WO2001010814A1 - Process for the preparation of naproxene nitroxyalkylesters - Google Patents

Process for the preparation of naproxene nitroxyalkylesters Download PDF

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Publication number
WO2001010814A1
WO2001010814A1 PCT/EP2000/007222 EP0007222W WO0110814A1 WO 2001010814 A1 WO2001010814 A1 WO 2001010814A1 EP 0007222 W EP0007222 W EP 0007222W WO 0110814 A1 WO0110814 A1 WO 0110814A1
Authority
WO
WIPO (PCT)
Prior art keywords
alkylene
carbon atoms
above defined
naphthyl
methoxy
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/EP2000/007222
Other languages
English (en)
French (fr)
Inventor
Francesca Benedini
Erminio Oldani
Graziano Castaldi
Antonio Tarquini
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nicox SA
Original Assignee
Nicox SA
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 to EP00951456A priority Critical patent/EP1200386B1/en
Priority to AT00951456T priority patent/ATE251109T1/de
Priority to SI200030256T priority patent/SI1200386T1/xx
Priority to HU0202435A priority patent/HU227109B1/hu
Priority to JP2001515282A priority patent/JP4667691B2/ja
Priority to BRPI0012915-1A priority patent/BRPI0012915B1/pt
Priority to AU64385/00A priority patent/AU778694B2/en
Priority to US10/031,412 priority patent/US6700011B1/en
Priority to DK00951456T priority patent/DK1200386T3/da
Priority to PL353092A priority patent/PL200165B1/pl
Priority to CA2380116A priority patent/CA2380116C/en
Priority to IL14763900A priority patent/IL147639A0/xx
Application filed by Nicox SA filed Critical Nicox SA
Priority to MXPA02001256A priority patent/MXPA02001256A/es
Priority to DE60005682T priority patent/DE60005682T2/de
Publication of WO2001010814A1 publication Critical patent/WO2001010814A1/en
Priority to NO20020515A priority patent/NO327669B1/no
Anticipated expiration legal-status Critical
Priority to US10/625,558 priority patent/US7238829B2/en
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C203/00—Esters of nitric or nitrous acid
    • C07C203/02—Esters of nitric acid
    • C07C203/04—Esters of nitric acid having nitrate groups bound to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/02—Preparation of esters of nitric acid

Definitions

  • the present invention relates to a new method for preparing nitroxyalkylesters of the 2 - ( S ) - ( 6 -methoxy- 2 - naphthyl ) -propanoic acid (naproxene) having an enantiomeric excess of the (S) form higher than or equal to 97%, preferably higher than or equal to 98%, combined with high yields, higher than 75-80%, preferably higher than 85%.
  • the reaction takes place in the presence of an organic nitrogenated base, such as for example 4 -dimethyl aminopyridine , morpholine, N-methyl morpholine or triethylamine.
  • an organic nitrogenated base such as for example 4 -dimethyl aminopyridine , morpholine, N-methyl morpholine or triethylamine.
  • An object of the present invention is a process to obtain nitroxyalkylesters of the 2 -( S )-( 6 -methoxy- 2 -naphthyl ) - propanoic acid having an enantiomeric excess higher than or equal to 97%, preferably higher than or equal to 98%, characterized in that an halide of the 2- ( S ) - ( 6 -methoxy- 2 - naphthyl ) -propanoic acid of formula A-Hal, wherein A is the acylic residue of said acid, is reacted in an inert organic solvent with an aliphatic nitroxyalkanol HO-Y-ON0 2 , wherein Y has one of the following meanings: a linear or optionally branched C 1 - C 2 Q I preferably C 2 -C 5 , alkylene; a cycloalkylene with ring from 3 to 8 carbon atoms, preferably from 5 to 7 carbon atoms,
  • T being alkylene as above dfeined and p an integer equal to zero or one, alkylene having the above mentioned meaning, nf ' is an integer from 1 to 6 , preferably from 1 to 4; in the presence of an inorganic base, to give the corresponding nitroxyalkylester of the 2- (S) - ( 6 -methoxy- 2 -naphthyl ) -propanoic acid of formula A-0-Y-ON0 2 , wherein A and Y are as above defined.
  • Y can also be a combination of two or more of the mentioned group.
  • the aliphatic nitroxyalcohol amount on molar basis is in the range 1-2, preferably 1.2-1.5, with respect to that of the acid halide.
  • inorganic bases hydroxides, oxides, carbonates and bicarbonates, silicates, aluminosilicates of the alkaline and alkaline -earth metals, or hydroxides, oxides, carbonates and bicarbonates of metals belonging to the group IIB, preferably zinc, or to groups Ilia or IVa , preferably tin, are meant.
  • the inorganic base amount is in molar ratio with the acid halide amount generally in the range 1-2, preferably 1.2-1.5.
  • aromatic hydrocarbons are meant, such as for example toluene and xylene, chlorinated or fluorinated organic solvents, for example methylene chloride, chlorobenzene , aliphatic esters for example C 1 -C acids esters with C- L -C 8 alcohols such as for example ethyl acetate and butyl acetate, etc.
  • the solvent amount is not critical and generally from 1 to 10 volumes of solvent are used, preferabaly from 2 to 5 volumes based on the acid halide weight.
  • the reaction is carried out at a temperature in the range -20°C and 50°C, preferably 0°C and 20°C.
  • nitroxyalkylesters of the 2 - ( S ) - ( 6 -methoxy- 2 - naphthyl ) -propanoic acid are recovered at the end of the reaction, after addition of water to the organic phase, separation of the phases and solvent evaporation. If necessary, a further purification can be carried out by chromatography on silica gel column in order to increase the product titre.
  • the compound can also be purified by crystallization from a suitable solvent.
  • Aliphatic nitroxyalcohols can be prepared according to the known methods in the prior art. See for example Gazzetta Chim. It. 1987, 117, 173 and WO 98/25,918.
  • Example 2 is repeated using toluene as solvent.
  • the nitroxyester yield is 76%, the (HPLC) purity > 99%.
  • the enatio eric excess is equal to 98%.
  • Example 2 is repeated but using as a base calcium carbonate. 4.6 g, equal to 13.3 mmoles of nitroxyester (yield 90%) are obtained, HPLC purity >99%, enantiomeric excess 98%.
  • EXAMPLE 5 is repeated but using as a base calcium carbonate. 4.6 g, equal to 13.3 mmoles of nitroxyester (yield 90%) are obtained, HPLC purity >99%, enantiomeric excess 98%.
  • Example 2 is repeated but using as a base calcium alumino- silicate. 4.6 g, equal to 13.3 mmoles of nitroxyester (yield 90%) are obtained, HPLC purity >99%, enantiomeric excess 98%.
  • Example 2 is repeated but using as a base triethylamine. The obtained mixture after the reaction is analyzed to evaluate the enantiomeric excess, which results equal to 80%.
  • EXAMPLE 8 (comparative)
  • Example 2 is repeated but using as a base diisopropylethylamine.
  • the mixture obtained after the reaction is analyzed to evaluate the enantiomeric excess, which results equal to 76%.
  • EXAMPLE 9 (comparative)
  • Example 2 is repeated but using as a base N- methylmorpholine.
  • the mixture obtained after the reaction is analyzed to evaluate the enantiomeric excess, which results equal to 56%.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
PCT/EP2000/007222 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters Ceased WO2001010814A1 (en)

Priority Applications (16)

Application Number Priority Date Filing Date Title
AT00951456T ATE251109T1 (de) 1999-08-04 2000-07-27 Verfahren zur herstellung von naproxennitroxyalkylestern
SI200030256T SI1200386T1 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
HU0202435A HU227109B1 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
JP2001515282A JP4667691B2 (ja) 1999-08-04 2000-07-27 ナプロキセンのニトロキシアルキルエステルの製造法
BRPI0012915-1A BRPI0012915B1 (pt) 1999-08-04 2000-07-27 Processo para obter nitroxialquilésteres do ácido 2-(s)-(6-metoxi-2-naftil)-propanóico
AU64385/00A AU778694B2 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
US10/031,412 US6700011B1 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
PL353092A PL200165B1 (pl) 1999-08-04 2000-07-27 Sposób wytwarzania estrów nitroksyalkilowych naproksenu oraz ester nitroksybutylowy kwasu 2-(S)-(6-metoksy-2-naftylo)propanowego o wysokim nadmiarze enancjomerycznym
DK00951456T DK1200386T3 (da) 1999-08-04 2000-07-27 Fremgangsmåde til fremstilling af nitroxyalkylestere af naproxen
EP00951456A EP1200386B1 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
IL14763900A IL147639A0 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
CA2380116A CA2380116C (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters
MXPA02001256A MXPA02001256A (es) 1999-08-04 2000-07-27 Procedimiento para la preparacion de esteres nitroxialquilicos de naproxeno.
DE60005682T DE60005682T2 (de) 1999-08-04 2000-07-27 Verfahren zur herstellung von naproxennitroxyalkylestern
NO20020515A NO327669B1 (no) 1999-08-04 2002-02-01 Fremgangsmate for fremstilling av naproxen-nitroksyalkylester, og slik forbindelse
US10/625,558 US7238829B2 (en) 1999-08-04 2003-07-24 Process for the preparation of naproxene nitroxyalkylesters

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITMI99A001753 1999-08-04
IT1999MI001753A IT1313596B1 (it) 1999-08-04 1999-08-04 Processo per la preparazione di nitrossialchil esteri del naproxene

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US10031412 A-371-Of-International 2000-07-27
US10/625,558 Division US7238829B2 (en) 1999-08-04 2003-07-24 Process for the preparation of naproxene nitroxyalkylesters

Publications (1)

Publication Number Publication Date
WO2001010814A1 true WO2001010814A1 (en) 2001-02-15

Family

ID=11383500

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2000/007222 Ceased WO2001010814A1 (en) 1999-08-04 2000-07-27 Process for the preparation of naproxene nitroxyalkylesters

Country Status (23)

Country Link
US (2) US6700011B1 (https=)
EP (2) EP1200386B1 (https=)
JP (2) JP4667691B2 (https=)
KR (1) KR100687820B1 (https=)
CN (1) CN1198786C (https=)
AT (2) ATE251109T1 (https=)
AU (1) AU778694B2 (https=)
BR (1) BRPI0012915B1 (https=)
CA (1) CA2380116C (https=)
DE (2) DE60005682T2 (https=)
DK (2) DK1200386T3 (https=)
ES (2) ES2243859T3 (https=)
HU (1) HU227109B1 (https=)
IL (1) IL147639A0 (https=)
IT (1) IT1313596B1 (https=)
MX (1) MXPA02001256A (https=)
NO (1) NO327669B1 (https=)
PL (1) PL200165B1 (https=)
PT (2) PT1384707E (https=)
RU (1) RU2248348C2 (https=)
TR (1) TR200200290T2 (https=)
WO (1) WO2001010814A1 (https=)
ZA (2) ZA200200478B (https=)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6297260B1 (en) 1998-10-30 2001-10-02 Nitromed, Inc. Nitrosated and nitrosylated nonsteroidal antiinflammatory compounds, compositions and methods of use
WO2003045896A1 (en) * 2001-11-27 2003-06-05 Astrazeneca Ab New process
WO2004020384A1 (en) 2002-08-29 2004-03-11 Nicox S.A. Process for preparing nitrooxyderivatives of naproxen
WO2004043897A1 (en) * 2002-11-14 2004-05-27 Dipharma S.P.A. A process for the purification of 1,4-butanediol mononitrate
US6825185B2 (en) 2000-12-21 2004-11-30 Nitromed, Inc. Substituted aryl compounds as novel cyclooxygenase-2 selective inhibitors, compositions and methods of use
US7163958B2 (en) 2002-07-03 2007-01-16 Nitromed Inc. Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
US7166618B2 (en) 1999-12-23 2007-01-23 Nitromed, Inc. Nitrosated and nitrosylated cyclooxygenase-2 inhibitors, compositions and methods of use
US7220749B2 (en) 2002-06-11 2007-05-22 Nitromed, Inc. Nitrosated and/or nitrosylated cyclooxygenase-2 selective inhibitors, compositions and methods of use
US7244753B2 (en) 2002-07-29 2007-07-17 Nitromed, Inc. Cyclooxygenase-2 selective inhibitors, compositions and methods of use
WO2009000723A1 (en) 2007-06-28 2008-12-31 Nicox S.A. Process for preparing 1,4-butandiol mononitrate
WO2009153668A3 (en) * 2008-06-20 2010-02-11 Nicox S.A. Method for purifying 4-(nitrooxy)butyl(2s)-2-(6-methoxy-2-naphthyl)propanoate
WO2011120695A1 (en) 2010-03-31 2011-10-06 Lonza Ltd Process for the production of esters of nitric acid
US8586790B2 (en) 2011-03-01 2013-11-19 Everlight Usa, Inc. Anhydride derivatives of 2-(S)-(6-methoxy-2-naphtyl)-propanoic acid, preparation method and use thereof
WO2014111957A1 (en) 2013-01-21 2014-07-24 Apparao Satyam Nitric oxide releasing prodrugs of therapeutic agents

Families Citing this family (4)

* Cited by examiner, † Cited by third party
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NZ569396A (en) * 2006-02-03 2011-06-30 Nicox Sa Use of nitrooxyderivative of drug for the treatment of muscular dystrophies
CN100427475C (zh) * 2006-11-30 2008-10-22 华南理工大学 萘普生-2-芳基吗啉乙酯及其制备方法与应用
WO2009149053A2 (en) * 2008-06-02 2009-12-10 Dr. Reddy's Laboratories Ltd. Naproxcinod process and solid dispersion
CA3167343A1 (en) 2020-02-10 2021-08-19 Brigitte DUQUESROIX-CHAKROUN Method for treating vaso occlusive crises associated with sickle cell disease

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FR2757159A1 (fr) * 1996-12-12 1998-06-19 Hoechst Marion Roussel Inc Nouveaux derives nitres analgesiques, anti-inflammatoires et anti-thrombotiques, leur procede de preparation, leur application comme medicaments

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US5703073A (en) * 1995-04-19 1997-12-30 Nitromed, Inc. Compositions and methods to prevent toxicity induced by nonsteroidal antiinflammatory drugs
CN1144092A (zh) * 1995-08-25 1997-03-05 蔡雄 可释放一氧化氮的新型非类固醇类抗炎药、它们的制备方法和用途
WO1997013519A1 (en) * 1995-10-09 1997-04-17 Russinsky Limited Esters of cyclooxygenase inhibitors and terpene derivatives as pharmaceutical products

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WO1992001668A1 (en) * 1990-07-26 1992-02-06 Italfarmaco S.P.A. Benzoic acid substituted derivatives having cardiovascular activity
WO1995009831A1 (en) * 1993-10-06 1995-04-13 Nicox S.A. Nitric esters having anti-inflammatory and/or analgesic activity and process for their preparation
WO1995030641A1 (en) * 1994-05-10 1995-11-16 Nicox S.A. Nitro compounds and their compositions having anti-inflammatory, analgesic and anti-thrombotic acitivities
WO1997016405A1 (en) * 1995-10-31 1997-05-09 Nicox S.A. New compounds and their compositions having anti-inflammatory and anti-thrombotic activities
FR2757159A1 (fr) * 1996-12-12 1998-06-19 Hoechst Marion Roussel Inc Nouveaux derives nitres analgesiques, anti-inflammatoires et anti-thrombotiques, leur procede de preparation, leur application comme medicaments

Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6297260B1 (en) 1998-10-30 2001-10-02 Nitromed, Inc. Nitrosated and nitrosylated nonsteroidal antiinflammatory compounds, compositions and methods of use
US6593347B2 (en) 1998-10-30 2003-07-15 Nitromed, Inc. Nitrosated and nitrosylated nonsteroidal antiinflammatory compounds, compositions and methods of use
US7432285B2 (en) 1999-12-23 2008-10-07 Nitromed, Inc. Nitrosated and nitrosylated cyclooxygenase-2 inhibitors, compositions and methods of use
US7166618B2 (en) 1999-12-23 2007-01-23 Nitromed, Inc. Nitrosated and nitrosylated cyclooxygenase-2 inhibitors, compositions and methods of use
US6825185B2 (en) 2000-12-21 2004-11-30 Nitromed, Inc. Substituted aryl compounds as novel cyclooxygenase-2 selective inhibitors, compositions and methods of use
JP2005510557A (ja) * 2001-11-27 2005-04-21 ニコックス・ソシエテ・アノニム 新規な方法
JP4771659B2 (ja) * 2001-11-27 2011-09-14 ニコックス・ソシエテ・アノニム 新規な方法
WO2003045896A1 (en) * 2001-11-27 2003-06-05 Astrazeneca Ab New process
US7220749B2 (en) 2002-06-11 2007-05-22 Nitromed, Inc. Nitrosated and/or nitrosylated cyclooxygenase-2 selective inhibitors, compositions and methods of use
US7589124B2 (en) 2002-06-11 2009-09-15 Nicox, S.A. Nitrosated and/or nitrosylated cyclooxygenase-2 selective inhibitors, compositions and methods of use
US8088762B2 (en) 2002-07-03 2012-01-03 Nicox S.A. Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
US8222277B2 (en) 2002-07-03 2012-07-17 Nicox S.A. Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
US7163958B2 (en) 2002-07-03 2007-01-16 Nitromed Inc. Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
US7883714B2 (en) 2002-07-03 2011-02-08 Nicox S.A. Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
US8304409B2 (en) 2002-07-03 2012-11-06 Nicox S.A. Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
US7244753B2 (en) 2002-07-29 2007-07-17 Nitromed, Inc. Cyclooxygenase-2 selective inhibitors, compositions and methods of use
US7199258B2 (en) 2002-08-29 2007-04-03 Nicox S.A. Process for preparing nitrooxyderivatives of naproxen
WO2004020384A1 (en) 2002-08-29 2004-03-11 Nicox S.A. Process for preparing nitrooxyderivatives of naproxen
CN1326830C (zh) * 2002-08-29 2007-07-18 尼科克斯公司 制备萘普生的硝基氧基衍生物的方法
AU2003266966B2 (en) * 2002-08-29 2009-08-06 Nicox S.A. Process for preparing nitrooxyderivatives of naproxen
KR101100064B1 (ko) 2002-08-29 2011-12-29 니콕스 에스. 에이. 나프록센의 니트로옥시유도체 제조방법
US7723382B2 (en) 2002-08-29 2010-05-25 Nicox S.A. Process for preparing nitrooxyalkyl substituted esters of carboxylic acids, intermediates useful in said process and preparation thereof
JP2005536558A (ja) * 2002-08-29 2005-12-02 ニコックス エス エイ ナプロキセンのニトロオキシ誘導体の製造法
JP2006506417A (ja) * 2002-11-14 2006-02-23 ディファルマ・ソシエタ・ペル・アチオニ １，４−ブタンジオール・モノニトレートの精製方法
US7947855B2 (en) 2002-11-14 2011-05-24 Dipharma S.P.A. Process for the purification of 1,4-butanediol mononitrate
HRP20050415B1 (en) * 2002-11-14 2008-07-31 Dipharma S.P.A. A process for the purification of 1,4-butanediol mononitrate
WO2004043897A1 (en) * 2002-11-14 2004-05-27 Dipharma S.P.A. A process for the purification of 1,4-butanediol mononitrate
WO2009000723A1 (en) 2007-06-28 2008-12-31 Nicox S.A. Process for preparing 1,4-butandiol mononitrate
CN101874014A (zh) * 2008-06-20 2010-10-27 尼科克斯公司 纯化(2s)-2-(6-甲氧基-2-萘基)丙酸4-(硝基氧基)丁酯的方法
WO2009153668A3 (en) * 2008-06-20 2010-02-11 Nicox S.A. Method for purifying 4-(nitrooxy)butyl(2s)-2-(6-methoxy-2-naphthyl)propanoate
US8329937B2 (en) 2008-06-20 2012-12-11 Nicox S.A. Method for purifying 4-(nitrooxy)butyl(2S)-2-(6-methoxy-2-naphthyl) propanoate
WO2011120695A1 (en) 2010-03-31 2011-10-06 Lonza Ltd Process for the production of esters of nitric acid
US8586790B2 (en) 2011-03-01 2013-11-19 Everlight Usa, Inc. Anhydride derivatives of 2-(S)-(6-methoxy-2-naphtyl)-propanoic acid, preparation method and use thereof
WO2014111957A1 (en) 2013-01-21 2014-07-24 Apparao Satyam Nitric oxide releasing prodrugs of therapeutic agents
US9844599B2 (en) 2013-01-21 2017-12-19 Apparao Satyam Nitric oxide releasing produgs of therapeutic agents

Also Published As

Publication number Publication date
DE60020753T2 (de) 2006-03-16
JP2003506425A (ja) 2003-02-18
CA2380116C (en) 2011-07-05
CN1198786C (zh) 2005-04-27
MXPA02001256A (es) 2005-06-06
EP1384707A1 (en) 2004-01-28
DE60020753D1 (de) 2005-07-14
HUP0202435A2 (hu) 2002-11-28
EP1200386A1 (en) 2002-05-02
ATE251109T1 (de) 2003-10-15
PL200165B1 (pl) 2008-12-31
RU2248348C2 (ru) 2005-03-20
JP4667691B2 (ja) 2011-04-13
KR100687820B1 (ko) 2007-02-28
DE60005682T2 (de) 2004-09-16
CA2380116A1 (en) 2001-02-15
HU227109B1 (en) 2010-07-28
IT1313596B1 (it) 2002-09-09
US7238829B2 (en) 2007-07-03
NO20020515D0 (no) 2002-02-01
DE60005682D1 (de) 2003-11-06
ITMI991753A0 (it) 1999-08-04
PT1384707E (pt) 2005-08-31
CN1367773A (zh) 2002-09-04
ES2208390T3 (es) 2004-06-16
ES2243859T3 (es) 2005-12-01
NO327669B1 (no) 2009-09-07
HUP0202435A3 (en) 2004-03-01
ITMI991753A1 (it) 2001-02-04
IL147639A0 (en) 2002-08-14
EP1200386B1 (en) 2003-10-01
BR0012915A (pt) 2002-06-04
EP1384707B1 (en) 2005-06-08
JP2011042690A (ja) 2011-03-03
BRPI0012915B1 (pt) 2015-09-01
ZA200304525B (en) 2004-04-28
KR20020013974A (ko) 2002-02-21
DK1384707T3 (da) 2005-08-15
DK1200386T3 (da) 2003-12-22
PT1200386E (pt) 2004-02-27
ATE297372T1 (de) 2005-06-15
US20050119339A1 (en) 2005-06-02
PL353092A1 (en) 2003-10-06
ZA200200478B (en) 2003-10-29
NO20020515L (no) 2002-02-01
TR200200290T2 (tr) 2002-05-21
AU778694B2 (en) 2004-12-16
US6700011B1 (en) 2004-03-02
AU6438500A (en) 2001-03-05

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