&


(19)

(11) EP 1 860 102 A1

(12) EUROPEAN PATENT APPLICATION

(43) Date of publication: (51) Int Cl.:

28.11.2007 Bulletin 2007/48 C07D 211/90 (2006.01)

(21) Application number: 06114517.3

(22) Date of filing: 24.05.2006

(84) Designated Contracting States: • Bertolino, Andrea

AT BE BG CH CY CZ DE DK EE ES FI FR GB GR 1145, Budapest (HU)
HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI • Lukács, Ferenc
SK TR 2143, Kistarcsa (HU)
Designated Extension States: • Garaczi, Sándor
AL BA HR MK YU 1048, Budapest (HU)
• Schneider, Géza
(71) Applicant: CF Pharma Ltd. 1097, Budapest (HU)
1097 Budapest (HU)
(74) Representative: UEXKÜLL & STOLBERG
(72) Inventors: Patentanwälte
• Bor, Ádám Beselerstrasse 4
2040, Budaörs (HU) 22607 Hamburg (DE)
• Orosz, György
1143, Budapest (HU) Remarks:
• Szücs, Stefánia Cserépi Amended claims in accordance with Rule 86 (2) EPC.
1204, Budapest (HU)

(54) Process for Producing Lercanidipine

(57) A process for preparing 1,4-dihydro-2,6-dime-

thyl-4- (3-nitrophenyl) -3,5-pyridinedicarboxylic acid 2-
[(3,3-diphenyl-propyl) methylamino]-1,1-dimethylethyl
ester (Lercanidipine) I, which comprises reacting 1,4-di-
hydro-2,6-dimethyl-4- (3-nitrophenyl) -3,5-pyridinedicar-
boxylic acid 1,1-dimethylethyl-2-methylamino ethyl me-
thyl ester IX or a salt thereof with a compound of the
general formula L-O-CH2-CH2-CHPh2 where L-O is a
leaving group.
EP 1 860 102 A1

Printed by Jouve, 75001 PARIS (FR)

 EP 1 860 102 A1

Description

[0001] The present invention relates to a process for preparing lercanidipine and its intermediates in high purity.
[0002] Lercanidipine (1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)
5 methylamino]-1,1-dimethylethyl methyl ester) is a highly lipophilic dihydropyridine calcium antagonist which is suitable
for treating hypertension. Lercanidipine has the following Formula I:

10

15

20

[0003] This compound is used in antihypertensive medication in numerous countries since 1997. Like other dihydro-
pyridine-type calcium channel blockers, Lercanidipine causes systemic vasodilation by blocking the influx of calcium
25 ions through L-type calcium channels in cell membranes. Due to its high lipophilicity it has a slower onset and longer
duration of action than other calcium antagonists of the dihydropyridine type.
[0004] Lercanidipine is commercially available from Recordati S.p.A. (Milan, Italy).
[0005] Although Corfini et al., Journal of Cardiovascular Pharmacology, 28(5), 687-694, 1996, showed that the
(S)-enantiomer of lercanidipine is more active than the (R)-enantiomer the (R,S) racemate is used in the medicament
30 Zanidip®.
[0006] The syntheses of lercanidipine was firstly described in EP 0 153 016 A2. Two alternative routes are disclosed
which involve the following reaction schemes:

35

40

45

50

55

2
 EP 1 860 102 A1

10

15

20

25

30

35

40

45

50
[0007] Lercanidipine was isolated in the form of an oily residue which was purified by flash chromatography. Flash
chromatography is difficult to apply on an industrial scale. Furthermore, the process reported in EP 0 153 016 A2 results
in the formation of side products which causes a low yield of the desired product.
[0008] US 5,912,351 describes an alternative process which involves reaction of 1,4-dihydro-2,6-dimethyl-5-methox-
55 ycarbonyl-4-(3-nitrophenyl) pyridine-3-carboxylic acid with thionyl chloride in dichloromethane and dimethylformamide
and subsequent esterification of the obtained acid chloride with 2,N-dimethyl-N-(3,3-diphenylpropyl)-1-amino-2-propyl
alcohol:

3
 EP 1 860 102 A1

10

[0009] The process is said to yield lercanidipine hydrochloride in an anhydrous non-hygroscopic crystalline form. The
15 product was purified by crystallization to give lercanidipine hydrochloride having a melting point of 186-188 °C, later
named Form (C). This process is said to give improved yields and to result in the formation of fewer side products.
However, the purity of the product is still not satisfactory and is not reproducible.
[0010] WO03/014084 discloses the preparation of various polymorphic forms of lercanidipine hydrochloride, Form (A)
having a melting point of 150-152 °C, Form (B) having a melting point of 131-135 °C, Form (I) having a melting point of
20 197-201 °C and Form (II) having a melting point of 207-211 °C, which are said to be reproducibly obtainable on commercial
scale. Forms (A) and (B) were produced from Form (C) by a protocol involving seven process steps. Forms (A) and (B)
can be converted to Forms (I) and (II).
[0011] WO03/014085 describes the formation of solvates of lercanidipine hydrochloride with various organic solvents,
and crystalline forms (III) and (IV) which are obtainable from the solvates by removing the solvation solvent. The solvates
25 and crystalline forms of lercanidipine hydrochloride were prepared by using Forms (I), (A) or (B) as starting material.
[0012] WO2006/021397 discloses the preparation of amorphous and crystalline acid addition salts of lercanidipine.
These salts are prepared by adding a solution of an acid to a solution of lercanidipine free base followed by the removal
of the solvent. Crystalline salts are obtained by recrystallization of the isolated salts from an aprotic and/or protic solvent.
[0013] WO2006/046830 discloses a method for preparing amorphous lercanidipine comprising the steps of (1) dis-
30 solving lercanidipine in an organic solvent; (2) forming a precipitate by the addition of a second solvent or concentration
the solution under reduced pressure to obtain a solid substance; (3) filtering, washing and drying the precipitate or drying
the solid substance.
[0014] Although the known processes often require numerous purification steps, none of the known methods is com-
pletely satisfactory as far as purity is concerned. It is therefore an object of the present invention to provide a new process
35 for the manufacture of lercanidipine which allows the production of the active ingredient on an industrial scale in high
purity and with a minimum number of purification steps.
[0015] According to the present invention this problem is surprisingly solved by a process for preparing lercanidipine
of formula I, i.e. 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methyl-
amino]-1,1-dimethylethyl methyl ester, which comprises reacting 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyrid-
40 inedicarboxylic acid 1,1-dimethylethyl-2-methylaminoethyl methyl ester IX or a salt thereof with a compound of the
general formula XI

L-O-CH2-CH2-CHPh2 XI

45 wherein L is a leaving group.

[0016] Compound IX can be used in the form of the free base but is preferably used in the form of an acid addition
salt. Preferred acid addition salts are the hydrochloride, tosylate, tartrate, citrate, more preferably the oxalate salt. These
salts can be prepared by reaction of the free base of compound IX with the corresponding acid.
[0017] The leaving group L of compound XI is preferably a triflate (trifluormethane sulfonic), brosylate (4-bromobenzene
50 sulfonic), or nasylate (naphthalensulfonic) group, more preferably a tosylate (4-methyl benzenesulfonic) group. The
preparation of compounds according to general formula XI can be achieved by known procedures starting at 3,3-diphenyl
propanol. The synthesis of the preferred tosylated compound 3-tosyloxy-3,3-diphenylpropane XIa can be achieved e.g.
by tosylating 3,3-diphenyl propanol according to Pitha et al., Collect. Czech. Chem. Commun. 25, 1960, 736-742. 3,3-
Diphenyl propanol is accessible e.g. by the method described in DE 766 207.
55 [0018] The reaction of compound IX with compound XI is preferably performed in a solvent selected from the group
consisting of toluene, xylene, dimethylformamide (DMF), dimethylacetamide (DMA), hexamethylphosphoric amide
(HMPT), N-methyl pyrrolidine and acetonitrile. The most preferred solvent is toluene.
[0019] The reaction temperature is preferably within a range of from 10 to 140 °C, more preferably 78 to 82 °C.

4
 EP 1 860 102 A1

[0020] It is preferred to perform the reaction in the presence of a base which is preferably selected from the group
consisting of alkali carbonates and alkaline-earth carbonates. Preferred alkali metal carbonates are sodium and potas-
sium carbonate, preferred alkaline-earth carbonates are magnesium and calcium carbonate. The most preferred car-
bonate is potassium carbonate.
5 [0021] It is also preferred to perform the reaction in the presence of a phase transfer catalyst. Preferably the catalyst
is selected from the group consisting of tetraalkyl quarternary ammonium salts, more preferably tetra(C2-6)-alkyl quar-
ternary ammonium salts. The most preferred phase transfer catalyst is tetrabutylammonium iodide.
[0022] Compound IX used in the above process is preferably prepared by esterification of 1,4-dihydro-2,6-dimethyl-
4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid monomethyl ester VIII with 1,1-dimethyl-2-methylaminoethanol X, or a
10 salt thereof, which can be prepared e.g. by the method described in US 2,252,713. Compound VIII is accessible according
to known procedures, e.g. by the method disclosed in DE 28 47 237.
[0023] Compound VIII is preferably first halogenated with a halogenating agent to give the acid halide derivative of
VIII. Preferably, the halogenation is a chlorination which results in the formation of 1,4-dihydro-2,6-dimethyl-4-(3-nitro-
phenyl)-3,5-pyridinedicarboxylic acid chloride monomethyl ester. Chlorination can be achieved by using known chlorin-
15 ating agents such as phosphorus pentachloride, phosphorus trichloride, phosphorus oxychloride, sulfuryl chloride and
in particular thionyl chloride. Halogenated compound VIII is then reacted with compound X. The reaction can be performed
in situ without prior isolation of halogenated compound VIII.
[0024] Alternatively, compound VIII can be activated by the addition of a suitable diimide such as N,N’-dicyclohexyl-
carbodiimide or by forming a mixed anhydride.
20 [0025] It is preferred to use compound X in the form of its triflate, hydrochloride or sulfate salt, and particularly preferred
in the form of its tosylate salt (1,1-dimethyl-2-methylaminoethanol tosylate). It was surprisingly found that e.g. the tosylate
salt of compound X can be O-acylated without protection of its amino group. The tosylate salt of X can be prepared from
2-chloro-1,1-dimethylethanol which can be synthesized according to the method described in US 2,252,713. The tosylate
salt can be purified and isolated in good yield. The tosylate salt of X is then reacted with compound VIII or preferably
25 halogenated compound VIII to give intermediate IX in pure form and with high yield.
[0026] The reaction of compound VIII with compound X is preferably performed in a solvent selected from the group
consisting of dimethylformamide (DMF), dimethylacetamide (DMA) and tetrahydrofuran (THF). The reaction temperature
is preferably within a range of from -20 to 30 °C.
[0027] The halogenation of compound VIII is preferably performed in a solvent selected from the group consisting of
30 dimethylformamide (DMF), dimethylacetamide (DMA), tetrahydrofuran (THF), N-methyl pyrrolidine and dimethylether
(DME). The reaction temperature is preferably within a range of from -20 to 30 °C.
[0028] The process of the present invention for the synthesis of lercanidipine by reaction of compound IX with compound
XI results in the formation of the desired product in good yield and in an unexpectedly high purity.
[0029] The stereo isomeric form of the product of course depends on the stereo isomeric form of the starting material.
35 If the racemate of compound VIII or IX is used, lercanidipine is also obtained in the form of the racemate. If the (R)-enan-
tiomer or the (S)-entantiomer of compounds VIII or IX is used in the process of the present invention, the (R)-enantiomer
or the (S)-enantiomer of lercanidipine can be obtained. The homochiral acids of compound VIII can be prepared by
resolution of racemic acid VIII according to the method reported by Ashimori at al., Chem. Pharm. Bull. 39, 108 (1991).
It is preferred to produce the (R,S) racemate of I, more preferably the (S)-enantiomer.
40 [0030] The process of the present invention results in the formation of lercanidipine I in the form of the free base. The
free base can be converted to an acid addition salt by adding an appropriate acid. Preferably, lercanidipine free base is
dissolved in an organic solvent, preferably an ether, more preferably methyl tertiary-butyl ether (MTBE), and an acid or
a solution of an acid in a solvent, preferably an organic solvent is added.
[0031] Suitable salts of lercanidipine include salts of inorganic acids such as hydrochloric acid, hydrobromic acid,
45 phosphoric acid and sulphuric acid; sulphonic acids such as methanesulphonic acid, benzenesulphonic acid, toluenesul-
phonic acid, and naphthalene-1,5-disulphonic acid; monocarboxylic acids, such as acetic acid, (+)-L-lactic acid, DL-
lactic acid, DL-mandelic acid, gluconic acid, cinnamic acid, salicylic acid, and gentisic acid; dicarboxylic acids, such as
oxalic acid, 2-oxo-glutaric acid, malonic acid, (-)-L-malic acid, mucic acid, (+)-L-tartaric acid, fumaric acid, maleic acid,
and terephthalic acid; tricarboxylic acids, such as citric acid; and aromatic sulphonimides such as saccharin. The prep-
50 aration of these addition salts of lercanidipine is disclosed in WO2006/021397.
[0032] Preferred salts of lercanidipine are the L-lactate, cinnamate, salicylate, maleate, saccharinate, besylate, na-
padisylate salts, in particular the oxalate salt and the hydrochloride salt.
[0033] Lercanidipine free base and the acid addition salts of lercanidipine can be produced in crystalline form and in
amorphous form. Amorphous forms can be prepared by the methods disclosed in WO2006/021397 and WO2006/046830.
55 [0034] Lercanidipine produced by the process of the present invention is preferably isolated by crystallization. Crys-
tallization is preferably carried out by use of water containing hydrochloric acid and sodium chloride as disclosed in EP
0 153 016 A2, or in a mixture of MTBE and isopropanol as described in.
[0035] The most preferred salt of lercanidipine is the hydrochloride hemihydrate salt. This salt is preferably obtained

5
 EP 1 860 102 A1

by crystallization from water containing hydrochloric acid and sodium chloride to give a product having a melting point
of 119-123 °C as disclosed in EP 0 153 016 A2.
[0036] Lercanidipine produced according to the method of the present invention can be further purified by converting
lercanidipine free base to a first acid addition salt, converting the first addition salt back to the free base, followed by
5 converting the free base to a second acid addition salt. The first acid addition salt is preferably the oxalate, the second
addition salt is preferably the hydrochloride. Lercanidipine subjected to this purification sequence has a very high purity
is suitable for production of pharmaceutical composition without further purification.
[0037] For the preparation of pharmaceutical compositions comprising lercanidipine as an active ingredient the ler-
canidipine prepared by the process of the present invention is mixed with at least one pharmaceutically acceptable
10 excipient, and the mixture of the active ingredient and the one or more excipients is then converted to a pharmaceutical
dosage form. Suitable excipients and dosage forms are disclosed e.g. in WO03/014084. Preferred dosage forms are
tablets, in particular film coated tablets.
[0038] Preferred excipients are pharmaceutically acceptable binders, such as lactose, hydroxypropylmethylcellulose
and povidone; disintegrants, such as sodium starch glycolate; lubricants, such as magnesium stearate, magnesium
15 palmitate and magnesium oleate; dispersing and suspending agents such as microcrystalline cellulose; plasticizers,
such as polyethylene glycol; colorants, such as ferric oxide(s) and titanium dioxide; and other additives such as talcum.
Suitable film forming agents are hydroxypropylmethylcellulose, ethylcellulose and polymethacrylates.
[0039] In the following the invention will be described by reference to figures and examples.
[0040] Figure 1 is a reaction scheme showing a preferred embodiment of the process of the present invention. 1,4-
20 Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid monomethyl ester VIII is transformed by reaction
with thionyl chloride to give 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic monomethyl ester acid
chloride. The acid chloride is then reacted in situ with the tosylate salt of 1,1-dimethyl-2-methylaminoethanol X to give
1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethyl-2-methylaminoethyl methyl ester
IX. Alkylation of compound IX with 3-tosyloxy-1,1-diphenylpropane XIa results in the formation of lercanidipine I free
25 base. The free base is purified by forming the oxalate salt which is then converted to the hydrochloride hemihydrate via
the free base. The final product is isolated in high yield and with high purity.

Examples

30 Example 1

1,1-Dimethyl-2-methylaminoethanol tosylate salt (Formula X)

[0041] 485 mmol distilled 1,1-dimethyl-2-methylaminoethanol (US 2,252,713; 1938) was solved in 50 ml ethylacetate
35 then 461 mmol p-toulenesulphonic acid hydrate in 270 ml ethylacetate was added between 50-60 °C. The solution was
cooled between 5-10 °C. The crystalline suspension was filtered. The product was washed with 100 ml cooled ethyla-
cetate.

Yield: 117.6 g (72.4 %)

40 Purity: min. 99.5 %
Melting point: 130-132 °C

Example 2

45 (R,S) 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethyl-2-methylaminoethyl methyl

ester oxalate (Formula IX oxalate)

[0042] 361 mmol (R,S) 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid monomethyl ester

(Formula VIII) (DE 2,847,237; 1938) was dissolved in a mixture of 600 ml abs. THF and 180 ml abs. DMF. The solution
50 was cooled between -10 to 0 °C and 379 mmol thionylchloride was added slowly maintaining the temperature below 0
°C. Following a 1 hour agitation 357.5 mmol 1,1-dimethyl-2-methylaminoethanol tosylate salt (Formula X; Example 1)
was added. The reaction mixture was stirred between 2-3 hours then 700 ml water and 700 ml dichloromethane were
added. The mixture was cooled below 0 °C and a 40 % aqueous solution of sodium hydroxide was added till pH 10-11.
The organic phase was separated. The aqueous phase was extracted with 2 x 300 ml dichloromethane. The combined
55 organic phases were washed with 3 x 300 ml 5 % aqueous solution of sodium hydrogencarbonate. The solution was
dried with sodium sulfate and evaporated. The residue was solved in 150 ml acetonitrile. 360 mmol oxalic acid dihydrate
in 150 ml acetonitrile was added to form the oxalate salt. The crystalline suspension was cooled between 12-15 °C. IX
oxalate was filtered, washed with 100 ml cooled acetonitrile and dried.

6
 EP 1 860 102 A1

Yield: 154.2 (85 %)

The product was recrystallized from 450 ml acetonitrile.
Yield: 130 g (71.6 %)
Purity: 99.8 % (HPLC)
5 Melting point: 161-162 °C

Example 3

3-Tosyloxy-1,1-diphenylpropane (Formula XI)

10
[0043] 1 mol 3,3-diphenylpropanol (DE 766,207; 1940) and 1.34 mol triethylamine were solved in 420 ml toluene then
1.1 mol p-toluenesulfonylchloride in 360 ml toluene was added maintaining the temperature between 20-26 °C. The
mixture was agitated 5 hours and 400 ml 1N hydrochloric acid was added. The organic phase was separated and washed
with 400 ml 5 % sodium hydrogencarbonate solution. The toluenic solution was evaporated. The residue was solved in
15 1,480 ml ethanol. The solution was cooled between -5 to -10 °C. The crystalline suspension was filtered and washed
with 500 ml cooled ethanol.

Yield: 307.4 g (83.9 %)

Purity: 99.9 % (HPLC)
20 Melting point: 49-51 °C

Example 4

(R,S) 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-

25 1,1-dimethylethyl methyl ester oxalate (Formula I oxalate)

[0044] 500 mmol IX oxalate salt (Example 2) and 500 mmol XI (Example 3) were suspended in 760 ml toluene then
5 mol dried potassium carbonate and 15 g tetrabutylammoniumiodide were added. The mixture was stirred at 78-82 °C
during 24 hours in N2 stream in dark while conversion was 55-65 %. The mixture was cooled, then 2,500 ml 0.1 N sodium
30 hydroxide solution and 500 ml toluene were added. The organic phase was separated. The aqueous phase was extracted
with 500 ml toluene. The combined organic phases were washed with 500 ml 0.1 N sodium hydroxide solution, 2 x 400
ml 10 % copper sulfate solution and 4 x 500 ml methanol-water mixture (1 : 2). The toluenic solution was extracted with
2 x 400 ml diluted hydrochloric acid - methanol mixture (2 : 1). The combined aqueous phase was treated with 10 %
sodium hydroxide solution up to pH 11 and extracted with 2 x 500 ml toluene. The organic phase was evaporated and
35 the residue was dissolved in 1000 ml MTBE. 300 mmol oxalic acid dihydrate in 210 ml isopropanol was added to the
solution. 2,100 ml MTBE was cooled between -15 to -20 °C and the solution of the oxalate salt was added maintaining
the temperature between -10 to -15 °C. The crystalline suspension was agitated 1 hour at -10 to -15 °C and filtered. The
product was washed with 4 x 500 ml cooled MTBE and was dried.

40 Yield: 181.5 g (51.7 % without recovery of IX or 76.1 % with recovery of IX, resp.)
Purity: 99.5 % (HPLC)
Melting point: 120 - 125 °C

Recovery of IX oxalate salt

45
[0045] In the above reaction unreacted IX was removed by extraction with the aqueous solution of copper sulfate. IX
was recovered by addition of ammonium hydroxide following extraction. The 800 ml 10 % copper sulfate solution con-
taining unreacted IX was treated with NH4OH solution until the Cu(OH)2 precipitate was dissolved. The solution was
extracted with 4 times 500 ml dichloromethane. The combined organic phases were evaporated. The residue was
50 dissolved in 100 ml acetonitrile. 200 mmol oxalic acid dihydrate in 100 ml acetonitrile was added to form the oxalate
salt. The crystalline suspension was cooled between 12 to 15 °C. IX oxalate salt was filtered and washed with 60 ml
cooled acetonitrile and was dried.

Yield: 81 g (160 mmol)

55
Recovery of XI

[0046] The toluenic solution, which was washed with sodium hydroxide, copper-sulfate and methanol-water solutions,

7
 EP 1 860 102 A1

was evaporated. The residue was solved in 300 ml ethanol. The solution was cooled between -5 to 10 °C. The crystalline
suspension was filtered and washed with 100 ml cooled ethanol.

Yield: 54.4 g (148 mmol)

5
Example 5

(R,S) 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-

1,1-dimethylethyl methyl ester hydrochloride hemihydrate (Formula I HCl ‘ H2O)
10
[0047] 10 mmol I oxalate (Example 4) was dissolved in 100 ml dichloromethane and 20 mmol potassium carbonate
in 20 ml water was added. The organic phase was separated. The aqueous phase was extracted with 2 x 10 ml dichlo-
romethane. The combined organic phases were treated with 20 ml 1N hydrochloric acid. The organic phase was separated
and was evaporated. The residue was treated with 2,000 ml of water containing 2 ml of 1N hydrochloride acid and 5 ml
15 of water saturated with sodium chloride to form I hydrochloride hemihydrate, which was filtered.

Yield: 6.2 g (95 %)

Purity: 99.8 % (HPLC)
Melting point: 118-122 °C
20
HPLC method: Column RP 18, 125 x 3 mm ID, 5 Pm, det: 233 nm
Eluent: 0.01 mol Na2HPO4/MeOH/can : 25/65/10 tr ~ 15 min.

[0048] IR, X-ray and DSC proved that the product was identical to the product which was prepared by the process
25 described in Example 16 of EP 0 153 016 A2.

Claims

30 1. A process for preparing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenyl-

propyl)methylamino]-1,1-dimethylethyl methyl ester of formula I, or a salt thereof,

35

40

45

which comprises reacting 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethyle-

thyl-2-methylaminoethyl methyl ester of formula IX, or a salt thereof,

50

55

8
 EP 1 860 102 A1

10

15 with a compound of the general formula XI

L-O-CH2-CH2-CHPh2 XI

wherein L is a leaving group.

20
2. The process of claim 1, wherein the salt of compound IX is the oxalate, tosylate, citrate, tartrate salt.

3. The process of claim 1 or 2, wherein the leaving group L is a tosylate, triflate, brosylate or nasylate group.

25 4. The process of any one of the preceding claims, wherein the reaction is conducted in a solvent selected from the
groups consisting of toluene, xylene, dimethylformamide (DMF), dimethylacetamide (DMA), hexamethylphosphoric
amide (HMPT), N-methyl pyrrolidine and acetonitrile.

5. The process of any one of the preceding claims, wherein the reaction is performed at a temperature of 10 to 140 °C.
30
6. A process for preparing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethylethyl-
2-methylaminoethyl methyl ester of formula IX, or a salt thereof,

35

40

45

wherein 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid monomethyl ester of formula VIII,

or an acid halide thereof,
50

55

9
 EP 1 860 102 A1

10

15 is reacted with 1,1-dimethyl-2-methylaminoethanol of formula X, or a salt thereof,

20

25

7. The process of claim 6, comprising halogenating compound VIII to give 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-

3,5-pyridinedicarboxylic acid halide monomethyl ester and reacting the acid halide of VIII with compound X or a salt
thereof.
30
8. The process of claim 7, wherein the halogenating agent is thionyl chloride, phosphorus pentachloride, phosphorus
trichloride, phosphorus oxychloride or sulfuryl chloride.

9. The process of any one of claims 6 to 8, wherein compound X is used in the form of its triflate, hydrochloride, sulfate
35 or tosylate salt.

10. The process of claim 6, wherein the reaction is performed in a solvent selected from the group consisting of THF,
DMF and DMA.

40 11. The process of claim 6 or 10, wherein the reaction is performed at a temperature of -20 to 30 °C.

12. The process of claim 7 or 8, wherein the reaction is performed in a solvent selected from the groups consisting of
DMF, THF, DME, N-methylpyrrolidine.

45 13. The process of claim 7, 8 or 12, wherein the reaction is performed at a temperature of -20 to 30 °C.

14. The process of any one of the preceding claims, further comprising converting the free base of compound I to a first
acid addition salt, converting the first addition salt back to the free base, followed by converting the free base to a
second acid addition salt.
50
15. The process of claim 14, wherein the first acid addition salt is the oxalate.

16. The process of claim 14 or 15, wherein the second addition salt is the hydrochloride hemihydrate.

55 17. The process of any one of the preceding claims, further comprising isolating the resultant product.

18. The process of claim 17, wherein the product is isolated by crystallization.

10
 EP 1 860 102 A1

19. The process of claim 17, wherein the product is isolated in amorphous form.

20. A process for preparing a pharmaceutical composition comprising 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-

pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)-methylamino]-1,1-dimethylethyl methyl ester as an active ingredi-
5 ent, comprising preparing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenyl-
propyl)methylamino]-1,1-dimethylethyl methyl ester according to any one of the preceding claims, mixing the same
with at least one pharmaceutically acceptable excipient and converting the mixture to a pharmaceutical dosage form.

21. 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethylethyl-2-methylaminoethyl me-

10 thyl ester of formula IX, or a salt thereof:

15

20

25 22. The compound of claim 21, which is an acid addition salt of the compound of formula IX.

23. The compound of claim 22, which is the tosylate, tartrate, citrate, or oxalate salt.

24. The use of the compound of any one of claims 21 to 23 for manufacturing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-
30 3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimethylethyl methyl ester of formula I.

Amended claims in accordance with Rule 86(2) EPC.

35 1. A process for preparing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenyl-

propyl)methylamino]-1,1-dimethylethyl methyl ester of formula I, or a salt thereof,

40

45

50
which comprises reacting 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethyle-
thyl-2-methylaminoethyl methyl ester of formula IX, or a salt thereof,

55

11
 EP 1 860 102 A1

10

with a compound of the general formula XI

15
L-O-CH2-CH2-CHPh2 XI

wherein L-O is a leaving group.

20 2. The process of claim 1, wherein the salt of compound IX is the oxalate, tosylate, citrate, tartrate salt.

3. The process of claim 1 or 2, wherein the leaving group L-O is a tosylate, triflate, brosylate or nasylate group.

4. The process of any one of the preceding claims, wherein the reaction is conducted in a solvent selected from the
25 groups consisting of toluene, xylene, dimethylformamide (DMF), dimethylacetamide (DMA), hexamethylphosphoric
amide (HMPT), N-methyl pyrrolidine and acetonitrile.

5. The process of any one of the preceding claims, wherein the reaction is performed at a temperature of 10 to 140 °C.

30 6. A process for preparing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethyle-

thyl-2-methylaminoethyl methyl ester of formula IX, or a salt thereof,

35

40

45

wherein 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid monomethyl ester of formula VIII,

or an acid halide thereof,

50

55

12
 EP 1 860 102 A1

10

is reacted with 1,1-dimethyl-2-methylaminoethanol of formula X, or a salt thereof,

15

20

25 7. The process of claim 6, comprising halogenating compound VIII to give 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-

3,5-pyridinedicarboxylic acid halide monomethyl ester and reacting the acid halide of VIII with compound X or a salt
thereof.

8. The process of claim 7, wherein the halogenating agent is thionyl chloride, phosphorus pentachloride, phosphorus
30 trichloride, phosphorus oxychloride or sulfuryl chloride.

9. The process of any one of claims 6 to 8, wherein compound X is used in the form of its triflate, hydrochloride,
sulfate or tosylate salt.

35 10. The process of claim 6, wherein the reaction is performed in a solvent selected from the group consisting of
THF, DMF and DMA.

11. The process of claim 6 or 10, wherein the reaction is performed at a temperature of -20 to 30 °C.

40 12. The process of claim 7 or 8, wherein the reaction is performed in a solvent selected from the groups consisting
of DMF, THF, DME, N-methylpyrrolidine.

13. The process of claim 7, 8 or 12, wherein the reaction is performed at a temperature of -20 to 30 °C.

45 14. The process of any one of the preceding claims, further comprising converting the free base of compound I to
a first acid addition salt, converting the first addition salt back to the free base, followed by converting the free base
to a second acid addition salt.

15. The process of claim 14, wherein the first acid addition salt is the oxalate.
50
16. The process of claim 14 or 15, wherein the second addition salt is the hydrochloride hemihydrate.

17. The process of any one of the preceding claims, further comprising isolating the resultant product.

55 18. The process of claim 17, wherein the product is isolated by crystallization.

19. The process of claim 17, wherein the product is isolated in amorphous form.

13
 EP 1 860 102 A1

20. A process for preparing a pharmaceutical composition comprising 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-

3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)-methylamino]-1,1-dimethylethyl methyl ester as an active in-
gredient, comprising preparing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-
diphenylpropyl)methylamino]-1,1-dimethylethyl methyl ester according to any one of the preceding claims, mixing
5 the same with at least one pharmaceutically acceptable excipient and converting the mixture to a pharmaceutical
dosage form.

21. An acid addition salt of l,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethyle-

thyl-2-methylaminoethyl methyl ester of formula IX:
10

15

20

25 22. The compound of claim 21, which is the tosylate, tartrate, citrate, or oxalate salt.

23. The use of 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 1,1-dimethylethyl-2-meth-

ylaminoethyl methyl ester of formula IX, or a salt thereof:

30

35

40

for manufacturing 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)

methylamino]-1,1-dimethylethyl methyl ester of formula I.
45
24. The use of claim 23, wherein the salt is acid addition salt.

25. The use of claim 24, wherein the salt is the tosylate, tartrate, citrate, or oxalate salt.

50

55

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17
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 EP 1 860 102 A1

REFERENCES CITED IN THE DESCRIPTION

This list of references cited by the applicant is for the reader’s convenience only. It does not form part of the European
patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be
excluded and the EPO disclaims all liability in this regard.

Patent documents cited in the description

• EP 0153016 A2 [0006] [0007] [0034] [0035] [0048] • WO 2006046830 A [0013] [0033]

• US 5912351 A [0008] • DE 766207 [0017] [0043]
• WO 03014084 A [0010] [0037] • US 2252713 A [0022] [0025] [0041]
• WO 03014085 A [0011] • DE 2847237 [0022] [0042]
• WO 2006021397 A [0012] [0031] [0033]

Non-patent literature cited in the description

• ALTHOUGH CORFINI et al. Journal of Cardiovas- • PITHA et al. Collect. Czech. Chem. Commun., 1960,
cular Pharmacology, 1996, vol. 28 (5), 687-694 vol. 25, 736-742 [0017]
[0005] • ASHIMORI. Chem. Pharm. Bull., 1991, vol. 39, 108
[0029]

19