Indian Patents. 262544:SULFAMATE AND SULFAMIDE DERIVATIVES FOR THE TREATMENT OF EPILEPSY AND RELATED DISORDERS

Title of Invention	SULFAMATE AND SULFAMIDE DERIVATIVES FOR THE TREATMENT OF EPILEPSY AND RELATED DISORDERS
Abstract	The present invention is directed to novel sulfarnide and sulfamate derivatives, pharmaceutical compositions containing them and their use in the treatment of epilepsy and related disorders.

Full Text	WO 2006/007435 PCT/US2005/021513 SULFAMATE AND SULFAMIDE DERIVATIVES FOR THE TREATMENT OF EPILEPSY AND RELATED DI BORDERS CROSS REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U. S. Provisional Application 60/580,178, filed on June 16, 2004, which is incorporated by reference herein in its entirety. FIELD OF THE INVENTION The present invention is directed to novel sulfamate and sulfamide derivatives, pharmaceutical compositions containing them and their use in the treatment of epilepsy and related disorders. BACKGROUND OF THE INVENTION Epilepsy describes a condition in which a person has recurrent seizures due to a chronic, underlying process. Epilepsy refers to a clinical phenomenon rather than a single disease entity, since there are many forms and causes of epilepsy. Using a definition of epilepsy as two or more unprovoked seizures, the incidence of epilepsy is estimated at approximately 0.3 to 0.5 percent in different populations throughout the world, with the prevalence of epilepsy estimated at 5 to 10 people per 1000. An essential step in the evaluation and management of a patient with a seizure is to determine the type of seizure that has occurred. The main characteristic that distinguishes the different categories of seizures is whether the seizure activity is partial (synonymous with focal) or generalized. Partial seizures are those in which the seizure activity is restricted to discrete areas of the cerebral cortex. If consciousness is fully preserved during the seizure, the clinical manifestations are considered relatively simple and the seizure is termed a simple-partial seizure. If consciousness is impaired, the 1 WO 2006/007435 PCT/US2005/021513 seizure is termed a complex-partial seizure. An important additional subgroup comprises those seizures that begin as partial seizures and then spread diffusely throughout the cortex, which are known as partial seizures with secondary generalization. Generalized seizures involve diffuse regions of the brain simultaneously in a bilaterally symmetric fashion. Absence or petit mal seizures are characterized by sudden, brief lapses of consciousness without loss of postural control. Atypical absence seizures typically include a longer duration in the lapse of consciousness, less abrupt onset and cessation, and more obvious motor signs that may include focal or lateralizing features. Generalized Tonic-clonic or grand mal seizures, the main type of generalized seizures, are characterized by abrupt onset, without warning. The initial phase of the seizure is usually tonic contraction of muscles, impaired respiration, a marked enhancement of sympathetic tone leading to increased heart rate, blood pressure, and pupillary size. After 10-20 s, the tonic phase of the seizure typically evolves into the clonic phase, produced by the superimposition of periods of muscle relaxation on the tonic muscle contraction. The periods of relaxation progressively increase until the end of the ictal phase, which usually lasts no more than 1 min. The postictal phase is characterized by unresponsiveness, muscular flaccidity, and excessive salivation that can cause stridorous breathing and partial airway obstruction. Atonic seizures are characterized by sudden loss of postural muscle tone lasting 1-2 s. Consciousness is briefly impaired, but there is usually no postictal confusion. Myoclonic seizures are characterized by a sudden and brief muscle contraction that may involve one part of the body or the entire body. (www.harrisonsonline.com, March 29, 2001) Carbonic anhydrase inhibitors (CAIs) have been widely used in medicine, mainly as antiglaucoma and antisecretory drugs or diuretic agents, and are valuable compounds. However, systemic antiglaucoma agents (such as acetazolamide) possess potentially unwanted side-effects including paresthesias, 2 WO 2006/007435 PCT/US2005/021513 nephrolithiasis and weight loss. Topiramate is a well known anticonvulsant drug that possesses single digit micromolar carbonic anhydrase inhibition, which is suspected as the cause of paresthesias noted by some patients taking topiramate. There remains a need to provide an effective treatment for epilepsy and related disorders, and preferably treatment which does not have the associated side-effects attributable to carbonic anhydrase inhibition. SUMMARY OF THE INVENTION The present invention is directed to novel sulfamate and sulfamide derivatives, pharmaceutical compositions containing them and their use in the treatment of epilepsy and related disorders. More particularly, the present invention is direction to compounds of formula (I) and compounds of formula (II) as hereinafter defined. i The present invention is directed to novel sulfamate derivatives, compounds of formula (I) wherein R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl; 3 a is an integer from 1 to 2; WO 2006/007435 PCT/US2005/021513 wherein b is an integer from 0 to 4; and wherein c is an integer from 0 to 2; 4 each R3 is independently selected form the group consisting of halogen, lower alkyl, hydroxy substituted lower alkyl, -O-(lowerialkyl), -S-(lower alkyl), nitro, cyano, amino, lower alkylamino, di(lower alkyl)amino and -C(0)0-(lower alkyl); WO 2006/007435 PCT/US2005/021513 The present invention is further directed to novel sulfamide derivatives, compounds of formula (li) wherein R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl; 5 R4 is selected from the group consisting of hydrogen and lower alkyl; a is an integer from 1 to 2; WO 2006/007435 PCT/US2005/021513 each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro; Illustrative of the invention is a pharmaceutical composition comprising a pharmaceutically acceptable carrier and any of the compounds described above. An illustration of the invention is a pharmaceutical composition made by mixing any of the compounds described above and a pharmaceutically acceptable carrier. Illustrating the invention is a process for making a pharmaceutical composition comprising mixing any of the compounds described above and a pharmaceutically acceptable carrier. Exemplifying the invention is a method of treating epilepsy and related disorders in a subject in need thereof comprising administering to the subject a therapeutically effective amount of any of the compounds or pharmaceutical compositions described above. 6 WO 2006/007435 PCT/US2005/021513 Another example of the invention is the use of any of the compounds described herein in the preparation of a medicament for treating epilepsy or a related disorder, in a subject in need thereof. DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to compounds of formula (I) and compounds of formula (II) As used herein, unless otherwise noted, "halogen" shall mean chlorine, bromine, fluorine and iodine. As used herein, unless otherwise noted, the term "alkyl" whether used alone or as part of a substituent group, includes straight and branched chains. For example, alkyl radicals include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, t-butyl, pentyl and the like. Unless otherwise noted, "lower" when used with alkyl means a carbon chain composition of 1-4 carbon atoms. 7 WO 2006/007435 PCT/US2005/021513 As used herein, unless otherwise noted, "alkoxy" shall denote an oxygen ether radical of the above described straight or branched chain alkyl groups. For example, methoxy, ethoxy, n-propoxy, sec-butoxy, t-butoxy, n-hexyloxy and the like. As used herein, the notation "" shall denote the presence of a stereogenic center. When a particular group is "substituted" (e.g., alkyl, aryl, etc.), that group may have one or more substituents, preferably from one to five substituents, more preferably from one to three substituents, most preferably from one to two substituents, independently selected from the list of substituents. With reference to substituents, the term "independently" means that when more than one of such substituents is possible, such substituents may be the same or different from each other. Under standard nomenclature used throughout this disclosure, the terminal portion of the designated side chain is described first, followed by the adjacent functionality toward the point of attachment. Thus, for example, a "phenyl-alkyl-amino-carbonyl-alkyl" substituent refers to a group of the formula Abbreviations used in the specification, particularly the Schemes and Examples, are as follows: DCC = Dicyclohexyl Carbodiimide DCE = Dichloroethane OCM = Dichloromethane 8 WO 2006/007435 PCT/US2005/021513 DIPEAorDlEA = Diisopropylethylamine DMF = N,N-Dimethylformamide DMSO = Dimethylsulfoxide EDC = Ethylcarbodiimide Et3NorTEA = Triethylamine Et2O = Diethyl ether EA or EtOAc = Ethyl acetate EtOH = Ethanol IPA = 2-propanol Hept = Heptane HOBT = 1-Hydroxybenzotriazole HPLC = High Pressure Liquid Chromatography LAH = Lithium Aluminum Hydride M or MeOH = Methanol NMR = Nuclear Magnetic Resonance Pd-C = Palladium on Carbon Catalyst RP HPLC = Reverse Phase High Pressure Liquid Chromatography RTorrt = Room temperature TEA = Triethylamine TFA = Trifluoroacetic Acid THF = Tetrahydrofuran TLC = Thin Layer Chromatography As used herein, unless otherwise noted, the terms "epilepsy and related disorders" or "epilepsy or related disorder" shall mean any disorder in which a subject (preferably a human adult, child or infant) experiences one or more seizures and / or tremors. Suitable examples include, but are not limited to, epilepsy (including, but not limited to, localization-related epilepsies, generalized epilepsies, epilepsies with both generalized and local seizures, and the like), seizures as a complication of a disease or condition (such as seizures associated with 9 WO 2006/007435 PCT/US2005/021513 encephalopathy, phenylketonuria, juvenile Gaucher's disease, Lundborg's progressive myoclonic epilepsy, stroke, head trauma, stress, hormonal changes, drug use or withdrawal, alcohol use or withdrawal, sleep deprivation, and the like), essential tremor, restless limb syndrome, and the like. Preferably, the disorder is selected from epilepsy (regardless of type, underlying cause or origin), essential tremor or restless limb syndrome, more preferably, the disorder is epilepsy (regardless of type, underlying cause or origin) or essential tremor. The term "subject" as used herein, refers to an animal, preferably a mammal, most preferably a human, who is or has been the object of treatment, observation or experiment. The term "therapeutically effective amount" as used herein, means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated. As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combinations of the specified ingredients in the specified amounts. Where the compounds according to this invention have at least one chiral center, they may accordingly exist as enantiomers. Where the compounds possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention. Furthermore, some of the crystalline forms for the compounds may exist as polymorphs and as such are intended to be included in the present invention. In addition, some of the compounds may form solvates with water (i.e., hydrates) or common organic 10 WO 2006/007435 PCT/US2005/021513 solvents, and such solvates are also intended to be encompassed within the scope of this invention. Where the processes for the preparation of the compounds according to the invention give rise to mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. The compounds may be prepared in racemicform, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution. The compounds may, for example, be resolved into their component enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (-)-di-p-toluoyl-D-tartaric acid and/or (+)-di-p-toluoyl-L-tartaric acid followed by fractional crystallization and regeneration of the free base. The compounds may also be resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column. During any of the processes for preparation of the compounds of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups may be removed at a convenient subsequent stage using methods known from the art. The present invention includes within its scope prodrugs of the compounds of this invention. In general, such prodrugs will be functional derivatives of the compounds which are readily convertible in vivo into the required compound. Thus, in the methods of treatment of the present invention, the term "administering" shall encompass the treatment of the various disorders 11 WO 2006/007435 PCT/US2005/021513 described with the compound specifically disclosed or with a compound which may not be specifically disclosed, but which converts to the specified compound in vivo after administration to the patient. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in Design of Prodrugs. ed. H. Bundgaard, Elsevier, 1985. The present invention provides pharmaceutical compositions comprising a compound of formula (I), a compound of formula (II) and / or a compound of formula (III) in association with a pharmaceutically acceptable carrier. Preferably these compositions are in unit dosage forms such as tablets, pills, capsules, powders, granules, sterile parenteral solutions or suspensions, metered aerosol or liquid sprays, drops, ampoules, autoinjector devices or suppositories; for oral parenteral, intranasal, sublingual or rectal administration, or for administration by inhalation or insufflation. Alternatively, the composition may be presented in a form suitable for once-weekly or once-monthly administration; for example, an insoluble salt of the active compound, such as the decanoate salt, may be adapted to provide a depot preparation for intramuscular injection. For preparing solid compositions such as tablets, the principal active ingredient is mixed with a pharmaceutical carrier, e.g. conventional tableting ingredients such as corn starch, lactose, sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalcium phosphate or gums, and other pharmaceutical diluents, e.g. water, to form a solid preformulation composition containing a homogeneous mixture of the principle ingredient. When referring to these preformulation compositions as homogeneous, it is meant that the active ingredient is dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective dosage forms such as tablets, pills and capsules. This solid preformulation composition is then subdivided into unit dosage forms of the type described above containing from about 1 to about 1000 mg of the active ingredient of the present invention. The tablets or pills of the novel composition can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action. For example, the tablet or pill can comprise an 12 WO 2006/007435 PCT/US2005/021513 inner dosage and an outer dosage component, the latter being in the form of an envelope over the former. The two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permits the inner component to pass intact into the duodenum or to be delayed in release. A variety of material can be used for such enteric layers or coatings, such materials including a number of polymeric acids with such materials as shellac, cetyl alcohol and cellulose acetate. The liquid forms in which the novel compositions of the present invention may be incorporated for administration orally or by injection include, aqueous solutions, suitably flavoured syrups, aqueous or oil suspensions, and flavoured emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil or peanut oil, as well as elixirs and similar pharmaceutical vehicles. Suitable dispersing or suspending agents for aqueous suspensions, include synthetic and natural gums such as tragacanth, acacia, alginate, dextran, sodium carboxymethylcellulose, methylcellulose, polyvinyl-pyrrolidone or gelatin. To prepare the pharmaceutical compositions of this invention, a compound of formula (I), a compound of formula (II) and / or a compound of formula (III) is intimately admixed with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques, which carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g., i.v. sterile injectable formulations will be prepared using appropriate solubilizing agents. A unit dose would contain about 10 to about 300 mg of the active ingredient. The tablets contain some or all of the following inactive ingredients: lactose hydrous, pregelatinized starch, microcrystalline cellulose, sodium starch glycolate, magnesium stearate, purified water, carnauba wax, hydroxypropyl methylcellulose, titanium dioxide, polyethylene glycol, synthetic iron oxide, and polysorbate 80. One skilled in the art will recognize that oral tablets containing a compound of formula (I), a compound of formula (II) and 13 WO 2006/007435 PCT/US2005/021513 / or a compound of formula (III) may be similarly prepared and may contain similar inactive ingredients. One skilled in the art will recognize that pharmaceutical compositions comprising more than one active ingredient may be similarly prepared according to known methods. In an embodiment of the present invention R1 is selected from the group consisting of hydrogen and methyl. In another embodiment of the present invention R2 is selected from the group consisting of hydrogen and methyl. In yet another embodiment of the present invention R1 and R2 are each hydrogen or R1 and R2 are each methyl. In an embodiment of the present invention -(CH2)a- is selected from the group consisting of-CH2- and -CH2-CH2-. In another embodiment of the present invention -(CH2)a- is -CH2-. In an embodiment of the present R4 is selected from the group consisting of hydrogen and methyl, preferably, R4 is hydrogen. In an embodiment of the present invention a is 1. In an embodiment of the present invention b is an integer from 0 to 2. In another embodiment of the present invention c is an integer from 0 to 2. In another embodiment of the present invention b is an integer from 0 to 1. In another embodiment of the present invention c is an integer from 0 to 1. In yet another embodiment of the present invention the sum of b and c is an integer form 0 to 2, preferably an integer form 0 to 1. In yet another embodiment of the present invention b is an integer from 0 to 2 and c is 0. 14 WO 2006/007435 PCT/US200S/021513 selected from the group consisting of 2-(chromanyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(benzo[1,3]dioxolyl), 2-(5-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxi'nyl), 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) and 2-(7-chloro-benzo[1,3]dioxolyl). In another embodiment of the present invention, 15 16 WO 2006/007435 PCT/US2005/021513 WO 2006/007435 PCT/US2005/021513 group consisting of 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(benzo[1,3]dioxolyl), 3-(3,4-dihydro-benzo[1,4]dioxepinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(chromanyl), 2-(5-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-benzo[1,3]dioxolyl), 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyl), 2-(5-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(8-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) and 2-(4-methyl-benzo[1,3]dioxolyl). the group consisting 2-(benzo[1,3]dioxolyl), 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl) and 2-(6,7-dichloro-2,3-dihydro-benzot1,4]dioxinyl). group consisting of 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxiny!) and 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl). In an embodiment of the present invention R3 is selected from the group consisting of halogen, lower alkyl, hydroxy substituted lower alkyl, -O-(lower alkyl), nitro, cyano, amino, lower alkylamino and di(lower alkyl)amino. In another embodiment of the present invention R3 is selected from the group consisting of halogen and nitro. In another embodiment of the present invention R3 is selected from the group consisting of chloro and nitro. 17 WO 2006/007435 PCT/US2005/021513 In an embodiment of the present invention R5 is selected from the group consisting of (II) halogen and lower alkyl. In another embodiment of the present invention R5 is selected from chloro, fluoro, bromo and methyl. selected from the group consisting of halogen, nitro, cyano, amino, lower alkyl, lower alkoxy and -C(O)O-(lower alkyl). In another embodiment of the present In an embodiment of the present invention, in the compound of formula (I), In an embodiment of the present invention, the stereo-center on the compound of formula (I) is in the S-configuration. In another embodiment of the present invention, the stereo-center on the compound of formula (I) is in the R-configuration. In an embodiment of the present invention, the stereo-center on the compound of formula (II) is in the S-configuration. In another embodiment of the present invention, the stereo-center on the compound of formula (II) is in the R-configuration. In an embodiment of the present invention the compound of formula (I) is present as an enantiomerically enriched mixture, wherein the % enantiomeric enrichment (%ee) is greater than about 75%, preferably greater than about 90%, 18 WO2006/007435 PCT/US2005/021513 more preferably greater than about 95%, most preferably greater than about 98%. In an embodiment of the present invention the compound of formula (II) is present as an enantiomerically enriched mixture, wherein the % enantiomeric enrichment (%ee) is greater than about 75%, preferably greater than about 90%, more preferably greater than about 95%, most preferably greater than about 98%. In an embodiment of the present invention are compounds of formula (I) wherein the MES activity at 100 mg/kg is greater than or equal to 3/5 mice. In another embodiment of the present invention are compounds of formula (II) wherein the MES activity at 100 mg/kg is greater than or equal to 3/5 mice. Representative compounds of the present invention, are as listed in Tables 1 and 2 below. Additional compounds of the present invention are as listed in Table 3. In Tables 1, 2 and 3 below, the column headed "stereo" defines the stereo-configuration at the carbon atom of the heterocycle attached at the starred bond. Where no designation is listed, the compound was prepared as a mixture of stereo-configurations. Where an "R" or "S" designation is listed, the stereo-configuration was based on the enantiomerically enriched starting material. 19 Table 1: Representative Compounds of Formula l\) 20 WO 2006/007435 PCT/US2005/021513 WO 2006/007435 PCT/US2005/021513 ;5 2-(2,3-dihydro-benzo[1,4]dioxinyl) R CH2 NH H H 6 2-(2,3-dihydro-benzo[1,4]dioxinyl) CH2 NH methyl methyl 7 2-(2,3-dihydro-benzo[1,4]dioxinyl) CH2 N(CH3) H H 8 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 9 2-(6-fluoro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 10 2-(chromanyl) CH2 NH H H 13 2-(5-fluoro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 14 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 15 2-(6-chloro-benzo[1,3]dioxolyl) CH2 NH H H 16 2-(2,3-dihydro-benzo[1,4]dioxinyl) CH2CH2 NH H H 18 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 19 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyi) S CH2 NH H H 20 2-(5-ch!oro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 22 2-(8-methoxy-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 24 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 21 22 WO 2006/007435 PCT/US2005/021513 29 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 30 2-(8-chloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H 33 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) S CH2 NH H H 35 2-(4-methyl-benzo[1,3]dioxolyl) CH2 NH H H Table 3 Additional Compounds of the Present Invention WO 2006/007435 PCT/US2005/021513 36 2-(7-amino-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H Compounds of formula (I) may be prepared according to the process outlined in Scheme 1. Scheme 1 Accordingly, a suitably substituted compound of formula (V), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (VI), a known compound or compound prepared by known methods, in the presence of a base such as NaH, TEA, DIPEA, pyridine, and the like, in an organic solvent such as DMF, DMSO, and the like, to yield the corresponding compound of formula (I). 23 Compounds of formula (II) may be prepared according to the process outlined in Scheme 2. WO 2006/007435 PCT/US2005/021513 Accordingly, a suitably substituted compound of formula (VII), a known compound or compound prepared by known methods, is reacted with sulfamide, a known compound, preferably wherein the sulfamide is present in an amount in the range of about 2 to about 5 equivalents, in an organic solvent such as THF, dioxane, and the like, preferably at an elevated temperature in the range of about 50°C to about 100°C, more preferably at about reflux temperature, to yield the corresponding compound of formula (Ma). Alternatively, a suitably substituted compound of formula (VII), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (VIII), a known compound or compound prepared by known methods, in the presence of a base such as TEA, DIPEA, pyridine, and the like, in an organic solvent such as DMF, DMSO, and the like, to yield the corresponding compound of formula (II). Scheme 3 Accordingly, a suitably substituted compound of formula (X), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (XI), a known compound or compound 24 WO 2006/007435 PCT/US2005/021513 prepared by known methods, in the presence of a base such as sodium methoxide, sodium ethoxide, sodium t-butoxide, potassium methoxide, potassium t-butoxide, and the like, in an organic solvent such as methanol, ethanol, IPA, and the like, preferably at an elevated temperature in the range of about 50°C to about 100°C, more preferably at about reflux temperature, to yield the corresponding compound of formula (XII). The compound of formula (XII) is reacted with a suitably selected reducing agent, such as LAH, and the like, in an organic solvent such as THF, diethyl ether, and the like, to yield the corresponding compound of formula (Va). Scheme 4 Accordingly, a suitably substituted compound of formula (XIII), a known compound or compound prepared by known method (for example as described in Scheme 3 above) is reacted with NH4OH, a known compound, optionally in an organic solvent such as acetonitrile, and the like, to yield the corresponding compound of formula (XIV). The compound of formula (XIV) is reacted with a suitably selected reducing agent, such as LAH, and the like, and the like, in an organic solvent 25 WO 2006/007435 PCT/US2005/021513 such as THF, diethyl ether, and the like, to yield the corresponding compound of formula (Vila). Scheme 5 Accordingly, a suitably substituted compound of formula (XV), a known compound or compound prepared by known methods is reacted with 3-chloro-2-chloromethyl-propene, a known compound, in the presence of a base such as potassium carbonate, sodium carbonate, sodium bicarbonate, TEA, DIPEA, and the like, in an organic solvent such as acetonitrile, THF, dioxane, and the like, preferably at an elevated temperature in the range of about 50°C to about 100°C, more preferably, at about reflux temperature, to yield the corresponding compound of formula (XVI). 26 WO 2006/007435 PCT/US2005/021513 The compound of formula (XVI) is reacted with borane, in an organic solvent such as THF, dioxane, and the like, to yield the corresponding compound of formula (XVII), which is preferably not isolated. The compound of formula (XVII) is reacted with aminosulfonic acid, preferably at an elevated temperature in the range of from about 50°C to about 100°, more preferably, at about reflux temperature, to yield the corresponding compound of formula (Vllb). Scheme 6 Accordingly, a suitably substituted compound of formula (XVIII), a compound prepared as in Scheme 5 above, is reacted with a peroxide, such as hydrogen peroxide, and the like, in the presence of a base such as NaOH, KOH, and the like, in an organic solvent such as chloroform, DCE, DCM, and the like, to yield the corresponding compound of formula (Vb). WO 2006/007435 PCT/US2005/021513 Scheme 7 28 Accordingly, a suitably substituted compound of formula (XIX), a known compound or compound prepared by known methods, is reacted with a suitably selected reducing agent, such as LAH, and the like, in an organic solvent such as THF, diethyl ether, and the like to yield the corresponding compound of formula (Vc). WO 2006/007435 PCT/US2005/02I513 Scheme 8 Accordingly, a suitably substituted compound of formula (XX), a known compound or compound prepared by known methods, is reacted with NH4OH, in the presence of a coupling agent such as DCC, and the like, optionally in an organic solvent such as acetonitrile, and the like, to yield the corresponding compound of formula (XXI). 29 The compound of formula (XXI) is reacted with a suitably selected reducing agent, such as LAH, and the like, in an organic solvent such as THF, diethyl ether, and the like, to yield the corresponding compound of formula (Vile). WO 2006/007435 PCT/US2005/0215I3 Accordingly, a suitably substituted compound of formula (XXII), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (XXIII), a known compound or compound prepared by known methods, in the presence of a base such as K2CO3, Na2CO3, NaHCC>3, and the like, in an organic solvent such as DMF, DMSO, acetonitrile, and the like, preferably, at an elevated temperature in the range of form about 50°C to about 100°C, more preferably, at an elevated temperature in the range of from about 50°C to about 75°C, to yield the corresponding compound of formula (Vd). Scheme 10 Accordingly, a suitably substituted compound of formula (XXIV) wherein J1 is a suitable leaving group such as Br, Cl, I, tosyl, mesyl, triflyl, and the like, a known compound or compound prepared by known methods (for example, by activating the corresponding compound wherein J1 is OH), is reacted with a cyanide such as potassium cyanide, sodium cyanide, and the like, in an organic solvent such as 30 WO 2006/007435 PCT/US2005/021513 DMSO, DMF, THF, and the like, to yield the corresponding compound of formula (XXV). The compound of formula (XXV) is reduced according to known methods, for example by reacting with a suitable reducing agent such as LAH, borane, and the like, to yield the corresponding compound of formula (Vile). Scheme 11 Accordingly, a suitably substituted compound of formula (XXVI), a known compound or compound prepared by known methods (for example according to the process outlined in Scheme 9 above) is activated, according to known 31 WO 2006/007435 PCT/US2005/021513 method, to yield the corresponding compound of formula (XXVII), wherein J2 is a suitable leaving group, such tosylate, Cl, Br, I, mesylate, triflate, and the like. The compound of formula (XXVII) is reacted with a phthalimide salt such as potassium phthlimide, sodium phthalimide, and the like, in an organic solvent such as DMF, DMSO, acetonitrile, and the like, preferably, at an elevated temperature in the range of from 50°C to about 200°C, more preferably, at about reflux temperature, to yield the corresponding compound of formula (XXVIII). The compound of formula (XXVI) is reacted with N2H4, a known compound, in an organic solvent such as ethanol, methanol, and the like, preferably, at an elevated temperature in the range of from about 50°C to about 100°C, more preferably, at about reflux temperature, and the like, to yield the corresponding compound of formula (Vlld). Scheme 12 Accordingly, a suitably substituted compound of formula (XXVII) wherein J2 is CN, a known compound or compound prepared by known methods, is hydrolyzed 32 WO 2006/007435 PCT/US2005/021513 according to known methods, for example by reacting with a suitable acid or base, to yield the corresponding compound of formula (XXIX). The compound of formula (XXIX) is reduced according to known methods, for example by reacting with a suitable reducing agent such as LAH, and the like, to yield the corresponding compound of formula (Ve). One skilled in the art will recognize that compounds of formula (V) and (VII) may be similarly prepared according to the processes outlined in Schemes 3 through 12 above, by selecting and substituting the corresponding naphthyl-fused compounds for the benzo-fused starting materials (e.g. the compounds of formula (X), (XIII), (XV), (XVIII), (XIX), (XX), (XXII), (XXIV), etc.). One skilled in the art will further recognize that wherein a single enantiomer (or a mixture of enantiomers wherein one enantiomer is enriched) of a compound of 33 WO 2006/007435 PCT/US2005/021513 formula (V) or a compound of formula (VII) is desired, the above processes as described in Schemes 1 through 12 may be applied by substituting the corresponding single enantiomer (or mixture of enantiomers wherein one enantiomer is enriched) for the appropriate starting material. The following Examples are set forth to aid in the understanding of the invention, and are not intended and should not be construed to limit in any way the invention set forth in the claims which follow thereafter. Example 1 ((3,4-Dihvdro-2H-benzorbin,41dioxepin-3-vl)methvl)sulfamide (Compound #3) Catechol (5.09 g, 46.2 mmol) and potassium carbonate were combined in acetonitrile and heated to reflux for one hour. 2-Chloromethyl-3-chloro-1-propene (5.78 g, 46.2 mmol) was added and the reaction was continued at reflux for 24 hours. The solution was cooled to room temperature and filtered. The filtrate was evaporated and the residue was diluted with water and extracted with diethyl ether (3 x). The combined organic solution was dried over MgSO4 and concentrated. Chromatography (2% ethyl ether in hexane) yielded 3-methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine as a colorless oil. MS (ESI): 163.2 (M+H+) 1H NMR (300 MHz, CDCI3), 5: 6.94 (m, 4H), 5.07 (s, 2H), 4.76 (s, 4H). 3-Methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine (5.00 g, 30.8 mmol) was dissolved in dryTHF (100 mL). Borane-THF (1.0 M in THF, 10.3 mL) was added at 0°C. The reaction was stirred at RT for 5 hours. Aminosulfonic acid (6.97 g, 61.6 mmol) was added. The reaction was heated to reflux overnight. The reaction was cooled to room temperature and aqueous sodium hydroxide 34 WO 2006/007435 PCT/US2005/021513 (3.0 M, 100 mL) was added. The solution was extracted with ethyl acetate (3 x 100 mL). The combined organic solution was dried over MgSO,. The solution was concentrated under vacuum and purified by chromatography (2% to 8% methanol in dichloromethane) to yield ((3,4-dihydro-2H-benzo[b][1,4]dioxepin-3-yl)methyl)amine as a colorless oil. MS (ESI): 180.1 (M+H+) 1H NMR (300 MHz, DMSO), 5: 6.92 (m, 4H), 4.21 (m, 2H), 4.07 (m, 2H), 3.33 (broad, 2H), 3.16 (d, J = 4 Hz, 1H), 2.72 (d, J = 4 Hz, 1H), 2.30 (m, 1H). ((3,4-Dihydro-2H-benzo[b][1,4]dioxepin-3-yl)methyl)amine (2.90 g, 16.2 mmol) and sulfamide (3.11 g, 32.4 mmol) were combined in dry dioxane (60 ml) and heated to reflux overnight. Chloroform was added and the precipitate was removed by filtration. The filtrate was concentrated under vacuum and purified by chromatography (2% to 8% acetone in dichloromethane) to yield the title compound as an off-white solid. 258.8 (M+H+) 1H NMR (300 MHz, DMSO), 8: 6.92 (m, 4H), 6.71 (broad, 1H), 6.59 (broad, 2H), 4.19 (m, 2H), 4.04 (m, 2H), 3.00 (m, 2H), 2.39 (m, 1H). EXAMPLE 2 N-(2,3-Dihvdro-benzon.41dioxin-2-vlmethvl)-sulfamide (Compound #1) Racemic 2,3-dihydro-1,4-benzdioxin-2-ylmethylamine (4.4 g, 26 mmol) and sulfamide (5.1 g, 53 mmol) were combined in 1,4 dioxane (100 mL) and refluxed for 2 h. The reaction was cooled to room temperature and a small amount of solid was filtered and discarded. The filtrate was evaporated in vacuo and the residue was purified using flash column chromatography (DCM:Methanol 35 WO 2006/007435 PCT/US2005/021513 -10:1) to yield a white solid. The solid was recrystallized from DCM to yield the title compound as a white solid. mp: 97.5 - 98.5°C Anal Calc: C, 44.25; H, 4.95; N, 11.47; S, 13.13 Anal Found: C, 44.28; H, 4.66; N, 11.21; S, 13.15 H1 NMR (DMSO d6) 8 6.85 (m, 4H), 6.68 (bd s, 3H, NH), 4.28 (m, 2H), 3.97 (dd, J = 6.9, 11.4 Hz, 1H), 3.20 (m, 1H), 3.10 (m, 1H). EXAMPLE 3 (BenzoH,31dioxol-2-vlmethvl)sulfamide (Compound #2) Catechol (10.26 g, 93.2 mmol), sodium methoxide (25% by weight in methanol, 40.3 g, 186 mmol), and methyl dichloroacetate (13.3 g, 93.2 mmol) were combined in dry methanol (100 ml_). The solution was heated to reflux overnight. The reaction was cooled to room temperature, acidified by addition of concentrated hydrochloric acid and then reduced in volume under vacuum to about 50 mL. Water was added and the mixture was extracted with diethyl ether (3 x 100 mL). The combined organic solution was dried with MgSO4, concentrated to a brown solid, and chromatographed (2% ethyl acetate in hexane) to yield benzo[1,3]dioxole-2-carboxylic acid methyl ester as a colorless oil. MS (ESI): 195.10 (M+H+). 1H NMR (300 MHz, CDCI3), 5: 6.89 (broad, 4H), 6.29 (s, 1H), 4.34 (q, J=7 Hz, 2H), 1.33(t, J=7Hz, 3H). To benzo[1,3]dioxole-2-carboxylic acid methyl ester (7.21 g, 40.0 mmol) was added ammonium hydroxide (29% in water, 10 mL) and enough acetonitrile to make the mixture homogeneous (~5 mL). The solution was stirred for two hours at room temperature and then distilled water was added. 36 WO 2006/007435 PCT/US2005/021513 Benzo[1,3]dioxole-2-carboxylic acid amide precipitated as a white solid and was collected by filtration and used without further purification. MS (ESI): 160.00 (M+H+) 1H NMR (300 MHz, DMSO), S: 7.99 (s, broad, 1H), 7.72 (s, broad, 1H), 6.94 (m, 2H) 6.86 (m, 2H), 6.30 (s, 1H). Benzo[1,3]dioxole-2-carboxylic acid amide (5.44 g, 32.9 mmol) was dissolved in tetrahydrofuran (THF, 100 mL). Lithium aluminum hydride (LAH, 1M in THF, 39.5 mL, 39.5 mmol) was added slowly to the solution at room temperature. The reaction was stirred at room temperature for 24 hours. Distilled water was added to destroy the excess LAH. Aqueous sodium hydroxide (3.0 M, 100 mL) was added and the solution was extracted with ethyl acetate (3 x 100 mL). The combined organic solution was washed with water and dried over MgSO4. The solvent was evaporated to yield C-benzo[1,3]dioxol-2-yl-methylamine as a colorless oil. MS (ESI): 152.1 (M+H+) 1H NMR (300 MHz, CDCI3), 5: 6.87 (m, 4H), 6.09 (t, J = 4 Hz, 1H), 3.13 (d, J = 4Hz, 2H) C-Benzo[1,3]dioxol-2-yl-methylamine (2.94 g, 19.4 mmol) and sulfamide (3.74 g, 38.9 mmol) were combined in dry dioxane (50 mL) and the solution was heated to reflux overnight. The reaction was concentrated and the residue was chromatographed (2% to 10% acetone in dichloromethane) to yield the title compound as a white solid. MS (ESI): 230.0 (M+H+) 1H NMR (300 MHz, CDCI3), 5: 6.87 (m, 4H), 6.25 (t, J = 4 Hz, 1H), 4.79 (broad, 1H), 4.62 (broad, 1H), 3.64 (d, J = 4 Hz, 2H). EXAMPLE 4 (2S)-(-)-N-(2.3-Pihvdro-benzon.41dioxin-2-vlmethvl)-sulfamide (Compound #4) 37 WO 2006/007435 PCT/US2005/021513 Catechol (13.2 g, 0.12 mol) and potassium carbonate (16.6 g, 0.12 mol) were stirred in DMF (250 mL) and (2R)-glycidyl tosylate (22.8 g, 0.10 mol) was added and the reaction was stirred at 60°C for 24 h. The reaction was cooled to room temperature and diluted with ice water (1 L) and extracted with diethyl ether (4 times). The combined organic solution was washed 3 times with 10% potassium carbonate, once with water, once with brine and evaporated in vacuo to yield a white solid which was purified by flash column chromatography (DCM:Methanol - 50:1) to yield ((2S)-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methanol as a solid. The solid (13.3 g, 68 mmol) was dissolved in pyridine (85 mL) cooled to 0°C, p-toluenesulfonyl chloride (13.0 g, 68 mmol) was added and the reaction mixture stirred at room temperature for 20h. The reaction was diluted with diethyl ether (1 L) and 1N HCI (1.2 L). The organic layer was separated and washed 2 times with 1N HCI (500 mL), 4 times with water (150 mL), once with brine, dried (MgSCU) and evaporated in vacuo to yield a white solid which was purified by flash column chromatography (Hept:EA - 2:1) to yield toluene-4-sulfonic acid (2S)-2,3-dihydro-benzo[1,4]dioxin-2-yImethyl ester as a white solid. The white solid was combined with potassium phthalimide (14.4 g, 78 mmol) in DMF (250 mL) and heated to reflux for 1 h, cooled to room temperature and poured into vigorously stirring water (1.5 L) and stirred 30 min. White solid was filtered and the solid was washed several times with water, 2% NaOH, and water again and let air dry to yield a (2S)-2-(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-isoindole-1,3-dione as white powdery solid. The powdery white solid was combined with hydrazine (2.75 g, 86 mmol) in EtOH (225 mL) and heated at reflux for 2 h, cooled to room temperature and 1N HCI added to pH 1.0 and stirred for 15 min. White solid was filtered and washed with fresh EtOH (solid discarded) and the filtrate was evaporated in 38 WO 2006/007435 PCT/US2005/021513 vacuo to a solid, which was partitioned between diethyl ether and dilute aqueous NaOH. The diethyl ether solution was dried (Na2SO4) and evaporated in vacuo to a yield a light yellow oil. The oil was purified by flash column chromatography (DCM:MeOH - 10:1) to yield an oil. A portion of the oil (4.82 g, 29 mmol) in 2-propanol (250 mL) was treated with 1N HCI (30 mL) and heated on steambath until homogeneous and then let cool to room temperature. After 3 h, the mixture was ice cooled for 2 h. A white flaky solid (the corresponding HCI salt of (2S)-C-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-methylamine) was filtered off and then recrystallized again from 2-propanol to yield a white solid. [a]D = -69.6 (c = 1.06, EtOH) The white solid was partitioned between DCM and dilute NaOH, and the DCM was dried (NaSO4) and evaporated in vacuo to yield (2S)-C-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-methylamine as an oil. [a]D = -57.8 (c = 1.40, CHCI3) The oil (2.1 g, 12.7 mmol) and sulfamide (2.44 g, 25.4 mmol) were refluxed in dioxane (75 mL) for 2 h and the crude product was purified by flash column chromatography (DCM:MeOH 10:1) to yield a white solid, which was recrystallized from DCM to yield the title compound as a white crystalline solid. mp 102-103°C [a]D = -45.1°(c= 1.05, M); 1H NMR (DMSOd6) 5 6.86 (m, 4H), 6.81 (bd s, 3H, NH), 4.3 (m, 2H), 3.97 (dd, J = 6.9, 11.4 Hz, 1H), 3.20 (dd, J = 5.5, 13.7 Hz, 1H), 3.10 (dd, J = 6.9, 13.7 Hz, 1H) Anal Calc: C, 44.25; H, 4.95; N, 11.47; S, 13.13 Anal Found: C, 44.20; H, 4.69; N, 11.40; S, 13.22. 39 WO 2006/007435 PCT/US2005/021513 EXAMPLE 5 N-(2.3-Dihvdro-benzon.41dioxin-2-vlmethvl)-N'.N' dimethylsulfamide (Compound #6) Racemic 2,3-dihydro-1,4-benzdioxin-2-ylmethylannine (8.25 g, 5.0 mmol) and triethylamine (1.52 g, 15 mmol) were combined in DMF (10 ml_) and cooled in an ice bath as dimethylsulfamoyl chloride (1.44 g, 10 mmol) was added. The reaction mixture was then stirred for 3 hr with continued cooling. The reaction mixture was partitioned between ethyl acetate and water, and the ethyl acetate solution was washed with brine, dried (MgSO4) and evaporated in vacuo to yield an oil. The oil was purified using flash column chromatography (ethyl acetate:Heptane -1:1) to yield a white solid, which was recrystallized (ethyl acetate/Hexane) to yield the title compound as a white floccular solid. mp 76 - 78°C MS 273 (MH+) Anal Calc: C, 48.52; H, 5.92; N, 10.29; S, 11.78 Anal Found: C, 48.63; H, 5.62; N, 10.20; S, 11.90 1H NMR (CDCI3) 5 6.87 (m, 4H), 4.59 (bd m, 1H, NH), 4.35 (m, 1H), 4.27 (dd, J = 2.3, 11.4 Hz, 1H), 4.04 (dd, J = 7.0, 11.4, 1H), 3.36 (m, 2H), 2.82 (s, 6H). EXAMPLE 6 N-te.S-Dihvdro-benzori^idioxin^-vlmethvll-N-methylsulfamide (Compound #7) 40 WO 2006/007435 PCT/US2005/021513 Racemic 2,3-dihydro-1,4-benzdioxin-2-ylmethylamine (825 mg, 5 mmol) was dissolved in ethyl formate (15 mL), refluxed for 30 min and evaporated in vacuo to yield N-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-formamide as an oil. The oil in diethyl ether (25 mL) was treated with 1M LAH in THF (9.0 mL, 9.0 mmol) at 0°C and stirred for 5 h at room temperature. The reaction was cooled in an ice bath and quenched with water (0.50 mL), followed by 3 N NaOH (0.50 mL) and water (0.50 mL). The mixture was then stirred at room temperature for 1 h. Solid was filtered and the filtrate was evaporated in vacuo to yield a residue which was partitioned between 1N HCI and diethyl ether. The aqueous phase was basified with 1N NaOH and extracted with diethyl ether. The organic phase was dried (MgSO4) and evaporated in vacuo to yield (2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-methyl-amine as an oil. MS180(MH+) 1H NMR (CDCI3) 5 6.85 (m, 4H), 4.30 (m, 2H), 4.02 (dd, J = 7.9, 11.6 Hz, 1H), 2.85 (m, 2H), 2.50 (s, 3H) The oil (380 mg, 2.1 mmol) and sulfamide (820 mg, 8.5 mmol) were combined in dioxane (15 mL), refluxed for 1.5 h and evaporated in vacuo to yield a crude residue. The residue was purified via column chromatography (ethyl acetate/Heptane 1:1) and the resultant solid was recrystallized from ethyl acetate/Hexane to yield the title compound as a white solid. mp 97-98°C MS 257 (M'1) Anal Calc: C, 46.50; H, 5.46; N, 10.85; S, 12.41 Anal Found: C, 46.48; H, 5.65; N, 10.90; S, 12.07 1H NMR (CDCI3) 6 6.86 (m, 4H), 4.52 (bs, 2H), 4.46 (m, 1H), 4.29 (dd, J = 2.3, 11.5 Hz, 1H), 4.05 (dd, J = 6.5, 11.5 Hz, 1H), 3.51 (dd, J = 6.7,14.9 Hz, 1H), 3.40 (dd, J = 5.9, 14.9 Hz, 1H), 2.99 (s, 3H). Example 7 f2S^-f-)-N-(6-Chloro-2,3-dihvdro-benzori,41clioxin-2-vlmethvn-sulfamide (Compound #8) 41 WO 2006/007435 PCT/US2005/021513 Following the procedure outlined in Example 4 above, 4-chlorocatechol was reacted to yield a mixture of (2S)-C-(7-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine and (2S)-C-(6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine (ca. 3:1 ratio of 6-chloro:7-chloro isomers by RP HPLC). The mixture was dissolved in 2-propanol (100 ml_) and 1N HCI in diethyl ether was added until pH = 1.0 was attained. The hydrochloride salt that precipitated was filtered (2.65 g) and re-crystallized from methanol/lPA to yield white crystals. The white crystals were partitioned between DCM and dilute NaOH. The DCM was dried and evaporated in vacuo to yield purified (2S)-C-(6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine as an oil. [a]D = -67.8 (c = 1.51, CHCI3) The oil (7.75 mmol) and sulfamide (1.50 g, 15.5 mmol) were combined in dioxane (50 ml_) and refluxed for 2.0 h, cooled to room temperature and evaporated in vacuo to yield a solid. The product was purified via flash column using DCM/methanol 20:1 to yield the title compound as a white solid. MS 277 (M-1) [cc]D = -59.9° (c = 1.11, M) 1H NMR (CDCI3) 5 6.90 (d, J = 2.2 Hz, 1H), 6.81 (m, 2H), 4.76 (m, 1H), 4.55 (s, 2H), 4.40 (m, 1H), 4.29 (dd, J = 2.4, 11.5 Hz, 1H), 4.05 (dd, J = 7.1, 11.5 Hz, 1H),3.45(m,2H) AnalCalc: C, 38.78; H, 3.98; N, 10.05 Anal Found: C, 38.80; H, 3.67; N, 9.99. The filtrates of the crystallized hydrochloride salt of (2S)-C-(6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine prepared above were recovered (ca. 1:1 of 6-chloro:7-chloro isomers) and evaporated in vacuo to yield a solid, which was partitioned between DCM (200 mL) and dilute NaOH (0.5 M, 50 ml_). The DCM solution was washed once with brine, dried (Na2SO4) and evaporated in 42 WO 2006/007435 PCT/US2005/021513 vacuo to yield an oil, which was purified via reverse phase HPLC (10 - 50% ACN with 0.16% TFA in water with 0.20% TFA) to yield (2S)-C-(7-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine as a residue. The residue was combined with sulfamide (0.90 g, 9.4 mmol) in dioxane (25 mL) and refluxed for 2.5 h, cooled to room temperature and evaporated in vacuo to yield an oil. The oil was purified by flash column chromatography using DCM/methanol - 10:1 to yield (2S)-(-)-N-(7-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide as a white solid. MS 277 (M'1) 1H NMR (CDCI3/CD3OD) 5 6.88 (d, J = 0.7 Hz, 1H), 6.81 (m, 2H), 4.37 (m, 1H), 4.30 (dd, J = 2.3, 11.6 Hz, 1H), 4.04 (dd, J = 7.0, 11.6 Hz, 1H), 3.38 (m, 2H). Example 8 Chroman-2-vlmethvlsulfamide (Compound #10) Chroman-2-carboxylic acid (4.5 g, 25 mmol) and HOBT (3.86 g, 25 mmol) were combined in DCM (40 mL) and DMF (10 mL). Dimethylaminopropyl ethylcarbodiimide (EDC, 4.84 g, 25 mmol) was added at room temperature and the reaction mixture was stirred for 30 min. Ammonium hydroxide (2.26 mL, 33.4 mmol) was added and the reaction mixture was stirred for 16h. The reaction mixture was diluted with DCM (50 mL) and water (50 mL) and the pH of the mixture was adjusted to about pH = 3.0 with 1N HCI. The DCM was separated and the aqueous phase extracted twice with DCM. The combined DCM phase was dried (Na2SO4) and evaporated in vacuo to yield an oil, which was purified with flash column chromatography (ethyl acetate) to yield an oil. The oil (5.35 g, 30 mmol) in THF (90 mL) was stirred as 1M LAH in THF (36 mL, 36 mmol) was added and the reaction mixture was then stirred at room temperature for 20 h. The reaction was quenched with water, stirred for 2 hours, 43 WO 2006/007435 PCT/US2005/021513 the solution decanted, dried (Na2SO4) and evaporated in vacuo to yield C-chroman-2-yl-methylamine as an oily amine. The oily amine (1.63 g, 10 mmol) and sulfamide (1.92 g, 20 mmol)were combined in dioxane (50 mL) and brought to reflux for 2 h. The solution was cooled and evaporated in vacuo to yield an oil, which was purified via column chromatography (DCM:Methanol 10:1) to yield a white solid. The solid was recrystallized from ethyl acetate/hexane to yield chroman-2-ylmethylsulfamide as a white solid. mp100-101°C MS 241 (M~1) Anal Calc: C, 49.57; H, 5.82; N, 11.56; S, 13.23 Anal Found: C, 49.57; H, 5.80; N, 11.75; S, 13.33. Example 9 Chroman-2-vlmethylsulfamate (Compound #11) Chroman-2-carboxylic acid (4.3 g, 24 mmol) in THF (70 mL) was combined with 1M LAH in THF (30 mL, 30 mmol) and stirred at room temperature for 2h. The reaction mixture was quenched with water and then stirred for 2 hours. The THF solution was decanted from the solid, which was washed with fresh THF. The combined THF solution was dried (Na2SO4) and evaporated in vacuo to yield chroman-2-yl-methano! as an oil. The chroman-2-yl-methanol (1.97 g, 12 mmol) in DMF (30 mL) was cooled with an ice bath to about 0°C under argon and combined with 95% NaH (0.39 g, 15.6 mmol), then stirred for 30 min. Sulfamoyl chloride (2.78 g, 24 mmol) was then added and the reaction mixture was stirred for 1 h. The reaction mixture was diluted with ethyl acetate (100 mL) and water (100 mL). The ethyl acetate solution was separated and the aqueous phase was extracted twice with ethyl 44 WO 2006/007435 PCT/US2005/021513 acetate. The combined ethyl acetate phase was dried (MgSO4) and evaporated in vacuo to yield an oil, which was purified by flash column chromatography (ethyl acetate/hexane 1:2) to yield a white solid, which was recrystallized from ethyl acetate/hexane to yield the title compound as a white solid. mp 87-90°C MS [M-H]-242.1 Anal Calc: C, 49.37; H, 5.39; N, 5.76; S, 13.18 Anal Found: C, 49.46; H, 5.17; N, 5.72; S, 13.09. Example 10 2-(2.3-Dihvdro-benzon.41dioxin-2-vn-ethvlsulfamide (Compound #16) Potassium cyanide (2.05 g, 31.5 mmol) was added to 2-bromomethyl-(2,3 dihydrobenzo[1,4]dioxine) (6.87 g, 30 mmol) in DMSO (90 mL) and stirred at ambient temperature for 20 h. The reaction mixture was then diluted with water (250 mL) and extracted twice with diethyl ether. The diethyl ether was washed with water, then washed twice with brine, dried (Na2SO4) and evaporated in vacuo to yield 2-cyanomethyl-(2,3 dihydrobenzo[1,4]dioxine) as a white solid. 1H NMR (CDCI3) 5 6.89 (m, 4H), 4.50 (m, 1H), 4.31 (dd, J = 2.3, 11.5 Hz, 1H), 4.08 (dd,J = 6.2, 11.6 Hz, 1H), 2.78 (d, J = 6.1, Hz, 2H) The 2-cyanomethyl-(2,3 dihydrobenzo[1,4]dioxine) was dissolved in THF (50 mL) and 1M BH3 in THF (80 mL, 80 mmol) was added and the reaction mixture refluxed for 5 h, then stirred at ambient temperature for 16h. With ice bath cooling, 2N HCI was added until pH = 1.0 was achieved. The reaction mixture was then stirred for 1h at room temperature and evaporated in vacuo to yield an oil. The oil was partitioned between 3N NaOH and diethyi ether, and the diethyl ether solution was washed with brine, dried (Na2SO4) and evaporated in vacuo to yield crude 2-(2,3 dihydrobenzo[1,4]dioxin-2-yl)ethylamine. 45 WO 2006/007435 PCT/US2005/021513 MS(M+H)+180. The crude 2-(2,3 dihydrobenzo[1,4]dioxin-2-yl)ethylamine in dioxane (100 mL) was combined with sulfamide (3.0 g, 31 mmol) and heated to reflux for 2 h. The solution was cooled and evaporated in vacuo to yield an orange solid, which was purified by column chromatography (DCM:MeOH -10:1) to yield a white solid. The solid was re-crystallized from DCM to yield the title compound as a solid. MS(M-1)257 MP101 -103°C(corr) 1H NMR (CDCI3): 5 6.86 (m, 4H), 4.70 (m, 1H), 4.52 (s, 2H), 4.30 (m, 2H), 3.94 (dd, J = 7.4, 11.3 Hz, 1H), 3.43 (dd, J = 6.4, 12.9 Hz, 2H), 1.94 (dd, J = 6.5, 12.9, 2H). Elemental Analysis: Measured: C, 46.48; H, 5.60; N, 10.81; S, 12.41 Calculated: C, 46.50; H, 5.46; N, 10.85; S, 12.41 Example 11 (2S)-(-)-N-(6,7 Dichloro-2,3-dihvdro-benzon,41dioxin-2-vlmethvl)-sulfamide (Compound #29) 4,5 Dichloroatechol (8.6 g, 48 mmol) and potassium carbonate (6.64 g, 48 mmol) were stirred in DMF (200 mL). (2R)-Glycidyl tosylate (9.12 g, 40 mmol) was added and the reaction mixture was stirred at 60°C for 24 h. The reaction mixture was cooled to room temperature and then diluted with ice water (600 mL) and extracted with diethyl ether (4 times). The combined organic solution was washed 3 times with 10% potassium carbonate, twice with brine, dried (MgSO4) and evaporated in vacuo to yield a viscous oil of (2S)-2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxine) methanol. 46 WO 2006/007435 PCT/US2005/021513 The (2S)-2-(6,7 dichloro-2,3-dihydro-benzo[1,4]dioxine) methanol oil (6.4 g, 27 mmol) was dissolved in pyridine (50 mL) cooled to 0°C. Then, p-toluenesulfonyl chloride (5.2 g, 27 mmol) was added and the reaction mixture was stirred at room temperature for 20h. The reaction mixture was diluted with diethyl ether and 1N HCI (750 mL) and the organic layer was separated and washed 2 times with 1N HCI (250 mL), once with water (150 mL), twice with brine, dried (MgSO4) and evaporated in vacuo to yield light yellow solid of toluene-4-sulfonic acid (2S)-6,7-dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl ester. 1H NMR (CDCI3): 5 7.79 (d, J = 8.3 Hz, 2H), 7.36 (d, J = 8.0 Hz, 2H), 6.94 (s, 1H), 6.83 (s, 1H), 4.37 (m, 1H), 4.2 (m, 3H), 4.03 (dd, J = 6.3, 11.7 Hz, 1H), 2.47 (s, 3H). Toluene-4-sulfonic acid (2S)-6,7-dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl ester (8.0 g, 20.5 mmol) was combined with potassium phthalimide (6.1 g, 33 mmol) in DMF (75 mL) and heated to reflux for 1 h, cooled to room temperature and poured into vigorously stirring water (0.5 L) and then stirred 30 min. White solid was filtered and the solid was washed several times with water, 2% NaOH, and water again and then let air dry to yield (2S)-2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-isoindole-1,3-dione (6.0 g, 80%) as a white powdery solid. The white powdery solid was combined with hydrazine (1.06 g, 33 mmol) in EtOH (80 mL) and heated at reflux for 2 h, then cooled to room temperature. 1N HCI was added to adjust the reaction mixture's pH to pH 1.0 and the reaction mixture was then stirred for 15 min. White solid was filtered and washed with fresh EtOH (solid discarded) and the filtrate was evaporated in vacuo to a solid, which was partitioned between diethyl ether and dilute aqueous NaOH. The diethyl ether solution was dried (Na2SO4) and evaporated in vacuo to a yield a viscous oil of (2S)-2-aminomethyl-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxine). 1H NMR (CDCI3): 5 6.98 (s, 1H), 6.96 (s, 1H), 4.25 (dd, J = 2.0, 11.2 Hz, 1H), 4.15 (m, 1H), 4.0 (m, 1H), 2.97 (d, J = 5.5 Hz, 2H) 47 WO 2006/007435 PCT/US2005/021513 A portion of the oil (3.8 g, 16 mmol) and sulfamide (3.1 g, 32.4 mmol) were refluxed in dioxane (100 mL) for 2 h and the crude product was purified by flash column chromatography (DCM:MeOH 20:1) to yield the title compound as a white solid, which was recrystallized from ethyl acetate / hexane to yield the title compound as a white crystalline solid. MS[M-H]-311.0 mp119-121°C [a]D = -53.4 °(c= 1.17, M) 1H NMR (DMSOd6): 5 7.22 (s, 1H), 7.20 (s, 1H), 6.91 (bd s, 1H), 6.68 (bd s, 2H), 4.35 (m, 2H), 4.05 (dd, J = 6.5, 11.5 Hz, 1H), 3.15 (m, 2H) Elemental Analysis: Measure: C, 34.52; H, 3.22; N, 8.95; Cl, 22.64; S, 10.24 Calculated: C, 34.64; H, 2.68; N, 8.87; Cl, 22.94; S, 10.35. Example 12 (2S)-(-)-N-(7-Amino-2.3-dihvdro-benzori,41dioxin-2-vlmethyl)-sulfamide (Compound #36) (2S)-(-)-N-(2,3-Dihydro-7-nitro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide (1.2 g, 4.15 mmol), was prepared from 4-nitrocatechol according to the process outlined in Example 4. The (2S)-(-)-N-(2,3-Dihydro-7-nitro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide, was then combined with 10% Pd/C in methanol (120 mL) and shaken under hydrogen atmosphere (39 psi) at room temperature for 3 h. The solids were filtered and washed with 10% M in DCM and the filtrate was evaporated in vacuo to yield crude product. The crude product was dissolved in 0.2 N HCI (25 mL), frozen and lyophilized to yield the title compound as a white flaky solid, as the corresponding hydrochloride salt. MS (M+H)+ 260 48 WO 2006/007435 PCT/US2005/021513 1H NMR (DMSO d6): 5 10.2 (bd s, 3H), 6.86 (m, 1H), 6.85 (s, 1H), 6.74 (dd, J = 2.5, 8.4 Hz, 1H), 4.22 (m, 2H), 3.88 (dd, J = 6.7, 11.4 Hz, 1H), 3.04 (m, 2H) Example 13 (2S)-(-)-N-(7-Methvl-2,3-dihvdro-benzon.41dioxin-2-vlmethvl>-sulfamide (Compound #19) Title compound was prepared according to the procedure described in Example 4 above, starting with 4-methylcatechol, to yield a white solid, which was recrystallized from ethyl acetate/ hexane to yield the title compound as a white solid. MS[M-H]"257 1H NMR (CDCI3): 6 6.76 (m, 1H), 6.66 (m, 2H), 4.80 (m, 1H), 4.57 (bd s, 1H), 4.40 (m, 1H), 4.28 (m, 1H), 4.03 (dd, J = 6.9, 11.4 Hz, 1H), 3.45 (m, 2H), 2.25 (s, 3H). Elemental Analysis Calculated: C, 46.50; H, 5.46; N, 10.85; S, 12.41 Found: C, 46.65; H, 5.60; N, 10.84; S, 12.61. Example 14 Sulfamic acid, 6.7 dichloro-2.3-dihvdro-benzoH.41dioxin-2-vlmethvl ester 49 (Compound #27) WO 2006/007435 PCT/US2005/021513 (2S)-6,7 dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethanol (2.0 g, 8.5 mmol), prepared according to the procedure described in Example 11 above, in DMF (20 mL) was cooled in an ice bath. Then, 95% sodium hydride (0.28 g, 11 mmol) was added under argon and the reaction mixture was stirred 30 min. Sulfamoyl chloride (1.97 g, 17 mmol) was added and the reaction mixture was stirred with ice bath cooling. After 1 h, the reaction mixture was diluted with water (50 mL) and extracted three times with ethyl acetate. The combined ethyl acetate was washed with brine, dried (Na2SO4) and evaporated in vacuo to an oil, which was purified by flash column chromatography (ethyl acetate/heptane 1:1) to yield a white solid. The white solid was recrystallized from benzene to yield the title compound as a white solid. mp109-111°C MS[M-H]"312 1H NMR (DMSOd6) 5 7.65 (s, 2H), 7.26 (s, 1H), 7.25 (s, 1H), 4.58 (m, 1H), 4.41 (dd, J = 2.5, 11.7 Hz, 1H), 4.28 (m, 2H), 4.11 (dd, J = 6.9, 11.7 Hz, 1H). Example 15 Sulfamic acid, 6-chloro-2.3-dihvdro-benzof1,41dioxin-2-ylmethvl ester (Compound #12) (2S)-6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethanol (6.4 g, 32 mmol) was prepared according to procedure as in Example 7 above, in DMF (80 mL) was cooled in an ice bath. Then, 95% sodium hydride (1.06 g, 42 mmol) was added over 20 min under argon and the reaction mixture was stirred 30 min. Sulfamoyl chloride (7.4 g, 64 mmol) was added over 10 min and the reaction mixture was stirred with ice bath cooling. After 1 h, the reaction was diluted with water (300 mL) and extracted three times with ethyl acetate. The combined ethyl acetate was washed with brine, dried (MgSO4) and evaporated in vacuo to yield 50 WO 2006/007435 PCT/US2005/021513 an oil, which was purified by flash column chromatography (ethyl acetate /hexane 1:2) to yield a white solid. The white solid was recrystallized from benzene 3 times to yield the title compound as a white solid. mp113-116°C MS[M-H]"278 [a]D = -41.0 °(c = 1.32, M) 1H NMR (CDCI3) 5 6.91 (d, J = 1.9 Hz, 1H), 6.84 (m, 2H), 4.82 (bd s, 2H), 4.50 (m, 1H), 4.41 (m, 2H), 4.31 (dd, J = 2.3, 11.6 Hz, 1H), 4.12 (dd, J = 6.3, 11.6 Hz, 1H) Elemental Analysis: Measured: C, 38.57; H, 3.42; N, 4.92; S, 11.53 Calculated: C, 38.65; H, 3.60; N, 5.01; S, 11.46 Example 16 In Vivo Assay: Maximal Electroshock Test (MES) Anticonvulsant activity was determined using the MES test, run according to the procedure described in detail below. Swinyard EA, Woodhead JH, White HS, Franklin MR. Experimental selection, quantification, and evaluation of anticonvulsants. In Levy RH, et al., eds. Antiepileptic Drugs. 3rd ed. New York: Raven Press, 1989:85-102 CF-1 male albino mice (25-35g) were fasted for 16 hours before testing. Mice were randomly selected into control and test groups, with the animals dosed with vehicle or test compound, at varying concentrations, respectively. On the study date, at 30 minutes prior to shock, the mice were orally dosed with vehicle (0.5% methylcellulose) or test compound (100-300 mg/kg). Seizures were induced by trans-comeal electric shock using a 60-Hz alternating current, 50 mA, delivered for 0.2 sec. The mice in the test groups were subjected to electrical stimulus at time intervals between 15 minutes and 4 hours following administration of test compound. The shock resulted in an immediate full body tonic extension. The test was complete when the entire course of the convulsion 51 WO 2006/007435 PCT/US2005/021513 has been observed (typically, less than 1 minute after electrical stimulation), and the mice were then immediately euthanized by carbon dioxide inhalation. Abolition of the full body tonic extensor component of the seizure was taken as the endpoint of the test. Absence of this component indicated that the test compound had the ability to prevent the spread of seizure discharge through neural tissue. The ED50 value of the test compound (calculated when appropriate) was the calculated dose required to block the hind limb tonic-extensor component of the MES-induced seizure in 50% of the rodents tested. A probit analysis was used to calculate the ED50 and 95% fiducial limits (FL). Representative compounds of the present invention were tested according to the procedure described above, with results as listed in Table 4 below. Results are listed as number of mice with full body tonic extension prevented / total number of mice tested @ a given time (at a given test compound dosage level). Table 4: MES Mouse Activity ID No. MES Activity 1 2/4@1h(300mg/kg) 2 4/4@2h(100mg/kg) 3 2/3@1h(300mg/kg) 4 5/5@1h(300mg/kg) 5 1/5 @ 2h (300 mg/kg) 6 4/5 @ 0.5h (300 mg/kg) 7 3/3 @ 0.5h (300 mg/kg) 8 3/5 @3h (100 mg/kg) 9 1/5 @1h (300 mg/kg) 10 1/5 @ 1h (100 mg/kg) 11 4/5 @1h (100 mg/kg) 12 3/5 @4h (100 mg/kg) 52 WO 2006/007435 PCT/US2005/021513 13 2/[email protected](10mg/kg) 14 3/5@4h(100mg/kg) 15 Inactive @ 100 mg/kg 16 5/5 @ 0.5h (300 mg/kg) 17 4/5 @0.5h (100 mg/kg) 18 Inactive @ 100 mg/kg 19 5/5 @ 0.5h (300 mg/kg) 20 1/5 @2h (100 mg/kg) 21 5/5 @2h (100 mg/kg) 22 1/5 @4h (100 mg/kg) 23 Inactive @ 100 and 300 mg/kg 24 5/5 @ 4h (300 mg/kg) 25 5/5 @4h (100 mg/kg) 26 Inactive @ 100 and 300 mg/kg 27 5/5 @4h (100 mg/kg) 28 4/5 @4h (100 mg/kg) 29 3/5 @4h (100 mg/kg) 30 1/5 @0.5h (100 mg/kg) 31 3/5 @0.5h (100 mg/kg) 32 Inactive @ 100 and 300 mg/kg 33 1/3 @ 2h (300 mg/kg) 34 Inactive @ 100 and 300 mg/kg 35 Inactive at 100 mg/kg 36 Inactive @ 100 and 300 mg/kg Example 17 As a specific embodiment of an oral composition, 100 mg of the Compound #8 prepared as in Example 7 is formulated with sufficient finely divided lactose to provide a total amount of 580 to 590 mg to fill a size O hard gel capsule. 53 WO 2006/007435 PCT/US2005/021513 While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, it will be understood that the practice of the invention encompasses all of the usual variations, adaptations and/or modifications as come within the scope of the following claims and their equivalents. 54 WO 2006/007435 PCT/US2005/021513 We Claim: 1. A compound of formula (II) wherein R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl; 55 R4 is selected from the group consisting of hydrogen and lower alkyl; a is an integer from 1 to 2; WO 2006/007435 PCT/US2005/021513 each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro; 2. A compound as in Claim 1 wherein R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl; R4 is selected from the group consisting of hydrogen and lower alkyl; 56 a is an integer from 1 to 2; WO 2006/007435 PCT/US2005/021513 wherein b is an integer from 0 to 2; and wherein c is an integer from 0 to 1; each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro; 3. A compound as in Claim 2 wherein R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl; R4 is selected from the group consisting of hydrogen and lower alkyl; a is an integer from 1 to 2; 57 WO 2006/007435 PCT/US2005/021513 wherein b is an integer from 0 to 2; and wherein c is 0; each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro; 4. A compound as in Claim 3 wherein R1 and R2 are each independently selected from the group consisting R4 is selected from the group consisting of hydrogen and methyl; 58 a is an integer from 1 to 2; WO 2006/007435 PCT/US2005/021513 benzo[1,4]dioxepinyl), 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(chromanyl), 2-(5-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-benzo[1,3]dioxolyl), 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyl), 2-(5-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl),2-(8-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) and 2-(4-methyl-benzo[1,3]dioxolyl); or a pharmaceutically acceptable salt thereof. 5. A compound as in Claim 4 wherein R1 and R2 are each independently selected from the group consisting of hydrogen and methyl; R4 is selected from the group consisting of hydrogen and methyl; a is an integer from 1 to 2; dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyI), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl) and 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl); or a pharmaceutically acceptable salt thereof. 59 WO 2006/007435 PCT/US2005/021513 6. A compound selected from the group consisting of A/-[(6-chioro-2,3-° dihydro-1,4-benzodioxin-2-yl)methyl]-sulfamide and pharmaceutically acceptable salts thereof. 7. A compound selected from the group consisting of and pharmaceutically acceptable salts thereof. 8. A compound of the formula (III) or a pharmaceutically acceptable salt thereof. 9. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound of Claim 1. 10. A pharmaceutical composition made by mixing a compound of Claim 1 and a pharmaceutically acceptable carrier. 11. A process for making a pharmaceutical composition comprising mixing a compound of Claim 1 and a pharmaceutically acceptable carrier. 12. A method of treating epilepsy or a related disorder, in a subject in need thereof comprising administering to the subject a therapeutically effective amount of the compound of Claim 1. 60 WO 2006/007435 PCT/US2005/021513 61 13. A method of treating epilepsy, in a subject in need thereof comprising administering to the subject a therapeutically effective amount of the compound of Claim 1. 14. A method as in Claim 12, wherein the disorder is selected from essential tremor or restless limb syndrome. 15. The use of compound as in Claim 1 in the preparation of a medicament for treating epilepsy or a related disorder, in a subject in need thereof. The present invention is directed to novel sulfarnide and sulfamate derivatives, pharmaceutical compositions containing them and their use in the treatment of epilepsy and related disorders.

Full Text

WO 2006/007435 PCT/US2005/021513
SULFAMATE AND SULFAMIDE DERIVATIVES FOR THE TREATMENT OF EPILEPSY AND RELATED DI BORDERS
CROSS REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U. S. Provisional Application 60/580,178, filed on June 16, 2004, which is incorporated by reference herein in its entirety.
FIELD OF THE INVENTION
The present invention is directed to novel sulfamate and sulfamide derivatives, pharmaceutical compositions containing them and their use in the treatment of epilepsy and related disorders.
BACKGROUND OF THE INVENTION
Epilepsy describes a condition in which a person has recurrent seizures due to a chronic, underlying process. Epilepsy refers to a clinical phenomenon rather than a single disease entity, since there are many forms and causes of epilepsy. Using a definition of epilepsy as two or more unprovoked seizures, the incidence of epilepsy is estimated at approximately 0.3 to 0.5 percent in different populations throughout the world, with the prevalence of epilepsy estimated at 5 to 10 people per 1000.
An essential step in the evaluation and management of a patient with a seizure is to determine the type of seizure that has occurred. The main characteristic that distinguishes the different categories of seizures is whether the seizure activity is partial (synonymous with focal) or generalized.
Partial seizures are those in which the seizure activity is restricted to discrete areas of the cerebral cortex. If consciousness is fully preserved during the seizure, the clinical manifestations are considered relatively simple and the seizure is termed a simple-partial seizure. If consciousness is impaired, the
1

WO 2006/007435 PCT/US2005/021513
seizure is termed a complex-partial seizure. An important additional subgroup comprises those seizures that begin as partial seizures and then spread diffusely throughout the cortex, which are known as partial seizures with secondary generalization.
Generalized seizures involve diffuse regions of the brain simultaneously in a bilaterally symmetric fashion. Absence or petit mal seizures are characterized by sudden, brief lapses of consciousness without loss of postural control. Atypical absence seizures typically include a longer duration in the lapse of consciousness, less abrupt onset and cessation, and more obvious motor signs that may include focal or lateralizing features. Generalized Tonic-clonic or grand mal seizures, the main type of generalized seizures, are characterized by abrupt onset, without warning. The initial phase of the seizure is usually tonic contraction of muscles, impaired respiration, a marked enhancement of sympathetic tone leading to increased heart rate, blood pressure, and pupillary size. After 10-20 s, the tonic phase of the seizure typically evolves into the clonic phase, produced by the superimposition of periods of muscle relaxation on the tonic muscle contraction. The periods of relaxation progressively increase until the end of the ictal phase, which usually lasts no more than 1 min. The postictal phase is characterized by unresponsiveness, muscular flaccidity, and excessive salivation that can cause stridorous breathing and partial airway obstruction. Atonic seizures are characterized by sudden loss of postural muscle tone lasting 1-2 s. Consciousness is briefly impaired, but there is usually no postictal confusion. Myoclonic seizures are characterized by a sudden and brief muscle contraction that may involve one part of the body or the entire body. (www.harrisonsonline.com, March 29, 2001)
Carbonic anhydrase inhibitors (CAIs) have been widely used in medicine, mainly as antiglaucoma and antisecretory drugs or diuretic agents, and are valuable compounds. However, systemic antiglaucoma agents (such as acetazolamide) possess potentially unwanted side-effects including paresthesias,
2

WO 2006/007435 PCT/US2005/021513
nephrolithiasis and weight loss. Topiramate is a well known anticonvulsant drug that possesses single digit micromolar carbonic anhydrase inhibition, which is suspected as the cause of paresthesias noted by some patients taking topiramate.
There remains a need to provide an effective treatment for epilepsy and related disorders, and preferably treatment which does not have the associated side-effects attributable to carbonic anhydrase inhibition.
SUMMARY OF THE INVENTION
The present invention is directed to novel sulfamate and sulfamide derivatives, pharmaceutical compositions containing them and their use in the treatment of epilepsy and related disorders. More particularly, the present invention is direction to compounds of formula (I) and compounds of formula (II) as hereinafter defined.
i
The present invention is directed to novel sulfamate derivatives, compounds of formula (I)

wherein
R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl;
3
a is an integer from 1 to 2;

WO 2006/007435 PCT/US2005/021513

wherein b is an integer from 0 to 4; and wherein c is an integer from 0 to 2;
4
each R3 is independently selected form the group consisting of halogen, lower alkyl, hydroxy substituted lower alkyl, -O-(lowerialkyl), -S-(lower alkyl), nitro, cyano, amino, lower alkylamino, di(lower alkyl)amino and -C(0)0-(lower alkyl);

WO 2006/007435 PCT/US2005/021513
The present invention is further directed to novel sulfamide derivatives, compounds of formula (li)

wherein
R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl;
5
R4 is selected from the group consisting of hydrogen and lower alkyl; a is an integer from 1 to 2;

WO 2006/007435 PCT/US2005/021513
each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro;

Illustrative of the invention is a pharmaceutical composition comprising a pharmaceutically acceptable carrier and any of the compounds described above. An illustration of the invention is a pharmaceutical composition made by mixing any of the compounds described above and a pharmaceutically acceptable carrier. Illustrating the invention is a process for making a pharmaceutical composition comprising mixing any of the compounds described above and a pharmaceutically acceptable carrier.
Exemplifying the invention is a method of treating epilepsy and related disorders in a subject in need thereof comprising administering to the subject a therapeutically effective amount of any of the compounds or pharmaceutical compositions described above.
6

WO 2006/007435 PCT/US2005/021513
Another example of the invention is the use of any of the compounds described herein in the preparation of a medicament for treating epilepsy or a related disorder, in a subject in need thereof.
DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to compounds of formula (I) and compounds of formula (II)

As used herein, unless otherwise noted, "halogen" shall mean chlorine, bromine, fluorine and iodine.
As used herein, unless otherwise noted, the term "alkyl" whether used alone or as part of a substituent group, includes straight and branched chains. For example, alkyl radicals include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, t-butyl, pentyl and the like. Unless otherwise noted, "lower" when used with alkyl means a carbon chain composition of 1-4 carbon atoms.
7

WO 2006/007435 PCT/US2005/021513
As used herein, unless otherwise noted, "alkoxy" shall denote an oxygen ether radical of the above described straight or branched chain alkyl groups. For example, methoxy, ethoxy, n-propoxy, sec-butoxy, t-butoxy, n-hexyloxy and the like.
As used herein, the notation "*" shall denote the presence of a stereogenic center.
When a particular group is "substituted" (e.g., alkyl, aryl, etc.), that group may have one or more substituents, preferably from one to five substituents, more preferably from one to three substituents, most preferably from one to two substituents, independently selected from the list of substituents.
With reference to substituents, the term "independently" means that when more than one of such substituents is possible, such substituents may be the same or different from each other.
Under standard nomenclature used throughout this disclosure, the terminal portion of the designated side chain is described first, followed by the adjacent functionality toward the point of attachment. Thus, for example, a "phenyl-alkyl-amino-carbonyl-alkyl" substituent refers to a group of the formula

Abbreviations used in the specification, particularly the Schemes and Examples, are as follows:
DCC = Dicyclohexyl Carbodiimide
DCE = Dichloroethane
OCM = Dichloromethane
8

WO 2006/007435

PCT/US2005/021513

DIPEAorDlEA = Diisopropylethylamine
DMF = N,N-Dimethylformamide
DMSO = Dimethylsulfoxide
EDC = Ethylcarbodiimide
Et3NorTEA = Triethylamine
Et2O = Diethyl ether
EA or EtOAc = Ethyl acetate
EtOH = Ethanol
IPA = 2-propanol
Hept = Heptane
HOBT = 1-Hydroxybenzotriazole
HPLC = High Pressure Liquid Chromatography
LAH = Lithium Aluminum Hydride
M or MeOH = Methanol
NMR = Nuclear Magnetic Resonance
Pd-C = Palladium on Carbon Catalyst
RP HPLC = Reverse Phase High Pressure Liquid
Chromatography
RTorrt = Room temperature
TEA = Triethylamine
TFA = Trifluoroacetic Acid
THF = Tetrahydrofuran
TLC = Thin Layer Chromatography
As used herein, unless otherwise noted, the terms "epilepsy and related disorders" or "epilepsy or related disorder" shall mean any disorder in which a subject (preferably a human adult, child or infant) experiences one or more seizures and / or tremors. Suitable examples include, but are not limited to, epilepsy (including, but not limited to, localization-related epilepsies, generalized epilepsies, epilepsies with both generalized and local seizures, and the like), seizures as a complication of a disease or condition (such as seizures associated with
9

WO 2006/007435 PCT/US2005/021513
encephalopathy, phenylketonuria, juvenile Gaucher's disease, Lundborg's progressive myoclonic epilepsy, stroke, head trauma, stress, hormonal changes, drug use or withdrawal, alcohol use or withdrawal, sleep deprivation, and the like), essential tremor, restless limb syndrome, and the like. Preferably, the disorder is selected from epilepsy (regardless of type, underlying cause or origin), essential tremor or restless limb syndrome, more preferably, the disorder is epilepsy (regardless of type, underlying cause or origin) or essential tremor.
The term "subject" as used herein, refers to an animal, preferably a mammal, most preferably a human, who is or has been the object of treatment, observation or experiment.
The term "therapeutically effective amount" as used herein, means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated.
As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combinations of the specified ingredients in the specified amounts.
Where the compounds according to this invention have at least one chiral center, they may accordingly exist as enantiomers. Where the compounds possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention. Furthermore, some of the crystalline forms for the compounds may exist as polymorphs and as such are intended to be included in the present invention. In addition, some of the compounds may form solvates with water (i.e., hydrates) or common organic
10

WO 2006/007435 PCT/US2005/021513
solvents, and such solvates are also intended to be encompassed within the scope of this invention.
Where the processes for the preparation of the compounds according to the invention give rise to mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. The compounds may be prepared in racemicform, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution. The compounds may, for example, be resolved into their component enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (-)-di-p-toluoyl-D-tartaric acid and/or (+)-di-p-toluoyl-L-tartaric acid followed by fractional crystallization and regeneration of the free base. The compounds may also be resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column.
During any of the processes for preparation of the compounds of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups may be removed at a convenient subsequent stage using methods known from the art.
The present invention includes within its scope prodrugs of the compounds of this invention. In general, such prodrugs will be functional derivatives of the compounds which are readily convertible in vivo into the required compound. Thus, in the methods of treatment of the present invention, the term "administering" shall encompass the treatment of the various disorders
11

WO 2006/007435 PCT/US2005/021513
described with the compound specifically disclosed or with a compound which may not be specifically disclosed, but which converts to the specified compound in vivo after administration to the patient. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in Design of Prodrugs. ed. H. Bundgaard, Elsevier, 1985.
The present invention provides pharmaceutical compositions comprising a compound of formula (I), a compound of formula (II) and / or a compound of formula (III) in association with a pharmaceutically acceptable carrier. Preferably these compositions are in unit dosage forms such as tablets, pills, capsules, powders, granules, sterile parenteral solutions or suspensions, metered aerosol or liquid sprays, drops, ampoules, autoinjector devices or suppositories; for oral parenteral, intranasal, sublingual or rectal administration, or for administration by inhalation or insufflation. Alternatively, the composition may be presented in a form suitable for once-weekly or once-monthly administration; for example, an insoluble salt of the active compound, such as the decanoate salt, may be adapted to provide a depot preparation for intramuscular injection. For preparing solid compositions such as tablets, the principal active ingredient is mixed with a pharmaceutical carrier, e.g. conventional tableting ingredients such as corn starch, lactose, sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalcium phosphate or gums, and other pharmaceutical diluents, e.g. water, to form a solid preformulation composition containing a homogeneous mixture of the principle ingredient. When referring to these preformulation compositions as homogeneous, it is meant that the active ingredient is dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective dosage forms such as tablets, pills and capsules. This solid preformulation composition is then subdivided into unit dosage forms of the type described above containing from about 1 to about 1000 mg of the active ingredient of the present invention. The tablets or pills of the novel composition can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action. For example, the tablet or pill can comprise an
12

WO 2006/007435 PCT/US2005/021513
inner dosage and an outer dosage component, the latter being in the form of an envelope over the former. The two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permits the inner component to pass intact into the duodenum or to be delayed in release. A variety of material can be used for such enteric layers or coatings, such materials including a number of polymeric acids with such materials as shellac, cetyl alcohol and cellulose acetate.
The liquid forms in which the novel compositions of the present invention may be incorporated for administration orally or by injection include, aqueous solutions, suitably flavoured syrups, aqueous or oil suspensions, and flavoured emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil or peanut oil, as well as elixirs and similar pharmaceutical vehicles. Suitable dispersing or suspending agents for aqueous suspensions, include synthetic and natural gums such as tragacanth, acacia, alginate, dextran, sodium carboxymethylcellulose, methylcellulose, polyvinyl-pyrrolidone or gelatin.
To prepare the pharmaceutical compositions of this invention, a compound of formula (I), a compound of formula (II) and / or a compound of formula (III) is intimately admixed with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques, which carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g., i.v. sterile injectable formulations will be prepared using appropriate solubilizing agents. A unit dose would contain about 10 to about 300 mg of the active ingredient. The tablets contain some or all of the following inactive ingredients: lactose hydrous, pregelatinized starch, microcrystalline cellulose, sodium starch glycolate, magnesium stearate, purified water, carnauba wax, hydroxypropyl methylcellulose, titanium dioxide, polyethylene glycol, synthetic iron oxide, and polysorbate 80. One skilled in the art will recognize that oral tablets containing a compound of formula (I), a compound of formula (II) and
13

WO 2006/007435 PCT/US2005/021513
/ or a compound of formula (III) may be similarly prepared and may contain similar inactive ingredients.
One skilled in the art will recognize that pharmaceutical compositions comprising more than one active ingredient may be similarly prepared according to known methods.
In an embodiment of the present invention R1 is selected from the group consisting of hydrogen and methyl. In another embodiment of the present invention R2 is selected from the group consisting of hydrogen and methyl. In yet another embodiment of the present invention R1 and R2 are each hydrogen or R1 and R2 are each methyl.
In an embodiment of the present invention -(CH2)a- is selected from the group consisting of-CH2- and -CH2-CH2-. In another embodiment of the present invention -(CH2)a- is -CH2-.
In an embodiment of the present R4 is selected from the group consisting of hydrogen and methyl, preferably, R4 is hydrogen.
In an embodiment of the present invention a is 1.
In an embodiment of the present invention b is an integer from 0 to 2. In another embodiment of the present invention c is an integer from 0 to 2. In another embodiment of the present invention b is an integer from 0 to 1. In another embodiment of the present invention c is an integer from 0 to 1. In yet another embodiment of the present invention the sum of b and c is an integer form 0 to 2, preferably an integer form 0 to 1. In yet another embodiment of the present invention b is an integer from 0 to 2 and c is 0.
14

WO 2006/007435 PCT/US200S/021513

selected from the group consisting of 2-(chromanyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(benzo[1,3]dioxolyl), 2-(5-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxi'nyl), 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) and 2-(7-chloro-benzo[1,3]dioxolyl). In another embodiment of the present invention,
15

16
WO 2006/007435 PCT/US2005/021513

WO 2006/007435 PCT/US2005/021513

group consisting of 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(benzo[1,3]dioxolyl), 3-(3,4-dihydro-benzo[1,4]dioxepinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(chromanyl), 2-(5-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-benzo[1,3]dioxolyl), 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyl), 2-(5-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(8-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) and 2-(4-methyl-benzo[1,3]dioxolyl).

the group consisting 2-(benzo[1,3]dioxolyl), 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl) and 2-(6,7-dichloro-2,3-dihydro-benzot1,4]dioxinyl).

group consisting of 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxiny!) and 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl).
In an embodiment of the present invention R3 is selected from the group consisting of halogen, lower alkyl, hydroxy substituted lower alkyl, -O-(lower alkyl), nitro, cyano, amino, lower alkylamino and di(lower alkyl)amino. In another embodiment of the present invention R3 is selected from the group consisting of halogen and nitro. In another embodiment of the present invention R3 is selected from the group consisting of chloro and nitro.
17

WO 2006/007435 PCT/US2005/021513
In an embodiment of the present invention R5 is selected from the group consisting of (II) halogen and lower alkyl. In another embodiment of the present invention R5 is selected from chloro, fluoro, bromo and methyl.

selected from the group consisting of halogen, nitro, cyano, amino, lower alkyl, lower alkoxy and -C(O)O-(lower alkyl). In another embodiment of the present

In an embodiment of the present invention, in the compound of formula (I),
In an embodiment of the present invention, the stereo-center on the compound of formula (I) is in the S-configuration. In another embodiment of the present invention, the stereo-center on the compound of formula (I) is in the R-configuration.
In an embodiment of the present invention, the stereo-center on the compound of formula (II) is in the S-configuration. In another embodiment of the present invention, the stereo-center on the compound of formula (II) is in the R-configuration.
In an embodiment of the present invention the compound of formula (I) is present as an enantiomerically enriched mixture, wherein the % enantiomeric enrichment (%ee) is greater than about 75%, preferably greater than about 90%,
18

WO2006/007435 PCT/US2005/021513
more preferably greater than about 95%, most preferably greater than about 98%.
In an embodiment of the present invention the compound of formula (II) is present as an enantiomerically enriched mixture, wherein the % enantiomeric enrichment (%ee) is greater than about 75%, preferably greater than about 90%, more preferably greater than about 95%, most preferably greater than about 98%.
In an embodiment of the present invention are compounds of formula (I) wherein the MES activity at 100 mg/kg is greater than or equal to 3/5 mice. In another embodiment of the present invention are compounds of formula (II) wherein the MES activity at 100 mg/kg is greater than or equal to 3/5 mice.
Representative compounds of the present invention, are as listed in Tables 1 and 2 below. Additional compounds of the present invention are as listed in Table 3. In Tables 1, 2 and 3 below, the column headed "stereo" defines the stereo-configuration at the carbon atom of the heterocycle attached at the starred bond. Where no designation is listed, the compound was prepared as a mixture of stereo-configurations. Where an "R" or "S" designation is listed, the stereo-configuration was based on the enantiomerically enriched starting material.
19
Table 1: Representative Compounds of Formula l\)

20
WO 2006/007435 PCT/US2005/021513

WO 2006/007435

PCT/US2005/021513

;5 2-(2,3-dihydro-benzo[1,4]dioxinyl) R CH2 NH H H
6 2-(2,3-dihydro-benzo[1,4]dioxinyl) CH2 NH methyl methyl
7 2-(2,3-dihydro-benzo[1,4]dioxinyl) CH2 N(CH3) H H
8 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
9 2-(6-fluoro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
10 2-(chromanyl) CH2 NH H H
13 2-(5-fluoro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
14 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
15 2-(6-chloro-benzo[1,3]dioxolyl) CH2 NH H H
16 2-(2,3-dihydro-benzo[1,4]dioxinyl) CH2CH2 NH H H
18 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
19 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyi) S CH2 NH H H
20 2-(5-ch!oro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
22 2-(8-methoxy-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
24 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
21

22
WO 2006/007435 PCT/US2005/021513

29 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
30 2-(8-chloro-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
33 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) S CH2 NH H H
35 2-(4-methyl-benzo[1,3]dioxolyl) CH2 NH H H
Table 3 Additional Compounds of the Present Invention

WO 2006/007435 PCT/US2005/021513

36 2-(7-amino-2,3-dihydro-benzo[1,4]dioxinyl) S CH2 NH H H
Compounds of formula (I) may be prepared according to the process outlined in Scheme 1.

Scheme 1
Accordingly, a suitably substituted compound of formula (V), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (VI), a known compound or compound prepared by known methods, in the presence of a base such as NaH, TEA, DIPEA, pyridine, and the like, in an organic solvent such as DMF, DMSO, and the like, to yield the corresponding compound of formula (I).
23
Compounds of formula (II) may be prepared according to the process outlined in Scheme 2.

WO 2006/007435 PCT/US2005/021513
Accordingly, a suitably substituted compound of formula (VII), a known compound or compound prepared by known methods, is reacted with sulfamide, a known compound, preferably wherein the sulfamide is present in an amount in the range of about 2 to about 5 equivalents, in an organic solvent such as THF, dioxane, and the like, preferably at an elevated temperature in the range of about 50°C to about 100°C, more preferably at about reflux temperature, to yield the corresponding compound of formula (Ma).
Alternatively, a suitably substituted compound of formula (VII), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (VIII), a known compound or compound prepared by known methods, in the presence of a base such as TEA, DIPEA, pyridine, and the like, in an organic solvent such as DMF, DMSO, and the like, to yield the corresponding compound of formula (II).

Scheme 3
Accordingly, a suitably substituted compound of formula (X), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (XI), a known compound or compound
24

WO 2006/007435 PCT/US2005/021513
prepared by known methods, in the presence of a base such as sodium methoxide, sodium ethoxide, sodium t-butoxide, potassium methoxide, potassium t-butoxide, and the like, in an organic solvent such as methanol, ethanol, IPA, and the like, preferably at an elevated temperature in the range of about 50°C to about 100°C, more preferably at about reflux temperature, to yield the corresponding compound of formula (XII).
The compound of formula (XII) is reacted with a suitably selected reducing agent, such as LAH, and the like, in an organic solvent such as THF, diethyl ether, and the like, to yield the corresponding compound of formula (Va).

Scheme 4
Accordingly, a suitably substituted compound of formula (XIII), a known compound or compound prepared by known method (for example as described in Scheme 3 above) is reacted with NH4OH, a known compound, optionally in an organic solvent such as acetonitrile, and the like, to yield the corresponding compound of formula (XIV).
The compound of formula (XIV) is reacted with a suitably selected reducing agent, such as LAH, and the like, and the like, in an organic solvent
25

WO 2006/007435 PCT/US2005/021513
such as THF, diethyl ether, and the like, to yield the corresponding compound of formula (Vila).

Scheme 5
Accordingly, a suitably substituted compound of formula (XV), a known compound or compound prepared by known methods is reacted with 3-chloro-2-chloromethyl-propene, a known compound, in the presence of a base such as potassium carbonate, sodium carbonate, sodium bicarbonate, TEA, DIPEA, and the like, in an organic solvent such as acetonitrile, THF, dioxane, and the like, preferably at an elevated temperature in the range of about 50°C to about 100°C, more preferably, at about reflux temperature, to yield the corresponding compound of formula (XVI).
26

WO 2006/007435 PCT/US2005/021513
The compound of formula (XVI) is reacted with borane, in an organic solvent such as THF, dioxane, and the like, to yield the corresponding compound of formula (XVII), which is preferably not isolated.
The compound of formula (XVII) is reacted with aminosulfonic acid, preferably at an elevated temperature in the range of from about 50°C to about 100°, more preferably, at about reflux temperature, to yield the corresponding compound of formula (Vllb).

Scheme 6
Accordingly, a suitably substituted compound of formula (XVIII), a compound prepared as in Scheme 5 above, is reacted with a peroxide, such as hydrogen peroxide, and the like, in the presence of a base such as NaOH, KOH, and the like, in an organic solvent such as chloroform, DCE, DCM, and the like, to yield the corresponding compound of formula (Vb).

WO 2006/007435 PCT/US2005/021513

Scheme 7
28
Accordingly, a suitably substituted compound of formula (XIX), a known compound or compound prepared by known methods, is reacted with a suitably selected reducing agent, such as LAH, and the like, in an organic solvent such as THF, diethyl ether, and the like to yield the corresponding compound of formula (Vc).

WO 2006/007435 PCT/US2005/02I513

Scheme 8
Accordingly, a suitably substituted compound of formula (XX), a known compound or compound prepared by known methods, is reacted with NH4OH, in the presence of a coupling agent such as DCC, and the like, optionally in an organic solvent such as acetonitrile, and the like, to yield the corresponding compound of formula (XXI).
29
The compound of formula (XXI) is reacted with a suitably selected reducing agent, such as LAH, and the like, in an organic solvent such as THF, diethyl ether, and the like, to yield the corresponding compound of formula (Vile).

WO 2006/007435 PCT/US2005/0215I3
Accordingly, a suitably substituted compound of formula (XXII), a known compound or compound prepared by known methods, is reacted with a suitably substituted compound of formula (XXIII), a known compound or compound prepared by known methods, in the presence of a base such as K2CO3, Na2CO3, NaHCC>3, and the like, in an organic solvent such as DMF, DMSO, acetonitrile, and the like, preferably, at an elevated temperature in the range of form about 50°C to about 100°C, more preferably, at an elevated temperature in the range of from about 50°C to about 75°C, to yield the corresponding compound of formula (Vd).

Scheme 10
Accordingly, a suitably substituted compound of formula (XXIV) wherein J1 is a suitable leaving group such as Br, Cl, I, tosyl, mesyl, triflyl, and the like, a known compound or compound prepared by known methods (for example, by activating the corresponding compound wherein J1 is OH), is reacted with a cyanide such as potassium cyanide, sodium cyanide, and the like, in an organic solvent such as
30

WO 2006/007435 PCT/US2005/021513
DMSO, DMF, THF, and the like, to yield the corresponding compound of formula (XXV).
The compound of formula (XXV) is reduced according to known methods, for example by reacting with a suitable reducing agent such as LAH, borane, and the like, to yield the corresponding compound of formula (Vile).

Scheme 11
Accordingly, a suitably substituted compound of formula (XXVI), a known compound or compound prepared by known methods (for example according to the process outlined in Scheme 9 above) is activated, according to known
31

WO 2006/007435 PCT/US2005/021513
method, to yield the corresponding compound of formula (XXVII), wherein J2 is a suitable leaving group, such tosylate, Cl, Br, I, mesylate, triflate, and the like.
The compound of formula (XXVII) is reacted with a phthalimide salt such as potassium phthlimide, sodium phthalimide, and the like, in an organic solvent such as DMF, DMSO, acetonitrile, and the like, preferably, at an elevated temperature in the range of from 50°C to about 200°C, more preferably, at about reflux temperature, to yield the corresponding compound of formula (XXVIII).
The compound of formula (XXVI) is reacted with N2H4, a known compound, in an organic solvent such as ethanol, methanol, and the like, preferably, at an elevated temperature in the range of from about 50°C to about 100°C, more preferably, at about reflux temperature, and the like, to yield the corresponding compound of formula (Vlld).

Scheme 12
Accordingly, a suitably substituted compound of formula (XXVII) wherein J2 is CN, a known compound or compound prepared by known methods, is hydrolyzed
32

WO 2006/007435 PCT/US2005/021513
according to known methods, for example by reacting with a suitable acid or base, to yield the corresponding compound of formula (XXIX).
The compound of formula (XXIX) is reduced according to known methods, for example by reacting with a suitable reducing agent such as LAH, and the like, to yield the corresponding compound of formula (Ve).
One skilled in the art will recognize that compounds of formula (V) and (VII)

may be similarly prepared according to the processes outlined in Schemes 3 through 12 above, by selecting and substituting the corresponding naphthyl-fused compounds for the benzo-fused starting materials (e.g. the compounds of formula (X), (XIII), (XV), (XVIII), (XIX), (XX), (XXII), (XXIV), etc.).
One skilled in the art will further recognize that wherein a single enantiomer (or a mixture of enantiomers wherein one enantiomer is enriched) of a compound of
33

WO 2006/007435 PCT/US2005/021513
formula (V) or a compound of formula (VII) is desired, the above processes as described in Schemes 1 through 12 may be applied by substituting the corresponding single enantiomer (or mixture of enantiomers wherein one enantiomer is enriched) for the appropriate starting material.
The following Examples are set forth to aid in the understanding of the invention, and are not intended and should not be construed to limit in any way the invention set forth in the claims which follow thereafter.
Example 1
((3,4-Dihvdro-2H-benzorbin,41dioxepin-3-vl)methvl)sulfamide
(Compound #3)

Catechol (5.09 g, 46.2 mmol) and potassium carbonate were combined in acetonitrile and heated to reflux for one hour. 2-Chloromethyl-3-chloro-1-propene (5.78 g, 46.2 mmol) was added and the reaction was continued at reflux for 24 hours. The solution was cooled to room temperature and filtered. The filtrate was evaporated and the residue was diluted with water and extracted with diethyl ether (3 x). The combined organic solution was dried over MgSO4 and concentrated. Chromatography (2% ethyl ether in hexane) yielded 3-methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine as a colorless oil.
MS (ESI): 163.2 (M+H+)
1H NMR (300 MHz, CDCI3), 5: 6.94 (m, 4H), 5.07 (s, 2H), 4.76 (s, 4H).
3-Methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine (5.00 g, 30.8 mmol) was dissolved in dryTHF (100 mL). Borane-THF (1.0 M in THF, 10.3 mL) was added at 0°C. The reaction was stirred at RT for 5 hours. Aminosulfonic acid (6.97 g, 61.6 mmol) was added. The reaction was heated to reflux overnight. The reaction was cooled to room temperature and aqueous sodium hydroxide
34

WO 2006/007435 PCT/US2005/021513
(3.0 M, 100 mL) was added. The solution was extracted with ethyl acetate (3 x 100 mL). The combined organic solution was dried over MgSO,*. The solution was concentrated under vacuum and purified by chromatography (2% to 8% methanol in dichloromethane) to yield ((3,4-dihydro-2H-benzo[b][1,4]dioxepin-3-yl)methyl)amine as a colorless oil.
MS (ESI): 180.1 (M+H+)
1H NMR (300 MHz, DMSO), 5: 6.92 (m, 4H), 4.21 (m, 2H), 4.07 (m, 2H), 3.33 (broad, 2H), 3.16 (d, J = 4 Hz, 1H), 2.72 (d, J = 4 Hz, 1H), 2.30 (m, 1H).
((3,4-Dihydro-2H-benzo[b][1,4]dioxepin-3-yl)methyl)amine (2.90 g, 16.2 mmol) and sulfamide (3.11 g, 32.4 mmol) were combined in dry dioxane (60 ml) and heated to reflux overnight. Chloroform was added and the precipitate was removed by filtration. The filtrate was concentrated under vacuum and purified by chromatography (2% to 8% acetone in dichloromethane) to yield the title compound as an off-white solid.
258.8 (M+H+)
1H NMR (300 MHz, DMSO), 8: 6.92 (m, 4H), 6.71 (broad, 1H), 6.59 (broad, 2H), 4.19 (m, 2H), 4.04 (m, 2H), 3.00 (m, 2H), 2.39 (m, 1H).
EXAMPLE 2 N-(2,3-Dihvdro-benzon.41dioxin-2-vlmethvl)-sulfamide (Compound #1)

Racemic 2,3-dihydro-1,4-benzdioxin-2-ylmethylamine (4.4 g, 26 mmol) and sulfamide (5.1 g, 53 mmol) were combined in 1,4 dioxane (100 mL) and refluxed for 2 h. The reaction was cooled to room temperature and a small amount of solid was filtered and discarded. The filtrate was evaporated in vacuo and the residue was purified using flash column chromatography (DCM:Methanol
35

WO 2006/007435 PCT/US2005/021513
-10:1) to yield a white solid. The solid was recrystallized from DCM to yield the title compound as a white solid.
mp: 97.5 - 98.5°C
Anal Calc: C, 44.25; H, 4.95; N, 11.47; S, 13.13
Anal Found: C, 44.28; H, 4.66; N, 11.21; S, 13.15
H1 NMR (DMSO d6) 8 6.85 (m, 4H), 6.68 (bd s, 3H, NH), 4.28 (m, 2H), 3.97 (dd, J = 6.9, 11.4 Hz, 1H), 3.20 (m, 1H), 3.10 (m, 1H).
EXAMPLE 3 (BenzoH,31dioxol-2-vlmethvl)sulfamide (Compound #2)

Catechol (10.26 g, 93.2 mmol), sodium methoxide (25% by weight in methanol, 40.3 g, 186 mmol), and methyl dichloroacetate (13.3 g, 93.2 mmol) were combined in dry methanol (100 ml_). The solution was heated to reflux overnight. The reaction was cooled to room temperature, acidified by addition of concentrated hydrochloric acid and then reduced in volume under vacuum to about 50 mL. Water was added and the mixture was extracted with diethyl ether (3 x 100 mL). The combined organic solution was dried with MgSO4, concentrated to a brown solid, and chromatographed (2% ethyl acetate in hexane) to yield benzo[1,3]dioxole-2-carboxylic acid methyl ester as a colorless oil.
MS (ESI): 195.10 (M+H+).
1H NMR (300 MHz, CDCI3), 5: 6.89 (broad, 4H), 6.29 (s, 1H), 4.34 (q, J=7 Hz, 2H), 1.33(t, J=7Hz, 3H).
To benzo[1,3]dioxole-2-carboxylic acid methyl ester (7.21 g, 40.0 mmol) was added ammonium hydroxide (29% in water, 10 mL) and enough acetonitrile to make the mixture homogeneous (~5 mL). The solution was stirred for two hours at room temperature and then distilled water was added.
36

WO 2006/007435 PCT/US2005/021513
Benzo[1,3]dioxole-2-carboxylic acid amide precipitated as a white solid and was collected by filtration and used without further purification.
MS (ESI): 160.00 (M+H+)
1H NMR (300 MHz, DMSO), S: 7.99 (s, broad, 1H), 7.72 (s, broad, 1H), 6.94 (m, 2H) 6.86 (m, 2H), 6.30 (s, 1H).
Benzo[1,3]dioxole-2-carboxylic acid amide (5.44 g, 32.9 mmol) was dissolved in tetrahydrofuran (THF, 100 mL). Lithium aluminum hydride (LAH, 1M in THF, 39.5 mL, 39.5 mmol) was added slowly to the solution at room temperature. The reaction was stirred at room temperature for 24 hours. Distilled water was added to destroy the excess LAH. Aqueous sodium hydroxide (3.0 M, 100 mL) was added and the solution was extracted with ethyl acetate (3 x 100 mL). The combined organic solution was washed with water and dried over MgSO4. The solvent was evaporated to yield C-benzo[1,3]dioxol-2-yl-methylamine as a colorless oil.
MS (ESI): 152.1 (M+H+)
1H NMR (300 MHz, CDCI3), 5: 6.87 (m, 4H), 6.09 (t, J = 4 Hz, 1H), 3.13 (d, J = 4Hz, 2H)
C-Benzo[1,3]dioxol-2-yl-methylamine (2.94 g, 19.4 mmol) and sulfamide (3.74 g, 38.9 mmol) were combined in dry dioxane (50 mL) and the solution was heated to reflux overnight. The reaction was concentrated and the residue was chromatographed (2% to 10% acetone in dichloromethane) to yield the title compound as a white solid.
MS (ESI): 230.0 (M+H+)
1H NMR (300 MHz, CDCI3), 5: 6.87 (m, 4H), 6.25 (t, J = 4 Hz, 1H), 4.79 (broad, 1H), 4.62 (broad, 1H), 3.64 (d, J = 4 Hz, 2H).
EXAMPLE 4 (2S)-(-)-N-(2.3-Pihvdro-benzon.41dioxin-2-vlmethvl)-sulfamide
(Compound #4)
37

WO 2006/007435 PCT/US2005/021513

Catechol (13.2 g, 0.12 mol) and potassium carbonate (16.6 g, 0.12 mol) were stirred in DMF (250 mL) and (2R)-glycidyl tosylate (22.8 g, 0.10 mol) was added and the reaction was stirred at 60°C for 24 h. The reaction was cooled to room temperature and diluted with ice water (1 L) and extracted with diethyl ether (4 times). The combined organic solution was washed 3 times with 10% potassium carbonate, once with water, once with brine and evaporated in vacuo to yield a white solid which was purified by flash column chromatography (DCM:Methanol - 50:1) to yield ((2S)-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methanol as a solid.
The solid (13.3 g, 68 mmol) was dissolved in pyridine (85 mL) cooled to 0°C, p-toluenesulfonyl chloride (13.0 g, 68 mmol) was added and the reaction mixture stirred at room temperature for 20h. The reaction was diluted with diethyl ether (1 L) and 1N HCI (1.2 L). The organic layer was separated and washed 2 times with 1N HCI (500 mL), 4 times with water (150 mL), once with brine, dried (MgSCU) and evaporated in vacuo to yield a white solid which was purified by flash column chromatography (Hept:EA - 2:1) to yield toluene-4-sulfonic acid (2S)-2,3-dihydro-benzo[1,4]dioxin-2-yImethyl ester as a white solid.
The white solid was combined with potassium phthalimide (14.4 g, 78 mmol) in DMF (250 mL) and heated to reflux for 1 h, cooled to room temperature and poured into vigorously stirring water (1.5 L) and stirred 30 min. White solid was filtered and the solid was washed several times with water, 2% NaOH, and water again and let air dry to yield a (2S)-2-(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-isoindole-1,3-dione as white powdery solid.
The powdery white solid was combined with hydrazine (2.75 g, 86 mmol) in EtOH (225 mL) and heated at reflux for 2 h, cooled to room temperature and 1N HCI added to pH 1.0 and stirred for 15 min. White solid was filtered and washed with fresh EtOH (solid discarded) and the filtrate was evaporated in
38

WO 2006/007435 PCT/US2005/021513
vacuo to a solid, which was partitioned between diethyl ether and dilute aqueous NaOH. The diethyl ether solution was dried (Na2SO4) and evaporated in vacuo to a yield a light yellow oil. The oil was purified by flash column chromatography (DCM:MeOH - 10:1) to yield an oil. A portion of the oil (4.82 g, 29 mmol) in 2-propanol (250 mL) was treated with 1N HCI (30 mL) and heated on steambath until homogeneous and then let cool to room temperature. After 3 h, the mixture was ice cooled for 2 h. A white flaky solid (the corresponding HCI salt of (2S)-C-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-methylamine) was filtered off and then recrystallized again from 2-propanol to yield a white solid.
[a]D = -69.6 (c = 1.06, EtOH)
The white solid was partitioned between DCM and dilute NaOH, and the DCM was dried (NaSO4) and evaporated in vacuo to yield (2S)-C-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-methylamine as an oil.
[a]D = -57.8 (c = 1.40, CHCI3)
The oil (2.1 g, 12.7 mmol) and sulfamide (2.44 g, 25.4 mmol) were refluxed in dioxane (75 mL) for 2 h and the crude product was purified by flash column chromatography (DCM:MeOH 10:1) to yield a white solid, which was recrystallized from DCM to yield the title compound as a white crystalline solid.
mp 102-103°C
[a]D = -45.1°(c= 1.05, M);
1H NMR (DMSOd6) 5 6.86 (m, 4H), 6.81 (bd s, 3H, NH), 4.3 (m, 2H), 3.97 (dd, J = 6.9, 11.4 Hz, 1H), 3.20 (dd, J = 5.5, 13.7 Hz, 1H), 3.10 (dd, J = 6.9, 13.7 Hz, 1H)
Anal Calc: C, 44.25; H, 4.95; N, 11.47; S, 13.13
Anal Found: C, 44.20; H, 4.69; N, 11.40; S, 13.22.
39

WO 2006/007435 PCT/US2005/021513
EXAMPLE 5
N-(2.3-Dihvdro-benzon.41dioxin-2-vlmethvl)-N'.N' dimethylsulfamide
(Compound #6)

Racemic 2,3-dihydro-1,4-benzdioxin-2-ylmethylannine (8.25 g, 5.0 mmol) and triethylamine (1.52 g, 15 mmol) were combined in DMF (10 ml_) and cooled in an ice bath as dimethylsulfamoyl chloride (1.44 g, 10 mmol) was added. The reaction mixture was then stirred for 3 hr with continued cooling. The reaction mixture was partitioned between ethyl acetate and water, and the ethyl acetate solution was washed with brine, dried (MgSO4) and evaporated in vacuo to yield an oil. The oil was purified using flash column chromatography (ethyl acetate:Heptane -1:1) to yield a white solid, which was recrystallized (ethyl acetate/Hexane) to yield the title compound as a white floccular solid.
mp 76 - 78°C
MS 273 (MH+)
Anal Calc: C, 48.52; H, 5.92; N, 10.29; S, 11.78
Anal Found: C, 48.63; H, 5.62; N, 10.20; S, 11.90
1H NMR (CDCI3) 5 6.87 (m, 4H), 4.59 (bd m, 1H, NH), 4.35 (m, 1H), 4.27 (dd, J = 2.3, 11.4 Hz, 1H), 4.04 (dd, J = 7.0, 11.4, 1H), 3.36 (m, 2H), 2.82 (s, 6H).
EXAMPLE 6
N-te.S-Dihvdro-benzori^idioxin^-vlmethvll-N-methylsulfamide
(Compound #7)

40

WO 2006/007435 PCT/US2005/021513
Racemic 2,3-dihydro-1,4-benzdioxin-2-ylmethylamine (825 mg, 5 mmol) was dissolved in ethyl formate (15 mL), refluxed for 30 min and evaporated in vacuo to yield N-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-formamide as an oil.
The oil in diethyl ether (25 mL) was treated with 1M LAH in THF (9.0 mL, 9.0 mmol) at 0°C and stirred for 5 h at room temperature. The reaction was cooled in an ice bath and quenched with water (0.50 mL), followed by 3 N NaOH (0.50 mL) and water (0.50 mL). The mixture was then stirred at room temperature for 1 h. Solid was filtered and the filtrate was evaporated in vacuo to yield a residue which was partitioned between 1N HCI and diethyl ether. The aqueous phase was basified with 1N NaOH and extracted with diethyl ether. The organic phase was dried (MgSO4) and evaporated in vacuo to yield (2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-methyl-amine as an oil.
MS180(MH+)
1H NMR (CDCI3) 5 6.85 (m, 4H), 4.30 (m, 2H), 4.02 (dd, J = 7.9, 11.6 Hz, 1H), 2.85 (m, 2H), 2.50 (s, 3H)
The oil (380 mg, 2.1 mmol) and sulfamide (820 mg, 8.5 mmol) were combined in dioxane (15 mL), refluxed for 1.5 h and evaporated in vacuo to yield a crude residue. The residue was purified via column chromatography (ethyl acetate/Heptane 1:1) and the resultant solid was recrystallized from ethyl acetate/Hexane to yield the title compound as a white solid.
mp 97-98°C
MS 257 (M'1)
Anal Calc: C, 46.50; H, 5.46; N, 10.85; S, 12.41
Anal Found: C, 46.48; H, 5.65; N, 10.90; S, 12.07
1H NMR (CDCI3) 6 6.86 (m, 4H), 4.52 (bs, 2H), 4.46 (m, 1H), 4.29 (dd, J = 2.3, 11.5 Hz, 1H), 4.05 (dd, J = 6.5, 11.5 Hz, 1H), 3.51 (dd, J = 6.7,14.9 Hz, 1H), 3.40 (dd, J = 5.9, 14.9 Hz, 1H), 2.99 (s, 3H).
Example 7 f2S^-f-)-N-(6-Chloro-2,3-dihvdro-benzori,41clioxin-2-vlmethvn-sulfamide
(Compound #8)
41

WO 2006/007435 PCT/US2005/021513

Following the procedure outlined in Example 4 above, 4-chlorocatechol was reacted to yield a mixture of (2S)-C-(7-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine and (2S)-C-(6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine (ca. 3:1 ratio of 6-chloro:7-chloro isomers by RP HPLC).
The mixture was dissolved in 2-propanol (100 ml_) and 1N HCI in diethyl ether was added until pH = 1.0 was attained. The hydrochloride salt that precipitated was filtered (2.65 g) and re-crystallized from methanol/lPA to yield white crystals. The white crystals were partitioned between DCM and dilute NaOH. The DCM was dried and evaporated in vacuo to yield purified (2S)-C-(6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine as an oil.
[a]D = -67.8 (c = 1.51, CHCI3)
The oil (7.75 mmol) and sulfamide (1.50 g, 15.5 mmol) were combined in dioxane (50 ml_) and refluxed for 2.0 h, cooled to room temperature and evaporated in vacuo to yield a solid. The product was purified via flash column using DCM/methanol 20:1 to yield the title compound as a white solid.
MS 277 (M-1)
[cc]D = -59.9° (c = 1.11, M)
1H NMR (CDCI3) 5 6.90 (d, J = 2.2 Hz, 1H), 6.81 (m, 2H), 4.76 (m, 1H), 4.55 (s, 2H), 4.40 (m, 1H), 4.29 (dd, J = 2.4, 11.5 Hz, 1H), 4.05 (dd, J = 7.1, 11.5 Hz, 1H),3.45(m,2H)
AnalCalc: C, 38.78; H, 3.98; N, 10.05
Anal Found: C, 38.80; H, 3.67; N, 9.99.
The filtrates of the crystallized hydrochloride salt of (2S)-C-(6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine prepared above were recovered (ca. 1:1 of 6-chloro:7-chloro isomers) and evaporated in vacuo to yield a solid, which was partitioned between DCM (200 mL) and dilute NaOH (0.5 M, 50 ml_). The DCM solution was washed once with brine, dried (Na2SO4) and evaporated in
42

WO 2006/007435 PCT/US2005/021513
vacuo to yield an oil, which was purified via reverse phase HPLC (10 - 50% ACN with 0.16% TFA in water with 0.20% TFA) to yield (2S)-C-(7-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-yl)-methylamine as a residue.
The residue was combined with sulfamide (0.90 g, 9.4 mmol) in dioxane (25 mL) and refluxed for 2.5 h, cooled to room temperature and evaporated in vacuo to yield an oil. The oil was purified by flash column chromatography using DCM/methanol - 10:1 to yield (2S)-(-)-N-(7-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide as a white solid.
MS 277 (M'1)
1H NMR (CDCI3/CD3OD) 5 6.88 (d, J = 0.7 Hz, 1H), 6.81 (m, 2H), 4.37 (m, 1H), 4.30 (dd, J = 2.3, 11.6 Hz, 1H), 4.04 (dd, J = 7.0, 11.6 Hz, 1H), 3.38 (m, 2H).
Example 8 Chroman-2-vlmethvlsulfamide (Compound #10)

Chroman-2-carboxylic acid (4.5 g, 25 mmol) and HOBT (3.86 g, 25 mmol) were combined in DCM (40 mL) and DMF (10 mL). Dimethylaminopropyl ethylcarbodiimide (EDC, 4.84 g, 25 mmol) was added at room temperature and the reaction mixture was stirred for 30 min. Ammonium hydroxide (2.26 mL, 33.4 mmol) was added and the reaction mixture was stirred for 16h. The reaction mixture was diluted with DCM (50 mL) and water (50 mL) and the pH of the mixture was adjusted to about pH = 3.0 with 1N HCI. The DCM was separated and the aqueous phase extracted twice with DCM. The combined DCM phase was dried (Na2SO4) and evaporated in vacuo to yield an oil, which was purified with flash column chromatography (ethyl acetate) to yield an oil.
The oil (5.35 g, 30 mmol) in THF (90 mL) was stirred as 1M LAH in THF (36 mL, 36 mmol) was added and the reaction mixture was then stirred at room temperature for 20 h. The reaction was quenched with water, stirred for 2 hours,
43

WO 2006/007435 PCT/US2005/021513
the solution decanted, dried (Na2SO4) and evaporated in vacuo to yield C-chroman-2-yl-methylamine as an oily amine.
The oily amine (1.63 g, 10 mmol) and sulfamide (1.92 g, 20 mmol)were combined in dioxane (50 mL) and brought to reflux for 2 h. The solution was cooled and evaporated in vacuo to yield an oil, which was purified via column chromatography (DCM:Methanol 10:1) to yield a white solid. The solid was recrystallized from ethyl acetate/hexane to yield chroman-2-ylmethylsulfamide as a white solid.
mp100-101°C
MS 241 (M~1)
Anal Calc: C, 49.57; H, 5.82; N, 11.56; S, 13.23
Anal Found: C, 49.57; H, 5.80; N, 11.75; S, 13.33.
Example 9 Chroman-2-vlmethylsulfamate (Compound #11)

Chroman-2-carboxylic acid (4.3 g, 24 mmol) in THF (70 mL) was combined with 1M LAH in THF (30 mL, 30 mmol) and stirred at room temperature for 2h. The reaction mixture was quenched with water and then stirred for 2 hours. The THF solution was decanted from the solid, which was washed with fresh THF. The combined THF solution was dried (Na2SO4) and evaporated in vacuo to yield chroman-2-yl-methano! as an oil.
The chroman-2-yl-methanol (1.97 g, 12 mmol) in DMF (30 mL) was cooled with an ice bath to about 0°C under argon and combined with 95% NaH (0.39 g, 15.6 mmol), then stirred for 30 min. Sulfamoyl chloride (2.78 g, 24 mmol) was then added and the reaction mixture was stirred for 1 h. The reaction mixture was diluted with ethyl acetate (100 mL) and water (100 mL). The ethyl acetate solution was separated and the aqueous phase was extracted twice with ethyl
44

WO 2006/007435 PCT/US2005/021513
acetate. The combined ethyl acetate phase was dried (MgSO4) and evaporated in vacuo to yield an oil, which was purified by flash column chromatography (ethyl acetate/hexane 1:2) to yield a white solid, which was recrystallized from ethyl acetate/hexane to yield the title compound as a white solid.
mp 87-90°C
MS [M-H]-242.1
Anal Calc: C, 49.37; H, 5.39; N, 5.76; S, 13.18
Anal Found: C, 49.46; H, 5.17; N, 5.72; S, 13.09.
Example 10 2-(2.3-Dihvdro-benzon.41dioxin-2-vn-ethvlsulfamide (Compound #16)

Potassium cyanide (2.05 g, 31.5 mmol) was added to 2-bromomethyl-(2,3 dihydrobenzo[1,4]dioxine) (6.87 g, 30 mmol) in DMSO (90 mL) and stirred at ambient temperature for 20 h. The reaction mixture was then diluted with water (250 mL) and extracted twice with diethyl ether. The diethyl ether was washed with water, then washed twice with brine, dried (Na2SO4) and evaporated in vacuo to yield 2-cyanomethyl-(2,3 dihydrobenzo[1,4]dioxine) as a white solid.
1H NMR (CDCI3) 5 6.89 (m, 4H), 4.50 (m, 1H), 4.31 (dd, J = 2.3, 11.5 Hz, 1H), 4.08 (dd,J = 6.2, 11.6 Hz, 1H), 2.78 (d, J = 6.1, Hz, 2H)
The 2-cyanomethyl-(2,3 dihydrobenzo[1,4]dioxine) was dissolved in THF (50 mL) and 1M BH3 in THF (80 mL, 80 mmol) was added and the reaction mixture refluxed for 5 h, then stirred at ambient temperature for 16h. With ice bath cooling, 2N HCI was added until pH = 1.0 was achieved. The reaction mixture was then stirred for 1h at room temperature and evaporated in vacuo to yield an oil. The oil was partitioned between 3N NaOH and diethyi ether, and the diethyl ether solution was washed with brine, dried (Na2SO4) and evaporated in vacuo to yield crude 2-(2,3 dihydrobenzo[1,4]dioxin-2-yl)ethylamine.
45

WO 2006/007435 PCT/US2005/021513
MS(M+H)+180.
The crude 2-(2,3 dihydrobenzo[1,4]dioxin-2-yl)ethylamine in dioxane (100 mL) was combined with sulfamide (3.0 g, 31 mmol) and heated to reflux for 2 h. The solution was cooled and evaporated in vacuo to yield an orange solid, which was purified by column chromatography (DCM:MeOH -10:1) to yield a white solid. The solid was re-crystallized from DCM to yield the title compound as a solid.
MS(M-1)257
MP101 -103°C(corr)
1H NMR (CDCI3): 5 6.86 (m, 4H), 4.70 (m, 1H), 4.52 (s, 2H), 4.30 (m, 2H), 3.94 (dd, J = 7.4, 11.3 Hz, 1H), 3.43 (dd, J = 6.4, 12.9 Hz, 2H), 1.94 (dd, J = 6.5, 12.9, 2H). Elemental Analysis:
Measured: C, 46.48; H, 5.60; N, 10.81; S, 12.41
Calculated: C, 46.50; H, 5.46; N, 10.85; S, 12.41
Example 11
(2S)-(-)-N-(6,7 Dichloro-2,3-dihvdro-benzon,41dioxin-2-vlmethvl)-sulfamide
(Compound #29)

4,5 Dichloroatechol (8.6 g, 48 mmol) and potassium carbonate (6.64 g, 48 mmol) were stirred in DMF (200 mL). (2R)-Glycidyl tosylate (9.12 g, 40 mmol) was added and the reaction mixture was stirred at 60°C for 24 h. The reaction mixture was cooled to room temperature and then diluted with ice water (600 mL) and extracted with diethyl ether (4 times). The combined organic solution was washed 3 times with 10% potassium carbonate, twice with brine, dried (MgSO4) and evaporated in vacuo to yield a viscous oil of (2S)-2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxine) methanol.
46

WO 2006/007435 PCT/US2005/021513
The (2S)-2-(6,7 dichloro-2,3-dihydro-benzo[1,4]dioxine) methanol oil (6.4 g, 27 mmol) was dissolved in pyridine (50 mL) cooled to 0°C. Then, p-toluenesulfonyl chloride (5.2 g, 27 mmol) was added and the reaction mixture was stirred at room temperature for 20h. The reaction mixture was diluted with diethyl ether and 1N HCI (750 mL) and the organic layer was separated and washed 2 times with 1N HCI (250 mL), once with water (150 mL), twice with brine, dried (MgSO4) and evaporated in vacuo to yield light yellow solid of toluene-4-sulfonic acid (2S)-6,7-dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl ester.
1H NMR (CDCI3): 5 7.79 (d, J = 8.3 Hz, 2H), 7.36 (d, J = 8.0 Hz, 2H), 6.94 (s, 1H), 6.83 (s, 1H), 4.37 (m, 1H), 4.2 (m, 3H), 4.03 (dd, J = 6.3, 11.7 Hz, 1H), 2.47 (s, 3H).
Toluene-4-sulfonic acid (2S)-6,7-dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl ester (8.0 g, 20.5 mmol) was combined with potassium phthalimide (6.1 g, 33 mmol) in DMF (75 mL) and heated to reflux for 1 h, cooled to room temperature and poured into vigorously stirring water (0.5 L) and then stirred 30 min. White solid was filtered and the solid was washed several times with water, 2% NaOH, and water again and then let air dry to yield (2S)-2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-isoindole-1,3-dione (6.0 g, 80%) as a white powdery solid.
The white powdery solid was combined with hydrazine (1.06 g, 33 mmol) in EtOH (80 mL) and heated at reflux for 2 h, then cooled to room temperature. 1N HCI was added to adjust the reaction mixture's pH to pH 1.0 and the reaction mixture was then stirred for 15 min. White solid was filtered and washed with fresh EtOH (solid discarded) and the filtrate was evaporated in vacuo to a solid, which was partitioned between diethyl ether and dilute aqueous NaOH. The diethyl ether solution was dried (Na2SO4) and evaporated in vacuo to a yield a viscous oil of (2S)-2-aminomethyl-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxine).
1H NMR (CDCI3): 5 6.98 (s, 1H), 6.96 (s, 1H), 4.25 (dd, J = 2.0, 11.2 Hz, 1H), 4.15 (m, 1H), 4.0 (m, 1H), 2.97 (d, J = 5.5 Hz, 2H)
47

WO 2006/007435 PCT/US2005/021513
A portion of the oil (3.8 g, 16 mmol) and sulfamide (3.1 g, 32.4 mmol) were refluxed in dioxane (100 mL) for 2 h and the crude product was purified by flash column chromatography (DCM:MeOH 20:1) to yield the title compound as a white solid, which was recrystallized from ethyl acetate / hexane to yield the title compound as a white crystalline solid.
MS[M-H]-311.0
mp119-121°C
[a]D = -53.4 °(c= 1.17, M)
1H NMR (DMSOd6): 5 7.22 (s, 1H), 7.20 (s, 1H), 6.91 (bd s, 1H), 6.68 (bd s, 2H), 4.35 (m, 2H), 4.05 (dd, J = 6.5, 11.5 Hz, 1H), 3.15 (m, 2H) Elemental Analysis:
Measure: C, 34.52; H, 3.22; N, 8.95; Cl, 22.64; S, 10.24
Calculated: C, 34.64; H, 2.68; N, 8.87; Cl, 22.94; S, 10.35.
Example 12
(2S)-(-)-N-(7-Amino-2.3-dihvdro-benzori,41dioxin-2-vlmethyl)-sulfamide
(Compound #36)

(2S)-(-)-N-(2,3-Dihydro-7-nitro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide (1.2 g, 4.15 mmol), was prepared from 4-nitrocatechol according to the process outlined in Example 4. The (2S)-(-)-N-(2,3-Dihydro-7-nitro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide, was then combined with 10% Pd/C in methanol (120 mL) and shaken under hydrogen atmosphere (39 psi) at room temperature for 3 h. The solids were filtered and washed with 10% M in DCM and the filtrate was evaporated in vacuo to yield crude product. The crude product was dissolved in 0.2 N HCI (25 mL), frozen and lyophilized to yield the title compound as a white flaky solid, as the corresponding hydrochloride salt.
MS (M+H)+ 260
48

WO 2006/007435 PCT/US2005/021513
1H NMR (DMSO d6): 5 10.2 (bd s, 3H), 6.86 (m, 1H), 6.85 (s, 1H), 6.74 (dd, J = 2.5, 8.4 Hz, 1H), 4.22 (m, 2H), 3.88 (dd, J = 6.7, 11.4 Hz, 1H), 3.04 (m, 2H)
Example 13
(2S)-(-)-N-(7-Methvl-2,3-dihvdro-benzon.41dioxin-2-vlmethvl>-sulfamide
(Compound #19)

Title compound was prepared according to the procedure described in Example 4 above, starting with 4-methylcatechol, to yield a white solid, which was recrystallized from ethyl acetate/ hexane to yield the title compound as a white solid.
MS[M-H]"257
1H NMR (CDCI3): 6 6.76 (m, 1H), 6.66 (m, 2H), 4.80 (m, 1H), 4.57 (bd s, 1H), 4.40 (m, 1H), 4.28 (m, 1H), 4.03 (dd, J = 6.9, 11.4 Hz, 1H), 3.45 (m, 2H), 2.25 (s, 3H).
Elemental Analysis
Calculated: C, 46.50; H, 5.46; N, 10.85; S, 12.41
Found: C, 46.65; H, 5.60; N, 10.84; S, 12.61.
Example 14
Sulfamic acid, 6.7 dichloro-2.3-dihvdro-benzoH.41dioxin-2-vlmethvl ester
49
(Compound #27)

WO 2006/007435 PCT/US2005/021513
(2S)-6,7 dichloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethanol (2.0 g, 8.5 mmol), prepared according to the procedure described in Example 11 above, in DMF (20 mL) was cooled in an ice bath. Then, 95% sodium hydride (0.28 g, 11 mmol) was added under argon and the reaction mixture was stirred 30 min. Sulfamoyl chloride (1.97 g, 17 mmol) was added and the reaction mixture was stirred with ice bath cooling. After 1 h, the reaction mixture was diluted with water (50 mL) and extracted three times with ethyl acetate. The combined ethyl acetate was washed with brine, dried (Na2SO4) and evaporated in vacuo to an oil, which was purified by flash column chromatography (ethyl acetate/heptane 1:1) to yield a white solid. The white solid was recrystallized from benzene to yield the title compound as a white solid.
mp109-111°C
MS[M-H]"312
1H NMR (DMSOd6) 5 7.65 (s, 2H), 7.26 (s, 1H), 7.25 (s, 1H), 4.58 (m, 1H), 4.41 (dd, J = 2.5, 11.7 Hz, 1H), 4.28 (m, 2H), 4.11 (dd, J = 6.9, 11.7 Hz, 1H).
Example 15
Sulfamic acid, 6-chloro-2.3-dihvdro-benzof1,41dioxin-2-ylmethvl ester
(Compound #12)

(2S)-6-Chloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethanol (6.4 g, 32 mmol) was prepared according to procedure as in Example 7 above, in DMF (80 mL) was cooled in an ice bath. Then, 95% sodium hydride (1.06 g, 42 mmol) was added over 20 min under argon and the reaction mixture was stirred 30 min. Sulfamoyl chloride (7.4 g, 64 mmol) was added over 10 min and the reaction mixture was stirred with ice bath cooling. After 1 h, the reaction was diluted with water (300 mL) and extracted three times with ethyl acetate. The combined ethyl acetate was washed with brine, dried (MgSO4) and evaporated in vacuo to yield
50

WO 2006/007435 PCT/US2005/021513
an oil, which was purified by flash column chromatography (ethyl acetate /hexane 1:2) to yield a white solid. The white solid was recrystallized from benzene 3 times to yield the title compound as a white solid.
mp113-116°C
MS[M-H]"278
[a]D = -41.0 °(c = 1.32, M)
1H NMR (CDCI3) 5 6.91 (d, J = 1.9 Hz, 1H), 6.84 (m, 2H), 4.82 (bd s, 2H), 4.50 (m, 1H), 4.41 (m, 2H), 4.31 (dd, J = 2.3, 11.6 Hz, 1H), 4.12 (dd, J = 6.3, 11.6 Hz, 1H) Elemental Analysis:
Measured: C, 38.57; H, 3.42; N, 4.92; S, 11.53
Calculated: C, 38.65; H, 3.60; N, 5.01; S, 11.46
Example 16 In Vivo Assay: Maximal Electroshock Test (MES)
Anticonvulsant activity was determined using the MES test, run according to the procedure described in detail below. Swinyard EA, Woodhead JH, White HS, Franklin MR. Experimental selection, quantification, and evaluation of anticonvulsants. In Levy RH, et al., eds. Antiepileptic Drugs. 3rd ed. New York: Raven Press, 1989:85-102
CF-1 male albino mice (25-35g) were fasted for 16 hours before testing. Mice were randomly selected into control and test groups, with the animals dosed with vehicle or test compound, at varying concentrations, respectively. On the study date, at 30 minutes prior to shock, the mice were orally dosed with vehicle (0.5% methylcellulose) or test compound (100-300 mg/kg). Seizures were induced by trans-comeal electric shock using a 60-Hz alternating current, 50 mA, delivered for 0.2 sec. The mice in the test groups were subjected to electrical stimulus at time intervals between 15 minutes and 4 hours following administration of test compound. The shock resulted in an immediate full body tonic extension. The test was complete when the entire course of the convulsion
51

WO 2006/007435

PCT/US2005/021513

has been observed (typically, less than 1 minute after electrical stimulation), and the mice were then immediately euthanized by carbon dioxide inhalation.
Abolition of the full body tonic extensor component of the seizure was taken as the endpoint of the test. Absence of this component indicated that the test compound had the ability to prevent the spread of seizure discharge through neural tissue. The ED50 value of the test compound (calculated when appropriate) was the calculated dose required to block the hind limb tonic-extensor component of the MES-induced seizure in 50% of the rodents tested. A probit analysis was used to calculate the ED50 and 95% fiducial limits (FL).
Representative compounds of the present invention were tested according to the procedure described above, with results as listed in Table 4 below. Results are listed as number of mice with full body tonic extension prevented / total number of mice tested @ a given time (at a given test compound dosage level).
Table 4: MES Mouse Activity
ID No. MES Activity
1 2/4@1h(300mg/kg)
2 4/4@2h(100mg/kg)
3 2/3@1h(300mg/kg)
4 5/5@1h(300mg/kg)
5 1/5 @ 2h (300 mg/kg)
6 4/5 @ 0.5h (300 mg/kg)
7 3/3 @ 0.5h (300 mg/kg)
8 3/5 @3h (100 mg/kg)
9 1/5 @1h (300 mg/kg)
10 1/5 @ 1h (100 mg/kg)
11 4/5 @1h (100 mg/kg)
12 3/5 @4h (100 mg/kg)
52

WO 2006/007435

PCT/US2005/021513

13 2/[email protected](10mg/kg)
14 3/5@4h(100mg/kg)
15 Inactive @ 100 mg/kg
16 5/5 @ 0.5h (300 mg/kg)
17 4/5 @0.5h (100 mg/kg)
18 Inactive @ 100 mg/kg
19 5/5 @ 0.5h (300 mg/kg)
20 1/5 @2h (100 mg/kg)
21 5/5 @2h (100 mg/kg)
22 1/5 @4h (100 mg/kg)
23 Inactive @ 100 and 300 mg/kg
24 5/5 @ 4h (300 mg/kg)
25 5/5 @4h (100 mg/kg)
26 Inactive @ 100 and 300 mg/kg
27 5/5 @4h (100 mg/kg)
28 4/5 @4h (100 mg/kg)
29 3/5 @4h (100 mg/kg)
30 1/5 @0.5h (100 mg/kg)
31 3/5 @0.5h (100 mg/kg)
32 Inactive @ 100 and 300 mg/kg
33 1/3 @ 2h (300 mg/kg)
34 Inactive @ 100 and 300 mg/kg
35 Inactive at 100 mg/kg
36 Inactive @ 100 and 300 mg/kg
Example 17
As a specific embodiment of an oral composition, 100 mg of the Compound #8 prepared as in Example 7 is formulated with sufficient finely divided lactose to provide a total amount of 580 to 590 mg to fill a size O hard gel capsule.
53

WO 2006/007435 PCT/US2005/021513
While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, it will be understood that the practice of the invention encompasses all of the usual variations, adaptations and/or modifications as come within the scope of the following claims and their equivalents.
54

WO 2006/007435 PCT/US2005/021513
We Claim:
1. A compound of formula (II)

wherein
R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl;
55
R4 is selected from the group consisting of hydrogen and lower alkyl; a is an integer from 1 to 2;

WO 2006/007435 PCT/US2005/021513
each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro;

2. A compound as in Claim 1 wherein
R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl;
R4 is selected from the group consisting of hydrogen and lower alkyl;
56
a is an integer from 1 to 2;

WO 2006/007435 PCT/US2005/021513

wherein b is an integer from 0 to 2; and wherein c is an integer from 0 to 1; each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro;

3. A compound as in Claim 2 wherein
R1 and R2 are each independently selected from the group consisting of hydrogen and lower alkyl;
R4 is selected from the group consisting of hydrogen and lower alkyl;
a is an integer from 1 to 2;
57

WO 2006/007435 PCT/US2005/021513

wherein b is an integer from 0 to 2; and wherein c is 0; each R5 is independently selected from the group consisting of halogen, lower alkyl and nitro;

4. A compound as in Claim 3 wherein
R1 and R2 are each independently selected from the group consisting R4 is selected from the group consisting of hydrogen and methyl;
58
a is an integer from 1 to 2;

WO 2006/007435 PCT/US2005/021513
benzo[1,4]dioxepinyl), 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(chromanyl), 2-(5-fluoro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-benzo[1,3]dioxolyl), 2-(7-nitro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyl), 2-(5-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl), 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl),2-(8-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-naphtho[2,3-b][1,4]dioxinyl) and 2-(4-methyl-benzo[1,3]dioxolyl);

or a pharmaceutically acceptable salt thereof.
5. A compound as in Claim 4 wherein
R1 and R2 are each independently selected from the group consisting of hydrogen and methyl;
R4 is selected from the group consisting of hydrogen and methyl;
a is an integer from 1 to 2;

dihydro-benzo[1,4]dioxinyl), 2-(2,3-dihydro-benzo[1,4]dioxinyl), 2-(6-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-chloro-2,3-dihydro-benzo[1,4]dioxinyl), 2-(7-methyl-2,3-dihydro-benzo[1,4]dioxinyI), 2-(6-bromo-2,3-dihydro-benzo[1,4]dioxinyl) and 2-(6,7-dichloro-2,3-dihydro-benzo[1,4]dioxinyl); or a pharmaceutically acceptable salt thereof.
59

WO 2006/007435 PCT/US2005/021513
6. A compound selected from the group consisting of A/-[(6-chioro-2,3-°
dihydro-1,4-benzodioxin-2-yl)methyl]-sulfamide and pharmaceutically acceptable
salts thereof.
7. A compound selected from the group consisting of

and pharmaceutically acceptable salts thereof. 8. A compound of the formula (III)

or a pharmaceutically acceptable salt thereof.
9. A pharmaceutical composition comprising a pharmaceutically acceptable
carrier and a compound of Claim 1.
10. A pharmaceutical composition made by mixing a compound of Claim 1
and a pharmaceutically acceptable carrier.
11. A process for making a pharmaceutical composition comprising mixing a
compound of Claim 1 and a pharmaceutically acceptable carrier.
12. A method of treating epilepsy or a related disorder, in a subject in need
thereof comprising administering to the subject a therapeutically effective amount
of the compound of Claim 1.
60

WO 2006/007435 PCT/US2005/021513
61
13. A method of treating epilepsy, in a subject in need thereof comprising
administering to the subject a therapeutically effective amount of the compound
of Claim 1.
14. A method as in Claim 12, wherein the disorder is selected from essential
tremor or restless limb syndrome.
15. The use of compound as in Claim 1 in the preparation of a medicament for
treating epilepsy or a related disorder, in a subject in need thereof.

The present invention is directed to novel sulfarnide and sulfamate derivatives, pharmaceutical
compositions
containing them and their use in the treatment of epilepsy and related disorders.

Documents:

« Previous Patent

Next Patent »

Patent Number

262544

Indian Patent Application Number

185/KOLNP/2007

PG Journal Number

35/2014

Publication Date

29-Aug-2014

Grant Date

27-Aug-2014

Date of Filing

16-Jan-2007

Name of Patentee

JANSSEN PHARMACEUTICA N.V.

Applicant Address

TURNHOUTSEWEG 30,B-2340,BEERSE

Inventors:

#	Inventor's Name	Inventor's Address
1	DAVID F.McCOMSEY	1125 VICTORIA ROAD,WARMINSTER,PA 18974
2	ALLEN B.REITZ	109 GREENBRIAR ROAD,LANSDALE,PA 18922
3	BRUCE E. MARYANOFF	4029 DEVONSHIRE DRIVE,FOREST GROVE,PA 18922
4	MICHAEL H. PARKER	3587 GRAY FOX DRIVE,CHALFONT,PA 18914

PCT International Classification Number

C07D321/08; A61K31/353; A61K31/357

PCT International Application Number

PCT/US2005/021513

PCT International Filing date

2005-06-16

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	60/580,178	2004-06-16	U.S.A.