AU2014202485A1 - Substituted triazolo-pyridazine derivatives - Google Patents

Abstract

This invention relates to novel substituted triazolo-pyridazines, their derivatives, and pharmaceutically acceptable salts thereof. This invention also provides compositions 5 comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering an al -GABA A receptor antagonist and/or a a2, 3 and a5 GABA-A receptor agonist. 531078 1 (GHMaiers- P86533 A[ J 1

Description

SUBSTITUTED TRIAZOLO-PYRIDAZINE DERIVATIVES CROSS-REFERENCE TO RELATED APPLICATION [1] The entire disclosure in the complete specification of our Australian Patent Application No. 2009285533 is by this cross-reference incorporated into the present 5 specification. [1a] This application claims the benefit of priority to United States Provisional Application Serial No. 61/093,293, filed August 29, 2008, the contents of which are incorporated herein by reference. -0 [2] This invention relates to novel substituted triazolo-pyridazines, their derivatives, and pharmaceutically acceptable salts thereof This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering an al -GABA-A .5 receptor antagonist. [3] L-838417, also known as 7-tert-butyl-3-(2,5-difluorophenyl)-6-(1-methyl-lH-1,2,4 triazol-5-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine, acts at the benzodiazepine site of the GABA-A receptor as an antagonist of al subtypes, and as a functionally selective allosteric agonist of the a2, a3 and a5 subtypes. o [4] L-838417 is currently a preclinical candidate for central nervous system disorders. Despite the beneficial activities of L-838417, there is a continuing need for new compounds that are al -GABA-A receptor antagonists. Brief Description of the Drawings [5] Figure 1 depicts the stability of compounds of the invention in human liver 25 microsomes over time. [6] Figure 2 depicts the stability of compounds of the invention in rat liver microsomes over time. [7] Figure 3 depicts the change in concentration of compounds of the invention in plasma following intravenous administration to rats. [8] Figure 4 depicts the change in concentration of compounds of the invention in plasma 30 following oral administration to rats. 1 5298591 1 (GHMailersn P8533 Al J Definitions [9] The term "treat" means decrease, suppress, attenuate, diminish, arrest, or stabilize the development or progression of a disease (e.g., a disease or disorder 5 la 5298591 1 (GHMatter PR86533 A J 1 delineated herein). [10] "Disease" means any condition or disorder that damages or interferes with the normal function of a cell, tissue, or organ. [11] It will be recognized that some variation of natural isotopic abundance occurs 5 in a synthesized compound depending upon the origin of chemical materials used in the synthesis. Thus, a preparation of L-838417 will inherently contain small amounts of deuterated isotopologues. The concentration of naturally abundant stable hydrogen and carbon isotopes, notwithstanding this variation, is small and immaterial as compared to the degree of stable isotopic substitution of compounds of this invention. 10 See, for instance, Wada, E et al, Seikagaku, 1994, 66:15; Gannes, LZ et a]. Comp Biochem Physiol Mol Integr Physiol, 1998, 119:725. In a compound of this invention, when a particular position is designated as having deuterium,, it is understood that the abundance of deuterium at that position is substantially greater than the natural abundance of deuterium, which is 0.015%. A position designated as 15 having deuterium typically has a minimum isotopic enrichment factor of at least 3000 (45% deuterium incorporation) at each atom designated as deuterium in said compound. [12] The term "isotopic enrichment factor" as used herein means the ratio between the isotopic abundance and the natural abundance of a specified isotope. 20 [13] In other embodiments, a compound of this invention has an isotopic enrichment factor for each designated deuterium atom of at least 3500 (52.5% deuterium incorporation at each designated deuterium atom), at least 4000 (60% deuteium incorporation), at least 4500 (67.5% deuterium incorporation), at least 5000 (75% deuterium), at least 5500 (825% deuterium incorporation), at least 6000 (90% 25 deuterium incorporation), at least 6333.3 (95% deuteium incorporation), at least 6466.7 (97% deuterium incorporation), at least 6600 (99% deuterium incorporation), or at least 6633.3 (99,5% deutedum incorporation). [141 In the compounds of this invention any atom not specifically designated as a particular isotope is meant to represent any stable isotope of that atom., Unless 30 otherwise stated, when a position is designated specifically as "H" or "hydrogen", the position is understood to have hydrogen at its natural abundance isotopic composition, Also unless otherwise stated, when a position is designated specifically as "D" or "deuterium" the position is understood to have deuterium at an abundance that is at 2 least 3340 times greater than the natural abundance of deuteriuni, which is 0,015% (i.e., at least 50.1% incorporation of deuteriu), [1$] The term "isotopologue" refers to a species that differs from a specific compound of this invention only in the isotopic composition themof, 5 [16] The term "compound," as used herein, refers to a collection of molecules having an identical chemical stmtme, except that there may be isotopic variation among the constituent atoms of the molecules. Thus, it will be clear to those of skill in the art that a compound represented by a particular chemical structure containing indicated deuterium atoms, will also contain lesser amounts of isotopologues having 10 hydrogen atoms at one or more of the designated deutedium positions in that structure. The relative amount of such isotopologues in a compound of this invention will depend upon a number of factors including the isotopic purity of deuterated reagents used to make the compound and the efficiency of incorporation of deuterium in the various synthesis steps used to prepare the compound. However, as set forth above 15 the relative amoutm of' such isotop&logues will be less than 49.9% of the compound. [17] The invention also includes salts of the compounds disclosed herein, [18] A salt of a compound of this invention is formed between an acid and a basic group of the compound, such as an amino functional group, or a base and an acidic group of the compound, such as a carboxyl functional group. According to another 20 embodiment, the compound is a pharmaceutically acceptable acid addition salt. [191 The ten "pharmaceutically acceptable," as used herein, refers to a component that is, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and other manmnals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. A 25 pharmaceuticallyy acceptable salt" means any non-toxic salt that, upon administration to a recipient, is capable of providing, either directly or indirectly, a compound of this invention. A "pharmaceutically acceptable counterion" is an ionic portion of a salt that is not toxic when released from the salt upon administration to a recipient, [201 Acids commonly employed to form pharmaceutically acceptable salts include 30 inorganic acids such as hydrogen bisuifide, hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid and phosphoric acid, as well as organic acids such as para-toluenesulfonic acid, salicylic acid, tartaric acid, bitartaric acid, ascorbic acid, maleic acid, besylic acid, furaric acid, glucon-ic acid, glucuronic acid, formic acid, glutamic acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, lactic 3 acid, oxalic acid, para-bromophenylsulfonic acd, carbonic acid, succinic acid, citric acid, benzoic acid and acetic acid, as well as related inorganic and organic acids. Such phannaceutically acceptable salts thus include sulfate, pyrosulfate, bisulfate, sulfite, bisulfite, phosphate, monohydrgenpbosphate, dihydrogenphosphate, 5 metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate, propionate, decanoate, caprylate, acrylate, format, isobntyrate, caprate, heptanoate, propiolate, oxalate, malonate, succinate, suberate, sebacate, fumarate, maleate, butyne-1,4ioate, hexyne-1,6-dicate, benroate, chlombenzoate, methylbenzoate, dinrobenzoate, hydroxybenzoate, methoxybenzoate, phthalate. tereplithalate, sulfonate, xylene 10 sulfonate, phenylacetate, phenylpropionate, phenylbutyrate, citrate. lactate, 0 hydroxybutyrate, glycolate, maleate, tactrate, methanesulfonate, propanesulfonate, naphthalene-1-sulfonate, nahthalene-2-nateonate, mandelate and other sals. In one embodiment, phannaceutically acceptable acid addition salts include those formed. with mineral acids such as hydrochloric acid and hydrobromic acid, and especially 15 those formed with organic acids such as maleic acid. 121] The compounds of the present invention (e~ge, compounds of Formula I), may contain an asymmetric carbon atom, for example, as the result of deuterium substitution or otherwise. As such, compounds of this invention can exist as either individual enantiomers, or mixtures of the two enantiomers,. Accordingly, a 20 compound of the present invention may exist as either a racemic mixture or a scaltemic mixture, or as individual respective stereoisomers that are substantially free from another possible stereoisomer. The term "substantially free of other steroisomers" as used herein means less than 25% of other stereoisomers, preferably less than 10% of other steroisomners, more preferably less than 5% of other 25 stereoisomers and most preferably less than 2% of other stereoisomers, or less than "X"% of other stereoisomers (wherein X is a number between 0 and 100, inclusive) are present, Methods of obtaining or synthesizing an individual enantiomer for a given compound are known in the art and may be applied as practicable to final compounds or to starting material or intermediates. 30 [221 Unless otherwise indicated, when a disclosed compound is named or depicted by a structure without specifying the stereochemis try and has one or more chiral centers, it is understood to represent all possible stereoisomers of the compound. [231 The term "stable compounds," as used herein, refers to compounds which possess stability sufficient to allow for their manufacture and which maintain the 4 integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., formulation into therapeutic products, intermediates for use in production of therapeutic compounds, isolatable or storable intermediate compounds, treating a disease or condition responsive to therapeutic agents). 5 [24] "D" refers to deuterium, "Stereisome refers to both enantiomers and diasteeomers. "Tet", and "C-" each refer to tertiary. "US"I refers to the United States of America, [25] Throughout this specification, a variable may be referred to generally (e.g."each R") or may be referred to specifically (e.g. R', Rt R", etc.). Unless 10 otherwise indicated, when a variable is referred to generally, it is meant to include all specific embodiments of that particular variable, Therapeutic Compounds [26] The present invention provides a compound of Formula I N N' F N 5-N Y2 15 F Formula I or a pharmaceutically acceptable salt thereof, wherein: R1 is CHi CDH 2 , CD28, or CDi) 3 R is a t-butyl group having 0-9 deuterium atoms; each Y is independently hydrogen or deuterium; and 20 when R 1 is CH 3 and each Y is hydrogen, then R: has 1-9 deuterium atoms. [27] One embodiment of this invention provides a compound of Formula I wherein R' is CH3 or CD.. In one aspect of this embodiment, Y" and Y are hydrogen In another aspect, Ya and Y ) are deuterium. In another aspect, Y2 is hydrogen. In another aspect, Y 2 is deuterhim. In another aspect, R 2 is -C(C1%) or -C(CD,) 3 . As ai 25 example of this aspect, W) is -C(CD3)3. [28] Another embodiment provides compounds wherein R 2 is ~C(CHT) or C(CD 3 ). As an example, RW is -C(CD) 3 . In one aspect of this embodiment, Y1a and Ya are hydrogen. In another aspect, Y" and Y are deuterium. In another aspect, Y2 is hydrogen, h, another aspect, Y is deuterium 5 [29] Another embodiment provides compounds wherein Y" and Y"' arc the same. In one aspect of this embodiment, Yit and Y are deuterium. In one aspect of this embodiment, Ris -C(CD 3

)

1 . 130] In yet another embodiment, the compound is selected from any one of the 5 compounds set forth in Table 1 below. Table 1: Examples of Conpounds of Formula I 101 CD, -C(CQ fU D D 107CH, C(CHb D D H 102 C~a C(CD3) D D H 110 C CH C(CD 3

)

3 H H D 114 CD- C(CDk H H H 108 CD, C(CD 3 D D D 109 CH-I CDD~ D D 110 Ct H&(QCD;4 H H D III CD-1 -CfCD- 3 ). H H D 112 C-3 Q~CD 3 )) D D D 113 CD- C(CH) H H D 114 C1-6 -C(CH>3 0 D D [31] In certain embodinents, the compound is selected from any one of 10 Compounds 102, 103, 104,105, 109, 110, 111 and 112, or pharmaceutical acceptable salts thereof. In other embodiments, the compound is selected from any one of Compounds 102, 103 and 105, or phamaceutically acceptable salts thereof In one aspect, the compound is selected fron Compound 103 or Compound 105, or pharmaceutically acceptable salts thereof. 15 [32] In another set of embodiments, any atam not designated as deutewum in any of the embodiments set forth above is present at its natural isotopic abundance. [33] The synthesis of compounds of Formula I can be readily achieved by synthetic chemists of ordinary skill following the Exemplary Synthesis and Examples disclosed herein. Other relevant procedures and intenmediates are disclosed, for instance in 20 PCT patent publication Nos. WO 98/04559 and WO 00/44752. [341 Such methods can be carried out utilizing corresponding deuterated and optionally, other isotope-containing reagents and/or intemediates to synthesize the compounds delineated herein, or invoking standard synthetic protocols known in the 6 art for introducing isotopic atoms to a chemical structure, Certain intermediates can be used with or without purification (e~g., filtration, distillation, sublimation, crystaization, trituration, solid phase extraction, and chromatography). 5 Exemplary Synthesis [35] Compounds of Formula I may be prepared according to the schemes shown below. Sch1.en_Qm oetCompaundso omaI Cl N (NH4) 2

SO

5 C N Rr'-CC 2 H +N AgNOQ, H 2 S0 4 C H2O, 70"C Rl Cl 0 10 1 12 H

R

1 <a yib F NH2 R OH N~ \, NR NC N F 15 F13 Y2 1 Et 5 N#HC- NaH, DMF xylene F 14 N N F Formula I 15 [36] The synthesis of compounds of Fonnula I can be accomplished generally as shown in Scheme 1 Intermediate 12 is prepared by radical alkylation of 3& dichloropyridazine 11 with the appropriately deuterated pivalic acid 10. D9-Pivalic acid is commercially available for the preparation of those compounds wherein R- is 20 C(CD,)s. The appropriately deuterated 3,6-dichloro-4-t-butylpyridazine 12 is then condensed with 25difluoribenzohydrazide 13 to provide 14 Displacement of the chloride with the anion generated from appropriately deuterated (2-methyl-2- 1,2,4 7 triazol-3-yl)metbanol 15 and NaH provides compounds of Formula 1. Aternatively, the conversion of 14 to compowids of Formula I is accomplished via the use of nBuLi in THF, or cesium carbonate in DMSO or under other similar conditions known to the skilled artisan. 5 Scheme 2. Synthesis of Compound 15, RT y y h yR1 Nia ylab N ' "''' N + H Na. MaCH HzOr~ N ~~R N:.Me5 H0 or D20N 16 17 15 10 [37] Scheme 2 illustrates the preparation of deuterated analogs of 1.5, As described by Dallacker F at aL, Chemiker-Zeitung 1986, 110:101-108 and Dallacker F et at Chemiker-Zeitung 1986, 110, p. 275-281, 12A4-tazole (16) reacts with R 1 -l to provide the appropriately deuterated methyl triazole 17, which is then treated with fonmaldehyde or deuterated formaldehyde to provide 15. One skilled in the art will 15 appreciate that deuterium exchange may potentially occur under these conditions to afford compounds wherein Y 2 is deuterium, [38] The specific approaches and compounds shown above are not intended to be limiting. The chemical structumes in the schemes herein depict variables that are hereby defined commensurately with chemical group definitions (moieties, atoms, 20 etc-.) of the corresponding position in the compound frmnulae herein, whether identified by the same variable name (i iet R R2, R, etc.) or not. The suitability of a chemical group in a compound structure for use in the synthesis of another compound is within the knowledge of one of ordinary skill in the art [39) Additianal methods of synthesizing compounds of Formula I and their 25 synthetic precurors, including those within routes not explicitly shown in schemes herein, are within the means of chemists of ordinary skill in the art. Synthetic chemistry transformations and protecting group methodologies (protection and deprotetion) useful in synthesizing the applicable compounds are known in the at and include, for example, those described in Larock R, Conprehensive Organc 30 Transformations, VCH Publishers (1989); Greene TW et al., Protective Groups in Organic Synthesis, 3d Ed., John Wiley and Sons (1999); Fieser L et al, Fieser and Fieser's Reagentsfor Organic Synthesis, John Wiley and Sons (1994); and Paquette 8 L, ed,, Encyclopedia ofReagents for Organic 5ynthesis, John Wiley and Sons (1995) and subsequent editions thereof. [40] Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. 5 Compositions [41] The invention also provides pyrogen-4ree compositions comprising an effective amount of a compound of Formula I (e.g,, including any of the formulae herein), or a pharmaceutically acceptable sa-of said compound; and an acceptable 10 canier, Preferably, a composition of this invention is formulated for pharmaceutical use ("a pharmaceutical composition"), wherein the carrier is a phnmnaceutically acceptable carrier, The carder(s) are "acceptable" in the sense of being compatible with the other ingredients of the formulation and, in the case of a pharnaceutically acceptable carrier, not deleterious to the recipient thereof in an amount used in the 15 medicament, [42] A pharmaceutically acceptable carrier includes adjuvants and vehicles that may be used in the pharmaceutical compositions of this invention. A pharmaceutical acceptable canrier includes one or more of salts, electrolytes, solubiliing agents, solvents, buffers, emulsifying agents, flavorings, colorings, sweeteners, filler, 20 lubricating agents, diluents, suspending agents, thickening agents, dispersing agents, wetting agents, bioavailability enhancers, and absorption promoters. Specific pharmaceutically acceptable carrier include, but are not limited to, 1,3-butanediol, 2 octyldodecanol, acacia, alumina, aluninum stearate, beeswax, benzyl alcohol, phosphates, cellulose-based substances, cetearyl alcohol, cetyl esters wax, cocoa 25 butter, colloidal silica, corn starch, disodium hydrogen phosphate, emulsifying wax, ethylene oxide-propylene oxide block copolymers, gelatin, glycerin, glycine, human senum albumin, ion exchangers, isotonic sodium chloride, lactose, lecithin, liquid petroleum long-chain alcohol, LUTROLT

M

. magnesiam separate, magnesium trisilicate, mannitol, mineral oil, oleic acid and its glyceride derivatives, olive oil or 30 castor oil especially in their polyoxyethylated versions, partial glyceride mixtures of saturated vegetable fatty acids, PLURONICT1, polyacrylates, polyethylene glycol, polyethylene-polyoxypropylene-block polymers, polysorbate 60, polyvinyl pyrrolidone, potassium hydrogen phosphate, potassium sorbate, propylene glycol, protanine sulfate, Ringers solution, serum proteins, sodium carboxymethylcellulose, 9 sodium chloride, sorbic acid, sorbitan monostearate, sucrose, tragacanth, Tween 80, water, waxes, white petroleum, wool fat, and zinc salts, 143] The pharmaceutical compositions of the invention include those suitable fbr oral, rectal, nasal, topical (including buccal and sublingual), vaginal, parenteral 5 (including subcutaneous, intramuscular, intravenous and intradermal) and transdermal administration. The choice of appropriate pharmaceutically acceptable cartier to employ with each type of composition is well known in the art. Similarly, methods for bringing together the active ingredients) and the carriers to create unit dosage forms of the vadIous phaanaceutical compositions of this invention are also well 10 known in the art, See, for example, Remington: The Science and Practice of Pharmacy, Lippincctt Williams & Wilkins, Batiore, MD (20th ed, 2000) [44] In another embodiment, a composition of this invention further comprises a second therapeutic agent. The second therapeutic agent may be selected from any compound or therapeutic agent known to have or that demonstrates advantageous 15 properties when administered with a compound having the same mechanism of action as L-838417. [45] Preferably, the second therapeutic agent is an agent useful in the treatment or prevention of a disease or condition selected from disorders of the central nervous system, including anxiety and convulsions; and neuropathic, inflammatory and 20 migraine associated pain. [40] In another embodiment, the invention provides separate dosage foms of a compound of this invention and one or more of any of the above-described second therapeutic agents, wherein the compound and second therapeutic agent are associated with one another. The temi "associated with one another" as used herein means that 25 the separate dosage forns are packaged together or otherwise attached to one another such that it is readily apparent that the separate dosage forms ar intended to be sold and administered together (within less than 24 hours of one another, consecutively or simultaneously). [471 In the pharmaceutical compositions of the invention, the compound of the 30 present invention is present in an effective amount, As used herein, the term "effective amount" refers to an amount which, when administered in a proper dosing regimen, is sufficient to reduce or ameliorate the severity, duration or progression of the disorder being treated, prevent the advancement of the disorder being treated, 10 cause the regression of the disorder being treated, or enhance or improve the prophylactic or therapeutic effect(s) of another therapy. [481 The interelationship of dosages for animals and humans (based on milligrams per meter squared of body surface) is described in Freireich et at, (1966) Cancer 5 Chemother. Rep 50: 219. Body surface area may be approximately determined from height and weight of the patient., See, e-g., Scientific Tables, Geigy Pharmaceuticals, Ardsley, NY, 1970, 537. 149] In one embodiment, an effective amount of a compound of this invention can range front about 0.01 to about 5000 rmg per treatment. In more specific embodiments 10 the range is from about 0,1 to 2500 mg, or front 0,2 to 1000 rmg, or most specifically from about I to 500 rmg. Treatment typically is administered one to three times daily. [501 Effective doses will also vary, as recognized by those skilled in the art, depending on the diseases treated, the severity of the disease, the route of administration, the sex, age and general health condition of the patient, excipient 15 usage, the possibility of co-usage with other therapeutic treatments such as use of other agents and the judgment of the treating physician. For example, guidance for selecting an effective dose can be determined by refenace to the prescribing information for L-838417. [51] For pharmaceutical compositions that comprise a second therapeutic agent, an 20 effective amount of the second therapeutic agent is between about 20% and 100% of the dosage normally utilized in a monotherapy regime using just that agent. Preferably, an effective amount is between about 70% and 100% of the normal monotherapeu tic dose. The normal monotherapeutic dosages of these second therapeutic agents are well known in the art. See, e.g, Wells et aL, eds, 25 Pharmacotherapy Handbook, 2nd edition, Appleton and Lange, Stamtford, Conn. (2000); PDR Pharmacqpceia, Tarascon Pocket Pharmacopoeia 2000, Deluxe Edition, Tarascon Publishing, Loma Linda, Calif. (2000), each of which references are incorporated herein by reference in their entirety. [52] It is expected that some of the second therapeutic agents referenced above will 30 act synergistically with the compounds of this invention. When this occurs, it will allow the effective dosage of the second therapeutic agent and/or the compound of this invention to be reduced from that required in a nonotherapy. This has the advantage of minimizing toxic side effects of Cither the second therapeutic agent of a compound of this invention, synergistic improvements in efficacy, improved ease of 11 administration or use and/or reduced overall expense of compound preparation or formulation. Methods of treatment 5 [53] In another embodiment, the invention provides a method of inhibiting the m- I subtype of the GABA-A receptor in4 a cell, comprising contacting a cell with one or more compounds of Fonmula I herein, In another embodiment, the invention provides a method of activating one or more of the a2, 3 and aS subtypes of the GABA-A receptor in a cell 10 f54] According to another embodiment, the invention provides a method of treating a patient suffering from, or susceptible to, a disease that is beneficially treated by L 838417 comprising the step of administering to said patient an effective amount of a compound of Formula I or salt thereof, or a composition of this invention. Such diseases are well known in the art and are disclosed in, but not limited to the 15 following patents and published applications: WO 1998004559, WO 2000044752, WO 2006061428. Such diseases include, but are not limited to, disorders of the central nervous system, including anxiety and convulsions; and neuropathic, inflammatory and migraine-associated pain. [55] Methods delineated herein also include those wherein the patient is identified 20 as in need of a particular stated treatment. Identifying a patient in need of such treatment can be in the judgment of a patient or a health care professional and can be subjective (e.g. opinion) or objective (e.g, measurable by a test or diagnostic method) [56] In another embodiment, any of the above methods of treatment comprises the further step of co-administering to said patient one or more second therapeutic agents. 25 The choice of second therapeutic agent may be made fromt any second therapeutic agent known to be useful for co-administration with L-838417. The choice of second therapeutic agent is also dependent upon the particular disease or condition to be treated. Examples of second therapeutic agents that may be employed in the methods of this invention are those set forth above for use in combination compositions 30 comprising a compound of this invention and a second therapeutic agent. [57] The term "c-adminisiered" as used herein means that the second therapenti agent may be administered together with a compound of this invention as part of a single dosage form (such as a composition of this invention comprising a compound of the invention and an second therapeutic agent as described above) or as separate, 12 multiple dosage forms. Alternatively, the additional agent may be administered prior to, consecutively with, or following the administration of a compound of this invention. In such combination therapy treatment, both the compounds of this invention and the second therapeutic agent(s) are administered by conventional 5 methods The administration of a composition of this invention, comprising both a compound of the invention and a second therapeutic agent, to a patient does not preclude the separate administation of that same therapeutic agent, any other second therapeutic agent or any compound of this invention to said patient at another time during a course of treatment, 10 158] Effective amounts of these second therapeutic agents are well known to those skilled in the art and guidance for dosing may be found in patents and published patent applications referenced herein, as well as in Wells et al, eds,, Pharmacotherapy Handbook, 2nd Edition, Appleton and Lange, Stamford, Conn. (2000); PDR Pharmacopoeia, Tarascon Pocket Pharmacopoeia 2000, Deluxe Edition, Tarascon 15 Publishing, Loma Linda, Calif. (2000), and other medical texts. However, it is well within the skilled arisan's purview to determine the second therapeutic agent's optimal effective-amount range. ($9] In one embodiment of the invention, where a second therapeutic agent is administemd to a subject, the effective amount of the compound of this invention is 20 less than its effective amount would be where the second therapeutic agent is not administered, In another embodiment, the effective amount of the second therapeutic agent is less than its effective amount would be where the compound of this invention is not administered. In this way, undesired side effects associated with high doses of either agent may be minimized. Other potential advantages (including without 25 limitation improved dosing regimens and/or reduced drug cost) will be apparent to those of skill in the art. [60] In yet another aspect, the invention provides the use of a compound of Formnuda I alone or together with one or more of the above-described second therapeutic agents in the manufacture of a medicament, either as a single composition 30 or as separate dosage forms, for treatment or prevention in a patient of a disease, disorder or symptom set forth above, Another aspect of the invention is a compound of Formula I or a pharmaceutical composition comprising a compound of Fonmala I for use in the treatment or prevention in a patient of a disease, disorder or symptom 13 thereof delineated herein. Pharmaceutical Kits [61] The present invention also provides kits for use to treat disorders of the central 5 nervous system, including anxiety and convulsions; and neuropathic, inflammatory and migraine associated pain. These kits comprise (a) a pharmaceutical composition comprising a compound of Formiula I or a salt thereof, wherein said pharmaceutical composition is in a container; and (b) instructions describing a method of using the pharmaceutical composition to treat disorders of the central nervous system, including 10 anxiety and convulsions; and neumpathic, inflammatory and migraine associated pain. [62] The container may be any vessel or other sealed or sealable apparatus that can hold said pharmaceutical composition. Examples include bottles, ampules, divided or multi-chambered holders bottles, wherein each division or chamber comprises a 15 single dose of said composition, a divided foil packet wherein each division comprises a single dose of said composition, or a dispenser that dispenses single doses of said composition. The container can be in any conventional shape or form as known in the art which is made of a pharmaceutically acceptable material, for example a paper or cardboard box, a glass or plastic bottle or jar, a r-sealable bag (for 20 example, to hold a "refill" of tablets for placement into a different container), or a blister pack with individual doses for pressing out of the pack according to a therapeutic schedule. The container employed can depend on the exact dosage form involved, for example a conventional cardboard box would not generally be used to hold a liquid suspension. It is feasible that more than one container can be used 25 together in a single package to market a single dosage form. For example, tablets may be contained in a bottle, which is in turn contained within a box. In one embodiment, the container is a blister pack. [63] The kits of this invention may also comprise a device to administer or to measure out a unit dose of the pharmaceutical composition. Such device may include 30 an inhaler if said composition is an inh&labie composition a syringe and needle if said composition is an injectable composition; a syringe, spoon, purnp, or a vessel with or without volume markings if said composition is an oral liquid composition; or any otter measuring or delivery device appropriate to the dosage fonnulation of the corpsition present in the kit. 14 [641 In certain embodiment, the kits of this invention may comprise in a separate vessel of container a pharmaceutical composition comprising a second therapeutic agent, Such as one of those listed above for use for co-administration wth a compound of this invention, 5 Examples [65] Example 1.Synthesis of 7ntert-Butvd).3-(2,5difiuorophenvD-6-((I methyl-1Hl, 2,4triazol -5-ynethoxv)-1 ,2Altriazolo['4, 3-lpyridazine (Compound i.1 Compound 103 was prepared frm appropriately deuterated intermediates as 10 generally outlined in Scheme 1 above. Cos N 103 [66 Step L. 4-(terButvL 3,64 dichloropdidazine (12a1. Concentrmed sulfuric acid (5:7 mL, 108 mmol) was added to a suspension of freshly purified 3,6dichior~ pyridazine, 11 (5.4 g, 33.5 mmol) in distilled water (130 mL). The mixtume was 15 warmed to 65 *C and trimethylacetic acid-do, 1{}a (6.0 g, 54 mal, CDN Isotopes, 99 aton% D) was added, followed by silver nitrate (1 A g, 7 mmol). A solution of ammonium peroxydisuIfate (12,3 g, 54 mmol) in distilled water (35 mL) was added to the mixture over a 10-15 minute period while keeping the reaction temperatue at 65 75 *C The mixture was stired for 30 minutes and cooled to room temperature. The 20 mixture was poured onto ice (100 g) and the mixture adjusted to pH = 9-10 with concentrated ammonium hydroxide. The aqueous mixture was extracted with dichloromethane (2 x 30 mL). The combined extracts were washed with IN sodium hydroxide (10 mL), dried over Na 2 SO,, filtered and concentrated under reduced pressure. The cmde product was purified by column chromatography on silica gel, 25 eludng with 10% ethyl acetatetheptanes to give 6.1 g (80%) of 12a as a colordess oiL [67] ,Ste 2.7ftrButv1ddY6cLoro-3-25-diqropenv)412,4triazolo[437 bipyridai 4a' A mixture of 12a (6 g, 28 mmnol) :13 (7.2 g. 42 mmcl. commercially available.), and triethylamine hydrochloride (5.8 g, 42 mmci) in xylene 1.5 (30 mL) was heated at 150 0 C with stirring for 36 hours. After cooling to room temperature the mixture was concentrated under reduced pressure. The residue was triturated with dichloromethane (40 mL), filtered, and the filtrate concentrated under reduced pressure, The crude product was purified by chromatography on silica gel, 5 elating with 20-50% ethyl acetate/heptanes to give 5,6 g (60%) of 14a as an off-white solid. [68] Step 3. 74terr-Butyl-d3425-difluoophenvl-64(Q-methyv l-I24 triazol-5-vlmethoxvbl;2,41tazoo4.3-blpyridazine(Compound 103) To a solution of (1-methyl-1H-12,4-trazo-5-yl)methanol15a (0.45 g, 4.0 mmol, 10 commercially available) in DMF (20 mL) was added 60% sodium hydide in mineral oil (017, 4.3 mmol). The mixture was stirred for 15 minutes and 14a (1.2 g, 3.6 mmol) was added, The mixture was stirred for 3 hours at room temperature, then diluted with water (100 mL). The precipitate was collected by filtration and washed several times with water, The crude product was purified by column chromatography 15 on silica gel eluting with 5% methanol/dichloromethane. The product was further purified by recrystallization from ethyl acetate-heptanes (1:1) to give 1.25 g (78%) of Compound 103 as a white solid. 1 1i-NMR (300 MHz, CDC 3 ): 6 3.91 (s, 314), 5,55 (s 2H), 7,23-728 (p, 2H), 7.62-7,68 (rn, 1H), 7.93 (s, 1IH), 8.00 (S, 1H). "C-NMR (75 MHz, CDCI 3 ): 8 34.55, 35L66, 59.37, 115.58 (dd,Jr=16.6,tz-=9.2), 117.63 (dd, 20 Ji= 2 5.8, J2=6 6 ), 11772 (dd, J=24.5, J 2 =12.2), 11872 (dd, J24. J2=.5), 12124, 137.85, 143,47, 145.00, 149.49, 15 1.13, 155.70 (d, J160.9), 159,01 (d, s=155.9), 158.70, HPLC (method: Waters Atlantis T3 2.1 x 50 mm 3 pm C1 8-RP cohmn gradient method 5-95% ACN + 0,1% formic acid in 14 min (1,0 mUiinin) with 4 mini hold at 95% ACN; Wavelength:254 nm): retention time: 5.41 min; 99.3% purity, MS 25 (M+H: 409,2. Elemental Analysis (CqHwDF 2

N

7 Q): Calculated: C=5588, H=4.69, N=24.01. Found: C=5i98, H=453, N=23.98, [691 Example 2. Synthesis ofl(Methvi- )-1H-i,2A-triazol-5-vl-1.1r methanol 05). Intermediate 15h was prepared from appropriately deuterated 30 intermediates as generally outlined in Scheme 2 above. 16 CDs N D N OH 1Sb [70] Stpj14M bdf1H41 _tazole (17a). In a flask equipped with a mechanical stirrer under a nitrogen atmosphere, 1,2,4-triazole 16 (6,0 g, 87 mol) was added to anbydrous THF (60 mL) followed by the addition of iodomethane-da (6.5 5 mL, 1.05 mol, Cambridge Isotopes, 99 atom% D) The cloudy mixture was cooled to o *C and 1,8-diazabicyclo[54,0iundec-7-ene "DBU" (13.2 mL, 0.87 rol) was added over 20 minutes. The mixture was allowed to slowly warm to room temperature and was stirred overnight. The mixture was then filtered through a Celite pad, and the filrate concentrated under reduced pressure to give 7.3 g (>100%) of crde 17a as a 10 yellow oil. GCMS shows a purity of 90%. The ratio of regioisomers was 12:1. [71] Step 2. (14MethyL ~ 4 t1H1,Agrazol-5- vfi l1-rmetanol(15h. A mixture of 17a (5 g, 58 mmol) and paraformaldehyde-dA (10 g, 333 mmol, Cambridge Isotopes, 99 atom% D) was heated in a sealed tube at 170 "C for 5 hours. The mixture was cooled to room temperature and diluted with dichloromethane (20 nL). The solid 15 was removed by filration and the filtrate was concentrated under reduced pressure, The crude product was purified by chromatography on a short column of silica gel elating with 75% THF/heptanes to give 4.8 g (71%) of 15b as an off-white solid. (721 Example I Synthesis of 7(rBL-di)-3(2&dfluorophenv{:fJ: 20 (methvl-d 1HL24-triiazol-5-v '01.I-d-methoxv 4]tazolol-bi yridaine (Compound 105). Compound 105 was prepared from appropriately deuterated intermediates as generally outlined in Scheme 1 above, QDA DsC i N DsC N N O N F N-N, Cc) F 105 7%T.n-Butylhd&l-3-(2,df5 rphny 4(1/mnethyl-d)-1Hl-1,2,4-triazollyft 1 LL 25 d -Mthoxy 2tl 3 ur n (Copgnd 105). To a solution of 15b (0.24 g, 20 mmol) in DMF (20 mL) was added 60% sodium hydride in mineral oil 17 (0.08, 2.1 mnmol). The mixture was stirred for 15 minutes and 14a (0.6 g, L8 mmol, see Example 1) was added. The mixture was stirred for 3 hours at room temperature, then diluted with water (100 nL). The precipitate was collected by filtration and washed several times with water. The crude product was purified by column 5 chromatography on silica gel eating with 5% mnethano/dichloromethane. The product was further purified by recrystaiziration from ethyl acetate/heptane (1:1) to give 0.52 g (70%) of Compound 105 as a white solid. HWNMR (300 MHz, CDC 3 ): 6 7.23 7.28 (m, 2H), 7.63-7.67 (m., 1H), 7,92 (s, I H), 8.00 (s, IH). '-NMR (75 MHz, CDCt): absence of signals at 35.66 and 59.37, HPLC methodd: Waters Atlands T3 10 2,1 x 50 mm 3 pm C18-RP column - gradient method 5-95% ACN +0,1% formic acid in 14 min (IO n/min) with 4 min hold at 95% ACN; Wavelength: 254 nm): retention time: 5,40 min; 99.0% purity. MS (M+): 414.3. Elemental Analysis (C1HIDMzF2N7O): Calculated: C=55.20, H4,63, N=23.72, F=9,19. Found: C=54,88, 1445, N=-23 46, F9,59. 15 {73) Examnle 4. Synthesis of (14etyl-d 1H-124-iazo-5-vimethanoi qgg), Intermediate Ie was prepared from appropriately denterated intermediates as generally outlined in Scheme 2 above. NrN N OH 20 (14(MethyA-d4-il2,4-triamiL5~Mlmethanol (15c. A mixture of 17a (5 g, 58 mmol, see Example 2) and paraformaldehyde (10 g, 333 mniol) was heated in a sealed tube at 170 0 C for 5 hours. The mixture was cooled to room temperature and diluted with dichloromethane (20 mL). The solid was removed by filtration and the filtrate was concentrated under reduced pressure., The crude product was purified by 25 chromatography on a short colhumm of silica gel, eluting with 5% methanol/dichloromethane to give 5.0 g (75%) of 15c as an off-white solid, 'H-NMR (300 MHz, CDCI): 8 5.55 (s, 2H), 7,23-7.28 (m, 2R), 7.62-7.67 (m, 11) 7.93 (a, iH), 8,00 (s, 1H1) IZCNMR (75 MHz, CDGb): 5 34:55, 59.36, 115.53 (,dd. t=16.6, J=8.8), 117,63 (dd, Jt 24

,

4 , J2=128), 117.71 (dd, Ji=24,1, h=8.0) 116.77 fdd, 30 Ji=23,9, =83), 121.75, 137.85, 143.48, 145,00, 149,50, 15115,15536 (d, J-163.5), 159.08 (d, J=156,9), 158.71 HPLC method: Waters Atlantis T3 2.1 x 50 mm 3 pm 18 C1 S-RP column - gradient method 5-95% ACN + 0.1% formic acid in 14 min (LO mrdmin) with 4 min hold at 95% ACN; Wavelength: 254 nm): retention time: 5.40 mfin; 99.6% purity, MS (M+H): 412.2. Elemental Analysis (CsqHD F2N0): Calculated: C=55.47, R=4.67, N=23.83, Found: C=55,49, H=4.76, N=23.87. 5 [74] Example S. Synthesis of 7-ter -Butyl-4d325ihornheny!6(1 (methvbdahl-L- 2,4trao5-lmtox i2triazoio[4, 3 -blpyridazine (Compound 104), Compound 104 was pepaed from appropriately deuteated intermediates as generally outlined in Scheme I above. C0s 0C A N N 0O N N F N -N CD' F 10 104 [75 -fite hvl d342,5-diftuoropheny}66t1 -(methv18-1 2.4-azol,5 yrnethoxlvii2,4tdiazoloI43-bpridazine (Comrpmnd 144), To a solution of 15c (046 g, 4,0 mnol) in DMF (20 ml) was added 60% sodium hydride in minenal oil (0.17, 43 mmol). The mixture was stirvd for 15 minutes and 14a (1.2 g, 3.6 mml, 15 see Example 1) was added. The mixture was stirred for 3 hours at room temperature, then diluted with water (100 ml), The precipitate was collected by filtration and washed seveml times with water. The crmde product was purified by column chromatography on silica gel eluting with 5% methanol/dichloromethane. The product was further purified by recrystallization from ethyl acetate/heptane (1:1) to give 1.31 20 g (88%) of Compound 104 as a white solid. [76] Fample 6. Synthesis of 7ytert-Butvk342-dinuorophenyly44(14methyl dg1AH-1 ,2A4-tdaol5-L)iSdmethoxv1L2AltriazoloF4,3-bpridazine (Compound 101). Compound 101 was prepared from appropriately deuterAted 25 intermediates as generally outlined in Scheme I above. 19 CH, CH 3 0

H

5 C N N F N-N, CDs F 101 7-tert-Buty-3425-dinuorophenyv)-64(04methy -da)-1H-L.4-triazol-5-vi1dr methoxy}41 1 2,4Wtriazolof4.34blpvridazine (Compound 101). To a solution of 15b (0.24 g, 4.0 rnmol, see Example 2) in DMF (10 mL) was added 60% sodium hydride 5 in mineral oil (O.0S 2.1 mmol). The mixture was tin-ed for 15 minutes and known compound 7tertutyl-6chlot-3-(2,5-difiuoropheny-[1 24]crazolo[43' b]pyridazine, 14b (0,58 g, 1.1 mmol, prepared as descibNed in patent application WO1998004559) was added, The mixture was stirred for 3 hours at room temperature, then diluted with water (100 mL). The prcipitate was collected by 1.0 filtration and washed several times with water, The crude product was purified by column chromatography on silica gel eluting with 75% THF/heptanes. The product was further purified by recrystallization from ethyl acetate/heptane (1:1) to give 0.53 g (72%) of Compound 101 as a white solid. 'H-NMR (300 MHz, CDCI): 6 1,41 (s, 9H). 7.23-7,28 (m, 2H), 7.62-7.68 (m, II), 7.92 (s, M), 8.00 (s, IH), "C-NMR (75 15 MHz, CDl): appearance of signal at 28.96, absence of signal at 35 66 and 59 36. HPLC (method: Waters Atlantis T3 2.1 x 50 mm 3 pm CI8-RP column - gradient method 5-95% ACN + 0.1% fornic acid in 14 min (1.0 mUin) with 4 min hold at 95% ACN; Wavelength: 254 nm): retention time: 5.2 min; 993% purity, MS (M+H): 405.3. Elemental Analysis (C 19

H

1 .DsF2N 7 O): Calculated: C=56,43, 20 H=i4.74, N=24.25, F=940, Found: C=56.22, HR473, N=23.87, F=9.35, [771 Example 7. Jf4mapgof metabolic Stability. Human liver microsomes (20 mg/mL) and rat liver microsormes (20 mg/mL) were obtained from Xcnotech, LLC (Lenexa, KS). $-nicotinamide adenine dinucleatide phosphate, reduced forn 25 (NADPH), magnesium chloride (MgC.), and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich. (78] )eterination of Metabolic Stability: 7.5 mM stock solutions of test compounds (L-838417, Compound 101, Compound 103, Compound 104 and 20 Compound 105) were prepared in DMSO. The 7.5 mM stock solutions were diluted to 12.5 pM in acetonitrile (ACN). The 20 mg/mL liver microsomes (either human or liver) were diluted to 2.5 mg/mL in 0.1 M potassium phosphate buffer, pH 7, containing 3 rmM MgCh. The diluted ricosomes (375 p) were added to wells of a 5 96-well deep-well polypropylene plate in triplicate, 10 pL of the 12.5 pM test compound was added to the microsomes and the mixture was pre-wamed for 10 minutes, Reactions were intiated by addition of 125 pL pre-warmed NADPH solution. The final reaction volume is 0,5 nL and contained 0.5 mg/mL human liver microsomes, 0.25 pTM test compound, and 2 mM NADPH in 0.1 M potassium 10 phosphate buffer, pHi 7.4, and 3 mM MgC1 2 , The reaction mixtures are incubated at 374C, and 50 pL aliquots were removed at 0, 5, 10, 20, and 30 minutes and added to shallow-well 96-well plates which contained 50 pL of ice-cold AC.N with intemal standard to stop the reactions. The plates were stored at 4"C for 20 minutes after which 100 pL of water was added to the wells of the plate before centrifugation to 15 pellet precipitated proteins., Supernatants were transferred to another 9&weli plate and analyzed for amounts of parent remaining by LC-MS/MS using an Applied Bio systems API 4000 mass spectrometer. 7-ethoxycoumarin (1 IM) was used as a positive control, [79] Data ana s'is: The in vitro t 1 s for test compounds were calculated from the 20 slopes of the linear regression of % parent remaining (in) vs incubation time relationship, using the fonnula: in vitro t a 0.693/k, where k =[slope of linear regression of % parent remainingjn) vs incubation time] Data analysis is performed using Microsoft Excel Software. 25 [I The results of these experiments are shown in Figures 1 (human liver rmicrosomes) and 2 (rat liver nuicrosomes). As shown in Figure 1, approximately 70% of L-838417 remained intact after 30 minutes of incubation with human i:iver microsomes. The half life of L-838417 was calculated to be, 54.4 minutes. In contrast, each of Compounds 101, 103, 104 and 105 were stable in human liver 30 microsomes (more than 80% of parent compound remained intact after 30 minute incubation). [$1] In rat liver muicrosomnes, approximately 70% of both L-838417 and Compound 101 remained intact after 30 minutes of incubation (Fig. 2). The calculated half-lives 21 were 50.5 minutes for 1838417 and 52,7 minutes for Compound 101. More than 80% of each of Compounds 103, 104 and 105 remained intact after 30 minutes of incubation, and each was considered stable in rat microsomes. 5 [8Z] Example . Pharmacokinetic and Bioavailability Analysis of Compounds 103 and 105 Following Orand nd intravenous Administration to Rats. Three male Sprague-Dawley rats (200-250 g each) were cannulated in the jugular vein and were administered a single dose containing 2mg/g each of L-838417, Compound 103 and Compound 105 (as a 1:1:1 mixture containing 2 ng/mL of each of the three 10 compounds in 10% dimethyl sulfoxide (DMSO), 10% N, N-dimethylacetamide (DMA), and 60% polyethylene glycol (PG) through the. jugular cannila. Truee additional male Spragne-Dawley rats (200-250 g each) were administered a single dust containing 2mg/kg each of L-838417, Compound 103 and Compound 105 (as a 1:11 mix tre containing 1 mg/mnL of each of the three compounds in 10% dimethyl 15 sulfoxide (DMSO), 10% N, Ndimethylacetamide (DMA), and 60% polyethylene glycol (PO) by oral gav age. [83] Blood (0.25 mL) from intravenously treated test rats was collected retr orbitally at 2, 5, 15, and 30 minutes, and 1, 2, 4, and 6 hours post-dosing, Blood (0.25 mL) from orally treated test rats was collected retro-orbitally at 5, 15, 30, and 45 20 minutes, and 1, 2, 4, and 6 hour post-dosing, Blood was collected into tubes containing K 2 EDTA as anticoagulant at the above mentioned time points. Blood samples were stored on ice and then centrifuged to obtain plasma. The plasma ( 0.125 pL) was aliquoted into deep 9-well plates and stored at -80"C until analysis by LC-MS/MS using an Applied Bio-systems API 4000 mass spectrometer. 25 [84] The results of the intravenous portion of this study are shown in Figure 3 and in Table 2, below. 22 Table 2. Pharmacokineties of 1-838417, Compound 103 and Compound 105 after Intravenous Administration to Sprague-Dawley Rats. L-838417 Compound 103 % Change Compound 105 % Chage over L- over L 838417 838417 zh) ON 1.25±0.14 +79 127*0-14 +81 CL 1-1 .ii OA8 &04 05 62 046 ±005 -60 (Uhdkg) AUAIoC6 831- 86 1920 200 +131 1957 ±190 +136 These results demonstrate that Campounds 103 and 105 each have an approximately 5 80% longer half-life and produce a greater than twoTold higher AUCo than undeuterated L-838417 following intravenous administration to rats, In addition, both Compound 103 and 105 are each cleared approximately 60% more slowly than L 838417. 10 [85] The results of the oral administration portion of this study are shown in Figure 4 and in Table 3, below. Table 3. Pharmacokinetics of L-838417, Compound 103 and Compound 105 after Oral Administration to Sprague-Dawley Rats, L-838417 Compound 103 % Compound % Change Change 10$ over L over L 838417 838417 C,(ng/mL) 128 40 277 76 +116 280 ±80 +119 XUCO_ _ 491± 95 1258 ± 289 +156 1248 & 272 +154 (hr*ng/mL) 15 These results show that Compounds 103 and 105 demonstrate a greater than two4bld higher C. following oral administration in rats than L-938417. in addition, the results show that Compounds 103 and 105 produce a greater than two and a half-fold higher AUCO4 than undeuterated L-838417 following oral administration. 23 [86] Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the illustrative examples, make and utilize the compounds of the present invention and practice the claimed methods, it should. be understood that the foregoing discussion and examples merely present a detailed 5 description of certain preferred embodiments. It will be apparnt to those of ordinary skill in the art that various modifications and equivalents can be made without departing from the spirit and scope of the invention, All the patents, journal articles and other documents discussed or cited above are herein incorporated by refermce, 24

Claims (13)

1. A compound of Formula I: N IO Y2b F Formula I 5 or a pharmaceutically acceptable salt thereof, wherein: R 1 is CH 3 , CDH 2 , CD 2 H, or CD 3 ; R2 is a t-butyl group having 0-9 deuterium atoms; each Y is independently hydrogen or deuterium; and when R' is CH 3 and each Y is hydrogen, then R 2 has 1-9 deuterium. 10

2. The compound of claim 1, wherein R' is CH 3 or CD 3 .

3. The compound of claim 1 or 2, wherein R 2 is -C(CH 3 ) 3 or -C(CD 3 ) 3 . 15

4. The compound of any one of claims 1 to 3, wherein Y' and Ylb are the same.

5. The compound of any one of claims 1 to 4, wherein R 2 is -C(CD 3 ) 3 .

6. The compound of claim 1, selected from any one of the compounds set forth 20 in table below: 25 Compound RL R ya Yib 7 2 101 CD 3 -C(CH 3 ) 3 D D H 102 CH 3 -C(CD 3 ) 3 D D H 103 CH 3 -C(CD 3 ) 3 H H H 104 CD 3 -C(CD 3 ) 3 H H H 105 CD 3 -C(CD 3 ) 3 D D H 106 CD 3 -C(CH 3 ) 3 H H H 107 CH 3 -C(CH 3 ) 3 D D H 108 CD 3 -C(CH 3 ) 3 D D D 109 CH 3 -C(CD 3 ) 3 D D D 110 CH3 -C(CD 3 ) 3 H H D I1 CD 3 -C(CD3) 3 H H D 112 CD 3 -C(CD 3 ) 3 D D D 113 CD 3 -C(CH 3 ) 3 H H D 114 CH3 -C(CH 3 ) 3 D D D or a pharmaceutically acceptable salt thereof.

7. The compound of any one of claims 1 to 6, wherein any atom not designated as deuterium in any of the embodiments set forth above is present at its natural 5 isotopic abundance.

8. A pyrogen-free composition comprising a compound of claim 1; and an acceptable carrier. 10

9. The composition of claim 8 formulated for pharmaceutical administration, wherein the carrier is a pharmaceutically acceptable carrier.

10. The composition of claim 9 additionally comprising a second therapeutic agent useful in the treatment or prevention of a disease or condition selected from 15 disorders of the central nervous system, neuropathic pain, inflammatory pain, and migraine-associated pain.

11. A compound of any one of claims 1 to 7 for use in: a. inhibiting the a-I subtype of the GABA-A receptor in a cell; or 20 b. activating one or more of the a2, a3 and a5 subtypes of the GABA-A receptor in a cell. 26

12. A composition of claim 8 or 9 for use in treating a disease or condition selected from disorders of the central nervous system, neuropathic pain, inflammatory pain, and migraine-associated pain. 5

13. A composition of claim 8 or 9 for use in treating a disease or condition selected from anxiety or convulsions. 27