Title of Invention	AN IMPROVED PROCESS FOR PREPARING TAMSULOSIN HYDROCHLORIDE
Abstract	The invention relates to an improved process for preparing Tamsulosin hydrochloride of Formula I.

Full Text

FIELD OF THE INVENTION The invention relates to an improved process for preparing the (i)-(-)- 5-[2- [[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesuIfonamide monohydrochloride of Formula 1. BACKGROUND OF THE INVENTION (7?)-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesulfonamide is known as Tamsulosin. Presently Tamsulosin is being marketed as its hydrochloride salt under the Trade name FLOMAX. It is an a-adrenergic antagonist used preferably for treating benign prostatic hyperplasia. US 4,703,063 describes two processes for the preparation of Tamsulosin, one of which involves the conversion of a hydroxy substituted analogue of Tamsulosin, i.e., a compound having the Tamsulosin structure but contains a hydroxyl substituent at a position a to the benzenesulfonamide ring, by halogenation followed by reduction and the other involves condensation of an appropriately substituted benzyl methyl ketone with the substituted phenoxy amine, followed by reduction of the resulting imino compound. The above described processes are non-stereospecific and the final product requires an additional step of resolution of enantiomers to specifically obtain (7?)-enantiomer tamsulosin. CA 1,282,077 discloses a process to prepare Tamsulosin wherein (7?)-enantiomer of sulfonamide amine has been condensed with ethoxy phenoxy bromide in dimethylformamide to obtain Tamsulosin (Scheme I), which was purified by crystallization before converting into hydrochloride salt. Scheme I As per the above described process, Tamsulosin hydrochloride is obtained in low yield, and therefore this process is not suitable for commercial production. WO 2002/068382 Al discloses a process to prepare sulfamoyl substituted phenethylamine derivatives including Tamsulosin. The described process involves a coupling reaction between (7f)-(-)-5-(2-aminopropyl)-2-methoxybenzenesulfonamide with an acid or a corresponding acid chloride or mixed anhydride to produce Tamsulosin amide and thereafter reduction of the obtained compound gives Tamsulosin. This coupling reaction presents the disadvantage that the acid or acid chloride or anhydride should be provided in a high purity in order to obtain a good yield in the coupling reaction; and it is known in the art that purification of such products is not always easy. WO 2004/022532 Al discloses a process to prepare Tamsulosin (Scheme II) wherein protected amine is used during condensation with ethoxy phenoxy derivative to obtain protected Tamsulosin. In this process, an additional step of removing the protecting group to obtain Tamsulosin is involved. This process involves the use of a protected amine derivative, which needs to be deprotected after the formation of Tamsulosin. EP 0 380 144 Bl describes a process for preparing Tamsulosin and the like, in stereospecific form, by reaction of a benzenesulfonamide amine with predetermined stereospecificity, with 2-(2-ethoxyphenoxy)ethyl halide, specifically the bromide. In this process, Tamsulosin base has been purified with column chromatography. WO 2004/016582 discloses a process to prepare Tamsulosin hydrochloride (Scheme III). This process involves two additional steps, first the protection of amine group before condensing with ethoxy phenoxy halide and thereafter the deprotection to obtain Tamsulosin. In all the examples given in this application, column chromatography has been used to purify Tamsulosin base before converting into hydrochloride salt. In view of the above difficulties, the instant invention describes a new economical and industrially advantageous method to prepare Tamsulosin by using alkaline earth metal oxides as acid neutralizing agent in the alkylation reaction. OBJECTIVE The objective of the present invention is to provide an improved process for preparing highly pure Tamsulosin hydrochloride in high yield. Yet another objective of the present invention is to provide a simple, industrially advantageous process to manufacture Tamsulosin hydrochloride. DETAILED DESCRIPTION OF THE INVENTION Specifically, the present invention involves reacting compound of Formula II with compound of Formula III in presence of an alkaline earth metal oxide selected from calcium oxide, barium oxide, magnesium oxide and the like. The said alkylation reaction is accomplished in presence of a solvent selected from CM alcohol such as methanol, ethanol, isopropanol, isobutyl alcohol and mixtures thereof, and preferably isobutyl alcohol. Typically the alkylation reaction is completed by heating under reflux at 60-100°C and preferably at 80-90°C. The major advantage realized in the present process is the use of alkaline earth metal oxide, an acid neutralizing agent, to promote the alkylation reaction. Alkaline earth metal salts are insoluble in the reaction medium and are removed easily by filtration after the alkylation reaction is over. In yet another embodiment of the present invention, the solvent employed during formation of Tamsulosin hydrochloride and during its purification is selected from CM alcohol such as methanol, ethanol, isopropanol, isobutyl alcohol and mixtures thereof, and preferably methanol. The invention is illustrated with the following examples, which are provided by way of illustration only and should not be construed to limit the scope of the invention. EXAMPLE 1 Step (i): PREPARATION OF CRUDE TAMSULOSIN HYDROCHLORIDE A mixture of (i?)-(-)-5-(2-aminopropyl)-2-methoxybenzenesuIfonamide (20 g, 0.082 mol), 2-(2-ethoxyphenoxy)ethyl methanesulfonate (19.18 g, 0.074 mol), calcium oxide (4.6 g, 0.821 mol) and isobutyl alcohol (300 ml) was heated at 80-85°C for 25 h. The reaction mass was filtered to remove calcium salts and the residue was washed with hot isobutyl alcohol (2x10 ml, 70°C). Thereafter, pH of the filtrate was adjusted to 1.0 using hydrochloric acid (10 g) at 60-65°C and the resulting product slurry was allowed to cool to 0-5°C. The solid thus obtained was filtered, washed with precooled isobutyl alcohol (2x10 ml, 5°C). Yield: 43 g (wet). Step (ii): PREPARATION OF PURE TAMSULOSIN HYDROCHLORIDE (#)-(-)-5-[2-[[2-(2-ethoxyphenoxy) ethyl] amino] propyl]-2- methoxybenzenesulfonamide hydrochloride (43 g, wet) was suspended in methanol (140 ml) and stirred at 55-60°C for 30 min. This suspension was cooled to 0-5°C, filtered and washed with precooled methanol (10 ml, 0°C). The filtered product (23 g) was dissolved in methanol (400 ml) at 55-60°C and treated with carbon (0.6 g) at the same temperature. Carbon was removed through hyflo and the residue was washed with hot methanol (2x25 ml, 60°C). The filtrate was concentrated under vacuum to a volume of about 150 ml. The product slurry was cooled and stirred at 0-5°C for 2 h. The mass was filtered, washed with precooled methanol (10 ml, 0°C) and dried to obtain Tamsulosin hydrochloride. Yield: 19 g. Chromatographic Purity: 99.76% (HPLC). EXAMPLE 2 Step (i): PREPARATION OF CRUDE TAMSULOSIN HYDROCHLORIDE A mixture of (i?)-(-)-5-(2-aminopropyl)-2-methoxybenzenesulfonamide (3 g, 0.0123 mol), 2-(2-ethoxyphenoxy)ethyl methanesulfonate (2.88 g, 0.011 mol), calcium oxide (0.52 g, 0.0093 mol) and ethanol (60 ml) was heated at 78-80°C for 35 h. The reaction mass was filtered and the residue was washed with hot ethanol (4 ml, 70°C). The pH of filtrate was adjusted to 1.0 using hydrochloric acid (1.68 g) at 60-65°C and the resulting product slurry was allowed to cool to 0-5°C. The solid thus obtained was filtered, washed with precooled ethanol (4 ml, 5°C). Yield: 6 g (wet) Step (H): PREPARATION OF PURE TAMSULOSIN HYDROCHLORIDE (i?)-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl] amino] propyl]-2- methoxybenzenesulfonamide hydrochloride (6 g, wet) was suspended in methanol (21 ml) and stirred at 55-60°C for 30 min. The suspension was cooled to 0-5°C, filtered and washed with precooled methanol (4 ml, 0°C). The filtered product (3.1 g) was dissolved in methanol (60 ml) at 55-60°C and treated with carbon (0.1 g) for 15 min. Carbon was removed by filtration and the filtrate was concentrated under vacuum to a volume of about 25 ml. The slurry was cooled and stirred at 0-5°C for 2 h. The product was filtered, washed with precooled methanol (4 ml, 0°C) and dried to obtain Tamsulosin hydrochloride. Yield: 2.65 g. Chromatographic Purity: 99.70% (HPLC). EXAMPLE 3 Step (i): PREPARATION OF CRUDE TAMSULOSIN HYDROCHLORIDE A mixture of (i?)-(-)-5-(2-aminopropyl)-2-methoxybenzenesuIfonamide (3 g, 0.0123 mol), 2-(2-ethoxyphenoxy)ethyl bromide (3.05 g, 0.0124 mol), calcium oxide * (0.52 g, 0.0093 mol) and isobutyl alcohol (45 ml) was heated at 80-90°C for 22 h. The reaction mass was filtered and the residue was washed with hot isobutyl alcohol (4 ml, 70°C). The pH of filtrate was adjusted to 1.0 with hydrochloric acid at 60-65°C and the contents were cooled to 0-5°C. The solid thus obtained was filtered, washed with precooled isobutyl alcohol (4 ml, 5°C). Yield: 7.5 g (wet) Step (ii): PREPARATION OF PURE TAMSULOSIN HYDROCHLORIDE (/?)-(-)-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesuIfonamide hydrochloride (7.5 g) was suspended in methanol (20 ml) and stirred at 55-60°C for 30 min. The suspension was cooled to 0-5°C and filtered. The product (3.5 g), thus obtained, was dissolved in methanol (60 ml) at 55-60°C and treated with carbon (0.1 g). Thereafter, carbon was removed through hyflo and the filtrate was concentrated to a volume of about 25 ml under vacuum. The product slurry was cooled to 0-5°C. The product was collected by filtration, washed with precooled methanol (4 ml, 0°C) and dried to obtain Tamsulosin hydrochloride. Yield: 2.45 g. Chromatographic Purity: 99.89% (HPLC). The process according to claim 1 wherein the alkaline earth metal salt is calcium oxide, magnesium oxide and barium oxide. 3. The process according to claim 1 wherein the solvent used in step (i) is selected from Ci-4 alcohol such as methanol, ethanol, isopropanol, isobutyl alcohol and mixtures thereof. 4. The process according to claim 3 wherein the solvent is isobutyl alcohol. 5. The process according to claim 1 wherein the reaction of compound of Formula II with a compound of Formula III is carried out at 80-90°C. 6. The process according to claim 1 wherein the solvent used in step (ii) is selected from Ci-4 alcohol, such as methanol, ethanol, isopropanol, isobutyl alcohol and mixtures thereof. 7. The process according to claim 1 to 5 wherein Tamsulosin hydrochloride is further purified by dissolving in a solvent selected from CM alcohol, such as methanol, ethanol, isopropanol, isobutyl alcohol and mixtures thereof, and precipitating the pure Tamsulosin hydrochloride. 8. An improved process for the preparation of Tamsulosin hydrochloride of Formula I, as defined in claim 1, substantially as herein described with reference to the examples. Dated this 8^ day of Septette* 2005.

Documents:

1270-CHE-2005 EXAMINATION REPORT REPLY RECEIVED 12-10-2012.pdf

1270-CHE-2005 FORM-3 12-10-2012.pdf

1270-CHE-2005 AMENDED CLAIMS 17-09-2012.pdf

1270-CHE-2005 AMENDED PAGES OF SPECIFICATION 17-09-2012.pdf

1270-CHE-2005 CORRESPONDENCE OTHERS 08-03-2013.pdf

1270-CHE-2005 EXAMINATION REPORT REPLY RECEIVED 17-09-2012.pdf

1270-che-2005 form-3 02-11-2010.pdf

1270-che-2005-abstract.pdf

1270-che-2005-claims.pdf

1270-che-2005-correspondnece-others.pdf

1270-che-2005-description(complete).pdf

1270-che-2005-form 1.pdf

1270-che-2005-form 5.pdf

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