Subtantially pure ropinirole hydrochloride, polymorphic form of ropinirole and process for their preparation
Ropinirole hydrochloride substantially free of impurities and a process for its preparation is provided. Also provided is ropinirole base substantially in polymorph Form A and a process for its preparation. Pharmaceutical compositions containing the same are also provided.
1 . Ropinirole base substantially in polymorph form A.
2 . The ropinirole base substantially in polymorph form A of claim 1 , characterized by having at least one of the following characteristics:
(a) an X-ray diffraction (XRD) pattern substantially in accordance with FIG. 1 ; and/or
(b) a Infra-Red (IR) spectrum substantially in accordance FIG. 2 .
3 . The ropinirole base substantially in polymorph form A of claim 1 , exhibiting a characteristic peak (expressed in degrees 2θ±0.2°θ) at about 6.81.
4 . The ropinirole base substantially in polymorph form A of claim 1 , exhibiting characteristic peaks (expressed in cm −1 ) at approximately about one or more of the positions: 3420, 2968, 2937, 2878, 2644, 1698, 1616, 1460, 1384, 1351, 1325, 1290, 1252, 1161, 1083, 967, 884, 839, 800, 705, 662 and 559.
5 . A pharmaceutical composition comprising a therapeutically effective amount of the ropinirole base substantially in polymorph form, A of claim 1 .
6 . A pharmaceutical composition comprising a therapeutically effective amount of the ropinirole base substantially in polymorph form A of claim 2 .
7 . A pharmaceutical composition comprising a therapeutically effective amount of the ropinirole base substantially in polymorph form A of claim 3 .
8 . A process for the preparation of ropinirole base substantially in polymorph form A, the process comprising:
(a) treating crude ropinirole base or a salt thereof with an inorganic base in a solvent; and
(b) recovering the ropinirole substantially in polymorphic Form A.
9 . The process of claim 8 , wherein the solvent is selected from the group consisting of water, water-miscible solvent, water-immiscible solvent and mixtures thereof.
10 . The process of claim 9 , wherein the water-miscible solvent is selected from the group consisting of methanol, ethanol, isopropanol, t-butanol, acetonitrile, 1,4-dioxane and mixtures thereof.
11 . The process of claim 9 , wherein the water-immiscible solvent is selected from the group consisting of ethyl acetate, ethyl acetoacetate, methylene chloride, ethylene chloride, chloroform, methyl tert butyl ether, toluene and mixtures thereof.
12 . The process of claim 5 , wherein the inorganic base is selected from the group consisting of an aqueous or solid alkaline earth metal hydroxide, alkali or alkaline earth metal carbonate and mixtures thereof.
13 . The process of claim 12 , wherein the alkaline earth metal hydroxide is selected from the group consisting of sodium hydroxide, potassium hydroxide, barium hydroxide, calcium hydroxide and mixtures thereof.
14 . The process of claim 12 , wherein the alkali or alkaline earth metal carbonate is selected from the group consisting of sodium bicarbonate, potassium carbonate, calcium carbonate, barium carbonate and mixtures thereof.
15 . Substantially pure ropinirole hydrochloride having less than about 0.15% weight of any one of 4-[2-(n-propylamino)ethyl]-1,3-dihydro-2H-indol-2-one, 4-(2-(dipropylamino)ethyl)-1-hydroxyindolin-2-one, and 4-ethyl-1,3-dihydro-2H-indol-2-one.
16 . The substantially pure ropinirole hydrochloride of claim 15 , having less than about 0.15% weight of each of 4-[2-(n-propylamino)ethyl]-1,3-dihydro-2H-indol-2-one, 4-(2-(dipropylamino)ethyl)-1-hydroxyindolin-2-one, and 4-ethyl-1,3-dihydro-2H-indol-2-one.
17 . A pharmaceutical composition comprising a therapeutically effective amount of the substantially pure ropinirole hydrochloride of claim 15 .
18 . A process for the preparation of substantially pure ropinirole hydrochloride, the process comprising:
(a) providing a solution comprising ropinirole base of Formula II in one or more organic solvents;
(b) extracting the solution with a base at a pH of about 10 to about 12;
(c) extracting the solution with an acid;
(d) substantially removing the solvent from the solution;
(e) dissolving the resulting solids in one or more polar solvents;
(f) adding hydrochloric acid under substantially dry conditions; and
(g) recovering the substantially pure ropinirole hydrochloride.
19 . Ropinirole hydrochloride prepared according to the process of claim 18 , having a purity of at least about 99.5% as determined by HPLC.