Patent Application
20080015359
The present invention relates to a process for the preparation of telmisartan [4′-[2-n-propyl-4-methyl-6-(1-methyl-benzimidazol-2-yl)benzimidazol-1-yl methyl]biphenyl-2-carboxylic acid] in a “one pot” synthesis, which is thus simple and cost effective, and produces telmisartan with high product yield and quality.
Telmisartan is known from EP 0502314B and has the following chemical structure of formula (I)
Telmisartan is an angiotensin II receptor antagonist, which by virtue of its pharmacological properties is particularly useful in the treatment of hypertension and cardiac insufficiency.
Chinese Patent CN 1344172 discloses the preparation of telmisartan in two steps: namely condensation and hydrolysis.
U.S. Pat. No. 5,591,762 discloses the preparation of telmisartan from its tertiary butyl ester. Hydrolysis is carried out using trifluoro acetic acid in dimethyl formamide at room temperature and maintained for about 12 hours. The crude product obtained is purified over a silica gel column and finally crystallized from acetone.
US 2002/0094997 is a divisional application of U.S. Pat. No. 6,358,986. US 2002/0094997 discloses polymorphs of telmisartan, particularly polymorphic form B, polymorphous mixtures and their preparation. Accordingly, telmisartan Form A is dissolved in a mixture of solvents consisting of water, formic acid and an organic solvent that is miscible therewith; the solution is heated followed by distillation and telmisartan containing Form A and Form B is precipitated from the mixture by addition of a base. The disclosure further refers to advantages of the polymorphic Form B mixture, for example it is easily filterable and has a low tendency to electrostatic charging. The disclosure still further refers to the fact that Form A, which is obtained according to the basic patent, is difficult to filter, is characterized by a very long drying time and exhibits a strong tendency to electrostatic charging. The two telmisartan polymorphs of Form A and B as characterised by US 2002/0094997 differ considerably in their melting point: Form B melts at 183° C. (determined by DSC), Form A at 269° C. (determined by DSC). The polymorphs A and B also differ in their IR spectrum. Pure polymorph A has a characteristic band at 815 cm−1 in the IR spectrum. In polymorph B, this oscillation is shifted to 830 cm−1.
In all the prior art processes, telmisartan is prepared in two or three steps, which is time consuming, product is lost during intermediate isolation, and as such there is a resulting low yield of the final product. It is also suggested in the prior art that the use of dimethyl formamide and alkali metal carbonates as solvent resulted in dimer formation, which also contributed to low yield.
The aim of the present invention is, therefore, to provide an improved process for the preparation of telmisartan. In particular, it is an aim of the present invention to prepare telmisartan in a one step process, thereby increasing the yield, decreasing the cost and avoiding filtration and drying problems.
Surprisingly, it has been found according to the present invention that telmisartan can be synthesised in one step from intermediates [1H -Benzimidazole-2-n-propyl-4-methyl-6-(1′-methyl benzimidazole-2′-yl)] and methyl-4-(bromomethyl)biphenyl-2-carboxylate.
According to the present invention, therefore, there is provided a process for the preparation of telmisartan of formula (I), or a pharmaceutically acceptable salt thereof
characterised in that 1H-Benzimidazole-2-n-propyl-4-methyl-6-(1′-methyl benzimidazole-2′yl) of formula (II), and methyl-4-(bromomethyl)biphenyl-2-carboxylate of formula (III), are subjected to condensation and hydrolysis in a single step (in other words, a “one pot” synthesis)
Intermediate compounds of formulae (II) and (III) are preferably reacted according to a process of the present invention in a polar aprotic solvent in the presence of a base. Polar aprotic solvents are well known in the art and can include, for example, dimethyl acetamide, dimethyl formamide, dimethyl sulphoxide, and the like, with the use of dimethyl formamide or dimethyl sulphoxide being preferred, especially dimethyl sulphoxide. Preferred bases for use in a method according to the present invention are alkali metal hydroxides.
A process according to the present invention is preferably carried out at a temperature in the range of about 10 to 80° C., with a preferred temperature being in the range of about 25 to 50° C. The reaction time for a process according to the present invention is typically in the range of from about a few minutes to a few hours, depending on the exothermicity of the reaction. Telmisartan is then typically isolated from the reaction mass by adjusting the pH using aqueous acids, suitably for example the pH is adjusted to be in the range of about 3 to 4.5 using acetic acid, optionally followed by extraction in a water-immiscible solvent.
Telmisartan can be isolated directly after pH adjustment by filtration without proceeding to extraction in a water-immiscible solvent. However, the use of the extraction phase is preferred because telmisartan as obtained directly after pH adjustment can be slimy in nature, thereby resulting in slow filtration properties. It is therefore preferable to extract telmisartan into a suitable solvent and isolate it from a non-solvent. A preferred water-immiscible solvent for extraction can be any of dichloromethane, ethyl acetate, chloroform or any other suitable water-immiscible solvent, with the use of dichioromethane being preferred. The organic layer is then suitably concentrated and isolated by addition of a suitable solvent, such as methanol, acetone, diisopropyl ether, acetonitrile or isopropyl acetate, with the use of acetone being preferred.
The present invention further provides telmisartan, or a pharmaceutically acceptable salt thereof, prepared by a process substantially as hereinbefore described. Telmisartan as prepared and isolated (typically employing acetone) by a process according to the present invention advantageously comprises free flowing polymorphic Form A, which can be similarly characterised by the melting point and IR properties as described above for Form A as defined in US 2002/0094997. Telmisartan Form A as provided by the present invention, however, is preferable over telmisartan Form A as prepared by prior art methods, in view of the free flowing properties of telmisartan as provided by the present invention compared to the poor flow characteristics of telmisartan Form A as provided by the prior art, for which the filtration rate can be very slow.
Telmisartan Form A as prepared by a process according to the present invention advantageously has a purity of at least about 97% and is typically obtained in a yield of about 80-88%.
The invention may also comprise further purification of telmisartan so as to achieve a highly pure compound. Preferably, telmisartan is subjected to purification by dissolving it in methanol and a methanolic ammonia mixture and isolating. Preferably, isolation is done by adjusting the pH using acetic acid, suitably to a pH of 3.5-4.0.
According to a preferred embodiment of the present invention, it may be desirable to isolate telmisartan as a pharmaceutically acceptable salt, such as the sodium or potassium salt of telmisartan. Telmisartan in salt form is suitably isolated from the reaction mass prior to pH adjustment.
Telmisartan, or a pharmaceutically acceptable salt thereof, has pharmaceutical utility as an angiotensin II receptor antagonist, and in view of the pharmacological properties thereof, telmisartan, or a pharmaceutically acceptable salt thereof, is suitable for the treatment of hypertension and cardiac insufficiency and also for treating ischaemic peripheral circulatory disorders, myocardial ischaemia (angina), for the prevention of the progression of cardiac insufficiency after myocardial infarction and for treating diabetic nephropathy, glaucoma, gastrointestinal diseases and bladder diseases. In particular, telmisartan, or a pharmaceutically acceptable salt thereof, as provided by the present invention is useful for the treatment of hypertension.
Telmisartan, or a pharmaceutically acceptable salt thereof, as provided by the present invention is also suitable for treating pulmonary diseases, e.g. lung oedema and chronic bronchitis, for preventing arterial restenosis after angioplasty, for preventing thickening of blood vessel walls after vascular operations, and for preventing arteriosclerosis and diabetic angiopathy. In view of the effects of angiotensin on the release of acetyl-choline and dopamine in the brain, telmisartan, or a pharmaceutically acceptable salt thereof, as provided by the present invention is also suitable for alleviating central nervous system disorders, e.g. depression, Alzheimer's disease, Parkinson syndrome, bulimia and disorders of cognitive function.
The present invention further provides, therefore, a pharmaceutically acceptable composition for administering to a patient, suffering from, or susceptible to, a disease state prevented, ameliorated or eliminated by the administration of an angiotensin II receptor antagonist, which composition comprises a therapeutically effective amount of telmisartan, or a pharmaceutically acceptable salt thereof, prepared according to the present invention, together with a pharmaceutically acceptable carrier, diluent or excipient therefor.
As used herein, the term “therapeutically effective amount” means an amount of telmisartan, or a pharmaceutically acceptable salt thereof, which is capable of preventing, ameliorating or eliminating a disease state for which administration of an angiotensin II receptor antagonist is indicated.
By “pharmaceutically acceptable composition” it is meant that the carrier, diluent or excipient is compatible with telmisartan, or a pharmaceutically acceptable salt thereof, and not deleterious to a recipient thereof. For this purpose, telmisartan, or a pharmaceutically acceptable salt thereof, optionally in conjunction with other active substances, such as hypotensives, diuretics and/or calcium antagonists, may be incorporated together with one or more inert conventional carriers and/or diluents, for example with corn starch, lactose, glucose, microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone, citric acid, tartaric acid, water, water/ethanol, water/glycerol, water/sorbitol, water/polyethylene-glycol, propylene-glycol, cetylstearyl alcohol, carboxymethylcellulose or fatty substances such as hard fat or suitable mixtures thereof, in conventional pharmaceutical preparations such as plain or coated tablets, capsules, powders, suspensions or suppositories.
The pharmaceutical compositions of the present invention may be prepared by conventional methods known in the art. For example, tablets may be prepared by mixing telmisartan, or a pharmaceutically acceptable salt thereof, according to the present invention, with known adjuvants and/or diluents and subsequently compressing the mixture in a conventional tabletting machine. The particular dosage form of telmisartan, or a pharmaceutically acceptable salt thereof, required to treat a disease state prevented, ameliorated or eliminated by the administration of an angiotensin II receptor antagonist as described herein in a patient, will depend on the particular disease state or condition, and the symptoms and severity thereof Dosage, routes of administration, and frequency of dosing are best decided by an attending physician.
The present invention further provides telmisartan, or a pharmaceutically acceptable salt thereof, prepared according to the present invention, for use in the manufacture of a medicament for the treatment of a disease state prevented, ameliorated or eliminated by the administration of an angiotensin II receptor antagonist as described herein.
The present invention also provides a method of treating a disease state prevented, ameliorated or eliminated by the administration of an angiotensin II receptor antagonist in a patient in need of such treatment, which method comprises administering to the patient a therapeutically effective amount of telmisartan, or a pharmaceutically acceptable salt thereof, prepared according to the present invention, substantially as hereinbefore described.
The present invention will now be further illustrated by the following Examples, which do not limit the scope of the invention in any way.
50 gm of [1H-Benzimidazole-2-n-propyl-4-methyl-6-(1′methyl benzimidazole-2′-yl)] was added to 200 ml dimethyl sulfoxide and 50 gm of potassium hydroxide. To this was added 60 gm of methyl-4-(bromomethyl)biphenyl-2-carboxylate at ambient temperature. The contents were stirred for 2 hours at 25-30° C., then heated to 40-50° C. and maintained for 2 hours. About 500 ml water was added to the reaction mixture at room temperature and acidified to pH 4 with acetic acid. The reaction mixture was filtered and washed with purified water, dried under reduced pressure at 50-60° C. to give 80 gm (88 %) of the title product.
50 gin of [1H-Benzimidazole-2-n-propyl-4-methyl-6-(1′-methyl benzimidazole-2′-yl)] was added to 200 ml dimethyl sulphoxide and 50 gm of potassium hydroxide. To this was added 60 gm of methyl-4-(bromomethyl)biphenyl-2-carboxylate at ambient temperature. The contents were stirred for 2 hours at 25-30° C. The contents were heated to 40-50° C. and maintained for 2 hours. About 500 ml water was added to the reaction mixture at room temperature and acidified with acetic acid to pH 3.8, extracted twice with 250 ml of dichloromethane and the combined extracts were concentrated and isolated by filtration after addition of 300 ml acetone, dried under reduced pressure at 50-60° C. to give 75 gm (80%) of the title product
50 gm of [1H -Benzimidazole-2-n-propyl-4-methyl-6-(1′-methyl benzimidazole-2′-yl)] was added to 200 ml dimethyl sulfoxide and 50 gm of sodium hydroxide. To this was added 60 gm of methyl-4-(bromomethyl)biphenyl-2-carboxylate at ambient temperature. The contents were stirred for 2 hours at 25-30° C. and then heated to 40-50 and maintained for 2 hours. About 500 ml water was added to the reaction mixture and acidified with acetic acid to pH 4.2, extract4ed twice with 250 ml of dichloromethane and the combined extracts were concentrated and isolated by filtration after addition of 300 ml acetone, dried under reduced pressure at 50-60° C. to give 75.0 gm (80%) of the title compound.
50 gm of [4′-[2-n-propyl-4-methyl-6-(1-methyl benzimidazol-2-yl)benzimidazol-1-yl methyl]biphenyl-2-carboxylic acid] (obtained according to any of Examples 1, 2 or 3) was added to 500 ml of methanol. To this was slowly added 50 ml of methanolic ammonia (10-15%) at 25-30° C. The contents were stirred for 30 minutes at 25-30° C. About 3 gm charcoal was added and stirred at 25-30° C. for 30 minutes. The reaction mixture was filtered over hyflo, bed washed with methanol. The clear filtrate pH was adjusted to 3.5-4.0 using acetic acid. The contents were stirred at 20-30° C. for 1 hour. Pure telmisartan was isolated by filtration, dried under reduced pressure at 50-60° C. to yield 45 gm (90%) of the title product with HPLC purity of about 99.3%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0410471.7 | May 2004 | GB | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/GB05/01799 | 5/10/2005 | WO | 1/11/2007 |
