Patent Application
20060241142
This invention relates to the treatment of diseases in which serotonin and Substance P or Neurokinin A are implicated, for example, in the treatment of disorders or conditions such as hypertension, depression, generalized anxiety disorder, phobias, posttraumatic stress syndrome, avoidant personality disorder, premature ejaculation, eating disorders, obesity, chemical dependencies, cluster headache, migraine, pain, Alzheimer's disease, obsessive-compulsive disorder, panic disorder, memory disorders, Parkinson's disease, endocrine disorders vasospasm, cerebellar ataxia, gastrointestinal tract disorders, negative symptoms of schizophrenia, premenstrual syndrome, fibromyalgia syndrome, stress incontinence, Tourette's syndrome, trichotillomania, kleptomania, male impotence, attention deficit hyperactivity disorder, chronic paroxysmal hemicrania and headache.
The mammalian neurokinins are peptide neurotransmitters found in the peripheral and central nervous systems. The three principal neurokinins are Substance P (SP), Neurokinin A (NKA) and Neurokinin B (NKB). N-terminally extended forms of at least NKA are known. Three receptor types are known for the principal neurokinins. Based upon their relative selectivities for the neurokinins SP, NKA and NKB, the receptors are classified as neurokinin 1 (NK1), neurokinin 2 (NK2) and neurokinin 3 (NK3) receptors, respectively. In the periphery, SP and NKA are localized in C-afferent sensory neurons, which neurons are characterized by non-myelinated nerve endings known as C-fibers, and are released by selective depolarization of these neurons, or selective stimulation of the C-fibers. C-Fibers are located in the airway epithelium, and the tachykinins are known to cause profound effects which clearly parallel many of the symptoms observed in asthmatics. The effects of release or introduction of tachykinins in mammalian airways include bronchoconstriction, increased microvascular permeability, vasodilation, increased mucus secretion and activation of mast cells. Neurokinin antagonists that interact with NK1, NK2 and NK3 receptors, having different chemical structures have been described.
NK1 activity is also implicated in depression and anxiety, mice with genetically altered NK1 receptors have decreased anxiety related behavior (Santarelli, L., et al., Proc. Nat. Acad. Sci. (2001), 98, 1912) and NK1 antagonists have been reported to be effective in an animal model of depression (Papp, M., et al., Behav. Brain Res. (2000), 115, 19).
Serotonin Selective Reuptake Inhibitors (SSRIs) are widely used for the treatment of major depressive disorder (MDD) and are considered well-tolerated and easily administered. SSRIs, however, have a delayed onset of action, are associated with undesirable side effects, such sexual dysfunction, and are ineffective in perhaps 30% of patients (M. J. Gitlin, M J, J. Clin. Psych., 55, 406-413, 1994).
Compounds with dual action as NK1 antagonists and serotonin reuptake inhibitors may, therefore provide a new class of antidepressants. Indeed, compounds combining NK1 antagonism and serotonin reuptake inhibition have been described (Ryckmans, T., et al., Bioorg. Med. Chem. Lett. (2002), 12, 261).
We have discovered naphthamide derivatives having both neurokinin 1 (NK1) antagonist activity and serotonin reuptake inhibitory (SRI) activity. Naphthamide derivatives of the invention are compounds in accord with structural diagram I:
wherein:
R1 independently at each occurrence is CN, CF3, OCF3, OCHF2, halogen, C2-4alkenyl, C2-4alkynyl, Ra, Rb, SRa, NRaRb, CH2NRaRb, ORa or CH2ORa, where Ra and Rb are independently at each occurrence hydrogen, C1-6alkyl, C(O)Rc, C(O)NHRc or CO2Rc, where Rc at each occurrence is C1-6alkyl; or, Ra and Rb together are (CH2)jG(CH2)k or G(CH2)jG, where G is oxygen or sulfur, j is 1, 2, 3 or 4, and k is 0, 1 or 2;
m is 1, 2 or 3 where at least one R1 moiety is other than hydrogen;
R2 and R3 are independently hydrogen, C1-6alkyl or C1-6alkyl substituted with C1-4alkoxy;
R4 independently at each occurrence is hydrogen, CN, CF3 OCF3, OCHF2, halogen, C1-4alkyl, C2-4alkenyl, C2-4alkynyl, SRa, NRaRb, CH2NRaRb, ORa or CH2ORa, where Ra and Rb are independently at each occurrence hydrogen, C1-6alkyl, C(O)Rc, C(O)NRc or CO2Rc where Rc at each occurrence is C1-6alkyl; or, Ra and Rb together are (CH2)jG(CH2)k or G(CH2)jG where G is oxygen or sulfur, j is 1, 2, 3 or 4, k is 0, 1 or 2, and
n is 0, 1, 2 or 3.
The invention also encompasses in vivo-hydrolysable precursors and pharmaceutically-acceptable salts of the naphthamide derivatives, pharmaceutical compositions and formulations containing them, methods of using them to treat diseases and conditions either alone or in combination with other therapeutically-active compounds or substances, processes and intermediates used to prepare them, uses of them as medicaments, uses of them in the manufacture of medicaments and uses of them for diagnostic and analytic purposes.
Compounds of the present invention are those in accord with structural diagram I:
wherein:
R1 at each occurrence is independently selected from CN, CF3, OCF3, OCHF2, halogen, C2-4alkenyl, C2-4alkynyl, Ra, Rb, SRa, NRaRb, CH2NRaRb, ORa or CH2ORa, where Ra and Rb are independently at each occurrence hydrogen, C1-6alkyl, C(O)Rc, C(O)NHRc or CO2Rc, where Rc at each occurrence is C1-6alkyl; or, Ra and Rb together are (CH2)jG(CH2)k or G(CH2)jG, where G is oxygen or sulfur, j is 1, 2, 3 or 4, and k is 0, 1 or 2;
m is 1, 2 or 3 where at least one R1 moiety is other than hydrogen;
R2 and R3 are independently hydrogen, C1-6alkyl or C1-6alkyl substituted with C1-4alkoxy;
R4 at each occurrence is independently selected from hydrogen, CN, CF3, OCF3, OCHF2, halogen, C1-4alkyl, C2-4alkenyl, C2-4alkynyl, SRa, NRaRb, CH2NRaRb, ORa or CH2ORa, where Ra and Rb are independently at each occurrence hydrogen, C1-6alkyl, C(O)Rc, C(O)NHRc or CO2Rc where Rc at each occurrence is C1-6alkyl; or, Ra and Rb together are (CH2)jG(CH2)k or G(CH2)jG, and
n is 0, 1, 2 or 3;
in vivo-hydrolysable precursors thereof, and pharmaceutically-acceptable salts thereof.
Other particular compound of the invention are those wherein:
R1 independently at each occurrence is CN, C1-6alkyl or ORc and m is 1, 2 or 3;
R2 and R3 are independently hydrogen or C1-6alkyl, and
R4 independently at each occurrence is halogen where n is 1 or 2; in vivo-hydrolysable precursors thereof, and pharmaceutically-acceptable salts thereof.
More particular compound of the invention are those wherein:
R1 independently at each occurrence is CN, ethyl or methoxy and m is 1, 2 or 3;
R2 and R3 are independently hydrogen or methyl, and
R4 independently at each occurrence is halogen where n is 1 or 2; in vivo-hydrolysable precursors thereof, and pharmaceutically-acceptable salts thereof.
Particular compounds of the invention are those wherein Ar, R1, R2 and R3 are moieties identified in Table 2 and Table 3, herein.
Particular compounds of the invention are those according to structural diagram II
wherein Ar is selected from phenyl, 3,4-dichlorophenyl, 3-fluorophenyl, 4-fluorophenyl 3,4-difluorophenyl, 4-methoxyphenyl, 3,4-dimethoxyphenyl, 3,4-methylenedioxyphenyl, 4-difluoromethoxyphenyl or 4-trifluoromethoxyphenyl; R1 is selected from H, methyl, ethyl or methoxy where m is 1 or 2 and R2 and R3 are independently is selected from H or methyl, and in vivo-hydrolysable precursors thereof, and pharmaceutically-acceptable salts thereof.
Most particular compounds of the invention are those described herein in vivo-hydrolysable precursors thereof, and pharmaceutically-acceptable salts thereof.
Pharmaceutically-acceptable salts of compounds in accord with structural diagram I include those made with inorganic or organic acids which afford a physiologically-acceptable anion, such as with, for example, hydrochloric, hydrobromic, sulfuric, phosphoric, methanesulfonic, sulfamic, para-toluenesulfonic, acetic, citric, lactic, tartaric, malonic, fumaric, ethanesulfonic, benzenesulfonic, cyclohexylsulfamic, salicyclic and quinic acids.
In order to use a compound in accord with structural diagram I or an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof for the therapeutic treatment or prophylactic treatment of mammals including humans, it is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition.
Therefore, another aspect the present invention is a pharmaceutical composition comprising a compound in accord with structural diagram I, an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof and a pharmaceutically-acceptable carrier.
Pharmaceutical compositions of this invention may be administered in standard manner for the disease condition that it is desired to treat, for example by oral, topical, parenteral, buccal, nasal, vaginal or rectal administration or by inhalation or insufflation. For these purposes the compounds of this invention may be formulated by means known in the art into the form of, for example, tablets, capsules, aq. or oily solutions, suspensions, emulsions, creams, ointments, gels, nasal sprays, suppositories, finely divided powders or aerosols or nebulisers for inhalation, and for parenteral use (including intravenous, intramuscular or infusion) sterile aq. or oily solutions or suspensions or sterile emulsions.
In addition to the compounds of the present invention the pharmaceutical composition of this invention may also contain, or be co-administered (simultaneously or sequentially) with, one or more pharmacological agents of value in treating one or more disease conditions referred to herein.
The pharmaceutical compositions of this invention will normally be administered to humans so that, for example, a daily dose of 0.01 to 25 mg/kg body weight (and preferably of 0.1 to 5 mg/kg body weight) is received. This daily dose may be given in divided doses as necessary, the precise amount of the compound received and the route of administration depending on the weight, age and sex of the patient being treated and on the particular disease condition being treated according to principles known in the art.
Typically unit dosage forms will contain about 1 mg to 500 mg of a compound of this invention. For example a tablet or capsule for oral administration may conveniently contain up to 250 mg (and typically 5 to 100 mg) of a compound in accord with structural diagram I or a pharmaceutically-acceptable salt thereof. In another example, for administration by inhalation, a compound in accord with structural diagram I or an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof may be administered in a daily dosage range of 5 to 100 mg, in a single dose or divided into two to four daily doses. In a further example, for administration by intravenous or intramuscular injection or infusion, a sterile solution or suspension containing up to 10% w/w (and typically 5% w/w) of a compound in accord with structural diagram I or an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof may be used.
Yet a further aspect of the present invention is a method of treating a disease condition wherein antagonism of NK1 receptors in combination with SRI activity is beneficial which method comprises administering to a warm-blooded animal an effective amount of a compound in accord with structural diagram I or an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof. The present invention also provides the use of a compound in accord with structural diagram I or an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof in the preparation of a medicament for use in a disease condition wherein antagonism of the NK1 receptors and SRI activity is beneficial.
The present invention also relates to a method for treating a disorder or condition selected from hypertension, depression in cancer patients, depression in Parkinson's patients, postmyocardial infarction depression, subsyndromal symptomatic depression, depression in infertile women, pediatric depression, major depression, single episode depression, recurrent depression, child abuse induced depression, post partum depression, generalized anxiety disorder, agoraphobia, social phobia, simple phobias, posttraumatic stress syndrome, avoidant personality disorder, premature ejaculation, anorexia nervosa, bulimia nervosa, obesity, addictions to alcohol, cocaine, heroin, phenobarbital, nicotine or benzodiazepines; cluster headache, migraine, pain, Alzheimer's disease, obsessive-compulsive disorder, panic disorder, dementia, amnestic disorders, age-related cognitive decline, dementia in Parkinson's disease, neuroleptic-induced parkinsonism, tardive dyskinesias, hyperprolactinaemia, vasospasm, cerebral vasculature vasospasm, cerebellar ataxia, gastrointestinal tract disorders, negative symptoms of schizophrenia, premenstrual syndrome, fibromyalgia syndrome, stress incontinence, Tourette's syndrome, trichotillomania, kleptomania, male impotence, attention deficit hyperactivity disorder, chronic paroxysmal hemicrania and headache associated with vascular disorders in a mammal, comprising administering an effective amount of a compound in accord with structural diagram I or a pharmaceutically-acceptable salt thereof effective in treating such disorder or condition and a pharmaceutically-acceptable carrier.
The present invention also relates to a pharmaceutical composition for treating a disorder or condition selected from hypertension, depression (e.g., depression in cancer patients, depression in Parkinson's patients, postmyocardial infarction depression, subsyndromal symptomatic depression, depression in infertile women, pediatric depression, major depression, single episode depression, recurrent depression, child abuse induced depression, and post partum depression), generalized anxiety disorder, phobias (e.g., agoraphobia, social phobia and simple phobias), posttraumatic stress syndrome, avoidant personality disorder, premature ejaculation, eating disorders (e.g., anorexia nervosa and bulimia nervosa), obesity, chemical dependencies (e.g., addictions to alcohol, cocaine, heroin, phenobarbital, nicotine and benzodiazepines), cluster headache, migraine, pain, Alzheimer's disease, obsessive-compulsive disorder, panic disorder, memory disorders (e.g., dementia, amnestic disorders, and age-related cognitive decline (ARCD)), Parkinson's diseases (e.g., dementia in Parkinson's disease, neuroleptic-induced parkinsonism and tardive dyskinesias), endocrine disorders (e.g., hyperprolactinaemia), vasospasm (particularly in the cerebral vasculature), cerebellar ataxia, gastrointestinal tract disorders (involving changes in motility and secretion), negative symptoms of schizophrenia, premenstrual syndrome, fibromyalgia syndrome, stress incontinence, Tourette's syndrome, trichotillomania, kleptomania, male impotence, attention deficit hyperactivity disorder (ADHD), chronic paroxysmal hemicrania and headache (associated with vascular disorders) in a mammal, preferably a human, comprising an effective amount of a compound in accord with structural diagram I or a pharmaceutically-acceptable salt thereof effective in treating such disorder or condition and a pharmaceutically-acceptable carrier.
Compounds in accord with structural diagram I and their in vivo-hydrolysable precursors or a pharmaceutically-acceptable salts may be made by processes as described and exemplified herein and by processes similar thereto and by processes known in the chemical art. If not commercially available, starting materials for these processes may be made by procedures which are selected from the chemical art using techniques which are similar or analogous to the synthesis of known compounds.
Pharmaceutically-acceptable salts may be prepared from the corresponding acid in a conventional manner. Non-pharmaceutically-acceptable salts may be useful as intermediates and as such are another aspect of the present invention.
It is well known in the art how to prepare optically-active forms (for example, by resolution of the racemic form or by synthesis from optically-active starting materials) and all optically active forms, enantiomers are compounds of this invention.
The following biological test methods, data and Examples serve to illustrate and further describe the invention.
The utility of a compound of the invention or an in vivo-hydrolysable precursor or a pharmaceutically-acceptable salt thereof (hereinafter, collectively referred to as a “Compound”) may be demonstrated by standard tests and clinical studies, including those disclosed in the publications described below.
Biological Assays:
SERT Binding Assay:
Frozen membrane preparations of a stably transfected HEK293 cell line expressing human 5-HTT receptors were purchased from Receptor Biology (PerkinElmer). Frozen alliquots were rapidly thawed, homogenized, and diluted in assay buffer (AB) containing 50 mM TRIS-HCL, 120 mM NaCl, 5 mM KCl and adjusted to pH 7.4 with NaOH. Final protein concentration was 40 μg/ml. Test compounds were evaluated in competition assays utlilizing [3H]-Imipramine Hydrochloride purchased from NEN (PerkinElmer) as the radioligand. The stock radioligand was diluted with AB for a final concentration of approximately 2 nM. Kd for [3H]-Imipramine Hydrochloride was determined to be 2.7 nM. The competition assays were performed on 96-well assay plates—two drugs per plate. Ten serial dilutions (normally 1 μM to 38 pM final concentration) from stock 10 mM solutions of compounds prepared in DMSO. All serial dilutions were made using 20% DMSO. DMSO content in assay is less than 1%. Incubation mixtures were prepared in quadruplicate in 96-well plates (Costar). Final assay volumes per well were 10 μL compound/nonspecific/control (1% DMSO), 20 μl membranes, 20 μL [3H]-Imipramine Hydrochloride, and 150 μl AB. Specific binding was defined by using 10 μM Imipramine. The binding reaction was initiated by adding membranes immediately after adding the radioligand to wells containing buffer plus either test compound, nonspecific, or control. The assay plates were placed on a plate shaker and shaken for thirty minutes while the reactions reached equilibrium. The plates were then filtered through Beckman GF/B filters, presoaked in 6% PEI, using a Packard Filtermate 196. Filters were washed 5× with 0.2 ml ice-cold wash buffer (5 mM Tris HCl, pH 7.4.) After filters dried, 35 μl of Microscint20 (Packard) was added to each well. The plates were then counted on a Packard TopCount to determine CPM's per well. Ki values were determined for each test compound utilizing the graphic and analytical software package, GraphPad Prism.
NK1 FLIPR Assay Using Fluo-4 Dye:
FLIPR assays are performed with a device marketed by Molecular Devices, Inc., designed to precisely measure cellular fluorescence in a high throughput whole-cell assay. (Schroeder et al., J. Biomolecular Screening, 1(2), p 75-80, 1996).
Compounds were evaluated for potency in blocking the response of U373 cells to the NK1 receptor agonist Acetyl-[Arg6, Sar9, Met(O2)11]-Substance P (ASMSP) using a FLIPR instrument.
U373 cells were loaded with Fluo-4 dye (Molecular Probes) for 45 min at 37° C. and exposed to graded concentrations of compounds for 15 min at room temperature before being challenged with 10 nM-12 nM ASMSP (an approximately EC80 concentration). Responses were measured as the peak relative fluorescence after agonist addition. pIC50s were calculated from eleven-point concentration-response curves for each compound.
Reagents:
Dye solution:
Fluo-4, AM dye, Molecular Probes F-14201. 50 μg lyophilized dye is dissolved in 23 μl DMSO plus 23 μL Pluronic F-127 (Molecular Probes P-3000). The 46 μL of solubilized fluo-4 dye is then added to 10 mL of working buffer solution to provide a working dye concentration of 5 μM. Each 10 mL of diluted dye is sufficient for a 384-well-plate of cells at 25 μL per well.
Agonist:
Acetyl-[Arg6, Sar9, Met(O2)11]-Substance P (ASMSP)
Stock solution of 3.33×10−2 M. Dissolve 100 mg in 3.05 mL DMSO and store in aliquots at 4° C.
Miscellaneous:
DMSO (to dissolve compounds and for tip wash)
Cell Culture and Plating Procedures:
U373 cells were grown in cell culture medium described above (30 mL per T-150 flask) and harvested when confluent as follows. Medium was removed by aspiration and cells were washed with 12 mL DPBS, 1× without Ca++ and Mg++. The DPBS was aspirated and replaced with 3 mL trypsin-EDTA. The cells plus trypsin/EDTA were incubated about 2 minutes at room temperature, until the cells detached from the flask. The harvesting reaction was quenched by addition of 9 mL culture medium and cells were resuspended by trituration. Cells were passaged at a transfer density of 1:4 every four days. For experiments, cells were counted, pelleted by centrifugation at 400× g for 5 min and resuspended in cell plating medium at a density of 480,000 cells/mL. 25 μL of this cell suspension was added to each well of a black-walled 384-well plate (Falcon Microtest, 35 3962) using a Labsystems Multidrop 384 to give 12,000 cells per well. Plates were incubated at 37° C. overnight (minimum 15 h, maximum 23 h) before use.
Compound and Agonist Preparation:
Compounds were dissolved in DMSO at a concentration of 10 mM and 120 μL of these solutions were transferred to the first well (column 1) of each row of a 96-well, round-bottomed, polypropylene storage plate (Costar 3365). Compounds on two such plates were then serially diluted simultaneously in DMSO using a Biomek 2000. 4 μl of each dilution was transferred to a deep well plate (Beckman Coulter 267006) which had been prepared previously to contain 400 μL of freshly made working buffer in each well. Concentrations resulting from this procedure are shown in Table 1. The final compound concentrations in the assay span 11 points, between 10 μM and 0.1 nM, in half-log increments.
The contents of the deep wells were mixed, and 45 μL of each dilution were transferred, in duplicate, to a 384-well polypropylene compound loading plate (Fisher 12-565-507) so that the 384-well plate contained duplicates of each of the compounds from both 96-well plates in the concentrations shown in table 1. Columns 23 & 24 of the plate contain no compound and serve as controls. Wells A-N in columns 23 and 24 were loaded with agonist only and therefore represent the maximal response. Wells O-P in columns 23 and 24 were loaded with only buffer, no agonist, and therefore represent the minimum response.
An ASMSP agonist loading plate was made by taking stock concentration of ASMSP and diluting in working buffer to give a concentration of 3.3×10−8 M. 45 μL of this solution were transferred to all wells of a 384-well polypropylene agonist loading plate (Fisher 12-565-507) except wells O23, O24, P23 & P24 which contained buffer alone and served as unstimulated controls.
Dye Loading Cells and Adding Compound:
For each 384-well assay plate of cells, 10 mL of diluted Fluo-4 dye was prepared as stated above in the methods/reagents section. First, each 384-well cell plate was washed once with working buffer on a CCS Packard plate washer. Any remaining post-wash buffer in the wells was removed by hand and 25 μL per well of Fluo-4 dye was added using a Labsystems Multidrop 384. The cell plate was returned to a 37° C. incubator for 45 min to allow the dye to permeate the cells. After 45 min of dye loading, the cell plates were washed twice with working buffer, leaving a 30 μL volume of buffer in each well. 5 μL of compound dilutions were transferred from the compound plate to the cell plate using a PlateMate Assay plates were incubated in the presence of compound for 15 min at room temperature in the dark, and then loaded onto FLIPR.
Recording Responses in FLIPR:
After the 15 min compound pre-incubation, the plates were loaded onto the FLIPR instrument, 15 μL of ASMSP agonist was added and the cellular response to the agonist was recorded for 90 seconds. The response is measured as the peak relative fluorescence after agonist addition.
Data analysis:
Results contained in the .stat files generated by FLIPR were pasted into an Excel analysis template and, after outliers were excluded, IC50 values were calculated within the template using XLfit. Individual IC50 values were reported, along with pIC50. When the two IC50's obtained for a compound differed by more than 3-fold that compound was assayed one or two more times to re-determine the value.
Compounds of the present invention exhibit a Ki in the range of 1 to 100 nM in the SERT assay and have an IC50 in the range 1 to 100 nM in FLIPR assay
The invention is illustrated by, but not limited to, the following examples in which descriptions, where applicable and unless otherwise stated, the following terms, abbreviations and conditions are used:
Abbreviations used herein are as follows: aq., aqueous; atm, atmospheric pressure; BOC, 1,1-dimethylethoxycarbonyl; DCM, dichloromethane; DMF, N,N-dimethylformamide; DMSO, dimethyl sulfoxide; EtOH, ethanol; Et2O, diethyl ether; EtOAc, ethyl acetate; h, hour(s); HPLC, high pressure liquid chromatography; HOBT, 1-hydroxybenzotriazole; MeOH, methanol; min, minutes; MS, mass spectrum; NMR, nuclear magnetic resonance; psi, pounds per square inch; RT, room temperature; sat., saturated; TEA, triethylamine; TFA, trifluoroacetic acid; THF, tetrahydrofuran.
Temperatures are given in degrees Celsius (° C.); unless otherwise stated, operations were carried out at room or ambient temperature (18-25° C.).
Organic solutions were dried over anhydrous sodium or magnesium sulfate; evaporation of solvent was carried out using a rotary evaporator under reduced pressure (4.5-30 mm Hg) with a bath temperature of up to 60° C.
Chromatography means flash column chromatography on silica gel unless otherwise noted; solvent mixture compositions are given as volume percentages or volume ratios.
When given, NMR data is in the form of delta values for major diagnostic protons (given in parts per million (ppm) relative to tetramethylsilane as an internal standard) determined at 300 MHz.
Melting points are uncorrected.
Mass spectra (MS) were obtained using an automated system with atmospheric pressure chemical ionization (APCI) unless otherwise indicated. Masses corresponding to the major isotopic component, or the lowest mass for compounds with multiple masses with nearly equivalent abundance (isotope splitting), are reported.
“Halogen” or “halo,” as used herein means, fluoro, chloro, bromo and iodo.
Where noted that a final compound was converted to the citrate salt, the free base was dissolved in methanol, DCM, or acetonitrile, combined with citric acid (1.0 equivalents) in methanol, concentrated under reduced pressure and dried under vacuum (25-60° C.). When indicated that the salt was isolated by filtration from Et2O, the citrate salt of the compound was stirred in Et2O for 4-18 h, recovered by filtration, washed with Et2O, and dried under vacuum (25-60° C.).
The title compound of the following structure
was prepared as a citrate hemihydrate, as follows. A solution containing 3-cyano-1-naphthoyl chloride (as described in U.S. Pat. No. 6,365,602) (141.2 mg, 0.655 mmol) and dry DCM (2 mL) was added in portions (0.25 mL) to a stirred solution containing 1-N-methyl-4-(3,4-dichlorophenyl)-4-(N-methylaminomethyl)piperidine (195.5 mg, 0.681 mmol), TEA (0.13 mL), and dry DCM (5 mL) at RT. After 72 h, the mixture was partitioned between DCM and 1M aq. HOAc, the organic layer was removed, and the aq. layer extracted with additional DCM (4×). The organic extracts were combined, washed (sat. aq. NaHCO3), dried, filtered, and concentrated. The residue was purified by chromatography (2-10% MeOH-DCM w/0.5% aq. NH3) and crystallization (DCM-hexane), converted to the citrate salt and isolated by filtration from Et2O to give the title compound as a white powder. MS m/z 466 (M+H). Analysis for C26H27Cl2N3O. 1.0 C6H8O7. 0.5 H2O: Calculated: C, 57.58; H, 5.13; N, 6.29. Found: C, 57.42; H, 5.05; N, 6.24.
The requisite 1-N-methyl-4-(3,4-dichlorophenyl)-4-(N-methylaminomethyl)piperidine was prepared as follows:
a) 1-N-Methyl-4-(3,4-dichlorophenyl)-4-(N-methylaminomethyl)piperidine.
A solution containing 1-N-methyl-4-(3,4-dichlorophenyl)-4-(ethoxycarbonylaminomethyl) piperidine (2.14 g, 6.2 mmol) and dry THF (20 mL) was added to a LiAlH4 and THF (40 mL) mixture at room temperature. The mixture was boiled under reflux for 1 h, cooled to RT, and carefully treated with Na2SO4. 10H2O (in portions) until no further gas evolution was noted. The mixture was stirred at RT for 18 h, filtered, and the solids washed with additional THF and toluene. The filtrates and washings were combined and concentrated to give the title compound as a light-yellow solid. The material was used without further purification. MS m/z 287 (M+H).
b) 1-Methyl-4-(3,4-dichlorophenyl)-4-(ethoxycarbonylaminomethyl)piperidine
A solution containing 1-N-methyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine (2.13 g, 7.80 mmol), TEA (1.36 mL), and dry DCM (15 mL) was cooled (ice bath), and a solution containing ethyl chloroformate (0.93 mL) and DCM (5 mL) was added dropwise over 20 min. After 40 min, cooling was removed and the solution was stirred at RT for an additional 3 h. The reaction was diluted with additional DCM, washed with sat. aq. NaHCO3 and brine, dried, filtered and concentrated. The residue was purified by chromatography (5-10% MeOH/DCM) to give the title compound as a viscous oil. MS m/z 345 (M+H).
c) 1-N-Methyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine
A mixture containing 1-N-methyl-4-(3,4-dichlorophenyl)-4-cyanopiperidine (2.1 g, 7.8 mmol), Raney Ni catalyst (1 g of 50% aq. slurry), EtOH (50 mL), and ammonium hydroxide (25 mL) was placed under a hydrogen atmosphere (50 psi) and agitated (Parr apparatus) for 18 h. The mixture was filtered through diatomaceous earth and concentrated to give the title compound as a viscous oil that was used without further purification. MS m/z 273 (M+H).
d) 1-N-Methyl-4-(3,4-dichlorophenyl)-4-cyanopiperidine.
According to procedures given in J. Het Chem., 20, 771 (1983); ibid., 23, 73 (1986), a mixture containing 3,4-dichlorophenylacetonitrile (4.9 g, 26.44 mmol), N-methyl-bis-(2-chloroethyl)amine hydrochloride (5.1 g, 26.49 mmol), hexadecyltributylphosphonium bromide (0.72 g, 1.43 mmol), and 50% aq. sodium hydroxide (30 mL) was heated at 100° C. for 1 hour, allowed to cool, treated with water (100 mL), and extracted with Et2O (3×). The ether extracts were combined, washed with water (1×), and extracted with 1N aq. HCl (5×). The acidic extracts were washed with Et2O, neutralized with solid sodium carbonate, and extracted with Et2O (2×). The ether extracts were dried, filtered and concentrated. The residual oil was purified by chromatography (0.5-2% MeOH/DCM) to give the title compound as a yellow oil. MS m/z 269 (M+H).
The title compound of the following structure
was prepared as a citrate hydrate, as follows. A solution containing 3-cyano-2-methoxy-1-naphthoyl chloride (described in international publication WO 00/20389) (151.9 mg, 0.618 mmol) and dry DCM (2 mL) was added in portions (0.25 mL) to a stirred solution containing 1-N-methyl-4-(3,4-dichlorophenyl)-4-(N-methylaminomethyl)piperidine (183.3 mg, 0.638 mmol), TEA (0.12 mL), and dry DCM (5 mL) at RT. After 72 h, the mixture was partitioned between DCM and 1M aq. HOAc, the organic layer was removed, and the aq. layer extracted with additional DCM (4×). The organic extracts were combined, washed (sat. aq. NaHCO3), dried, filtered, and concentrated. The residue was purified by chromatography (2-10% MeOH-DCM w/0.5% aq. NH3), converted to the citrate salt and isolated by filtration from Et2O to give the title compound (white powder) as a mixture of (E) and (Z) amides. MS m/z 496 (M+H). Analysis for C27H27Cl2N3O2. 1.0 C6H8O7. 1.0 H2O: Calculated: C, 56.10; H, 5.28; N, 5.95. Found: C, 56.44; H, 5.10; N, 5.98.
The title compound of the following structure
was prepared as a citrate, as follows. A solution containing 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (329 mg, 0.579 mmol) and DCM (5 mL) was stirred at room temperature and TFA (5 mL) was slowly added. After 18 h, the solution was concentrated, and the residue partitioned between DCM and sat. aq. NaHCO3. The organic layer was removed and the basic aq. layer was extracted with additional DCM (2×). The organic extracts were combined, dried, filtered, and concentrated. The residue was purified by chromatography (0-5% MeOH/DCM w/0.5% aq. NH3) and converted to the citrate salt to give the title compound as a white powder. MS m/z 468 (M+H).
The requisite 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine was prepared as follows:
a) 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl) piperidine.
To a stirred solution containing 1-N-BOC-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine (260.8 mg, 0.726 mmol), 3-cyano-2-methoxy-1-naphthoic acid (164.6 mg, 0.724 mmol), HOBT hydrate (290 mg, 1.89 mmol), N-methylmorpholine (0.17 mL), and DCM (15 mL) was added 1-(3-(dimethylamino)propyl-3-ethylcarbodiimide hydrochloride (215.5 mg, 1.12 mmol). After 72 h, the mixture was diluted with 30% hexane/EtOAc, washed successively with water (2×), 0.1 N aq. HCl (2×), sat. aq. NaHCO3, dried, filtered, and concentrated. The residue was purified by chromatography (0-1% MeOH/DCM) to give the title compound as a white, foamy solid. MS m/z 468.
b) 1-N-BOC-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine
A mixture containing 1-N-BOC-4-(3,4-dichlorophenyl)-4-cyanopiperidine (5.25 g, 14.78 mmol), Raney Ni catalyst (5 g of 50% aq. slurry), EtOH (175 mL), and ammonium hydroxide (88 mL) was placed under a hydrogen atmosphere (50 psi) and agitated (Parr apparatus) for 18 h. The mixture was filtered through diatomaceous earth, concentrated, and purified by chromatography (0-5% MeOH/DCM) to give the title compound as an off-white solid. MS m/z 344 (M+1-CH3). 1H NMR (CDCl3) δ 7.44 (d, 1H), 7.38 (d, 1H), 7.15 (m, 1H), 3.7 (br d, 2H), 3.07 (m, 2H), 2.76 (s, 2H), 2.08 (br d, 2H), 1.71 (m, 2H), 1.44 (s, 9H).
c) 1-N-BOC-4-(3,4-dichlorophenyl)-4-cyanopiperidine
A solution containing bis(2-chloroethyl)-N-BOC amine (described in U.S. Pat. No. 5,661,163) (8.15 g, 33.67 mmol), 3,4-dichlorophenylacetonitrile (5.05 g, 27.17 mmol), and DMSO (50 mL) was stirred at RT and solid cesium carbonate (17.6 g, 54.02 mmol) was added (in portions) over 10 minutes. After 20 h, additional cesium carbonate (1.7 g,) was added, and the mixture stirred for an additional 72 h. The mixture was partitioned between water and EtOAc, the aq. layer was removed, and the organic layer washed successively with additional water, 0.1M aq. HCl (2×), sat. aq. NaHCO3, and brine. The organic layer was dried, filtered, concentrated, and the residue triturated (3:1 hexane/ethyl acetate) to give the title compound as an off-white solid, m.p. 142-145° C. MS m/z 255. 1H NMR (CDCl3) δ 7.55 (d, 1H), 7.49 (d, 1H), 7.32 (m, 1H), 4.3 (br d, 2H), 3.18 (br t, 2H), 2.07 (d, 2H), 1.89 (m, 2H), 1.48 (s, 9H).
The title compound of the following structure
was prepared as a citrate, as follows. A solution containing 4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl) piperidine (103 mg, 0.22 mmol), formic acid (0.25 mL), and 37% aq. formaldehyde (2 mL) was heated at 100° C. for 18 h, then cooled and concentrated. The residue was partitioned between DCM and sat. aq. NaHCO3 and the organic layer was removed. The basic aq. layer was extracted with additional DCM (2×), and the combined organic extracts were dried, filtered, and concentrated. The residue was purified by chromatography (Chromatotron—silica rotor) (5% MeOH/DCM w/0.5% aq. NH3) and converted to the citrate salt to give the title compound as a white powder. MS m/z 482 (M+H).
The title compound of the following structure
was prepared as a citrate, as follows. In the same manner as Example 3, but using 1-N-BOC-4-(4-chlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (350 mg, 0.655 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound as a white powder. MS m/z 434 (M+H).
The requisite 1-N-BOC-4-(4-chlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine was prepared as follows:
a) 1-N-BOC-4-(4-chlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine.
In the same manner as Example 3a, but using 1-N-BOC-4-aminomethyl-4-(4-chlorophenyl) piperidine (244 mg, 0.75 mmol), 3-cyano-2-methoxy-1-naphthoic acid (170 mg, 0.748 mmol), HOBT hydrate (281 mg, 1.83 mmol), N-methylmorpholine (0.165 mL), 1-(3-(dimethylamino)propyl-3-ethylcarbodiimide hydrochloride (240 mg, 1.25 mmol), and DCM (10 mL), to yield the title compound as a foamy solid. MS m/z 434.
b) 1-N-BOC-4-aminomethyl-4-(4-chlorophenyl) piperidine.
In the same manner as Example 3b, but using 1-N-BOC-4-(4-chlorophenyl)-4-cyanopiperidine (1.05 g, 3.26 mmol), Raney Ni catalyst (1.4 g of 50% aq. slurry), EtOH (50 mL), and ammonium hydroxide (25 mL), to yield the title compound as a viscous oil. MS m/z 310 (M+H-Me).
c) 1-N-BOC-4-(4-chlorophenyl)-4-cyanopiperidine.
A solution containing bis(2-chloroethyl)-N-BOC amine (3.72 g, 15.38 mmol), 4-chlorobenzyl cyanide (2.10 g, 13.88 mmol), and anhydrous DMF (15 mL) was stirred and NaH (60% dispersion in mineral oil) (1.6 g, 40 mmol) was added in portions over 1 h. The mixture was heated at 60-65° C. for 1 h, stirred at RT for 72 h, then was poured into ice/water and extracted with EtOAc (2×). The organic extracts were washed (water and brine), dried, filtered, and concentrated. The residue was purified by chromatography (8:1:1 hexane/DCM/EtOAc) to give the title compound as a yellow solid. MS m/z 221.
The title compound of the following structure
was prepared as a citrate, as follows. In the same manner as Example 4, but using 4-(4-chlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (71.5 mg, 0.165 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound as a white powder. MS m/z 448 (M+H).
The title compound of the following structure
was prepared as a citrate, as follows. A solution containing 4-(4-chlorophenyl)-4-(3-(3-cyano-2-methoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl) piperidine (38.5 mg, 0.089 mmol), 2-bromoethyl methyl ether (55.5 mg, 0.40 mmol), TEA (0.075 mL), and DMF (0.5 mL) was heated (microwave) at 60° C. for 1.25 h, stirred at RT overnight, diluted with EtOAc, then washed successively with water (2×) and sat. aq. NaHCO3. The organic phase was dried, filtered, and concentrated. The residue was purified by chromatography (2-5% MeOH/DCM w/0.5% aq. NH3), converted to the citrate salt, and isolated by filtration from Et2O to give the title compound as a white powder. MS m/z 492 (M+H).
The title compound of the following structure
was prepared as a citrate, as follows. In the same manner as Example 3, but using 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2,4-dimethoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (801 mg, 1.34 mmol), TFA (25 mL), and DCM (25 mL), the citrate salt of to yield the title compound as a white, foamy solid. MS m/z 498 (M+H).
The requisite 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2,4-dimethoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine was prepared as follows: 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2,4-dimethoxynaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine.
A solution containing 3-cyano-2,4-dimethoxy-1-naphthoyl chloride (described in international publication WO 00/20389) (408.3 mg, 1.48 mmol) and dry DCM (2.5 mL) was added in portions (0.25 mL) to a stirred, cooled (ice bath) solution containing 1-N-BOC-4-(3,4-dichlorophenyl)-4-aminomethyl)piperidine (537 mg, 1.49 mmol), TEA (0.42 mL), and dry DCM (20 mL). After 1 h, the reaction was warmed to RT, stirred an additional 1.5 h, then concentrated. The residue was partitioned between water and EtOAc and the organic phase was removed and washed successively with 0.1N aq. HCl (2×), water, sat. aq. NaHCO3 (2×), and brine. The organic phase was dried, filtered, concentrated, and the residue purified by chromatography (0-1% MeOH/DCM) to give the title compound as an off-white, foamy solid. MS m/z 498.
The title compound of the following structure
was prepared as a citrate, as follows. In the same manner as Example 3, but using 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-ethylnaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (166.8 mg, 0.294 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound as a white powder. MS m/z 466 (M+H).
The requisite 1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-ethylnaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine was prepared as follows:
1-N-BOC-4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-ethylnaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine.
In the same manner as Example 3a, but using 1-N-BOC-4-aminomethyl-4-(3,4-dichlorophenyl) piperidine (375 mg, 1.04 mmol), 3-cyano-2-ethyl-1-naphthoic acid (described in international publication WO 00/20389, (233 mg, 1.04 mmol), HOBT hydrate (399 mg, 2.6 mmol), N-methylmorpholine (0.23 mL), 1-(3-(dimethylamino)propyl-3-ethylcarbodiimide hydrochloride (330 mg, 1.72 mmol), and DCM (10 mL), to yield the title compound as a foamy solid. MS m/z 466.
The title compound of the following structure
was prepared as a citrate, as follows. In the same manner as Example 4, but using 4-(3,4-dichlorophenyl)-4-(3-(3-cyano-2-ethylnaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (69 mg, 0.148 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound as a white powder. MS m/z 480 (M+H).
The title compound of the following structure
was prepared as a citrate salt as follows. To a solution containing 3-cyano-1-naphthoic acid (0.435 g, 2.21 mmol), 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine (0.539 g, 2.43 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.676 g, 3.53 mmol) and 1-hydroxybenzotriazole (0.600 g, 4.44 mmol) in DCM (20 mL) was added TEA (0.92 mL, 6.60 mmol). The solution was stirred at room temperature overnight. The mixture was partitioned between DCM and sat. NaHCO3, the organic layer was removed, and the aq. layer extracted with DCM (2×). The organic extracts were combined, dried, filtered, and concentrated. The residue was purified by chromatography (1-5% MeOH-DCM w/1% aq. NH3) to give the title compound as a white solid (0.7 g, 79% yield). MS m/z 402.50 (M+H). The citrate salt was obtained by standard procedure.
The requisite 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine was prepared as follows:
a) 1-N-Methyl-4-(4-fluorophenyl)-4-cyanopiperidine
To a solution containing mechlorethamine hydrochloride (1.923 g, 9.99 mmol) and 4-fluorophenyl acetonitrile (1.35 g, 9.99 mmol) in DMF (30 mL) was added sodium hydride (1.6 g, 40 mmol) slowly at 0° C. The resulting suspension was stirred and heated at 60° C. for 24 hrs. The reaction mixture was quenched with ice water, extracted with EtOAc (3×). The organic extracts were combined, washed with sat. NaCl (3×), dried, filtered, and concentrated. The residue was purified by chromatography (2-5% MeOH-DCM) to give the title compound as a yellow oil (1.788 g, 82% yield). MS m/z 219.38 (M+H).
b) 1-N-Methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine
To a solution of 1-N-methyl-4-(4-fluorophenyl)-4-cyanopiperidine (1.788 g, 8.20 mmol) in dry THF (25 mL) was added LAH (1M in THF, 25 mL, 24.6 mmol). The solution was stirred at room temperature overnight. The reaction was quenched by adding water (2.5 mL), followed by 15% NaOH (2.5 mL) and water (2.5 mL). The mixture was then filtered through diatomaceous earth, washed with EtOAc, dried, filtered, and concentrated to give the title compound as a yellow oil (1.619 g, 89% yield). MS m/z 223.45 (M+H).
The title compound of the following structure
was prepared as a citrate salt in the same manner as Example 11, but using 3-cyano-2-methoxy-1-naphthoic acid (100 mg, 0.44 mmol), 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine (107 mg, 0.48 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (135 mg, 0.704 mmol), 1-hydroxybenzotriazole (119 mg, 0.88 mmol), DCM (5 mL), and TEA (0.184 mL, 1.32 mmol), to yield the title compound as a white solid. 74% yield, MS m/z 432.46 (M+H).
The title compound of the following structure
was prepared as a citrate salt as follows. To a solution containing 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine (98 mg, 0.441 mmol) and TEA (0.13 mL, 0.933 mmol) in DCM (5 mL) was added 3-cyano-2-ethyl-1-naphthoyl chloride (108 mg, 0.443 mmol) in DCM (1 mL) at 0° C. The solution was stirred at 0° C. for 30 min and room temperature overnight. The mixture was partitioned between DCM and sat. NaHCO3, the organic layer was removed, and the aq. layer extracted with DCM (2×). The organic extracts were combined, dried, filtered, and concentrated. The residue was purified by chromatography (1-5% MeOH-DCM w/1% aq. NH3) to give the title compound as a light yellow solid (156 mg, 82% yield). MS m/z 430.51 (M+H). The citrate salt was obtained by standard procedure.
The title compound of the following structure
was prepared as a citrate salt as follows. To a solution of 1-N-methyl-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-(3-oxo-2-azaprop-1-yl))piperidine (366 mg, 0.912 mmol) in dry DMF (9 mL) was added NaH (44 mg, 1.1 mmol). The mixture was stirred at room temperature for 30 min and cooled to 0° C. Methyl iodide (0.085 mL, 1.36 mmol) was added and the mixture was stirred at 0° C. for 30 min, room temperature overnight. The mixture was partitioned between EtOAc and water, the organic layer was removed, and the aq. layer extracted with EtOAc (2×). The organic extracts were combined, washed with sat. NaCl (3×), dried, filtered, and concentrated. The residue was purified by chromatography (1-5% MeOH-DCM w/1% aq. NH3) to give the title compound as a white solid (164 mg, 43% yield). MS m/z 416.54 (M+H). The citrate salt was obtained by standard procedure.
The compounds of Examples 15 through 38 were prepared by processes similar to those given in Examples 11-14 but with replacement of 4-fluorophenyl acetonitrile with an appropriately substituted phenyl acetonitrile, compounds of Examples 15 through 38 and intermediates listed in Table 2 were obtained.
The title compound of the following structure
was prepared as a citrate in the same manner as Example 3, but using 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine (158 mg, 0.324 mmol), to yield the title compound as a white powder. MS m/z 388 (M+H).
The requisite 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine was prepared as follows:
a) 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine.
In the same manner as Example 3a, but using 1-N-BOC-4-amionmethyl-4-(4-fluoro)piperidine (1.68 g, 5.45 mmol), 3-cyano-1-naphthoic acid (980 mg, 4.97 mmol), HOBT (1.34 g, 9.92 mmol), triethylamine (2.08 mL), 1-(3-(dimethylamino)propyl-3-ethylcarbodiimide hydrochloride (1.52 g, 7.93 mmol), and DCM (30 mL), to yield the title compound as a foamy solid. MS m/z 388 (M+H-BOC).
b) 1-N-BOC-4-aminomethyl-4-(4-fluorophenyl) piperidine.
In the same manner as Example 3b, but using 1-N-BOC-4-(4-fluorophenyl)-4-cyanopiperidine (4.64 g, 15.2 mmol), Raney Ni catalyst (1.4 g of 50% aq. slurry), EtOH (30 mL), and ammonium hydroxide (20 mL), to yield the title compound as a viscous oil. MS m/Z 209 (M+H-BOC).
c) 1-N-BOC-4-(4-fluorophenyl)-4-cyanopiperidine.
To a solution of 4-(4-fluorophenyl)-4-cyanopiperidine (3.63 g, 17.8 mmol) in THF (90 mL) was added BOC-anhydride (3.88 g, 17.8 mmol) and DIPEA (3.10 mL, 17.8 mmol). The resulting solution was stirred at room temperature for overnight and poured into 0.1 N HCl. The aq. layer was extracted with EtOAc (2×80 mL). Combined EtOAc were dried over MgSO4, filtered and concentrated. The residue was purified by chromatography (1% MeOH/DCM) to give the title compound as a yellow oil. MS m/z 205 (M+H-BOC).
d) 4-(4-fluorophenyl)-4-cyanopiperidine
A solution containing bis(2-chloroethyl)amine hydrochloride (4.0 g, 22.4 mmol), 4-fluorobenzyl cyanide (3.03 g, 22.4 mmol), and anhydrous DMF (100 mL) was stirred at 0° C. and NaH (60% dispersion in mineral oil) (3.6 g, 90 mmol) was added in portions. The mixture was heated at 60° C. overnight, then was poured into ice/water and extracted with EtOAc (2×). The organic extracts were washed (water and brine), dried, filtered, and concentrated. The residue was purified by chromatography (1% MeOH/DCM) to give the title compound as a yellow oil. MS m/z 205 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 3, but using 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-(3-oxo-2-N-methyl-2-azaprop-1-yl))piperidine (1.5 g, 2.99 mmol), to yield the title compound as a white powder. MS m/z 402 (M+H).
The requisite 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-3-oxo-2-N-methyl-2-azaprop-1-yl))piperidine was prepared in the same manner as Example 14 but using 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine.
The title compound of the following structure
was prepared as a citrate in the same manner as Example 3, but using 3-cyano-2-methoxy-1-naphthoic acid instead of 3-cyano-1-naphthoic acid in 3a, to yield the title compound as a white powder. MS m/z 418 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 3, to yield the title compound as a white powder. MS m/z 416 (M+H).
The requisite 1-N-BOC-4-(4-fluorophenyl)-4-(3-(3-cyano-2-ethylnaphth-1-yl)-3-oxo-2-azaprop-1-yl)piperidine was prepared in the same manner as Example 13, but using 1-N-BOC-4-amionmethyl-4-(4-fluoro)piperidine instead of 1-N-methyl-4-amionmethyl-4-(4-fluoro)piperidine.
The title compound of the following structure
was prepared as a citrate in the same manner as Example 42, but using 3-cyano-2,4-dimethoxy-1-naphthoyl chloride instead of 3-cyano-2-ethyl-1-naphthoyl chloride, to yield the title compound as a white powder. MS m/z 448 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 13, but using 3-cyano-2,4-dimethoxy-1-naphthoyl chloride instead of 3-cyano-2-ethyl-1-naphthoyl chloride, to yield the title compound as a white powder. MS m/z 462 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 11, but using 4-fluoro-1-naphthoic acid instead of 3-cyano-1-naphthoic acid, to yield the title compound as a white powder. MS m/z 395 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 14, but using 1-N-methyl-4-(4-fluorophenyl)-4-(3-(4-fluoronaphth-1-yl)-(3-oxo-2-azaprop-1-yl))piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-(3-oxo-2-azaprop-1-yl))piperidine, to yield the title compound as a white powder. MS m/z 409 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 45, but using 1-N-methyl-4-(3,4-difluorophenyl)-4-(aminomethyl)piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine, to yield the title compound as a light yellow powder. MS m/z 480 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 11, but using 1-N-ethyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine, to yield the title compound as a white powder. MS m/z 416 (M+H).
The requisite 1-N-ethyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine was prepared as follows:
a) 1-N-Ethyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine
To a solution of 1-N-(1-oxoethyl)-4-(4-fluorophenyl)-4-cyanopiperidine (3.4 g, 13.8 mmol) in THF (50 mL) was added LAH (1 N in THF, 55 mL, 55.2 mmol). The solution was heated to 70° C. for 3 hours. The reaction was quenched by adding water (5.5 mL), 15% NaOH (5.5 mL) and water (5.5 mL). The mixture was filtered through diatomaceous earth, washed with EtOAc. The organic layer was dried, filtered and concentrated. The residue was purified by chromatography (5%, 10% MeOH/DCM, 20% MeOH/DCM with 2% NH4OH) to give the title compound as a yellow oil. MS m/z 237 (M+H).
b) 1-N-(1-Oxoethyl)-4-(4-fluorophenyl)-4-cyanopiperidine
To a solution of 4-(4-fluorophenyl)-4-cyanopiperidine (3.33 g, 16.3 mmol) and triethylamine (4.77 mL, 34.2 mmol) in DCM (90 mL) was added acetyl chloride (1.16 mL, 16.3 mmol) at 0° C. The solution was stirred at 0° C. for 0.5 hour and room temperature for 17 h. NaHCO3 (sat.) was added. The mixture was extracted with DCM (2×), dried, filtered and concentrated. The residue was purified by chromatography (30%, 50%, 60%, 80% and 90% EtOAc/hexane) to give the title compound as a yellow oil. MS m/z 247 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 12, but using 1-N-ethyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine, to yield the title compound as a white powder. MS m/z 446 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 14, but using 1-N-ethyl-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-(3-oxo-2-azaprop-1-yl))piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(3-(3-cyanonaphth-1-yl)-(3-oxo-2-azaprop-1-yl))piperidine, to yield the title compound as a white powder. MS m/z 430 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 13, but using 1-N-ethyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine, to yield the title compound as a light yellow powder. MS m/z 444 (M+H).
The title compound of the following structure
was prepared as a citrate in the same manner as Example 45, but using 1-N-ethyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine instead of 1-N-methyl-4-(4-fluorophenyl)-4-(aminomethyl)piperidine, to yield the title compound as a white powder. MS m/z 476 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-ethyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine (76 mg, 0.265 mmol) and 3-cyano-2-methoxy-1-naphthoyl chloride (71 mg, 0.29 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (116 mg) (63%) as a white powder. MS m/z 496 (M+H).
The requisite 1-N-ethyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine was prepared as follows:
a) 1-N-ethyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine
To a stirred solution containing 1-N-(1-oxoethyl)-4-(3,4-dichlorophenyl)-4-cyanopiperidine (623 mg, 2.097 mmol) and dry THF (10 mL), a solution of BH3 in THF (20 mL of 1M) was slowly added. The solution was heated under reflux for 21 h, cooled to ambient, and cautiously treated with 1 N aq. HCl (10 mL). After 0.5 h, the volume was reduced by evaporation, sat. aq. NaHCO3 was added (until basic), and the mixture was extracted with DCM (4×). The extracts were dried (MgSO4), filtered, and concentrated. The residue was treated with 8 N aq. HCl (25 mL), stirred with intermittent heating for 72 h., basified (33% aq. NaOH), and extracted with DCM (4×). The DCM extracts were washed (brine), dried (MgSO4), filtered, and concentrated. The residue was purified by chromatography (0-5% MeOH/DCM w/1% NH3) to give the title compound (315 mg) (52%) as an off-white solid. MS m/z 287 (M+H).
b) 1-N-(1-oxoethyl)-4-(3,4-dichlorophenyl)-4-cyanopiperidine
A stirred solution containing 4-(3,4-dichlorophenyl)-4-cyanopiperidine (535 mg, 2.097 mmol), TEA (0.44 mL), and dry DCM (15 mL) was cooled (ice bath) and acetyl chloride (210 mg, 2.67 mmol) was added dropwise. After 1 h, the mixture was warmed to RT, stirred for an additional 18 h, diluted with DCM, and washed with sat. aq. NaHCO3. The organic phase was dried (MgSO4), filtered, and concentrated. The residue was purified by chromatography (0-2% MeOH/DCM) to give the title compound (quantitative) as an off-white, solid. MS m/z 297 (M+H).
c) 4-(3,4-dichlorophenyl)-4-cyanopiperidine
A solution containing 1-N-BOC-4-(3,4-dichlorophenyl)-4-cyanopiperidine (Example 3c) (5.54 g, 15.59 mmol), TFA (50 mL), and DCM (50 mL) was stirred at RT for 18 h, then concentrated. The residue was treated with water, sodium bicarbonate, and sat. aq. sodium bicarbonate (until basic), then extracted with DCM (3×). The DCM extracts were dried (Na2SO4), filtered, and concentrated. The residue was purified by chromatography (0-5% MeOH/DCM) to give the title compound (3.81 g) (95%) as an off-white solid. MS m/z 255 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-ethyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine (151 mg, 0.525 mmol) and 3-cyano-1-naphthoyl chloride (124 mg, 0.577 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound 115 mg) (76%) as a white powder. MS m/z 466 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 11, but using 1-N-methyl-4-aminomethyl-4-(3,4-dichlorophenyl)piperidine (237 mg, 0.867 mmol) and 3-cyano-1-naphthoic acid (168 mg, 0.852 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (306 mg) (57%) as a white powder. MS m/z 452 (M+H).
The title compound of the following structure
was prepared as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(3-fluorophenyl)piperidine (172 mg, 0.775 mmol) and 3-cyano-1-naphthoyl chloride (164.5 mg, 0.763 mmol), the title compound (139 mg) (45%) was obtained as a white powder. MS m/z 402 (M+H).
The requisite 1-N-methyl-4-aminomethyl-4-(3-fluorophenyl)piperidine was prepared as follows:
a) 1-N-methyl-4-cyano-4-(3-fluorophenyl)piperidine
In the same manner as Example 11a, but using 3-fluorophenylacetonitrile (5.05 g, 37.4 mmol), and following short-path distillation, the title compound (7.96 g) (97%) was obtained as a colorless liquid. MS m/z 219 (M+H).
b) 1-N-methyl-4-aminomethyl-4-(3-fluorophenyl)piperidine
In the same manner as Example 11b, but using 1-N-methyl-4-cyano-4-(3-fluorophenyl)piperidine (3.08 g, 14.1 mmol), and following short-path distillation, the title compound (2.95 g) (94%) was obtained as a colorless liquid. MS m/z 223 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(3-fluorophenyl)piperidine (166.2 mg, 0.748 mmol) and 3-cyano-2-methoxy-1-naphthoyl chloride (178.8 mg, 0.728 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (325 mg) (72%) as a white powder. MS m/z 432 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(3-fluorophenyl)piperidine (151.9 mg, 0.683 mmol) and 3-cyano-2-ethyl-1-naphthoyl chloride (163.2 mg, 0.67 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (272 mg) (65%) as a white powder. MS m/z 430 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(3-fluorophenyl)piperidine (154.8 mg, 0.696 mmol) and 3-cyano-2,4-dimethoxy-1-naphthoyl chloride (187.3 mg, 0.679 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (247 mg) (55%) as a white powder. MS m/z 462 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-phenylpiperidine (159 mg, 0.776 mmol) and 3-cyano-1-naphthoyl chloride (164.5 mg, 0.763 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (278 mg) (65%) as a white powder. MS m/z 384 (M+H).
The requisite 1-N-methyl-4-aminomethyl-4-phenylpiperidine was prepared as follows:
a) 1-N-methyl-4-cyano-4-phenylpiperidine
In the same manner as Example 11a, but using phenylacetonitrile (4.4 g, 37.6 mmol), and following short-path distillation, the title compound (7.05 g) (93%) was isolated as a colorless liquid. MS m/z 201 (M+H).
b) 1-N-methyl-4-aminomethyl-4-phenylpiperidine
In the same manner as Example 1c, but using 1-N-methyl-4-cyano-4-phenylpiperidine (3.09 g, 15.4 mmol), and following short-path distillation, the title compound (2.71 g) (94%) was isolated as a colorless liquid. MS m/z 205 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-phenylpiperidine (151 mg, 0.738 mmol) and 3-cyano-2-methoxy-1-naphthoyl chloride (175 mg, 0.713 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (381 mg) (90%) as a white powder. MS m/z 414 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-phenylpiperidine (140.4 mg, 0.687 mmol) and 3-cyano-2-ethyl-1-naphthoyl chloride (163.2 mg, 0.67 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (257 mg) (64%) as a white powder. MS m/z 412 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-phenylpiperidine (147.5 mg, 0.722 mmol) and 3-cyano-2,4-dimethoxy-1-naphthoyl chloride (187.3 mg, 0.679 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (171 mg) (39%) as a white powder. MS m/z 444 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-(N-methylaminomethyl)-4-phenylpiperidine (109 mg, 0.497 mmol) and 3-cyano-1-naphthoyl chloride (107 mg, 0.497 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (141 mg) (48%) as a white powder. MS m/z 398 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(4-fluorophenyl)piperidine (107.5 mg, 0.484 mmol) and 3-methoxy-4-methyl-1-naphthoyl chloride (108.5 mg, 0.462 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (217 mg) (78%) as a white powder. MS m/z 421 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(4-fluorophenyl)piperidine (107 mg, 0.48 mmol) and 4-chloro-3-methoxy-1-naphthoyl chloride (115.5 mg, 0.453 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (187 mg) (67%) as a white powder. MS m/z 441 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(4-fluorophenyl)piperidine (122 mg, 0.549 mmol) and 3-cyano-4-methyl-1-naphthoyl chloride (110.9 mg, 0.483 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (224 mg) (76%) as a white powder. MS m/z 416 (M+H).
The title compound of the following structure
was prepared as a citrate salt, as follows. In the same manner as Example 13, but using 1-N-methyl-4-(methylaminomethyl)-4-(4-fluorophenyl)piperidine (132 mg, 0.558 mmol) and 3-cyano-4-methyl-1-naphthoyl chloride (108 mg, 0.47 mmol), the citrate salt was isolated by filtration from Et2O to give the title compound (250 mg) (88%) as a white powder. MS m/z 430 (M+H).
The title compound of the following structure
was prepared as follows. In the same manner as Example 13, but using 1-N-methyl-4-aminomethyl-4-(4-fluorophenyl)piperidine (174.6 mg, 0.785 mmol) and 4-bromo-1-naphthoyl chloride (177 mg, 0.656 mmol), the title compound (214 mg) (71%) was obtained as a white powder. MS m/z 455 (M+H).
The title compound of the following structure
was prepared as follows. In the same manner as Example 13, but using 1-N-methyl-4-(methylaminomethyl)-4-(4-fluorophenyl)piperidine (188 mg, 0.796 mmol) and 4-bromo-1-naphthoyl chloride (179 mg, 0.664 mmol), the title compound (270.8 mg) (86%) was obtained as a white powder. MS m/z 469 (M+H).
The compounds of Examples 71 through 79 were prepared by processes similar to those given in Examples 11-14 but with replacement of 4-fluorophenyl acetonitrile with an appropriately substituted phenyl acetonitrile, compounds of Examples 71 through 79 and intermediates listed in Table 3 were obtained.
Following conventional procedures well known in the pharmaceutical art, the following representative pharmaceutical dosage forms containing a compound in accord with structural diagram I may be prepared:
The pharmaceutical dosage form is administered to a patient in need thereof at a frequency depending on the patient and the precise disease condition being treated.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0202567-4 | Aug 2002 | SE | national |
| 020986-6 | Oct 2002 | SE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/SE03/01329 | 8/26/2003 | WO | 11/4/2005 |
