CA2343168A1

CA2343168A1 - Piperidine derivatives

Info

Publication number: CA2343168A1
Application number: CA002343168A
Authority: CA
Inventors: Andrea Cesura; Torsten Hoffmann; Stephan Roever; Jurgen Wichmann
Original assignee: Individual
Current assignee: F Hoffmann La Roche AG
Priority date: 1998-09-07
Filing date: 1999-09-02
Publication date: 2000-03-16
Also published as: MA26683A1; ZA200101830B; CN1316994A; TR200100660T2; WO2000014067A1; EP1109786A1; BR9913106A; AU5858199A; PE20001028A1; AR022083A1; KR20010073115A; JP2002524446A; CO5150201A1

Abstract

The present invention relates to compounds of general formula (I), wherein R 1 is tetrahydronaphtyl; or -(CH2)n-C6H5-R4 wherein n is 0-4 and R4 is H, lower alkyl, or lower alkoxy; or C5-C12 cycloalkyl, optionally substituted by lowe r alkyl; R2 is H, OH, lower alkoxy, lower alkenyloxy or lower alkyl; R3 is C5- C7 cycloalkyl or phenyl, optionally substituted by OH, halogen, lower alkoxy, lower alkenyloxy, lower alkyl or -O-(CH2)n-C6H5 wherein n is 0-3; and their pharmaceutically acceptable acid addition salts. The compounds of general formula (I) are suitable for the treatment of memory and attention deficits, psychiatric, neurological and physiological disorders, such as anxiety and stress disorders, depression, memory loss due to Alzheimer's disease or othe r dementias such as vascular dementia and AIDS dementia complex, Parkinson's disease, epilepsy and convulsions, acute and/or chronic pain conditions, withdrawal symptoms of addictive drugs and reduction of their abuse/craving, control of water balance, Na+ excretion, arterial blood pressure disorders a nd metabolic disorders such as obesity.

Description

Piperidine Derivatives The present invention relates to novel compounds of the general formula R' I
N

wherein R~ is tetrahydronaphtyl;
or -(CHa)n-CsHs-R4 wherein n is 0-4 and R~ is H, lower alkyl, or lower alkoxy;
or Cs-Cia cycloalkyl, optionally substituted by lower alkyl;
R2 is H, OH, lower alkoxy, lower alkenyloxy or lower alkyl;
l0 R3 is Cs-C~ cycloalkyl or phenyl, optionally substituted by OH, halogen, lower alkoxy, lower alkenyloxy, lower alkyl or -0-(CH2)n-CsH~ wherein n is 0-3;
and to pharmaceutically acceptable acid addition salts thereof.
The compounds of formula I and their salts are distinguished by valuable therapeutic properties. It has surprisingly been found that the compounds of the present invention are a~;onist/antagonists of the OFQ receptor.
Consequently they will be mseful in the treatment of memory and attention WO 00/14067 _ 2 _ PCT/EP99/06442 deficits, psychiatric, neurological and physiological disorders, especially, but not limited to, amelioration of symptoms of anxiety and stress disorders, depression, memory loss due to Alzheimer's disease or other dementias such as vascular dementia and AIDS dementia complex, Parkinson's disease, epilepsy and convulsions, acute a~id/or chronic pain conditions, withdrawal symptoms of addictive drugs and reduction of their abuse/craving, control of water balance, Na' excretion and arterial blood pressure disorders and metabolic disorders such as obesity.
Orphanin FQ (OFQ:), a seventeen amino-acid-long peptide ~o (F-G-G-F-T-G-A-R-K-S-A-R-K-L-A-N-Q), has been isolated from rat brain and is a natural ligand for a (~-protein coupled receptor (OFQ-R), found at high levels in brain tissue.
OFQ exhibits agoni;~tic activity at the OFQ-R both in vitro and in vivo.
Julius (Nature 377;176, [1995)) discusses the discovery of OFQ noting that this peptide shares greatest sequence similarity with dynorphin A, an established endogenous ligand for opioid receptors. OF~I inhibits adenylate cyclase in CHO(LC 132+) cells in culture and induces hyperalgesia when administered intra-cerebroventricularly to mice. The pattern of results indicate that this heptadecapeptide is an endogenous agonist of the LC 132 receptor and it appears to have pro-nociceptive properties. It has been described that when injected intra-cerebroventricularly in mice, OFG~ slows down locomotive activity and induces hyperalgesia and it has been concluded that OFQI may act as a brain neurotransmitter to modulate nociceptive and locomotive behavior.
Exemplary preferred are compounds of the formula I wherein Rl is CS C12 cycloalkyl, optionally su~~stituted by lower alkyl, for example the following compounds:
(3RS,4RS)-1-cyclononyl-4-(2-hydroxy-phenyl)piperidin-3-of hydrochloride (1:1);
3o 1-cyclodecyl-4-(2-methoxy-phenyl)-piperidine hydrochloride (1:1);
(3RS,4RS)-1-cyclodecyl-4-(2-isopropyl-phenyl)piperidin-3-of hydrochloride (l:l);

WO 00/14067 _ 3 - PCT/EP99/06442 (3RS,4RS)-4-(2-hydr<>xy-phenyl)-1-(cis-and-(trans-4-isopropylcyclohexyl)-piperidin-3-of hydrochloride (1:1);

2-(1-cyclodecyl-piperudin-4-yl)-phenol hydrochloride (1:1);
(3RS,4RS)-1-cyclodecyl-4-(2-methoxy-phenyl)-piperidin-3-of hydrochloride (1:1);
1-cyclodecyl-4-cyclohexyl-piperidine hydrochloride (1:1);
(3RS,4RS)-1-cyclononyl-4-(2-methoxy-phenyl)-piperidin-3-of hydrochloride (1:1);
(3RS,4RS)-4-(2-allyloxy-phenyl)-1-cyclodecyl-piperidin-3-of hydrochloride io (1:1);
1-cyclodecyl-4-phenyl-piperidine hydrochloride (1:1);
(3RS,4RS)-1-cyclononyl-4-(2-isopropyl-phenyl)-piperidin-3-of hydrochloride (1:I); and (3RS,4RS)-1-cyclodec;yl-4-(2-hydroxy-phenyl)piperidin-3-of hydrochloride ~5 (1:1).
Objects of the preser.~t invention are the novel compounds of formula I per se and pharmaceutically acceptable addition salts thereof, racemic mixtures and their corresponding enantiomers, the preparation of the above-mentioned compounds, medicaments containing them and their manufacture as well as 2o the use of the above-mentioned compounds in the control or prevention of illnesses, especially of illr.~esses and disorders of the kind referred to earlier.
The following definii:ions of the general terms used in the present description apply irrespective of whether the terms in question appear alone or in combination.
25 As used herein, the i;erm "lower alkyl" denotes a straight- or branched-chain alkyl group containing from 1 to 6 carbon atoms, for example, methyl, ethyl, propyl, isopropyl, n-butyl, i-butyl, 2-butyl, t-butyl.
The compounds of formula I and their pharmaceutically acceptable salts can be prepared by methods known in the art, for example by processes WO 00/14067 _ 4 _ PCT/EP99/06442 described below, which comprise reductively aminating a compound of formula II
H
I
N

I I
R
with a compound of formula wherein R', R2 and :R3 are as described above.
The amination taker place in two steps wherein an imine is formed as intermediate product which further undergoes reduction in the presence of a reductive agent such as sodium cyanoborohydride, molecular hydrogen or to nickel.
The amination agent II can be prepared by known methods, for example from compounds of formula III by means of a hydrogenation reaction:
H
,N I
N
cat wherein R2 and R3 are as described above and, in the case R3 is cycloalkyl or phenyl substituted by a -O-CHZ CsHs, the cleavage of the -CH2 CsHs group takes place during reaction.
The reaction takes place in the presence of hydrogen and a suitable hydrogenation catalyst such as palladium on activated charcoal.
Compounds of formula I, wherein R2 is hydroxy and/or R3 is cycloalkyl or 2o phenyl substituted by hydroxy or halogen may be converted into compounds of WO 00/14067 _ 5 - PCT/EP99/06442 formula I, wherein Rz is lower alkoxy, lower alkenyloxy or lower alkyl and/or R3 is cycloalkyl or phenyl substituted by lower alkoxy, Iower alkenyloxy, lower alkyl or -O-(CHZ)o-CsHS, b;y reacting them for example with alkyl halides, alkenyl halides, phenalky~1 halides or lower alcohols in an inert solvent such as anhydrous tetrahydrofur~m.
Compounds of formula III can be obtained according to literature procedures (e.g. Juan C. Jean and Lawrence D. Wise, J. Heterocyclic Chem.
1987, 24, 1317-1319).
If desired, compounds of formula I can be converted into pharma-1o ceutically acceptable acid addition salts. The salt formation is effected at room temperature with methods which are known per se and which are familiar to any person skilled in the art. Not only salts with inorganic acids, but also salts with organic acids come into consideration. Hydrochlorides, hydrobromides, sulphates, nitrates, citrates, acetates, maleates, succinates, methanesulphonates, p-toluenesulphonates and the like are examples of such salts.
As mentioned earlier, the compounds of formula I and their pharma-ceutically usable addition salts possess valuable pharmacodynamic properties.
It has been found that thE: compounds of the present invention are 2o agonist/antagonists of the OFQ receptor and have effects in animal models of memory and attention deficits, psychiatric, neurological and physiological disorders, such as anxiet3~, stress disorders, depression, memory loss due to Alzheimer's disease or other demential such as vascular dementia and AIDS
dementia complex, Parkuison's disease, epilepsy and convulsions, acute and/or chronic pain conditions, v~~ithdrawal symptoms of addictive drugs and reduction of their abuse/craving, control of water balance, Na' excretion, arterial blood pressure disorders and metabolic disorders such as obesity.
The compounds werE~ investigated in accordance with the tests given hereinafter:
3o Methods of OFQ-R Binding Assay Cell Culture HEK-293 cells adapted to suspension growth (293s) were cultured in HL
medium plus 2% FBS. Th.e cells were transfected with the rat OFQ receptor cDNA (LC132), FEBS Lei;t. 347, 284-288, 1994, cloned in the expression vector WO 00/14067 _ 6 - PCT/EP99/06442 pCEP4 (Invitrogen, SanI>iego, CA, USA) using lipofectin (Life Technologies, Bethesda, MD, USA). Tr~~nsfected cells were selected in the presence of hygromycin (1000 U/ml) (Calbiochem, SanDiego, CA, USA). A pool of resistant cells was tested for OFQ-R expression by binding of [3H]-OFG.~ (Amersham PLC, Buckinghamshire, :England). These cells (293s-OF~I-R) were expanded for large scale culture and membrane preparation.
Membrane preparation 293s-OFQ-R cells were harvested by centrifugation, washed 3 times with phosphate buffered saline (PBS) before resuspension in buffer A (50 mM
1o Tris-HCl, pH 7.8, 5 mM IVIgCI2, 1 mM EGTA) and disruption with a tissue homogenizer (30 seconds, setting 4, Pt 20, Kinematica, Kriens-Lucern, Switzerland). A total me~a~brane fraction was obtained by centrifugation at 49,000 x g at 4°C. This procedure was repeated twice and the pellet was resuspended in buffer A. Aliquots were stored at -70°C and protein concentrations were determined using the BCATM Protein Assay Reagent (Pierce, Rockford, IL) following the manufacturer's recommendations.
Binding Assays [3H]-OFQ competition studies were carried out with 77 ug membrane protein in a final assay volume of 0.5 ml buffer A plus 0.1% BSA and 0.01%
2o bacitracin (Boehringer-Mannheim, Mannheim, Germany) for one hour at room temperature. 50 nM unlabeled OFQ was used to define the non-specific binding. The assays werE~ terminated by filtration through Whatman GF/C
filters (Unifilter-96, Canberra Packard S.A., Zurich, Switzerland) pretreated with 0.3% polyethylenim.ine (Sigma, St. Louis, MO, USA) and 0.1% BSA
(Sigma) for 1 hour. The filters were washed 6 times with 1 ml of ice bold 50 mM Tris-HCl pH 7.5. The retained radioactivity was counted on a Packard Top-Count microplate scintillation counter after addition of 40 ul of Microscint 40 (Canberra Packard). 'Che effects of compounds were determined using at least 6 concentrations in triplicate, and determined twice. ICSp values were determined by curve fitting and these values were converted to K; values by the method of Cheng anti Prusoff, Biochem. Pharmacol., 22, 3099, 1973.
The affinity to the t~FQ-receptor, given as pKi, is in the range of 6,0 to 8,0, for example the pKi for the compounds mentioned below is as follows:

Example OFQ pKi 4 7.5 36 7.0 19 6.5 4 (3RS,4RS)-1-Cyclononyl-4-(2-hydroxy-phenyl)-piperidin-3-of hydrochloride (1:1) 36 (3RS,4RS)-1-Cyclodc:cyl-4-(2,6-dimethoxy-phenyl)-piperidin-3-of hydrochloride (1:1) 19 Mixture of (3RS,4R:i)-4-(2-Methoxy-phenyl)-1-(cis- and -(trans-4-isopropyl-cyclohexyl)-piperidin-3-of hydrochloride (1:1) The compounds of formula I as well as their pharmaceutically usable acid addition salts can be used as medicaments, e.g. in the form of pharmaceutical preparations. The pharmaceutical preparations can be administered orally, e.g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions. Z'he administration can, however, also be effected rectally, e.g. in the form of suppositories, or parenterally, e.g. in the firm of injection solutions.
The compounds of formula I and their pharmaceutically usable acid addition salts can be processed with pharmaceutically inert, inorganic or organic excipients for they production of tablets, coated tablets, dragees and hard gelatine capsules. lactose, corn starch or derivatives thereof, talc, stearic 2o acid or its salts etc can be used as such excipients e.g. for tablets, dragees and hard gelatine capsules.
Suitable excipients for soft gelatine capsules are e.g. vegetable oils, waxes, fats, semi-solid and liquid polyols etc.

WO 00/14067 _ $ _ PCT/EP99106442 Suitable excipients fir the manufacture of solutions and syrups are e.g.
water, polyols, saccharose, invert sugar, glucose etc.
Suitable excipients fir injection solutions are e.g. water, alcohols, polyols, glycerol, vegetable oils etc.
Suitable excipients for suppositories are e.g. natural or hardened oils, waxes, fats, semi-liquid or liquid polyols etc.
Moreover, the pharmaceutical preparations can contain preservatives, solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or to antioxidants. They can also contain still other therapeutically valuable substances.
The dosage can vary within wide limits and will, of course, be fitted to the individual requirements i:n each particular case. In general, in the case of oral administration a daily do;>age of about 10 to 1000 mg per person of a compound of general formula I should be appropriate, although the above upper limit can also be exceeded when it appears to be indicated.
The following examples illustrate the present invention, but are not intended to be limiting in any manner.
Example 1 2-(1-Cvclodecyl-nineridin-4-yl)-uhenol hydrochloride (1:1) a) 1-Benzyl-4-(2-benzylogy-phenyl)-1,2,3,6-tetrahydro-pyridine The title compound was prepared in comparable yield according to a literature procedure (Juan C. Jean and Lawrence D. Wise, J. Heterocyclic Chem. 1987, 24, 1317 - 1319) in two stE~ps starting from 2-benzyloxybromobenzene instead of 2-bromoanisole. The product was obtained as a light brown oil.
MS m/e (%): 356 (M+H', 100).
b) 2-Piperidin-4-yl-phenol To a solution of 37.6 g (0.105 mol) of 1-benzyl-4-(2-benzyloxy-phenyl)-1,2,3,6-tetrahydro-pyridine in 380 ml of methanol were added 7.0 g of 10 % of 3o palladium on activated charcoal. The reaction mixture was hydrogenated WO 00/14067 _ 9 _ PCT/EP99/06442 (room temperature, 5 bar) until the theoretical amount of hydrogen was taken up (about 20 h). The catalyst was filtered off and was washed three times with 50 ml portions of methanol. The filtrate was evaporated in vacuo and purified by flash-chromatography to give 14.8 g (80%) of the title compound as a light brown foam.
MS m/e (%): 177 (M+, 100).
c) 2-(1-Cyclodecyl-pipeW din-4-yl)-phenol To a suspension of 1.0 g (~~.64 mmol) 2-piperidin-4-yl-phenol in 870 mg (5.64 mmol) cyclodecanone werE~ added 8.0 g (28 mmol) tetraisopropyl orthotitanate.
1o After stirring for 4 days ai; room temperature, a viscous oil was obtained.
A
solution of 250 mg (3.95 nimol) sodium cyanoborohydride in 4 ml ethanol was added dropwise within 3-~~ min. Stirring was continued for 2 h at room temperature and 10 ml 2.;5 M ammonia in ethanol were added. The precipitate was filtered off and the filtrate evaporated. The residue was purified by flash-chromatography to give 1.37 g (7?%) of the title compound as a light yellow foam.
MS m/e (%): 316 (M+H', 100).
d) 2-(1-Cyclodecyl-piperidin-4-yl)-phenol hydrochloride (I:1) To a solution of 100 mg (0.32 mmol) 2-(1-cyclodecyl-piperidin-4-yl)-phenol in 2o ml ether were added 1 ml 2.3 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vc~cuo and the residue was re-suspended in 10 ml ether. Filtration of the precipitate and washing with ether gave 101 mg (91%) of the title compound as a white powder.
MS m/e (%): 316 (M+H', 100).
Example 2 1-Cvclodecyl-4-(2-methoxy-uhenyl)-niueridine hydrochloride (1:1) To a solution of 100 mg (0.32 mmol) 2-(1-cyclodecyl-piperidin-4-yl)-phenol (example lc) in 1 ml anhydrous tetrahydrofuran at 0°C were added 76 mg (0.38 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for lh 3o at this temperature and 55 mg (0.38 mmol) methyl iodide were added. After WO 00/14067 _ 1~ _ PCT/EP99/06442 stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
The solvent was removed and the residue was purified by flash-chromatography to give 'l4 mg of an oil. The amine was dissolved in 5 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in vaccuo to give 42 mg (36%) of the title compound as a white powder.
MS m/e (%): 330 (M+H', 100).
Esamule 3 4-(2-Allyloxy-phenyl)-1-cyclodecyl-pit~eridine hydrochloride (1:1) To a solution of 200 mg (0.64 mmol) ) 2-(1-cyclodecyl-piperidin-4-yl)-phenol (example 1c) in 2 ml anhydrous tetrahydrofuran at 0°C were added 152 mg (0.76 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for lh at this temperature and 92 mg (0.76 mmol) allyl bromide were added. After i5 stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
The solvent was removed and the residue was purified by flash-chromatography to give :164 mg of an oil. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The 2o precipitate was filtered off, washed with ether and dried in vczcuo to give mg (55%) of the title compound as a white powder.
MS m/e (%): 356 (M+H', 100).
Example 4 (3RS.4RS)-1-Cyclononyl-4-(2-hydroxy-phenyl)-niperidin-3-of 25 hydrochloride (1:1) a) (3RS,4RS)-1-Benzyl-4-(2-benzylogy-phenyl)-piperidin-3-of hydrochloride (1:1) The title compound was prepared in comparable yield according to a literature procedure (Juan C. Jean and Lawrence D. Wise, J. Heterocyclic Clxem. 1987, 30 24, 1317 - 1319) in three steps starting from 2-benzyloxybromobenzene instead of 2-bromoanisole. The product was obtained as white crystals.

WO 00/14067 _ 11 _ PCT/EP99/06442 MS m/e (%): 374 (M+H', 100).
b) (3RS,4RS)-4-(2-Hydrogy-phenyl)-piperidin-3-of hydrochloride (1:I) To a solution of 46.5 g (0.1.1 moI) of (3RS,4RS)-1-benzyl-4-(2-benzyloxy-phenyl)-piperidin-3-of hydrochloride (1:1) in 1100 ml of methanol were added 8.5 g of 10 % of palladium on acti~~ated charcoal. The reaction mixture was hydrogenated (room temperature, 5 bar) until the theoretical amount of hydrogen was taken up (about 20 h). The catalyst was filtered off and was washed three times with 7L00 ml portions of methanol. The filtrate was evaporated in uacuo to give 21.0 g (99%) of the title compound as a white powder.
MS m/e (%): 193 (M', 78), 164 (58), 44 (100).
c) (3RS,4RS)-4-(2-Hydroxy-phenyl)-piperidin-3-of To a solution of 3.17 g (1.38 mmol) (3RS,4RS)-4-(2-hydroxy-phenyl)-piperidin-3-0l hydrochloride (l:l) in 30 ml methanol were added 1.5 g sodium carbonate.
After stirring for lh at room temperature, the sodium salts were filtered off and washed with 10 ml of ethanol. The filtrate was concentrated, diluted with ethanol and filtered again.. The filtrate was evaporated to give 2.7 g (quantitative) of the title compound as a white solid.
MS m/e (%): 194 (M+H', 100).
2o d) (3RS,4RS)-1-cyclononyl-4-(2-hydrogy-phenyl)-piperidin-3-of To a suspension of 520 m~; (2.69 mmol) (3RS,4RS)-4-(2-hydroxy-phenyl)-piperidin-3-of in 380 mg (L55 mmol) cyclononanone were added 3.80 g (13 mmol) tetraisopropyl orth.otitanate. After stirring for 2 days at room temperature, a viscous oil. was obtained. A solution of I20 mg (1.9 mmol) sodium cyanoborohydride in 1 ml ethanol was added dropwise within 3-4 min.
Stirring was continued fo:r 6 h at room temperature and 2 ml 2.5 M ammonia in ethanol were added. The precipitate was filtered off and the filtrate evaporated. The residue vvas purified by flash-chromatography to give 435 mg (51%) of the title compound as a light yellow foam.
3o MS m/e (%): 318 (M+H', 1.00).

WO 00/14067 - 12 _ PCT/EP99/06442 e) (3RS,4RS)-1-Cyclononyl-4-(2-hydroxy-phenyl)-piperidin-3-of hydrochloride (1:1) To a solution of 100 mg (0.32 mmol) (3RS,4RS)-1-cyclononyl-4-(2-hydroxy-phenyl)-piperidin-3-of in 10 ml ether were added 1 ml 2.3 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in uacuo and the residue was re-suspended in 10 ml ether. Filtration of the precipitate and washing with ether gave 9$ mg (88%) of the title compound as a white powder.
MS m/e (%): 318 (M+H', 100).
1o Example 5 (3RS,4RS)-1-Cyclono=wl-4-(2-methoxy-phenyl)-nineridin-3-of hydrochloride (1:1) To a solution of 110 mg (0.35 mmol) (3RS,4RS)-1-cyclononyl-4-(2-hydroxy-phenyl)-piperidin-3-of (e:!cample 4d) in 1 ml anhydrous tetrahydrofuran at 0°C
were added 85 mg (0.42 :mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for lh at i;his temperature and 59 mg (0.42 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
The solvent was removed and the residue was purified by flash-2o chromatography to give '74 mg of an oil. The amine was dissolved in 5 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in vacuo to give 70 mg (54%) of the title compound as a white powder.
MS m/e (%): 332 (M+H', 100).
Examvle 6 (3RS.4RS)-1-Cvclodecvl-4-(2-hvdroxv-phenyl)-pineridin-3-of hydrochloride (1:1) To a suspension of 2.50 ~; (12.9 mmol) (3RS,4RS)-4-(2-hydroxy-phenyl)-piperidin-3-of (example ~Ec) in 2.00 g (12.9 mmol) cyclodecanone were added 4.58 g (16.1 mmol) tetraiaopropyl orthotitanate. After stirring overnight at room temperature, a viscous oil was obtained. A solution of 570 mg (9 mmol) WO 00/14067 _ 13 _ PCT/EP99/06442 sodium cyanoborohydride in 10 ml ethanol was added dropwise within 1 min.
Stirring was continued a1; room temperature overnight and 50 ml of 1 N
hydrochloric acid solution were added. After 30 min, the precipitate was filtered off and washed with 1 N hydrochloric acid solution to give 2.81 g (59%) of the title compound as a light brown foam.
MS m/e (%): 332 (M+H', 100).
Examule 7 (3RS.4RS)-1-Cvclodec~l-4-(2-ethoxy-vhenyl)-hiperidin-3-of hydrochloride (1:1) 1o a) (3RS,4RS)-1-Cyclodeeyl-4-(2-hydroxy-phenyl)-piperidin-3-of To a solution of 570 mg (1.55 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-hydroxy-phenyl)-piperidin-3-of hydrochloride (I:I) (example 6) in 20 ml ethanol were added 1.5 g sodium carbonate. After stirring for 1h at room temperature, the sodium salts were filtered off and washed with 10 ml of ethanol. The filtrate was evaporated to give 57L0 mg (quantitative) of the title compound as a white solid.
MS m/e (%): 332 (M+H', 100).
b) (3RS,4RS)-1-Cyclodecyl-4-(2-ethoxy-phenyl)-piperidin-3-of To a solution of 204 mg (0.62 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-hydroxy-2o phenyl)-piperidin-3-of in 1 ml anhydrous tetrahydrofuran at 0°C were added I47 mg (0.74 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for 1h at this temperature and 74 mg (0.68 mmol) ethyl bromide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
The solvent was removed and the residue was purified by flash-chromatography to give 51 mg (23%) of the title compound as a colourless oil.
MS m/e (%): 360 (M+H', 100).
c) (3RS,4R.S)-1-Cyclodecyl-4-(2-ethogy-phenyl)-piperidin-3-of hydrochloride (1:1) WO 00/14067 _ 14 _ PCT/EP99/06442 To a solution of 7 mg (0.0~; mmol) (3RS,4RS)-1-cyclodecyl-4-(2-ethoxy-phenyl)-piperidin-3-of in 1 ml ether were added 0.2 ml 2.5 N hydrochloric acid in ether.
After stirring for 30 min, Excess hydrochloric acid and ether were removed in vacuo and the residue wa.; re-suspended in 2 ml ether. Filtration of the precipitate and washing vczth ether gave 7 mg (quantitative) of the title compound as white crystals.
MS m/e (%): 360 (M+H', 100).
Examule 8 (3RS.4RS)-1-Cyclodecyl-3-ethoxv-4-(2-ethoxy-nhenyl)-niperidine 1o hydrochloride (1:1) a) (3RS,4RS)-1-Cyclodecyl-3-etho8y-4-(2-ethogy-phenyl)-piperidine The title compound was obtained as side product during the isolation and purification of (3RS,4RS)-:1-Cyclodecyl-4-(2-ethoxy-phenyl)-piperidin-3-of (example 7b). Flash-chromatography gave 93 mg {38 mg) of the title compound, as a light brown oil.
MS m/e (%): 388 (M+H', 100).
b) (3RS,4RS)-1-Cyclodecyl-3-ethoxy-4-(2-ethoxy-phenyl)-piperidine hydrochloride ( 1:1 ) To a solution of 10 mg (O.CI25 mmol) (3RS,4RS)-1-cyclodecyl-3-ethoxy-4-(2-2o ethoxy-phenyl)-piperidine in 1 ml ether were added 0.2 ml 2.5 N
hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vaccuo and the residue was re-suspended in 2 ml ether. Filtration of the precipitate and washing with ether gave 10 mg (quantitative) of the title compound as white crystals.
MS m/e (%): 388 (M+H', 100).
Example 9 (3RS.4RS)-4-(2-Ailvlox~~-nhenvl)-1-cyclodecvl-pioeridin-3-of hydrochloride (1:1) a) (3RS,4RS)-4-(2-A.llyloxy-phenyl)-1-cyclodecyl-piperidin-3-of To a solution of 645 mg (7..96 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-hydroxy-phenyl)-piperidin-3-of (example 7a) in 6 ml anhydrous acetone were added 298 mg (2.15 mmol) potassium carbonate and 260 mg (2.15 mmol) allyl bromide.
After stirring at 60°C overnight, the product was extracted with three 10 ml portions of ethyl acetate, washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 557 mg (76%) of the title compound as a white powder.
MS m/e (%): 372 (M+H', 1.00).
b) (3RS,4RS)-4-(2-Allyloa~y-phenyl)-1-cyclodecyl-piperidin-3-of to hydrochloride (1:1) To a solution of 133 mg (CL36 mmol) (3RS,4RS)-4-(2-allyloxy-phenyl)-I-cyclodecyl-piperidin-3-of in 2.5 ml tetrahydrofuran were added 2 ml 2.5 N
hydrochloric acid in ether'. After stirring for 30 min, excess hydrochloric acid and ether were removed in vczcuo and the residue was re-suspended in 10 ml ether. Filtration of the precipitate and washing with ether gave 100 mg (68%) of the title compound as white crystals.
MS m/e (%): 372 (M+H+, 7.00).
Example 10 (3RS,4RS)-4-(2-Allylox~ nhenvl)-1-cvclodecvl-3-methoxy-niperidine 2o hydrochloride (1:1) To a solution of 133 mg ((1.36 mmol) (3RS,4R5)-4-(2-allyloxy-phenyl)-1-cyclodecyl-piperidin-3-of (example 9a) in 1.5 ml anhydrous tetrahydrofuran at 0°C were added 85 mg (0.43 mmol) potassium bis(trimethylsilyl)amide.
Stirring was continued for 1h at this temperature and fil mg (0.43 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 ml water, the product was extracted with three 10 ml portions of ether, dried (magnesium sulfate) and evaporated. The residue was 3o purified by flash-chromatography to give 77 mg of an oil. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in uacuo to give 67 mg (4~l%) of the title compound as a white powder.

WO 00/14067 _ 16 _ PCT/EP99/06442 MS m/e (%): 386 (M+H', 100).
Example 11 (3RS.4RS)-1-Cyclodecyl-3-methoxv-4-(2-propogv-phenyl)-piperidine hydrochloride (1:1) To a solution of 30 mg (O.CI7 mmol) of (3RS,4RS)-4-(2-allyloxy-phenyl)-1-cyclodecyl-3-methoxy-piperidine hydrochloride (1:I) (example 10) in 1.5 ml of methanol were added 10 zng of 10 % of palladium on activated charcoal. The reaction mixture was hydrogenated (room temperature, 1 bar) overnight. The catalyst was filtered off and was washed three times with 1 ml portions of methanol. The filtrate was evaporated an ua~cuo to give 23 mg (77%) of the title compound as a white powder.
MS m/e (%): 388 (M+H', 100).
Example 12 (3RS.4RS)-4-(2-Benzvloxv-phenvD-1-evclodecvl-pineridin-3-of hydrochloride (I:1) To a solution of 721 mg (1.96 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-hydroxy-phenyl)-piperidin-3-of hydrochloride (1:1) (example 6) in 3 ml anhydrous dimethylformamide were .added 810 mg (5.88 mmol) potassium carbonate and 370 mg (2.16 mmol) benzyl bromide. After stirring at 60°C overnight, the 2o product was extracted with three 10 ml portions of ethyl acetate, washed with brine, dried (magnesium e,ulfate) and evaporated. The residue was purified by flash-chromatography to give 90 mg of a light yellow solid. The amine was dissolved in 10 ml ether a:nd 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in vacuo to give 63 mg (7 i~) of the title compound as a white powder.
MS m/e (%): 422 (M+H', 100).
Example 13 (3RS.4RS)-1-CycloundE~cyl-4-~,2-hydroxy-phenyl)-niueridin-3-of hydrochloride (1:1) 3o a) (3RS,4RS)-1-Cycloundecyl-4-(2-hydroxy-phenyl)-piperidin-3-of WO OOI14067 _ 17 _ PCT/EP99/06442 To a suspension of 300 mg (I.55 mmol) (3RS,4RS)-4-(2-hydroxy-phenyl)-piperidin-3-of (example 4c) in 260 mg (1.55 mmol) cycloundecanone were added 2.20 g (7.8 mmol) tetraisopropyl orthotitanate. After stirring for 6 days at room temperature, a viscous oil was obtained. A solution of 70 mg (1.1 mmol) sodium cyanoborohydridE: in 1 ml ethanol was added dropwise within 3-4 min.
Stirring was continued far 6 h at room temperature and 2 ml 2.5 M ammonia in ethanol were added. The precipitate was filtered off and the filtrate evaporated. The residue was purified by flash-chromatography to give 138 mg (26%) of the title compound as a light yellow foam.
to MS m/e (%): 346 (M+H', :L00).
b) (3RS,4RS)-1-Cycloundecyl-4-(2-hydroxy-phenyl)-piperidin-3-of hydrochloride (1:1) To a solution of 7 mg (0.02 mmol) (3RS,4RS)-1-cycloundecyl-4-(2-hydroxy-phenyl)-piperidin-3-of in 1 ml ether were added 0.2 ml 2.3 N hydrochloric acid ~5 in ether. After stirring fo:r 30 min, excess hydrochloric acid and ether were removed in vacuo and thE~ residue was re-suspended in 1 ml ether. Filtration of the precipitate and washing with ether gave 7 mg (quantitative) of the title compound as a white powder.
MS m/e (%): 346 (M+H', :L00).
2o Ezample 14 ~3RS.4RS)-1-Cycloundecyl-4-(2-methoxy-phenyl)-vineridin-3-of hydrochloride (1:1) To a solution of 110 mg (0.31 mmol) (3RS,4RS)-1-cycloundecyl-4-(2-hydroxy-phenyl)-piperidin-3-of (example 13a) in 1 ml anhydrous tetrahydrofuran at 0°C
25 were added 65 mg (0.34 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for lh at this temperature and 4$ mg (0.34 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 ml water, the product was extracted with three 10 ml 3o portions of ether, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 70 mg of an oil. The amine was dissolved in 5 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added WO 00/14067 _ 18 _ PCT/EP99/06442 dropwise. The precipitate was filtered off, washed with ether and dried in vaccuo to give 65 mg (55°h) of the title compound as a white powder.
MS m/e (%): 360 (M+H', 100).
Example 15 Mixture of (3RS.4RS)- and (3SR.4SR)-4-(2-hydroxy-phenyl)-1-f (R.S)-1.2.3.4-tetrahvdro-naphthalen-2-yll-giperidin-3-oI hydrochloride (1:1) a) Mixture of (3RS,4RS)- and (3SR,4SR)-4-(2-hydro~y-phenyl)-1-[(RS)-1,2,3,4-tetrahydro-naphthalen-2-yl]-piperidin-3-of To a mixture of 300 mg (1.55 mmol) (3RS,4RS)-4-(2-hydroxy-phenyl)-piperidin-3-0l (example 4c) and 2317 mg (1.55 mmol) j3-tetralone were added 2.20 g (7.8 mmol) tetraisopropyl ort:hotitanate. After stirring for 5 days at room temperature, a viscous o:il was obtained. A solution of 70 mg (1.1 mmol) sodium cyanoborohydride in 1 ml ethanol was added dropwise within 3-4 min.
Stirring was continued for 6 h at room temperature and 2 ml 2.5 M ammonia in ethanol were added. T'he precipitate was filtered off and the filtrate evaporated. The residue was puxified by flash-chromatography to give 100 mg (20%) of the title compound as a light brown foam.
MS m/e (%): 324 (M+H', 100).
b) Mixture of (3RS,4RS)- and (3SR,4SR)-4-(2-hydrogy-phenyl)-1-[(RS)-1,2,3,4-tetrahydro-naphthalen-2-yl]-piperidin-3-of hydrochloride (1:1) To a solution of 7 mg (0.02 mmol) of the mixture of (3RS,4RS)- and (3SR,4SR)-4-(2-hydroxy-phenyl)-1-[f.RS)-1,2,3,4-tetrahydro-naphthalen-2-yl]-piperidin-3-of in 1 ml ether were added 0.2 ml 2.3 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vacuo and the residue was re-suspended in 1 ml ether. Filtration of the precipitate and washing with ether gave 7 mg (quantitative) of the title compound as a white powder.
MS m/e (%): 324 (M+H', 100).
Ezamnle 16 3o Mixture of (3RSi4RS)- and (3SR,4SR~-4-(2-methoxv-nhenvl)-1-f (RS)-1.2.3.4-tetrahydro-nanhthalen-2-yll-pineridin-3-of hydrochloride (1:1) To a solution of 78 mg (0.24 mmol) of the mixture of (3RS,4RS)- and (3SR,4SR)-4-(2-hydroxy-F~henyl)-1-[(RS)-1,2,3,4-tetrahydro-naphthalen-2-yl]-piperidin-3-of (example 15a) in 0.8 ml anhydrous tetrahydrofuran at 0°C
were added 55 mg (0.27 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for lh at this temperature and 38 mg (0.27 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 mI water, the product was extracted with three 10 ml portions of ether, dried (naagnesium sulfate) and evaporated. The residue was 1o purified by flash-chromatography to give 38 mg of a foam. The amine was dissolved in 3 ml ether acid 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in Uczcuo to give 40 mg (44%) of the title compound as a light brown powder.
MS m/e (%): 338 (M+1i', :L00).
~5 Example 1?
Mixture of (3RS.4R,S)- end (3SR,4SR?-4-S2-h~xy-phenyl)-1-f (RS)-1.2,3,4-tetrahvdro-na~hthalen-1-yll-pineridin-3-of hydrochloride (1:1) WO 00/14067 - 20 _ PCT/EP99/06442 To a solution of 4 mg (0.01 mmol) of the mixture of (3RS,4RS)- and (3SR,4SR)-4-(2-hydroxy-phenyl)-1-[(R;i)-1,2,3,4-tetrahydro-naphthalen-1-yl]-piperidin-3-of in 1 ml ether were added 0.2 ml 2.3 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vacuo and the residue was re-suspended in 1 ml ether. Filtration of the precipitate and washing with ether gave 4 mg (quantitative) of the title compound as a white powder.
MS m/e (%): 324 {M+H', 100).
Examiple 18 1o Mixture of (3RS,4R,S)-4-(2-Hvdrosv-phen~~l)-1-(cis- and -(trans-4-isopropyl-evclohexvl)-piperidin-3-of hydrochloride (1:1) a) Mixture of (3RS,4RS)-~4-(2-hydroxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohesyl)-pi.peridin-3-of To a suspension of 2.50 g (:12.9 mmol) ) (3RS,4RS)-4-(2-hydroxy-phenyl)-~5 piperidin-3-oI (example 4c) in 1.88 g (12.9 mmol) 4-isopropylcyclohexanone were added 9.16 g (32.2 mmol) tetraisopropyl orthotitanate. After stirring overnight at room temperature, a viscous oil was obtained. A solution of 570 mg (9 mmol) sodium cyanoborohydride in 10 ml ethanol was added dropwise within 1 min. Stirring was continued at room temperature overnight and 50 2o ml of 1 N hydrochloric acid. solution were added. After 30 min, the precipitate was filtered off and washed with 1 N hydrochloric acid solution to give 1.51 g of a white solid. The mother liquor was extracted with dichloromethane and the extract was combined with the first precipitate. Purification by flash-chromatography gave 1.90 g (46%) of the title compound as a white solid.
25 MS m/e (%): 318 (M+H', 100).
b) Mixture of (3RS,4RS)-4-(2-Iiydrosy-phenyl)-1-(cis- and -(tran.s-4-isopropyl-cyclohesyl)-piperidin-3-of hydrochloride (1:1) To a solution of 10 mg (0.03 mmol) of the mixture of (3RS,4RS)-4-(2-hydroxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of in 1 mi ether 3o were added 0.2 ml 2.5 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vacuo and the residue was re-suspended in 1 ml ether. Filtration of the precipitate and washing with ether gave 10 mg (quantit~~tive) of the title compound as a white powder.

WO 00/14067 _ 21 _ PCT/EP99l06442 MS m/e (%): 318 (M+H", 100).
Example 19 Mixture of (3RS,4RS)-4-(2-Methoxy-phenyl)-1-(cis- and -(traps-4-isopronyl-cyclohexyl)-t~iperidin-3-of hydrochloride (1:1) To a solution of 75 mg (0.24 mmol) of the mixture of (3RS,4RS)-4-(2-hydroxy-phenyl)-1-(cis- and -(trap,s-4-isopropyl-cyclohexyl)-piperidin-3-of (example 18a) in 1 ml anhydrous tetrah;ydrofuran at 0°C were added 103 mg (0.52 mmol) potassium bis(trimethyls:ilyl)arnide. Stirring was continued for 1h at this temperature and 70 mg (n.49 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
The solvent was removed and the residue was purified by flash-chromatography to give 7 mg of an oil. The amine was dissolved in 1 ml ether and 0.2 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered o:ff, washed with ether and dried in vacuo to give 7 mg (8%) of the title compound as a white powder.
MS m/e (%): 332 (M+H", :L00).
Example 20 Mixture of (3RS,4RS)-4-(~2-allyloxy-phenyl)-1-(cis- and -(traps-4-2o isopropyl-evclohexyl)=ciperidin-3-of hydrochloride (1:1) a) Mixture of (3RS,4RS)-4-(2-allyloxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-;piperidin-3-of To a solution of 700 mg (;~.2 mmol) of the mixture of (3RS,4RS)-4-(2-hydroxy phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of (example 18a) in 3 ml anhydrous dimetlzylformamide were added 610 mg (4.4 mmol) potassium carbonate and 320 mg (2.64 mmol) allyl bromide. After stirring at 60°C overnight, the solvent was removed and the residue was purified by flash-chromatography to give 125 mg ( 16%) of the title compound as a colourless foam.
3o MS m/e (%): 358 (M+H', L00).

WO 00/14067 _ 22 _ PCT/EP99/06442 b) Mixture of (3RS,4RS)-4-(2-allylozy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of hydrochloride (1:1) To a solution of 5 mg (O.Ol.4 mmol) of the mixture of (3RS,4RS)-4-(2-allyloxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of in 1 ml ether were added 0.2 ml 2.3 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vacuo and the residue was re-suspended in 1 mI ethe:r. Filtration of the precipitate and washing with ether gave 5 mg (quantitative) of the title compound as a white powder.
MS m/e (%): 358 (M+H', 1~D0).
to Example 21 Mixture of (3RS.4RS)-4-~(2-Allvloxv-uhenyl)-1-(cis- and traps-4-isopropvl-cvclohexvl)-3-methoxv-niperidine hydrochloride (1:1) To a solution of 50 mg (O.1.4 mmol) of the mixture of (3RS,4RS)-4-(2-allyloxy-phenyl)-I-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of (example 20a) in 0.5 ml anhydrous tetrahydrofuran at 0°C were added 33 mg (0.17 mmol) potassium bis(trimethylsi:lyl)amide. Stirring was continued for lh at this temperature and 24 mg (0.17 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
2o After addition of 2 ml water, the product was extracted with three 10 ml portions of ether, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 30 mg of an oil. The amine was dissolved in 2 ml ether and 0.5 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered oif, washed with ether and dried in vacuo to give 32 mg (56%) of the title compound as a white powder.
MS m/e (%): 372 (M+H', 100).
Example 22 Mixture of (3RS,4RS)-4-(2-benzyloxy-phenyl)-1-(cis- and -(traps-4-isonropyl-eyclohexyl)-~iperidin-3-of hydrochloride (1:1) 3o a) Mixture of (3RS,4RS)-4-(2-benzyloxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of WO 00/14067 _ 23 - PCT/EP99/06442 To a solution of 397 mg (1.25 mmol) of the mixture of (3RS,4RS)-4-(2-hydroxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of (example 18a) in 3 ml anhydrous dimethylformamide were added 912 mg (6.6 mmol) potassium carbonate and f:50 mg (2.64 mmol) benzyl bromide. After stirring at 60°C overnight, the solvent was removed and the residue was purified by flash-chromatography to give 228 mg (45%) of the title compound as a colourless foam.
MS m/e (%): 408 (M+H~, 1(10).
b) Mixture of (3RS,4R,S)-4-(2-benzyloxy-phenyl)-1-(cis- and -(traps-4-1o isopropyl-cyclohexyl)-piperidin-3-of hydrochloride (i:I) To a solution of 7 mg (0.017 mmol) of the mixture of (3RS,4RS)-4-(2-benzyloxy-phenyl)-1-(cis- and -(traps-4-isopropyl-cyclohexyl)-piperidin-3-of in 1 ml ether were added 0.2 ml 2.3 N h:~drochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vacuo and the residue was re-suspended in 1 ml ether'. Filtration of the precipitate and washing with ether gave 7 mg (quantitat;ive) of the title compound as a white powder.
MS m/e (%): 408 (M+H', 1(10).
Example 23 (3RS,4RS)-1-Benzyl-3-methoxy-4-(2-methoxy-phenyl)-nineridine 2o hydrochloride (1:1) a) (3RS,4RS)-1-Benzyl-4-(2-methosy-phenyl)-piperidin-3-of The title compound was prepared in comparable yield according to a literature procedure (Juan C. Jean a:nd Lawrence D. Wise, J. Heterocyclic Chem. 1987, 24, 1317 - 1319) in three steps starting from 2-bromoanisole. The product was obtained as a white powder.
MS nz/e (%): 298 (M+H', 100).
b) (3RS,4RS)-1-Benzyl-3-methoxy-4-(2-methogy-phenyl)-piperidine hydrochloride ( 1:1 ) To a solution of 149 mg (0.5 mmol) (3RS,4RS)-1-benzyl-4-(2-methoxy-phenyl)-3o piperidin-3-of in 1.5 ml anhydrous tetrahydrofuran at 0°C were added 126 mg (0.6 mmol) potassium bis(t;rimethylsilyl)amide. Stirring was continued for lh WO 00/14067 _ 24 _ PCT/EP99/06442 at this temperature and 85 mg (0.6 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 ml water, the product was extracted with three 10 ml portions of ether, dried ynagnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 128 mg of an oil. The amine was dissolved in 10 ml ether .and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in uacuo to give 130 mg (75%) of the title compound as a white powder.
to MS m/e (%): 312 (M+H', 100).
Example 24 3RS,4RS)-3-Methoxy-1-(2-methoxy-benzyl)-4-(2-methoxy-nhenyl)-piperidine hydrochlox~ide 1:1 a) (3RS,4RS)-3-Methoxy-4-(2-methoxy-phenyl)-piperidine i5 To a solution of 4.03 g (ll.fi mol) (3RS,4RS)-1-benzyl-3-methoxy-4-(2-methoxy-phenyl)-piperidine hydrochloride (1:1) (example 23b) in 100 ml of methanol were added 1.0 g of 10 % of palladium on activated charcoal. The reaction mixture was hydrogenated (room temperature, 1 bar) for 20 h. The catalyst was filtered off and was washed three times with 10 ml portions of methanol.
2o The filtrate was concentrated to a total volume of ca. 50 ml and 1.3 g sodium carbonate were added. After stirring the suspension for additional 2 h, the solvent was removed under reduced pressure and the residue was re-suspended in 50 ml dichloromethane. Inorganic salts were filtered off and the filtrate was evaporated to give 2.20 g (74%) of the title compound as a light 25 yellow oil.
MS m/e (%): 221 (M', 17), 189 (100), 178 (62).
b) (3RS,4R,S)-3-Methoxy-1-(2-methoxy-benzyl)-4-(2-methoxy-phenyl)-piperidine hydrochloride (1:1) To a solution of 111 mg (0.5 mmol) (3RS,4RS)-3-methoxy-4-(2-methoxy-3o phenyl)-piperidine in 1.5 ml methanol were added 75 mg (0.55 mmol) 2-methoxybenzaldehyde. The reaction mixture was stirred for 5 min at room temperature and 63 mg ( 1.0 mmol) sodium cyanoborohydride were added.

WO 00/14067 _ 25 _ PCT/EP99/06442 After reaction overnight, 1 ml 2.3 M hydrochloric acid in methanol was added.
The reaction mixture was evaporated, re-dissolved in 5 ml water and was washed with ether. The aqueous solution was adjusted to pH 10 by addition of solid potassium hydroxide and was extracted with dichloromethane, dried (magnesium sulfate), evaporated and purified by flash-chromatography to give 100 mg of an oil. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M
hydrochloric acid in ether' was added dropwise. The precipitate was filtered off, washed with ether and dazed in uc~cuo to give 70 mg (35%) of the title compound as a white powder.
to MS m/e (%): 342 (M+H', 1.00).
Example 25 (3RS.4RS)-3-Methoxy-4-(2-methoxy-phenyl)-1-(3-uhenyl-nropyl)-niperidine hydrochloride (1:1) To a solution of 111 mg (CL5 mmol) (3RS,4RS)-3-methoxy-4-(2-methoxy-phenyl)-piperidine (example 24a) in 1.5 ml methanol were added 74 mg (0.55 mmol) 3-phenylpropionaldehyde. The reaction mixture was stirred for 5 min at room temperature and 63 mg (1.0 mmol) sodium cyanoborohydride were added. After reaction ove~:night, 1 ml 2.3 M hydrochloric acid in methanol was added. The reaction mixture was evaporated, re-dissolved in 5 ml water and was washed with ether. 'fhe aqueous solution was adjusted to pH 10 by addition of solid potassium hydroxide and was extracted with dichloromethane, dried (magnesium sulfate) and evaporated to give 155 mg of an oil. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in vc~cuo i;o give 150 mg (80%) of the title compound as a white powder.
MS m/e (%): 340 (M+H', 1.00).
Example 26 ~3RS,4RS)-1-(4-tert-Butyl-benzyl)-3-methoxy-4-(2-methoxv-phenyl)-3o piperidine hydrochloride 1:1 To a solution of I11 mg (CL5 mmol) (3RS,4RS)-3-methoxy-4-(2-methoxy-phenyl)-piperidine (exam;ple 24a) in 1.5 ml methanol were added 89 mg (0.55 mmol) 4-tent-butylbenzalnehyde. The reaction mixture was stirred for 5 min at WO 00/14067 _ 26 _ PCT/EP99/06442 room temperature and 63 mg (1.0 mmol) sodium cyanoborohydride were added. After reaction ovei~ight, 1 ml 2.3 M hydrochloric acid in methanol was added. The reaction mixture was evaporated, re-dissolved in 5 ml water and was washed with ether. The aqueous solution was adjusted to pH 10 by addition of solid potassium hydroxide and was extracted with dichloromethane, dried (magnesium sulfate), evaporated and purified by flash-chromatography to give 100 mg of an oil. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in Uacuo to give 110 l0 mg (55%) of the title compound as a white powder.
MS m/e (%): 368 (M+H', 100).
Example 27 (3RS,4RS)-3-Allyloxy-1-benzvl-4-(2-methoxy-phenyl)-nineridine hydrochloride (1:1) To a solution of 149 mg (0.5 mmol) (3RS,4RS)-1-benzyl-4-(2-methoxy-phenyl)-piperidin-3-of (example 23a) in 1.5 ml anhydrous tetrahydrofuran at 0°C
were added 126 mg (0.6 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for lh at this tE;mperature and 73 mg (0.6 mmol) allyl bromide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the 2o reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 ml wager, the product was extracted with three 10 ml portions of ether, dried (magnesium sulfate) and evaporated. T'he residue was purified by flash-chromatography to give 149 mg of an oil. The amine was dissolved in 10 ml ether a.nd 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in Uacuo to give 150 mg (80%) of the title compound as a white powder.
MS m/e (%): 338 (M+H', 1.00).
Examx~Ie 28 (3RS,4RS)-1-Cyclodecyl-4-(2-methoxy~henyl)-niveridin-3-of 3o hydrochloride (1:1) a) (3RS,4RS)-4-(2-Meth~oxy-phenyl)-piperidin-3-of hydrochloride (1:1) WO 00/14067 _ 27 _ PCT/EP99/06442 A solution of 5.95 g (20 m~mol) of (3RS,4RS)-1-benzyl-4-(2-methoxy-phenyl)-piperidine-3-of (example 23a) in 100 ml 1 N hydrochloric acid solution in ethanol was stirred for 30 min. The solvent and excess hydrochloric acid were removed in vacuo. The re.;idue was dissolved in 100 ml of methanol and 1.5 g of 10 % of palladium on activated charcoal were added. The reaction mixture was hydrogenated (room temperature, 1 bar) for 20 h. The catalyst was filtered off and was washed three times with 10 ml portions of methanol. The filtrate was evaporated in vacuo to give 4.7 g (96%) of the title compound as a white powder.
o MS m/e (%): 207 (M', 19), I78 (100).
b) (3RS,4RS)-4-(2-Methoxy-phenyl)-piperidin-3-of To a suspension of 4.7 g (~:0 mmol) (3RS,4RS)-4-(2-methoxy-phenyl)-piperidin-3-0l hydrochloride (1:1) in 40 ml methanol were added 2.1 g sodium carbonate.
After stirring for lh at room temperature, the sodium salts were filtered off and washed with 10 ml of methanol. The filtrate was concentrated, diluted with 2-propanol and filtered again. The filtrate was evaporated to give 4.10 g (quantitative) of the title compound as a white solid.
MS m/e (%): 208 (M+H', 100).
c) (3RS,4RS)-1-Cyclodecyl-4-(2-methoxy-phenyl)-piperidin-3-of 2o To a suspension of 4.14 g ~;20 mmol) (3RS,4RS)-4-(2-methoxy-phenyl)-piperidin-3-oI in 3.09 g (20 mmol) cyclodecanone were added 7.12 g (25 mmol) tetraisopropyl orthotitana.te. After stirring overnight at room temperature, a viscous oil was obtained. ~~ solution of 880 mg (14 mmol) sodium cyanoborohydride in 20 m.l ethanol was added dropwise within 3-4 min.
Stirring was continued for 4$ h at room temperature and 10 ml of 25 %
hydrochloric acid were added. After 30 min, the precipitate was filtered off and 200 ml 2.5 M ammonia in ethanol were added. The precipitate was filtered off again and the filtrate evaporated. The residue was purified by flash-chromatography to give 5.40 g (78%) of a light yellow oil that crystallized upon standing at room temperature.
MS m/e (%): 346 (M+H', 100).
d) (3RS,4RS)-1-Cyclodecyl-4-(2-methoxy-phenyl)-piperidin-3-of hydrochloride (1:1) To a solution of 270 mg (0.78 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-methoxy-phenyl)-piperidin-3-of in 7.0 ml ether were added 2 ml 2.5 N hydrochloric acid in ether. After stirring for 30 min, excess hydrochloric acid and ether were removed in vacuo and the residue was re-suspended in 20 ml ether. Filtration of the precipitate and washing with ether gave 298 mg (quantitative) of the title compound as a white powder.
MS m/e (%): 346 (M+H', 100).
Example 29 (3RS,4RS)-3-Methoxy-l.-cvclodecyl-4-(2-methoxy-phenyl)-piueridine 1o hydrochloride (1:1) To a solution of 173 mg (0.5 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-methoxy-phenyl)-piperidin-3-of (example 28c) in 1.5 ml anhydrous tetrahydrofuran at 0°C were added 126 mg (0~.6 mmol} potassium bis(trimethylsilyl)amide.
Stirring was continued for lh at this temperature and 85 mg (0.6 mmol) methyl iodide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 ml water, the product was extracted with three 10 ml portions of ether, dried (magnesium sulfate) and evaporated. The residue was 2o purified by flash-chromatography to give 120 mg of an oil. The amine was dissolved in 10 ml ether a:nd 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in uacuo to give 133 mg (67%) of the title compound as a white powder.
MS m/e (%): 360 (M+H', 100).
Examine 30 (3RS,4RS)-3-Allyloxy-1-cyclodecyl-4-(2-methoxy-uhenyl)-uineridine hydrochloride (1:I) a) (3RS,4RS)-3-Allyloxy-1-cyclodecyl-4-(2-methoxy-phenyl)-piperidine To a solution of 146 mg (1.0 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-methoxy-3o phenyl)-piperidin-3-of (example 28c) in 3.0 ml anhydrous tetrahydrofuran at 0°C were added 256 mg (1.2 mmol) potassium bis(trimethylsilyl)amide.

Stirring was continued for lh at this temperature and 145 mg (1.2 mmol) allyl bromide were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction :mixture was allowed to warm up to room temperature overnight.
After addition of 4 ml watE:r, the product was extracted with three 20 xnl pox-tions of ether, dried (magnesium sulfate) and evaporated. The residue was pux-ified by flash-chromatography to give 280 mg (73%) the title compound as a colourless oil.
MS m/e (%): 386 (M+H', 100).
1o b) (3RS,4RS)-3-Allyloxy~~1-cyclodecyl-4-(2-methoxy-phenyl)-piperidine hydrochloride (1:1) To a solution of 100 mg (0.26 mmol) (3RS,4RS)-3-allyloxy-1-cyclodecyl-4-(2-methoxy-phenyl)-pipex~idine in 10 ml ether was added dropwise 1 ml of 2.3 M
hydrochloric acid in ether. The precipitate was filtered ofl; washed with ether and dried in vacuo to give 109 mg (quantitative) of the title compound as a white powder.
MS m/e (%): 386 (M+H~, 100).
Example 31 ~3RS,4RS)-1-Cyclodecyl-4-(2-methoxy-phenyl)-3-nropoxv-nineridine 2o hydrochloride (1:1) To a solution of 77 mg (0.2 mmol) (3RS,4RS)-3-allyloxy-1-cyclodecyl-4-(2-methoxy-phenyl)-piperidine (example 30a) in 10 ml of ethyl acetate were added 40 mg of 10 % of palLladium on activated charcoal. The reaction mixture was hydrogenated (room temperature, 1 bar) for 20 h. The catalyst was filtered off and was washed three fiimes with I xnl portions of ethyl acetate. The filtrate was evaporated in uacuo to give 78 mg of an oil. The amine was dissolved in 10 ml ether and 1 xnl of 2.3 M: hydrochloxzc acid in ether was added dropwise.
The precipitate was filtered off; washed with ether and dx-ied in va~cuo to give 85 mg (quantitative) of the title compound as a white powder.
so MS m/e (%): 388 (M+H', 1()0).

WO 00/14067 - 3~ - PCT/EP99/06442 Example 32 (3RS.4RS)-1-Cvclodecvl-4-(2-isoprovvl-phenyl)-nineridin-3-of hydrochloride (1:1) a) (3RS,4RS)-1-Benzyl-4-(2-isopropyl-phenyl)-piperidin-3-of The title compound was prepared in comparable yield according to a literature procedure (Juan C. Jean wind Lawrence D. Wise, J. Heterocyclic Chem. 1987, 24, 1317 - 1319) in three steps starting from 2-bromoisopropylbenzene instead of 2-bromoanisole. The product was obtained as a white solid.
MS m/e (%): 310 (M+H', 100).
1o b) (3RS,4RS)-4-(2-Isopropyl-phenyl)-piperidin-3-of hydrochloride (1:1) A solution of 10.9 g (32 nvnol) of (3RS,4RS)-1-benzyl-4-(2-isopropyl-phenyl)-piperidin-3-of in 100 ml 1 N hydrochloric acid solution in ethanol was stirred for 30 min. The solvent ar.~d excess hydrochloric acid were removed in va~cuo.
The residue was dissolved in 300 ml of methanol and 2.4 g of 10 % of palladium on activated charcoal were added. The reaction mixture was hydrogenated (room temperature, 5 bar) for 20 h. The catalyst was filtered off and was washed three times with 50 ml portions of methanol. The filtrate was evaporated in Uacuo to give 5.9 g (74%) of the title compound as a white powder.
2o MS m/e (%): 219 (M', 17), 202 (21), 190 (39), 172 (42), 44 (100).
c) (3RS,4RS)-4-(2-Isopropyl-phenyl)-piperidin-3-of To a suspension of 5.75 g x;22.6 mmol) (3RS,4RS)-4-(2-isopropyl-phenyl)-piperidin-3-of hydrochloride (I:1) in I50 ml ethanol were added 3.6 g sodium carbonate. After stirring fir 2h at room temperature, the sodium salts were filtered off and washed with 10 ml of ethanol. The filtrate was concentrated, diluted with 2-propanol and filtered again. The filtrate was evaporated to give 4.93 g (quantitative) of this title compound as a white solid.
MS m/e (%): 220 (M+H', 100).
d) (3RS,4RS)-1-Cyclodecyl-4-(2-isopropyl-phenyl)-piperidin-3-of To a suspension of 500 mg (2.28 mmol) (3RS,4RS)-4-(2-isopropyl-phenyl)-piperidin-3-of in 350 mg (2.28 mmol) cyclodecanone were added 3.24 g (11.4 mmol) tetraisopropyl orthotitanate. After stirring for 5 days at room temperature, a viscous oil was obtained. A solution of 100 mg {1.59 mmol) sodium cyanoborohydride in 2 ml ethanol was added dropwise within 3-4 min.
Stirring was continued for 4 h at room temperature and 25 ml of 2.3 N
hydrochloric acid in ethanol were added. After heating for 3 h at 60°C, the solution was adjusted to p:Ei 8 by addition of 25 % sodium hydroxide solution and filtered. The filtrate was extracted with ethyl acetate, the organic phase 1o washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 415 mg (51%) of the title compound as a white solid.
MS m/e (%): 358 (M+H', 1()0).
e) (3RS,4RS)-1-Cyclodec;yl-4-(2-isopropyl-phenyl)-piperidin-3-of hydrochloride (1:1) To a solution of 30 mg (0.08 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-isopropyl-phenyl)-piperidin-3-of in 3 mI ethanol were added dropwise 0.3 ml of 2.3 M
hydrochloric acid in ethanol. The solution was stirred for 30 min at room temperature and was evaporated. The residue was suspended in ether and was 2o stirred for 1 h. The precipitate was filtered off, washed with ether and dried in vacuo to give 23 mg (70%) of the title compound as a white powder.
MS m/e (%): 358 (M+H', 100).
Example 33 (3RS,4RS)-1-Cyclodec~~l-4-(2-isoyrouyl-phen~~l)-3-methoxy-pineridine hydrochloride (1:1) To a solution of 200 mg (0.56 mmol) (3RS,4RS)-1-cyclodecyl-4-(2-isopropyl-phenyl)-piperidin-3-of (exa.mple 32d) in 2 ml anhydrous tetrahydrofuran at 0°C
were added 134 mg (0.67 mmol) potassium bis(trimethylsilyl)amide. Stirring was continued for 1h at this temperature and 80 mg (0.56 mmol) methyl iodide 3o were added. After stirring for 30 minutes at 0°C, the ice bath was removed and the reaction mixture was allowed to warm up to room temperature overnight.
After addition of 2 ml wat~:r, the product was extracted with three 10 ml portions of ether, dried (magnesium sulfate) and evaporated. The residue was WO 00/14067 _ 32 _ PCT/EP99/06442 purified by flash-chromatography to give 50 mg of an oil. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M hydrochloric acid in ether was added dropwise. The precipitate was filtered off, washed with ether and dried in vacuo to give 34 mg (15%) of the title compound as a white powder.
MS m/e (%): 372 (M+H', 1170).
Example 34 (3RS,4RS)-1-Cyclononyl-4-(2-isopropyl-phenyl)-piperidin-3-of hydrochloride (1:1) To a suspension of 200 mg (0.91 mmol) (3RS,4RS)-4-{2-isopropyl-phenyl)-piperidin-3-of (example 32c) in 160 mg (1.14 mmol) cyclononanone were added 1.29 g (4.56 mmol) tetraisopropyl orthotitanate. After stirring for 6 days at raom temperature, a viscous oil was obtained. A solution of 24 mg (0.64 mmol) sodium borohydride in 2 rr~l ethanol was added dropwise within 3-4 min.
Stirring was continued for 1 h at room temperature and 10 ml of 2.3 N
hydrochloric acid in ethanol were added. After heating far 4 h at 60°C, the solution was adjusted to p:Ei 8 by addition of 25 % sodium hydroxide solution and filtered. The filtrate was extracted with ethyl acetate, the organic phase washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 160 mg of a Iight yellow oil. The amine was dissolved in 10 ml ethanol and 1 ml of 2.3 M hydrochloric acid in ethanol was added dropwi se. The solution was stirred for 30 min at room temperature and was evaporated. The residue was suspended in ether and was stirred for 1 h. The precipitate was filtered off, washed with ether and dried in vacuo to give 175 mg (51%~) of the title compound as a white powder.
MS m/e (%): 344 (M+H', 11)0).
Ezamnle 35 1-Cvclodecvl-4-(2,6-dimethoxv-nhenyl)-piperidine hydrochloride (1:1) a) 1-Benzyl-4-(2,6-dimethoxy-phenyl)-1,2,3,6-tetrahydro-pyridine The title compound was prepared in comparable yield according to a literature procedure (Juan C. Jean and Lawrence D. Wise, J. Heterocyclic Chem. 1987, 24, 1317 - 1319) in two steps starting from 1,3-dimethoxyphen-2-ylmagnesium bromide instead of 2-meth.oxyphenylmagnesium bromide. The product was obtained as white needles.
MS m/e (%): 310 (M+H', 100).
b) 4-(2,6-Dimethoxy-phenyl)-piperidine A solution of 3.4 g (11 mmol) of 1-benzyl-4-(2,6-dimethoxy-phenyl)-1,2,3,6-tetrahydro-pyridine in 10() ml 1 N hydrochloric acid solution in ethanol was stirred for 30 min. The solvent and excess hydrochloric acid were removed in uacuo. The residue was dissolved in 110 ml of methanol and 0.9 g of 10 % of palladium on activated charcoal were added. The reaction mixture was 1o hydrogenated (room tempE:rature, 5 bar) for 20 h. The catalyst was filtered off and was washed three times with 50 ml portions of methanol. The filtrate was evaporated in vdcuo and the product was purified by flash-chromatography to give 1.34 g (57%) of the title compound as a white powder.
MS m/e (%): 222 (M+H', 1170).
c) 1-Cyclodecyl-4-(2,6-dimethosy-phenyl)-piperidine hydrochloride (1:1) To a suspension of 200 mg (0.9 mmol) 4-(2,6-dimethoxy-phenyl)-piperidine in 140 mg (0.9 mmol) cyclodecanone were added 1.28 g (4.52 mmol) tetraisopropyl orthotitanate. After stirring for 4 days at room temperature, a viscous oil was 2o obtained. A solution of 40 mg (0.63 mmol) sodium cyanoborohydride in 1 ml ethanol was added dropwise within 3-4 min. Stirring was continued for 5 h at room temperature and 10 ml of 2.3 N hydrochloric acid in ethanol were added.
After heating for 3 h at 60°C, the solution was adjusted to pH 8 by addition of % sodium hydroxide solution and filtered. The filtrate was extracted with 25 ethyl acetate, the organic ;phase washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 18 mg of white crystals. The amine was dissolved in 10 ml ether and 1 ml of 2.3 M
hydrochloric acid in ether was added dropwise. The solution was stirred for 30 min at room temperature ,and was evaporated. The residue was suspended in 3o ether and was stirred for 1. h. The precipitate was filtered off, washed with ether and dried in uacuo to give 20 mg (6%) of the title compound as a white powder.
MS m/e (%): 360 (M+H', 1170).

Example 36 ~3RS,4RS)-I-Cvclodecv~l-4-(2.6-dimethoxv-nhenvl)-uineridin-3-of hydrochloride (i:1) a) (3RS,4RS)-I-Benzyl-4-(2,6-dimethozy-phenyl)-piperidin-3-of hydrochloride (1:1) The title compound was prepared in comparable yield according to a literature procedure (Juan C. Jean and Lawrence D. Wise, J. Heterocyclic Chem. 1987, 24, 1317 - 1319) in three steps starting from 1,3-dimethoxyphen-2-ylmagnesium bromide instead of 2-methoxyphenylmagnesium bromide. The l0 product was obtained as white crystals.
MS m/e (%): 328 (M+H', 100).
b) (3RS,4RS)-4-(2,6-Dim.ethoxy-phenyl)-piperidin-3-of hydrochloride (1:1) To a solution of 2.9 g (8 mmol) of (3RS,4RS)-1-benzyl-4-(2,6-dimethoxy-phenyl)-piperidin-3-of hydrochloride (1:1) in 80 ml of methanol were added 600 mg of 10 % of palladium on activated charcoal. The reaction mixture was hydrogenated (room temperature, 5 bar) until the theoretical amount of hydrogen was taken up (about 20 h). The catalyst was filtered off and was washed three times with :?0 ml portions of methanol. The filtrate was 2o evaporated in Uacuo to give 1.88 g (87%) of the title compound as a light yellow powder.
MS m/e (%): 237 (M', 27), 208 (100).
c) (3RS,4RS)-4-(2,6-Dimethoxy-phenyl)-piperidin-3-of To a suspension of 1.78 g (6.53 mmol) (3RS,4RS)-4-(2,6-dimethoxy-phenyl)-piperidin-3-of hydrochloride (l:l) in 25 ml ethanol were added 1.0 g sodium carbonate. After stirring for 2h at room temperature, the sodium salts were filtered off and washed with 10 ml of ethanol. The filtrate was concentrated, diluted with 2-propanol and filtered again. The filtrate was evaporated to give 1.46 g (quantitative) of the title compound as a light yellow solid.
MS m/e (%): 238 (M+H', 100).
d) (3RS,4RS)-I-Cyclodecyl-4-(2,6-dimethogy-phenyl)-piperidin-3-of To a suspension of 500 mg (2.1 mmol) (3RS,4RS)-4-(2,6-dimethoxy-phenyl)-piperidin-3-of in 325 mg (2.1 mmol) cyclodecanone were added 3.0 g (10.5 mmol) tetraisopropyl orthotitanate. After stirring for 4 days at room temperature, a viscous oil was obtained. A solution of 93 mg (1.5 mmol) sodium cyanoborohydride in 1.5 ml ethanol was added dropwise within 3-4 min. Stirring was continued for 2 h at room temperature and 25 ml of 2.3 N
hydrochloric acid in ethanol were added. After heating for 2 h at 60°C, the solution was adjusted to pH 8 by addition of 25 % sodium hydroxide solution and filtered. The filtrate w;~s extracted with ethyl acetate, the organic phase io washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 218 mg (27%) of the title compound as a yellow oil.
MS m/e (%): 376 (M+H', 100).
e) (3RS,4RS)-1-Cyclodecyl-4-(2,&dimethozy-phenyl)-piperidin-3-of hydrochloride (1:1) To a solution of 30 mg (0.08 mmol) (3RS,4RS)-1-cyclodecyl-4-(2,6-dimethoxy-phenyl)-piperidin-3-of in 3 :ml ethanol were added dropwise 0.3 ml of 2.3 M
hydrochloric acid in ethanol. The solution was stirred for 30 min at room temperature and was evaporated. The residue was suspended in ether and was 2o stirred for 1 h. The precipitate was filtered off, washed with ether and dried in vacuo to give 20 mg (61%) of the title compound as a white powder.
MS m/e (%): 376 (M+H', 100).
Ezam~le 37 1-Cvclodecvl-4-nhenyl-ni,Eeridine hydrochloride (1:1,~
To a suspension of 200 mg (1.24 mmol) 4-phenylpiperidine in 230 mg (1.49 mmol) cyclodecanone were added 1.76 g (6.2 mmol) tetraisopropyl orthotitanate. After stirring for 5 days at room temperature, a viscous oil was obtained. A solution of 235 mg (6.2 mmol) sodium borohydride in 10 ml ethanol was added dropwise within 3-4 min. Stirring was continued for 2 h at room 3o temperature and 10 ml concentrated ammonia solution were added. The inorganic precipitate was filtered off and washed with dichloromethane. The filtrate was extracted with dichloromethane, the organic phase washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by WO 00/14067 _ 36 - PCT/EP99/06442 flash-chromatography to give 270 mg of a yellow solid. The amine was dissolved in 10 ml ethanol and 1 ml of 2.3 M hydrochloric acid in ethanol was added dropwise. The solution was stirred for 30 min at room temperature and was evaporated. The residue was suspended in ether and was stirred for 1 h.
The precipitate was filtere~3 off, washed with ether and dried in vacuo to give 200 mg (48%) of the title compound as a white powder.
MS m/e (%): 300 (M+H', 100).
Exainnle 38 1-Cyclodecyl-4-cyclohexyl-piperidine hydrochloride (1:1) To a suspension of 200 mg (1.12 mmol) 4-cyclohexylpiperidine in 220 mg (1.43 mmol) cyclodecanone were added 1.67 g (6.0 mmol) tetraisopropyl orthotitanate. After stirring for 5 days at room temperature, a viscous oil was obtained. A solution of 225 mg (6.0 mmol) sodium borohydride in 10 ml ethanol was added dropwise within 3-4 min. Stirring was continued for 2 h at room temperature and 10 ml concentrated ammonia solution were added. The inorganic precipitate was f filtered off and washed with dichloromethane. The filtrate was extracted with dichloromethane, the organic phase washed with brine, dried (magnesium sulfate) and evaporated. The residue was purified by flash-chromatography to give 80 mg of a light yellow solid. The amine was dissolved in 10 ml ethanol and 1 ml of 2.3 M hydrochloric acid in ethanol was added dropwise. The solution was stirred for 30 min at room temperature and was evaporated. The residue was suspended in ether and was stirred for 1 h.
The precipitate was filtered off, washed with ether and dried in vacuo to give 78 mg (19%) of the title compound as a white powder.
MS m/e (%): 305 (M', 18), 206 (100).

Claims

1. Compounds of the general formula wherein R1 is tetrahydronaphtyl;
or -(CH2)n-C6H5-R4 wherein n is 0-4 and R4 is H, lower alkyl, or lower alkoxy;
or C5-C12 cycloalkyl, optionally substituted by lower alkyl;
R2 is H, OH, lower alkoxy, lower alkenyloxy or lower alkyl;
R3 is C5-C7 cycloalkyl or phenyl, optionally substituted by OH, halogen, lower alkoxy, lower alkenyloxy, lower alkyl or -O-(CH2)n-C6H6 wherein n is 0-3;
and their pharmaceutically acceptable acid addition salts.

2. Compounds according to claim 1 wherein R1 is C5-C12 cycloalkyl, optionally substituted by lower alkyl.

3. Compounds according to claim 2, being (3RS,4RS)-1-cyclononyl-4-(2-hydroxy-phenyl)piperidin-3-ol;
1-cyclodecyl-4-(2-methoxy-phenyl)-piperidine;
(3RS,4RS)-1-cyclodecyl-4-(2-isopropyl-phenyl)piperidin-3-ol;
(3RS,4RS)-4-(2-hydroxy-phenyl)-1-(cis-and-(trans-4-isopropylcyclohexyl)-piperidin-3-ol;

2-(1-cyclodecyl-piperidin-4-yl)-phenol;
(3RS,4RS)-1-cyclodecyl-4-(2-methoxy-phenyl)-piperidin-3-ol;
1-cyclodecyl-4-cyclohexyl-piperidine;
(3RS,4RS)-1-cyclononyl-4-(2-methoxy-phenyl)-piperidin-3-ol;
(3RS,4RS)-4-(2-allyloxy-phenyl)-1-cyclodecyl-piperidin-3-ol;
1-cyclodecyl-4-phenyl-piperidine;
(3RS,4RS)-1-cyclononyl-4-(2-isopropyl-phenyl)-piperidin-3-ol; and (3RS,4RS)-1-cyclodecyl-4-(2-hydroxy-phenyl)piperidin-3-ol.

4. Compounds according to anyone of claims 1-3 for use as therapeutic active substances, in particular for memory and attention deficits, psychiatric, neurological and physiological disorders, such as anxiety and stress disorders, depression, memory loss due to Alzheimer's disease or other dementias such as vascular dementia and AIDS dementia complex, Parkinson's disease, epilepsy and convulsions, acute and/or chronic pain conditions, withdrawal symptoms of addictive drugs and reduction of their abuse/craving, control of water balance, Na+ excretion, arterial blood pressure disorders and metabolic disorders such as obesity.

5. A medicament containing one or more compounds of any one of claims 1 to 3 or a pharmaceutically acceptable salt thereof.

6. A medicament according to claim 5 for the treatment of Orphanin FQ
(OFQ) receptor related diseases, which include memory and attention deficits, psychiatric, neurological and physiological disorders, such as anxiety and stress disorders, depression, memory loss due to Alzheimer's disease or other dementias such as vascular dementia and AIDS dementia complex, Parkinson's disease, epilepsy and convulsions, acute and/or chronic pain conditions, withdrawal symptoms of addictive drugs and reduction of their abuse/craving, control of water balance, Na+ excretion, arterial blood pressure disorders and metabolic disorders such as obesity.

7. A process for preparing a compound of formula I as defined in claim 1, which process comprises reductively aminating a compound of formula II

with a compound of formula wherein R1, R2 and R3 are as claimed in claim 1.

8. The use of one or more compounds according to claims 1 to 3, or pharmaceutically acceptable salts thereof, for the manufacture of medicaments.

9. The use according to claim 8 for the manufacture of a medicament for the treatment of memory and attention deficits, psychiatric, neurological and physiological disorders, such as anxiety and stress disorders, depression, memory loss due to Alzheimer's disease or other dementias such as vascular dementia and AIDS dementia complex, Parkinson's disease, epilepsy and convulsions, acute and/or chronic pain conditions, withdrawal symptoms of addictive drugs and reduction of their abuse/craving, control of water balance, Na+ excretion, arterial blood pressure disorders and metabolic disorders such as obesity.

10. Compounds of the general formula I, obtained by the process of claim 7 or by equivalent processes.

11. The invention substantially as described herein.