Title of Invention

PROCESS FOR THE PREPARATION OF AMORPHOUS FLUVASTATIN SODIUM

Abstract The present invention relates to a novel process for the preparation of the HMG-CoA reductase inhibitor, fluvastatin, more specifically to a process for the preparation of amorphous form of fluvastatin sodium.
Full Text Process for the preparation of amorphous Fluvastatin sodium FIELD OF THE INVENTION
The instant invention relates to a novel process for the preparation of the HMG-CoA reductase inhibitor, fluvastatin, more specifically to a process for the preparation of amorphous fluvastatin sodium. BACKGROUND OF THE INVENTION
Fluvastatin, of which the full chemical name is R*f S*-(E)-(. +>.)-7-[3-(4-fluorophenyl)-l-(l-methyl-ethyl)-lH-indol-2-yl]-3,5-dihydroxy-6-heptenoic acid, as well as its sodium salt, are disclosed in EP-A-0 114 027. Fluvastatin is an inhibitor of 3-hydroxy-3-methyl-glutaryl coenzyme A (HMG-CoA) reductase, which is a key enzyme in the regulation of cholesterol biosynthesis. Fluvastatin can be used pharmaceutically particularly as a hypercholesterolemic, hyperlipoproteinemic and antiatherosclerotic agent.
The present invention relates to a novel process for the preparation fluvastatin form A. Polymorphism is the existence of more than one crystal structure for a compound. Since properties can and do vary with crystal structure, polymorphism can influence many important properties of pharamceuticals: bioavailability, dissolution rate, compressibility, solubility, stability, filtering and drying characteristics etc. Different combination of experimental techniques (microscopy, variable temperature X-ray structure determination, spectroscopic and calorimetric methods) are used to discover, prepare, characterize, and study polymorphs of compounds of pharamceutical importance.
Many pharmaceutical materials exhibit polymorphism during heating and this refers to the generation of thermodynamically unstable

melting forms. These polymorphic forms can be produced due to the given thermal history of the material. Different polymorphic forms can have differing solubilities and this can have a potentially major effect on the bioavailability of the drug when ingested. One polymorphic form may dissolve rapidly while another is very slow to dissolve. It is essential to screen pharmaceuticals for polymorphism for process optimization and for quality assurance purposes.
Fluvastatin sodium is specifically claimed as a substance in patent US 5,354,772.
Polymorphic forms of Fluvastatin sodium are claimed in various patent applications viz. WO 97/49681, WO 02/36563 and WO 03/013512.
WO 97/49681 (equivalent patents US 6,124,340 and EP 0 907 639) claims fluvastatin sodium crystalline form B. The PCT publication has compared properties of form B with form A. In accordance to WO 97/49681, the form A could be obtained by lyophilization process disclosed in U.S. Pat. No. 4,739,073. Several of these prior art process often result in a mixture of amorphous form and different crystalline form.
The present invention provides a robust process for the preparation of fluvastatin sodium in a amorphous form. The amorphous form of fluvastatin sodium thus prepared is substantially free from the anti-isomer. SUMMARY OF THE INVENTION
The invention relates to a novel process for the preparation of amorphous form of sodium fluvastatin.

DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to a novel process for the preparation of the HMG-CoA reductase inhibitor, fluvastatin, more specifically to a process for the preparation of amorphous form of fluvastatin sodium.
The instant invention discloses a process for the preparation of amorphous form of fluvastatin sodium comprising of:
(a) dissolving the sodium fluvastatin in methanol followed by stirring,
(b)concentrating the methanol extract to get a residue, (c) isolating the residue to get amorphous form of fluvastatin sodium. The process further comprising of
(d) subjecting the isolated amorphous form of fluvastatin sodium to drying. The process where the amorphous fluvastatin sodium in step (c) is isolated by filtration.
The process where the amorphous form of fluvastatin sodium is vacuum dried.
The instant invention has following advantages over prior art:
1. The process is robust resulting in amorphous form only.
2. The product prepared by the process is chemically stable.
3. The process is simple and economic
4. The process is environmentally friendly.
The present invention is further illustrated by the following non-limiting examples.
EXAMPLES Example 1

To a solution of t-butyl (E)-3,5-dihydroxy-7-[3'-(4"-fluorophenyl)-l'-methylethyl-ind6l-2'--yl]hept-6-enoate (1.0 Kg) in methanol (10 L), a solution of sodium hydroxide (90 g) in methanol (1.0 L) was added stirred for 2 h. The reaction mixture was concentrated . The residue was dissolved in methanol (5.0 L) and filtered over celite bed. The clear filtrate concentrated to syrup. Methanol (3.0 L) was added to the residue and stirred for 30 minutes. The mixture was concentrated and residue was dried in vacuum drier. The XRD pattern of the product showed that the product corresponds to amorphous fluvastatin sodium. Yield: 480 g. Example 2
Fluvastatin sodium form A (1.0 Kg) was dissolved in methanol (10 L) and filtered over celite bed. The clear filtrate concentrated to syrup. Methanol (5.0 L) was added to the residue and stirred for 30 minutes. The mixture was concentrated and residue was dried in vacuum drier. The XRD pattern of the product showed that the product corresponds to amorphous fluvastatin sodium.Yield: 980 g.







We claim:
1. A process for the preparation of amorphous form of fluvastatin
sodium comprising of:
(a) dissolving the sodium fluvastatin in methanol followed by
stirring, (b)concentrating the methanol extract to get a residue, (c) isolating the residue to get amorphous form of fluvastatin
sodium.
2. A process of claim 1, further comprising
- subjecting the isolated amorphous form of fluvastatin sodium to drying.
3. A process of claim 1, wherein the residue of step (b) is optionally dried under vacuum to get amorphous fluvastatin sodium.
4. A process of claim 1, wherein the amorphous fluvastatin sodium in step (c) is isolated by filtration.
5. A process of claim 2, wherein the amorphous form of fluvastatin sodium is vacuum dried. ♦
Dated this 09th day of April 2007
OfAnand And Anand Advocates Attorney for the Applicant

Documents:

1443-CHENP-2007 AMENDED CLAIMS 18-10-2010.pdf

1443-CHENP-2007 AMENDED PAGES OF SPECIFICATION 18-10-2010.pdf

1443-CHENP-2007 EXAMINATION REPORT REPLY RECIEVED 18-10-2010.pdf

1443-chenp-2007 form-3 18-10-2010.pdf

1443-CHENP-2007 OTHER PATENT DOCUMENT 18-10-2010.pdf

1443-chenp-2007 other patent document-1 18-10-2010.pdf

1443-CHENP-2007 POWER OF ATTORNEY 18-10-2010.pdf

1443-CHENP-2007 CORRESPONDENCE OTHERS 06-10-2010.pdf

1443-chenp-2007-abstract.pdf

1443-chenp-2007-claims.pdf

1443-chenp-2007-correspondnece-others.pdf

1443-chenp-2007-description(complete).pdf

1443-chenp-2007-form 1.pdf

1443-chenp-2007-form 3.pdf

1443-chenp-2007-form 5.pdf

1443-chenp-2007-pct.pdf


Patent Number 245135
Indian Patent Application Number 1443/CHENP/2007
PG Journal Number 01/2011
Publication Date 07-Jan-2011
Grant Date 04-Jan-2011
Date of Filing 09-Apr-2007
Name of Patentee BIOCON LIMITED
Applicant Address 20TH KM HOSUR ROAD ELECTRONICS CITY P.O BANGALORE 560 100 KARNATAKA
Inventors:
# Inventor's Name Inventor's Address
1 SRINATH SUMITHRA BIOCON LIMITED 20TH KM HOSUR ROAD ELECTRONICS CITY P.O BANGALORE 560 100 KARNATAKA
2 PUTHIAPRAMPIL TOM THOMAS BIOCON LIMITED 20TH KM HOSUR ROAD ELECTRONICS CITY P.O BANGALORE 560 100 KARNATAKA
3 CHANDRAPA RAVINDRA BIOCON LIMITED 20TH KM HOSUR ROAD ELECTRONICS CITY P.O BANGALORE 560 100 KARNATAKA
4 GANESH SAMBASIVAM BIOCON LIMITED 20TH KM HOSUR ROAD ELECTRONICS CITY P.O BANGALORE 560 100 KARNATAKA
PCT International Classification Number C07D 209/24
PCT International Application Number PCT/IN2004/000310
PCT International Filing date 2004-10-05
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 NA