WO2007086948A1

WO2007086948A1 - Dnt-fumarate and methods of preparation thereof

Info

Publication number: WO2007086948A1
Application number: PCT/US2006/036975
Authority: WO
Inventors: Santiago Ini; Mili Abramov; Tamas Koltai
Original assignee: Teva Pharmaceutical Industries Ltd.; Teva Pharmaceuticals Usa, Inc.
Priority date: 2006-01-23
Filing date: 2006-09-21
Publication date: 2007-08-02
Also published as: EP1844034A1; US20070191471A1; IL192553A0; MX2007011611A

Abstract

(S)-N,N-Dimethyl-3-(l-naphthalenyloxy)-3-(2-thienyl)propanamine fumarate (DNT-fumarate) and polymorphs of DNT-fumarate, compositions of DNT-fumarate and its polymorphs, processes for the preparation of DNT-fumarate and its polymorphs, and processes for the preparation of duloxetine hydrochloride from DNT-fumarate are provided.

Description

DNT-FUMARATE AND METHODS OF PREPARATION THEREOF

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims the benefit of the following United States Provisional Patent Application No.: 60/761568 filed January 23, 2006 and 60/771078 filed February 6, 2006. The contents of which are incorporated herein by reference.

FIELD OF THE INVENTION

[0001] The invention is directed to an intermediate for the synthesis of duloxetine. hi particular, the invention is directed to the duloxetine intermediate DNT-fumarate, to the solid state chemistry of DNT-fumarate, and to processes for preparing DNT-fumarate and to converting DNT-fumarate into duloxetine HCl.

BACKGROUND OF THE INVENTION

[0002] Duloxetine HCl (duloxetine hydrochloride) is a dual reuptake inhibitor of the neurotransmitters serotonin and norepinephrine. It is used for the treatment of stress urinary incontinence (SUI), depression, and pain management. Duloxetine hydrochloride is known by the chemical name (S)-(+)-N-methyl-3-(l- naphthalenyloxy)-3-(2-thienyl) propanamine hydrochloric acid salt, and has the following structure.

[0003] Duloxetine, as well as processes for its preparation, is disclosed in

U.S. Patent No. 5,023,269. EP Patent No. 457559 and U.S. Patents Nos. 5,491,243 and 6,541,668 also provide synthetic routes for the preparation of duloxetine. U.S. Patent No. 5,023,269 discloses preparing duloxetine by reacting (S)-(-)-N,N-Dimethyl-3-(2-thienyl)-3-hydroxypropanamine with fluoronaphtalene (Stage a), followed by demethylation with phenyl chloroforaiate or trichloroethyl chloroformate (Stage b) and basic hydrolysis (Stage c), according the following scheme.

Stage a

DNT

HCI/solvents

Stage d

DLX-HCI DLX-base

R= Phenyl, trichloroethyl

The conversion of duloxetine to its hydrochloride salt in ethyl acetate (Stage d) is described in U.S. Patent No. 5,491,243 and in Wheeler, W.J., et al, J. Label. Cpds.

Radiopharm, 1995, 36, 312.

[0004] As illustrated in the above scheme, DNT is an intermediate in the preparation of duloxetine. DNT has an N,N-dimethyl group instead of a secondary amine.

[0005] U.S. Patent No. 5,023,269 describes the preparation of DNT-oxalate from DNT. See Example 1.

[0006] The oxalate salt of U.S. Patent No. 5,023,269 is problematic for use on an industrial process. Oxalic acid has to be used to prepare the oxalate. Oxalic acid is highly toxic. Therefore, there is a need in the art to prepare duloxetine HCl with a relative high purity with a process that is suitable for industrial scale. [0007] Stereochemical purity is of importance in the field of pharmaceuticals, where many of the most prescribed drugs exhibit chirality, and the two isomers exhibit different potency. Furthermore, optical purity is important since certain isomers may actually be deleterious rather than simply inert. Therefore, there is a need to obtain the desired enantiomer of duloxetine HCl in high enantiomeric purity.

[0008] A composition of DNT is often contaminated with enantiomeric impurity. This enantiomeric impurity generally carries over to the final pharmaceutical product, i.e., duloxetine HCl. The present Applicants have found out that formation of the oxalate salt as carried out in EP Patent No. 457559 does not reduce the amount of the enantiomeric impurity (enantiomer R). There is a need in the art for a process that reduces the quantity of enantiomer R present in DNT.

SUMMARY OF THE INVENTION

[0009] In one embodiment, the invention provides a compound (DNT- fumarate) having the following formula:

[00010] In another embodiment, the invention provides a process for preparing duloxetine hydrochloride comprising preparing a solution of DNT in a solvent selected from the group consisting of _Ci_-8 alcohols, C_3-7 esters, C_3-8 ethers, C_3-7 ketones, C_6-12 aromatic hydrocarbons, acetonitrile, water, and mixtures thereof, combining the solution with fumaric acid to form a reaction mixture, precipitating DNT-fumarate from the reaction mixture, and converting the crystalline DNT- fumarate to the duloxetine hydrochloride.

[00011] In another embodiment, the invention provides a crystalline form of

DNT-fumarate:

characterized by a powder XRD with peaks at about 9.7°, 16.5°, 17.4°, 21.2°, and 24.1° 20 ± 0.2° 20.

[00012] In another embodiment, the invention provides a process for preparing a pharmaceutically acceptable salt of duloxetine, comprising combining DNT, a solvent selected from the group consisting OfC_1-8 alcohols, C_3-7 esters, C_3-8 ethers, C_3-7 ketones, C_6-12 aromatic hydrocarbons, acetonitrile, water and mixtures thereof with fumaric acid to form a reaction mixture, precipitating DNT-fumarate from the reaction mixture, converting the DNT-fumarate to DNT, converting the DNT to duloxetine, and converting the duloxetine to the pharmaceutically acceptable salt of duloxetine.

BRIEF DESCRIPTION OF THE FIGURE

Figure 1 illustrates the powder X-ray diffraction pattern for DNT-fumarate Form Fum2.

DETAILED DESCRIPTION OF THE INVENTION [00013] The present invention provides DNT-fumarate, which can be represented by the formula C₂₃H_2SNO₅S and the structure:

[00014] DNT-fumarate is preferably isolated as a solid, and, more preferably as a crystal. The use of DNT-fumarate as an intermediate salt for preparation of DNT, which is an intermediate of duloxetine, allows for obtaining such hydrochloride salt in relatively high purity without the drawbacks of the oxalate salt. [00015] Use of the DNT-fumarate salt provides an enantiomeric cleaning effect not observed with the oxalate salt. The cleaning effect results from the process of forming crystalline DNT-fumarate which produces a greater ratio of the S enantiomer relative to the R enantiomer, than was present in the DNT starting material. [00016] DNT-fumarate can be characterized by data selected from: ¹H NMR

(400 MHz, DMSO d₆) δ(ppm): 8.26 (dd, /=6.12 Hz, /=3.36 Hz, IH), 7.82 (dd, /=8.00 Hz, /=3.17 Hz, IH), 7.50 (dd, /=8.00 Hz, /=3.22 Hz, 2H), 7.43 (m, 2H), 7.31 (t, J=7.88 Hz, IH), 7.22 (d, J=2.96 Hz, IH), 7.00 (d, J=7.66 Hz, IH), 6.97 (t, J=3.8 Hz, IH), 6.60 (s, 2H), 6.00 (dt, /=6.25 Hz, /=2.32 Hz, IH), 3.26 (m, IH)₅ 3.16 (m, IH), 2.75 (s, 6H), 2.56 (m, IH), 2.38 (m, IH); ¹³C (¹H)NMR (100 MHz): δ 166.8, 152.6, 143.8, 134.6, 127.8, 127.2, 126.8, 126.4, 126.2, 125.8, 122.1, 120.9, 107.8, 73.3, 53.9, 42.6, 33.4; and FAB MS: m/z 312 ([M-H]⁺, 100%). The DNT-fumarate is preferably solid, more preferably crystalline. [00017] The present invention also provides a process for preparing

DNT-fumarate. DNT-fumarate may be prepared by combining DNT and fumaric acid to create a reaction mixture. DNT fumarate forms in such reaction mixture through contact of DNT with fumaric acid.

[00018] In one embodiment, a solution or suspension of DNT in a solvent is combined with fumaric acid to form a reaction mixture. The fumaric acid may be either added as a solid or as a solution or suspension in an organic solvent. The solvent maybe selected from the group consisting OfC_1-8 alcohols, C_3-7 esters, C_3-8 ethers, C_3-7 ketones, C_6-12 aromatic hydrocarbons, acetonitrile, water and mixtures thereof Preferably, the solvent is selected from a group consisting of acetone, n-BuOH, ethyl acetate, MTBE, toluene and water. More preferably, the solvent is selected from the group consisting of ethyl acetate, acetone, and n-BuOH. [00019] In one embodiment, fumaric acid, DNT and at least one solvent are combined to form a reaction mixture. DNT fumarate then precipitates out of such a mixture. Generally, fumaric acid is added to a solution of DNT in an organic solvent, followed by precipitation of DNT-fumarate. The reaction mixture may be stirred before, during, or after precipitation. Such precipitation may occur on its own or be induced. The process is generally carried out at a temperature of from about room temperature to about the reflux temperature of the solvent.

odiment, the mixture of fumaric acid and DNT in a solvent are heated to obtain a reaction mixture. The temperature for heating can be dependent on the solvent, and generally ranges from about room temperature to about the reflux temperature of the solvent. DNT fumarate forms in the reaction mixture. The reaction mixture may be cooled for a subsequent period to facilitate precipitation. Cooling may be carried out at a temperature of about 5O⁰C or less, such as about room temperature. The reaction mixture may be stirred before, during or after precipitation. Cooling is generally carried out at a temperature of about 5O⁰C or less, such as room temperature.

[00021] The above embodiments, with or without heating, may be carried out without a solvent. In this method, DNT is used both as a reagent and a solvent; fumaric acid and DNT are combined to form a reaction mixture followed by precipitation.

[00022] The resulting precipitate from any of the above embodiments may be recovered by conventional techniques, such as filtration. The precipitate may be dried under ambient or reduced pressure, or elevated temperature. In one embodiment, the precipitate is dried at room temperature at a pressure of less than about lOOmmHg. [00023] The DNT-fumarate of the invention can be prepared in different polymorphic forms. Polymorphism, the occurrence of different crystal forms, is a property of some molecules and molecular complexes. A single molecule, such as DNT-fumarate may give rise to a variety of crystalline forms having distinct crystal structures and physical properties like melting point, X-ray diffraction pattern, infrared absorption fingerprint, and solid state NMR spectrum. One crystalline form may give rise to thermal behavior different from that of another crystalline form. Thermal behavior can be measured in the laboratory by such techniques as capillary melting point, thermogravimetric analysis ("TGA"), and differential scanning calorimetry ("DSC"), which have been used to distinguish polymorphic forms. [00024] The difference in the physical properties of different crystalline forms results from the orientation and intermolecular interactions of adjacent molecules or complexes in the bulk solid. Accordingly, polymorphs are distinct solids sharing the same molecular formula, yet having distinct physical properties that can be advantageous in certain applications compared to other crystalline forms of the same compound or complex. Therefore, processes for the preparation of polymorphic forms of DNT-fumarate are desirable. P' C ^"I^" ./" LP S O IB ./" Ξl 6975

[00025] One such crystalline form of DNT-fumarate, herein defined as Form

Fum2, is characterized by a powder XRD pattern with peaks at about 9.7°, 16.5°, 17.4°, 21.2°, and 24.1° 20 ± 0.2° 20. The crystalline Form Fum2 maybe further characterized by X-ray powder diffraction peaks at about 18.7°, 19.3°, 22.4°, 23.1°, and 26.4° 20 ± 0.2° 20. DNT-fumarate Form Fum2 can also be characterized by an X-ray powder diffraction pattern substantially as depicted in Figure 1. Form Fum2 may be prepared by any of the processes set out above.

[00026] Preferably, the DNT-fumarate, Form Fum2, resulting from the above processes is present in a composition, such as a batch, having a polymorphic purity of at least about 10 percent by weight, more preferably, at least about 25 percent by weight, and most preferably at least about 50 percent by weight of a single crystalline form.

[00027] Preparation of the fumarate salt can also lower the amount of the

^• undesired R-enantiomer present in DNT. Such reduction in the level of undesired R- enantiomer can be calculated according to the following formula:

Preferably the molar amount of R-enantiomer present in the DNT-fumarate, compared to the starting material, is less than about 70 percent, more preferably, less than about 40 percent, even more preferably, less than about 17 percent of the molar amount present in such starting material. The process of the invention can lower the level of the undesired R-enantiomer below the detection limit.

[00028] Repetitions of the processes for preparation of DNT-fumarate can increase the enantiomeric purity even further, preferably to an undetectable amount of the undesired R-enantiomer. In other words, the processes can further comprise combining DNT-fumarate with a base, combining the DNT-base with fumaric acid to form a reaction mixture, precipitating DNT-fumarate from the reaction mixture, and recovering the DNT-fumarate.

[00029] To decrease the level of the R-enantiomer of DNT-fumarate even further, the DNT-fumarate prepared with the process of the invention may be crystallized from one or more polar solvents, such as C_1-8 alcohols, e.g., n-butanol, C_3-7 esters, e.g., ethyl acetate, water, and mixtures thereof. The crystallization may be performed by dissolving DNT-fumarate in the organic solvent, preferably at a temperature of about room temperature to about reflux temperature, followed by cooling. The obtained DNT-fumarate is recovered by any method known in the art, such as filtering, and may be washed and dried.

[00030] The DNT-fumarate of the present invention, including Form Fum2, will generally have a maximal particle size of less than about 500 μm, preferably less than about 300 μm, more preferably less than about 200 μm, and most preferably less than about 100 μm. A particularly preferred crystalline Form Fum2 of DNT-fumarate has a maximal particle size of less than about 50 μm. The particle size of DNT- fumarate crystalline forms may be measured by methods including, but not limited to, sieves, sedimentation, electrozone sensing (coulter counter), microscopy, and Low Angle Laser Light Scattering (LALLS).

[00031] The DNT-fumarate of the present invention is useful as an intermediate in the preparation of pharmaceutically acceptable salts of duloxetine, particularly the hydrochloride salt. The conversion can be carried out by combining DNT-fumarate, water, a base such as ammonium hydroxide, and toluene to obtain a two phase system, separating the organic phase containing DNT and toluene, and converting the DNT to duloxetine HCl. The DNT-fumarate used in this process is preferably the DNT-fumarate prepared as described above. As such, it has a low content of the R-enantiomer, and, therefore, the duloxetine HCl obtained from the DNT-fumarate of the invention also has a decreased R-enantiomer content. [00032] The conversion of DNT to a pharmaceutically acceptable salt of duloxetine may be performed by any method known in the art, such as the one described in U.S. Patent No. 5,023,269 or in co-pending U.S. Patent Application No. 11/318,365, filed on December 23, 2005, for making duloxetine HCl. Preferably, the conversion is performed by dissolving DNT in an organic solvent, and combining it with an alkyl haloformate. That step will yield duloxetine alkyl carbamate, which can be combined with an organic solvent and a base, to yield duloxetine. The duloxetine may then be converted to a pharmaceutically acceptable salt. More preferably, the conversion is performed by dissolving DNT in a water immiscible organic solvent; adding alkyl chloroformate at a temperature of about 5°C to less than about 80⁰C to obtain duloxetine alkyl carbamate, combining the duloxetine alkyl carbamate with an organic solvent and a base; maintaining the reaction mixture at reflux temperatures for at least 1 to 3 hours; cooling, and adding water and an additional amount of an "T / USKlB / 3BΨ7 S organic solvent; recovering duloxetine; combining the duloxetine with a solvent; adding hydrochloric acid until a pH of about 3 to about 4 is obtained; maintaining the reaction mixture to obtain a solid residue; and recovering duloxetine HCl. [00033] Pharmaceutical compositions can be made using the pharmaceutically acceptable salts of duloxetine from the processes described above. A pharmaceutical composition may comprise a pharmaceutically acceptable salts of duloxetine from the processes described above, and a pharmaceutically acceptable excipient. Preferably, a pharmaceutical composition can be made by combining the duloxetine HCl produced by the above method with a pharmaceutically acceptable excipient. These pharmaceutical compositions contain less than about 50%, more preferably less than about 15%, even more preferably less than about 5%, and even more preferably less than about 0.04% of enantiomeric impurity. Most preferably such impurity is undetectable by HPLC.

[00034] In addition to the active ingredient(s), the pharmaceutical compositions of the present invention contain one or more excipients or adjuvants. Selection of excipients and the amounts to use may be readily determined by the formulation scientist based upon experience and consideration of standard procedures and reference works in the field.

[00035] Diluents increase the bulk of a solid pharmaceutical composition, and may make a pharmaceutical dosage form containing the composition easier for the patient and care giver to handle. Diluents for solid compositions include, for example, microcrystalline cellulose (e.g. Avicel^®), microfme cellulose, lactose, starch, pregelitinized starch, calcium carbonate, calcium sulfate, sugar, dextrates, dextrin, dextrose, dibasic calcium phosphate dihydrate, tribasic calcium phosphate, kaolin, magnesium carbonate, magnesium oxide, maltodextrin, mannitol, polymethacrylates (e.g. Eudragit^®), potassium chloride, powdered cellulose, sodium chloride, sorbitol, and talc.

[00036] Solid pharmaceutical compositions that are compacted into a dosage form, such as a tablet, may include excipients whose functions include helping to bind the active ingredient and other excipients together after compression. Binders for solid pharmaceutical compositions include acacia, alginic acid, carbomer (e.g. carbopol), carboxymethylcellulose sodium, dextrin, ethyl cellulose, gelatin, guar gum, hydrogenated vegetable oil, hydroxyethyl cellulose, hydroxypropyl cellulose (e.g. Klucel^®), hydroxypropyl methyl cellulose (e.g. Methocel^®), liquid glucose, / U SO S /3 B '975 magnesium aluminum silicate, maltodextrin, methylcellulose, polymethacrylates, povidone (e.g. Kollidon^®, Plasdone^®), pregelatinized starch, sodium alginate, and starch.

[00037] The dissolution rate of a compacted solid pharmaceutical composition in the patient's stomach may be increased by the addition of a disintegrant to the composition. Disintegrants include alginic acid, carboxymethylcellulose calcium, carboxymethylcellulose sodium (e.g. Ac-Di-Sol^®, Primellose^®), colloidal silicon dioxide, croscarmellose sodium, crospovidone (e.g. Kollidon^®, Polyplasdone^®), guar gum, magnesium aluminum silicate, methyl cellulose, microcrystalline cellulose, polacrilin potassium, powdered cellulose, pregelatinized starch, sodium alginate, sodium starch glycolate (e.g. Explotab^®), and starch.

[00038] Glidants can be added to improve the flowability of a non-compacted solid composition and to improve the accuracy of dosing. Excipients that may function as glidants include colloidal silicon dioxide, magnesium trisilicate, powdered cellulose, starch, talc, and tribasic calcium phosphate.

[00039] When a dosage form such as a tablet is made by the compaction of a powdered composition, the composition is subjected to pressure from a punch and die. Some excipients and active ingredients have a tendency to adhere to the surfaces of the punch and die, which can cause the product to have pitting and other surface irregularities. A lubricant can be added to the composition to reduce adhesion and ease the release of the product from the die. Lubricants include magnesium stearate, calcium stearate, glyceryl monostearate, glyceryl palmitostearate, hydrogenated castor oil, hydrogenated vegetable oil, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc, and zinc stearate. [00040] Flavoring agents and flavor enhancers make the dosage form more palatable to the patient. Common flavoring agents and flavor enhancers for pharmaceutical products that may be included in the composition of the present invention include maltol, vanillin, ethyl vanillin, menthol, citric acid, fumaric acid, ethyl maltol, and tartaric acid.

[00041] Solid and liquid compositions may also be died using any pharmaceutically acceptable colorant to improve their appearance and/or facilitate patient identification of the product and unit dosage level. P C T/ U S Cl 6 / 3 B ¹¹IiI 7 B

[00042] In liquid pharmaceutical compositions of the present invention, the active ingredient and any other solid excipients are suspended in a liquid carrier such as water, vegetable oil, alcohol, polyethylene glycol, propylene glycol or glycerin. [00043] Liquid pharmaceutical compositions may contain emulsifying agents to disperse uniformly throughout the composition an active ingredient or other excipient that is not soluble in the liquid carrier. Emulsifying agents that may be useful in liquid compositions of the present invention include, for example, gelatin, egg yolk, casein, cholesterol, acacia, tragacanth, chondrus, pectin, methyl cellulose, carbomer, cetostearyl alcohol, and cetyl alcohol.

[00044] Liquid pharmaceutical compositions of the present invention may also contain a viscosity enhancing agent to improve the mouth-feel of the product and/or coat the lining, of the gastrointestinal tract. Such agents include acacia, alginic acid bentonite, carbomer, carboxymethylcellulose calcium or sodium, cetostearyl alcohol, methyl cellulose, ethylcellulose, gelatin guar gum, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, maltodextrin, polyvinyl alcohol, povidone, propylene carbonate, propylene glycol alginate, sodium alginate, sodium starch glycolate, starch tragacanth, and xanthan gum. [00045] Sweetening agents such as sorbitol, saccharin, sodium saccharin, sucrose, aspartame, fructose, mannitol, and invert sugar may be added to improve the taste.

[00046] Preservatives and chelating agents such as alcohol, sodium benzoate, butylated hydroxy toluene, butylated hydroxyanisole, and ethylenediamine tetraacetic acid may be added at levels safe for ingestion to improve storage stability. [00047] According to the present invention, a liquid composition may also contain a buffer such as gluconic acid, lactic acid, citric acid or acetic acid, sodium gluconate, sodium lactate, sodium citrate, or sodium acetate. [00048] Selection of excipients and the amounts used may be readily determined by the formulation scientist based upon experience and consideration of standard procedures and reference works in the field.

[00049] The solid compositions of the present invention include powders, granulates, aggregates, and compacted compositions. The dosages include dosages suitable for oral, buccal, rectal, parenteral (including subcutaneous, intramuscular, and intravenous), inhalant, and ophthalmic administration. Although the most suitable administration in any given case will depend on the nature and severity of the condition being treated, the most preferred route of the present invention is oral. The dosages may be conveniently presented in unit dosage form and prepared by any of the methods well known in the pharmaceutical arts.

[00050] Dosage forms include solid dosage forms like tablets, powders, capsules, suppositories, sachets, troches, and losenges, as well as liquid syrups, suspensions, and elixirs.

[00051] The dosage form of the present invention may be a capsule containing the composition, preferably a powdered or granulated solid composition of the invention, within either a hard or soft shell. The shell may be made from gelatin, and, optionally, contain a plasticizer such as glycerin and sorbitol, and an opacifying agent or colorant.

[00052] The active ingredient and excipients may be formulated into compositions and dosage forms according to methods known in the art.

[00053] A composition for tableting or capsule filling can be prepared by wet granulation. In wet granulation, some or all of the active ingredients and excipients in powder form are blended, and then further mixed in the presence of a liquid, typically water, that causes the powders to clump into granules. The granulate is screened and/or milled, dried, and then screened and/or milled to the desired particle size. The granulate may then be tableted or other excipients may be added prior to tableting, such as a glidant and/or a lubricant.

[00054] A tableting composition can be prepared conventionally by dry blending. For example, the blended composition of the actives and excipients may be compacted into a slug or a sheet, and then comminuted into compacted granules. The compacted granules may subsequently be compressed into a tablet.

[00055] As an alternative to dry granulation, a blended composition may be compressed directly into a compacted dosage form using direct compression techniques. Direct compression produces a more uniform tablet without granules.

Excipients that are particularly well suited for direct compression tableting include microcrystalline cellulose, spray dried lactose, dicalcium phosphate dihydrate and colloidal silica. The proper use of these and other excipients in direct compression tableting is known to those in the art with experience and skill in particular formulation challenges of direct compression tableting. [00056] A capsule filling of the present invention may comprise any of the aforementioned blends and granulates that were described with reference to tableting, however, they are not subjected to a final tableting step.

[00057] The following non-limiting examples are merely illustrative of the preferred embodiments of the present invention, and are not to be construed as limiting the invention, the scope of which is defined by the appended claims.

EXAMPLES Instruments

[00058] X-Ray powder diffraction (XRD) data was obtained using a Scintag

X-ray powder diffractometer model X'TRA equipped with a Cu-tube solid state detector. A round standard aluminum sample holder with rough zero background quartz plate with a cavity of 25 (diameter) x 0.5 mm (depth) was used. The scanning parameters included: range: 2° to 40° 20; scan mode: continuous scan; step size: 0.05°; and a rate of 57minute.

HPLC method for measuring enantiomeric purity: Column: Diacel Chiral OD 250 x 4.65 μm

Eluent: Hexane (900 ml): IPA (100 ml): DEA(2 ml)

Flow: 1 ml/minute

Detection: 230 nm

Sample cone: 0.5 mg/ml Sample vol: 100 μl Column temp: 2O⁰C Detection limit: 0.02% Preparation of DNT-fumarate Examples 1-5:

[00059] Fumaric acid (1.53 g) was added to a solution of 4 g of DNT (2.3% enantiomer R) dissolved in 40 ml of the appropriate solvent, and stirred for about 1 hour. After filtration, the product was dried in a vacuum oven (10 mm Hg) at 50°C for 16 hours, and analyzed by XRD and HPLC. The results are set forth in Table 1.

Table 1

Examples 6-9:

[00060] Fumaric acid (1.53 g) was added to a solution of 4 g of DNT (2.3% enantiomer R) dissolved in 40 ml of the appropriate solvent, and the mixture was heated to reflux for about 10 minutes. After cooling to room temperature, the mixture was stirred for about 1 hour. After filtration, the product was dried in a vacuum oven (10 mm Hg) at 50°C for 16 hours, and analyzed by XRD and HPLC. The results are set forth in Table 2.

Table 2

Example 10:

[00061] Fumaric acid (1.53 g) was added to a suspension of 3 g of DNT (2.3% enantiomer R) in 30 ml of water, and the mixture was heated to reflux for about 10 minutes. After cooling to room temperature, the mixture was stirred for an additional 1 hour, filtrated, and washed with water. After drying, in a vacuum oven (10 mm Hg) at 50°C for 16 hours, 1.5 g (88% yield, 1.37% enantiomer R) of product were obtained. The product was analyzed by XRD and found to be Form Fum2 after the drying.

Preparation of DNT Example 11 : P C T/ U S O B .■^■'" 3 B 97 S

[00062] A 2 liter reactor equipped with mechanical stirrer is charged with a mixture of 107 g DNT-fumarate, 600 ml water, 96 ml of a 22 percent solution of ammonium hydroxide, and 1 liter toluene. The mixture is stirred at 25°C for 20 to 30 minutes, and the organic phase is separated and washed with water (3 x 300 ml). The toluene solution of DNT can be used for the preparation of duloxetine hydrochloride step without evaporation.

Preparation of DNT Oxalate

Example 12:

[00063] To a solution of 2.1 g of DNT-base (12% enantiomer R) dissolved in

12 ml of ethyl acetate was added a solution of 0.6 g of oxalic acid in 12 ml of ethyl acetate. The resulting mixture was stirred at room temperature for an hour, filtrated and washed with ethyl acetate. After drying, in a vacuum oven for overnight, 2 g

(77% yield) of DNT-oxalate were obtained containing 12% of enantiomer R.

Example 13

[00064] A 100 ml three necked flask, equipped with mechanical stirrer, thermometer, dean stark, and condenser, was charged with 5 g of DNT and 25 ml of toluene. The clear solution was heated, and an azeotropic distillation was performed for about 30 to about 60 minutes. After cooling to room temperature, 4.6 ml of ethyl chloroformate were added during over a period of 1 to 2 hours, and the reaction mixture was stirred at room temperature over night.

[00065] Diluted NH₄OH was added to the reaction mixture, which was stirred for an additional 30 minutes. After phase separation, the organic phase was washed with water (3 x 20 ml), dried over Na₂SO₄, filtered, and concentrated to dryness to give 5.2 g of a brownish oil. (88% chemical yield).

Example 14

[00066] A 100 ml three necked flask equipped, with mechanical stirrer, thermometer, and condenser, was charged with 2.5 g duloxetine ethyl carbamate and

20 ml toluene. The mixture was stirred, and 4.8 g of KOH were added in portions, followed by reflux for about 3 hours.

[00067] After cooling, 30 ml of water, followed by 20 ml of toluene, were added, and the resulting organic phase was washed with water (3 x 20 ml), dried over FMC T /\ J SO 6 / 3 S 97^' EiI

Na₂SO₄, filtered and concentrated to dryness to give 1.70 g of an oily product.

(85.31% yield).

Example 15

[00068] To a solution of 1 g of duloxetine in 10 ml MEK was slowly added

0.32 ml of a 37 percent hydrochloric acid solution. The mixture was stirred until a solid formed. The resulting solid was filtered, and dried in a vacuum oven to give

0.50 g of (S)-(+)-duloxetine hydrochloride. (94.64% yield).

[00069] While it is apparent that the invention disclosed herein is well calculated to fulfill the objects stated above, it will be appreciated that numerous modifications and embodiments may be devised by those skilled in the art. Therefore, it is intended that the appended claims cover all such modifications and embodiments as falling within the true spirit and scope of the present invention.

Claims

What is claimed:

1. A compound (DNT-ramarate) having the following formula:

2. The compound of claim 1, wherein the compound is isolated.

3. The compound of claim 2, wherein the compound is isolated as a crystal.

4. A composition comprising the compound of any of claims 1-3, wherein the compound is present in said composition with at least about 99.96% enantiomeric purity by HPLC.

5. A composition comprising the compound of any of claims 1-3, wherein the compound is present in said composition with at least about 95% enantiomeric purity by HPLC.

6. A composition comprising the compound of any of claims 1-3, wherein the compound is present in said composition with at least about 85% enantiomeric purity by HPLC.

7. A composition comprising the compound of any of claims 1-3, wherein the compound is present in said composition with at least about 50% enantiomeric purity by HPLC.

8. A composition comprising the compound of any of claims 1-3, wherein the R- enantiomer of DNT-fumarate is not detectable by HPLC.

9. A process for preparing DNT-fumarate of any of claims 1-8 comprising combining DNT with fumaric acid to form a reaction mixture, precipitating DNT fumarate from the reaction mixture, and recovering the DNT fumarate.

10. The process of claim 9 wherein the reaction mixture contains a solvent selected from the group consisting OfC_1-8 alcohols, C_3-7 esters, C_3-8 ethers, C_3-7 ketones, C_6-12 aromatic hydrocarbons, acetonitrile, water, and mixtures thereof.

11. The process of claim 10, wherein the solvent is at least one of acetone, n- BuOH, ethyl acetate, MTBE, toluene, and water.

12. The process of claim 10, wherein the solvent is at least one of n-BuOH, ethyl acetate, and acetone.

13. The process of any of claims 10-13 wherein the DNT and the fumaric acid in the solvent are heated to obtain a mixture, followed by precipitation of the fumarate.

14. The process of claim 13, wherein the heating is carried out at about room temperature to about reflux temperature of the solvent.

15. The process of any of claims 13-14 wherein the mixture is cooled to precipitate the DNT-fumarate.

16. The process of any of claims 9-15, wherein the level of the DNT-fumarate R- enantiomer of the precipitate is less than about 70% of the R-enantiomer content of the DNT starting material in relation to the S-enantiomer.

17. The process of any of claims 9-15, wherein the level of the DNT-fumarate R- enantiomer of the precipitate is less than about 40% of the R-enantiomer content of the DNT starting material in relation to the S-enantiomer.

18. The process of any of claims 9-15, wherein the level of the DNT-fumarate R- enantiomer of the precipitate is less than about 17% of the R-enantiomer content of the DNT starting material in relation to the S-enantiomer.

19. The process of any of claims 9-15, wherein the level of the DNT-fumarate R- enantiomer of the precipitate is not detectable by HPLC.

20. The process of any of claims 9-19 further comprising combining DNT- fumarate with a base, combining the DNT-base with fumaric acid to form a reaction mixture, precipitating DNT-fumarate from the reaction mixture, and recovering the DNT-fumarate.

21. The process of any of claims 9-20, wherein the process results in a crystalline form characterized by a powder XRD with peaks at about 9.7°, 16.5°, 17.4°, 21.2°, and 24.1° 20 ± 0.2° 20.

22. The process of claim 21, wherein the crystalline form is obtained in a composition with at least 50% polymorphic purity.

23. A process for preparing duloxetine hydrochloride comprising preparing a solution of DNT in a solvent selected from the group consisting of C_1-8 alcohols, C_3-7 esters, C_3-8 ethers, C_3-7 ketones, C_6-12 aromatic hydrocarbons, acetonitrile, water, and mixtures thereof, combining the solution with fumaric acid to form a reaction mixture, precipitating DNT-fumarate from the reaction mixture, and converting the crystalline DNT-fumarate to the duloxetine hydrochloride.

24. A crystalline form of DNT-fumarate:

^y C T/ U S O B /^" 3 B B 7 S characterized by a powder XRD with peaks at about 9.7°, 16.5°, 17.4°, 21.2°, and

24.1° 20 ± 0.2° 20.

25. The crystalline form of claim 24, further characterized by powder XRD peaks at about 18.7°, 19.3°, 22.4°, 23.1°, and 26.4° 20 ± 0.2° 20.

26. The crystalline form of claim 24 in a crystalline form characterized by an powder XRD pattern substantially as depicted in Figure 1.

27. A process for preparing duloxetine or a pharmaceutically acceptable salt thereof comprising converting the crystalline form of any of claims 24-26 to said duloxetine or said pharmaceutically acceptable salt thereof.

28. A process for preparing a pharmaceutically acceptable salt of duloxetine, comprising combining DNT, a solvent selected from the group consisting of C_1-8 alcohols, C_3-7 esters, C_3-8 ethers, C_3-7 ketones, C_6-12 aromatic hydrocarbons, acetonitrile, water and mixtures thereof with fumaric acid to form a reaction mixture, precipitating DNT-fumarate from the reaction mixture, converting the DNT-fumarate to DNT, converting the DNT to duloxetine, and converting the duloxetine to the pharmaceutically acceptable salt of duloxetine.

29. A pharmaceutical composition comprising the pharmaceutically acceptable salt of duloxetine prepared by the process of any of the preceding claims and at least one pharmaceutically acceptable excipient.

30. The pharmaceutical composition of claim 29, wherein the level of the DNT- fumarate R-enantiomer content of the precipitate is at less than about 50% by HPLC in relation to the corresponding S-enantiomer.

31. The pharmaceutical composition of claim 30, wherein the level of the DNT- fumarate R-enantiomer content of the precipitate is at less than about 15% by HPLC in relation to the corresponding S-enantiomer.

32. The pharmaceutical composition of claim 31, wherein the level of the DNT- fumarate R— enantiomer content of the precipitate is at less than about 5% by HPLC in relation to the corresponding S-enantiomer.

33. The pharmaceutical composition of claim 32, wherein the level of the DNT- fumarate R-enantiomer content of the precipitate is at less than about 0.04% by HPLC in relation to the corresponding S-enantiomer.

34. The pharmaceutical composition of claim 33, wherein the level of the DNT- maleate R-enantiomer content of the precipitate is undetectable by HPLC.

35. A process for preparing the pharmaceutical composition of any of claims 29- 34 comprising admixing duloxetine HCl with at least one pharmaceutically acceptable excipient.

36. Use of the composition of any of claims 29-34 in the manufacture of a medicament for inhibiting uptake of neurotransmitters serotonin and norepinephrine in a mammal.