Title of Invention	2-,3-, 4-, OR 5-SUBSTITUTED-N1-(BENZENSULFONYL)INDOLES AND THEIR USE IN THERAPY
Abstract	This invention relates to 2-, 3-, 4- or 5-substituted-NI-(benzensulfonyl)indoles compounds of the general formula (I) and to pharmaceutical compositions comprising the same. The said compounds have affmity for the 5-HT6 receptor and are useful for the treatment and prophylaxis of d.isorders relating to the said receptor, such as obesity and CNS disorders.

Full Text

TECHNICAL FIELD The present invention relates to novel 2-3-, 4- or 5-substituted-Nl-(benzensulfonyl)indole compounds, to pharmaceutical compositions comprising the compounds and to the use of the compounds for the preparation of a medicament for the treatment of obesity and CNS disorders as well as method of treatment of these disorders. BACKGROUND ART Obesity is a condition characterized in an increase in body fat content resulting in excess body weight above accepted norms. Obesity is the most important nutritional disorder in the western world and represents a major health problem in all industrialized countries. This disorder leads to increased mortality due to increased incidences of diseases such as cardiovascular disease, digestive disease, respiratory disease, cancer and NIDDM (type [I diabetes). Searching for compounds, which reduce body weight has been going on for many decades. One line of research has been activation of serotonergic systems, either by direct activation of serotonin receptor subtypes or by inhibiting'serotonin reuptake. The exact receptor subtype profile required is however not known. Serotonin (5-bydroxytryptamine or 5-HT), a key transmitter of the peripheral and central nervous system, modulate a wide range of physiological and pathological functions, including anxiety, sleep regulation, aggression, feeding and depression. Multiple serotonin receptor subtypes have been identified and cloned. One of these, the 5-HT(j receptor, was cloned by several groups in 1993 (M Ruat, E Traiffort, J-M \rrang, J Taidivel-Lacombe, J Diaz, R Leurs, J-C Shwartz. Biochem. Biophys. Res. Zommitn. 1993, 193 (1) 268-276; M Sebben, H Ansanay, J Bockaert, A Dumuis, VeiiroRepon 5, 2553-2557 (1994).) This receptor is positively coupled to adenylyl :yclase and displays affinity for antipsychotics such as clozapine. Recently, the effect of i-HT(j antagonist and 5-HT£ antisense oligonucleotides to reduce food intake in rats as been reported (JC Bentlcy, CA Mardsen, AJ Sleight and KC Fone. Effect of 5-HT6 ntagonist Ro 04-6790 on food consumption in rats trained to a fixed feeding regime. Br Pharmacol. 1999 Suppl. 126, P66; JC Bentley, AJ Sleight, CA Mardsen, KLCF Fone. 5-HT& antisense oligonucleotide ICV affects rat performance in the water maze and feeding. J Psychopimrmacol Snppt A64, 1997, 255). Compounds with enhanced affinity and selectivity for the 5-HT6 receptor have been identified, e.g. in WO 00/34242 and by M. Isaac, A. Si^si, 1". Xin, N. Mac Lean, .1. Wilson, fC. McCallum, H. Wang and L. Demchyshyn: 6-Bicyciopiperazinyl-l-arylsulfonylindoles and 6-Bicyclopiperidinyl-l-arylsulfonylivKioles derivatives as novel, potent and selective 5-HT& receptor antagonists; Bioorgamc & Medicinal Chemistiy Letters 2000, 10,1719-1721. DETAILED DESCRIPTION OF THE INVENTION According to the present invention it has been found that the compounds of formula (I) show affinity for ihe 5-HTG receptor as antagonists at a low nanomolar range. The 5-HT6 antagonist compounds of the present invention are useful for the treatment or prophylaxis of obesity and for the treatment or prophylaxis of memory and CNS disorders (schizophrenia, Parkinson's disease and depression), Attention Deficit Hyperactive Disorders (ADHD), drug abuse. According to the invention a compound of the general formula (I) is provided: wherein Ar is (1) phenyl, (2) naphlhyl, (3) a 5- to 10-membered monocyclic or bicyclic heterocyclic ring having 1 to 4 leteroaloms selected from the group consisting of oxygen, sulfur, or nitrogen, or (4) -R°-phenyl; vherein each of phenyl, naphlhyl. and heterocyclic ring is independently optionally ubstituted with halogen, C|.„ alkyl. CF.i. hydroxyl, CMl alkoxyl, OCF3, COCF3, CN, NO;, phenyloxy, phenyl, C[,G alkylsulfonyl, C;.& alkeny], -NR7R8, Ci-c alkylcarboxyl, formyl, -C,.6 alkyl-NH-CO-phenyl, -CG alkyl-CO-NH-phenyl, -NH-CO-C,^ alkyl, -CO-NR7RB, or SR7; wherein each of R7 and Rs is independently H or C,_0 alkyl; and Ry is Ci.(, alkyl or C^-r, alkenyl, each of which being optionally substituted with phenyl or phenyloxy; R' is H, phenyl, I, or C|.f, alkyl; R3 is H or 3-(l-azabicyclo[2.2.2]oct-2-en)yl; R is H or a heterocyclic ring selected from the group consisting of: t * or a pharmaceutically acceptable salt, hydrate, or stereoisomer thereof, with the proviso that when R^ is alkyl R^ is not H. The term "C^ alkyl" denotes a straight or branched alkyl group having from 1 to 6 carbon atoms. Examples of said lower alkyl include methyl, ethyl, n-propyl, iso- propyl, n-butyl, iso-butyl, sec-butyl, t-butyl and straight- and branched-chain pentyl and hexyl. The term "C[.g alkoxy" denotes a straight or branched alkoxy group having from 1 to 6 c;;ibon aLoms. Examples of said lower alkoxy include rnetboxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec-butoxy, t-butoxy and straight- and branched-chain pentoxy and hexoxy. The term "halogen" shall mean fluorine, chlorine, bromine or iodine. The term "heterocyclic ring" includes unsaturated, as well as saturated or partially saturated he'*croc_>L'lic rings. Preferred compounds of the invention are compounds of the general formula (I) wherein: Ar is (1) phenyl, (2) 1-naphthyl or 2-naphthyl, (3) a 5- to 10-membered monocyclic or bicyclic heterocyclic ring having 1 to 4 heteroatoms selected from the group consisting of oxygen, sulfur, or nitrogen, or (4) -R9-phenyl; wherein each of phenyl, naphthyl, and heterocyclic ring is independently optionally substituted with F,-C1, Br, C,.* alky!, CF3, hydroxy], C].6 alkoxy!, OCF:, phenyl, C24 alkenyl, -NR7RS, -NH-CO-C,.(, alkyl, or SR7, wherein each of R7 and Rs is independently H or C,-6 alkyl: and R° is C|.: alkyl; R2 is H, phenyl, I, or C|.& alkyl; R4 is selected from the group consisting of: Other preferred compounds of the invention include those wherein: (a) Ar is phenyl, optionally substituted with F, Ct, Br, methyl, CF-,, d.4 alkoxyl, OCF3, CN, NO2, phenyloxy, phenyl, methylsulfonyl, or -NR7R', where each of R7 and Rs is independently H or methyl. (b) Ar is 1-naphlhyl or 2-naphthyl, each of which being optionally substituted with F, CI, Br, methyl, CF3, CM alkoxyl, OCF3, CN, K02. phenyloxy, phenyl, methylsulfonyl, or-NR R , where each of R7 and R8 is independently H or methyl. (c) Ar is a heterocyclic ring selected from the group consisting of furyl, pyrrolyl, triazolyl, diazolyl, oxazoiyl, thiazolyl, oxadiazolyl, isothiazolyl, isoxazoly!, thiadiazolyl, pyridyl, pyrimidyl, pyrazinyl, thienyl, imidazolyl, pyrazolyl, indolyl, quinolinyl, isoqiiinolinyl, benzofuryl, benzothienyl, and benzoxadiazolyl, each of which being optionally substituted with halogen, C1-6 alkyl, CF3, hydroxyl, C[.6 alkoxyl, OCF3, CN, NO;, phenyloxy, phenyl, C|-&alkylsulfonyl, C2-6 alkenyl, -NR'RS, C|.e alkylcarboxyl, foi-myl, -NH-CO-Ct.e alkyl, -CO-NR7Rs, or SR7; wherein each of R7 and R8 is independently H orG-6 alkyl. (d) Ar is a heterocyclic ring selected from the group consisting of pyridyl, thienyl, imidazolyl, pyrazolyl, benzothienyl, and benzoxadiazolyl, each of which being optionally substituted with halogens or Ci-& alkyl. (e) Ar is 2-pyridyl, 3-pyridyl, or 4-pyridyl. (f) Ar is a 5- to 7-membered aromatic, partially saturated, or completely saturated heterocyclic ring having 1 to 4 heteroatoms selected from the group consisting of O, S, or NR'°, where R10 is H, C,.& alkyl, -CO-CF3, or absent. (g) Ar is -R9-phenyl, wherein R is C1.3 alkyl or C2-3 alkenyl, each of which being optionally substituted with phenyl, and wherein phenyl is optionally substituted with F, CI, Br, methyl, CF}. Cw alkoxyl, OCF], CN, NO2, phenyloxy, phenyl, methylsulfonyl, or -NR7R3; each of R7 and R8 being independently H or CK, alkyl. Additional preferred compounds of the invention are compounds of the general formula (I) wherein each of R4 and R' is independently a heterocyclic ring selected from the group consisting of: wherein R1' is H, O.i alkyl, or benzyl. The following compounds are particularly preferred embodiments of the invention: l-(phenylsidfonyt)-4-(l-piperazinyl)-lH-indole, l-[(4-fluorophenyl)su!fonyl]-4-(l-piperaziny])-lH-indole, l-[{5-chloro-3-methyl-l-benzothien-2-yl)sulfonyl]-4-(l-piperazinyl)-lH-indole, 3-(l-azabicyclo[2.2.2]oct-2-eri-3-yl)-l-(phenylsLilfonyl)-lH-indole 5-methoxy-1 -(phenylsuIfonyl)-4-( I -piperazinyl)-l H-indole, 4-(4-eIliyl-l-piperazinyl)-l-(phenylsulfonyl)-lH-indole, l-[(4-methylphenyi)sLilfonyI]-4-(4-methyl-l-piperazinyl)-lH-indole, 1 -(phenylsulfonyl)-5-Cl -piperazinyl)-! "H-indole, 4-(2.5-dirnethyi-I-piperazinyI)-l-(phenylsulfonyl)-lH-indole, 4-(2,6-dimethy!-l-piperazinyl)-I-(phen.ylsulfonyl)-lH-indoIe, 4-(l,4-diazepan-l-yl)-l-(phenylsulfonyl)-lH-indoie, 2-[l-(phenylsulfonyI)-lH-indoI-4-yl]octabydropyrrolo[l,2-a]pyrazinel-(2-naphthylsulfonyO^^l-piperazmyiyiH-indole, l-(l-naphthylsulfonyl)-4-(I-piperazinyI)-lH-indole, l-[{4-metiiyIpheny!)sulfonyl]-4-(l-piperazinyl)-lH-indole, N'{l-Azabicyclo[2.2.2]oct-3-yI)-N-{l-[(4-methylphenyi)suIfonyl]-lH-indol-4-yl famine, 2-Ethyl-4-(4-ethyi-l -piperazinyO-1 -[(phenyl)suifonyl]-1 H-indoie; 2-elhyl-1 -(4-methyl-phenylsul fonyl)-4-{ 1 -piperazinyl)- IH-indole, 4-(2,5-dimethyl-t-piperazinyl)-2-emyl-l-(phenyisulfonyi)-lH-indole. 4-(4-ethyi-1-piperazinyl)-5-nuoro-l-[(4-niethylphenyl)sulfonylj-IH-indole, 5-nuoro-4-(I-piperazinyl)-l-{[4-{tnfluoroniethyl)phenyl]sitlfonyl[-lH-indole, 5-cl]loro-l-(phenyisulfonyn-4-( I-piperazinyl)-IH-indole, 5-cl]loro-I-(phenylsulfonyl)-4-( I-piperazinyl)-! H-indole, 1-[(5-chloro-3-methyl-1-benzolhien-2-yl)su!fonyl]-5-niethoxy-4-(l-piperazinyl)-! H-isdole, l-[(5-chloro-3-niethyl-l-benzothien-2-yl)sulfonyl]-5-(l-piperazinyl)-! H-indole, 1 -[(4-methylphenyl)sul fonyI]-4-(3-methyl-1 -piperazinyl)- i H-indole, I-[(4-methylpheny])sul fonyl]-4-(4-piperidinyio\y)-l H-indoIc, l-[(4-methylphenyl)sLilfonyl]-4-(3-methyl-! -piperazinyl)-1 H-indole. Most preferred embodiments of the invention are the compounds !-(phenyIsu!fonyI)-4-(l-piperazinyl)-! H-indole hydrochloride, l-[(2J5-dimethoxyphenyI)su!fonyl]-4-(l-piperazinyl)-lH-indoie hydrochloride, 4-(l-piperazinyI)-l-(3-pyridinyIsiilfonyl)-l H-indole hydrochloride. Certain compounds of formula (J) are capable of existing in stereoisomer^ forms including diastereomers and enantiomers and the invention extends to each of these stereoisomer^ forms and to mixtures thereof including racemates. The different stereoisomer^ forms may be separated from each other by conventional methods. Any given isomer may be obtained by stereospecific or asymmetric synthesis. The invention also extends to any tautomeric forms and mixtures thereof. The compounds of the formula (I) can form acid addition salts with acids such as conventional pharmaceutical^ acceptable acids, for example maleic, hydrochloric, hydrobromic, phosphoric, acetic, fumaric, salicylic, citric, lactic, mandelic, tartaric and methanesulfomc. Compounds of formula (I) may also form solvates such as hydrates and the invention also extends to these forms. When referred to herein, it is understood that the term "'compound of formula ([) : The compounds according to formula (I) can conveniently be administered in a pharmaceutical composition containing the compound in combination with pharmacologically and pharmaceutical!}' acceptable carriers. Such pharmaceutical compositions can be prepared by methods and contain carriers or excipients which are well known in the art. A generally recognized compendium of such melhods and ingredients is Remington's Pharmaceutical Sciences by E.W. Martin (MarkPubl. Co., 15lh Ed., 1975). The compounds and compositions can be administered orally, parenterally (for example, by intravenous, intraperitoneal or intramuscular injection), transdermally, or rectally. For oral therapeutic administration, the active compound may be combined with one or more excipients and used in the form of digestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. Such compositions and preparations should contain at least 0.1% of active compound. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2 lo about 60% of the weight of a given unit dosage form. The amount of active compound in such therapeutically useful compositions is such that ait effective dosage level v,'i![ be obtained. The tablets, troches, pills, capsules, and the like may also contain the following: binders such as gum tragacanth, acacia, com starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as com starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such x. sucrose, fiiictose, lactose or aspartame 01 .1 flavoring agent such as pcppenninL oil of wintergreen, or cherry flavoring may be added- When the unil dosage form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier, such as a vegetable oil or a polyethylene glycol. Various other materials may be present as coatings or to otherwise modify the physical form of the solid unit dosage form. For instance, tablets, pills, or capsules may be coated with gelatin, wax, shellac or sugar and the like. A syrup or elixir may contain the active compound, sucrose or fructose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavoring such as cherry or orange flavor. Of course, any material used in preparing any unit dosage form should be pharmaceutically acceptable and substantially non-toxic in the amounts employed, hi addition, the active compound may be incorporated into sustained-re lease preparations and devices. The compounds or compositions can also be administered intravenously, or intraperitoneally by infusion or injection. Solutions of the active compound or its salts can be prepared in water, optionally mixed with a nontoxic surfactant. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, triacetin, and mixtures thereof and in oils. Useful dosages of the compounds of formula I can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known to the art; for example, see U.S. Pat. No. 4,938,949. The compound can be administered in unit dosage form; for example, containing about 0.05 mg to about 500 mg, conveniently about 0.1 nig to about 250 mg, most conveniently, about 1 mg £0 about ] 50 mg of active ingredient per unit dosage form. The desired dose may be presented in a single dose or as divided doses administered at appropriate intervals. The compositions can be administered orally, sublingually, transdermally, or parenterally at dose levels of about 0.01 to about 150 mg/kg, preferably about 0.1 to about 50 mg/kg, and more preferably about-0.1 to about 30 mg/kg of mammal body weight. TABLE I Compounds prepared according to synthetic schemes I or 2. All compounds in Table I are hydrochlorides salts. General synthetic schemes Scheme 1: (i) NaH, THF, TBDMSC1 or TIPSC1 in CH;CL2; (it) X = Br. t-Bu3P, Pd(OAc);, Diamine of choice, NaOt-Bu, xylene; (iii) BmNF IM, THF or NaF, Ethyl Acetate; (iv) Ar-SO:CI, Py or NaOH or NaH CH2Ch; (v) HCl in ether. Scheme 2: (i) (CF3SO:hO, EtjN, CHzCh; (ii) Ar-S02Cl, Py or NaOH or NaH CH2C1:; (iii)X = Br: t-Bu^P, Pd(OAc):, Diamine of choice, Na-Ot-Bu, xylene; (iv) HCi in ether. The assigned structures were confirmed by standard spectroscopical methods and elemental analysis and/or high resolution MS. NMR spectra were obtained on Bntker 500 MHz or JEOL 270 MHz spectrometers at 25°C, and the chemical shift values are reported as parts per million (5). MS spectra were acquired on a 2690 Separation Module (Waters) with a Platform LCZ ' (Micromass). Flash chromatography was performed on Silica gel 60 (Merck) or LiChroprep RP-18 (Merck). HPLC analysis were accomplished on a HP Seriesl 100, with a GROM-SIL 100 ODS-0 AB column, 4.6x50mm. The HPLC purifications were performed on preparalive HPLC/ Mass system using YMC Combi prep ODS-AQ ' column, 56x20 mm, Gilson pumps, Dynamax UV-I detector and Finnigan Mass detector. The used eluents were H2O and CHiCN, both with 0.1% TFA. The purity of the compounds was determined by HPLC. Elemental analysis was performed at Structural Chemistry Department, Biovitrum AB, Stockholm. Melting points, when given, were obtained on a Biichi or a Gallenkamp melting point apparatus and are uncorrected. General Synthetic Methods Method J: Buchwald coupling between aryltriflates or arylahalides and amines To a solution of the aryitriflate (1 equiv.) in xylene are added, under N2 flush, Pd(OAc)2 (0.6 equiv.), (^>2,2'-bis(diphenyiphosphino)-l,r-binaphthyl (BINAP) (0.1 equiv.) and Cs;C03 (3 equiv.), followed by amine (2 equiv.). The mixtures are heated to 100 °C-120 °C under stirring (TLC monitoring). Purification by flash chromatography [SiOn, CHCb toMeOH:CHCl3:aq NH3 (10:90: 0.4%)] afforded the final compounds. The final compounds are converted into their hydrochloride salts by dissolving the free bases in methanol and diethyl ether (1:9) followed by the addition of HC1 in diethyl ether. Method 2: Buchwald coupling between arylhalides and amines To a mixture of 4-bromoindoles (1 equiv), /-B113P (0.05 equiv.) or2-(dicyclohexylphosphino)biphenyl (0.05 equiv.), and Pd (OAc)i ( 0.02 equiv.) in xylene are added amines (2.S equiv.) and NaO/-Bu (2.8 equiv.). The reactions are heated at 120 °C foi"4h, filtered through celite and the solvent is removed. The crude mixtures are purified by column chromatography (SiO;, CH;CWheptane 1:4) to yield final compounds. The final compounds are converted in their hydrochloride salts according to the same procedure as described in Method 1. Method 3: Sulfonylation in the presence of NaOH Arylsulfonyl chlorides (0.75 mmol) arc added to a cold (0°C) solution of indole derivales (0.5 mmol), grounded NaOH (3 mmol) and tetrabutyl ammonium hydrogen sulfate (0.05 mmol) in CH2Ch (3 mL). I lie mixtures are shaken for 30 min at 0°C and 30 min at room temperature. Each mixture is then filtered through a bed of hydromatrix (Varian; 3 cm) and silica gel (0.5 cm). The system is washed with CH2C1; (2 x 3 mL) and the solvent is evaporated in vacuum. The resulting residues (Final products as free base) are dissolved in CH2CL (3 mL) and HCI in ether is added (2 mL) and shaken for 2 h at room temperature. The resulting precipitates are collected by filtration to give the Final compounds as hydrochloride salts. The purity of the compounds is analyzed by LC and eventually purified by LC/MS if required. Method 4: Sutfonylation in the presence of NaH Sulfonylchlorides (1.5 equiv.) are added to indoles derivatives (lequiv.) and NaH 60% dispersion in oil (2 equiv.) in CH^CL containing DMF (1%). After 1 h at room temperature the reactions are quenched with water, filtered and the solvent is removed. Purification by column chromatography (SiO:, CH:Cb:MeOH 9:1:0.4 % NH3) gave the final compounds. The final compounds are transformed into their hydrochloride salts by the procedure described in Method 1. Method 5: Sulfonylatioii of sodium salt of 4-(4-?-butyloxycarbonyl)-piperazinyl-indole (stock solution A). NaH (163 mg, 6.5 mmol) is added to a solution of 4-(4-/-butyloxycarbonyI)-piperazinyI-indole (1.50 g, 6.50 mmol) in THF (45 mL). The reaction is stirred at room temperature for 0.5 h. The suspension is diluted to 60 mL with THF and distributed into 30 reaction vials (stock solution A), Diverse sulfonylchlorides ( 0.25 mmol) in THF (2 mL) are added to the stock solution A (2 mL). The reactions are shaken for 3 h followed by addition of MeOH(100 (.iL). Polystyrene-trisamme (PS-trisamine) is added to the mixtures and the reactions are agitated at room temperature over night. The mixtures are filtered through a short silica column and the volatiles are removed. The crude products are dissolved in MeOH (2 mL) followed by addition of HCl/ether 2 M (4 mL). After 0.5 h the sample was centrifugated and the supernatant was decanted after 0.5 hrs. The remaining solid was washed with (ether) and dried //; vacuo to afford the hydrochloride salts. EXAMPLE I (Intermediate) 4-Bromo-I-{tri-isopropylsilyl}-lH-indole (Scheme 1) The NaH 60% dispersion in oil (0.94 g, 23.4 mmol) was added to a solution of 4- ' bromoindole(3.07g, 15.6 mmol) and Iriisopropylsilyl chloride (3.62 g, IS.8 mmol) in CHiCb (50 mL) and DMF (2 mL). The reaction was stirred at room temperature for 1 h and quenched with water. The insoluble material was filtered off and the solvent was removed. Purification by column chromatography (SiOz, CHiCN/heptane 1:4) yielded 3.44 g (63%) of the title compound: 'H NMR (CDCI3) 6 7.42-6.63 (m, 5H), 1.66 (sept, J = S Hz, 3H), 1.10 (d, J= 8 Hz, 1SH; MS (ESI) 354.4 (M + H)4; Purity (HPLC) >95%. EXAMPLE 2 (Intermediate) N-tert-Butyl-trimethylsilyl-4-chloroindole (Scheme 1) 4-ChtoroindoIe (131.1 g, 0.871 mol) was dissolved in dry THF (0.5 L). The solution was chilled to 0 °C (ice bath, stirring). t-BuOK (97.6 g, 0.871 mol) was added in one portion and the stirring was continued for additional 5 minutes. Tert-butyldimerhylchlorosilane (131.3 g, 0.S71 mol) was added portionwise over 10 min with a good stirring. The reaction is exothermic. After 30 minutes the reaction was quenched with water (20 ml) and pH was adjusted to 8-9 and extracted with ethyl acetate (3 x 50 mL). The organic phases were dried (MgSOJ, filtered and the volatiles were eliminate by vacuum. The residue was triturated and crystallized from heptane to yield 1S1 g (78%) of the title compound. ] H NMR (CDCI3) 5 7.45 (dd, J = 7.9 Hz, J = 0.8 Hz, 1H), 7.25 (d, J = 3.0 Hz, 1H), 7.1S-7.07 (m, 2H), 6.77 (d, 1H), 0.96 (s, 9H), 0.62(s,6H); I3cNMR(CDCl3) 141.S; 131.7; 130.3; 125.9; 122.0; 119.7; 112.5; 103.5; 26.3; 19.5;-3.9; MS (ESI) 266.1(M + H). EXAMPLE 3 (Intermediate) 4-(4-Methy)-]-Piperazinyl)-]-(triisopropylsilyl)-lH-indole (Scheme 1) The compound was prepared according to Method 2 from 4-bromo-l-(triisopropylsilyl)indole (0.090 g, 0.255 mmol), /-Bu3P (3.6 mg, 0.014 mmol), and Pd (OAc): (1 mg, 0.0036 mmol) in xylene (3 mL) and 4-methyl-l-piperazine (0.135 g, 0.73 mmol) and NaOf-Bu (69 mg, 0.72 mmol). The crude was purified by column chromatography (SiO;, Cf-LCMieptane 1:4) to yield 90 mg (S4%) of pure material: 'H NMR (CD3OD) 6 7.19-6.56 (m, 5H), 3.3 N3.25 (m, 4HJ, 2.71-2.63 (m, 4H), 2.36 (s, 3H), 1.76 (sept, 7=8 Hz, 3H), 1.11 (d,./=3Hz, 1SH); MS (ESI) 372.5 (M + H)+; Purity (HPLC)>95%. EXAMPLE 4 (Intermediate) N-tert-ButyldirnethylsilyI-4-(4-Boc-piperazinyl)-indole (Scheme 1) The compound was prepared according to Method 2 from N-tert-butyldimethylsilyl -4-cViioromtiote (\00 g. 2>76 mmol, 1 equiv.), tert-buty\ \-piperazmecarboxylate {84 g, 451 mmol), Palladium(II) acetate (1.26 g., 5.62 mmol, 2%), 2-(dicyclohexylphosphino)-biphenyl (3.95 g.. 11.28 mmol, 4 mol %), tert-BuONa (50 g, 520 mmol, 1.4equiv.) in toluene. The solution was cooled to room temperature and KH^POa (150 mL, 13 % aqueous solution) was added and pH was adjusted (pH = 8-9 ) followed by extraction with toluene (2 x 100 mL), dried (MgSOj) and evaporated. The residue was crystallized from heptane to yield 124.4 g (79.6%). *H NMR (CDCI3) 5 7.20 (d,J= 8.4 Hz, 1H), 7.13 (d, .7=3.2 Hz, IH), 7.06 (t: 1H), 6.60-6.57 (m, 2H), 3.65 (t, 4H), 3.16 (t, 4H), 1.48 (s,9H), 0.91 (s, 9H), 0-5S (s: 6H); 13C NMR (CDCI3) 5 155.0; 145.5, 142.2, 129.9; 124.9; 122.0; 109.3; 107.2: 102.9; 79.8; 77.3; 51.5; 28.5; 26.4; 19.5; -3.8; MS (ESI)416.4(M+H). EXAMPLE 5 (Intermediate) 4-{4-Boc-piperazinyl)-indoIe (Scheme 1) A mixture of N-tert-butyIdimethyIsiiyl-4-(4-tert-buty]oxyIcarbonate-piperazinyl)-indole (4) (116.9 g., 2S1 mmol), NaF (30 g., 714 mmol), AcOEt (440 g), water (200 mL) and BU4NSO4 (2 g, 6 mmol) was heated under powerful stirring at 50-60uC under Ni for 2 h. The organic phase was separated and the water phase was extracted once more by AcOEt (100 mL). The organic phases were dried (MgS04), evaporated and co-evaporated with ethanol. The residue was crystallized from ethenhexane (1:3) to yield 81.0 g (95.6%) of the title compound. ' H NMR (CDCI3) 5 8.59 (bs, 1H); 7.12-7.02 (m, 3H), 6.53 (d, J = 6.9 Hz, 1H). 753 (t, 1H). 3.69 (t, 4H), 3 A9 (t, 4H), 1.53 (s. 9H); '3CNMR(CDCI3)6 155.1; 145-5; 137.1; 123.2; 122.6; 121.4; 106.9; 106.5; I00.S; 80.0; 77.*; 51.4; 28.6; MS (ESI) 302.2 (M + H). EXAMPLE 6 (Intermediate) ■ 4-(4-MetIiyl-l-piperazinyl)-lH-indoIe (Scheme 1) A mixture of 4-()-metliyl-l-piperaziny])-l-(triisopropylsilyl)-lH-indole (] 10 mg, 0.296 mmol) and Bu4NF 1M in THF (1 mL) was stirred at room temperature for ! h. A mixture of CHiCN/heptane !:| (10 mL) was added followed by filtration through silica The product was purified by column chromatography (SiOj, CtLCli'. MeOH 9:1: 0.4% NH3) to yield 60 mg (94 %) of the title product: 'H NMR (CD^OD) § 7.11-6.41 (m, 5H), 3.30-3.23 (m, 4H), 2.71-2.66 (m, 4H), 2.37 (s, 3H); MS (ESI) 216.4 (M + H)+; Purity (HPLC) >95%. EXAMPLE 7 l-Phenyisulfonyl-4-piperazinylindole dihydrochloride The title compound was prepared from 4-boc-piperazinyI-indole and phenylsulfonylchlonde according to Method 3: 'H NMR (DMSO-d6) 5 9.64 (brs, 2H), 7.98-7.94 (m, 4H), 7.80-7.77 (m, 1H), 7.70-7.65 {m, 1H), 7.63-7.55 (m, 3H), 7.27-7.22 (m, 1H), 6.95 (d, J = 3.76 Hz, 1H), 6.81-6.77 (m, 1H), 3-31-3.20 (m, 4H); UC NMR (DMSO-do) 5 144.79, 137.02, 135.22, 134.62, 129.82, 126.65, 125.63, 125.54, 123.49, 111.15, 107.87, 107.76,47.81,42.86. Anal. (C^H^N^S 2HCI ' 0.5 H20) C, H, N- EX .AMPLE 8 I-)(2,5-D]"metho\yplienyl)sulfony[)-4-(l-pipcrazinyl)-1H-indole hydrochloride (Scheme, 1) The title compound was prepared from 4-(4-boc-piperazinyl)-indoIe and 2,5-dimethoxyphenyl)sulfonyl chloride according to Method 3: 'H NMR (500 MHz, DMS(M0S8.95(br, 1 H), 7.71 (d,J=5Hz, 1 H), 7.52 (d, 7= 5 Hz, 1 H), 7.38 (d,J = 8 Hz, I H), 7.27 (d, 7=8 Hz, 1 H), 7.14 (l, J= 8 Hz, 1 H), 7.13 (d,J=SHz, 1 H), 6.86 (d,J=5Hz, i H).6.77(d,J=SHz, 1 H), 3.SI (s, 3 H), 3.64 (s, 3 H), 3.40-3.20 (m. 8 H); MS (ESI+) for miz 402 (M+H)+. EXAMPLE 9 1-{Mesitylsulfonyl)-4-(l-pipera2iny])-IH-indole hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyI)-indole and mesilylsulfonylchloride according to Method 3: 'H NMR (270 MHz, DMSO-d6) 5 9.10 (br, 1 H),7.71 (d,7=5Hz, t H), 7.40-7.20 (m, 3 H), 7.00-6.S0 (m. 2 H), 6.51 (d,7=S Hz, 1 H), 3.30-3.20 (m, S HI. 2.41 (s. 6 H), 2.27 (s, 3 U); MS (ESI!) for m/z 384 (M+H)+- EXAMPLE10 l-(l-NaphthyisuIfonyl)-4-(l-pipera2inyl)-IH-indoIe hydrochloride (Scheme 1) The title compound was prepared according 4-(4-boc-piperazinyl)-indole and naphthylsiilfonylchloride according to Method 3: 'H NMR (270 MHz, DMSO-rfs) 5 9.03 (br, 1 H), 8.63 (d, 7= 8 Hz, 1 H), 8.43 (d, 7 = 8 Hz, 1 H), S.34 (d, 7 = 8 Hz, 1 H), S.15-S.05 (m, 2H), 7,80-7-65 (m, 3 H)5 7.41 (d,7=8Hz, 1 H), 7.1S (t, J= 8 Hz, I H), 6.93 (d, 7=5 Hz, 1 H), 6.74 (d, 7 = 8 Hz, 1 H), 3.30-3.20 (m, S H); MS (ESI+) for m/z 392 (M+H)+. EXAMPLE 11 N,N-Dimethyl-5-{[4-(I-piperazinyl)-lH-indol-l-yIJsulfonyl}-l-naphthalenamine hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperaziiiyl)-indole and 5-N3N-dimetliyl-naphthalenamine-1 -sulfonylchJoride according lo Method 3: !H NMR (270 MHz,DMSO-rf6)5 9.25(br, 1H), 8.63 (d, 7 = 8 Hz, 1 H), S.4I (d,7=8 Hz, 1 H), 8.29 (d,7=SHz. 1 H), S.12(m, 2 H), 7.S0-7.65 (m, 3 H), 7.41 (d, 7=8 Hz, 1 H), 7.18(1,7 = ■ SHz. 1 H), 6.93 (d, 7= 5 Hz, 1 H), 6.74 (d, 7-8 Hz, ! H), 3.30-3.20 (m, 3 H), 2.82 (m, 6 H); MS (ESI+) for mJz 435 (M+Hf. EXAMPLE 12 J-|(4-Propoxyphenyl)sulfonyl|-4-(]-pipera2inyl)-JH-indole hydrochloride (Scheme 1) The title compound was prepared according from 4-(4-boc-piperazinyl)-indole and 4-propoxyphenylsylfonyl chloride according Jo Method 3: *H NMR (270 MHz, DMSO-d6) S 9.03 (br, 1 H), 7.89 (d, J= 8 Hz, 2 H), 7.78 (d, J = 5 Hz, 1 H), 7.61 (d, J= 8 Hz, 1 H), 7.25 (t, J= 8 Hz, 1 H), 7.07 (d, /= 8 Hz, 2 H), 6.93 (d, J= 5 Hz, I H), 6.67 (d, J= 8 Hz; I H), 4.01 (t, J = 7 Hz, 2 H), 3.28 (m, 8 H), 1.66 (m, 2 H), L .38 (m, 2 H), 0,88 (t, J = 7 Hz, 2 H). MS (ESI+) for m/z 414 (M+H)+. EXAMPLE 13 l-[(2,5-Diciiloro-3-thienyl)sulfonyl]-4-(l-piperazinyl)-]H-indole hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 2,5-dichloro-3- thienylsulfonyl chloride according to Method 3-. 'H NMR (270 MHz, DMSO-ffc) 5 9.24 (br, 1 H),7.78(d,J=5Hz, 1 H), 7.72 (s, \ H), 7.57 (d,J= S Hz, 1 H), 7.29 (t, J= % Hz, 1H), 7.01(d,7=5Hz, 1 H), 6.86 (d,J= 8 Hz, 1 H),3.31 (m, 8 H). MS (ESI+) for m/r 416 (M+H)+. EXAMPLE 14 l-[(4-Methoxyphenyl)sulfonyI]-4-(l-piperazinyI)-l H-indole hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperaziny!)-indole and 4- methoxyphenylsulfonyl chloride according to Method 3: 'H NMR (270 MHz, DMSO- ^)5 9.07(br, I H), 7.90 (d,/= 8 Hz, 2 H), 7.78 (d, J= 5 Hz, 1 H), 7.61 (d,y= S Hz, 1 H), 7.25(t,J=8Hz, 1 H), 7.09 (d, J= 8 Hz, 2 H), 6.92 (d, 7= 5 Hz, 1 H), 6.6S (d, J= 8 Hz, 1 H), 3.79 (s, 3H), 3.24 (m, 8 H); MS (£SI+) form/r371 (M+H)+. EXAMPLE 15 l-|(2,4-Difluorophenyl)sulfoiiyl|-4-(l-pipera2myl)-lH-inclole hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 2,4-di- fluorophenylsulfonylchloride according to Method 3: 'H NMR (270 MHz, DMSO-d6) 5 9.41 (br, 1 H), 8.24 (m, 1 H), 7.75 (m, 1 H), 7.58 (m, 1 H), 7.47 -7.33 (m, 2 H), 7.23 (t, •7=8 Hz, 1 H), 6.99 (d, J= 5 Hz, 1 H), 6.70 (d,y=8 Hz, 1 H), 3.25 (in, 8 H). MS (ESI+) for m/z 378 (M+H)+. EXAMPLE 16 l-(II,r-Biphenyl]-4-yI-sulfony])-4-(l-piperazinyl)~IH-indole hydrochloride (Scheme 1) The title compound was prepared from 4-{4-boc-piperazinyl)-indole and 1,1 '-biphenyl- 4-ylsulfoayl chloride according to Method 3: 'H NM& (270 MHz, DMSO-rffi) S 9.26 (br, 1 H), 8.04 (m, 2 H), 7,88 (m, 3 H), 7.67 (m, 3 H), 7.46 (m, 3 H), 7.27 (t, J= S Hz, 1 H), 6.96(d,y=5Hz, 1 H), 6.S0 (d, J= 8 Hz, 1 H), 3.25 (m, 8 H); MS (ESI+) (ox m/z 41S(M+H)+. EXAMPLE 17 I -|(3,4-Dimethoxyphenyl)sulfonyI]-4-(l-piperazinyl)-] H-indole hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperaziny))-indole and 3,4-dimethosyphenylsulfonyl chloride according to Method 3: !H MMR (270 MHz, DMSO- ;M+H)+. EXAMPLE IS 5-Methyl-2-methoxyl-{|4-(l-piperazinyl)-lH-indol-l-yl|sulfony!}pheny! ether hydrochloride (Scheme I) The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 5-methyl-2-methoxyphenylsulfonyl chloride according to Method 3: [H NMR (270 MHz, DMSO-rf„) 5 9.45 (br, 1 H), 7.92 (d,J= 8 Hz, 1 H), 7.70 (d,J= 5 Hz, 1 H), 7.30 (d, J= 8 Hz, 1 H), 7.13(t,./= 8 Hz, 1 H), 7.01-6.92 (m,2H), 6.83 (d, 7=5 Hz, 1 H): 6.73 (d, J= 8 Hz, 1 H), 3.70 (s, 3 H), 3.26 (m, 8 H), 3.32 (s, 3 H); MS (ESI+) for m/z 386 (M+H)"EXAMPLE 19 l-[(2,5-DichIorophenyl)suIfonyl|-4-(l-piperazinyl)-lH-indole hydrochloride ' (Scheme 1) The title compound was prepared according from 4-(4-boc-piperazinyl)-indole and 2,5-dichlorophenylsulfonyl chloride according to Method 3: lH NMjR (270 MHz, DMSO-d6) S 9.09 (br, 1 H), 8.25 (d, J= 3 Hz, 1 H), 7.91-7.81 (m, 2H), 7.72 (d,J= 8 Hz, 1 H), 7.36 (d, J = 8 Hz, 1 H), 7.23 (t, J= 8 Hz, 1 H), 6.98 (d, J= 3 Hz, 1 H), 6.82 (d, J= 8 Hz, 1 H), 3.26 (m, 8 H). EXAMPLE 20 l-[(5-Chloro-l,3-dimethyl-lH-pyrazol-4-yl)su!fonyl|-4-(l-piperazinyl)-lH-indole hydrochloride (Scheme 1) The title compound was prepared from 4~(4-boc-piperazinyI)-indoie and 5-chloro-l,3-dimethyl-lH-pyra2ol-4yl-sulfonyl chloride according to Method 3: (H NMR (270 MHz, DMSO-4s)S9.17(br, 1 H), 7.78 (d, J= 3 Hz, 1 H), 7.49 (d, 7= 8 Hz, 1 H). 7.28 (t, 7 = 8 Hz, 1 H),6.93(d,J=3 Hz. 1 H), 6.87 (d,J= 8 Hz, 1 H), 3.72 (s, 3H), 3.2S (m, 8 H), 2.34 (s, 3H); MS (ES1+) for m/z 394 (M+H)+ EXAMPLE 21 l-[(3-Chloro-2-methylphenyI)sulfonyl|-4-(l-piperazinyl)-IH-indole hydrochloride {Scheme I) The compound was prepared from 4-{4-boc-piperaziny!)-indole and 3-chloro-2-methoxylphenylsulfonyl chloride according to Method 3: 'H NMR (270 MHz, DMSO-rf«s) 5 9.21 (br, IH), 7.89(d,J=3Hz, 1 H), 7.82 {t,J= 8 Hz, 1 H), 7.51 (t, J=Z Hz, 1 H), 7.19 (d; .7=8 Hz, 1 H),7.10(t,y=8Hz, 1H), 7.01 (d, .7=3 Hz, 1H),6.SI (d,y=S Hz, 1 H), 3.29 (m, 8 H), 2.54 (s, 3 H), MS (ES1+) for m/i 390 (M+H)EXAMPLE 22 2-Chloro-5-(4-{|4-(l-piperazinyl)-lH-indol-l-yl]suIfonyl}phenoxy)benzonitrile hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 2-chloro-5-[(4-(piperazinyl)-lH-indol-l-yl]-sulfonyl chloride according to Method 3: 'H NMR (270 MHz, DMSO-rfs) 6 9.20 (br, 1 H), 8,06 (d,/= S Hz, 2 H), 7-81 (d,y=3Hz,l H), 7.75-7.55 (m, 3 H), 7.30 - 7.15 (m, 4 H), 6.97 (d, J= 3 Hz, 1 H), 6.82 (d, J= 8 Hz, 1 H), 3.27 (m, 8 H); MS (ESL+) for m/z 493 (M)\ 495. EXAMPLE 23 4-Bromo-2-{[4-(J-piperazinyl)-lH-indol-l-yl]sulfonyl}pheny] methyl ether hydrochloride (Scheme 1) The title compound was prepared from 4-(4-bQc-piperazmyl)-ind.ole and 4-bromo-2-phenylmemylethersulfonyl chloride according to Method 3: lH NMR (270 MHz, DMSO-rffl) 8 9.40 (br, 1 H), 8.12 (d,/=3 Hz. 1 H), 7.88 (d, J= 8 Hz, 1 H), 7.72 (d, 7 = 5 Hz, 1 H), 7.37 (d, 7= 8 Hz, I H), 7.25 - 7.10 (m, 2 H)„ 6.89 (d,J= 3 Hz, 1 H), 6.78 (d,7=SHz, 1 H), 3.71 (s,3H), 3.29 (m, 8 H); MS (ESI+) for m/z 450 (M)+, 452. EXAMPLE 24 4-(l-PiperazinyI)-l-(3-pyridinylsulfonyl)-lH-indole hydrochloride {Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 3-pyndinylsulfony! chloride according to Method 3: 'H NMR. (270 MHz, DMSO-fW 5 9.37 (br, 1 HJ.9.IS(d,y=3Hz, 1 H), 8.86 (J, J= 5 Hz, I HJ, 8.39 (d,7=8 Hz, 1 H), 7.85 (d, 7=3 Hz, I H), 7.70-7.60 (m, 2 H), 7.27 ((,./= S Hz, 1 H), 7.00 (d, J= 3 Hz, 1 H), 6.82 (d, 7=8 Hz, 1 H), 3.24 (m, 8 H); MS (ESI+) forw/z 343 (M+H)*. EXAMPLE 25 7-{[4-(l-Piperazinyl)-lH-mdol-l-yl]suIfonyl}-2-(trifluoroacetyl)-l)2,3,4-tetrahydroisoquinoline hydrochloride (Scheme I) The title compound was prepared from 4-(4-boc-piperazinyI)-indole and 2-(trifluoroacetyl)-l,2,3,4-tetrahydroisoquinoIinsulfonyl Ghloride according to Method 3: 'H NMR (500 MHz, DMSO-rf6) The experiment was done at 100°C 5 9.25 (br, 1 H), 7.94 (br, 1 H), 7.75 (d, 7=8 Hz, 1 H), 7.71 (d, .7=3 Hz, 1 H), 7.63 (d, 7= 8 Hz, 1 H), 7.41 (d,7=SHz, 1H), 7.26(t,7=8Hz, 1 H), 6.90 (d, 7= 3 Hz, 1 H),6.81 (d,7=8 Hz, 1 H), 4.80 (s, 2 H), 3.79 (m, 2 H), 3.35 - 3.25 (m, 8 H), 2.97 (m, 2 H); MS (ESI+) for mh 493 (M+H)+. EXAMPLE 26 Methyl 2-{[4-(1-piperazinyl)-lH-indol-l-yljsulfonyl}phenyl sulfone hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperaziny!)-indole and 2-methylsulfonyl-phenytsulfonyl chloride according to Method 3: lH NMR (270 MHz, DMSCWe) 6 9.22 (br, I H), 8.29 (d,7= 8 Hz, 1 H), 7.99 (t, 7- S Hz, 1 H), 7.90-7.80 (m, 2 H), 7.43 (d, 7 = S Hz, 1 H), 7.30 -7.15 (m, 2 H), 7.04 (d, 7= 3 Hz, 1 H), 6.85 (d, 7= 8 Hz, 1 H), 3.56 (s, 3 H), 3.29 (m, S H); MS (ESI+) for m/z 420 (M+H)+ EXAMPLE 27 ]-|(4-fluorophenyl)sulfonyl|-4-(l-piperazinyl)-IH-indole hydrochloride (Scheme 1) The title compound was prepared from 4-(4-boc-piperazinyi)-indole and 2-methylsulfonyi-phenylstilfonyl chloride according to Method 4 yield the hydrochloride (yield 70%), HPLC purity >95%; 'H NMR (DMSO-r/tf) 5 3.26 (bs, 8H), 6.80 (bs, 1H), 6.95 (bs, 1H), 7.26 (bs, IH), 7.61 (app t, 2H), 7.S0 (bs, lH),S.06(bs, lH),9.30(bs, IH); IJCNMR(DMSO-f/6)§ 165.20, 144.94, 135.14, 133.31, 130.06 (2C), 125.62 (2C), 123.50, 117.25, 117.06,111.15, 107.92, 107.71, 47.82 (2C), 42.98 (2C); MS (posES-FIA) m/z 360 (M+H). EXAMPLE 28 l-|(5-chIoro-3-methyl-3-benzothien-2-yl)su[fonyl]-4-(]-piperazinyl)-]H-indole hydrochloride (Scheme 1) The title compound was prepared 4-(4-boc-piperazinyl)-indoIe and l-[(5-chloro-3-methyl-l-ben.zothien-2-yl)sulfonyl chloride according to Method 4 to afford the hydrochloride salt (yield 45%), HPLC purity >95%; 'H NMR (DUSO-dS) 8 2.65 (s, 3H), 3.26 (bs, 8H), 6.S2 (app d, IH), 7.00 (appd, IH), 7.28 (app t, IH), 7.60 (app dd, 2H), 7.87 (app d, IH), 8.08-8.12 (m, 2H); l3C NMR (DMSO-rf6) 5 145.05, 139.82, 139.35, 137.46, 135,14, 133.31, 130.96, 128.70 (2C), 125.62, 124.89, 124.12, 123.52, 111.42, 107.91, 107.71, 47.87 (2C), 43.03 (2C), 12.27; MS (posES-FIA) m/z 446 (M+H). EXAMPLE 29 4-(4-Methyl-l-piperazinyl)-l-(4-methylbenzenesulfonyl)-lH-indole hydrochloride (Scheme 1) The title compound was prepared 4-(4-methyl-l-piperazinyl)-lH-indole and p-methylbenzenesulfonyl chloride according to Method 4 (45 %); !H NMR(CD3OD) 5 7.S1-6.77 (m, 9H), 3.62-3.02 (m, 8H), 2.98 (s, 3H), 2.34 (s, 3H); MS (ESI) 370.5 (M + H)+; Purity (HPLC) >95%. EXAMPLE (Intermediate) 30 Synthesis of 4-(trinuoromethyIsuIfonyloxy)indolc (Scheme 2) EhN(l.6mL, 11.3 mmol) was added to a solution of 4-hydroxylindole (l.Og, 7.5 mmol) in CH^Cb (20 mL). The reaction was cooled (ice bath) followed by the careful addition of a solution N-pheny[-bis(trif]uoromethanesulfonamide) (2.6$, 7.5 mmol) in CHiCk The reaction was washed with aqueous IGCOj after 10 minutes, dried (K;C03) and filtered. The volatiles were eliminated by vacuum to give 2.9 g of a light brown oil that was purified by flash chromatography (SiCh, CHCb)- This gave 2.47g (62%) of the title product as a light orange oil. Purity according to GC analysis was 92%. 'H NMR (MeOH-d3):6 7.45(d, IH),7.35(d, 1H), 7.15 ft, 1H), 7.00 (d, lH),6.50(d, 1H). EXAMPLE (Intermediate) 31 Synthesis of 4-(tr i flu or o methyls u Ifonyloxy)(N-(4-trifluoromethyl)phenylsulfonyt)indoie (Scheme 2) A solution of4-(trifluoromethylsulfonyloxy)indole (2.28 g, S.6 mmol) in CH^Cbwas added dropwise over 10 minutes to a mixture ofNaH (619 mg, 25.8 mmol prewashed with heptane) in CH:Cb (20 mL) and DMF (0.5 mL) under N?. A solution of 4-(trifluoromethyi)-benzenesulfonyl chloride (2.31 g, 9.5 mmol) in CH2CI2 (1 mL) was then added slowly at 0°C. The mixture was left at room temperature under stirring for 1 h. The reaction was then quenched carefully with water, the organic phase isolated, dried, filtered through silica and concentrated to yield 3.3 g crude product as a red oil. The product was purified by flash chromatography (SiO:, heptane to heptane/EtOAc 10:1 to yield 2.43 g (59%) of the title product as a colorless oil. HPLC analysis 100%. MS m/z =496 (M + Na+). 'H NMR (MeOH-d3): 5 8.20 (d, 2H), S.l (d, 1H), 7.85 (m, 3H), 7.45 (t, 1H), 7.30 (d, 1H), 6.85 (d, 1H). EXAMPLE 32 4-Piperazino-N-(4-trifluoromethyl)phenylsulfony[)indole hydrochloride (Scheme 2) The title compound was prepared from 4-(trifluoromethylsulfonyloxy)(N-(4-trifiiioromethyl)-phenylsulfonyl)indoIe (200 mg, 0.42 mmol) and piperazine (72 mg, 0.S4 mmol) according to Method I. Purification by flash chromatography (SiO:, CHCI3 toMeOH:CHCI3 10:90: 0.4% aq NH3) afforded to 10 mg of a yellow oil. This was dissolved in ethanol and KCl/ether was added and allowed to stir for a few hours. The solid was filtered to yield 10 mg final product as a beige solid that was further purified by preparative HPLC to give, after formation of the HCI salt, the final product (3S mg, 51 %) as an off-white solid. HPLC 97 %. MS (posEf) m/z=410 (M+H). lHNMR (CDjOD) 5 8.12 (d, 2H. J = 8.3 Hz), 7.84 (d, 2H, J = 8.3 Hz), 7.76-7.68 (m, 2H), 7.33-7.27 (m, 1H>, 6.88- 6.85 (m, 2H) 3.44-3.30 (m, 8H, partly hidden). EXAMPLE 33 4-(3-MethyIpiperazine)-(N-(4-trinuoromelliyl)phenylsuIfonyl)indole dihydrochloride (Scheme 2) The title compound was prepared from 4-(tnnuoromethylsuIfonyloxy)(N-(4-trif!uoromethyl>phenylsulfonyl)indole and rac-2-methyIpiperazine according to Method 1. Filtration through silica using CHCI3 to MeOH:CHCl3 10:90: 0.4% aq NH3 as eluent gave 48 mg of final product as a beige solid, mp 145°C (dec); 'H NMR (MeOH-d3): 5 8.10 (d, 2H), 7.85 (d, 2H), 7.75 (d, 1H), 7.65 (d, 1H), 7.30 (t, 1H), 6.S5 (m, 2H), 3.50 (m, 5H), 3.00 ft, 1H), 2.85 (t, 1H), 1.35 (d, 3H);). HPLC 94%; MS (posEI) m/z=424 (M+H). Anal. (C:oH2oF3N303S.2HCl) C,H,N,S. N calcd. 8.47, found 9.32. EXAMPLE (Intermediate) 34 4-Bromo-l-(benzenesuIfonyl)-lH-indole (Scheme 2) 4-Bromo-l-(benzenesulfonyl)-lH-indole was prepared from 4-bro mo indole and phenylsulfonylchloride according to Method 4 to afford 3.1 g (91 %) of a light purple solid: 'HNMR (CDC13) 5 7.94 (d, J = 8 Hz, 1H), 7.S9-7.84 (m, 2H), 7.62 (d, 4 Hz, 1H), 7.57-7.51 (m, 1H), 7.46-7.37 (m, 3H), 7.19-7.13 (m, 1H), 6.72 (dd, J = 1, 4 Hz, 1H); MS (ESI) 419.9+421.9 (M + H)+; Purity (HPLC) >95%. EXAMPLE (intermediate) 35 4-Bromo-l-(2-methyl-benzenesulfonyl)-lH-indole (Scheme 2) The compound was prepared from 4-bromoindole (l.02g, 5.25 mmol) ando-methylbenzenesulfonyl chloride (a 9:1 mixture of o/lho and para methyl isomers) (1.29 g, 6.78 mmol) according lo method 4. Purification by column chromatography (SiO:, CHiCkheptane) gave 1.6 g (S7 %) of the title compound which contains ca !0 % of the /?-melhyl isomer) as a light purple viscous oil: 'HNMR (CDJODJ 5 7.94-6.68 (m, 9H), 2.52 (s, 3H); MS (ESI) 352.3 (M + H)+; Purity (HPLC) >95%. EXAMPLE 36 4-(4-Methyl-l-piperazinyi)-l-(2-methyibeii2enesulfonyl)-lH-indoIe (Scheme 2) The title compound was prepared from 4-bromo-l-(2-methyl-benzenesulfonyI)-lH-indole (0.! 35 mg, 0.385 mmol) and 4-methyI-1 -piperazine (0.143 mg, 0.77 mmol) according to Method 2. The product purified by flash column chromatography (SiO?, CHzCkMeOH 9:1: 0.4% NH3) and convened into its HC1 salt to afford 15 mg (10 %): lHNMR (CD3OD) 6 7.97-6.79 (m, 9H), 3.72-3.07 (m, 8H), 3.01 (s, 3H), 2.48 (s, 3H); MS (ESI) 370.0 (M + H)+; Purity (HPLC) >95%. EXAMPLE 37 4-(4-Ethyl-l-piperazinyl)-l-(2-methyibenzenesulfonyl)-lH-indoIe (Scheme 1) The compounds was prepared from 4-bromo-3-(2-methyI-benzenesulfonyl)-lH-indo!e and 4-ethyl-l-piperazine according to Method I. The product was isolated by column chromatography (SiO?, CH2Ch:MeOH/heptane:0.4% NH3) and converted into its hydrochloride salt by addition of HCl/ether to give 8-5 mg (40%) of a white solid: lHNMR (CD3OD) 8 7.95-6.61 (m, 9H), 3.41-3.26 (m, 8H), 3.20-3.07 (m, 2H), 2.47 (s, 3H), 1.42 (t, J= 1 Hz, 3H); MS (ESI) 384.0 (M + H)+; Purity (HPLC) >95%. EXAMPLE 38 4-(l-Piperazinyl)-l-(2-methylbenzenesulfonyI)-lH-indole (Scheme 1) The title compound was prepared from 4-bromo-l-(2-methyI-benzenesulfony])-lH-indole and piperazine according to Method 1 to give 25 mg (12 %) of a whitesolid: 'HNMR (CD3OD) 5 7.91-6.79 (m, 9H), 3.49-3.30 (m, SH). 2.4S (s, 3H); MS (ESI) 356.1 (M + H)+; Purity (HPLC) >95%. EXAMPLE 39 4-{5-Aza-indolizidinyl)-l-(2-methylben2enesulfonyl)-lH-indole (Scheme 1) The title compound was prepared from 4-bromo-l-(2-methyl-benzenesulfonyl).lH-indole and 5-aza-indolizidinyl according to Method 1 to give 30 mg (13 %)ofa white solid: 'H NMR on Tree base (CDCI3) 5 7.85-7.66 (m, 9H), 3.63-3.47 (m, 1H), 3.16-2.93 (m,3H), 2.67-2.45 (m, 5H), 2.51 (s, 3H), 2.33-2.19 (m, 2H), 1.92-1.74 (m,4H), 1.52-1.44 (m. 1H); MS (ESI) 396.0 (M + H)+; Purity (HPLC) >95%. EXAMPLE 40 4-(4-Methyl-l-homopiperazinyl)-I-(2-methyIbenzenesulfonyl)-lH~indole (scheme The compounds was prepared from 4-bromo-l-(2-methyl-benzenesulfony])-lH-indoIe and 4-methyI-I-homopiperazine according Method I to give 20 mg (13%) of a white solid: ]H NMR (CD3OD) § 7.91-6.73 (m, 9H), 3.74-3.45 (m, SH), 3.00 (s, 3H), 2.47 (Sj 3H), 2.34-2.26 (m, 2H); MS (ESI) 384.0 (M + Hf; Purity (HPLC) >95%. EXAMPLE 41 4-(3-Methyl-l-piperazinyl)-l-(2-methylbenzenesulfonyI)-lH-indole (Scheme 1) The compound was prepared from 4-bromo-l-(2-methyl-benzenesulfonyl)-lH-indole and 3-methylpiperazine according to Method 1 to give 110 mg (38 %) of a white solid: 'HNlvlR (CD3OD) 5 7.92-6.82 (m, 9H), 3.64-3.39 (m, 5H), 3.12-3.03 (m, 1H), 2.92-2.83 (m, 1H), 2.47 (s, 3H), 1.40 (d,/= 7 Hz, 3H); MS (ESI) 370.0 (M + H)+; Purity (HPLC) 94 %. EXAMPLE 42 4-(c/5-3,5-Dimethyl-l-piperaziny!)-l-(2-metliyIbenzenesulfonyt)-lH-indoIe (Scheme 1) The compound was prepared according from 4-bromo-l-(2-methyl-benzenesulfonyl)-IH-indoleand w-3,5-dimethyl-[-piperazine according to Method 1 to give 10 nig (4 %) of a while solid: 'HNMR (CD:,OD) 6 7.90-6.S2 {m, 9H), 3.69-3.5S (m. 4H), 2.S3- 2.74 (m, 2H), 2.45 (s, 3H), 1.41 (d,J= 7 Hz, 6H); MS (ESI) 492.1 (M + H)*; Purity (HPLC) 95%. EXAMPLE 43 4-(4-Isopropyl-l-piperazinyl)-l-(2-methylbenzenesulfonyl)-lH-indole (Scheme 1) The compound was prepared from 4-bromo-l-(2-methy[-benzenesutfonyl)-lH-indole and 4-isopi'opyl-l-piperazine according to Method 1 to give 75 mg (56 %) of a white solid: lH NMR (CDjOD) 5 7.92-6.S1 (m, 9H), 3.75-3.56 (m, 5H), 3.4S-3.40 (m, 2H). 3.19-3.09 (m, 2H), 2.47 (s, 3H), 1.44 (d, J= 7 Hz, 6H); MS (ESI) 398.1 (M + H)+; Purity (HPLC) >95%. EXAMPLE 44 4-((lS,4S)-2-Metliyl-2,5-diazabicycIo|2.2.1iheptyl)-l-(2-methyIbenzenesulfonyl)-]H-indole (Scheme 1) The compound was prepared from 4-bromo-1 -(2-methyl-benzenesulfony!)-1 H-indo!e and (lS,4S)-2-methyi-2,5-diazabicyclo[2.2.1]heptane according to Method I to give 25 mg (19 %) of a white solid: 'H NMK (CD3OD) 5 7.91-6.44 (m, 9H), 4.67-4.63 (m, 1HJ, 4.35-4.33 (m, 1H), 4.09-4.07 (m, 1H), 3.99-3.95 (m, 1H), 3.72-3.70 (m, 1H), 3.21-3.17 (m, 1H), 2.95 (s, 3H), 2.33-2.31 (m, 2H); MS (ESI) 382.1 (M + H)+; Purity (HPLC) >95%. EXAMPLE 45 4-(4-Mcthyl-l-homopiperaziny!)-l-(benzenesulfonyl)-lH-indole (Scheme 1) The compound was prepared from 4-bromo-l-(benzenesLi!fonyI)-lH-indole and 4-methyl-1-homopiperazine according to Method 1 to give 4 mg (2 %) of a white solid: 'H NMR for free base (CDCI3) 5 7.86-7.! 1 (m, SH), 6.71 (d, J = 4 Hz, 1H) 6.54 (d, J = 8 Hz, 1H), 3.60-3.57 (m, 2H), 3.52-3.4S (m, 2H), 2.S1 -2.78 (m. 2H), 2.68-2.64 (m, 2H), 2.39 (s, 3HJ, 2.04-2.00 (m, 2HJ; MS (ESI) 370.1 (M + H)+; Purity (HPLC) >95%. EXAMPLE 46 4-(c/j3,5-Dime(hyl-l-piperazinyl)-I-(benzenesulfonyl)-lH-indole (Scheme 1) The title compound was prepared from 4-bromo-I-(benzenesu[fonyl)-IH-indole and cis 3,?-diinelhyl-I-pipeiazi]ie according Lo Method i to give 138 nig (52 %) of a white solid: 'HNMR (CD3OD) 5 7.93-6.S2 (m, 10 H), 3.64-3.59 (m, 4 H), 2.77-2.68 (m, 2 H), 1.36 (d, J = 6 Hz, 6 H); MS (ESI) 370.0 (M + H)+; Purity (HPLC) >95%. EXAMPLE 47 4-(4-Ethyl-l-piperazinyl)-l-(benzenesulfonyl)-lH-indole (Scheme 1) The title compound was prepared from 4-bromo-l-(benzenesulfonyl)-lH-indole and 4-ethyipiperazine according to Method 1 to afford 129 mg (48 %) of a white solid: 'H NMR (CD3OD) 5 7.94-6.81 (m, 10 H), 3.69-3.62 (m, 4 H), 2.34-3.26 (partly hidden) (m, 4 H), 3.14-3.04 (m, 2 Jfi), 1.40 (t, J = 7 Hz, 3 H); MS (ESI) 370.1 (M + H~f; Purity (HPLC) >95%. EXAMPLE 48 4-PiperazinyI-l-(4-ni(ro-benzenesuIfonyl)-lH-indoIe (Scheme 1) The title compound was prepared according to Method 5 from 4-nitrobenzenesulfonyl chloride and the sodium salt of 4-(4-/-butyIoxycarbonyl)-piperazinyl-indole (stock solution A) to give 60.3 mg (86 %) as HCI salt: !HNMR (CD:OD) 5 8.34 (d, 2 H, J = 9.0 Hz), 8.1S (d, 2 H, J = 9.0 Hz), 7.76-7.69 (m, 2 H), 7.33-7.27 (m, 1H), 6.90- 6.85 (m, 2 H) 3.44-3.30 (m, S H, partly obscured); MS (ESI) 3S6.9 (M + H)4"; Purity (HPLC) 95%. EXAMPLE 49 4-PiperazinyM-(4-bromo-benzenesiilfonyl)-lH-indole (Scheme 1) The title compound was prepared according to Method 5 from 4-bromobenzenesulfonyl chloride and the sodium salt of 4-(4-/-butyloxycarbonyl)-piperazinylindole (stock solution A) to give 40.3 mg (53 %) as HCI salt; 'HNMR. (CD;,OD) 5 7.81-7.61 (m, 6 H), 7.30-7.24 (m, 1 H), 6.S6- 6.83 +; Purity (HPLC) 98 %. EXAMPLE 50 4-Piperazinyl-l-(4-chloro-benzenesulfonyI)-lH-indole (Scheme 1) The title compound was prepared according to Method 5 from 4-chloro-benzenesulfonyI chloride and the sodium salt of 4-(4-/-butyIoxycarbonyl)-piperazinyI-indole (stock solution A) to give 42 mg (61 %) as HCI salt: 'HNMR (CD3OD) 6 7.88 (d,2H, J = 8.7 Hz), 7.72-7.63 (m, 2 H), 7.50 (d, 2H,J = 8.7 Hz), 7.30-7.24 (m, 1 H), 6.86-6.84 (m, 2 H) 3.44-3.31 (m, 8 H); MS (ESI) 375.9, 377.9 (M + H)+; Purity (HPLC) 95%. EXAMPLE 51 4-PiperazinyI-l-(£'2-phenyl-ethensulfonyl)-IH-indoIe (Scheme 1) The title compound was prepared according to Method 5 from l-(£ 2-phenyl-ethensuifonyi chloride and the sodium salt of 4-(4-/-butyloxycarbonyl)-piperazinyl-indoie (stock solution A) to give 8 mg (11 %) as HCI salt: 'HNMR (CD3OD) 6 7.78 (d, I H, J =15.4 Hz) 7.68-7.25 (m, 9 H), 7.16 (d, 1H,J= 15.4), 6.8S-6.84 (m, 2 H) 3.46-3.34 (m, 8 H); MS (ESI) 368.0 (M + H)+; Purity (HPLC) 97%. EXAMPLE 52 4-Piperazinyl-I-(3-trifluorometliyI-benzenesulfonyI)-l H-indole (Scheme 1) The title compound was prepared according to Method 5 from 3-trifluoromethyl-benzenesulfonyl chloride and the sodium salt of 4-(4-/-butyloxycarbonyl)-piperazinyI-indole (stock solution A) to give 42 mg (61 %) of a white solid: 'HNMR (CD^OD) 6 8.21-8.16 (m, 2 H) 7.96-7.93 (m, 1 H), 7.34-7,27 (m, 1 H). 6.89- 6.S5 (m, 2 H) 3.44-3.32 (m, 8 H); MS (ESI) 410.0 (M + Hj+; Purity (HPLC) 95%. EXAMPLE 53 4-Piperazinyl-l-(4-cyanobeiizenesulfonyl)-lH-indoIe {Scheme I) The title compound was prepared according to Method 5 from 4-cyanobenzenesulfonyl chloride and the sodium salt of 4-(4-/-butyloxycarbonyl)-piperazinyl-indole (stock solution A) to give 28 mg (42.%) of a white solid: MS (ESI) 367.0 (M + H)*; Purity (HPLC) 95 %. EXAMPLE 54 4-Piperazinyl-l-(4-chloro-7-chloro-2,l,3-benzoxadiazole sulfonyl)-lH-indole (Scheme !) The title compound was prepared according to Method 5 from 4-chtoro-7-chlorosuifonyl-2;l;3-benzoxadiazole sulfonylchloride and the sodium salt of 4-(4-f-butyloxycarbonyl)-piperazinyI-indole (stock solution A) to give 12 mg(16 %) of a white solid: 'HNMR (CD3OD) S 8.42 (d, 2 H, J = 7.1 Hz), 7.84-7.63 (m, 3 H), 7.27-7.21 (m, 1 H), 6.85- 6.81 (m, 2 H) 3.43-3.27 (m, 8 H, partly hidden); MS (ESI) 41 8.0 (M + H)+; Purity (HPLC) 91 %. EXAMPLE 55 4-PiperazinyI-l-(3-cyanobenzenesuIfonyl)-lH-indole (Scheme 1) The title compound was prepared according to Method 5 from 4-trifHiorom ethyl-benzenesulfonyl chloride and sodium salt of 4-(4-/-bufy!oxycarbonyl)-piperazinyl-indole (stock solution A) to give 68 mg (50 %) of a white solid: MS (ESI) 367.1 (M + H)+; Purity (HPLC) 93%. EXAMPLE 56 4-PiperazinyI-J-(4-phenoxybertzenesulfonyl)-IH-indoIe (Scheme 1) The title compound was prepared according to Method 5 from 4-phenoxybenzenesulfonyl chloride and sodium salt oF4-(4-/-butyIoxycarbonyl)-piperazinyl-indole (slock solution A) to give 68 mg (S7 %) of a while solid: "HNMR (CD3OD) 7.82-7.59 (m, 4 H), 7.76-7.34 (m. 4 H), 6.88- 6.7S (m, 6 H) 3.45-3.30 (m, 8 H); MS (ESI) 434.1 (M + H)*; Purity (HPLC) 95%. EXAMPLE 57 4-Piperazinyl-l-(4-clilorophenylmethanesulfonyl)-lH-indoIe (Scheme 1) The title compound was prepared according to Method 5 from 4-chlorophenylmcthanesulfonyl chloride and sodium salt of 4-(4-/-butyloxycarbony!)-piperazinyl-indole (stock solution A) to give 3 mg(4 %) of a white solid: 'H NMR (CD3OD) 5 7.44 (d, I H, J = 8.2 Hz) 7.24-7.18 (m, 4 H), 6.87-6.84 (m, 3 H), 6.69-6.67 (m, I H) 4.72 (s, 2 H) 3.43-3.31 (m, 8 H, partly hidden); MS (ESI) 390.0, 392.1 (M + H)4; Purity (HPLC) 91%. EXAMPLE 58 4-Piperazinyl-l-(4-methylphenytmethanesulfonyl)-l H-indole (Scheme t) The title compound was prepared according to Method 5 from 4-methylphenylmethanesulfonyl chloride and sodium salt of 4-(4-/-butyloxycarbonyl)-piperazinyi-indole (stock solution A) to give 9 mg(13 %) of a white solid: 'HNMR (CD3OD) 5 7.46 (d, 1 H, J = 8.4 Hz) 7.24-7.18 (m, 1 H), 7.06 (d, 1 H, J = 4.0 Hz) 6.95-6.S5 (m, 3 H), 6.76-6.64 (m, 3 H) 4.65 (s, 2 H) 3.47-3.35 (m, 8 H) 2.24 (s, 3 H); MS (ESI) 370.1 (M + H)+; Purity (HPLC) 95 %. EXAMPLE 59 4-Piperazinyl-I-(l,l-diphenylethanesulfonyl)-lH-indoIe (Scheme 1) The title compound was prepared according to Method 5 from 1,1-diphenylethanesulfonyl chloride and the sodium salt of 4-(4-/-butyloxycarbonyI)-piperazinyl-indole (stock solution A) to give 57 mg (71 %) of a white solid: HNMR (CD3OD)5 7.59(d, 1 H, J = 8.4 Hz), 7.31-7.25 (m, 1 H), 7.12-7.05 fm, 10 H), 6.86-6.S3 (m, 1 H) 6.50-6.48 (m, 1 H) 6.42 (t, 1 H, J = 6.6 Hz) 4.28 (d, 2 H, J = 6.6 H2) 3.47-3.32 (m, 8 H); MS (ESI) 446.1 JU EXAMPLE 60 4-Piperazinyl-l-(4-trifluoromethoxybenzenesulfony[)-lH-i'ndole (Scheme 1) The title compound was prepared according to Method 5 from 4-trifluoromethoxybenzenesulfonyl chloride and the sodium salt of 4-(4-/-butyloxycarbonyl)-piperaziny!-indole (stock solution A) to give 46 mg (60 %) of a white solid: 'HNMR (CD3OD) 5 8.07-S.04 (m, 2 H), 7.75-7.72 (m, 1 H) 7.67-7.68 (m, 1 H> 7.43-7.40 (m, 2 H), 7.32-7.20 (m, 1 H) 6.87- 6.8S (m, 2 H) 3.44-3.31 (m, 8 H, partly hidden); MS (ESI) 426.1 (M + H)+; Purity (HPLC) 93%. EXAMPLE 61 4-PiperazinyM-(5-[(benzoylamino)methyl]thiophene-2-sulfonyl)-]H-indole (Scheme 1) The title compound was prepared according to Method 5 from 5-[(benzoylamino)methyl]thiophene-2-sulfonylchloride and the sodium salt of 4-(4'f-butyloxycarbonyl)-p'perazinyl-indole (stock solution A) to give 5 mg (6 %) of a white solid: 'H NMR (CD3OD) 5 7.79-7.42 (m, 8 H), 7.30-7.24 (m, 1 H) 7.00-6.98 (m, 1 H) 6.85-6.81 (m, 2 H) 3.39-3.28 (m, 8 H, partly hidden); MS (ESI) 481.1 (M + H)4; Purity (HPLC) 91%. EXAMPLE 62 l-[(N-methyl-lH-imidazol-4-yi)sulfonylI-4-(l-piperaziny!)-lH-indole hydrochloride The compound was prepared from 4-(4-boc-piperazinyl)-indole 1-methyl-lH-imidazol-4-yi)sulfonyl chlonde according to Method 3:Yield: 74 %.'H NMR (270 MHz, DMSO-d6) 5 9.23 (br, 1 H), 8.25 (s, 1 H), 7.75 (s, 1 H), 7.61 (d, J= 3 Hz, 1 H), 7.53 (d, J= 8 Hz, I H),7.22(t,y=8Hz, 1 H), 6.86 (d, J=2 Hz, 1 H), 6.79 (d, J=8 Hz, 1 H),3-65(s 3H), 3.27 (m, S H); MS (ESI+) for w/r 346 (M+H)*. Scheme 3 (i) (iPr)iSi, NaH, dimethylformamide/dichlorometane; R5 (when it is different than K) (tBu)3P, Pd(OAch, NaOtBu; (iii) Bu4NF in THE, acetonitrile; (iv) R1 (ArSOi- as indicated in Table il), NaOH, dichlorometane. EXAMPLE 63 (Intermediate) 5-Bromo-l-triisopropyIsilyl-indole 5-BromoindoIe (3.92 g; 20 mmol) was dissolved in DCM (100 mL) and DMF (1 mL). NaH (0.8S g, 22 mmol; 60% in oil) was added to the cooled solution. After stirring for 1 5 minutes, triisopropylsilyl chloride (3.86 g, 20 mmol) was added dropwise to the reaction mixture. After 3 h, water (1 mL) was added, followed byMgS04. The mixture was filtered and concentrated arid the residue put through a silica column with hexane as eluent. The product was obtained as a pale yellow oil (5.96 g, 17 mmol, yield S5 %). 'H NMR(CDC13)5 1.13(18H,d,J=S), 1.67 (3 H, m), 6.55 (1 H, d, J=3), 7.21 (1 H, dd, J=9, 2), 7.24 (1 H, d, .1=3), 7.36 {\ H, d, J=9) and 7.74 (1 H, d, J=2). EXAMPLE 64 (Intermediate) 5-(4-Methylpiperazin-l-yl)-indole 5-Bromo-l-triisopropylsilyl-indole (5.8 g, 16,4 mmol), N-methylpiperazine (l.S g, 18 mmol), NaOt-Bu (2.2 g, 23 mmol), Pd(OAc)2 (37 mg, 0.16 mmol), P/-Bu3 (66 mg, 0.33 mmol) and xylene (30 mL) were mixed and heated to 130 QC under stirring for 5 h. The crude material was chromatographed on a silica column using DCM/MeOH 95/5 as eluent. Concentration of the main fractions left 5.6 g of an oil which was dissolved in MeCN (10 mL), 20 mLof a ! M solution of tetrabutylammonium fluoride in TKF was added and the mixture left over-night. The reaction mixture was put on a silica column and eluted with DCM/MeOH 95/5 to give the product as an oil (3 g, 9.3 mmol; yield 57 %) 'HNMR (CDCI3) 5 2.37 (3 H, s), 2.64(4 H, t, J=5), 3.19 (4 H, t, J=5), 6.44-6.4S (1 H, m), 6.95-7.00 (1 H. m), 7.16(1 H, d, J=3), 7.18 (1 H, d, J=2), 7.29 (1 H, d, J=9) and S.I2(1 H, bs). Intermediates 65-67 were prepared using the same method as for intermediate 64. EXAMPLE 65 (Intermediate) 5-(4-Isopropylpiperazin-l-yl)-indole (0.46 g, 1.9 mmol; yield 63%), !H NMR (CDC!3) 8 1.12 (6 H, d, J=7), 2.70-2.78 (5 H, m), 3.15-3.22 (4 H, m), 6.45-6.49 (I H, m), 6.97-7.01 (I H, dm), 7.14-7.19 (2 H, m), 7.30(1 H,d,J=9) and 8.05(1 H, bs). EXAMPLE 66 (Intermediate) 5-(4-Benzylpiperazin-l-yl)-indole (3.6 g, 12.4 mmol; yield 55 %), ]H NMR (CDC!3) 5 2.67 (4 H, t, J=5), 3.18 (4 H, t, J=5), 3.60 (2 H, s), 6.44-6.47 (I H, m), 6.97 (2 H, dd, J~9, 3), 7.13-7.17 (2 H, m), 7.25-7.39 (5 H,m) and 8.01 (1 H, bs). EXAMPLE 67 (Intermediate) 5-(4-Propylpiperazin-l-yl)-indole (0.54 g, 2.2 mmol; yield 24 %), 'H NMR (CDCN) & 0.94 (3 H, t, J=7), 1.53-1.62 (2 H, m), 2.37-2.43 (2 H, m), 2.65-2.73 (4 H, m), 3.17-3.22 (4 H, m), 6.45-6.48 (1 H, m), 6.96-7.00 (1 H, dm), 7.14-7.19 (2 H, m), 7.30 (1 H, d, J^9) and 8.13 (1 H, bs). EXAMPLE 68 t\-BenzenesulfonyI-5-(4-methylpiperazin-l-yl)-indole 5-(4-Methylpiperazin-l-yl)-indole (215 mg, lmmol), benzenesulfonylchloride (265 mg, 1.5 mmol) and Aliquat 336 (10 mg) were dissolved in DCM (10 mL). Aqueous NaOH [20 %, 2 mL) was added and the mixture was stirred vigorously for 6 li. The organic layer was separated, dried and concentrated to give the crude as an oil that was purified jn a silica column using DCM and MeOH as eluent. The pure fractions were :oncen(rated to give an oil (260 mg, 0.66 mmol) lH NMR (CDC13) 5 2.35 (3 H, s), 2.59 4 H, t, J=5), 3.IS (4 H, t, J=5), 6.57 (1 H, d. J=4), 6.9S-7.03 (2 H, m), 7.38-7.54 (4 H, m), 7.S2-7.90 (3 H, m); MS (posES-FIA) 355.1345 M+; Purity (HPLC chromsil C18) >98%. Examples 69-87 were prepared using the same method as for Example 1. Examples 72-87 are reported as hydrochloride salts. EXAMPLE 69 N-(4-Methylbenzenesulfony0-5-(4-methylpiperazin-l-yl)-indole (0.24 g, yield 59 %) SH NMR (CDC13) 5 2.33 (3 H, s), 2.37 (3 H, s), 2.61 (4 H, t, J=5), 3.18 (4 H, t, J=5), 6.55 (1 H, d, J=3), 6.98-7.30 (2 H, m), 7.19 (2 H, d, 7.47 (1H, d, J=4), 7.72 (2 H, d, J=9) and 7.86 (1 H, d, 3=9); MS (posES-FIA) 369.1502 M+; Purity (HPLC chromsil CI8)>98%. EXAMPLE 70 N-Benzeiiesulfonyl-5-(4-isopropylpiperazin-l-yl)-indole (0.24 g, yield 57 %), >H NMR (CDC13) 5 1.12 (6 H, d, J=7), 2.68-2.77 (5 H, m), 3.15-3.25 (4 H, m), 6.57 (1 H, d, J=5), 6.98-7.04 (2 H, m), 7.39-7.44 (2 H, m), 7.46-7.54 (1 H, m) and 7.S1-7.S9 (3 H, m); MS (posES-FIA) 383.1655 M+; Purity (HPLC chromsil C1S)>98%. EXAMPLE 71 N-(4-Methylbenzenesulfonyl)-5-(4-isopropylpiperazin-l-yl>indole (0.29 g, yield 67 %}, 'H NMR(CDCl3)o 1.11 (6 H, d, J=6), 2.33 (3 H, s), 2.67-2.7S (5 H, m), 3.15-3.25 (4 H, m), 6.54 (1 H, d, J=4), 6.97-7.03 (2 H, m), 7.19 (2 H, d, J=8), 7.46(1 H,d,J=4), 7.67-7.81 (3 H, m) and 7.86 (1 H, d, J=9); MS (posES-FLA) 397.1823 M+; Purity (HPLC chromsil CIS) >90%. EXAMPLE 72 N-(3,4-Dimetho\ybenzenesuIfonyl)-5-(4-propyIpiperazin-l-yl)-indole, hydrochloride (0.27 g, yield 67 %), 'H NMR (CDCh) 5 1.10 (3 R t, .1-7), 1.93-2.03 (2 H, ni), 3.10-3.20 (2 H, m), 3.63-3.70 (4 H, m), 3.SS (3 H, s), 3.90 (3 R s), 4.30-4.42 (2 H, m), 4.82-! 4.94 (2 H, m), 6.76 (I H, d, J=4), 6.S7-6.94 (2 R m), 7.53-7.60 (2 H, m), 7,72-7.76 (1 H, m). 7.83-7.88(1 H, m), 8.08-8.12 (I H, m), 8.16-8.20(1 R m) and 13.45(1 H, bsj; MS (posES-FIA) 443.1871 M+; Purity (HPLC chromsil C1SJ >75%. EXAMPLE 73 N-(3-FluorobenzenesuIfonyl)-5-(4-propy!piperazin-l-yl)-indole, hydrochloride (0.16 g, yield 67 %), 'H NMR (MeOH d6) 5 1.02 (3 H, t, J=7), 1.72-1.84 (2 H, m), 3,02-3.IS (4 R m), 3.19-3.26 (2 R m), 3.60-3,68 (2 H, m); 3.71-3.80 (2 R m), 6.67 (I H, d, i=4), 7.08-7.13 (1 H, m), 7.15-7.18 (] H, m), 7.30-7.37 (1 H, m), 7.46-7.54 (1 R m), 7.58-7.64 (2 R m), 7.66-7.72 (1 H, m) and 7.86-7.91 (1 R m); MS (posES-FrA) 401.1585 M+; Purity (HPLC chromsil C18) >90%. EXAMPLE 74 N-(4-Propylbenzenesulfonyl)-5-(4-rnethyIpiperazin-l-yI)-indole, hydrochloride (0.15 g, yield 38 %) 'HNMRfCDCb) 5 0.90 (3 H, t, J=7), 1.56-1.66 (2 R m), 2.60 (2 R t, J=&), 2.98 (3 R s), 3.56-3.68 (4 R m), 4.27-4.40 (2 R m), 4.64-4.74 (2 H, m), 6.74 (1 H, "d, J=3), 7.25-7.29 (2 H, m), 7.71-7.81 (4 H, m), 8.06-8.13 (2 R m) and 13.89 (1 H, bs); MS (posES-FLA) 397.1813 M*; Purity (HPLC chromsil CI8) >93%. EXAMPLE 75 N-(l-NaphtalenesuIfonyl)-5-(4-methylpiperazin-I-yl)-indole, hydrochloride (0. IS g, yield 45 %) !H NMR (CDCh) 5 2.97 (3 R s), 3.59 (4 H, t, J^l5}, 4.35-4.46 (2 R m). 4.68-4.7S (2 R m), 6.75 (1 R d, .1=3), 7.50-7.76 (4 H, m), 7.SS-7.9S (3 H, m), 8.11-8.15 (2 H, m), 8.34-8.38(1 R m), 8.62(1 R d, J=9J and 13.94(1 Rbs);MS (posES-FIA) 405.1503 M+; Purity (HPLC chromsil CIS) >90%. EXAMPLE 76 N-(Bipheny\-4-su\fony\)-5-(4-methylpipeicazm-\ -yl)-indole, hydrochloride (0.13 g, yield 30 %) !H NMR (MeOH-d6) 6 2.93 (3 H, s), 3.05-3.) 5 (2 H, m), 3.20-3.30 (2 H, m), 3.50-3.60 (2 H, in), 3.70-3.80 (2 H, m), 6.66 (1 H, d. .1=5), 7.11 (1 H, dd, J=9, 3), 7.16 (1 H, d, J=3), 7.32-7.43 (3 H, m), 7.51-7.56 (2 H, mj. 7.61 (1 H.d, J=4), 7.66-7.70 (2 H, m) and 7.8S-7.94 (3 H, m); MS (posES-FIA) 431.1662 M+; Purity (HPLC chromsil CI 8) >98%. EXAMPLE 77 N-(4-Methoxybenzenesulfonyl)-5-(4-methylpiperazin-l-yl)-indole, hydrochloride (0.17 g, yield 44 %) 'H NMR (CDC13) 5 2.9S (3 H, s), 3.55-3.68 (4 H, m), 3.82 (3 H, s), 4.30-4.45 (2 H, m), 4.66-4.76 (2 H, m), 6.72 (1 H, d, J=4), 6.93 (2 H, d, J=9), 7.71 (I H,d,J=4); 7.74-7.79(1 H, m), 7.83 (2 H, d, J=9), 8.10 (2 H, d, J=9) and 13.97 (1 H, bs); MS (posES-FIA) 385.1456 M* Purity (HPLC chromsil CIS) >95%. EXAMPLE 78 N-P^-DimethoxybenzenesuIfonyO-S-^-methylpiperazin-J-ylHndole, hydrochloride (0.13 g, yield 28 %) 'H NMR (CDC13) 5 2.9S (3 H, s), 3.55-3.70 (4 H, m), 3.SS (3 H, s)7 3.89 (3 H, s), 4.32-4.45 (2 H, m), 4.66-4.78 (2 H, m), 6.75 (1 H, d, J=4), 6.S5-6.93 (2 H, m), 7.53-7.58 (1 H, m), 7.73 (1 H, d, J=4), 7.77-7.82 (1 H, m), 8.0S-S.I4 (2 H, m) and 13.97 (1H, bs); MS (posES-FIA) 415.1561 M+; Purity (HPLC chromsil CIS) >80%. EXAMPLE 79 N-(2,4-Dinuorobenzenesulfonyl)-5-(4-methylpiperazin-l-yl)-indole, hydrochloride (0.23 g, yield 53 %) 'H NMR (CDCl3) 5 2.2.99 (3 H, s), 3.55-3.6S (4 H, m), 4.35-4.45 (2 H. m), 4.71-4.S2 (2 H. m), 6.77 (1 H, d, J=4), 6.S4-6.93 (2 H, m), 7.04-7.12 (1 H, m), 7.75-7.S2 (2 H, m). 7.9S (1 H, d, J=9), 8.10-S.20 (2 H, m) and 13.SS (1 H, bs); MS (posES-FIA) 391.1155 M*: Purity (HPLC chromsil CIS) >SS%. EXAMPLE 80 N-(4-MethoNybenzenesiilfony0-5-(4-benzy)piperazin-l-yl)-iiidole, hydrochloride (0.34 g, yield 61 %). 'H NMR (CD3OD) 5 3.26-3.29 (8 H, m), 3.76 (3 H, s), 4,40(2 H, s), 6.93(1 H,d,J=9), 7.08(1 H, dd, J=9, 3), 7.17 (1 H, d, J=3), 7.46-7.51 (3 H. m), 7.52-7.57 (3 H, m), 7.76 (2 H, d, J=9) and 7.86 (1 H, d, J=9); MS (posES-FIA) 461.1763 M±; Purity (HPLC chromsil CIS)>90%. EXAMPLESl N-(2,4-Difluorobenzenesulfonyl)-5-(4-benzylpiperazin-l-yl)-indole, hydrochloride (0.30 g, yield 64 %). 'H NMR (CD3OD) 5 3.30-3.80 (8 H, m), 4.40 (2 H, s), 6.66 (1 H, d, J=4), 7.04-7.15 (3 H, m), 7.30 (1 H, d, J-3), 7.43-7.47 (3 H, m), 7.52-7.56 (2 H, m), 7.57-7.66 (1 H, m), 7.74 (1 H, d, J=9) and 8.06-8.14 (1 H, m); MS (posES-FIA) 467.1492 M+; Punty (HPLC chromsil CI8) >98%. EXAMPLE 82 N-(4-Butoxybenzenesulfonyl)-5-(4-benzylpiperazin-l-yl)-indole, hydrochloride (0.30 g, yield 64 %). ]H NMR (DMSO d0) 5 0.86 (3 H, t, J=7), 1.29-1.42 (2 H, m), 1.55- 1.69 (2 H, m), 3.05-3.37 (6 H, m), 3.60-3.70 (2 H, m), 3.97 (2 H, t, J=6), 4,35 (2 H, s), 6.69 (1 H, d, J=3), 7.02-7.15 (4 H, m), 7.43-7.50 (3 H, m), 7.65-7.71 (3 H, m), 7.78-7.S6 (3 H, m) and 11.45 (1 H, bs); MS (posES-FIA) 503.2236 M+; Purity (HPLC chromsil C18) >95%. EXAMPLE S3 N-{3,4-Dimethoxybenzenesulfonyl)-5-(4-benzylpiperazin-l-yl)-indole, hydrochloride (0.36 g, yield 6S %). lH NMR (DMSO d6) 5 3,10-3.40 (6 H, m), 3.65-3.S5 (2 H, mj, 3.76 (6 H, s). 4.35 (2 H, s), 6.70 (1 H, d, J=4), 7.04-7.14 (3 H. m), 7.34 (I H, d, J-2), 7.42-7.47 (3 H. m), 7.50 (I H, dd, J=9, 2), 7.65-7.70 (2 H, m). 7.73 (I H. d. J=4), 7.S3 (1H, d, J=9J and 11.65 (I H, bs); MS (posES-FIA) 491.18 75 M+; Purity (HPLC chromsilC18)>9S%. EXAMPLE 84 N-(BiphenyM-sulfonyl)-5-(4-benzyIpiperazin-l-yl)-indole, hydrochloride (0.35 g, yield 64 %). !H NMR(DMSO d6) 5 3.10-3.20 (4 H, m), 3.30-3.40 (2 H, m), 3.70-3.80 (2 H, m), 4.36 (2 H, s), 6.74 (! H, d, J=4), 7.05-7.13 (2 H, m), 7.40-7.50 (6 H, m), 7.5S-7.63 (2 H, m), 7.63-7.68 (2 H, mj, 7.76 (1 H, d, J=4), 7.82-7.87 (3 H, m), 7.98 (2 H, d, 3=9) and 10.81 (1 H, bs); MS (posES-FIA) 507.1981 M+; Purity (HPLC chromsi!C18)>9S%. EXAMPLE 85 N-(Napthalene-2-sulfonyl)-5-(4-benzylpiperazin-J-yI)-indoie, hydrochloride (0.40 g, yield 55 %). 'H NMR (DMSO d0) 5 3.05-3.35 (6 H, m), 3.66 (2 H, d, J=l2), 4.33 (2 H,s), 6.71 (1 H, d, J=4); 6.99 (1 H, dd; J=9; 2), 7.10 (1 H, d, J=4), 7.41-7.45 (3H, m), 7.58-7.75 (6 H, m), 8.00 (1 H, d, J-4), 8.07 (1 H, d. >8), 8.29 (1 H, d, J=9), 8.32 (1 H, d, J=7), 8.62 (1 H, d, J=9J and 11.53 (I H, bs); MS (posES-FIA) 481.1842 M+; Purity (HPLC chromsil CIS) >9S%. EXAMPLE 86 N-(4-PropylbenzenesulfonyI)-5-(4-benzylpiperazin-l-yl)-indole, hydrochloride (0.49 g, yield 63 %). 'H NMR (DMSO d0) 5 0.81 (3 H, t, J=7), 1.44-1.56 (2 H, m), 2.54 (2.H, t, J=8), 3.10-3.27 (6 H, m), 3.2S-3.3S (2 H, m), 4.35 (2 H, s), 6.70 (1 H, d, J-4), 7.05-7.09(1 H, 01X7.10-7.12(1 H, mj, 7.37 (2 H,d,J=8), 7.43-7.48(3 H, m), 7.63-7.67 (2 H,m), 7.69(1 H,d,J=4), 7.77-7.84(3 H, m), and 11.37(1 H, bs); MS (posES-FIA) 473.2152 M4"; Purity (HPLC chromsil CIS) >98%. EXAMPLE 87 N-(3-Fluarobenzenesulfoiiyl)-5-(4-benzy!piperazin-l-ylHndole, hydrochloride (0.36 g, yield 70 %). lH NMR (DMSO d6) 5 3.10-3.23 (2 H, m), 3.26-3.40 (4 H, m), 3.65-3.77 (2 H, m), 4.37 (2 H, s), 6.75 (I H, d, J=4), 7.! 1 (1 H, dd, J=9, 2), 7.17 (1 H, d, .1=2), 7.40-7.45 (3 H, m), 7.48-7.56 {1 H, m), 7.58-7.65 (1 H, m), 7.65-7.71 (2 H, m), 7.73-7.78 (2 H, m), 7.80-7.86 (2 H, m) and 11.79 (1 H, bs); MS (posES-FIA) 449.1595 £ M+; Purity (HPLC chromsil CIS) >98%. EXAMPLE 88 N-(4-Metl]0\ybenzenesu[fonyl)-5-(piperazin-l-yi)-indoIe, hydrochloride ) N-(4-Methoxybenzenesulfonyl)-5-(4-benzyIpiperazin-l-yl)-indole (0.25g, 0.54 mmot) was dissolved in DCM (4 mL), a-chloroethyl chloroformate (0.150 g, 1.05 mmol) was added and the mixture left at room temperature for 2 h after which it was concentrated. MeOH (10 mL) was added and the mixture refluxed for 2 hrs and then concentrated to give the product (0.22 g, quantitative yield). 'H NMR (MeOH d6) 5 3.39-3.47 (8 H, m), 3.77 (3 H, s), 6.64 (1 H, d, J=3), 6.94 (2 H, d, J=9), 7.15 (1 H, dd, J-9, 2), 7.26 (1 H, d, 1=2), 7.59 (1 H, d, J=4), 7.80 (2 H, d, J=9) and 7.90 (1 H, d, J=9); MS (posES-FIA) 371.1304 M+; Purity (HPLC chromsil CI8) >98%. Examples 89-95 were prepared using the same procedure as in example 88. EXAMPLE 89 N-fi^-DifiuorobenzenesulfonylJ-S-tpiperazin-l-yO-indole, hydrochloride (Isolated 0.20 g). 'H NMR (CDC13) 5 3.49-3.54 (4 H, m), 3-57-3.62 (4 H, m), 6.71 (1 H.d.-M), 7.04-7,15 (2 H,m), 7.28(1 H, dd, J=9,3), 7.51 (1 H, d, J=3), 7.62-7.65 (1 H, m), 7.81 (I H,d, 1=9) and 8.08-8.16(1 H, m); MS (posES-FIA) 377.1012 NT; Purity (HPLC chromsil CIS) >98%. EXAMPLE 90 N-{4-ButoxybenzenesuIfonyI)-5-(piperazin-l-yl)-indole, hydrochloride (Isolated 0.30 g) LH NMR (DMSO dCl) 5 0.84 (3 H, t. J=S). 1.23-1.39 (2 H, m). 1.55-1.65 (2 H, m), 3.22-3.30 (4 H, m), 3.40-3.48 (4 H, m), 3.95 (2 H. U=7), 6.73(1 H, d. J=4), 7,00 (2 H, d, J=9), 7.19(1 H, df J=9), 7.29 (1 H, bs), 7.71(1 H, d, J=4), 7.S4 (3 H, d, J=9) and 9.64 (1 H, bs); MS (posES-FIA) 413.1770 M+; Purily (HPLC chromsil CIS) >88%. EXAMPLE 91 N-(3,4-Dimethoxybenzenesulfonyl)-5-(piperazin-l~yI)-indole, diliydrochloride (Isolated 0.24 g ). 'HNMR (DMSO d„) 5 3.28-3.36 (4 H, m), 3.48-3.55 (4 H, m), 3.75 (3 H, s), 3.76 (3 H, s), 6.76 (1 H, d, J=4), 7.05 (1 H, d, J=9), 7.23-7.44 (3 H, m), 7,53 (1 H, dd, J^9, 3), 7.80 (1 H, d, J=4), 7.93 (1 H, d, J=9), and 9.81 (2 H, bs); MS (posES-FIA) 401.1401 M+; Purity (HPLC chromsil CIS) >9S%. EXAMPLE 92 N-(Bipheny[-4-sulfonyl)-5-(piperazin-l-yE)-indole, dihydrochloride (Isolated 0.21 g). lH NMR (DMSO d6) 5 3.16-3.23 (4 H, m), 3.27.3.32 (4 H, m), 6.74 (1 H, d, 1=4), 7.07-7.14 (2 H, m), 7.38-7.49 (3 H, m), 7.63-7.68 (2 H, m), 7.75 (I H, d, J=4), 7.S2-7.87 (3 H, m), 7.98 (2 H, d, J=9) and 9.00 (2 H, bs); MS (posES-FIA) 417.1519 M+; Purity (HPLC chromsil C18) >98%. EXAMPLE 93 N-(Napthalene-2-sulfonyl)-5-(piperazin-l-yl)-indole? dihydrochloride (Isolated 0.25 g). 'H NMR (DMSO d„) 8 3.15-3.25 (4 H, m), 3.30-3.36 (4 H, m), 6.73 (1 H, d, J=4), 7,05 (1 H, dd, J=9, 3), 7.17 (1 H, d, J=3), 7.61-7.74 (4 H, m), 8.02 (1 H, d, J=4), 8.07(1 H,d,J=8), 8.30(1 H, d, J=S), S.33 (1 H, d, J=S), S.62 (1 H, d, .1=9) and 9.46 (2 H, bs); MS (posES-FIA) 391.1349 M+; Purily (HPLC chromsil CI8J >9S%. EXAMPLE 94 N-(4-Propylbenzenesulfotiyi)-5-(piperazin-l-yl)-indole, dihydrochloride (isolated 0.24 g). lH NMR (DMSO do) 5 0.S0 (3 H, t, J=S), 1.44-1.55 (2 H. m), 2.53 (2 H, t, J=S), 3.1 S-3.26 (4 H, m), 3.36-3.42 (4 H. m). 6.73 (1 H, d, .1=4), 7.14 (I H, dd, J=9, 2), 7.21 (1 H. d, J=3), 7.36 (2 H, d, J=S), 7.71 (1 H, d, J=4), 7.79-7.85 (3 H, m), 9.52 (2 H, bs); MS (posES-FIA) 383.1679 M*; Purity (HPLC chromsi] CI8) >98%. EXAMPLE 95 N-(3-Fluorobenzenesulfonyl)-5-(piperazin-l-yl)-indole, dihydrochloride (Isolated 0.18 g). 'H NMR (DMSO d6) S 3.3 [-3.28 (4 H, m), 3.32-3.43 (4 H, m), 6.77 (1 H, d, J=4), 7.14 (1 H, dd, J=9, 3), 7.19 (1 H, d, J=2), 7.50-7.5S (1 H, m), 7.59-7.66 (1 H, m), 7.73-7.79 (2 H, m), 7.80-7.87 (1 H, m) and 9.53 {2 H, bs); MS (posES-FIA) 359.1109 M+; Purity (HPLC chromsi 1 C18) >98%. EXAMPLE 96 N-Benzenesulfonyl-5-(piperazin-l-yl)-indole, dihydrochloride l-Benzenesiilfonyl-5-bromo-indole (0.336 g, 1 mmol), piperazine (0.516 g, 6 mmol), CsC03 (0.456 g, 1.4 mmol), Pd2(dba)3 (46 mg, 0.05 mmol), BINAP (62 mg, 0.1 mmol) and xylene (10 mL) were mixed and heated to 120 °C under stirring for 18 h. The product was isolated as the hydrochloride salt (0.05 g). ]H NMR (CDCU) 5 3.00-3.16 (8 H, m), 6.57 (1 H, d, J=3), 6.99 (1 H, s), 7.02 (1 H, d, J=3), 7.40 (2 H, t, 1=8), 7.47-7.53 (2 H, m) and 7.81-7.90 (3 H, m); MS (posES-FIA) 341.11S7 JVf; Purity (HPLC chromsi! C18)>98%. Preparation of 3-substituted-l-aryIsulfonyl indole, hydrochloride. (i)^-Fluoro-sulfonylchloride, NaH, DMF. EXAMPLE 91 (Intermediate) .3-(l-azabicycloI2.2.2|oct-2-en-3-yl)-IH-indole, oxalate The compound was obtained according to the procedure described in the literature ( ////', V.O. Synthesis 1979, 136; Boettcher. H.; Seyfried. C; Minck, K.O.; Wolf, H. P. Cer. Offen. (1991). DE 90-4009565). ' H NMR (400 MHz, DMSO-rfd) 8 I L .48 (s, 1 H), 7.75 -7.70(m,2 H), 7.42 (d, 7= 8 Hz, 1 H), 7.20-7.05 (m, 2 H), 6.92 (s, 1 H), 3.34 (s, IH), 3,26 (br, 2 H), 2.84 (br, 2 H), 1.88 (br, 2 H), 1.63 (br, 2H). EXAMPLE 98 3-(l-Azabicyclo[2.2.2]oct-2-en-3-yl)-l-[(4-fluorophenyI)sulfonyI]-lH-indole At 0aC 3-(3-indolyl)-2,3-dihydroqmnuclidine (179 mg, 0.80 mmol) was added to a suspension ofNaH (20 mg, 0.85 mmol) in DMF (1 mL) and stirred for 15 min. Then the 4-fluoroplienylsulfonyl chloride (174 mg, 0.90 mmol) was added and the resulting solution was stirred for 30 min at 0°C and 3h at room temperature. The DMF was evaporated and the resulting solid was chromatographed (Eluant CHiCI; / MeOH, 90/10) to afford 100 mg (32%) of the desired compound. 'H NMR (270 MHz, DMSO-d6) 5 8.25 - 8.10 (m, 3 H), 7.99 (d, J= 8 Hz, 1 H), 7.83 (d, J= 8 Hz, 1 H), 7.65 - 7.30 (m, 3 H), 7.20-7.05 (m, 2 H), 3,18 (br, 2 H), 2.75 (br, 2 H), 1.78 (br, 2 H), 1.50 (br, 2H); MS (ESJ+) for m/z 383 (M+Hf ■ EXAMPLE 99 (Intermediate) tert-Butyl 4-|2-iodo-l-(phenylsulfonyl)-]H-indoM-yl]-l-piperazinecarboxyiate A mixture of buty[magnesium chloride (1 mL, Immol, 2.0 M in ether) and di-isopropyl amine (0.279 mL, 2 mmol) in dry THF (5 mL) was stirred for 4 h under inert atmosphere at room temperature. A solution of tert-butyl 4-[l-(phenylsulfonyl)-!H-indol-4-yl]-1-piperazinecarboxyiate (220 mg, 0.5 mmol) in THF (2 mL) was added slowly and the resulting mixture stirred for 2 h at room temperature. A solution of iodine (380 mg, 2.2 mmol) in THF (2 mL) was added dropwise and the mixture was stirred overnight. After evaporation of the solvent in vacuo, the residue was treated with an aqueous solution ofNHjCl (10 mL). The mixture was extracted with CH2C\2 (3x10 mL) and the combined organic layers were dried (MgSOa) and concentrated in vacuo. The residue was purified by column chromatography (SiO:) using CH2CI2 as eluent to give 100 mg (35%). 'H NMR (500 MHz, CDCb) 5 S.05-7.80 (m, 3 H), 7.60-7.35 (m, 3 H). 7.19(t,./= S Hz, 1 H), 6.9S(s, I H). 6.72 (d,y= S Hz, i H), 3.62 (m, 4 Hi, 3.05 (m, 4H), l.47{m, 9 H); MS (ESI+) for mh 56S (M+H)+. . EXAMPLE 100 2-lodo-I-(pheiiylsulionyl)-4-(l-pipciazinyl)-in-indo|e hydrochloride In CH2CI3 (1 mL) tcrt-butyl 4-[2-iodo-l-{pheny!suIfonyl)-IH-indol-4-yl]-l-piperazinecarboxylate (25 mg, 0.044 mmol) and HC1 in ether (1 mL) were added and shaken for 2 h at room temperature. Tlie resulting precipitate was filtered off and washed with ether giving 20 mg of the desired compound, 'H NMR (270 MHz, DMSO-d6) 5 9.02 (br, 1H), 7.90-7.S0 {in, 3 H), 7.75-7.55 (m, 3 H), 7.32 (s, ] H), 7.22 ((, J= S Hz, lH),6.79(d,/=8Hz,l K), 3.35-310 (m, S H); MS (ESI+) for w/z468 (M+H)+. EXAMPLE 101 (Intermediate) tert.-Butyl 4-[2-phenyl-Hphenylsulfonyl)-lH-indoI-4-yll-l-piperazinecarboxylate tert-Butyl 4-[2-iodo-I-(phenylsi.!lfonyl)-lH-indol-4-yl]-l-piperazinecarboxylate(40 mg, 0.07 mmol), phenyl boronic acid (12 mg, 0.1 mmol), Pd(PPh3j4 {2 mg, 0.002 mmol) and a 2M aqueous solution of K0CO3 (0.075 mL) were stirred for 3 days at 80 °C in dimethoxyethane (2 mL),. After evaporation of the solvent, the crude was purified by column chromatography (SiO;) and led to 30 mgof the desired" compound (80%). 'H NMR (270 MHz, DMSO-40 5 8.02 (d, J= S Hz, 1 H), 7.55-7.20 (m, 11 H), 6.78 (t,J = 8 Hz, 1 H), 7.57 (s, 1 H), 3.58 (m, 4 H), 3.02 (m, 4 H), 1.48 (m, 9 H). MS (ESI+) for m/z 518 (M+Hf. EXAMPLE 102 2-Phenyl-l-(pheny)5ulfonyl)-4-Q-piperazinyl)-lH-indole hydrochloride tert-Butyl 4-[2-phenyi-l-(plienylsulfony!)-lH-indol-4-yl]-l-piperazinecarbo,\:ylate (30 mg, 0.058 mmol) was dissolved in CH:Cb (1 mL) followed by addition of HC1 in ether (1 mL). The reaction was shaken for 2 h at room temperature. The resulting precipitate was filtered off and washed with ether giving 20 mg of the desired compound (S0%). 'H NMR (270 MHz, DMSO-rfrt) 5 9.02 (br, 1 H), 7.90-7.S0 (m, 3 H), 7.75-7.55 (m, 3 H), 7.32 (s, I H), 7.22(1, J=& Hz, 1 H), 6.79 (d,J= S Hz. 1 H), 3.35-310 (m, S H). MS (ESI+) for m/z 41S (M+H)*. EXAMPLE 103 (Intermediate) 4-Tnnuorometliaiiesulfonyloxy-2-methyl-l-tetrabutyldimethyIsilylindole 4-Hydroxy-2-methylindoIe (3.0g, 20 mmol) was dissolved in 30 mL of DCM followed by addition of triethylamine (4.2 mL). Solution was cooled (ice bath) and a solution of trifluoromethanesulfonic anhydride (6.3 g, 22 mmol) in DCM (6 mL) was slowly added under stirring. After 10 minutes the solution was washed by aqueous KJCOJ, dried (KJCOJ) and solvent was evaporated. Compound was dissolved in THF (10 mL) and NaH (0.8 g of 80% suspension in oil) was added. TBDMSC1 (3.3g, 22 mmol) in THF (5 mL) was added. The solution was diluted by 20 mL of DCM, washed by aqueous NHjCl. Organic phase was dried and evaporated. The compound was purified by chromatography (Si02 hexane-ether). Yield 5.7 g (75%): lH NMR (CDCI3) 5 7.48 (d, J = 7.9 Hz, 1 H), 7.10-6.96 (m, 2 H), 6.44 (s, 1 H), 2.50 (s, 3 H), 0.96 (s, 9 H), 0.64 (s, 6 H); MS (ESI) 381.1 (M + H). EXAMPLE 104 (Intermediate) 4- (N-Boc-piperazinyl)-2-methyl-l-tetrabutyldimcthylsi]ylindoIe 4- trifluoromethanesulfonyloxy-2-methyl-l-tetrabutyldimethylsilylindole (1.0 g, 2.6 mmol) and boc-piperazine (0.73 g, 3.9 mmol) were reacted according to Method 1 to give 0.75 g (67%) of a solid-. *HKMR (CDCI3) 5 7.20 (d, J= 8.2 Hz, 1 H), 6.96 (t, H), 6.55 (d,J= 7.4 Hz, 1 H), 6.31 (s, I H), 3.63 (pt, 4H), 3.11 (pt, 4H), 2.47 (s, 3 H), 1.48 (s, 9 H), 0.94 (s, 9 H), 0.64 {s, 6 H); MS (ESI) 417.4 (M + H). EXAMPLE 105 4-Piperazinyl-2-methyl-l-benzosulfonylindole trifluoroacetate t- (N-Boc-piperazinyl)-2-niethyl-l-tetrabu(yldimethylsiIylindole (0.2 g, 0.4S mmol) vas dissolved in ethyl acetate (5 ml) followed by the addition of a solution of sodium luoride(0.1 g) in water (1 mL). Mixture was vigorously stirred (50°C) for 2 h. The irganic phase was separated, dried and evaporated. The crude was dissolved in DCM 10 mL) followed by the addition of benzosulfonylchloride (0.1 g, 0.5S mmol) and aqueous NaOH (0.5 mL, 50% water solution). The mixture was vigorously stirred for 1 h. Water (5 mL) was added, the organic phase was separated, dried and evaporated. The crude was dissolved in DCM (10 mL) and trifluoroacetic acid (1 mL) was added. After 3 h solvent was evaporated and compound was crystallized from ethanol. Yield 60 nig (54%): 1H NMR (CDCI3) 8 7.83-7.77 (m, 3 H), 7.59-7.56 (m, I H), 7.50-7.46 (m, 2 H), 7.19(1, 1 H),6.8I (d,y=7.8Hz, 1 H), 6.52 (s, 1 H),3.41 (pi, 4 H), 3-30 (pt, 4 H), 2.61 (s, 3 H); 13rNMR(CDCl3) 6 143.7, 138.8, 138.0, 136.6, 133.9, 129.2, 126.1, 124.3, 123.5, 111.5, 110.0, 107.3,48. 5, 43.8, 14.6; MS (ESI) 356.4 (M + H). EXAMPLE 106 (Intermediate) N-(t-ButyI-dimethylsilyl-4-(4-boc-homopiperazinyl)-indole The title compound was prepared according as Example 4. 'H NMR (D20) 5 9.37 (bs, 2 H) NH; 7.95 (m, 2 H); 7.73-7.56 (m, 4 H); 7.44 (d, J = 8.2, \ H); 7.18 (t, J = 8.2, I H); 6.84 (m, 1 H); 6.65 (d, J = 7.9, I H); 3.65 (m, 2 H); 3.46 (m, 2 H); 3.3! (m, 2 H); 3.19 (m, 2 H); 2.13 (m, 2 H). I3C NMR (D30) : 145.7, 137.5, 136.3, 135.2, 130.4, 127.3, 126.2, 125.1,121.3, 109.3, 105.4, 100.0,50.8,48.7,46.6, 45.1,25.6. MS (ESI) 356 (M+H). EXAMPLE 107 (Intermediate) I- PhenylsuIfonyl-N-(t-butyl-dimethylsi[yl-4-(4-boc-hoffiopiperazinyl)-indoIe 'H NMR CCDCb) 5 7.86 (m, 2 H); 7.54-7.3S (m, 6 H); 7.4 (t, J = 8.2. 1 H); 6.65-6.62 (m, I H); 3.63-3.41 (m, S H); 1.97 (m, 2 H); 1.43 (s, 9 H); MS (ESI) 456 (M+H). EXAMPLE 108 1- Phenylsulfonyl-4-(homopiperazinyI)-indole hydrochloride 'H NMR (CDCh): 7.24 (m, 2 H); 7.09-7.07 ( m, 6 H); 7.01 (t, J - 8.1, 1 H); 6.53 (m, 1 H); 3.69-3.28 (ni, 8 H); 2.06 (m, 2 H);l .42 (s, 9 H); 0.91 (s, 9 H); 0.56 (s, 6 H). MS(£SI)430(M+H). Pharmacological tests Tlie ability of a compound of the invention to bind the 5HTG receptor can be determined using //( vivo and /// vitro assays known in the art. The biological activity of compounds prepared in the Examples was tested using different tests. 5-HTG Intrinsic Activity Assay Antagonists at the 5HT& receptor were characterized by measuring inhibition of 5-HT induced increase in cAMP in HEK 293 cells expressing the human 5-HT& receptor (see Boess et al. (1997) Neuropharmacology 36: 713-720). Briefly, H£K293/5-HTfi cells were seeded in polyiysine coated 96-weIl plates at a density of 25 000 / well and grown in DMEM {Dubecco's Modified Eagle Medium) (without phenol-red) containing 5% dialyzed Foetal Bovine Serum for 48 hours at 37°C in a 5% CO: incubator. The medium was then aspirated and replaced by 0.1 ml assay medium (Hanks Balance Salt Solution containing 20 mM HEPES, 1.5 mM isobutylmethylxanthine and 1 mg/ml bovine serum albumin). After addition of test substances, 50 nl dissolved in assay medium, the cells were incubated for 10 min at 37°C in a 5% CO: incubator. The medium was again aspirated and the cAMP content was determined using a radioactive cAMP kit (Amersham Pharmacia Biotech, BfOTRAfC RPA559). The potency of antagonists was quantified by determining the concentration that caused 50% inhibition i of 5-HT (at [5-HT]= 8 times EC50) evoked increase in cAMP, using the formula iCi=IC5o/{H-[5HT]/EC5o). Typically, the 5-HT6 receptor affinity values (Kf) were in the range of from 0.1 nMto2uM. Method for in vivo assay of reduction of food intake Animals Obese (ob/ob) mouse is selected as the primary animal model for screening as this mutant mouse consumes high amounts of food resulting in a high signal to noise ratio. To further substantiate and compare efficacy data, the effect of the compounds on food consumption is also studied in wild type (C57BL/6J) mice. The amountof food consumed during 15 hours of infusion of compounds is recorded. Male mice (obese C57BL/6JBom-Lepob and lean wild-type C57Bl/6JBom; Bomholtsgaard, Denmark) 8-9 weeks with an average body weight of 50 g (obese) and 25 g (lean) are used in all the studies. The animals are housed singly in cages at 23±l°C, 40-60 % humidity and have free access to water and standard laboratory chow. The 12/12-h light/dark cycle is set to lights off at 5 p.m. The animals are conditioned for at least one week before start of study. Compounds The test compounds are dissolved in solvents suitable for each specific compound such as cyclodextrin, cyclodextrin/methane sulfonic acid, polyethylene glycol/methane sulfonic acid, saline. Fresh solutions are made for each study. Doses of 30, 50 and 100 mgkg"lday"1 are used. The purity of the test compounds is of analytical grade. Minipump implantation The animals are weighed at the start of the study and randomized based on body weight. Alzet osmotic minipumps (Model 2001D; infusion rate 8 ul/h) are used and loaded essentially as recommended by the Alzet technical information manual (Alza Scientific Products, 1997; Teeuwes and Yam, 1976). Continuous subcutaneous infusion with 24 hours duration is used. The minipumps are either filled with different concentrations of tesl compounds dissolved in vehicle or with only vehicle solution and maintained in vehicle pre-warmed to 37°C (approx. Ih). The minipumps are implanted subcutaneously in the neck/back region under short acting anesthesia (metofane/enflurane). This surgical procedure lasts approximately 5 min. It takes about 3 h to reach steady state delivery of the compound. Food intake measurements The weight of the food pellets are measured at 5 p.m. and at 8 p. m. for two days before (baseline) and one day after the implantation of the osmotic minipumps. The weigh-in is performed with a computer assisted Mettier Toledo PR 5002 balance. Occasional spillage is corrected for. At the end of the study the animals are killed by neck dislocation and trunk blood sampled for later analysis of plasma drug concentrations. Determination of plasma concentration The plasma sample proteins are precipitated with methanol, centrifuged and the supernatant is transferred to HPLC vials and injected into the liquid chromatography /mass spectrometric system. The mass spectrometer is set for electrospray positive ion mode and Multiple Reaction Monitoring is used. A linear regression analysis of the standards forced through the origin is used to calculate the concentrations of the unknown samples. Statistical evaluation Food consumption for 15 hours is measured for the three consecutive days and the percentage of basal level values is derived for each animal from the day before and after treatment. The values are expressed as mean ± SD and ± SEM from eight animals per dose group. Statistical evaluation is performed by Kruskal-Wallis one-way ANOVA using the per cent basal values. If statistical significance is reached at the level of p WE CLAIM: 1. A compound of forniLila (I): wherein Ar is (1) phenyl. (2) naphthyl, (3) a 5-to lO-membered monocvclic or bicyclic heterocyclic ring having 1 lo 4 heteroatoms selected from the group consisting of oxygen, sulfur, or nitrogen, or (4) -R'-phenyl; wherein each of phenyl, naphthyl, and heterocyclic ring is independently optionally 2. The compound as claimed in claim I, wherein Ar is (1) phenyl, (2) l-naphthyl or 2-naphthyl. (3) a 5-to 10-membered monocyclic or bicyclic heterocyclic ring having 1 to 4 heteroatoms selected from the group consisting of oxygen, sulfur, or nitrogen, or (4)-R'-phenyl: wherein each of phenyl, naphthyl, and heterocyclic ring is independently optionally substituted with F, CI. Br, C|_6 alkyl, CF3. hydroxyl, C|.t, alkoxyl, OCF3, phenyl, C2-& alkenyl, -NR^R^ -NH-C0-C,-6 alkyl. or SR^ wherein each of R' and R** is independently H orC|.6 alkyl: and R' is Ci.i alkyl: R" is H. phenyl, I. or C|.6 alkyl; R is selecied from the group consisting of: 3. The compound as claimed in claim I, wherein Ar is phenyl, optionally substituted with F. CI. Br, methyl. CF3, CM alkoxyl, OCFi, CN, NOz.phenyloxy, phenyl, methylsulfonyl. or -NR^R^, where each of R' and R' is independently H or methyl. 4. The compound as claimed in claim 1, wherein Ar Is 1 -naphthyl or 2-naphthyl. each of which being optionally substituted with F. CI, Br, methyl, CFi. Ci-i alkoxyl, OCF3. CN. N02,phenylo\y. phenyl, methylsulfonyl. or -NR^R^ where each of R^ and R'^ is independently li or methyl. 5. fhe compound as claimed in claim 1. wherein Ar is a heterocyclic ring selected from the group consisting of furyl, pyrrolyl, triazolyl. diazolyl, oxazolyl. thia/olyl. oxadiazolyl, isothiazolyl. isoxazolyl. thiadiazolyl. pyridyl, pyrimidyl, pyra/inyl. thienyi. imidazolyl. pyra/olyl, indolyl, qninolinyl, isoquinolinyl, ben/ofuryl, benzothienyl, and benzoxadiazolyl. each of which being optionally substituted with halogen, Cn, alkyl. 6. The compoLind as claimed in claim 5, wherein Ar is a helerocycHc ring selected from the group consisting of pyridyl. thienyl. imidazolyl, pyra/olyl, benzothieiivl, and benzoxadiazoiji, each ofwhich being optionally substituted with halogens or C|.6 alkyl. 7. The compound as claimed in claim 6, wherein Ar is 2-pyridyl, 3-pyrid\ I. or 4- pyridyl. 8. The compound as claimed in claim I, wherein Ar is a 5- to 7-membered aromatic, partially saturated, or completely saturated heterocyclic ring having 1 to 4 10. The compound as claimed in any one of claims 1 to 9. wherein each of R" and R-' is H. 11. The compound as claimed in any one of claims 1 to 10. wherein each of R"'and R"^ is independently a heterocyclic ring selected from the group consisting of wherein R^ is 11. C1-3 alkyl, or benzyl. 12. The compound as claimed in claim I, wherein Ar is phenyl, optionally methyl: each of R" and R" is H; and each of R'^ and R^ is independently a heterocyclic ring selected from the group consisting of: 13. The compound as claimed in claim 1, wherein Ar is 1-naphthyl or 2-na|3hthyl, each of which being optionally suhstituted with F, CI, Br, methyl, CF^, Ci.j alkoxyl. OCFi, CN, NO? phenyloxy, phenyl, methylsulfonyl, or -NR'R , where each of R^ and R is independently M or methyl; each of R" and R^ is H; and each of R' and R^ is independently a hetcroc\clic ring selected from the gronp consisting of: wherein R" is H, C1-3 alkyl, or benzyl. 14. The compound as claimed in claim I. wherein Ar is a heterocyclic ring selected from the group consisting of pyridyl. ihienyl. imidazolyl. pyrazoiyi, bcnzothienyl. and benzoxadiazolyl, each of which being optionally substituted with halogens or C|_(, alkyl: each of R' and R' is H: and each of R"* and R" is independently a heterocyclic ring selected from the group consisting of; 15. The compound as claimed in claim 14. wherein Ar is 2-pyridyl, 3-pyridyl, or 4- pyridyl; each of R" and R3 is H: and each of R** and R' is independently a heterocyclic ring selected from the group consisting of: wherein R' is H. C1.3 alkyl, or benzyl. 16. The compound as claimed in claim I. wherein Ar is -R'-phenyl; each of R' and R3 is H: and each of R and R3 is independently a heteroc>clic ring selected from the group consisting of: wherein R' is H, C1.3 alkyl, or benzyl; R' is C1-3 alkyl or Ci.salkenyl. each of which being optionally substituted with phenyl; and phenyl is optionally substituted with F, CI, Br. methyl, CK3. C1-4 alkoxyl, OCF3, CN. NOi, phenyloxy. phenyl, methylsulfonyl. or-NR3R3 each of R' and R* being independently H or C,.3 alkyl. 17. The compound as claimed in claim I. said compound being l-phenylsulfon>l-4-piperazinylindole hydrochloride. l-[(2,5-dimethoxyphenyl)sulfonyl]-4-(l-piperazinyl)-lH-indole hydrochloride, 1 -(mesitylsulfonyl)-4-(I -piperazinyl)-1 H-indole hydrochloride. I -(! -naphthylsulfony l)-4-( I -piperazinyl)-1 H-indole hydrochloride. N.N-dimethyl-5-{[4-(l-piperazinyl)-!H-indol-l-yl]su!fonylf-l-naphthalenamine hydrochloride. I -[(4-propoxyphenyl)sulfonyl]-4-( I -piperazinyl)-1 H-indole hydrochloride. 1 -[(2.5-dichloro-3-thienyl)sulfonyl]-4-( I -piperazinyl)-1 H-indole hydrochloride, 1 -[(4-methoxyphenyl)sulfonyl]-4-( I -pipera/inyl)-1 H-indole hydrochloride. 1-[(2.4-dinuorophcnyl)sulfony 11-4-( I-piperazinyl)-Hl-indole hydrochloride. 1 -([1.1 '-biphcii} n-4-ylsLilfonyl)-4-(J-piperazinvI)-1 H-indolc hydrochloride, l-[(3,4-dimethoxyphcnyl)sulfonyl]-4-(l-piperazinyl)-in-indolt; hydrochloridt;. 5-melh\l-2-methoxyl-!|4-(l-pipcrazinyl)-lII-indol-l-yl]sulfonyi}phenyl ether hydrochloride, I -[(2.5-dichlorophenyl)sulfonyl]-4-( 1 -ptperazinyl)-1 H-indole hydrochloride, l-[(5-chloro-l,3-dimethyl-IH-pyrazol-4-yl)sulfonyIJ-4-(l-piperazinyl)-IH-indole hydroehloride, l-[{3-chloro-2-methylphenyl)sulfonyl]-4-(l-piperazinyl)-IH-indole hydrochloride, 2-chloro-5-(4-{|4-(l-pipcra2inyl)-IH-indol-l-yl]sLilfonyl}phenoxy)benzonitrile hydrochloride. 4-bromo-2-{[4-(l-piperazinyl)-IH-indol-]-yl]sulfonyl}phenyl methyl etiier hydrochloride, 4-( I -piperazinyO-l -(3-pyridylsuirony I)-1 H-indole hydrochloride, 7-{[4-(l-piperazinyl)-IH-indol-l-yl]sulfonyl}-2-(tritluoroacetyl)-l.2.3.4-telrahydroisoquinoline hydrochloride, methyl 2-||4-{I-piperazinyl)-]H-indol-l-yl]suironyl}phenyl sulfone hydrochloride, ]-[(4-fluorophenyl)suironyl]-4-(l-piperazinyl)-]H-indote hydrochloride. ! -[(5-chloro-3-methyl-1 -ben/othien-2-yl)sulfonyl |-4-( I -piperazinyl)-11 l-indole hydrochloride, 4-(4-methyl-l-piperazinyl)-!-(4-methylbcn/enesuiron\l)-l H-indole hydrochloride h\drochloridc. 4-piperazino-N-(4-trinLioromethyl)phenylsu!tbnyl)indole hydrochloride. 4-(3-methylpiperazine)-(N-(4-trit1uoromethyI)phenylsulfonyl)indo!e dihydrochloride, 4-(4-melhyl-l-pipera/inyl)-l-(2-methylbenzenesulfonyl)-1 H-indole hydrochloride. 4-(4-clhy 1-1 -piperazinyl)-1 -(2-methylbenzenesulfonyl)-1 H-indole hydrochloride, 4-(l-piperazinyl)-!-(2-methylbenzenesulfonyl)-1 H-indole hydrochloride. 4-(5-aza-indolizidinyl)-l-(2-methylbenzenesLilfonyl)-lH-indole hydrochloride. 4-(4-methyl-1 -homopiperazinyI)-1 -(2-methylbenzenesLilfonyl)-11 l-indole hydrochloride, 4-(3-meihyl-1-pipera/inyI)-l-(2-methylben/.enesulfonyl)-l H-indole hydrochloride, 4-(t/.v-3.5-dimeihyl-I-piperazinyl)-l-(2-mcthylberizenesuIfonyl)-IH-indo!e hydrochloride, 4-(4-isopropyl-1 -piperazinyl)-1 -(2-methylbenzenesulfony!)-l H-indolc hydrochloride, 4-((lS.4S)-2-methyl-2,5-dia7abicyclo[2.2.IJhep[yl)-l-(2-methy[benzenesulfonyl)-lH-iiidole hydrochloride, 4-(4-methyl-l-homopipcrazinyI)-]-(benzenesulfonyl)-lH-ind()le hydrochloride, 4-(cw 3,5-dimeihyl-l-piperazinyl)-l-(benzenesulfonyl)-IH-indoie hydrochloride, 4-(4-ethyl-1 -piperazinyl)-1 -(benzenesulfonyl)-1 H-indole hydrochloride, 4-piperazinyl-l-(4-nitro-benzenesulfonyl)-III-indole hydrochloride, 4-piperazinyl-]-(4-bromo-benzenesulfonyl)-lll-indole hydrochloride, 4-piperazinyl-1 -(4-chloro-benzenesulfonyl)-1 H-indole hydrochloride. 4-piperazinyl-l-(£' 2-phcny!-ethensiilfonyl)-II-l-indole hydrochloride, 4-piperazinyl-l-(3-trifluoromethyl-ben/enesulfonyl)-l H-indole hydrochloride. 4-piperazinyl-1 -(4-cyanobenzenesiilfony!)-1 H-indole hydrochloride. 4-piperazinyl-l-(4-chloro-7-chloro-2,1.3-ben/oxadiazole sulfon\i)-1 H-indole hydrochloride. 4-piperazinyl-l-(3-cyanobenzenesulfonyl)-l H-indole h\drochloride. 4-pipera7.inyl-1-(4-phenoxybcnzenesuironyl)-1 H-indole hydrochloride, 4-piperazinyl-l-(4-chlorophenylmethanesLilfonyl)-lH-indole hydrochloride. 4-piperazinyl-l -(4-melhy!phenylmethanesulfonyl)-1 H-indole hydrochloride, 4-pipera/-inyl-l-(l.]-d!phenylethanesulfonyl)-lH-indole hydrochloride. 4-piperaziny!-l-(4-trifluoromelhoxybcnzenesiiironyl)-1 H-indole hydrochloride. 4-piperazinyl-l-(5-[(benzoylamino)methyl]lhiophene-2-SLilfonyl)-1 H-indole hydrochloride. I -[(N-methyl-111-imida/-ol-4-yl)sulfony l]-4-( I -piperazinyl)-111-indole hydrochloride, N-ben/enesulfonyl-5-(4-methylpipera/in-l-yl)-indole. N-(4-methylbenzenesultbnyl)-5-(4-methylpiperazin-l-yl)-indole. N-bcnzenesnlfony!-5-(4-isopropylpiperazin-1-yl)-indolc, N-(4-melhylbenzenesidronyl)-5-(4-isopropylpiperazin-l-\l)-indole. N-(3,4-dimetho\yben/enesulfonyl)-5-(4-propylpipcrazin-l->'l)-indole. hydrochloride. N-{3-f[uoroben/.enesulfonyl)-5-(4-propylpipera?in-l-yl)-indole, hydrochloride. N-{4-propylbenzenesulfonyl)-5-(4-meThylpiperazin-l-yl)-indole. hydrochloride. N-{l-naphtalencsulfonyl)-5-(4-melhylpipcrazin-l-yl)-induIe. hydrochloride, N-(biphenyl-4-sultbnyl)-5-{4-methylpiperazin-l-\l)-ir!dotc, hydrochloride. N-(4-methoxybenzenesulfonyl)-5-(4-melhylpipera7.in-!-yl)-indole. hydrochloride, N-(3,4-dimelho.\ybenzenesiiJfony])-5-(4-melhy]piperazin-I-y])-indolc. hydrochloride, N-(2,4-ditluorobenzenesLdfonyl)-5-(4-methylpipcrazin-l-yl)-indolc, hydrochloride. N-(4-methQxybejizenesij)fonyJ)-5-(4-benzyJpiperazin-)-yl)-indole. hydrochloride, N-(2.4-difluorobenzenesLi!fonyl)-5-(4-benzylpiperazin-l-yl)-indole, hydrochloride, N-(4-butoxyber)zenesi)]for)y))-5-(4-benzy]piperazir)-)-yl)-indole. hydrochloride, N-(3.4-dinielhoxyben/.encsulfonyl)-5-(4-ben/,y|piperazin-l-yl)-indole. hydrochloride. N-(biphe)jyl-4-s!j!fonyl)-5-(4-bei]zylpiperazij)-l-}l)-indole, bydrocblDridc, N-(naptha!ene-2-sulfonyl)-5-(4-benzylpipcrazin-1 -yl)-indo!e. hydrochloride, N-(4-propylben/-enesulfonyl)-5-(4-benzylpiperazin-l-yl)-indole. hydrochloride, N-(3-nuoroben/enesulfonyl)-5-(4-benzylpipera/in-l-yl)-indolc, h\drochloride. N-(4-methoxybenzenesult'onyl)-5-(piperazin-l-yl)-indole, hydrochloride, K-(2.4-dinLioroben/-enesulfonyl)-5-(piperazin-i-\l)-indole, hydrochloride. N-(4-butoxybenzenesulfonyl)-5-(piperazin-1 -yl)-indole, hydrochloride, N-(3,4-dimethoxybenzenesulfotiyl)-5-(piperazin-1 -yl)-indole, dihydrochloride, N-(biphenyl-4-sultbnyl)-5-(piperazin-l-yl)-indole. dihydrochloride, N-(napthalene-2-sultbnyl)-5-{pipera/in-l-\l)-indolc, dihydrochloride. N-(4-propylbenzcnesulfonyl)o-(piperazin-l-\l)-indole, dihydrochloride. N-(3-nuorobenzenesulfonyl)-5-(piperazin-1 -yl)-indole. dihydrochloride, N-ben/.enesLilfonyl-5-(pipera/.in-l-yl)-indole. dihydrochloride. 3-(l-azabicyclo|2.2.2]oct-2-en-3-yl)-l-[{4-flLiorophenyl)sulfonyl]-iH-mdolc. 2-iodo-l-(phen\lsulfonyl)-4-(I-piperazmyl)-l H-indole hydrochloride. 2-phenyl-1 -(phcnylsLilfonyl)-4-( I -piperazinyl)-111-indole hydrochloride. 4-piperazinyl-2-methyl-l -henzosultbnylindole trifluoroacetate, or I -phenylsulfonyl-4-(homopiperazinyl)-indole hydrochloride. 18. The compound as claimed in claim I. said compound being I -(phenylsulfonyl)-4-(l-piperazinyl)-lH-indo!e. 19. The compound as claimed in claim I, said compound being l-[(2,5-dimethoxyphenyl)sulfonyl]-4-(l-piperazinyl)-lH-indole. 20. The compound as claimed in claim 1, said compound being 4-(l-piperazinyl)-l-(3-pyridylsultbnyl)-11 l-indole hydrochloride.

Documents:

0573-chenp-2003 abstract.jpg

0573-chenp-2003 abstract.pdf

0573-chenp-2003 assignment.pdf

0573-chenp-2003 claims-duplicate.pdf

0573-chenp-2003 claims.pdf

0573-chenp-2003 correspondence-others.pdf

0573-chenp-2003 correspondence-po.pdf

0573-chenp-2003 description(complete)-duplicate.pdf

0573-chenp-2003 description(complete).pdf

0573-chenp-2003 form-1.pdf

0573-chenp-2003 form-13.pdf

0573-chenp-2003 form-26.pdf

0573-chenp-2003 form-3.pdf

0573-chenp-2003 form-5.pdf

0573-chenp-2003 others.pdf

0573-chenp-2003 pct.pdf

0573-chenp-2003 petition.pdf