Process for the preparation of pure and stable crystalline Raltegravir potassium form 3

Abstract

The present invention provides improved, commercially viable and consistently reproducible processes for the preparation of pure and stable crystalline Raltegravir potassium Form 3 and pharmaceutical composition thereof.

Claims

1. A process for the preparation of crystalline Raltegravir potassium Form 3 comprising: (i) contacting Raltegravir in ketone or ether solvent and/or mixtures thereof, wherein the ketone is selected from acetone, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), or mixtures thereof, and the ether solvent is selected from dimethyl ether, diethyl ether, methyl tert-butyl ether (MTBE), or mixtures thereof; (ii) heating the reaction mass of step (i) to obtain clear solution; (iii) adding aqueous alcoholic potassium base; and (iv) isolating crystalline Raltegravir potassium Form 3 from the reaction mixture thereof.

2. The process of claim 1, wherein the solvent in step (i) is selected from a mixture of acetone and methyl ethyl ketone or a mixture of acetone and methyl tert-butyl ether.

3. The process of claim 2, wherein the solvent in step (i) is a mixture of acetone and methyl ethyl ketone.

4. The process of claim 1, wherein step (ii) is carried out at a temperature of 30 C. to reflux temperature of solvent.

5. The process of claim 1, wherein the potassium base employed in step (iii) is selected from potassium hydroxide, potassium ethoxide, potassium methoxide.

6. The process of claim 1, wherein a molar ratio of the potassium base employed in step (iii) with respect to Raltegravir free acid is 0.2 to 1.2 molar equivalents.

7. The process of claim 1, wherein the isolation in step (iv) is carried out by filtration, concentration or evaporation.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1: illustrates X-ray powder diffraction pattern of pure and stable crystalline Raltegravir potassium Form 3.

(2) FIG. 2: illustrates DSC curve for pure and stable crystalline Raltegravir potassium Form 3.

(3) FIG. 3: illustrates X-ray powder diffraction pattern of substantially pure Raltegravir potassium Form 3.

(4) FIG. 4: illustrates DSC curve for substantially pure Raltegravir potassium Form 3.

(5) FIG. 5: illustrates TGA of substantially pure Raltegravir potassium Form 3.

SUMMARY OF THE INVENTION

(6) The present invention provides process for the preparation of pure and stable crystalline Raltegravir potassium Form 3.

(7) The present invention also provides pharmaceutical compositions comprising said pure and stable crystalline Raltegravir potassium Form 3.

(8) The present invention also provides substantially pure crystal line Raltegravir potassium Form 3 and process for the preparation thereof.

DETAILED DESCRIPTION

(9) As used herein, the term substantially pure is further defined as Raltegravir potassium salt, having a purity of greater than or equal to 95%, preferably a purity of greater than or equal to about 99% and more preferably a purity of greater than or equal to about 99.5%, when measured by HPLC.

(10) While working on the process development for Raltegravir it has been found that the present process for the preparation of crystalline Raltegravir potassium Form 3 does not have the disadvantages of the earlier mentioned methods. Raltegravir potassium Form 3 obtained from the present process is stable at accelerated conditions as well.

(11) It is also found that to achieve reproducibility of stable and pure crystalline Form 3 of Raltegravir potassium, maintaining the critical process parameters like stirring and cooling temperatures; solvent system and volume of solvent ratio used for dissolving Raltegravir free acid and dissolving source of potassium base; water content of solvents used and isolation conditions are very important.

(12) In one embodiment, the present invention provides an improved process for the preparation of pure and stable crystalline Raltegravir potassium Form 3 comprising the steps of:

(13) (i) contacting Raltegravir in ketone or ether solvent and/or mixtures thereof;

(14) (ii) heating the reaction mass of step (i) to obtain clear solution;

(15) (iii) adding aqueous alcoholic potassium base; and

(16) (iv) isolating Raltegravir potassium Form 3 from the reaction mixture thereof.

(17) According to present invention, the organic solvent used in step (i) is selected from ketone, ethers or mixtures thereof; wherein ketone is selected from acetone, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK) and the like or mixtures thereof; ether solvent is selected from dimethyl ether, diethyl ether, THF, dioxane, methyl ter-butyl ether (MTBE) and the like. Preferably the organic solvent used is acetone, methyl ethyl ketone, methyl isobutyl ketone, MTBE or mixtures thereof.

(18) In one embodiment the solvent used in step (i) is selected from mixture of acetone and methyl ethyl ketone or mixture of acetone and methyl ter-butyl ether. The volume ratio of first solvent to second solvent can be from 10-80 volumes to 90-20 volumes, preferably the ratio of first solvent to second solvent can be 25-75 volumes to 75-25 volumes.

(19) In another embodiment, the first solvent can be acetone and second solvent can be methyl ethyl ketone or methyl ter-butyl ether. In further embodiment, the first solvent can be methyl ethyl ketone and second solvent can be acetone or methyl ter-butyl ether. In still further embodiment, the first solvent can be methyl ter-butyl ether and second solvent can be acetone or methyl ethyl ketone.

(20) The reaction of step (ii) can be heated from 30 C. to reflux temperature of solvent system used to get clear solution.

(21) Potassium base used in step (iii) is selected from potassium hydroxide; potassium alkoxide such as potassium ethoxide, potassium methoxide and the like. The aqueous alcoholic potassium base used in step (iii) can be aqueous methanolic potassium base. The aqueous percentage in alcohol solvent is not more than 15%.

(22) The molar ratio of potassium base employed in step (iii) with respect to Raltegravir free acid is in the range of 0.2 to 1.2 molar equivalents.

(23) The reaction of step (iii) can be done at 5 to 30 C.; preferably at below room temperature.

(24) The isolation of pure and stable crystalline Raltegravir potassium Form 3 in step (iv) is carried out by conventional techniques filtration, concentration, evaporation followed by drying of the product obtained.

(25) In another embodiment of the invention, the present invention provides pure and stable crystalline Raltegravir potassium Form 3, characterized by PXRD (powder X-ray diffraction chromatogram) which shows peaks expressed as 2 at 7.2, 7.7, 10.6, 13.7 and 24.30.2 degrees. The XRPD of pure and stable crystalline Raltegravir potassium Form 3 is depicted in FIG. 1.

(26) The pure and stable crystalline Raltegravir Form 3 is further characterized by PXRD peaks at about 8.1, 18.9, 19.7, 20.7 and 26.30.2 degrees 2 values.

(27) The pure and stable crystalline Raltegravir Form 3 is further characterized by the DSC curve, obtained at a heating rate of 10 C./min, exhibiting a single endotherm with onset temperature of about 285.59 C. as depicted in FIG. 2.

(28) According to the present invention, the pure and stable crystalline Raltegravir potassium Form 3 obtained by the process of the present invention is having an assay of greater than about 98.2%, or greater than about 99.9%, when measured by using high performance liquid chromatography (HPLC) and maximum impurity observed is below 0.10% even at accelerated conditions.

(29) Physical Stability

(30) Within the context of the present disclosure, pure and stable crystalline Raltegravir potassium Form 3 of the present invention may exhibit long-term physical and chemical stability. As an example, Table 1 below shows data collected on pure and stable crystalline Raltegravir potassium Form 3 prepared by the processes disclosed hereinabove. The pure and stable crystalline Raltegravir potassium Form 3 tested shows no significant degradation or change in PXRD pattern (e.g., is stable at 1, 3 and 6 months storage) when stored at 252 C./605%, 302 C./655%, and at 40 C./755% relative humidity (RH).

(31) TABLE-US-00001 TABLE 1 Crystalline Raltegravir potassium Form 3 Moisture content Related substance Condition (%) [by HPLC] PXRD At 40 2 C./75 5% RH Initial 0.3 All impurities below 0.10% Crystalline Form 3 1 month 0.04 All impurities below 0.10% Stable 3 month 0.4 All impurities below 0.10% Stable 6 month 0.4 All impurities below 0.10% Stable At 30 2 C./65 5% RH Initial 0.3 All impurities below 0.10% Crystalline Form 3 1 month 0.6 All impurities below 0.10% Stable 3 month 0.2 All impurities below 0.10% Stable 6 month 0.6 All impurities below 0.10% Stable At 25 2 C./60 5% RH Initial 0.3 All impurities below 0.10% Crystalline Form 3 1 month 0.1 All impurities below 0.10% Stable 3 month 0.3 All impurities below 0.10% Stable 6 month 0.4 All impurities below 0.10% Stable

(32) In another embodiment, the present invention provides a pharmaceutical composition comprising pure and stable crystalline Raltegravir potassium Form 3 with pharmaceutically acceptable excipients.

(33) The pure and stable crystalline Raltegravir potassium Form 3 can be formulated into various pharmaceutical compositions like powder, granules, capsules, tablets, pellets etc.

(34) Pharmaceutically acceptable excipients may be utilized as required for conversion of the pure and stable Crystalline Raltegravir potassium Form 3 into the final pharmaceutical dosage forms and include, for example, any one or more of diluents, binders, stabilizers, lubricants, glidants, disintegrating agents, surfactants, and other additives that are commonly used in solid pharmaceutical dosage form preparations.

(35) In another embodiment, the invention provides a process for the preparation of substantially pure crystalline Raltegravir potassium Form 3 comprising the steps of:

(36) (i) providing a solution of Raltegravir and a potassium base in a suitable solvent;

(37) (ii) cooling the reaction mixture of step (i); and

(38) (iii) isolating Raltegravir potassium Form 3 from the reaction mixture thereof.

(39) The suitable solvent employed in step (i) is selected from water, acetone, tetrahydrofuran, iso-propanol, n-propanol, ethyl acetate and/or mixtures thereof.

(40) Potassium base employed in step (i) is selected from potassium hydroxide; potassium alkoxides such as potassium ethoxide, potassium methoxide and the like. The molar ratio of potassium base employed with respect to Raltegravir free acid is in the range of 0.2 to 1.2 molar equivalents.

(41) The reaction involving formation of potassium salt in step (ii) carried out at a temperature of 0 to 40 C. more preferably at 0 to 20 C. Reaction mixture is further cooled to 0 to 5 C.

(42) The reaction mixture is stirred at ambient temperature for 1 to 8 hours, preferably for 1-2 hours after addition of the potassium base.

(43) The isolation of the crystalline solid is carried out by conventional techniques known in the prior art such as filtration, concentration, evaporation etc followed by drying.

(44) In another embodiment of the invention, the present invention provides substantially pure crystalline Raltegravir potassium Form 3, characterized by XRPD which comprises of peaks expressed as 2 at 5.5 7.7, 10.55, 12.10, 13.64, 15.46, 24.22 and 31.240.2 degrees. The XRPD of substantially pure crystalline Raltegravir potassium Form 3 is depicted in FIG. 3.

(45) A DSC curve, obtained at a heating rate of 10 C./min, exhibiting a single endotherm with a peak temperature of about 290 C. as depicted in FIG. 4.

(46) The invention is further illustrated by following examples, which should not be construed as limiting to the scope of invention.

EXAMPLES

(47) The X-ray diffraction patterns were measured using Philips X'Pertpro machine with following measurement parameters:

(48) Scan axis: Gonio

(49) Step size: 0.0080

(50) Scan type: continuous

(51) DL lergence slit size: 0.2393

(52) Anode material: Cu

(53) Radiation type: K-alpha 1

(54) Scan: 3.49 to 402

(55) Spinning: Yes

(56) Measurement temperature: 25 C.

Example 1

(57) 30 gm of Raltegravir was charged in 510 ml of acetone and the mixture was stirred and cooled. 15 ml of aq KOH was added to this solution maintaining the temperature at 15 C. The obtained solid was filtered and dried under vacuum to get 24.2 g of crystalline Raltegravir potassium Form 3.

Example 2

(58) 100 g of Raltegravir potassium was charged in 1400 ml of water and the mixture was stirred at 20 C. to get a clear solution. The solution was concentrated under vacuum. To the obtained solid was added 1250 ml n-propanol and the mixture was concentrated. The solid obtained was dried under vacuum to get 90-100 g of crystalline Raltegravir potassium Form 3.

Example 3

(59) 5 g of Raltegravir was dissolved in 85 ml of acetone and MTBE at 50 C. and the mixture was further stirred at 25 C. 0.66 g of KOH dissolved in 2.7 ml aq methanol and the slurry was stirred. After completion of the reaction the mass was filtered, washed with solvent and dried at 40 C. to get 2.2 g of pure and stable crystalline Raltegravir potassium Form 3.

Example 4

(60) 30 g of Raltegravir was dissolved in 510 ml of acetone and MEK at 50 C. to get a clear solution. 3.97 g of KOH dissolved in 16.2 ml aq methanol was added to the solution under stirring. After completion of the reaction the mass was filtered, washed with solvent and dried at 40 C. to get 25.8 g of pure and stable crystalline Raltegravir potassium Form 3.

Example 5

(61) 30 g of Raltegravir was dissolved in 480 ml of acetone and MEK at 45 C. to get a clear solution. 3.97 g of KOH dissolved in 16.2 ml aq methanol was added to the solution under stirring. After completion of the reaction the mass was filtered, washed with solvent and dried at 40 C. to get 25.8 g of pure and stable crystalline Raltegravir potassium Form 3.

Example 6

(62) 40 g of Raltegravir was dissolved in 680 ml of acetone and MEK at 50 C. to get a clear solution. 5.29 g of KOH dissolved in 21.6 ml aq methanol was added to the solution under stirring. After completion of the reaction the mass was filtered, washed with solvent and dried at 40 C. to get 35.2 g of pure and stable crystalline Raltegravir potassium Form 3.

Example 7

(63) 3 Kg of Raltegravir was dissolved in 48 lit of acetone and MEK at 50 C. to get a clear solution. 397 g of KOH dissolved in 1.62 lit aq methanol was added to the solution under stirring. After completion of the reaction the mass was filtered, washed with solvent and dried at 40 C. to get 2.70 kg of pure and stable crystalline Raltegravir potassium Form 3.