WO2001040211A1 - A PROCESS FOR THE PREPARATION OF {2-[4-(α-PHENYL-p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR - Google Patents

A PROCESS FOR THE PREPARATION OF {2-[4-(α-PHENYL-p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR Download PDF

Info

Publication number
WO2001040211A1
WO2001040211A1 PCT/HU2000/000123 HU0000123W WO0140211A1 WO 2001040211 A1 WO2001040211 A1 WO 2001040211A1 HU 0000123 W HU0000123 W HU 0000123W WO 0140211 A1 WO0140211 A1 WO 0140211A1
Authority
WO
WIPO (PCT)
Prior art keywords
phenyl
ethoxy
formula
chloro
acetamide
Prior art date
Application number
PCT/HU2000/000123
Other languages
French (fr)
Inventor
József Reiter
Péter Trinka
Ferenc Bartha
Gyula Simig
Kálmán NAGY
Györgyi VERECZKEYNÉ DONÁTH
Norbert Németh
György CLEMENTIS
Péter TÖMPE
Pál VÁGÓ
Original Assignee
EGIS Gyógyszergyár Rt.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from HU9904438A external-priority patent/HU226641B1/en
Priority claimed from HU9904439A external-priority patent/HU226639B1/en
Priority to US10/148,704 priority Critical patent/US6908999B2/en
Priority to SI200030569T priority patent/SI1233954T1/en
Priority to JP2001541895A priority patent/JP4763954B2/en
Priority to SK752-2002A priority patent/SK285641B6/en
Priority to AT00981508T priority patent/ATE280165T1/en
Priority to UA2002065341A priority patent/UA72949C2/en
Application filed by EGIS Gyógyszergyár Rt. filed Critical EGIS Gyógyszergyár Rt.
Priority to PL354677A priority patent/PL200046B1/en
Priority to DE60015177T priority patent/DE60015177T2/en
Priority to EP00981508A priority patent/EP1233954B1/en
Priority to AU18742/01A priority patent/AU1874201A/en
Publication of WO2001040211A1 publication Critical patent/WO2001040211A1/en
Priority to HR20020470A priority patent/HRP20020470B1/en
Priority to BG106760A priority patent/BG65455B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents

Definitions

  • the invention refers to a novel process for the preparation of ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ acetic acid of the formula
  • the invention also refers to novel ⁇ 2-[4-( ⁇ -phenyl-p-chloro- be ⁇ zyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ acetam ⁇ des of the formula wherein
  • R* ⁇ and R 2 represent, independently, a C ⁇ -4 alkyl group optionally substituted by a phenyl group, a C 2 . 4 alkenyl group or a cyclohexyl group, or
  • R- ! and R 2 form together with the adjacent nitrogen atom a morphohno group, and acid addition salts thereof which are useful intermediates in the synthesis of ceti ⁇ zine
  • Y stands for a group of the formula -OR 1 or an ammo group, wherein R 1 means an alkyl group, is hydrolized to obtain the compound of the formula I
  • the potassium salt of ceti ⁇ zine is obtained in a yield of 59 %
  • the potassium salt is formed in a yield of 81 %
  • the desired dihydrochlo ⁇ de of ceti ⁇ zi ⁇ e is obtained in a yield of 80 %
  • the total yield of the known process amounts to 38 2 %
  • a rather great drawback of the known process consists in the fact that the esters of the formula V used as the starting compound can be prepared only with difficulties and in a poor yield
  • ceti ⁇ zine can be prepared also from the acetic amide of the formula V, wherein Y stands for an ammo group, by hydrolysis
  • Y stands for an ammo group
  • the acetamide of the formula V can be also prepared from the corresponding methyl ester of the formula V, wherein Y means a methoxy group, by reaction with ammonia in a yield of 54 % Taking into consideration the low yield (27 8 %) of the preparation of the methyl ester, the total yield is as low as 15 0 % Consequently, the latter known synthesis of ceti ⁇ zine is uneconomical, too
  • chloroethoxy-acetonit ⁇ le can be prepared from ethylene chlorohyd ⁇ n in two steps using the very poisonous copper(l) cyanide in a total yield of 58 %
  • the aim of the invention is to provide an economical process for the preparation of ceti ⁇ zine that satisfies the most severe quality requirements
  • the invention includes the ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)- p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetam ⁇ des of the formula II that are novel compounds
  • the starting compound is an acetamide of the formula II or an acid addition salt thereof formed with an inorganic or an organic acid, and the starting compound is subjected to alkaline or acidic hydrolysis in a manner known per se, if, desired, in the presence of a phase transfer catalyst
  • the product formed is converted to a pharmaceutically suitable acid addition salt or metal salt and/or the base is liberated from the acid addition salt or metal salt thereof in a manner known per se
  • N,N-d ⁇ methyl- ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)- p ⁇ peraz ⁇ n-1 -yl]-ethoxy ⁇ acetamide is used as the acetamide of the formula II
  • the hydrolysis of the ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ - acetamides of the formula II is carried out in an aqueous solution of an alkali metal hydroxide, preferably sodium or potassium hydroxide, wherein the concentration of the alkali in the solution amounts to 2-25 % by mass, preferably 6-16 % by mass, suitably about 12 % by mass, generally at 40-110 °C, preferably at 70-110 °C, suitably at the boiling point of the solution
  • the product is separated as follows the reaction mixture is diluted with water, acidified with hydroch
  • a further possibility is that - after the hydrolysis and adjustment of the pH value to 3 8-4 0 - the solution of ceti ⁇ zine base in dichloromethane is extracted with preferably 5-30 % hydrochloric acid, the aqueous solution is concentrated under reduced pressure to reduce the water content to 20-25 % by mass and then the procedure described above is followed to obtain cetinzine dihydrochlo ⁇ de
  • the honey-like residue obtained after the evaporation of the solution of cetinzine base in dichloromethane can be dissolved in a water-miscible organic solvent, preferably acetone, methyl ethyl ketone or tetrahydrofuran, and then the thus-obtained solution of the cetinzine base in the organic solvent is treated with the hydrochloric acid
  • a water-miscible organic solvent preferably acetone, methyl ethyl ketone or tetrahydrofuran
  • the hydrolysis of the acetic amide of the formula II is carried out with an aqueous solution of an inorganic acid, preferably hydrochloric acid or sulfu ⁇ c acid at 40-110 °C, preferably 70- 110 °C, suitably at the boiling point of the solution
  • an inorganic acid preferably hydrochloric acid or sulfu ⁇ c acid at 40-110 °C, preferably 70- 110 °C, suitably at the boiling point of the solution
  • a 2-25 % by mass, preferably 10-20 % by mass, suitably about 15 % by mass solution of the inorganic acid is employed
  • the acidic hydrolysate obtained is diluted with water, the pH is adjusted to a value of 3 8-4 0 by the addition of aqueous sodium hydroxide solution, and then the procedure described in connection with the alkaline hydrolysis is followed
  • phase transfer catalyst a phase transfer catalyst, and, if desired, also a cosolvent
  • phase transfer catalyst a tetraalkyl- ammonium halide, preferably tetrabutylammonium chloride, t ⁇ ethylbenzylammonium chloride or t ⁇ octylmethylammonium chloride (Aliquat 336) or a crown ether, preferably 15-crown-5 or 18-crown-6 can be used
  • the cosolvent can be an organic solvent being miscible with water such as ethanol, butanol, ethylene glycol or dioxane
  • an acid addition salt of the acetamide of the formula II prepared with an organic acid is used as the starting compound, this organic acid crystallizes from the reaction mixture after the precipitation of the product with an acid
  • the precipitated organic acid can be separated by filtration before the extraction of the product with dichloromethane to achieve an easier separation of the phases
  • the reaction mixture can be worked up without the separation of the organic acid, too
  • the process of the invention is economical, can be easily carried out and provides cetinzine or the acid addition salt thereof in a very pure form
  • a second aspect of the invention refers to the novel intermediates of the formula II, wherein R- and R 2 are as defined above, and acid addition salts thereof formed with inorganic or organic acids
  • the invention includes the isomers of the ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ - acetamides of the formula II and mixtures thereof
  • the C 1-4 alkyl group optionally substituted by a phenyl group may have a straight or branched chain such as a methyl, ethyl, isopropyl, tert -butyl or benzyl group etc
  • the C 2 . alkenyl group is, for example, an allyl or a methallyl group
  • Preferred compound of the formula II is (RS)-N,N-d ⁇ methyl- ⁇ 2- [4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1-yl]ethoxy ⁇ acetamide
  • the ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ - acetamide of the formula II is prepared by reacting the alkali metal salt of the ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1 - yl] ⁇ ethanol of the formula III with a 2-haloacetam ⁇ de of the formula IV, wherein R-, and R 2 are as defined in connection with formula II, X stands for a halo atom, preferably a chloro atom, in an organic aprotic solvent, and, if desired, converting the obtained base of the formula II to an acid addition salt with an inorganic or organic acid or liberating the base from the acid addition salt thereof
  • the reaction is carried out at a reaction temperature that is not higher than 120 °C, preferably at 60-90 °C
  • the alkali metal salt of the (2-[4-( ⁇ -phenyl-p-chlorobenzyl)- p ⁇ peraz ⁇ n-1-yl] ⁇ ethanol of the formula III is prepared in an indifferent aprotic solvent using an alkali metal hydride, amide or alcoholate, preferably sodium hydride, sodium amide or sodium methylate
  • the indifferent aprotic solvent is an organic aprotic solvent being indifferent from the point of view of the reaction, preferably benzene, toluene, xylene or N,N-d ⁇ methyl- formamide
  • novel ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)p ⁇ peraz ⁇ n-1 -yl]- ethoxyj-acetamides of the formula II are separated from the reaction mixture in a manner known per se
  • the compound of the formula II is subjected to distribution between water and a water-immiscible organic solvent, the phases are separated, and the organic phase containing the compound of the formula II is evaporated
  • the contaminants are removed from the organic solution by adjusting the pH to a value of 6 2-6 7, preferably about 6 4 with an aqueous solution of an inorganic or organic acid, preferably hydrochloric acid, performing the extraction and separating the phases.
  • a further portion of water is added to the organic solution, the pH is adjusted to about 4 by the addition of the aqueous acid, thus, converting the product to the acid addition salt thereof that is dissolved in the aqueous phase
  • the base is liberated with an alkali, preferably an aqueous sodium hydroxide solution and extracted again with a water-immiscible organic solvent, preferably dichloromethane
  • the residue is dissolved in a lower alkanol, preferably isopropanol, and the solution obtained is treated with an alkanol containing hydrogen chloride, preferably
  • the residue is dissolved in cold hydrochloric acid, the water is distilled off under reduced pressure, and, to the residue, a d ⁇ (lower alkyl) ketone, preferably acetone is added to crystallize the dihydrochlo ⁇ de
  • the 2-haloacetam ⁇ des of the formula IV are also known from the literature [W E Weaver and W M Whaley J Amer Chem Soc , 69, 516 (1947), J Kasprzyk et al , J Heterocycl Chem , 30, 1 19 (1993)] and can be easily prepared by the method described in the above references, respectively.
  • Example 2 The procedure described in Example 1 is followed with the difference that the honey-like residue is dissolved in 30 ml of methanol, and, to the solution obtained, 80 ml of methanol containing 27 % of hydrogen chloride are added, then the dihydrochlo ⁇ de is separated as described in Example 1 Thus, 108.9 g (75 6 %) of the title compound are obtained, m.p.: 185-190 °C.
  • Example 1 The phases are separated, the aqueous phase is extracted with 50 ml of toluene The combined toluene solutions are washed with 50 ml of saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, then the procedure described in Example 1 is followed
  • Example 1 The procedure of Example 1 is followed with the difference that the reaction is carried out on a scale of 0 025 moles, the honey-like base (10 3 g, 98 %) is dissolved in 10 ml of isopropanol, to the solution obtained, 2 9 g (0 024 moles) of fuma ⁇ c acid are added, and the mixture is heated until dissolution To the warm solution, 40 ml of ethyl acetate are added and the product is allowed to crystallize After cooling, the crystals are filtered, and washed with ethyl acetate Thus, 11 2 g (84 0 %) of the title compound are obtained, m p 138-141 °C
  • Example 1 The procedure described in Example 1 is followed with the difference that the reaction is performed on a scale of 0 025 moles, and, instead of N,N d ⁇ methyl-2-chloroacetam ⁇ de, 4 11 g (0 0275 moles) of N,N-d ⁇ ethyl-2-chloroacetam ⁇ de are used
  • the honey-like base (9 98 g, 89 9 %) is not converted to the dihydrochlo ⁇ de, but purified by chromatography on a silica gel column that is eluted with chloroform containing 1 -10 % of methanol by continuously enhancing the polarity of the mixture.
  • Example 3 The procedure of Example 3 is followed with the difference that, instead of the N,N-diethyl-2-chloroacetamide, 4.77 g (0.0275 moles) of N,N-diallyl-2-chloroacetamide are employed.
  • the honey-like base (10.5 g, 89 %) obtained at the end of working up the reaction mixture is purified by chromatography on a silica gel column using a mixture of chloroform and 2 % of methanol as the eluent.
  • 9.45 g (80.1 %) of the title compound are obtained as a pale yellow honey-like product.
  • Example 2 The procedure described in Example 1 is followed with the difference that the reaction is performed on a scale of 0 05 moles, and, instead of the N,N-d ⁇ methyl-2-chloroacetam ⁇ de, 8 9 g (0 05 moles) of chloroacetyl morpholide are used.
  • the honeylike base (10 4 g, 45 4 %) obtained at the end of working up the reaction mixture is purified by chromatography on a silica gel column using a mixture of ethyl acetate and 10 % of methanol as the eluent
  • Example 2 The procedure described in Example 1 is followed with the exception that the reaction is performed on a scale of 0 05 moles, and, instead of the N,N-d ⁇ methyl-2-chloroacetam ⁇ de, 13 7 g (0 05 moles) of N,N-d ⁇ benzyl-2-chloroacetam ⁇ de are used.
  • the honey-like base 25 1 g, 88 5 %) obtained at the end of working up the reaction mixture is purified by chromatography on a silica gel column that is eluted with mixtures of ethyl acetate and n-hexane by continuously enhancing the polarity of the mixture
  • 17 0 g (57 %) of the title compound are obtained as a honey-like product
  • v C O 1654 cm "1 pmr (CDCI 3 ) ⁇ 2 35 (b
  • Example 13 The procedure described in Example 13 is followed with the difference that, instead of the (RS)-N,N-d ⁇ methyl- ⁇ 2-[4-( ⁇ - phenyl-p-chloro-benzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetamide dihydrochlo ⁇ de, 83 2 g (0 2 moles) of (RS)-N,N-d ⁇ methyl- ⁇ 2-[4- ( -phenyl-p-chloro-benzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetamide base are used Thus, 75 0 g (81 3 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
  • Example 13 The procedure described in Example 13 is followed with the difference that, instead of the (RS)-N,N-d ⁇ methyl- ⁇ 2-[4-( ⁇ - phenyl-p-chloro-benzyl)p ⁇ peraz ⁇ n-1-yl]ethoxy ⁇ -acetam ⁇ de dihydrochloride, 106 4 g (0 2 moles) of (RS)-N,N-d ⁇ methyl- ⁇ 2- [4-( ⁇ -phenyl-p-chloro-benzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetamide fumarate is used, and, after adjusting the pH of the reaction mixture to 3 8, the precipitated fuma ⁇ c acid is filtered to facilitate the extraction with dichloromethane Thus, 71 8 g (77 8 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
  • Example 14 The procedure described in Example 14 is followed with the difference that, instead of the (RS)-N,N-d ⁇ methyl- ⁇ 2-[4-( ⁇ - phenyl-p-chloro-benzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetamide, 104 4 g (0 2 moles) of (RS)-N,N-d ⁇ ethyl- ⁇ 2-[4-( ⁇ -phenyl-p- chloro-benzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetam ⁇ de are used, 100 ml of dioxane are employed as cosolvent, and, during the alkaline hydrolysis, the reaction mixture is boiled for 4 hours Thus, 69 1 g (74 9 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
  • Example 14 The procedure described in Example 14 is followed with the difference that, instead of the (RS)-N,N-d ⁇ methyI- ⁇ 2-[4-( ⁇ - phenyl-p-chloro-benzyl)p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetam ⁇ de, 107 7 g (0 2 moles) of (RS)- ⁇ 2-[4-( ⁇ -phenyl-p-chlorobenzyl)- p ⁇ peraz ⁇ n-1 -yl]ethoxy ⁇ -acetyl morpholide are used, and the hydrolysis is carried out for 5 hours under boiling Thus, 72 4 g (78 4 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084 Example 19
  • Example 13 The procedure described in Example 13 is followed with the difference that, after the hydrolysis, the reaction mixture is diluted with 3500 ml of water, extracted with 600 ml of ethyl acetate and 200 ml of dnsopropyl ether, the residues of the organic solvents are removed from the aqueous solution under reduced pressure, and the procedure of Example 13 is continued Thus, 68 1 g (73 8 %) of the title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
  • Example 13 The procedure described in Example 13 is followed with the difference that, after the hydrolysis, the reaction mixture is diluted with 3500 ml of water, cooled to 0 °C, the precipitated crystalline cetinzine sodium salt is allowed to sediment for 1 hour, filtered, then dissolved in 1000 ml of water, the pH is adjusted to a value of 3 8 by the addition of hydrochloric acid, then the procedure of Example 13 is continued Thus, 65 7 g (71 2 %) of the title compound are obtained The purity of the product corresponds to the quality requirements given in Eur. Pharm., 3, 1997, 1084.
  • Example 13 The procedure described in Example 13 is followed with the difference that the hydrolysis is carried out with 170 ml (2.0 moles) of concentrated hydrochloric acid, and, at the end of the hydrolysis, the pH of the reaction mixture is adjusted to the desired value of 3.8 with about 270 ml of 40 % aqueous sodium hydroxide solution. Thus, 70.6 g (76.5 %) of the title compound are obtained, m.p.: 225-228 °C. The purity of the product corresponds to the quality requirements given in Eur. Pharm., 3, 1997, 1084.
  • Example 13 The procedure described in Example 13 is followed with the difference that the hydrolysis is carried out with 170 ml (0.9 moles) of 50 % sulfuric acid, and, at the end of the hydrolysis, the pH of the reaction mixture is adjusted to the desired value of 3.8 with about 260 ml of 40 % aqueous sodium hydroxide solution. Thus, 67.3 g (72.9 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
  • Example 13 The procedure described in Example 13 is followed with the difference that, in addition to the aqueous sodium hydroxide solution, also 2 g of Aliquat 336 (t ⁇ octylmethyl ammonium chloride) are added to the reaction mixture Thus, 74 9 g (81 2 %) of the title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
  • Example 25 The procedure described in Example 13 is followed with the difference that, in addition to the aqueous sodium hydroxide solution, also 1 g of 15-crown-5 (1 ,4,7, 10,13-pe ⁇ taoxacyclo- pentadecane) is added to the reaction mixture. Thus, 76 1 g (82 5 %) of the title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084 Example 25
  • Example 13 The procedure described in Example 13 is followed with the difference that the hydrolysis is carried out with 280 ml of 40 % aqueous potassium hydroxide solution. Thus, 75.0 g (81.3 %) of the title compound are obtained, m.p.: 226-228 °C. The purity of the product corresponds to the quality requirements given in Eur. Pharm., 3, 1997, 1084.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

The invention refers to a novel process for the preparation of cetirizine of formula (I) as well as to novel {2-[4-(α-phenyl-p-chloro-benzyl)piperazin-1-yl]ethoxy}acetamides of formula II, wherein R1 and R2 represent, independently, a C1-4 alkyl group optionally substituted by a phenyl group, a C2-4 alkenyl group or a cyclohexyl group, or R1 and R2 form together with the adjacent nitrogen atom a morpholino group. According to the novel process, an acetamide of formula (II) is hydrolized, if desired in the presence of a phase transfer catalyst, to obtain cetirizine.

Description

A PROCESS FOR THE PREPARATION OF {2-[4-(α-PHENYL- p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY} ACETIC ACID
AND NOVEL INTERMEDIATES THEREFOR
Field of the invention
The invention refers to a novel process for the preparation of {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]ethoxy} acetic acid of the formula
Figure imgf000002_0001
{2-[4-( -Phenyl-p-chlorobenzyl)pιperazιn-1 -yl]ethoxy} acetic acid is known under the international non-propnetory name cetinzine that is widely used as the ingredient of antiallergic pharmaceutical compositions
The invention also refers to novel {2-[4-(α-phenyl-p-chloro- beπzyl)pιperazιn-1 -yl]ethoxy}acetamιdes of the formula
Figure imgf000003_0001
wherein
R*ι and R2 represent, independently, a Cι-4 alkyl group optionally substituted by a phenyl group, a C2.4 alkenyl group or a cyclohexyl group, or
R-! and R2 form together with the adjacent nitrogen atom a morphohno group, and acid addition salts thereof which are useful intermediates in the synthesis of cetiπzine
Background of the invention
Several methods are known for the preparation of cetiπzine of the formula I According to European Patent Application No 58, 146 (Chem Abstr , 98, 34599r), an ester or an amide of the formula
Figure imgf000003_0002
wherein Y stands for a group of the formula -OR1 or an ammo group, wherein R1 means an alkyl group, is hydrolized to obtain the compound of the formula I
Starting from the methyl ester of the formula V, after hydrolysis with potassium hydroxide, the potassium salt of cetiπzine is obtained in a yield of 59 % From the potassium salt the corresponding acid is formed in a yield of 81 %, and the desired dihydrochloπde of cetiπziπe is obtained in a yield of 80 % Thus, the total yield of the known process amounts to 38 2 % A rather great drawback of the known process consists in the fact that the esters of the formula V used as the starting compound can be prepared only with difficulties and in a poor yield Thus, the 1 -[(4-chloro-phenyl)phenylmethyl]pιperazιne of the formula
Figure imgf000004_0001
is reacted with methyl 2-chloroethoxyacetate of the formula
^^ o COOMe VII
Cl ^^ ^-^
to obtain the corresponding methyl ester of the formula V - after chromatography - in a yield of as low as 10 6 %
In the European Patent Application referred to above the possibility is mentioned that cetiπzine can be prepared also from the acetic amide of the formula V, wherein Y stands for an ammo group, by hydrolysis However, neither any Example, nor yield data are given for the hydrolysis of the acetic amide of the formula V According to a later communication (Synthesis, 1995, 766), the acetamide of the formula V is hydrolized in hydrochloric acid at 50 °C to obtain cetiπzine in a yield of 71 %
Even three methods are known for the preparation of the acetamide of the formula V For example, the 1 -[(4-chloro- phenyl)phenylmethyl]-pιperazιne of the formula VI is reacted with 2-chloroethoxy-acetamιde of the formula
Figure imgf000005_0001
in the presence of an acid binding agent to obtain the acetamide of the formula V in a yield of 47 % According to a second method, the {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn- 1 -yl]}ethanol of the formula
Figure imgf000005_0002
is converted to the sodium salt with sodium hydride, and the salt is reacted with a chloroacetamide of the formula
Figure imgf000006_0001
wherein X represents a chloro atom, R-j and R2 stand for a hydrogen atom However, the yield of the reaction is merely 1 1 % According to the third method, the acetamide of the formula V can be also prepared from the corresponding methyl ester of the formula V, wherein Y means a methoxy group, by reaction with ammonia in a yield of 54 % Taking into consideration the low yield (27 8 %) of the preparation of the methyl ester, the total yield is as low as 15 0 % Consequently, the latter known synthesis of cetiπzine is uneconomical, too
The process of UK-P No 2 225 320 (Chem Abstr , 1 13, 191395s) aims at the elimination of the disadvantages of the above known processes by preparing cetiπzine from the {2-[4- (α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]}ethanol of the formula III which is converted to the potassium salt with potassium tert - butylate The potassium salt is reacted with sodium chloro- acetate to obtain cetiπzine dihydrochloπde in a yield of 48 8 % In addition, 5 1 % of a second generation product are obtained Also an improved process is described for the preparation of the {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]}ethanol of the formula III according to which 1 -[(4-chlorophenyl)phenyl- methyl]pιperazιne of the formula VI is reacted with ethylene chlorohydπne in a yield of 90 4 %, the total yield of the synthesis, referred to the piperaz e derivative of the formula VI, is merely 48 7 %
The latter known process has a further drawback The reaction of the ethanol derivative of the formula III with sodium chloro- acetate can be carried out in a relatively acceptable yield if the reactants are added in several portions to the solution of the ethanol derivative of the formula III The addition of the reactants is to be programmed on the basis of a continuous monitoring of the composition of the reaction mixture This technology is rather awkward, especially on industrial scale
The latter known process is tried to be improved by the method described in PL-P No 163415 (Chem Abstr , 123, 55923s) according to which the reaction is performed in a system consisting of two phases, in the presence of an indifferent organic solvent and aqueous sodium hydroxide solution to obtain cetiπzine dihydrochloπde in a yield of 60 % Although this method is less complicated than the one known from UK-P No 2 225 320, the total yield amounts to only 54 % as calculated for the ethanol derivative of the formula III that can be prepared in the most favourable way
A further method for the preparation of cetiπzine is known from UK-P No 2 225 321 (Chem Abstr , 113, 191396t) according to which the the 1-[(4-chloro-phenyl)phenylmethyl]-pιperazιne of the formula VI is reacted with chloroethoxyacetonitπle to obtain the nitπle derivative of the formula
Figure imgf000008_0001
that is hydrolized in acidic or alkaline medium to cetiπzin In this way, cetiπzin dihydrochloπde is obtained from the nitπie derivative of the formula IX in a total yield of 60 5 % in case of the acidic hydrolysis, and in a total yield of 65 6 % in case of the alkaline hydrolysis
However, the reaction of 1 -[(4-chlorophenyl)phenylmethyl]- piperazine of the formula VI with chloroethoxyacetonitπle produces the nitπle derivative in a yield of 86 4 % thereby reducing the total yield of the synthesis to 52 2 % and 56 6 %, respectively
It should be also taken into consideration that, according to the literature [E J Salmi, R Leimu and H Kallio, Suomen Kemistilehti, 17B, 17-19 (1944)], chloroethoxy-acetonitπle can be prepared from ethylene chlorohydπn in two steps using the very poisonous copper(l) cyanide in a total yield of 58 %
Finally, a simple method of preparation is aimed by the process known from published European Patent Application No 801 ,064 according to which cetiπzine is prepared from 1 -[(4- chlorophenyl)phenylmethyl]-pιperazιne of the formula VI with 2- chloroethoxyacetic acid in an indifferent solvent in the presence of an acid binding agent The publication has only one example that does not contain either yield or quality data for the product Furthermore, a great drawback of this method consists in the unavailability of 2-chloroethoxyacetιc acid on an industrial scale
The aim of the invention is to provide an economical process for the preparation of cetiπzine that satisfies the most severe quality requirements
Summary of the invention
It has been found that the above aim is achieved if, in the process for the preparation of {2-[4-(α-phenyl-p- chlorobenzyl)pιperazιn-1 -yl]ethoxy}acetιc acid of the formula I or a pharmaceutically suitable acid addition salt or metal salt thereof through hydrolyzing a corresponding acetamide in alkaline or acidic medium, and, if desired, converting the product formed to an acid addition salt or metal salt and/or liberating the base from the acid addition salt or metal salt, a compound of the formula II or an acid addition salt thereof is used as the acetamide, and, if desired, the hydrolysis is carried out in the presence of a phase transfer catalyst
The invention includes the {2-[4-(α-phenyl-p-chlorobenzyl)- pιperazιn-1 -yl]ethoxy}-acetamιdes of the formula II that are novel compounds
Description of the preferred embodiments
In the process of the invention, the starting compound is an acetamide of the formula II or an acid addition salt thereof formed with an inorganic or an organic acid, and the starting compound is subjected to alkaline or acidic hydrolysis in a manner known per se, if, desired, in the presence of a phase transfer catalyst
If desired, the product formed is converted to a pharmaceutically suitable acid addition salt or metal salt and/or the base is liberated from the acid addition salt or metal salt thereof in a manner known per se
The hydrolysis of the {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn- 1 -yl]ethoxy}-acetamιdes of the formula II takes place surprisingly fast and completely, without the formation of byproducts, in 1 -8 hours depending on the character of R-i and R2 From the reaction mixture, cetiπzine or the dihydrochloπde thereof can be simply separated in a very pure form that satisfies the extremely severe HPLC quality requirements of European Pharmacopoeia, 3, (1997) at 1084
For the expert it is surprising that the hydrolysis of the {2-[4-(α- phenyl-p-chlorobenzyl)pιperazιn-1 -yl]ethoxy }-acetamιdes of the formula II proceeds so fast since it is known from the literature that dialkyl acetamides are stable compounds, the hydrolysis of which takes place slowly and requires strong reaction conditions For example, N,N,N',N'-tetraethyl-5,5-dιmethyl-3,7- dioxanone diamide was hydrolized in 3 N aqueous sodium hydroxide under boiling for 5 days to obtain the corresponding dicarboxylic acid in a yield of 91 5 % [J Chem Soc Perkin Trans I , 1981 , 741-745, Chem Abstr , 95, 42286q (1981)] However, after boiling for 5 days, only 39 8 % of the corresponding N,N,N',N'-tetramethyl derivative was converted to the corresponding dicarboxylic acid that was separated as the methyl ester Moreover, when, for example, the threo- 10,11-dιhydroxy-N,N-dιmethyl-nonadecaneamιde was boiled in ethanol with 2 N aqueous sodium hydroxide solution for 1 hour, no decomposition was experienced to form the corresponding carboxylic acid [J Chem Soc , 1961 , 351 -356, Chem Abstr , 55, 12276g (1961)] This is the cause of the practice according to which carboxylic amides are hydrolized to carboxylic acid with a concentrated alkali or rather in a concentrated acidic medium in the presence of nitrites [Houben-Weyl Methoden der Organischen Chemie, Vol 8, 432, A R Katπtzky et al , Comprehensive Organic Functional Group Transformations, Vol 5, 34-36 (1995)]
Preferably, N,N-dιmethyl-{2-[4-(α-phenyl-p-chlorobenzyl)- pιperazιn-1 -yl]-ethoxy} acetamide is used as the acetamide of the formula II According to a preferred method of the invention, the hydrolysis of the {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]ethoxy}- acetamides of the formula II is carried out in an aqueous solution of an alkali metal hydroxide, preferably sodium or potassium hydroxide, wherein the concentration of the alkali in the solution amounts to 2-25 % by mass, preferably 6-16 % by mass, suitably about 12 % by mass, generally at 40-110 °C, preferably at 70-110 °C, suitably at the boiling point of the solution After the alkaline hydrolysis, the product is separated as follows the reaction mixture is diluted with water, acidified with hydrochloric acid to a pH value of 3 8-4 0, the cetiπzin base is dissolved in an organic solvent being immiscible with water, preferably dichloromethane, the organic solution is evaporated to dryness under reduced pressure, and the remaining honey-like residue is dissolved in 5-36 %, preferably 10-20 %, suitably about 16 % hydrochloric acid Then, a water- miscible organic solvent, preferably acetone, methyl ethyl ketone or tetrahydrofuran is added to the solution to crystallize the dihydrochloπde, or the hydrochloric acidic solution is concentrated under reduced pressure until a water content of 20-25 % by mass, and the above water-miscible organic solvent is added to the concentrated solution, and the honeylike cetiπzine dihydrochloπde is recrystallized
A further possibility is that - after the hydrolysis and adjustment of the pH value to 3 8-4 0 - the solution of cetiπzine base in dichloromethane is extracted with preferably 5-30 % hydrochloric acid, the aqueous solution is concentrated under reduced pressure to reduce the water content to 20-25 % by mass and then the procedure described above is followed to obtain cetinzine dihydrochloπde
The honey-like residue obtained after the evaporation of the solution of cetinzine base in dichloromethane can be dissolved in a water-miscible organic solvent, preferably acetone, methyl ethyl ketone or tetrahydrofuran, and then the thus-obtained solution of the cetinzine base in the organic solvent is treated with the hydrochloric acid The acidic solution is worked up by any of the procedure described above to obtain cetinzine dihydrochloπde
According to a further preferred method of the invention, the hydrolysis of the acetic amide of the formula II is carried out with an aqueous solution of an inorganic acid, preferably hydrochloric acid or sulfuπc acid at 40-110 °C, preferably 70- 110 °C, suitably at the boiling point of the solution In general, a 2-25 % by mass, preferably 10-20 % by mass, suitably about 15 % by mass solution of the inorganic acid is employed To separate the product, the acidic hydrolysate obtained is diluted with water, the pH is adjusted to a value of 3 8-4 0 by the addition of aqueous sodium hydroxide solution, and then the procedure described in connection with the alkaline hydrolysis is followed
Either the alkaline or the acidic hydrolysis can be performed in the presence of a phase transfer catalyst, and, if desired, also a cosolvent As the phase transfer catalyst a tetraalkyl- ammonium halide, preferably tetrabutylammonium chloride, tπethylbenzylammonium chloride or tπoctylmethylammonium chloride (Aliquat 336) or a crown ether, preferably 15-crown-5 or 18-crown-6 can be used The cosolvent can be an organic solvent being miscible with water such as ethanol, butanol, ethylene glycol or dioxane
If, in the process of the invention, an acid addition salt of the acetamide of the formula II prepared with an organic acid is used as the starting compound, this organic acid crystallizes from the reaction mixture after the precipitation of the product with an acid In this case the precipitated organic acid can be separated by filtration before the extraction of the product with dichloromethane to achieve an easier separation of the phases However, the reaction mixture can be worked up without the separation of the organic acid, too
Thus, the process of the invention is economical, can be easily carried out and provides cetinzine or the acid addition salt thereof in a very pure form
A second aspect of the invention refers to the novel intermediates of the formula II, wherein R- and R2 are as defined above, and acid addition salts thereof formed with inorganic or organic acids The invention includes the isomers of the {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]ethoxy}- acetamides of the formula II and mixtures thereof
In formula II, in the definition of R-, and R2, the C1-4 alkyl group optionally substituted by a phenyl group may have a straight or branched chain such as a methyl, ethyl, isopropyl, tert -butyl or benzyl group etc The C2. alkenyl group is, for example, an allyl or a methallyl group
Preferred compound of the formula II is (RS)-N,N-dιmethyl-{2- [4-(α-phenyl-p-chlorobenzyl)pιperazιn-1-yl]ethoxy} acetamide
The {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]ethoxy}- acetamide of the formula II is prepared by reacting the alkali metal salt of the {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 - yl]}ethanol of the formula III with a 2-haloacetamιde of the formula IV, wherein R-, and R2 are as defined in connection with formula II, X stands for a halo atom, preferably a chloro atom, in an organic aprotic solvent, and, if desired, converting the obtained base of the formula II to an acid addition salt with an inorganic or organic acid or liberating the base from the acid addition salt thereof
The reaction is carried out at a reaction temperature that is not higher than 120 °C, preferably at 60-90 °C
The alkali metal salt of the (2-[4-(α-phenyl-p-chlorobenzyl)- pιperazιn-1-yl]}ethanol of the formula III is prepared in an indifferent aprotic solvent using an alkali metal hydride, amide or alcoholate, preferably sodium hydride, sodium amide or sodium methylate The indifferent aprotic solvent is an organic aprotic solvent being indifferent from the point of view of the reaction, preferably benzene, toluene, xylene or N,N-dιmethyl- formamide
The novel {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]- ethoxyj-acetamides of the formula II are separated from the reaction mixture in a manner known per se According to a preferred method, the compound of the formula II is subjected to distribution between water and a water-immiscible organic solvent, the phases are separated, and the organic phase containing the compound of the formula II is evaporated
According to an especially preferred method of separation, during the above distribution of the compound of the formula II between water and a water-immiscible organic solvent the contaminants are removed from the organic solution by adjusting the pH to a value of 6 2-6 7, preferably about 6 4 with an aqueous solution of an inorganic or organic acid, preferably hydrochloric acid, performing the extraction and separating the phases Then a further portion of water is added to the organic solution, the pH is adjusted to about 4 by the addition of the aqueous acid, thus, converting the product to the acid addition salt thereof that is dissolved in the aqueous phase After the separation of the phases, the base is liberated with an alkali, preferably an aqueous sodium hydroxide solution and extracted again with a water-immiscible organic solvent, preferably dichloromethane After the evaporation of the solution, the residue is dissolved in a lower alkanol, preferably isopropanol, and the solution obtained is treated with an alkanol containing hydrogen chloride, preferably isopropanol containing hydrogen chloride to obtain the dihydrochloπde that is precipitated in crystalline form by the addition of a solvent that does not dissolve the product, preferably a dι(lower alkyl) ketone, suitably acetone
According to another preferred separation method of the dihydrochloπde of the acetamide of the formula II, after the evaporation of the solution of the base in an organic solvent, the residue is dissolved in cold hydrochloric acid, the water is distilled off under reduced pressure, and, to the residue, a dι(lower alkyl) ketone, preferably acetone is added to crystallize the dihydrochloπde
Thus, the acetamide of the formula II is obtained in a very pure form that is suitable for the preparation of pure cetinzine
The {2-[4-(α-phenyl-p-chlorobenzyl)pιperazιn-1 -yl]} ethanol of the formula III used as the starting compound for the preparation of the acetamide of the formula II has been known in the literature for a long time [H Morren et al , Belg Chem Industrie, XIX, 1176-1185 (1954), Chem Abstr , 53, 2240e (1959)] For the preparation of very pure cetinzine it is especially preferred to use (2-[4-(α-phenyl-p-chlorobenzyl)- pιperazιn-1 -yl]}ethanol dihydrochloπde monohydrate [m p 196-205 °C (under decomposition), water content (according to Karl Fischer) 4 6 %]
The 2-haloacetamιdes of the formula IV are also known from the literature [W E Weaver and W M Whaley J Amer Chem Soc , 69, 516 (1947), J Kasprzyk et al , J Heterocycl Chem , 30, 1 19 (1993)] and can be easily prepared by the method described in the above references, respectively.
The invention is further elucidated by the following Examples
Preparation of the {2-[4-(α-phenyl-p-chloro-benzyl)- piperazin-1 -yl]ethoxy}acetamides of the formula II
Example 1
(RS)-N,N-Dιmethyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1 -yl]ethoxy}-acetamιde dihydrochloπde
To a solution of 99 3 g (0 3 moles) of (RS)-{2-[4-(α-phenyl-p- chloro-benzyl)pιperazιn-1 -yl]}ethanol in 500 ml of toluene, 25 8 g (0 33 moles) of 50 % sodium amide suspension in toluene are added at 25 °C under nitrogen stream The reaction mixture is placed into an oil bath heated to 105 °C and reacted for 3 hours During the reaction, the inner temperature of the reaction mixture remains 80-85 °C Then the reaction mixture is cooled to 40 °C, 40 1 g (0.33 moles) of N,N-dιmethyl-2-chloro- acetamide are added to it, drop by drop, and stirred at 50 °C for further 2 hours 120 g of crushed ice are added to the reaction mixture, and the pH is adjusted to 6 4 by the addition of 8 ml of concentrated hydrochloric acid The phases are separated, 150 ml of water are added to the toluene phase, and the pH of the mixture is adjusted to 4 by the addition of about 21 ml of concentrated hydrochloric acid The aqueous phase is separated, 300 ml of dichloromethane are added to it, and the pH is adjusted to a value between 7-8 by the addition of about 28 ml (0 28 moles) of 40 % aqueous sodium hydroxide solution The organic phase is separated, extracted with 40 ml of saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure The honey-like residue (124 g, 99 %) is dissolved in 50 ml of isopropanol, and, to the solution obtained, 90 ml of isopropanol containing 25 % by mass of hydrogen chloride are added, drop by drop, at room temperature under stirring To the reaction mixture, 1000 ml of acetone are added under vigorous stirring, and the mixture is stirred for a further hour The precipitated crystals are filtered, washed 3 times using 50 ml of acetone each time, then with 100 ml of dusopropyl ether
Thus, 120 g (81 8 %) of (RS)-N,N-dιmethyl-{2-[4-(α-phenyl-p- chloro-benzyl)pιperazιn-1 -yl]ethoxy } -acetamide dihydro- chloπde are obtained, m p 182-190 °C The spectral data of the base ιr (KBr) v C=O 1658 cm"1 pmr (CDCI3) δ ppm 2 41 (bs, 4H, piperazine 3,5-NCH2), 2 53 (t,
J=5 8 Hz, 4H, piperazine 2,6-NCH2), 2 62 (t, J=7 0 Hz, 2H, ethoxy NCH2), 2 92 and 2 98 (double s, 2x3H, NCH3), 3 63 (t,
J=7 0 Hz, 2H, ethoxy OCH2), 4 14 (s, 2H, COCH2), 4 20 (s, 1 H,
CH), 7 15-7 37 (m, 9H, ArH)
Example 2
(RS)-N,N-Dιmethyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1 -yl]ethoxy }-acetamιde dihydrochloπde
The procedure described in Example 1 is followed with the difference that the honey-like residue of the base is dissolved in 100 ml of 20 % hydrochloric acid, the solution obtained is concentrated at 10-20 °C under reduced pressure until the water content is reduced to about 5 %, the residue is dissolved in 100 ml of isopropanol, to the solution obtained, 1000 ml of acetone are added, and again the procedure of Example 1 is followed Thus, 1 10 g =76 4 %) of the title compound are obtained, m p 184-189 °C
Example 3
(RS)-N,N-Dιmethyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1 -yl]ethoxy}-acetamιde dihydrochloπde
The procedure described in Example 1 is followed with the difference that the honey-like residue is dissolved in 30 ml of methanol, and, to the solution obtained, 80 ml of methanol containing 27 % of hydrogen chloride are added, then the dihydrochloπde is separated as described in Example 1 Thus, 108.9 g (75 6 %) of the title compound are obtained, m.p.: 185-190 °C.
Example 4
(RS)-N,N-Dιmethyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1 -yl]ethoxy}-acetamιde dihydrochloπde
126.8 g (0.3 moles) of (RS)-{2-[4-(α-phenyl-p-chloro-benzyl)- pιperazin-1 -yl]}ethanol dihydrochloride monohydrate are dissolved in 300 ml of water, and, to the solution obtained, 100 g of crushed ice are added. To the solution obtained, 200 ml of toluene are added, and the pH is adjusted to 8 by the addition of about 60 ml of 40 % by mass aqueous sodium hydroxide solution. The phases are separated, the aqueous phase is extracted with 50 ml of toluene The combined toluene solutions are washed with 50 ml of saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, then the procedure described in Example 1 is followed
Thus, 129.2 g (88 1 %) of the title compound are obtained, m.p : 185-190 °C Purity above 99 6 % as determined by HPLC Example 5
(RS)-N,N-Dιmethyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1-yl]ethoxy} -acetamide fumarate
The procedure of Example 1 is followed with the difference that the reaction is carried out on a scale of 0 025 moles, the honey-like base (10 3 g, 98 %) is dissolved in 10 ml of isopropanol, to the solution obtained, 2 9 g (0 024 moles) of fumaπc acid are added, and the mixture is heated until dissolution To the warm solution, 40 ml of ethyl acetate are added and the product is allowed to crystallize After cooling, the crystals are filtered, and washed with ethyl acetate Thus, 11 2 g (84 0 %) of the title compound are obtained, m p 138-141 °C
Example 6
(RS)-N,N-Dιethyl-{2-[4-(α-phenyl-p-chloro-beπzyl)pιperazιn-1- yl]ethoxy}-acetamιde
The procedure described in Example 1 is followed with the difference that the reaction is performed on a scale of 0 025 moles, and, instead of N,N dιmethyl-2-chloroacetamιde, 4 11 g (0 0275 moles) of N,N-dιethyl-2-chloroacetamιde are used In working up the reaction mixture, the honey-like base (9 98 g, 89 9 %) is not converted to the dihydrochloπde, but purified by chromatography on a silica gel column that is eluted with chloroform containing 1 -10 % of methanol by continuously enhancing the polarity of the mixture.
Thus, 9.16 g (82.5 %) of the title compound are obtained as a pale yellow honey-like product. Rf=0.45 (Kieselgel Merck plate, chloroform: methanol = 9:1). ir (Kbr): v C=O 1646 cm"1. pmr (CDCI3): δ ppm 1.10 and 1.15 (double t, J=7.0 Hz, 2x3H, CH3), 2.42 (bs, 4H, piperazine 3,5-NCH2), 2.54 (bs, 4H, piperazine 2,6-NCH2), 3.30 and 3.33 (double m, 2x2H, ethyl NCH2), 3.65 (t, J=5.9 Hz, 2H, ethoxy OCH2), 4.14 (s, 2H, COCH2), 4.20 (s, 1 H, CH), 7.17-7.37 (m, 9H, ArH).
Example 7
(RS)-N,N-Diallyl-{2-[4-(α-phenyl-p-chloro-benzyl)piperazin-1- yl]ethoxy} -acetamide
The procedure of Example 3 is followed with the difference that, instead of the N,N-diethyl-2-chloroacetamide, 4.77 g (0.0275 moles) of N,N-diallyl-2-chloroacetamide are employed. The honey-like base (10.5 g, 89 %) obtained at the end of working up the reaction mixture is purified by chromatography on a silica gel column using a mixture of chloroform and 2 % of methanol as the eluent. Thus, 9.45 g (80.1 %) of the title compound are obtained as a pale yellow honey-like product. Rf = 0.5 (Kieselgel Merck plate, chloroform: methanol = 9:1). ir (KBr): v C=O 1657 cm"1, pmr (CDCI3): δ 2.42 (bs, 4H, piperazine 3,5-NCH2), 2.53 (bs, 4H, piperazine 2,6-NCH2), 2 62 (t, J=5 8 Hz), 2H, ethoxy NCH2),
3 65 (t, J=5 8 Hz, 2H, ethoxy OCH2), 3 86 (t, J=5 8 Hz), 2H, NCH2), 3 96 (t, J=5 8 Hz), 2H, NCH2), 4 15 (s, 2H, COCH2),
4 20 (s, 1 H, CH), 5 16 (m, 4H, CCH2), 5 72 (m, 2H, CH), 7 17- 7 38 (m, 9H, ArH)
Example 8
(RS)-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy}- acetyl morpholide
The procedure described in Example 1 is followed with the difference that the reaction is performed on a scale of 0 05 moles, and, instead of the N,N-dιmethyl-2-chloroacetamιde, 8 9 g (0 05 moles) of chloroacetyl morpholide are used The honeylike base (10 4 g, 45 4 %) obtained at the end of working up the reaction mixture is purified by chromatography on a silica gel column using a mixture of ethyl acetate and 10 % of methanol as the eluent
Thus, 8 3 g (36 2 %) of the title compound are obtained as an oily product Rf = 0 35 (Kieselgel Merck plate, chloroform methanol = 9 1) ιr (KBr) v C=O 1655 cm pmr (CDCI3) δ 2 41 (bs, 4H, piperazine 3,5-NCH2), 2 53 (bs,
4H, piperazine 2,6-NCH2), 2 61 (t, J=5 6 Hz, 2H, ethoxy NCH2),
3 50 (m, 4H, morpholino NCH2), 3 57 (m, 4H, morpholino
OCH2), 3 62 (t, J=5 6 Hz, 2H, ethoxy OCH2), 4 13 (s, 2H, COCH2), 4 20 (s, 1 H, CH), 7 16-7 36 (m, 9H, ArH) ms (CI) (M+1)+ = 458
Example 9
(RS)-N,N-Dιcyclohexyl-{2-[4-(α-phenyl-p-chloro-benzyl)- pιperazιπ-1 -yl]ethoxy}-acetamιde
The procedure described in Example 1 is followed with the difference that the reaction is carried out on a scale of 0 02 moles, and, instead of the N,N-dιmethyl-2-chloroacetamιde, 5 2 g (0 02 moles) of N,N-dιcyclohexyl-2-chloroacetamιde is used Thus, 9 8 g (88 9 %) of the title compound are obtained as an honey-like product Purity 99 % as determined by HPLC ιr (KBr) v C=O 1656 cm 1 pmr (CDCI3) δ 1 23 (m, 4H, cyclohexyl 4-CH2), 1 46-1 78 (m, 16H, cyclohexyl 2,3,5, 6-CH2), 2 45 (bs, 4H, piperazine 3,5- NCH2), 2 59 (bs, 4H, piperazine 2,6-NCH2), 2 67 (m, 2H, ethoxy NCH2), 3 48 (m, 2H, cyclohexyl CH), 3 67 (m, 2H, ethoxy OCH2), 4 08 (s, 2H, COCH2), 4 21 (s, 1 H, CH), 7 17-7 36 (m, 9H, ArH)
Example 10
(RS)-N,N-Dιcyclohexyl-{2-[4-(α-phenyl-p-chloro- benzyl)pιperazιn-1 -yl]ethoxy }-acetamιde dimaleinate
1 1 g of the honey-like base obtained as described in Example 9 are dissolved in 3 ml of isopropanol, to the solution obtained, a solution of 0 23 g of maleic acid in 2 ml of isopropanol are added at room temperature, and the reaction mixture is stirred at room temperature for 14 hours The crystals precipitated are filtered, and washed with some isopropanol
Thus, 0 81 g (60 8 /) of the title product are obtained, m p 149-152 °C Purity 99 6 % as determined by HPLC
Example 1 1
(RS)-N,N-Dιbenzyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1 -yl]ethoxy} -acetamide
The procedure described in Example 1 is followed with the exception that the reaction is performed on a scale of 0 05 moles, and, instead of the N,N-dιmethyl-2-chloroacetamιde, 13 7 g (0 05 moles) of N,N-dιbenzyl-2-chloroacetamιde are used The honey-like base (25 1 g, 88 5 %) obtained at the end of working up the reaction mixture is purified by chromatography on a silica gel column that is eluted with mixtures of ethyl acetate and n-hexane by continuously enhancing the polarity of the mixture Thus, 17 0 g (57 %) of the title compound are obtained as a honey-like product Rf = 0 7 (Kieselgel Merck plate, ethyl acetate methanol = 1 1 ) ιr (KBr) v C=O 1654 cm"1 pmr (CDCI3) δ 2 35 (bs, 4H, piperazine 3,5-NCH2), 2 49 (bs, 4H, piperazine 2,6-NCH2), 2 59 (t, J=5 5 Hz, 2H, ethoxy NCH2), 3 68 (t, J=5 5 Hz, 2H, ethoxy OCH2), 4 16 (s, 1 H, CH), 4 25 (s, 2H, COCH2), 4 43 (s, 2H, PhCH2), 4 55 (s, 2H, PhCH2), 7 16- 7 37 (m, 9H, ArH)
Example 12
(RS)-N,N-Dιmethyl-{2-[4-(α-phenyl-p-chloro-benzyl)pιperazιn- 1 -yl]ethoxy}-acetamιde dihydrochloπde
To a solution of 99 3 g (0 3 moles) of (RS)-{2-[4-(α-phenyl-p- chloro-benzyl)pιperazιn-1 -yl]}ethanol in 500 ml of toluene, 17 8 g (0 33 moles) of sodium methylate are added at 25 °C under vigorous stirring and nitrogen stream The reaction mixture is heated to boiling and 200 ml of solvent are distilled off, then 500 ml of absolute toluene are added at the same rate as the distillation proceeds, thus, maintaining the volume of the reaction mixture between 250-350 ml At the end of the addition of the toluene, no methanol can be detected in the distillate Heating of the reaction mixture is stopped, 200 ml of absolute toluene are added, the temperature of the mixture is adjusted to 40 °C and 40 1 g (0 33 moles) of N,N-dιmethyl-2-chloro- acetamide are added, drop by drop, and the reaction mixture is stirred at 50 °C for further 2 hours The reaction mixture is worked up as described in Example 1
Thus, 120 g (81 8 %) of (RS)-N,N-dιmethyl-{2-[4-(α-phenyl-p- chloro-benzyl)pιperazιn-1 -yl]ethoxy }-acetamιde dihydrochloπde are obtained the purity of which is identical with that of the product of Example 1
Preparation of the {2-[4-(α-phenyl-p-chlorobenzyl)- piperazin-1-yl]ethoxy} acetic acid of the formula I
Example 13
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1 -yl]ethoxy}- acetic acid dihydrochloπde
To a solution of 97 8 g (0 2 moles) of (RS)-N,N-dιmethyl-{2-[4- (α-phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy} -acetamide dihydrochloπde in 340 ml of water, a solution of 80 g (2 0 moles) of sodium hydroxide in 200 ml of water is added under stirring, and the suspension is boiled for 2 5 hours while nitrogen stream is bubbled through it The reaction mixture is allowed to cool to 40 °C, diluted with 500 ml of water, made acidic until a pH of 3 8 by the addition of 120 ml of concentrated hydrochloric acid, and extracted with 400 ml of dichloromethane, then with 200 ml of dichloromethane The combined organic phases are evaporated under reduced pressure, the residue is dissolved in 50 ml of water, acidified by the addition of 24 ml of concentrated hydrochloric acid, and evaporated to dryness under reduced pressure The thick oily residue is dissolved in 50 ml of acetone, to the solution obtained further 550 ml of acetone are added, and the mixture is stirred for 1 hour The precipitated crystalline product is filtered, washed with acetone, then with diethyl ether, and dried under reduced pressure
Thus, 74 3 g (80 5 %) of the pure title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 14
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1 -yl]ethoxy}- acetic acid dihydrochloπde
The procedure described in Example 13 is followed with the difference that, instead of the (RS)-N,N-dιmethyl-{2-[4-(α- phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy} -acetamide dihydrochloπde, 83 2 g (0 2 moles) of (RS)-N,N-dιmethyl-{2-[4- ( -phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy} -acetamide base are used Thus, 75 0 g (81 3 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 15
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιπ-1-yl]ethoxy}- acetic acid dihydrochloπde
The procedure described in Example 13 is followed with the difference that, instead of the (RS)-N,N-dιmethyl-{2-[4-(α- phenyl-p-chloro-benzyl)pιperazιn-1-yl]ethoxy}-acetamιde dihydrochloride, 106 4 g (0 2 moles) of (RS)-N,N-dιmethyl-{2- [4-(α-phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy} -acetamide fumarate is used, and, after adjusting the pH of the reaction mixture to 3 8, the precipitated fumaπc acid is filtered to facilitate the extraction with dichloromethane Thus, 71 8 g (77 8 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 16
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1 -yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 14 is followed with the difference that, instead of the (RS)-N,N-dιmethyl-{2-[4-(α- phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy} -acetamide, 104 4 g (0 2 moles) of (RS)-N,N-dιethyl-{2-[4-(α-phenyl-p- chloro-benzyl)pιperazιn-1 -yl]ethoxy}-acetamιde are used, 100 ml of dioxane are employed as cosolvent, and, during the alkaline hydrolysis, the reaction mixture is boiled for 4 hours Thus, 69 1 g (74 9 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 17
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1 -yl]ethoxy}- acetic acid dihydrocnloπde The procedure described in Example 14 is followed with the difference that, instead of the (RS)-N,N-dιmethyl-{2-[4-(α- phenyl-p-chloro-benzyl)pιperazιn-1-yl]ethoxy} -acetamide, 110 0 g (0 2 moles) of (RS)-N,N-dιallyl-{2-[4-(α-phenyl-p- chloro-benzyl)pιperazιn-1-yl]ethoxy} -acetamide are used, 100 ml of dioxane are employed as cosolvent, and, during the alkaline hydrolysis, the reaction mixture is boiled for 10 hours Thus, 64 0 g (69 3 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 18
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1-yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 14 is followed with the difference that, instead of the (RS)-N,N-dιmethyI-{2-[4-(α- phenyl-p-chloro-benzyl)pιperazιn-1 -yl]ethoxy}-acetamιde, 107 7 g (0 2 moles) of (RS)-{2-[4-(α-phenyl-p-chlorobenzyl)- pιperazιn-1 -yl]ethoxy}-acetyl morpholide are used, and the hydrolysis is carried out for 5 hours under boiling Thus, 72 4 g (78 4 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084 Example 19
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1 -yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that, after the hydrolysis, the reaction mixture is diluted with 3500 ml of water, extracted with 600 ml of ethyl acetate and 200 ml of dnsopropyl ether, the residues of the organic solvents are removed from the aqueous solution under reduced pressure, and the procedure of Example 13 is continued Thus, 68 1 g (73 8 %) of the title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 20
(RS)-{2-[4-( -phenyl-p-chlorobenzyl)-pιperazιn-1-yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that, after the hydrolysis, the reaction mixture is diluted with 3500 ml of water, cooled to 0 °C, the precipitated crystalline cetinzine sodium salt is allowed to sediment for 1 hour, filtered, then dissolved in 1000 ml of water, the pH is adjusted to a value of 3 8 by the addition of hydrochloric acid, then the procedure of Example 13 is continued Thus, 65 7 g (71 2 %) of the title compound are obtained The purity of the product corresponds to the quality requirements given in Eur. Pharm., 3, 1997, 1084.
Example 21
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-piperazin-1 -yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that the hydrolysis is carried out with 170 ml (2.0 moles) of concentrated hydrochloric acid, and, at the end of the hydrolysis, the pH of the reaction mixture is adjusted to the desired value of 3.8 with about 270 ml of 40 % aqueous sodium hydroxide solution. Thus, 70.6 g (76.5 %) of the title compound are obtained, m.p.: 225-228 °C. The purity of the product corresponds to the quality requirements given in Eur. Pharm., 3, 1997, 1084.
Example 22
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-piperazin-1 -yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that the hydrolysis is carried out with 170 ml (0.9 moles) of 50 % sulfuric acid, and, at the end of the hydrolysis, the pH of the reaction mixture is adjusted to the desired value of 3.8 with about 260 ml of 40 % aqueous sodium hydroxide solution. Thus, 67.3 g (72.9 %) of the title compound are obtained, m p 225-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 23
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1 -yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that, in addition to the aqueous sodium hydroxide solution, also 2 g of Aliquat 336 (tπoctylmethyl ammonium chloride) are added to the reaction mixture Thus, 74 9 g (81 2 %) of the title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084
Example 24
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-pιperazιn-1-yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that, in addition to the aqueous sodium hydroxide solution, also 1 g of 15-crown-5 (1 ,4,7, 10,13-peπtaoxacyclo- pentadecane) is added to the reaction mixture Thus, 76 1 g (82 5 %) of the title compound are obtained, m p 226-228 °C The purity of the product corresponds to the quality requirements given in Eur Pharm , 3, 1997, 1084 Example 25
(RS)-{2-[4-(α-phenyl-p-chlorobenzyl)-piperazin-1-yl]ethoxy}- acetic acid dihydrochloride
The procedure described in Example 13 is followed with the difference that the hydrolysis is carried out with 280 ml of 40 % aqueous potassium hydroxide solution. Thus, 75.0 g (81.3 %) of the title compound are obtained, m.p.: 226-228 °C. The purity of the product corresponds to the quality requirements given in Eur. Pharm., 3, 1997, 1084.

Claims

Claims:
1. A process for the preparation of {2-[4-(α-phenyl-p-chloro- benzyl)piperazin-1-yl]ethoxy} acetic acid of the formula
Figure imgf000036_0001
or a pharmaceutically suitable acid addition salt or metal salt thereof through hydrolyzing a corresponding acetamide in alkaline or acidic medium, and, if desired, converting the product formed to an acid addition salt or metal salt and/or liberating the base from the acid addition salt or metal salt, characterized in that a {2-[4-(α-phenyl-p-chloro- benzyl)piperazin-1-yl]ethoxy} acetamide of the formula
Figure imgf000036_0002
wherein
R-i and R2 represent, independently, a Cι- alkyl group optionally substituted by a phenyl group, a C2- alkenyl group or a cyclohexyl group, or Ri and R2form together with the adjacent nitrogen atom a morpholino group, or an acid addition salt thereof is used as the acetamide, and, if desired, the hydrolysis is carried out in the presence of a phase transfer catalyst.
2. A process as claimed in Claim 1 , characterized in that the {2-[4-(α-phenyl-p-chloro-benzyl)piperazin-1 -yl]ethoxy}- acetamide of the formula II is (RS)-N,N-dimethyl-{2-[4-(α- phenyl-p-chloro-benzyl)piperazin-1-yl]ethoxy} acetamide.
3. A {2-[4-(α-phenyl-p-chloro-benzyl)piperazin-1 -yl]ethoxy}- acetamide of the formula II, wherein Ri and R2 are as defined in Claim 1 , or an acid addition salt thereof.
4. (RS)-N,N-Dimethyl-{2-[4-(α-phenyl-p-chloro-benzyl)- piperazin-1-yl]ethoxy} acetamide or an acid addition salt thereof.
5. A process for the preparation of a {2-[4-(α-phenyl-p-chloro- benzyl)piperazin-1-yl]ethoxy}-acetamide of the formula II, wherein Ri and R2 are as defined in Claim 1 , or an acid addition salt thereof, characterized in that an alkali metal salt of the {2-[4-(α-phenyl-p-chlorobenzyl)piperazin-1-yl]} ethanol of the formula
Figure imgf000038_0001
is reacted with a 2-haloacetamιde of the formula
/ R1
CON
N , IV
wherein Ri and R2 are as defined above, X stands for a halo atom, preferably a chloro atom, and, if desired, the obtained base of the formula II is converted to an acid addition salt with an inorganic or organic acid or the base is liberated from the acid addition salt thereof
PCT/HU2000/000123 1999-11-30 2000-11-29 A PROCESS FOR THE PREPARATION OF {2-[4-(α-PHENYL-p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR WO2001040211A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
EP00981508A EP1233954B1 (en) 1999-11-30 2000-11-29 A process for the preparation of 2- 4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl]ethoxy acetic acid and novel intermediates therefor
AU18742/01A AU1874201A (en) 1999-11-30 2000-11-29 A process for the preparation of (2-(4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl)ethoxy) acetic acid and novel intermediates therefor
PL354677A PL200046B1 (en) 1999-11-30 2000-11-29 A PROCESS FOR THE PREPARATION OF {2−[4−(α−PHENYL−p−CHLOROBENZYL)PIPERAZIN−1−YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR
JP2001541895A JP4763954B2 (en) 1999-11-30 2000-11-29 Process for the production of {2- [4- (α-phenyl-p-chlorobenzyl) piperazin-1-yl] ethoxy} acetic acid and novel intermediates therefor
SK752-2002A SK285641B6 (en) 1999-11-30 2000-11-29 A process for the preparation of {2-[4-(alpha-phenyl-p- chlorobenzyl)piperazin-1-yl]ethoxy}acetic acid and novel intermediates therefor
AT00981508T ATE280165T1 (en) 1999-11-30 2000-11-29 METHOD FOR PRODUCING 2-(4-(ALPHA-PHENYL-P-CHLOROBENZYL)PIPERAZINE-1-YL)ETHOXYACETIC ACID AND INTERMEDIATE PRODUCTS THEREFOR
UA2002065341A UA72949C2 (en) 1999-11-30 2000-11-29 A PROCESS FOR THE PREPARATION OF {2-[4-(a-PHENYL-P-CHLOROBENZENE-1-YL]-ETHOXY}ACETIC ACID AND INTERMEDIARY COMPOUNDS
US10/148,704 US6908999B2 (en) 1999-11-30 2000-11-29 Process for the preparation of {2-[4-α-phenyl-p-chlorobenzyl)piperazin-1-yl]ethoxy} acetic acid and novel intermediates therefor
SI200030569T SI1233954T1 (en) 1999-11-30 2000-11-29 A process for the preparation of 2- 4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl)ethoxy acetic acid and novel intermediates therefor
DE60015177T DE60015177T2 (en) 1999-11-30 2000-11-29 PROCESS FOR PREPARING 2- [4- (ALPHA-PHENYL-P-CHLOROBENZYL) PIPERAZINE-1-YL] ETHOXY ACETIC ACID AND INTERMEDIATES THEREFOR
HR20020470A HRP20020470B1 (en) 1999-11-30 2002-05-28 A PROCESS FOR THE PREPARATION OF {2-[4-(alpha-PHENYL-p-CHLORBENZYL)-PIPERAZIN-1-YL]ETHOXY} ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR
BG106760A BG65455B1 (en) 1999-11-30 2002-05-30 A PROCESS FOR THE PREPARATION OF {2-[4-(ALPHA-PHENYL-p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREOF

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
HUP9904438 1999-11-30
HUP9904439 1999-11-30
HU9904438A HU226641B1 (en) 1999-11-30 1999-11-30 Process for producing {2-[4-(alpha-phenyl-p-chloro-benzyl)-piperazine-1-yl]-ethoxy}-acetic acid
HU9904439A HU226639B1 (en) 1999-11-30 1999-11-30 {2-[4-(alpha-phenyl-p-chloro-benzyl)-piperazine-1-yl]-ethoxy}-acetic acid-amides and process for producing them

Publications (1)

Publication Number Publication Date
WO2001040211A1 true WO2001040211A1 (en) 2001-06-07

Family

ID=90000077

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/HU2000/000123 WO2001040211A1 (en) 1999-11-30 2000-11-29 A PROCESS FOR THE PREPARATION OF {2-[4-(α-PHENYL-p-CHLOROBENZYL)PIPERAZIN-1-YL]ETHOXY}ACETIC ACID AND NOVEL INTERMEDIATES THEREFOR

Country Status (15)

Country Link
US (1) US6908999B2 (en)
EP (1) EP1233954B1 (en)
JP (1) JP4763954B2 (en)
AT (1) ATE280165T1 (en)
AU (1) AU1874201A (en)
BG (1) BG65455B1 (en)
CZ (1) CZ304892B6 (en)
DE (1) DE60015177T2 (en)
HR (1) HRP20020470B1 (en)
PL (1) PL200046B1 (en)
RU (1) RU2248974C2 (en)
SI (1) SI1233954T1 (en)
SK (1) SK285641B6 (en)
UA (1) UA72949C2 (en)
WO (1) WO2001040211A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003009849A1 (en) * 2001-07-26 2003-02-06 Ucb, S.A. Process for the preparation of 2-(2-(4-(bis(4-fluorophenyl)methyl)-piperazin-1-yl)ethoxy)acetic acid derivatives or corresponding salt forms thereof and intermediates therefor
WO2003104211A2 (en) * 2002-06-05 2003-12-18 Dr. Reddy's Laboratories Limited Crystalline [2-[4-[(4-chlorophenyl)-phenyl methyl]-1-piperazinyl] ethoxy] acetic acid dihydrochloride
WO2007066162A1 (en) * 2005-12-08 2007-06-14 Egis Gyógyszergyár Nyilvanosan Mukodo Reszvenytarsasag Process for the preparation of a pharmaceutical intermediate

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU227319B1 (en) * 2005-12-08 2011-03-28 Egis Gyogyszergyar Nyrt Process for the production of (2-chloro-ethoxy)-acetic acid-n,n-dimethylamide and its intermediate and the novel intermediate
KR102034448B1 (en) 2017-12-20 2019-10-18 주식회사 포스코 Steel and method for the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0058146A1 (en) * 1981-02-06 1982-08-18 U C B, S.A. 2-(4-(Diphenylmethyl)-1-piperazinyl)-acetic acids and their amides, process for their preparation and pharmaceutical compositions
WO1997037982A1 (en) * 1996-04-10 1997-10-16 Ucb S.A. Novel substituted [2-(1-piperazinyl)ethoxy]methyl

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA82752B (en) * 1981-02-06 1982-12-29 Ucb Sa 2-(4-(diphenylmethyl)-1-piperazinyl)-acetic acids and their amides
US5347060A (en) * 1991-07-24 1994-09-13 Mobil Oil Corporation Phase-transfer catalysis with onium-containing synthetic mesoporous crystalline material
GB9305282D0 (en) * 1993-03-15 1993-05-05 Ucb Sa Enantiomers of 1-(4-chlorophenyl)phenylmethyl)-4-(4-methylphenyl)sulphonyl)piperazine
CA2180993A1 (en) * 1996-07-11 1998-01-12 Yong Tao Methods for the manufacture of cetirizine

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0058146A1 (en) * 1981-02-06 1982-08-18 U C B, S.A. 2-(4-(Diphenylmethyl)-1-piperazinyl)-acetic acids and their amides, process for their preparation and pharmaceutical compositions
WO1997037982A1 (en) * 1996-04-10 1997-10-16 Ucb S.A. Novel substituted [2-(1-piperazinyl)ethoxy]methyl

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
OPALKA, C. J. ET AL: "A novel synthesis of the enantiomers of an antihistamine drug by piperazine formation from a primary amine", SYNTHESIS, vol. 7, 1995, pages 766 - 768, XP000979124 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003009849A1 (en) * 2001-07-26 2003-02-06 Ucb, S.A. Process for the preparation of 2-(2-(4-(bis(4-fluorophenyl)methyl)-piperazin-1-yl)ethoxy)acetic acid derivatives or corresponding salt forms thereof and intermediates therefor
WO2003104211A2 (en) * 2002-06-05 2003-12-18 Dr. Reddy's Laboratories Limited Crystalline [2-[4-[(4-chlorophenyl)-phenyl methyl]-1-piperazinyl] ethoxy] acetic acid dihydrochloride
WO2003104211A3 (en) * 2002-06-05 2004-12-23 Reddys Lab Ltd Dr Crystalline [2-[4-[(4-chlorophenyl)-phenyl methyl]-1-piperazinyl] ethoxy] acetic acid dihydrochloride
WO2007066162A1 (en) * 2005-12-08 2007-06-14 Egis Gyógyszergyár Nyilvanosan Mukodo Reszvenytarsasag Process for the preparation of a pharmaceutical intermediate
EA014530B1 (en) * 2005-12-08 2010-12-30 Эгиш Дьёдьсердьяр Ньильваношан Мюкёдё Ресвеньтаршашаг Process for the preparation of pharmaceutical intermediate

Also Published As

Publication number Publication date
ATE280165T1 (en) 2004-11-15
UA72949C2 (en) 2005-05-16
SK7522002A3 (en) 2002-11-06
PL354677A1 (en) 2004-02-09
CZ304892B6 (en) 2015-01-07
HRP20020470A2 (en) 2004-04-30
US20030092911A1 (en) 2003-05-15
US6908999B2 (en) 2005-06-21
PL200046B1 (en) 2008-11-28
AU1874201A (en) 2001-06-12
JP2003515600A (en) 2003-05-07
BG65455B1 (en) 2008-08-29
BG106760A (en) 2003-04-30
JP4763954B2 (en) 2011-08-31
DE60015177T2 (en) 2005-10-27
EP1233954A1 (en) 2002-08-28
EP1233954B1 (en) 2004-10-20
RU2002118101A (en) 2004-01-20
CZ20021712A3 (en) 2002-09-11
SK285641B6 (en) 2007-05-03
SI1233954T1 (en) 2005-02-28
DE60015177D1 (en) 2004-11-25
RU2248974C2 (en) 2005-03-27
HRP20020470B1 (en) 2009-04-30

Similar Documents

Publication Publication Date Title
EP1252151B1 (en) A process for the preparation of quetiapine and intermediates therefor
CZ222392A3 (en) Amino substituted piperazine derivatives
JP2000508634A (en) Newly substituted [2- (1-piperazinyl) ethoxy] methyl compound
EP2024369A2 (en) Novel process for the preparation of sildenafil citrate
EP1233954B1 (en) A process for the preparation of 2- 4-(alpha-phenyl-p-chlorobenzyl)piperazin-1-yl]ethoxy acetic acid and novel intermediates therefor
US7915421B2 (en) Method for preparing phenyl acetic acid derivatives
WO2007066162A1 (en) Process for the preparation of a pharmaceutical intermediate
IL182439A (en) Intermediates useful for the preparation of aripiprazole and methods for the preparation of the intermediates and aripiprazole
Adamo et al. An Improved Resolution Of 2-Methyl Piperidine And Its Use in The Synthesis Of Homochiral Trans-2, 6-Dialkyl Piperidines
US4767767A (en) 2-pyrrolidinylethyl-2-(7-trifluoromethyl-4-quinolyl-aminobenzoate having analgesic, antipyretic and anti-inflammatory activities
JPH09110832A (en) Production of 4-acylamino-2,2,6,6-tetramethylpiperazine
NZ202857A (en) Preparation of beta-((2-methylpropoxy)methyl)-n-phenyl-n-(phenylmethyl)-1-pyrrolidineethanamine hydrochloride hydrate
EP2121643B1 (en) New process for the preparation of levocetirizine and intermediates thereof
HU226641B1 (en) Process for producing {2-[4-(alpha-phenyl-p-chloro-benzyl)-piperazine-1-yl]-ethoxy}-acetic acid
HU226639B1 (en) {2-[4-(alpha-phenyl-p-chloro-benzyl)-piperazine-1-yl]-ethoxy}-acetic acid-amides and process for producing them
EP2297122B1 (en) New process for the preparation of levocetirizine and intermediates thereof
SU523634A3 (en) Method for preparing benzylamine derivatives or their salts
JP2013006804A (en) Method for producing benzophenone derivative
WO2013002253A1 (en) Method for producing benzophenone derivative
BE536889A (en)
SI22586A (en) New procedure for preparation of levocetirizine and its intermediates

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

ENP Entry into the national phase

Ref document number: 2002 200200695

Country of ref document: RO

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: PV2002-1712

Country of ref document: CZ

WWE Wipo information: entry into national phase

Ref document number: 2000981508

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 7522002

Country of ref document: SK

Ref document number: P20020470A

Country of ref document: HR

ENP Entry into the national phase

Ref document number: 2001 541895

Country of ref document: JP

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2000 106760

Country of ref document: BG

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2002 2002118101

Country of ref document: RU

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 10148704

Country of ref document: US

WWP Wipo information: published in national office

Ref document number: 2000981508

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: PV2002-1712

Country of ref document: CZ

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWG Wipo information: grant in national office

Ref document number: 2000981508

Country of ref document: EP