Indian Patents. 263360:" PROCESS FOR THE PREPARATION OF THE ALPHA CRYSTALLINE FORM OF THE ARGININE SALT OF PERINDOPRIL OF COMPOUND OF FORMULA (I)"

Title of Invention	" PROCESS FOR THE PREPARATION OF THE ALPHA CRYSTALLINE FORM OF THE ARGININE SALT OF PERINDOPRIL OF COMPOUND OF FORMULA (I)"
Abstract	α crystalline form of the compound of formula (I): characterised by its powder X-ray diffraction diagram. Medicaments.

Full Text	α CRYSTALLINE FORM OF THE ARGININE SALT OF PERINDOPRIL, A PROCESS FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT The present invention relates to the a crystalline form of the arginine salt of perindopril of formula (I): (Formula Removed) to a process for its preparation and to pharmaceutical compositions containing it. Perindopril and its pharmaceutically acceptable salts, and more especially its arginine salt, have valuable pharmacological properties. Their principal property is that of inhibiting angiotensin I converting enzyme (or kininase II), which allows, on the one hand, impedance of the conversion of the decapeptide angiotensin I to the octapeptide angiotensin II (a vasoconstrictor) and, on the other hand, prevention of the degradation of bradykinin (a vasodilator) to an inactive peptide. Those two actions contribute to the beneficial effects of perindopril in cardiovascular diseases, more especially in arterial hypertension and heart failure. Perindopril, its preparation and its use in therapeutics have been described in European Patent specification EP 0 049 658. The arginine salt of perindopril has been described in European Patent specification EP 1 354 873. In view of the pharmaceutical value of that compound, it has been of prime importance to obtain it with excellent stability, mainly in terms of hygroscopicity, of processability of the powder, of filtrability of the solid, of grindability, and of solvent retention. Obtaining a well-defined crystalline form allows those requirements to be met. Patent specification EP 1 354 873 describes the arginine salt of perindopril. That document does not, however, specify the conditions for obtaining that salt in a well-defined crystalline form. The Applicant has now found that the arginine salt of perindopril can be obtained in a well-defined crystalline form that, as a result, has valuable characteristics for filtration, drying and ease of formulation. More specifically, the present invention relates to the a crystalline form of the compound of formula (I), characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of angle 2 theta (°): 4.5, 7.9 and 13.5. Preferably, the present invention relates to the a crystalline form of the compound of formula (I), characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of angle 2 theta (°):4.5,7.9,13.5, 17.5 and 20.6. Even more preferably, the present invention relates to the a crystalline form of the compound of formula (I), characterised by the following powder X-ray diffraction diagram measured using a diffractometer (copper anti-cathode) and expressed in terms of inter-planar distance d, Bragg's angle 2 theta, intensity and relative intensity (expressed as a percentage of the most intense line) : (Table Removed) The invention relates also to a process for the preparation of the a crystalline form of the compound of formula (I), wherein perindopril is dissolved in water with L-arginine, and then an apolar solvent and a polar solvent are added and the crystals obtained are filtered off, washed and then dried. Among the apolar solvents there may be mentioned, by way of example, methylcyclohexane, cyclohexane and toluene. Among the polar solvents there may be mentioned, by way of example, dimethyl sulphoxide, N,N-dimethylformamide, N,N-dimethylacetamide and N-methyl-2- pyrrolidinone. The crystals so obtained are in a compact form composed of baguettes. According to one embodiment of the invention, perindopril is dissolved in water with L-arginine and then methylcyclohexane and dimethyl sulfoxide are added and the crystals obtained are filtered off, washed and then dried. The invention relates also to pharmaceutical compositions comprising as active ingredient the a crystalline form of the compound of formula (I) together with one or more appropriate, inert, non-toxic excipients. Among the pharmaceutical compositions according to the invention there may be mentioned, more especially, those that are suitable for oral, parenteral (intravenous or subcutaneous) or nasal administration, tablets or dragees, sublingual tablets, capsules, lozenges, suppositories, creams, ointments, dermal gels, injectable preparations, drinkable suspensions. The dosage used can be varied according to the nature and severity of the disorder, the administration route and the age and weight of the patient. It varies from 1 to 500 mg per day in one or more administrations. The pharmaceutical compositions according to the invention may also contain a diuretic such as indapamide. The following Examples illustrate the invention. The powder X-ray diffraction spectrum was measured under the following experimental conditions : Siemens D5005 diffractometer; scintillation detector; Copper anti-cathode, voltage 40KV, intensity 30mA ; Mounting θ-θ, fixed specimen; Temperature : ambient; Measurement range : 3° to 30°; Increment between each measurement: 0.04°; Measurement time per step :4 s; Fixed slits : 1.6 mm; Kß filter (Ni); No internal reference; Zeroing procedure using Siemens slits; Experimental data processed using EVA software (version 9.0). EXAMPLE 1 : a crystalline form of perindopril arginine salt 1.5 kg of water, 328 g of perindopril and 155 g of L-arginine are introduced into a reactor at ambient temperature and with stirring. When a clear solution is obtained, 630 g of methylcyclohexane are added, and then 4.7 kg of dimethyl sulphoxide are added slowly. The mixture is then stirred until the temperature of the heterogeneous mixture stabilises at around 20.0°C, after which the mixture is filtered and the solid obtained is washed and dried. The crystals so obtained are in a compact form composed of baguettes. The water content of the resulting product is approximately 3.2%, which corresponds to a monohydrate. Powder X-ray diffraction diagram : The powder X-ray diffraction profile (diffraction angles) of the a form of perindopril arginine salt is given by the significant lines collated in the following table together with the intensity and relative intensity (expressed as a percentage of the most intense line). (Table Removed) EXAMPLE 2 : Pharmaceutical composition Preparation formula for 1000 tablets each containing 4 mg of active ingredient: Compound of Example 1 4 g Hydroxypropylcellulose 2 g Wheat starch 10 g Lactose 100 g Magnesium stearate 3 g Talc 3 g CLAIMS 1. α crystalline form of the arginine salt of perindopril, of formula (I) : (Formula Removed) characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of Bragg's angle 2 theta (°) : 4.5, 7.9 and 13.5. 2. α crystalline form of the compound of formula (I) according to claim 1, characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of Bragg's angle 2 theta (°) : 4.5, 7.9, 13.5, 17.5 and 20.6. 3. α crystalline form of the compound of formula (I) according to claim 1, characterised by the following powder X-ray diffraction diagram measured using a diffractometer (copper anti-cathode) and expressed in terms of inter-planar distance d, Bragg's angle 2 theta, intensity and relative intensity (expressed as a percentage of the most intense line): (Table Removed) 4. Process for the preparation of the a crystalline form of the compound of formula (I) according to any one of claims 1 to 3, wherein perindopril is dissolved in water with L-arginine, and then an apolar solvent and a polar solvent are added and the crystals obtained are filtered off, washed and then dried. 5. Process according to claim 4, wherein the apolar solvent is selected from methylcyclohexane, cyclohexane and toluene. S. Process according to either claim 4 or claim 5, wherein the polar solvent is selected from dimethyl sulphoxide, N,N-dimethylformamide, N,N-dimethylacetamide and N-methyl-2-pyrrolidinone. 7. Process according to claim 4, wherein the apolar solvent is methylcyclohexane and the polar solvent is dimethyl sulphoxide. 3. Pharmaceutical composition comprising as active ingredient the compound according to any one of claims 1 to 3, in combination with one or more pharmaceutically acceptable, inert, non-toxic carriers. 9. Pharmaceutical composition accerdins to claim 8.charaotprised in that it also contains a diuretic. 10. Pharmaceutical composition according to claim 9, characterised in that the diuretic is indapamide. 11. Use of the compound according to any one of claims 1 to 3 in the manufacture of a medicaments for use as inhibitors of angiotensin I converting enzyme. 12. Use of the compound according to any one of claims 1 to 3 in the manufacture of medicaments for use in the treatment of cardiovascular diseases.

Full Text

α CRYSTALLINE FORM OF THE ARGININE SALT OF PERINDOPRIL,
A PROCESS FOR ITS PREPARATION AND
PHARMACEUTICAL COMPOSITIONS CONTAINING IT
The present invention relates to the a crystalline form of the arginine salt of perindopril of formula (I):

(Formula Removed)
to a process for its preparation and to pharmaceutical compositions containing it.
Perindopril and its pharmaceutically acceptable salts, and more especially its arginine salt,
have valuable pharmacological properties.
Their principal property is that of inhibiting angiotensin I converting enzyme (or
kininase II), which allows, on the one hand, impedance of the conversion of the
decapeptide angiotensin I to the octapeptide angiotensin II (a vasoconstrictor) and, on the
other hand, prevention of the degradation of bradykinin (a vasodilator) to an inactive
peptide.
Those two actions contribute to the beneficial effects of perindopril in cardiovascular
diseases, more especially in arterial hypertension and heart failure.
Perindopril, its preparation and its use in therapeutics have been described in European Patent specification EP 0 049 658.
The arginine salt of perindopril has been described in European Patent specification EP 1 354 873.
In view of the pharmaceutical value of that compound, it has been of prime importance to obtain it with excellent stability, mainly in terms of hygroscopicity, of processability of the powder, of filtrability of the solid, of grindability, and of solvent retention.
Obtaining a well-defined crystalline form allows those requirements to be met.
Patent specification EP 1 354 873 describes the arginine salt of perindopril. That document does not, however, specify the conditions for obtaining that salt in a well-defined crystalline form.
The Applicant has now found that the arginine salt of perindopril can be obtained in a well-defined crystalline form that, as a result, has valuable characteristics for filtration, drying and ease of formulation.
More specifically, the present invention relates to the a crystalline form of the compound of formula (I), characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of angle 2 theta (°): 4.5, 7.9 and 13.5.
Preferably, the present invention relates to the a crystalline form of the compound of formula (I), characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of angle 2 theta (°):4.5,7.9,13.5, 17.5 and 20.6.
Even more preferably, the present invention relates to the a crystalline form of the compound of formula (I), characterised by the following powder X-ray diffraction diagram measured using a diffractometer (copper anti-cathode) and expressed in terms of inter-planar distance d, Bragg's angle 2 theta, intensity and relative intensity (expressed as a percentage of the most intense line) :
(Table Removed)
The invention relates also to a process for the preparation of the a crystalline form of the compound of formula (I), wherein perindopril is dissolved in water with L-arginine, and then an apolar solvent and a polar solvent are added and the crystals obtained are filtered off, washed and then dried.
Among the apolar solvents there may be mentioned, by way of example,
methylcyclohexane, cyclohexane and toluene.
Among the polar solvents there may be mentioned, by way of example, dimethyl
sulphoxide, N,N-dimethylformamide, N,N-dimethylacetamide and N-methyl-2-
pyrrolidinone.
The crystals so obtained are in a compact form composed of baguettes.
According to one embodiment of the invention, perindopril is dissolved in water with L-arginine and then methylcyclohexane and dimethyl sulfoxide are added and the crystals obtained are filtered off, washed and then dried.
The invention relates also to pharmaceutical compositions comprising as active ingredient the a crystalline form of the compound of formula (I) together with one or more appropriate, inert, non-toxic excipients. Among the pharmaceutical compositions according to the invention there may be mentioned, more especially, those that are suitable for oral, parenteral (intravenous or subcutaneous) or nasal administration, tablets or dragees, sublingual tablets, capsules, lozenges, suppositories, creams, ointments, dermal gels, injectable preparations, drinkable suspensions.
The dosage used can be varied according to the nature and severity of the disorder, the administration route and the age and weight of the patient. It varies from 1 to 500 mg per day in one or more administrations.
The pharmaceutical compositions according to the invention may also contain a diuretic such as indapamide.
The following Examples illustrate the invention.
The powder X-ray diffraction spectrum was measured under the following experimental conditions :
Siemens D5005 diffractometer; scintillation detector;
Copper anti-cathode, voltage 40KV, intensity 30mA ;
Mounting θ-θ, fixed specimen;
Temperature : ambient;
Measurement range : 3° to 30°;
Increment between each measurement: 0.04°;
Measurement time per step :4 s;
Fixed slits : 1.6 mm;
Kß filter (Ni);
No internal reference;
Zeroing procedure using Siemens slits;
Experimental data processed using EVA software (version 9.0).
EXAMPLE 1 : a crystalline form of perindopril arginine salt
1.5 kg of water, 328 g of perindopril and 155 g of L-arginine are introduced into a reactor at ambient temperature and with stirring. When a clear solution is obtained, 630 g of methylcyclohexane are added, and then 4.7 kg of dimethyl sulphoxide are added slowly. The mixture is then stirred until the temperature of the heterogeneous mixture stabilises at around 20.0°C, after which the mixture is filtered and the solid obtained is washed and dried.
The crystals so obtained are in a compact form composed of baguettes.
The water content of the resulting product is approximately 3.2%, which corresponds to a
monohydrate.
Powder X-ray diffraction diagram :
The powder X-ray diffraction profile (diffraction angles) of the a form of perindopril arginine salt is given by the significant lines collated in the following table together with the intensity and relative intensity (expressed as a percentage of the most intense line).
(Table Removed)
EXAMPLE 2 : Pharmaceutical composition
Preparation formula for 1000 tablets each containing 4 mg of active ingredient:
Compound of Example 1 4 g
Hydroxypropylcellulose 2 g
Wheat starch 10 g
Lactose 100 g
Magnesium stearate 3 g
Talc 3 g

CLAIMS
1. α crystalline form of the arginine salt of perindopril, of formula (I) :
(Formula Removed)
characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of Bragg's angle 2 theta (°) : 4.5, 7.9 and 13.5.
2. α crystalline form of the compound of formula (I) according to claim 1, characterised by the following powder X-ray diffraction peaks, measured using a diffractometer with a copper anti-cathode and expressed in terms of Bragg's angle 2 theta (°) : 4.5, 7.9, 13.5, 17.5 and 20.6.
3. α crystalline form of the compound of formula (I) according to claim 1, characterised by the following powder X-ray diffraction diagram measured using a diffractometer (copper anti-cathode) and expressed in terms of inter-planar distance d, Bragg's angle 2 theta, intensity and relative intensity (expressed as a percentage of the most intense line):
(Table Removed)
4. Process for the preparation of the a crystalline form of the compound of formula (I) according to any one of claims 1 to 3, wherein perindopril is dissolved in water with L-arginine, and then an apolar solvent and a polar solvent are added and the crystals obtained are filtered off, washed and then dried.
5. Process according to claim 4, wherein the apolar solvent is selected from methylcyclohexane, cyclohexane and toluene.
S. Process according to either claim 4 or claim 5, wherein the polar solvent is selected from dimethyl sulphoxide, N,N-dimethylformamide, N,N-dimethylacetamide and N-methyl-2-pyrrolidinone.
7. Process according to claim 4, wherein the apolar solvent is methylcyclohexane and the polar solvent is dimethyl sulphoxide.
3. Pharmaceutical composition comprising as active ingredient the compound according to any one of claims 1 to 3, in combination with one or more pharmaceutically acceptable, inert, non-toxic carriers.
9. Pharmaceutical composition accerdins to claim 8.charaotprised in that it also contains a diuretic.
10. Pharmaceutical composition according to claim 9, characterised in that the diuretic is indapamide.
11. Use of the compound according to any one of claims 1 to 3 in the manufacture of a medicaments for use as inhibitors of angiotensin I converting enzyme.
12. Use of the compound according to any one of claims 1 to 3 in the manufacture of medicaments for use in the treatment of cardiovascular diseases.

Documents:

6868-delnp-2008-Abstract-(11-10-2012).pdf

6868-delnp-2008-abstract.pdf

6868-delnp-2008-Claims-(11-10-2012).pdf

6868-delnp-2008-Claims-(25-09-2013).pdf

6868-delnp-2008-claims.pdf

6868-delnp-2008-Correspondence Others-(25-09-2013).pdf

6868-delnp-2008-Correspondence-Others-(11-10-2012).pdf

6868-delnp-2008-correspondence-others.pdf

6868-delnp-2008-Description (Complete)-(11-10-2012).pdf

6868-delnp-2008-description (complete).pdf

6868-delnp-2008-form-1.pdf

6868-delnp-2008-form-18.pdf

6868-delnp-2008-Form-2-(11-10-2012).pdf

6868-delnp-2008-form-2.pdf

6868-delnp-2008-Form-3-(11-10-2012).pdf

6868-delnp-2008-Form-3-(25-09-2013).pdf

6868-delnp-2008-form-3.pdf

6868-delnp-2008-form-5.pdf

6868-delnp-2008-GPA-(11-10-2012).pdf

6868-delnp-2008-pct-210.pdf

6868-delnp-2008-Petition-137-(11-10-2012).pdf

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Patent Number

263360

Indian Patent Application Number

6868/DELNP/2008

PG Journal Number

44/2014

Publication Date

31-Oct-2014

Grant Date

22-Oct-2014

Date of Filing

11-Aug-2008

Name of Patentee

LES LABORATOIRES SERVIER

Applicant Address

12, PLACE DE LA DEFENSE, F-92415 COURBEVOIE CEDEX, FRANCE.

Inventors:

#	Inventor's Name	Inventor's Address
1	GERARD COQUEREL	192, RUE DE 1'EGLISE, 76520 BOOS, FRANCE.
2	LOIC LEFEBVRE	APT 146, 17 PARC DE LA RISLE, 76130 MONT SAINT AIGNAN, FRANCE
3	JEAN-CLAUDE SOUVIE	RESIDENCE GARDEN PARK B 19, AVENUE NORMAN PRINCE 64000 PAU, FRANCE
4	PASCALE AUTHOUART	12, RUE DU VILLAGE, 76430 LES TROIS PIERRES, FRANCE

PCT International Classification Number

C07D 209/42

PCT International Application Number

PCT/FR2007/000335

PCT International Filing date

2007-02-26

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	06/01748	2006-02-28	France