF3, OCF3, OCHF2, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3- C8)-R9 may be ed with O, CO, S, SO, SO2, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 alkoxy, CN, SO2R8, )2, SO2N(R8)2, heterocycloalkyl, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R7 is C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from 0 to 3 inclusive.

31. The compound of claim 30, wherein R2 is C1-C6 alkyl, C1-C6 fluoroalkyl, cycloalkyl, aryl, heterocycloalkyl, aryl, or a straight chain )-R9, branched (C1- C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched )-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

32. The compound of claim 30, wherein R2 is CH3, , CH(CH3)2, CH2CH(CH3)2, CH2CHF2, CH2CF3, CH(CH3)CH2F, CH2CN, CH2CH2OH, CH2C(CH3)2OH, COCH2CH3, or COCH(CH3)2.

33. The compound of claim 30, n R5 is H, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 fluroroalkyl, halo, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)- R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

34. The compound of claim 30, n R5 is H, CH3, OCH3, OCH2CH3, CF3, Cl, F, or CH2OH.

35. The compound of claim 30, wherein R6 is H, C1-C6 alkoxy, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 units may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

36. The compound of claim 30, wherein R6 is H, CH2OH, OCH2CH3, OtBu, OCH(CH3)2, OCH2C(CH3)2OCH3, CH(OH)CH(CH3)2, OCH2C(CH3)2OH, 2OH, 2OCH3, OCH2CH2OH, OCH2CH2CH2OH, CCCH2OCH3, SO2CH3, CH(CH3)2, SO2CH(CH3)2, SO2CH2CH3, SO2C(CH3)3, CON(CH2CH3)2, OH O S NH N O O O O C(CH3)2CO2CH3, , , , , O , S O O , or HO .

37. The compound of claim 30, wherein R7 is halo.

38. The compound of claim 30, wherein R7 is F.

39. The compound of claim 30, wherein the R5 moiety is: O O O O , F , OMe , Cl , O O OH S O O , , , , O OH S N OH , O , O , , O O OH O O O , , OMe , HO , O O S S O O OH , OH , , F , S O OH , O , O , OMe , O O O NH O OH , , OH , , OH O O O OH, OH , , , OMe O O O Cl OMe , , O , , O S O O O O S S HO , , O , O , O CF3 HO , or .

40. The compound of claim 30, wherein the compound has formula IB: (R7)p wherein: R2 is H, C1-C6 alkyl, C1-C6 fluoroalkyl, an optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or ally tuted heterocycloalkyl, or a straight chain )-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1- C8)-R9 or cyclic (C3-C8)-R9 may be ed with O, CO, S, SO, SO2, N, CF2, or NR8; R5 is H, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 fluoroalkyl, halo, CF3, OCF3, OCHF2, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3- C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 alkoxy, CN, SO2R8, CON(R8)2, SO2N(R8)2, heterocycloalkyl, or a straight chain (C1-C8)-R9, ed (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R7 is C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from 0 to 3 inclusive.

41. The compound of claim 40, wherein R2 is C1-C6 alkyl, C1-C6 fluoroalkyl, or a straight chain (C1-C8)-R9, branched )-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be ed with O, CO, S, SO, SO2, N, CF2, or NR8.

42. The compound of claim 40, wherein R2 is CH3, CH2CH3, CH(CH3)2, CH2CH(CH3)2, 2, CH2CF3, CH(CH3)CH2F, CH2CN, CH2CH2OH, CH2C(CH3)2OH, COCH2CH3, or COCH(CH3)2.

43. The compound of claim 40, wherein R5 is H, C1-C6 alkyl, C1-C6 , C1-C6 fluroroalkyl, halo, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)- R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

44. The nd of claim 40, wherein R5 is H, CH3, OCH3, OCH2CH3, CF3, Cl, F, or CH2OH.

45. The compound of claim 40, wherein R6 is H, C1-C6 alkoxy, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

46. The compound of claim 40, wherein R6 is H, CH2OH, OCH2CH3, OtBu, OCH(CH3)2, OCH2C(CH3)2OCH3, CH(OH)CH(CH3)2, OCH2C(CH3)2OH, C(CH3)2OH, OCH2CH2OCH3, OCH2CH2OH, OCH2CH2CH2OH, CCCH2OCH3, SO2CH3, CH(CH3)2, SO2CH(CH3)2, SO2CH2CH3, SO2C(CH3)3, CON(CH2CH3)2, OH O S NH N O O O O C(CH3)2CO2CH3, , , , , O , S O O , or HO .

47. The nd of claim 40, wherein R7 is halo.

48. The compound of claim 40, wherein R7 is F.

49. The nd of claim 40, wherein the R5 moiety is: O O O O , F , OMe , Cl , O O OH S O O , , , , O OH S N OH , O , O , , O O OH O O O , , OMe , HO , O O S S , O , OH , OH F , S O OH , O , O , OMe , O O O NH O OH , , OH , , OH O O O OH, OH , , , OMe O O O Cl OMe , , O , , O S O O O O S S HO , , O , O , O CF3 HO , or .

50. The compound of claim 1, wherein the compound has formula IC: (R7)p Het wherein, the Het ring is a mono or bicyclic ally tuted heterocyclic or optionally substituted aryl ring; R2 is H, C1-C6 alkyl, C1-C6 fluoroalkyl, an optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heterocycloalkyl, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1-C8)- R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R5 is H, C1-C6 alkyl, C1-C6 alkoxy, halo, CF3, OCF3, OCHF2, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched )-R9 or cyclic (C3- C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 alkoxy, CN, SO2R8, )2, SO2N(R8)2, heterocycloalkyl, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, ed (C1-C8)-R9 or cyclic )-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8 R7 is C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from 0 to 3 inclusive.

51. The compound of claim 50, wherein the Het ring is an ally substituted thiazole, optionally substituted pyridine, optionally substituted pyrazole, optionally substituted oxazole, or optionally substituted oxadiazole.

52. The compound of claim 50, wherein p is 0 or 1.

53. The compound of claim 50, n, R7 is C1-C6 alkyl.

54. The compound of claim 50, wherein, R7 is CH3, CH2CH3, CH(CH3)2, or tBu.

55. The compound of claim 50, wherein the Het ring is N N N S N N , , N , , , , O O O O O N HN N N N N N N N H , , , , , , , N N HN N N O N N N N , , , , or .

56. The compound of claim 50, wherein R2 is C3-C6 alkyl or a straight chain (C1-C8)- R9, branched (C1-C8)-R9, or cyclic (C1-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

57. The compound of claim 50, wherein R2 is CH2CH3, tBu, CH2CHF2, , or

58. The compound of claim 50, wherein R5 is H, C1-C6 alkyl, C1-C6 alkoxy, or halo.

59. The compound of claim 50, wherein R5 is H, CH3, OCH3, F, or Cl.

60. The compound of claim 50, wherein R6 is H, C1-C6 alkoxy, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

61. The compound of claim 50, wherein R6 is OCH(CH3)2, C(CH3)2OH, OCH2CH2OH, O O S S N OCH2CH2CH2OH, O , or O .

62. The nd of claim 1, wherein the nd has formula ID: (R7)p Het wherein, the Het ring is a mono or bicyclic optionally substituted heterocyclic or optionally substituted aryl ring; R2 is H, C1-C6 alkyl, C1-C6 fluoroalkyl, an optionally tuted aryl, optionally substituted heteroaryl, or optionally substituted heterocycloalkyl, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight )-R9, branched (C1-C8)- R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R5 is H, C1-C6 alkyl, C1-C6 alkoxy, halo, CF3, OCF3, OCHF2, or a ht chain (C1-C8)-R9, branched )-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3- C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8; R6 is H, C1-C6 alkyl, C1-C6 , CN, SO2R8, CON(R8)2, SO2N(R8)2, heterocycloalkyl, or a straight chain (C1-C8)-R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8 R7 is C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, halo, CN, OH, OR8, N(R8)2, CF3, OCF3, or OCHF2; and p is an integer from 0 to 3 inclusive.

63. The compound of claim 62, wherein the Het ring is an ally substituted thiazole, optionally substituted pyridine, optionally substituted pyrazole, optionally substituted oxazole, or ally tuted oxadiazole.

64. The compound of claim 62, wherein p is 0 or 1.

65. The compound of claim 62, wherein R7 is C1-C6 alkyl.

66. The compound of claim 62, wherein R7 is CH3, CH2CH3, CH(CH3)2, or tBu.

67. The compound of claim 62, wherein the Het ring is N N N N S N N , , N , , , , O O O O O N HN N N N N N N N H , , , , , , , HN N N N N N N , , , or .

68. The compound of claim 62, n R2 is C1-C6 alkyl or a straight chain (C1-C8)- R9, branched (C1-C8)-R9, or cyclic (C3-C8)-R9 wherein up to two CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be ed with O, CO, S, SO, SO2, N, CF2, or NR8.

69. The compound of claim 62, wherein R2 is CH2CH3, tBu, CH2CHF2, CH2CF3, or

70. The compound of claim 62, wherein R5 is H, C1-C6 alkyl, C1-C6 alkoxy, or halo.

71. The nd of claim 62, wherein R5 is H, CH3, OCH3, F, or Cl.

72. The compound of claim 62, wherein R6 is H, C1-C6 alkoxy, or a straight chain (C1-C8)-R9, ed )-R9, or cyclic (C3-C8)-R9 wherein up to three CH2 units of the straight (C1-C8)-R9, branched (C1-C8)-R9 or cyclic (C3-C8)-R9 may be replaced with O, CO, S, SO, SO2, N, CF2, or NR8.

73. The compound of claim 62, wherein R6 is OCH(CH3)2, C(CH3)2OH, OCH2CH2OH, O O S S N OCH2CH2CH2OH, O , or O .

74. The compound of claim 1, wherein the compound is selected from the following table: 1 2 3 4 5 6 7 8 10 11 12 ———— ———— 327— 328— ———— 330— 331— ———— 3333 ———— ———— ———— ———— ———— 339— ————

75. A pharmaceutical ition comprising the nd of claim 1 and a pharmaceutically acceptable carrier.

76. A method of inhibiting a voltage-gated sodium ion channel in: a biological sample; comprising contacting the biological sample, with the nd or composition of claim 1, and wherein the biological sample is located in vitro.

77. The method of claim 76, wherein the voltage-gated sodium ion channel is NaV 1.7.

78. The use of a compound according to claim 1, in the manufacture of a medicament for treating or lessening the severity of a condition selected from acute, chronic, neuropathic, or inflammatory pain, arthritis, migraine, cluster headaches, trigeminal neuralgia, herpatic gia, general gias, epilepsy or epilepsy ions, neurodegenerative disorders, psychiatric disorders, anxiety, depression, dipolar disorder, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, multiple sis, irritable bowel syndrome, incontinence, visceral pain, osteoarthritis pain, postherpetic neuralgia, diabetic athy, radicular pain, sciatica, back pain, head or neck pain, severe or table pain, nociceptive pain, breakthrough pain, postsurgical pain, cancer pain, , cerebral ischemia, traumatic brain injury, ophic lateral sclerosis, stress- or exercise induced angina, palpitations, hypertension, migraine, and abormal gastro-intestinal motility.

79. The use of claim 78, n the condition is selected from femur cancer pain; nonmalignant chronic bone pain; rheumatoid arthritis; osteoarthritis; spinal stenosis; neuropathic low back pain; athic low back pain; myofascial pain syndrome; fibromyalgia; temporomandibular joint pain; chronic visceral pain, abdominal pain; pancreatic; IBS pain; chronic and acute headache pain; migraine; tension headache, including, cluster headaches; chronic and acute neuropathic pain, post-herpatic neuralgia; diabetic neuropathy; HIV-associated neuropathy; trigeminal neuralgia; Charcot-Marie Tooth neuropathy; tary sensory neuropathies; peripheral nerve injury; l neuromas; ectopic proximal and distal discharges; lopathy; chemotherapy induced neuropathic pain; radiotherapy-induced neuropathic pain; post-mastectomy pain; central pain; spinal cord injury pain; post-stroke pain; thalamic pain; complex regional pain syndrome; phantom pain; intractable pain; acute pain, acute post-operative pain; acute musculoskeletal pain; joint pain; mechanical low back pain; neck pain; tendonitis; injury/exercise pain; acute visceral pain, abdominal pain; pyelonephritis; appendicitis; cholecystitis; intestinal obstruction; hernias; chest pain, cardiac pain; pelvic pain, renal colic pain, acute obstetric pain, labor pain; cesarean section pain; acute inflammatory, burn and trauma pain; acute intermittent pain, endometriosis; acute herpes zoster pain; sickle cell anemia; acute pancreatitis; breakthrough pain; orofacial pain including sinusitis pain, dental pain; multiple sclerosis (MS) pain; pain in depression; leprosy pain; Behcet's disease pain; adiposis dolorosa; phlebitic pain; Guillain-Barre pain; painful legs and moving toes; Haglund syndrome; erythromelalgia pain; Fabry's disease pain; bladder and urogenital e, y incontinence; ctivity bladder; l bladder syndrome; interstitial cyctitis (IC); prostatitis; complex regional pain syndrome (CRPS), type I and type II; widespread pain, paroxysmal extreme pain, pruritis, tinnitis, or angina-induced pain.

80. The use of a compound according to claim 1 in the manufacture of a medicament for inhibiting a voltage gated sodium ion channel.

81. A compound according to claim 1, substantially as herein described with reference to any one of the examples and/or figures.

82. A pharmaceutical composition according to claim 75, ntially as herein bed with reference to any one of the examples and/or figures.

83. A method according to claim 76, substantially as herein described with nce to any one of the es and/or figures.

84. The use according to claim 78, substantially as herein described with reference to any one of the examples and/or figures.