SK283894B6 - Spôsob výroby 5-[2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo [4,3-d]pyrimidin-7-ónu - Google Patents

Spôsob výroby 5-[2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo [4,3-d]pyrimidin-7-ónu Download PDF

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Publication number
SK283894B6
SK283894B6 SK1783-2001A SK17832001A SK283894B6 SK 283894 B6 SK283894 B6 SK 283894B6 SK 17832001 A SK17832001 A SK 17832001A SK 283894 B6 SK283894 B6 SK 283894B6
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SK
Slovakia
Prior art keywords
acid
compound
formula
carbon atoms
chloride
Prior art date
Application number
SK1783-2001A
Other languages
English (en)
Slovak (sk)
Inventor
Peter James Dunn
Albert Shaw Wood
Original Assignee
Pfizer Research And Development Company N. V./S. A.
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10795332&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK283894(B6) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Research And Development Company N. V./S. A. filed Critical Pfizer Research And Development Company N. V./S. A.
Publication of SK283894B6 publication Critical patent/SK283894B6/sk

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    • 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
    • C07D295/22—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 hetero atoms directly attached to ring nitrogen atoms
    • C07D295/26—Sulfur atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (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)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Urology & Nephrology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Steroid Compounds (AREA)
SK1783-2001A 1996-06-14 1997-06-10 Spôsob výroby 5-[2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo [4,3-d]pyrimidin-7-ónu SK283894B6 (sk)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9612514.1A GB9612514D0 (en) 1996-06-14 1996-06-14 Novel process

Publications (1)

Publication Number Publication Date
SK283894B6 true SK283894B6 (sk) 2004-04-06

Family

ID=10795332

Family Applications (5)

Application Number Title Priority Date Filing Date
SK743-97A SK283893B6 (sk) 1996-06-14 1997-06-10 Spôsob výroby 5-[2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]- pyrimidin-7-ónu a medziprodukty tohto spôsobu
SK1786-2001A SK283896B6 (sk) 1996-06-14 1997-06-10 Kyselina 2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl) benzoová
SK1787-2001A SK283897B6 (sk) 1996-06-14 1997-06-10 4-[2-Etoxy-5-(4-metylpiperazin-1-ylsulfonyl)benzamido]-1-metyl-3- n-propylpyrazol-5-karboxamid
SK1784-2001A SK283895B6 (sk) 1996-06-14 1997-06-10 Spôsob výroby 5[2-etoxy-5-(4-metylpiperazinu-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3- d]pyrimidin-7-ónu
SK1783-2001A SK283894B6 (sk) 1996-06-14 1997-06-10 Spôsob výroby 5-[2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo [4,3-d]pyrimidin-7-ónu

Family Applications Before (4)

Application Number Title Priority Date Filing Date
SK743-97A SK283893B6 (sk) 1996-06-14 1997-06-10 Spôsob výroby 5-[2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]- pyrimidin-7-ónu a medziprodukty tohto spôsobu
SK1786-2001A SK283896B6 (sk) 1996-06-14 1997-06-10 Kyselina 2-etoxy-5-(4-metylpiperazin-1-ylsulfonyl) benzoová
SK1787-2001A SK283897B6 (sk) 1996-06-14 1997-06-10 4-[2-Etoxy-5-(4-metylpiperazin-1-ylsulfonyl)benzamido]-1-metyl-3- n-propylpyrazol-5-karboxamid
SK1784-2001A SK283895B6 (sk) 1996-06-14 1997-06-10 Spôsob výroby 5[2-etoxy-5-(4-metylpiperazinu-1-ylsulfonyl)- fenyl]-1-metyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3- d]pyrimidin-7-ónu

Country Status (48)

Country Link
US (2) US5955611A (ru)
EP (2) EP0916675B1 (ru)
JP (2) JP2866841B2 (ru)
KR (1) KR100207352B1 (ru)
CN (2) CN1106399C (ru)
AP (1) AP717A (ru)
AR (1) AR003401A1 (ru)
AT (2) ATE246194T1 (ru)
AU (1) AU697684B2 (ru)
BG (1) BG62554B1 (ru)
BR (1) BR9703580A (ru)
CA (1) CA2207694C (ru)
CO (1) CO4780028A1 (ru)
CZ (1) CZ290942B6 (ru)
DE (2) DE69700321T2 (ru)
DK (2) DK0812845T3 (ru)
DZ (1) DZ2247A1 (ru)
EA (1) EA000102B1 (ru)
EG (1) EG24123A (ru)
ES (2) ES2134051T3 (ru)
GB (1) GB9612514D0 (ru)
GR (1) GR3031087T3 (ru)
HK (1) HK1033459A1 (ru)
HN (1) HN1997000072A (ru)
HR (1) HRP970326B1 (ru)
HU (1) HU224497B1 (ru)
ID (1) ID18745A (ru)
IL (3) IL125411A (ru)
IN (5) IN187350B (ru)
IS (2) IS1922B (ru)
MA (1) MA24205A1 (ru)
MX (1) MX9704433A (ru)
NO (2) NO304551B1 (ru)
NZ (1) NZ328084A (ru)
OA (1) OA10426A (ru)
PE (2) PE20011303A1 (ru)
PL (1) PL189333B1 (ru)
PT (1) PT916675E (ru)
RS (2) RS49924B (ru)
SA (1) SA97180124B1 (ru)
SG (1) SG50024A1 (ru)
SI (2) SI0916675T1 (ru)
SK (5) SK283893B6 (ru)
TN (1) TNSN97102A1 (ru)
TR (1) TR199700470A2 (ru)
UA (1) UA27085C2 (ru)
UY (2) UY24585A1 (ru)
ZA (1) ZA975259B (ru)

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060222647A1 (en) * 1993-05-27 2006-10-05 Beavo Joseph A Methods and compositions for modulating the activity of PDE5
ID22834A (id) * 1997-04-25 1999-12-09 Pfizer Pirazolopimidinona untuk kelainan seksual
CN1309561A (zh) * 1997-05-29 2001-08-22 持田制药株式会社 ***机能障碍治疗剂
US6399618B1 (en) 1997-07-09 2002-06-04 Cardiome Pharma Corp Compositions and methods for modulating sexual activity
GB9722520D0 (en) 1997-10-24 1997-12-24 Pfizer Ltd Compounds
PT1049695E (pt) 1997-11-12 2002-07-31 Bayer Ag Imidazotriazinonas 2-fenil substituidas enquanto inibidores de fosfodiesterase
DK1073658T3 (da) * 1998-04-20 2003-12-08 Pfizer Pyrazolopyrimidinon-cGMP PDE5-inhibitorer til behandling af sexualforstyrrelse
CA2235642C (en) 1998-05-15 2007-11-13 Torcan Chemical Ltd. Processes for preparing sildenafil
DK1109814T3 (da) * 1998-09-04 2004-08-02 Ortho Mcneil Pharm Inc 5-Heterocyclylpyrazolo[4,3-d]pyrimidin-7-oner til behandling af mandlig erektil dysfunktion
GB9822238D0 (en) * 1998-10-12 1998-12-09 Pfizer Ltd Process for preparation of pyrazolo[4,3-D]pyrimidin-7-ones and intermediates thereof
GB9823102D0 (en) 1998-10-23 1998-12-16 Pfizer Ltd Pharmaceutically active compounds
GB9823103D0 (en) 1998-10-23 1998-12-16 Pfizer Ltd Pharmaceutically active compounds
GB9823101D0 (en) 1998-10-23 1998-12-16 Pfizer Ltd Pharmaceutically active compounds
KR100353014B1 (ko) * 1998-11-11 2002-09-18 동아제약 주식회사 발기부전 치료에 효과를 갖는 피라졸로피리미디논 화합물
US6087362A (en) * 1999-03-16 2000-07-11 Pentech Pharmaceuticals, Inc. Apomorphine and sildenafil composition
AU5204800A (en) * 1999-06-21 2001-01-09 Biochemical Pharmaceutical Factory of Zhuhai Sez, The Process for preparing sildenafil, and troche which comprises sildenafil and apomorphine
CN1094492C (zh) * 1999-06-21 2002-11-20 杭州神鹰医药化工有限公司 西地那非的制备方法
CN1077108C (zh) * 1999-07-13 2002-01-02 成都地奥制药集团有限公司 用于制备药物昔多芬的前体化合物
WO2001019827A1 (en) * 1999-09-13 2001-03-22 Cipla Ltd. A novel process for the synthesis of sildenafil citrate
US6075028A (en) * 1999-09-23 2000-06-13 Graham; Richard Method of treating Tourette's syndrome and related CNS disorders
TWI265925B (en) * 1999-10-11 2006-11-11 Pfizer Pyrazolo[4,3-d]pyrimidin-7-ones useful in inhibiting type 5 cyclic guanosine 3',5'-monophosphate phosphodiesterases(cGMP PDE5), process and intermediates for their preparation, their uses and composition comprising them
NZ517324A (en) 1999-10-11 2003-09-26 Pfizer 5-(2-substituted-5-heterocyclylsulphonylpyrid-3-YL)- dihydropyrazolo[4,3-d]pyrimidin-7-ones as phosphodiesterase inhibitors
WO2001098303A1 (en) * 2000-06-22 2001-12-27 Pfizer Limited Novel process for the preparation of pyrazolopyrimidinones
US6667398B2 (en) 2000-06-22 2003-12-23 Pfizer Inc Process for the preparation of pyrazolopyrimidinones
US6730786B2 (en) 2000-06-22 2004-05-04 Pfizer Inc Process for the preparation of pyrazolopyrimidinones
GB0015462D0 (en) * 2000-06-22 2000-08-16 Pfizer Ltd Novel process for the preparation of pyrazolopyrimidinones
EP1176147A1 (en) * 2000-07-28 2002-01-30 Pfizer Limited Process for the preparation of pyrazolo[4,3-d]pyrimidin-7-ones and intermediates thereof
EP1176142A1 (en) * 2000-07-28 2002-01-30 Pfizer Inc. Process for the preparation of pyrazoles
US6407259B1 (en) 2000-07-28 2002-06-18 Pfizer Inc. Process for the preparation of pyrazoles
US6821978B2 (en) 2000-09-19 2004-11-23 Schering Corporation Xanthine phosphodiesterase V inhibitors
CN1127506C (zh) * 2001-06-29 2003-11-12 刘宝顺 一种治疗阳痿的新化合物
CN1315835C (zh) * 2001-08-28 2007-05-16 先灵公司 多环鸟嘌呤磷酸二酯酶v抑制剂
SI1509525T1 (sl) 2002-05-31 2006-12-31 Schering Corp Postopek priprave inhibitorjev ksantinske fosfodiesteraze V in njihovih prekurzorjev
DE10232113A1 (de) 2002-07-16 2004-01-29 Bayer Ag Vardenafil Hydrochlorid Trihydrat enthaltende Arzneimittel
CN100374441C (zh) 2003-06-06 2008-03-12 天津倍方科技发展有限公司 二氢吡咯[2，3-d]嘧啶-4-酮衍生物，其制备方法及其制药用途
CN100360531C (zh) * 2003-12-18 2008-01-09 中国人民解放军军事医学科学院放射与辐射医学研究所 用于预防或治疗阳萎和***的新吡唑并嘧啶类化合物
ATE387203T1 (de) * 2004-01-05 2008-03-15 Teva Pharma Prozesse zur herstellung von sildenafil-base und zitratsalz
EP1779852A3 (en) * 2004-01-05 2007-05-09 Teva Pharmaceutical Industries Ltd. Processes for the production of sildenafil base and citrate salt
DE102005009240A1 (de) 2005-03-01 2006-09-07 Bayer Healthcare Ag Arzneiformen mit verbesserten pharmakokinetischen Eigenschaften
WO2008074194A1 (fr) * 2006-12-21 2008-06-26 Topharman Shanghai Co., Ltd. Procédé de préparation du sildénafil et de ses intermédiaires
ES2310144B1 (es) 2007-06-15 2010-01-12 Galenicum Health, S.L. Intermedios para la preparacion de un inhibidor de la fosfodiesterasa tipo 5.
EP2374460A4 (en) 2008-12-12 2013-08-21 Rhein Siegfried Sa De Cv SILDENAFIL COMPOSITION WITH PULSED RELEASE AND METHOD FOR PRODUCING THIS COMPOSITION
MX2010006227A (es) 2010-06-07 2011-12-14 World Trade Imp Exp Wtie Ag Nuevos derivados 1,4-diazepanos, inhibidores de pde-5.
CN102993205B (zh) * 2012-12-27 2015-04-15 华润赛科药业有限责任公司 一种高收率制备高纯度西地那非游离碱的纯化方法
CN103044330B (zh) * 2013-01-14 2018-11-13 常州亚邦制药有限公司 西地那非中间体4-氨基-1-甲基-3-正丙基吡唑-5-甲酰胺的绿色合成新工艺
CN105085526B (zh) * 2014-05-15 2017-08-01 重庆圣华曦药业股份有限公司 一种改进的西地那非制备方法
CN105753870B (zh) * 2016-04-01 2018-05-22 重庆康刻尔制药有限公司 一种西地那非杂质f及其制备方法和应用
WO2017168174A1 (en) 2016-04-02 2017-10-05 N4 Pharma Uk Limited New pharmaceutical forms of sildenafil
CN105837578A (zh) * 2016-04-05 2016-08-10 重庆康刻尔制药有限公司 一种西地那非杂质d的合成方法
WO2018069316A2 (en) 2016-10-10 2018-04-19 Transgene Sa Immunotherapeutic product and mdsc modulator combination therapy
CN113493459B (zh) * 2020-04-07 2022-12-13 广州白云山医药集团股份有限公司白云山制药总厂 Pde5抑制剂化合物及其制备方法和应用
CN112961160A (zh) * 2021-03-05 2021-06-15 遂成药业股份有限公司 一种西地那非的改良合成工艺
CN113754612B (zh) * 2021-10-26 2023-09-26 山东安舜制药有限公司 一种西地那非中间体的制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4871843A (en) * 1983-10-18 1989-10-03 Dropic-Societe Civile De Gestion De Droits De Propriete Industrielle Cyclic benzenesulfonamides, process for their preparation and their use as active substance of pharmaceutical compositions
GB9013750D0 (en) * 1990-06-20 1990-08-08 Pfizer Ltd Therapeutic agents
GB9114760D0 (en) * 1991-07-09 1991-08-28 Pfizer Ltd Therapeutic agents
GB9301192D0 (en) * 1993-06-09 1993-06-09 Trott Francis W Flower shaped mechanised table
ID22834A (id) * 1997-04-25 1999-12-09 Pfizer Pirazolopimidinona untuk kelainan seksual
US6087368A (en) * 1998-06-08 2000-07-11 Bristol-Myers Squibb Company Quinazolinone inhibitors of cGMP phosphodiesterase

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EP0916675B1 (en) 2003-07-30
IN187318B (ru) 2002-03-23
AU2487897A (en) 1997-12-18
CO4780028A1 (es) 1999-05-26
DK0916675T3 (da) 2003-10-27
ATE246194T1 (de) 2003-08-15
DE69700321T2 (de) 1999-11-04
IS1922B (is) 2004-03-15
TNSN97102A1 (fr) 2005-03-15
RS20060484A (en) 2007-04-10
DE69723846D1 (de) 2003-09-04
TR199700470A2 (xx) 1998-01-21
HU9701048D0 (en) 1997-08-28
PL189333B1 (pl) 2005-07-29
RS49653B (sr) 2007-09-21
JP3058863B2 (ja) 2000-07-04
SA97180124A (ar) 2005-12-03
HK1033459A1 (en) 2001-08-31
AU697684B2 (en) 1998-10-15
DZ2247A1 (fr) 2002-12-18
IN187317B (ru) 2002-03-23
US5955611A (en) 1999-09-21
IS1923B (is) 2004-03-15
SI0812845T1 (en) 1999-12-31
MA24205A1 (fr) 1997-12-31
DE69700321D1 (de) 1999-08-19
EG24123A (en) 2008-07-06
CZ290942B6 (cs) 2002-11-13
ES2134051T3 (es) 1999-09-16
GB9612514D0 (en) 1996-08-14
IS6634A (is) 2002-11-25
HRP970326B1 (en) 2000-10-31
JP2866841B2 (ja) 1999-03-08
SK283896B6 (sk) 2004-04-06
EA000102B1 (ru) 1998-08-27
IL125411A0 (en) 1999-03-12
SK283893B6 (sk) 2004-04-06
JPH1081688A (ja) 1998-03-31
PT916675E (pt) 2003-11-28
ATE182150T1 (de) 1999-07-15
NO972481D0 (no) 1997-05-30
GR3031087T3 (en) 1999-12-31
CN1106399C (zh) 2003-04-23
EA199700061A1 (ru) 1997-12-30
SG50024A1 (en) 1998-06-15
BG62554B1 (bg) 2000-02-29
HN1997000072A (es) 1997-12-26
CN1282740A (zh) 2001-02-07
EP0812845A1 (en) 1997-12-17
SK283897B6 (sk) 2004-04-06
MX9704433A (es) 1998-11-30
PE20011303A1 (es) 2001-12-25
PE1299A1 (es) 1999-01-13
NZ328084A (en) 1998-08-26
NO985064L (no) 1997-12-15
IS4503A (is) 1997-12-15
CZ181197A3 (cs) 1998-03-18
BG101569A (en) 1998-01-30
CA2207694C (en) 1999-11-23
IL121000A (en) 2000-02-29
HUP9701048A2 (hu) 1998-12-28
EP0916675A3 (en) 1999-07-14
AR003401A1 (es) 1998-08-05
SI0916675T1 (en) 2003-12-31
HUP9701048A3 (en) 2000-10-30
EP0812845B1 (en) 1999-07-14
JPH11171879A (ja) 1999-06-29
NO972481L (no) 1997-12-15
ID18745A (id) 1998-05-07
YU25497A (sh) 1998-12-23
HRP970326A2 (en) 1998-06-30
AP717A (en) 1999-01-04
IN187350B (ru) 2002-03-30
SK283895B6 (sk) 2004-04-06
SA97180124B1 (ar) 2006-02-08
BR9703580A (pt) 1998-11-10
KR100207352B1 (en) 1999-07-15
IN187320B (ru) 2002-03-23
DE69723846T2 (de) 2004-03-04
UA27085C2 (ru) 2000-02-28
HU224497B1 (hu) 2005-10-28
PL320555A1 (en) 1997-12-22
EP0916675A2 (en) 1999-05-19
NO985064D0 (no) 1998-10-30
ZA975259B (en) 1997-12-15
IL125411A (en) 2000-02-29
DK0812845T3 (da) 1999-11-29
CN1149206C (zh) 2004-05-12
UY24612A1 (es) 2000-09-29
SK74397A3 (en) 1998-06-03
UY24585A1 (es) 1997-12-02
IL121000A0 (en) 1997-11-20
NO304551B1 (no) 1999-01-11
NO306115B1 (no) 1999-09-20
AP9701009A0 (en) 1997-07-31
US6066735A (en) 2000-05-23
CN1168376A (zh) 1997-12-24
OA10426A (en) 2001-12-07
IN187319B (ru) 2002-03-23
KR980002051A (ko) 1998-03-30
RS49924B (sr) 2008-09-29
CA2207694A1 (en) 1997-12-14
ES2201397T3 (es) 2004-03-16

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