Improved Process for the preparation of highly pure Pitavastatin and its pharmaceutically acceptable salts Field of the Invention:
The present invention relates to an improved process for the preparation of highly pure pitavastatin and its pharmaceutically acceptable salts as well as their polymorphic forms. Pitavastatin is chemically known as (3R,5S)-7-[2-cyclopropyl-4-(4-fluorophenyl) quinolin-3-yll-3,5-dihydroKy-6(E)-hepteooic acid. Pitavastatin and its pharmaceutically acceptable salts are represented by the following general structural formula-1.

Pitavastatin is a synthetic lipid-lowering agent that acts as an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase inhibitor). This enzyme catalyzes the conversion of HMG-CoA to mevaionate. The HMG-CoA reductase inhibitors are commonly referred to as "statins". Statins are therapeutically effective drugs used for reducing low density lipoprotein (LDL) particle concentration in the blood streanr of patients who are at risk for cardiovascular disease. Pitavastatin is used in the treatment of hypercholesterolemia (heterozygous familial and nonfamiliai) and mixed dyslipidemia (Fredrickson Type lla and lib).
The compound of the present invention inhibits the HMG-CoA reductase, which plays a main role in the synthesis of cholesterol, and as a consequence they suppress the biosynthesis of cholesterol. Therefore, they are useful in the treatment of hypercholesterolemia, hyperlipoproteinemia, and atherosclerosis.

Background of the Invention:
US Patent 5856336 claimed quinoline type mevalonolactones, specifically pitavastatin. The disclosed process involves the usage of expensive reagent like sodium hydride, n-butyl lithium and borane derivatives, reagents that are difficuh to use on a commercial scale.
International publication WO 95/11898 claims a process for the preparation of condensed pyridine type mevalonolactone intermediates using wittig reagent. In the said process the triphenyl phosphonium bromide intermediate compound of formula-7 was condensed with tertiary butyl 2-((4R, 6S)-6-formyl-2,2-dimethyl-l,3-dioxan-4-yl)acetate compound of formuIa-8 in presence of n-BuLi. And the said patent discloses a process for the preparation of lactone intermediate but the conversion of lactone intermediate to pitavastatin calcium salt has not been disclosed. The usage of bases like n-BuLi is not recommendable for commercial scale up processes. Hence this process is commercially not a viable process.
International publication WO 2005/033083 claims process for the preparation of pure 3,5-dihydroxy-6-heptenoic acid derivatives by optical resolution using column separation process, which is not viable of commercial scale.
International publication WO 2005/054207 claims process for the preparation of pyrimidine derivatives and its intermediates using wittig reagent.
Our international application WO 2007/132482 claims a novel process for the preparation of pitavastatin and its pharmaceutically acceptable salts using wittig reaction. Another international publication WO 2007/125547 claims a process for the preparation of statins free of Z-isomer via julia-olefmation.
Polymorphism is the formation of a variety of crystalline forms of the same compound having distinct crystal structures and physical properties like mehing points, X-ray diffraction pattern, infrared absorption pattern in fingerprint region, and solid state NMR spectrum. One crystalline form may give rise to thermal behavior different from that of another crystalline form. Different crystalline forms or polymorphs of the same pharmaceutical compounds can and reportedly do have different aqueous solubility. The difference in the physical properties of different crystalline forms results in some forms having distinct advantageous physical properties compared to other crystalline fonus of

the same compound. The discovery of new polymorphic forms of pharmaceutically useful compounds provides a new opportunity to improve the performance characteristics of a pharmaceutical product. Those skilled in the art can understand that crystallization of an active pharmaceutical ingredient offers the best method for controlling important qualities like chemical quality, particle size, and polymorphic content. There is a need in the art for the preparation of new polymorphic forms of Pitavastatin and its pharmaceutically acceptable salts, and the intermediates which are used in the preparation of pitavastatin and its pharmaceutically acceptable salts.
Accordingly, there remains a need for an improved process for the preparation of pitavastatin and its pharmaceutically acceptable salts that avoids the problems of the prior art, on a commercial scale in a convenient and cost efficient manner.
Brief description of the Invention:
The present invention relates to an improved process for the preparation of pitavastatin and its pharmaceutically acceptable salts, compounds of general formula-1, preferably calcium salt, compound of forrnula-1 c.
The first aspect of the present invention provides an improved process for the preparation of pitavastatin and its pharmaceutically acceptable sahs, compounds of general formula-1, preferably pitavastatin calcium compound of formula-lc, which comprises of the following steps;
a) Reacting the triphenyl [2-cycloprOpyl-4-{4-fluorophenyl)-quinoline-3-yl-methyl)-
phosphonium] bromide compound of formula-2 with tertiary butyl 2-((4R,6S)-6-
formyl-2,2-dimethyl-l,3-dioxan-4-yl)acetate compound of formula-3 in presence of
suitable base in a suitable solvent, followed by recrystallisation from a suitable
solvent, to provide (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl) quinoUn-3-
yl)-vinyI]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound
offormula-4,
b) subjecting compound of formula-4 to acidic conditions to remove the acetonide
protection, followed by recrystallisation from a suitable solvent, to provide
pitavastatin tertiary butyl ester compound of formula-5.

c) hydrolyzing the pitavastatin tertiary butyl ester compound ot tormufa-? with a suitable base in a suitable solvent, subsequent treatment with a suitable organic amine, followed by recrystallisation from a suitable solvent to provide corresponding organic amine salt of pitavastatin compound of general formula-6,
d) treating the organic amine salt compound of general formula-6 with a suitable base to provide corresponding alkali metal salt of pitavastatin, which on treating in-situ with calcium source to provide pitavastatin calcium compound of formula-lc.
The second aspect of the present invention provides an improved process for the preparation of pitavastatin and its pharmaceutical! y acceptable salt compound of general formula-1, preferably pitavastatin calcium salt compound of formula-lc, which comprises of the following steps
a) Reacting the triphenyl [2-cyclopropyl-4-{4-fluorophenyl)-quinoline-3-yl-methyl)-phosphonium] bromide compound of formula-2 with tertiary butyl 2-((4R,6S)-6-formyl-2,2-dime\.hyl-l ,3-dioxan-4-yl)acetate compound of formula-3 in presence of a suitable base in a suitable solvent, followed by recrystallisation from a suitable solvent, to provide (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl) quinolin-3-yl)-vinyi]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound of formula-4,
b) subjecting compound of formula-4 to acidic conditions to remove the acetonide protection, followed by recrystallisation from a suitable solvent, to provide pitavastatin tertiary butyl ester compound of formula-5,
a) hydrolyzing pitavastatin tertiary butyl ester with a suitable aqueous base to provide corresponding alkali salt of pitavastatin, which on treating in-situ with a calcium source to provide pitavastatin calcium compound of formula-1 c.
The third aspect of the present invention provides an improved process for the preparation of highly pure triphenyl [2-cyclopropyl-4-(4-fluorophenyl)-quinoline-3-yl-methyl)-phosphonium] bromide compound of formuIa-2, which comprises of the following steps;

a) Reacting cyclopropyl methyl ketone compound of formula-7 with dimethylcarbonate in presence of a suitable base in a suitable solvent to provide methyl 3-cyclopropyl-3-oxopropanoate compound of formula-8,
b) reacting the compound of formula-8 with 2-amino-4'-fluorobenzophenone compound of formula-9 in presence of an acid with or without a solvent to provide methyl 2-cyclopropyl-4-(4-fluorophenyI) quinoline -3-carboxylate compound of formula-10,
c) reducing the compound of formula-10 with a suitable reducing agent in a suitable solvent, followed by recrystallisation from a suitable solvent, to provide a (2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-yl)methanol compound of formula-11,
d) reacting the compound of fonnuia-11 with phosphorous tribromide in a suitable solvent, subsequent treatment with triphenyl phosphene in a suitable solvent, followed by recrystallisation from a suitable solvent to provide triphenyl [2-cycIopropyl-4-(4-fluorophenyl)-quinoline-3-yl-methyl)-phosphonium] bromide compound of formula-2.
The fourth aspect of the present invention is to provide crystalline form of (4R,6S)-(E)-6-{2-(2-cyclopropyN4-(4-fluorophenyl)quinolin-3-yl)-vinyI]-2,2-dimethyl -[l,3]-dioxane-4-yl}-acetic acid tertiary butyl ester compound of formula-9.
The further aspects of the present invention provides crystalline forms of pitavastatin tertiary butyl ester compound of formula-5, pitavastatin methyl amine salt compound of formula-6a; pitavastatin compound of formula-la; pitavastatin sodium compound of formula-lb.
Advantages of the present invention
• Economical and commercially viable process
• Involves the usage of inexpensive raw materials, such as triphenyl phosphine and alkali/alkaline earth metal bases like carbonate bases.
• Avoids the usage of wittig-Homer type reagent and pyrophoric n-butyl lithium, which are not recommendable in commercial scale.

• The present invention provides highest purity of pitavastatin and hs intermediates by removing/controlling the impurities by simple purification technique at origin of the impurities.
• The present invention provides crystalline form of triphenyl [2-cyclopropyl-4-(4-fluorophenyI)-quinoline-3-ylmethyl)-phosphonium] bromide salt as well as crystalline forms of dihydroxy tertiary butyl ester, pitavastatin methyl amine, pitavastatin free acid and pitavastatin sodium.
Brief description of the drawings
Figure-la: Illustrates the Powder X-ray diffraction pattern of (4R,6S)-{E)-6-{2-(2-
cyclopropyl-4-(4-fluorophenyl) quinolin-3-yl)-vinyl]-2,2-dimethyl-[l,3]-dioxan-4-yl}-
acetic acid tertiary butyl ester compound of formula-4.
Figure-lb: Illustrates the Powder X-ray diffraction pattern of pitavastatin tertiary butyl
ester compound of formu!a-5.
Figure-2a: Illustrates the Powder X-ray diffraction pattern of Pitavastatin methyl amine
salt compound of formula-6a
Figure2b: Illustrates the Powder X-ray diffraction pattern of Pitavastatin free acid
compound of formula-la
Figure-3a: Illustrates the Powder X-ray diffraction pattern of Pitavastatin sodium
compound of formula-lb
Figure-3b: Illustrates the Powder X-ray diffraction pattern of prior art crystalline form of
Pitavastatin calcium compound of formula-Ic having water content 11.6.
Figure-4a: Illustrates the Powder X-ray diffraction pattern of prior art crystalline form of
Pitavastatin calcium compound of formula-Ic having water content 8.2.
Figure-4b: SST resolution chromatogram
Detailed description of the Invention
As used herein the term "alkyl" refers to straight or branched or cyclic Ct-Cn alkyl.
As used herein the term "aryl" refers to C^-Cn aromatic group include phenyl, tolyl, xylyl, biphenyl, naphthyl and the like. The aryl may have 1 to 3 substituents

independently selected from the group consisting of lower alkyl, halogen, amino, cyano, hydroxy.
As used herein the term "araikyl" refers to C|-C6 lower alkyl substituted C(,-C]2 aromatic aryl group defined above. For example are benzyl, phenylethyl, phenylpropyl and the hke each of which may have 1 to 3 substituents independently selected from the group consisting of lower alkyl, halogen, amino, cyano, hydroxy and the like.
As used herein the term "alcohol solvents" refers to methanol, ethanol, n-propanol, isopropanol and n-butanol and the like.
As used herein the term "hydrocarbon solvents" refers to toluene, xylene, cyclohexane, hexane, heptane and the like.
As used herein the term "polar aprotic solvents" refers to dimethyl sulfoxide, dimethylacetamide, dimethyl formamide, tetrahydrofuran, acetonitrile and the like.
As used herein the term "chloro solvents" refers to methylene chloride, ethylene dichloride, carbon tetra chloride, chloroform and the like.
As used herein the term "nitrile solvents" refers to acetonitrile and the like.
As used herein the term "alkali metal hydroxides" refers to sodium hydroxide, potassium hydroxide and the like.
As used herein the term "alkali metal carbonates" refers to sodium carbonate, potassium carbonate, cesium carbonate and the like.
As used herein the term "alkali metal bicarbonates" refers to sodium bicarbonate, potassium bicarbonate and the like.
As used herein the term "alkali metal alkoxides" refers to sodium methoxide, sodium tertiary butoxide and potassium tertiary butoxide and the like.
As used herein the term "inorganic acids" refers to hydrochloric acid, hydrobromic acid, sulfuric acid and the like
As used herein the term "organic amines" refers to methyl amine, ethyl amine, n-propyl amine, isopropyl amine, n-butyl amine, tertiary butyl, (+/-)-sec-butyl amine, octyl amine, 2-ethyl hexylamine, benzyl amine, a-methyl-benzylamine, phenyl ethylamine, dibenzylamine, N-methylbenzylamine, N,N-dimethylbenzyiamine, N,N-diethyl benzyl amine, N-ethyl-N-methylbenzylamine, tribenzyl amine, cyclopentylamine, cyclohexylamine, cycloheptylamine, N-methylcyclopentylamine, N-ethylcyclohexyl

amine, N-ethyl cycloheptylamine, dicyclohesylamme, N.Nniimethylcyclo pentylamine, N,N-dimethyl cyclohexylamine, N,N-diethylcycloheptylamine and the like.
The present invention relates to an improved process for the preparation of pitavastatin and its pharmaceuticaliy acceptable salt compounds represented by the following structural formula-1.
F
M
-In
Formula -1 Wherein n = 1, M is H^^, Na\ K^
n - 2, M is Mg^^ Ca^^
Accordingly the first aspect of the present invention provides an improved process for the preparation of pitavastatin and its pharmaceuticaliy acceptable salt compounds of general formuIa-1, preferably pitavastatin calcium salt compound of formual-lc,
OH OH O
+2
F
Ca
-^ 2
Formula-Ic which comprises of the following steps;
a) reacting the triphenyl [2-cyclopropyl-4-(4-fluorophenyl)-quinoline-3-yi-methyl)-
phosphonium] bromide salt compound of formula-2
F ■^
P^-PhBr-Pli
Ph
Formula-2

with tertiary butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-l,3-dioxan-4-yl)acetate compound of formula-3
O^ O
Formula-3 in presence of a base in a suitable solvent, followed by recrystallisation from a suitable solvent to provide (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl) quinolin-3-yI)-vinyI]-2,2-dimethyi-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound of formula-4,
F

Formula-4 b) reacting (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl)quino]in-3-yl)-vinyl]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acelic acid tertiary butyl ester compound of fonnula-4 with an acid in a suitable solvent, followed by recrystallisation from a suitable solvent to provide pitavastatin tertiary butyl ester compound of formula-5.


Formula-5 c) hydrolysis of pitavastatin tertiary butyl ester compound of formula-5 in presence of a suitable base in a suitable solvent, followed by subsequent treatment with a suitable organic amine, recrystaliization of the obtained solid from a suitable solvent to provide corresponding pitavastatin organic amine salt compounds of general formula-6,
F
OH OH O
OH.RNHR'
Formula-6

wherein R = alkyl or aryl or aralkyl or substituted aryl and R' is optionally hydrogen or alkyl or aryl or aryl alkyl or substituted aryl; d) hydrolyzing the compound of general formula-6 with a suitable base in a suitable solvent to provide corresponding alkali metal salt of pitavastatin, which on treating in-situ with a calcium source to provide pitavastatin calcium salt compound of formula-Ic.
The second aspect of the present invention is to provide an improved process for
the preparation of pitavastatin or its pharmaceutically acceptable salt compound of
general formula-1, preferably pitavastatin calcium salt compound of formu!a-lc, which
comprises of the following steps;
a) reacting the triphenyl [2-cyclopropyl-4-(4-f]uorophenyl)-quinoIine-3-yl-methyI)-
phosphonium] bromide salt compound of formuia-2
F
P;-Ph Br-Ph
Forraula-2 with tertiary butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-l,3-dioxan-4-yi)acetate
compound of formula-3
O^ 0
Formula-3 in presence of a base in a suitable soWent, followed by recrystallisation from a suitable solvent to provide {4R,6S)-{E)-6-{2-{2-cyclopropyl-4-(4-fluorophenyl) quinolin-3-yl)-vinyl]-2,2-dimethyl-[l,3]-dioxan'4-yl}-acetic acid tertiary butyl ester
compound of formula-4,
F

Formula-4

b) reacting (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yI)-vinyl]-
2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound of
fonnula-4 with a suitable acid in a suitable solvent, followed by recrystallisation from
a suitable solvent to provide pitavastatin tertiary butyl ester compound of formula-5,
F

Formula-5 c) hydrolyzing the compound of general formula-5 with a suitable alkali metal base in a suitable solvent to provide corresponding alkali metal salt of pitavastatin, which on in-situ treatment with a calcium source to provide pitavastatin calcium compound of formula-Ic.
Wherein in step a) of first and second aspect of the invention, the condensation of triphenyl[2-cyclopropyl-4-(4-f]uorophenyl)-quinoline-3-ylmethyl)-phosphonium] bromide salt compound of formula-2 with tertiary butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-l,3-dioxan-4-yl)acetate compound of formula-3, the base is selected from alkali metal hydroxides or alkali metal carbonates or alkali metal bicarbonates, preferably potassium carbonate and the suitable solvent is selected from polar aprotic solvents or alcohol solvents preferably polar aprotic solvents like dimethyl sulfoxide. Thus obtained compound of formula-4 is recrystallised from a suitable solvents selected from alcohols or hydrocarbons to remove the corresponding Z-isomer of the compound of formula-4, herein designated as "Impurity-A", preferably using alcoholic solvents like methanol.
In step b) of first and second aspect of the invention, the deprotecdon of acetonide in compound of formula-4 is carried out in presence of a suitable acid selected from inorganic acids or organic acids, preferably organic acids like oxalic acid in a suitable solvent selected from alcoholic solvents or hydrocarbon solvents, nitrile solvents, preferably alcoholic solvents like methanol to provide pitavastatin tertiary butyl ester compound of formiila-5, which on further recrystallized from a suitable solvent like alcoholic solvents or hydrocarbon solvents, preferable hydrocarbon solvents like toluene,

to remove the corresponding anti-isomer impurity compound of formula-5; herein designated as "Impuritj'-B".
In step c) of first aspect of the invention, the hydrolysis of pitavastatin tertiary butyl ester compound of formula-5 is carried out in presence of a base selected from alkali metal hydroxides or alkali metal carbonates or alkali metal bicarbonates, preferably alkali metal hydroxide like sodium hydroxide in presence of a suitable solvent selected from hydrocarbon solvents or polar aprotic solvents nitrile solvents, preferably acetonitrile to provide corresponding alkali metal sah of pitavastatin, which on in-situ treatment with suitable organic amine provides corresponding organic amine salt of pitavastatin compound of general formula-6. The obtained organic amine compound of general formula-6 is recrystallised from a suitable solvents selected from alcoholic solvents or hydrocarbon solvents or polar aprotic solvents or nitrile solvents, preferably nitrile solvent like acetonitrile to remove the formed lactone impurity herein designated as "Impurity-C" and there by controlling the formation of corresponding amide impurity herein designated as "Impurity-D".
In step d) of first aspect and step c) of the second aspect of the invention, hydrolysis of compound of general formula-6 or formula-5 with an alkali metal base selected from alkali metal hydroxides or alkali metal carbonates or alkali metal bicarbonates, preferably sodium hydroxide in presence of a polar solvent like water to provide corresponding alkali metal salt of phavastatin, which on in-situ treatment with calcium source like calcium chloride, calcium acetate and calcium bromide, preferably calcium chloride to provide pitavastatin calcium salt compound of formula-Ic.
Optionally the alkali metal salt of pitavastatin like potassium salt of pitavastatin and sodium sah of pitavastatin obtained in step d) of first aspect and step c) of second aspect of the invenfion are isolated as a crystalline solid. Thus obtained crystalline alkali metal salt can be converted into pitavastatin calciiun compound of formula-Ic.
The third aspect of the present invention provides an improved process for the preparation of highly pure triphenyl [2-cyclopropyi-4-(4-fluorophenyl)-quinoline-3-ylmethyl)-phosphonium] bromide compound of formula-2.


Formula-2 which comprises of the following steps;
a) reacting cyclopropyl methyl ketone compound of formula-7 with dimethyl carbonate in presence of a suitable base in a suitable solvent to provide a highly pure methyl 3-cyclopropyl-3-oxopropanoate compound of formula-8,
0 0
OCH3
Formula -8 b) reacting the methyl 3-cyclopropyl-3-oxopropanoate compound of formula-8 with
2-amino-4'-fluorobenzophenone compound of formula-9,
F


in presence of acid like sulfuric acid with or without a solvent to provide methyl 2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-carboxylate compound of formula-10,
COOCHi
F
Formula-10 c) reducing the methyl 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxylate compound of formula-10 with a suitable reducing agent in a suitable solvent, followed by recrystallisation from a suitable solvent to provide (2-cyclopropyI-4-(4-fluorophenyl)quinoline-3-yl)methanol compound of formula-11,

CH.OH
Formula-11 d) reacting (2-cyclopropyi-4-(4-fluorophenyl) quinoline-3-yl)methanol compound of formula-U with phosphorous tribromide in a suitable solvent, subsequent treatment with triphenyl phosphene in a suitable solvent, followed by recrystallisation from a suitable solvent to provide pure triphenyl[2-cyclopropyl-4-(4-fluorophenyl)-quinoline-3-ylmethyl)-phosphonium] bromide salt compound of formula-2.
Wherein in step a) cyclopropyl methyl ketone compound of formula-7 on reaction with dimethyl carbonate in presence of a suitable base selected from alkali metal hydroxides or alkali metal alkoxides or alkali metal carbonates or alkali metal bicarbonates preferably potassium tertiary butoxide in a suitable solvent selected from hydrocarbon solvents, preferably toluene provides highly pure methyl 3-cyclopropyl-3-oxopropanoate compound of formula-8. The dicyclopropyl compound having the following structure is formed as an impurity in this stage,

Wherein in step b the methyl 3-cyclopropyl-3-oxopropanoate compound of formula-S reacting with 2-amino-4'-fluorobenzophenone compound of formula-9 in presence of a suitable acid selected from sulfuric acid, para toluene sulfonic acid, methane sulfonic acid and the like, whh or without a solvent to provide methyl 2-cyclopropyl-4-(4-fluorophenyI) quinoline -3-carboxylate compound of formula-IO. The suitable solvent used for this step is selected from alcoholic solvents or hydrocarbon solvents, preferably methanol.
Wherein in step c) the reduction of methyl 2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-carboxylate compound of formula-IO is carried out with DIBAL-H or vitride in a suitable hydrocarbon solvent preferably toluene to provide (2-cyclopropyl-4-(4-fluorophenyl) quinoline-3-yl)methanol compound of formula-6, the obtained compound is recrystallized from a suitable solvent selected from hydrocarbon solvents, preferably

cyclohexane to provide pure compound of formula-6 free of dihydro impurity having the following structural formula.
F
j] CHzOH
H Dihydro impurity
Wherein in step d) (2-cyclopropyl-4-{4-tluorophenyl) quinoline-3-yl)methanol compound of formula-6 is reacted with phosphorous tribromide in a suitable chioro solvent, preferably methylene chloride to provide a bromo compound, which on subsequent reaction with the reagents like triphenyl phosphine, tributyl phosphine, preferably triphenyl phosphine in a suitable solvent selected from non-polar solvents such as toluene, o-xylene, chlorobenzene and the like or from the chioro solvents, preferably methylene chloride to provide triphenyl [2-cyclopropyl-4-(4-fluorophenyl)-quinoline-3-ylmethyl)-phosphonium] bromide salt compound of formula-7 which is purified in a suitable solvent selected from hydrocarbon solvents like benzene, toluene, xylene, and cyclohexane preferably toluene.
The fourth aspect of the present invention provides a novel crystalline form of (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-{4-fluorophenyl)qmnolin-3-yl)-vinyt]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound of formula-4.
The crystalline form of compound of formula-4 of the present invention is obtained by recrystalliation of compound of formula-4 from suitable alcoholic solvents, preferably methanol. The crystalline compound of formula-4 is characterized by its powder x-ray diffractogram having the peaks at 7.89, 9.98, 11.53, 14.87, 15.96, 17.51, 18.17, 19.18, 19.99, 20.86, 24.76 and 27.68 ± 0.2 degrees of 26 values (as illustrated in figrure-la), its IR spectrum having peaks at 3061, 2991, 2976, 1721, 1601, !488 and 1197 cm'' and hs DSC thermo gram having endothermic peak at about 114.59°C.
The fifth aspect of the present invention provides a novel crystalline form of pitavastatin tertiary butyl ester compound of formula-5.

The novel crystalline form of pitavastalin tertiary butyl ester compound of formula-5 of the present invention is obtained by recrystallisation of compound of formula-5 from a suitable solvent selected from hydrocarbon solvent, preferably toluene. This crystalline compound of formu!a-10 is characterized by its powder x-ray dif&actogram peaks at 8.07, 10.19, 12.15, 14.52, 16.25, 17.45, 17.90, 19.49, 21.84 and 25.3 ± 0.2 degrees of 29 values (as illustrated in figure-lb), its IR spectrum having peaks at 3413, 3005, 2971, 1733, 1604, 1512, 1489, 1152 and 766 cm"' and its DSC thermo gram having endolhermic peak at about 121.78°C.
The sixth aspect of the present invention is to provide crystalline form of pitavastatin methyl amine sah compound of formula-6a.
F
OH OH 0
OH.CH3NH2
Formula-6a The crystalline pitavastatin methylamine compound of formula-6a of the present invention is characterized by its powder x-ray diffractogram having the peaks at 8.61, 10.69,16.11, 17.46, 18.13,19.81, 20.97, 24.98, 25.76, 29.22 and 36.7 ± 0.2 degrees of 26 values (as illustrated in figure-2a), its IR spectrum having peaks at 3423, 3085, 3004, 2937, 1627, 1601, 1489, 1271, 1121 and 763 cm"' and its DSC thermo gram having endothermic peak at about 151.16°C.
The seventh aspect of the present invention is to provide a novel crystalline form of pitavastatin free acid compound of formula-la.
The crystalline free acid of pitavastatin compound of formula-la was obtained by hydrolyzing the pitavastatin tertiary butyl ester compound of formula-5 with a suitable alkali metal base in a suitable alcoholic solvent, preferably methanol to provide corresponding metal salt of pitavastatin, which on subsequent treatment with a suitable acid provides crystalline pitavastatin free acid, compound of formula-la.


Formula-la The crystalline pitavastatin free acid compound of formula-la of the present invention is characterized by its powder x-ray diffractogram having the peaks at 5.56, 10.57, 11.73, 13.15, 18.17, 19.36, 20.01, 21.98, 24.18, 24.73, 31.85 and 45.59 ± 0.2 degrees of 26 values ( as illustrated in figure-2b).
The eighth aspect of the present invention provides a crystalline form of pitavastatin sodium salt, compound of formula-lb.
OH OH 0
o-Na+
Formula-lb
The crystalline form of ptiavastatin sodium is obtained by treating the pitavastatin tertiary butyl ester compound of fonnula-10 with sodium hydroxide in a suitable alcoholic solvent.
The crystalline pitavastatin sodium compound of formula-lb of the present invention is characterized by its powder x-ray diffractogram having peaks at 8.72, 10.42, 13.70, 19.47, 20.53, 21.78, 23.37 and 25.10 ± 0.2 degrees of 26 values (as illustrated in figure-3a).
We have prepared pitavastatin calcium as per example-2 of EP 0520406 Bl, which involves the isolation of pitavastatin calcium from water and the obtained pitavastatin calcium is analyzed by PXRD. The powder X-ray diffractogram of the obtained crystalline pitavastatin calcium is illustrated in figure-4a.
Similarly, we have isolated the pitavastatin calcium from water and analyzed the obtained solid by PXRD. The powder X-ray diffractogram of thus obtained cr}'sta]line pitavastatin calcium is illustrated in figure-3b. Hence both the crystalline forms of pitavastatin calcium illustrated in figure-3b and figure-4a are prior art crystalline forms.

The impurities A to D are shown in the following table with structural formula:




NHR
COOClCH,);
Impurity-A

Impurity-B

Impurity-C

Impurity-D

Other than the above impurities, the following impurities {3R,5R,6E)-7-[2-cyclopropyt-4-(4-Fluorophenyl) quinolin-3-yl]-3,5-dihydroxy-6-heptenoic acid calcium (herein designated as Impurity-E), racemic pitavastatin calcium (herein designated as impurity-F), Monocalcium bis[(3R,5S,6Z)-7-[2-cyclopropyl-4-(4-fuorophenyl)-3-quinolinyl]-3,5-dihydroxy-6-heptenoate (herein designated as Impurity-G), (3R, 5S, 6E)-7[2-cyclopropyl-4-(phenyl)quinoiin-3-yI]-3,5-dihydroxy-6-heptenoic acid calcium sah (herein designated as Impurity-H), (3R,5S,E)-tert-butyl 7-(2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl)-3,5-dihydroxyhept-6-enoate (herein designated as Impurity-I) and (3R,5S,6E)-methyl-7-(2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-y!)-3,5-dihydroxyhept-6-enoate (herein designated as Impurity-J). All the above impurities are identified and well characterized. The structures of the impurities are represented are as follows.




Impurity-E

Impurity-F

Ca

2+

Impurity-G

^C(CH3)5
OCH,
Ca

+2

Impurity-H

Impurity-I

Impurity-J

The present invention is schematically represented as follows:


CH,OH
Fomiula-6 6a) oi^ani amine - Mclhyl niiiiiic

XRD analysis of pitavastatin, its pharmaceutically acceptable salts as well as their intermediates were carried out using SIEMENS/D-5000 X-Ray diffractometer using Cu, Ka radiation of wavelength 1.54 A° and continuous scan speed of 0.045°/min. FI-IR spectrum of pitavastatin, its pharmaceutically acceptable salts as well as their intermediates were recorded on Thermo model Nicolet-380 as KBr pellet. The thermal analysis of pitavastatin, its pharmaceutically acceptable salts as well as their intermediates were carried out on Waters DSC Q-10 model differential scanning calorimeter.

Related substances and photo (UV) degradation impurities of the pitavaslatin calcium are measured by HPLC, as per the following conditions. Apparatus: A liquid chromatograph is equipped with variable wavelength UV-detector. Column: ACE C18 250 x 4.0 mm, 5 jim; Flow rate: 1.2 ml/min; Wavelength: 250 nm; Temperature: 50°C; Injection volume 20 jiL; Run lime 60 min; Product retention time: 14.0 minutes; using water:acetonitrile as a diluent; Elution: gradient;

Impurity RRT
Impurity-C (Lactone) 1.73
Impurity-D (Amide) 0.759
Impurity-E (Antiisomer) 1.09
Impurity-G (Z-isomer) 1.59
Impurity-H (Desfluoro) 0.67
Impurity-I (Tertiary butyl ester) 1.91
Triphenyl phosphene salt 1.79
Dihydroxy protected tertiary butyl ester(Formula-4) 2.62

The process described in the present invention was demonstrated in examples illustrated below. These examples are provided as illustration only and therefore should not be construed as limitation of the scope of the invention.
Examples:
Example-1: Preparation of Methyl 3-cyclopropyl-3-oxopropanoate
To the solution of dimethyl carbonate (361 g) in toluene (!250 ml) added cyclopropyi methyl ketone(i25 g) and stirred for 15 min at 25°C. Cooled (he reaction mixture to 10°C, added potassium tert.butoxide (100 g) to it under nitrogen atmosphere. Heated the reaction mixture to TS^C and stirred for 14 hrs. Cooled the reaction mixture to 25°C and slowly poured it into chilled water (750 ml). Cooled the reaction mixture to 0°C and adjusted the pH to 2.5 by using 50% HCl solution. Raised the temperature to 25°C and stirred for 45 minutes. Separated the both organic and aqueous layers. Extracted the aqueous layer with toluene (500 ml). Washed the organic layer with water (500 ml). Distilled off the toluene completely from organic layer under reduced pressure to get the title compound. Yield; 130 g; G.C. purity: 93.85%
Exainple-2: Preparation of methyl 2-cyclopropyM-(4-fluorophenyl) quinoline -carboxylate.
To the solution of 2-amino-4'-fluorobenzophenone (100 g) in methanol (500 ml) added Methyl 3-cyclopropyl-3-oxopropanoate (132 g), sulfuric acid (5 ml) and stirred for 15 minutes at 25°C. Heated the reaction mixture to 65°C for 22 hrs. Distilled off the methanol completely under reduced pressure. Cooled the reaction mixture to 25''C, added water (500 ml) and stirred for 30 minutes. Cooled the reaction mixture to 0°C and pH adjusted to 6.0 with sodium carbonate solution. Stirred the reaction mixture for 45 minutes at 25°C. Filtered the cake and washed with water. Spin dry the compound for 60 minutes. To this compound added methanol (150 ml) and stirred for 1 hr at 25°C. FiUered the solid and washed with methanol (50 ml). Dried the obtained solid to get the title compound. Yield: 14l.6g; MR: 123-125°C; Purity by HPLC: 99.69%

Example-3: Preparation of methyl 2-cyclopropyl-4-(4-fluorophenyl) quinoline carboxylatc.
To the solution of 2-amino-4'-ftuorobenzophenone (iOO g) in acetic acid (500 ml) added methyl 3-cyclopropyl-3-oxopropanoate (132 g), sulfuric acid (5 ml) and stirred for 15 minutes at 25''C. Heated the reaction mixture to ]00°C for 10 hrs. Cooled the reaction mixture to 0-5°C and pH adjusted to neutral condhions with 40% sodium hydroxide solution. Filtered the solid formed and washed with water. The wet solid was dissolved in methylene chloride and separated the water from it. Silica slurry was given to the reaction mixture and filtered it. Methylene chloride was distilled off and the compound was co-distilled with methanol. To the compound added methanol (150 ml) and stirred for 1 hr at 25°C. Filtered the solid and washed with methanol (50 ml). Dried the obtained solid to get the title compound. Yield: 101 g.
Example-4: Preparation of methyl 2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-carboxylate.
The title compound is prepared analogous manner to example-3 using p-toluene sulfonic acid in place of sulfuric acid. Yield: 100.5 g.
Example-5: Preparation of (2-cyelopropyl-4-(4-fluorophenyl) quinoline -3-yl) methanol:
To 50 g of methyl 2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-carboxylate added toluene (250 ml) and stirred for 15 minutes at 25°C. Cooled the reaction mixture to 0°C. Added 300 ml of DIBAL H (25% solution in toluene) to the reaction mixture slowly in 45 minutes at the same temperature. Stirred the reaction mixture for 1 hr at 0°C. Quenched the reaction mixture with HCl (110 ml) solution at 10°C and stirred for 15 minutes. Raised the temperature to 25°C and stirred for 30 minutes. Separated the both aqueous and organic layers. Extracted the aqueous layer with toluene (400 ml), Adjusted the pH of the reaction mixture with 10% sodium bicarbonate solution (200 ml). Washed the organic layer with saturated sodium chloride solution (200 ml). Distilled off the solvent completely to obtain a solid. Added cyclohexane (50 ml) to the solid and distilled

it. To the residue added cyclohexane (150 mi) and stir for 30 minutes at 45°C. Cooied the
reaction mixture to 25°C and stirred for 1 hr. at the same temperature. Filtered the cake,
washed with cyclohexane (50 ml) and then dried to get the title compound.
Yield: 44 g.
MR: 125-135°C
Purity by HPLC: 99.83%; Des-fluoro: 0.12%
Example-6: Preparation of triphenyl (2-cyclopropyl-4-(4-nuorophenyl) quinoline -3-yI)-phosphonium bromide:
To 100 g of (2-cyclopropyl-4-(4-fluorophenyl) quinoHne -3-yl)methanoi added dichloromethane (400 ml). Stirred the reaction mixture for 30 minutes. To this reaction mixture added a solution of phosphorous iribromide (16.2 ml) in dichloromethane (100 ml) slowly at 25°C and stirred for 1 hr at same temperature. Quenched the reaction mixture with 10% sodium bicarbonate solution and adjusted the pH to neutral at 20°C, Stirred the reaction mixture to 15 minutes. Separated the both aqueous and organic layers. Extracted the aqueous layer with dichloromethane (100 ml). Washed the organic layer with 10% hypo solution. Then again washed the organic layer with saturated sodium chloride solution. Heated the reaction mixture to 40°C. To the reaction mixture added triphenyJ phosphene (90 g) in dichloromethane (]00 mi). Distilled off the solvent completely under reduced pressure. Added toluene (100 ml) to the reaction mixture and stirred for 15 minutes. Distilled off the toluene completely. Cooled the reaction mixture to 40°C, added toluene (500 ml) and heated for 1 hr at 75°C. Cooled the reaction mixture to 25°C and stirred for 1 hr. Filtered the reaction mixture and washed the compound with toluene and dried. The compound obtained as a crystalline solid. Yield: 200 g. MR:215-218°C Purity by HPLC: 99.61%, desfluoro-0.08%;
Example-7: Preparation of triphenyl (2-eyclopropyl-4-(4-fluorophenyl) quinoline -3-yl)-phosphonium bromide (One pot process)
To 50 g of methyl 2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-carboxylate added toluene (500 ml) and stirred for 15 minutes at 25°C. Added 145 ml of vitride (65%

solution in toluene) to the reaction mixture slowly in 45 minutes at the same temperature under nitrogen atmosphere. Stirred the reaction mixture for 4 hrs at 25°C. Quenched the reaction mixture with hydrochloric acid (55 ml) solution stirred for 30 minutes. Separated the both aqueous and organic layers. Extracted the aqueous layer with ethyl acetate. Neutralized the reaction mixture with 10% sodium bicarbonate solution. Washed the organic layer with saturated sodium chloride solution. Distilled the solvent completely under reduced pressure. To the above obtained compound added 250 ml of dichloromethane was added. To this reaction mixture phosphorous tri bromide was slowly added and stirred for 3 hrs. Adjusted the pH with 10% sodium bicarbonate solution. Separated the both aqueous and organic layers. Aqueous layer was extracted with dichloromethane and washed with hypo solution. Again the reaction mixture was washed with sodium chloride solution. Heated the reaction mixture to 40°C. To this added a solution of triphenyl phosphene (38.4 g) in dichloromethane (50 ml). Stirred the reaction mixture for 2 hrs. Distilled off the solvent completely under reduced pressure. To this added 250 ml of toluene and stirred for 2 hrs. Filtered the solid precipitated and dried it. The title compound obtained as a crystalline solid. Yield: 88 g. MR:215-218°C.
Example-8: Preparation of (4R,6S)-(E)-6-{2-(2-cycIopropyl-4-(4-fluorophenyl) qumolin-3-yl)-vinyl]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester.
To the solution of triphenyl (2-cyclopropyl-4-(4-fluorophenyl) quinoline -3-yl)-phosphonium bromide (60 g) in DMSO (100 ml) added a solution of tert-butyl 2-((4R,6S)-6-formyl-2,2-dimethyl-l,3-dioxan-4-yl)acetate (25 g) in DMSO (50 ml). Heated the reaction mixture to 75°C and added potassium carbonate (20 g) to it. Stirred the reaction mixture for 7 hrs at 75°C. Cooled the reaction mixture to 25°C, added water (250 ml) and stirred for 90 minutes at same temperature. Filter the solid precipitated and washed with water (200 ml). To the obtained wet solid added methanol (250 ml) and stirred for 45 minutes at 65°C. Cooled the reaction mixture to 25°C and stirred for 90 minutes. Filtered the compound and washed with methanol (25 ml) and dried. The compound obtained as a crystalline solid.

Yield: 35 g.
M.R;U1-1]3°C
Purity by HPLC: 97.65%; Impurity-A: 0.40%, Impurity-J: 0.90%
Example-9: Preparation of pitavastatin tert butyl ester.
To the solution of (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl)-viny!]-2,2-dimethyl-[l,31-dioxan-4-yl}-acetic acid tertiary butyl ester (150 g) in methanol (750 ml) added a solution of oxalic acid (90 g) in water (630 ml). Stirred the reaction mixture for 6 hrs at 35°C. Cooled the reaction mixture to IO°C. Adjusted the pH to 7.0 by using sodium carbonate solution (72 g in 360 ml of water). Stirred the reaction mixture for 45 minutes at 10°C. Heated the reaction mixture to 30''C and stirred for 2 hrs. Filtered the solid and washed with water (100 ml). To the wet solid added water (2250 ml) and stirred for 2.5 hrs at 30°C. Filtered the reaction mixture and washed the solid with water (100 ml). To the wet solid added toluene (75 ml) and stirred for 30 minutes at 75°C. Cooled the reaction mixture to 0°C and stirred for 3 hrs at same temperature. Filtered the solid and washed with cyclohexane (150 ml). Suck dried the compound for 1 hr. under reduced pressure. To this solid added toluene (75 ml) and stirred for 30 minutes at 75°C, Cooled the reaction mixture to O^C and stirred for 3 hrs at same temperature, Filtered the solid and washed with cyclohexane (150 ml) and dried the compound. Compound obtained as a crystalline solid. Yield: 110g.;M.R: 120-122°C. Purity by HPLC: 99.67%; Impurity-C: 0.05%, des-fluro: 0.08%; Impurity-J: 0.04%
Example-10: Preparation of pitavastatin tert butyl ester (with HCI).
The title compound is prepared analogous manner to example-3 using hydrochloric acid for deprotection in place oxalic acid. Yield: 105 g.
Example-ll: Preparation of pitavastatin methyl amine salt.
150 g of pitavastatin tert butyl ester was dissolved in acetonitrile (1500 ml). To this solution added sodium hydroxide solution (45 g in 450 ml of water) at 30°C slowly and stirred the reaction mixture for 1.5 hrs at same temperature. Cooled the reaction

mixture to 0°C and added sodium chloride {280 g) to h. Adjusted the pH to 4.0 with 10% HCI solution (60 ml in 600 ml of water). Stirred the reaction mixture for 15 minutes and separated the both aqueous and organic layers at 0°C. To the organic layer methyl amine (36 ml) was added at 0°C and stirred for 30 minutes. Stirred for another 30 minutes at 30°C. Distilled off the solvent completely under reduced pressure. To the reaction mixture added acetonitrile (150 ml) and distilled off completely. To the reaction mixture added acetonitrile (750 ml) and stirred for 1 hr at 30°C. Cooled the reaction mixture to Q°C and stirred for 1.5 hrs at same temperature. Filtered the reaction mixture and washed with chilled acetonitrile (150 ml) and dried it. The compound obtained as a crystalline solid.
Yield: llOg M.R: 146-149°C.
Example-12: Preparation of pitavastatin free acid.
From pitavastatin calcium salt: 20 g of pitavastatin calcium salt was taken in 100 ml of dichloro methane and stirred for 10 minutes. Cooled the reaction mixture to 0°C and adjusted the pti to 3.0 with 20% aqueous HCI solution. 60 g of sodium chloride is added to the reaction mixture and stirred for 10 minutes. Raised the temperature to 25°C and stirred for 30 minutes. Filtered the solid precipitated. Water was added to the solid and stirred for 10 minutes. Filtered the solid and washed with water. Dried the obtained solid to get the title compound. Yield: 17 g; M.R:125-130°C
From pitavastatin tertiary butyl ester: 50 g of pitavastatin tert-butyl ester was taken in 250 ml of methanol and stirred for 10 minutes at 25°C. 6 g of sodium hydroxide is dissolved in 60 ml of water and slowly added to the reaction mixture. Stirred the reaction mixture to 2 hrs at 25°. Distilled of the solvent completely under reduced pressure. To the obtained solid added 50 ml of dichloro methane and stirred for 10 minutes. Cooled the reaction mixture to 0°C and adjusted the pH to 3.0 with 20% aqueous HCI solution. 60 g of sodium chloride is added to the reaction mixture and stirred for 15 minutes. Raised the temperature to 25°C and stirred for 30 minutes. Filtered the solid precipitated. Water was

added to the solid and stirred for 10 minutes. Fihered the solid and washed with water. Dried the obtained solid to get the title compound. Yield: 42 g M.R:125-130°C
Example-13: Preparation of pitavastatin sodium salt.
10 g of pitavastatin tert-butyl ester was taken in 100 ml of methanol and stirred for 10 minutes at 25°C. 3 g of sodium hydroxide is dissolved in 30 ml of water and slowly added to the reaction mixture. Stirred the reaction mixture to 2 hrs at 25°. Distilled off the solvent completely under reduced pressure. The obtained solid was washed with water and dried the compound. The title compound obtained as a crystalline solid. Yield: 7 g. M.R: 100-110°C
EKampIe-14: Preparation of pitavastatin calcium salt.
20 g of pitavastatin methyl amine salt was dissolved in water (120 ml). To this solution added sodium hydroxide solution (1.76 g in 20 ml water) and stirred for 45 minutes at 3D°C.Tert butyl acetate (40 ml) was added to the reaction mixture and stirred for 15 minutes. Separated the tert butyl acetate from the reaction mixture. Removed the methyl amine and tert butyl acetate traces with nitrogen expelling upto the pH reaches to 9.0. Filtered the reaction mixture and washed with water (20 ml). Calcium chloride (3.9 g) was dissolved in water (20 ml) and added to the reaction mixture at 35''C and stirred for 45 minutes at same temperature. Filtered the solid and dried the crystals. Yield: 15 g.; MR: 206-209°C.
Example-15: Preparation of pitavastatin calcium salt
10 g of pitavastatin tert-butyl ester compound was dissolved in 50 ml of methanol and stirred for 10 minutes. Cooled the reaction mixture to 0°C and added aqueous sodium hydroxide solution (3 g of NaOH in 30 ml of water) slowly to it at the same temperature. Stirred the reaction mixture for 90 minutes at 0°C. Distilled off the solvent completely from reaction mixture. To the obtained residue added water (60 ml) and stirred for 15 minutes. The pH of the reaction mixture was adjusted to 9.0 by using 10% HCl solution

at 10°C. Heated the reaction mixture to 30°C and washed it by using tert-buty! acetate. Expelled the tert-butyl acetate by using nitrogen gas. Added 160 ml of water to the reaction mixture and adjusted the pH to 9.0 by using 10% NaOH solution. Then treated the reaction mixture with aqueous calcium chloride solution (1.92 g of CaCl; in 100 ml of water). Stirred the reaction mixture for 40 minutes at 25°C. Then cooled the reaction mixture to]0°-15°C and stirred overnight at the same temperature. Filtered the solid precipitated, washed with water and dried the compound. The compound obtained as a crystalline solid. The powder X-ray diffractogram of the above obtained compound is perfectly matched with the prior art crystalline form of pitavastatin calcium. Yield: 9.2 g.
Purity by HPLC: 99.75%; Impurity-H: 0.09%; Impurity-E: 0.06%; Impurity-C: 0.02% Water content: 11.6%
Example-16: Preparation of prior art crystalline form of pitavastatin calcium as per the example 2 of EP 0520406B1.
To a 12 g of (E)-3(R)-5(S)-dihydroxy-7-[4'-(4"-fluorophenyl)-2'-cyclDpropyl quinoline-3'-yl]hept-6-ene acid D(+) phenethylamine salt compound((-)l (+)I1), 24.3 ml of a IN sodium hydroxide aqueous solution and 200 mi of water were added and stirred to dissolve the compound. To this solution an aqueous calcium chloride solution obtained by dissolving 1.47 g of dry calcium chloride to 200 ml of water, was dropwise added. This reaction solution was stirred overnight, and the resulting white precipitate was collected by filtration to obtain 9.0 g of white crystals. MR: 190-192°C (decomposed). Water content: 8.2%
Exampie-17: UV degradation study of pitavastatin calcium:
0.1 g of pitavastatin calcium salt was dissolved in 100 ml of water and acetonitrile mixture and irradiated with UV light (130 W, 30°C) for 48 hrs. Acetonitrile and water were evaporated under vaccum. The two photo degradants of pitavastatin are obtained.

Photo degradation compounds RRT
Compound-A 0.281
Compound-B 1.543

We Claim:
1. An improved process for the preparation of pitavastatin and its pharmaceutically acceptable salt compounds of general formula-1,

in presence of a base in a suitable solvent, followed by recrystallisation from a suitable solvent to provide {4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl) quinolin-3-yl)-vinyl]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound of formula-4,
F
0 0^0 0
Formula-4

b) reacting (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yi)-
vinyl]-2,2-dimethyl-[i,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound of formula-4 with an acid in a suitable solvent, followed by recrystaUisation from a suitable solvent to provide pitavastatin tertiary butyl ester compound of formula-5,
F

Formula-5
c) hydrolysis of pitavastatin tertiary butyl ester compound of formula-5 in presence
of a suitable base in a suitable solvent, followed by subsequent treatment with a
suitable organic amine, recrystallization of the obtained solid from a suitable
solvent to provide corresponding pitavastatin organic amine salt compounds of
general formula-6,
F
OH OH O
OH.RNHR'
Formula-6 wherein R = alkyl or aryl or aralkyi or substituted aryl and R is optionally hydrogen or alkyl or aryl or aryl alkyl or substituted aryl;
d) hydrolyzing the compound of general formula-6 with a suitable base in a suitable
solvent to provide corresponding alkali metal salt of pitavastatin, which on
treating in-situ with a calcium source to provide pitavastatin calcium salt
compound of formula-lc.
2. An improved process for the preparation of pitavastatin and its pharmaceutically acceptable salts compound of general formula-1, which comprises of the following steps;

a) reacting the triphenyl [2-cyciopropyl-4-(4-fluorophenyl)-quinoline-3-yl-methyl)-
phosphonium] bromide salt compound of formula-2

b) reacting (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fiuorophenyl)quinolin-3-yl)-
vinyi]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester compound
of formula-4 with a suitable acid in a suitable solvent, followed by
recrystaliisation from a suitable solvent to provide pitavastatin tertiary butyl ester
compound of formula-5,
y^^ OH OH o
Formula-5
c) hydrolyzing the compound of general formula-5 with a suitable alkali metal base
in a suitable solvent to provide corresnondina alkali metal salt of nitavastatin.

which on in-silu treatment with a calcium source provides pitavastatin calcium compound of formula-lc.
3. The process according to claim 1 and 2, wherein
in step a), the base is selected from alkali meta! carbonates and the solvent is selected from polar aprotic solvent;
in step b), the acid is selected from hydrochloric acid, hydrobromic acid, acetic acid,
sulfuric acid, oxalic acid, para toluene sulfonic acid, poly phospharic acid, methane
sulphonic acid, maleic acid, malic acid, fumaric acid and formic acid; and the suitable
solvent is selected from alcoholic solvents or hydrocarbon solvents;
in step Ic), the base is selected from alkali metal hydroxides or alkali metal
carbonates or alkali metal bicarbonates; and the suitable solvent is selected from
nitrile solvents; and the organic amine is selected from methyl amine, ethyl amine,
n-propyl amine, isopropyl amine, n-butyl amine, tertiary butyl, {+/-)-sec-butyl amine,
octyl amine, 2-ethyl hexylamine, benzyl amine, a-methyl-benzylamine, phenyl
ethylamine, dibenzylamine, N-methylbenzylamine, N,N-dimethylbenzylamine, N,N-
diethyl benzyl amine, N-ethyl-N-methylbenzylamine, tribenzyl amine,
cyclopentylamine, cyclohexylamine, cycioheptylamine, N-methylcycIopentylamine,
N-ethylcyclohexyl amine, N-ethyl cycioheptylamine, dicyclohexylamine, N,N-
dimethylcyclo pentylamine, N,N-dimelhyl cyclohexylamine, N,N-
diethylcycloheptylamine.
in step Id) & 2c), the alkali metal base selected from alkali metal hydroxides or alkali metal carbonates or alkali metal bicarbonates; and the solvent is polar solvent and the calcium source is selected from calcium chloride, calcium acetate.
4. The process according to any of the proceeding claims, wherein the obtained pitavastatin calcium containing less than about 0.1 area-% by HPLC of each of impurities C, D, E, G, H, I and (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl) quinolin-3-yl)-vinyI]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester having the following structure.


5. The process according to any of the proceeding claims, wherein the obtained
pitavastatin calcium containing less than about 0.05 area-% by HPLC of each of
impurities C, D, E, G, H, I and (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-(4-fluorophenyl)
quinolin-3-yl)-vinyl]-2,2-dimethyl-[l,3]-dioxan-4-yl}-acetic acid tertiary butyl ester.
6. The process according to any of the proceeding claims, wherein the obtained
pitavastatin calcium is free of the impurities D, G, I and (4R,6S)-(E)-6-{2-(2-
cyclopropyl-4-(4-fluorophenyl) quinoUn-3-yl)-vinyt]-2,2-dimethyl-[l,3]-dioxan-4-
yl}-acetic acid tertiary butyl ester.

8. The process according to ciaim 7, where in
in step a) the suitable base is selected from alkali metal hydroxides or alkali metal
alkoxides or alkali metal carbonates or alkali metal bicarbonates; and the solvent is
selected from hydrocarbon solvents;
in step b) the acid is selected from sulfuric acid, poly phosphoric acid, methane
sulfuric acid, para toJuene sulfuric acid; and the suitable solvent is selected from
alcoholic solvents or hydrocarbon solvents;
in step c) the reducing agent is selected from DIBAL-H or vitride and the suitable
organic solvent is selected from hydrocarbon solvents;
in step d) the suhable solvent is selected from chloro solvents; and the wittig reagent
is selected from tripJieny] phosphine, tributyl phosphine.
9. Crystalline form of (4R,6S)-(E)-6-{2-(2-cyclopropyl-4-{4-fluorophenyl)quinolin-3-
yI)-vinyl]-2,2-dimethyl-fl,3]-dioxane-4-yI}-acetic acid tert. butyl ester compound of
formula-4 characterized by any one of the following
i) its powder X-ray diffractogram having peaks at about 7.89, 9.98, 11.53, 14.87, 15.96, 17.51,18.17, 19.18,19.99,20.86, 24.76 and 27.68 ± 0.2 degrees of 29;
ii) its IR spectrum shows the values of the said compound are 3061, 2991, 2976, 1721, 1601, 1488 and 1197 cm"';
iii) its DSC thermo gram having endothermic peak at about 121.78°C.
10. Crystalline form of pitavastatin tertiary butyl ester compound of formula-5
characterized by any one of the following;
i) Its powder X-ray diffractogram having peaks at about 8.07, 10.19, 12.15, 14.52, 16.25, 17.45, ]7.90, 19.49, 21.84and 25.3 ± 0.2 degreesof2e;
ii) its IR spectrum shows the values of the said compound are 3413, 3005, 2971, 1733, 1604, 1512,1489, 1152 and 766 cm"';
iii) its DSC thermo gram having endothermic peak at about 121.78°C.

11. Crystalline form of pitavastatin methyl amine salt compound of formula-6a
characterized by any one of the following;
i) Its powder X-ray diffractogram having peaks at about 8.61, 10.69, 16.11, 17.46, 18.13, 19.81, 20.97, 24.98, 25.76, 29.22 and 36.7 ± 0.2 degrees of 26;
ii) its IR spectrum shows the values of the said compound are 3423, 3085, 3004, 2937, 1627, 1601, 1489, 1271, 1121 and 763 cm-';
iii) its DSC thermo gram having endothermic peak at about 151.16°C.
12. Crystalline form of pitavastatin free acid compound of formula-la is characterized by
its powder X-ray diffractogram having peaks at about 5.56, 10.57, 11.73, 13.15,
18.17, 19.36, 20.01,21.98,24.18,24.73, 31.85 and 45.59 ±0.2 degrees of 26.