HUP0001547A2 - Az S-omeprazol új formája - Google Patents

Az S-omeprazol új formája

Info

Publication number
HUP0001547A2
HUP0001547A2 HU0001547A HUP0001547A HUP0001547A2 HU P0001547 A2 HUP0001547 A2 HU P0001547A2 HU 0001547 A HU0001547 A HU 0001547A HU P0001547 A HUP0001547 A HU P0001547A HU P0001547 A2 HUP0001547 A2 HU P0001547A2
Authority
HU
Hungary
Prior art keywords
omeprazole
neutral
organic solvents
solution
solid
Prior art date
Application number
HU0001547A
Other languages
English (en)
Inventor
Martin Bohlin
Karol Horvath
Sverker Von Unge
Original Assignee
Astra Aktiebolag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=20405146&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HUP0001547(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astra Aktiebolag filed Critical Astra Aktiebolag
Publication of HUP0001547A2 publication Critical patent/HUP0001547A2/hu
Publication of HU0001547D0 publication Critical patent/HU0001547D0/hu
Publication of HUP0001547A3 publication Critical patent/HUP0001547A3/hu
Publication of HU227589B1 publication Critical patent/HU227589B1/hu

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics

Abstract

A találmány tárgyát az (S)-omeprazol neutrális alakjának új, szilárdhalmazállapotú, legalább részben kristályos formája, eljárás ennekelőállítására és ezt a formát tartalmazó gyógyszerkészítményekképezik. A találmány szerint úgy járnak el, hogy a) neutrális (S)-omeprazol egy vagy több szerves oldószerrel készített oldatát nagyontöményre bepárolják, további oldószert adva hozzá folytatják abepárlást mindaddig, amíg szilárd, amorf, neutrális (S)-omeprazolkeletkezik; vagy b) az (S)-omeprazolt egy vagy több szervesoldószerrel és adott esetben vízzel készített oldatábólkristályosítják; vagy c) az (S)-omeprazol alkalikus sójának vízzel ésadott esetben egy vagy több szerves oldószerrel készített oldatából az(S)-omeprazolt megfelelő savval kicsapják. Ó
HU0001547A 1996-12-20 1997-12-16 Crystal form of (s)-omeprazole HU227589B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9604793A SE510666C2 (sv) 1996-12-20 1996-12-20 Nya Kristallmodifikationer
PCT/SE1997/002125 WO1998028294A1 (en) 1996-12-20 1997-12-16 A novel compound form

Publications (4)

Publication Number Publication Date
HUP0001547A2 true HUP0001547A2 (hu) 2002-05-29
HU0001547D0 HU0001547D0 (hu) 2002-05-29
HUP0001547A3 HUP0001547A3 (en) 2002-06-28
HU227589B1 HU227589B1 (en) 2011-09-28

Family

ID=20405146

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0001547A HU227589B1 (en) 1996-12-20 1997-12-16 Crystal form of (s)-omeprazole

Country Status (37)

Country Link
US (1) US6162816A (hu)
EP (1) EP0946547B1 (hu)
JP (1) JP4402174B2 (hu)
KR (1) KR20000069595A (hu)
CN (1) CN1109684C (hu)
AR (1) AR010361A1 (hu)
AT (1) ATE236898T1 (hu)
AU (1) AU730129B2 (hu)
BR (1) BR9714059A (hu)
CA (1) CA2274076C (hu)
CZ (1) CZ294784B6 (hu)
DE (1) DE69720774T2 (hu)
DK (1) DK0946547T3 (hu)
EE (1) EE03923B1 (hu)
EG (1) EG24414A (hu)
ES (1) ES2194231T3 (hu)
HK (1) HK1022909A1 (hu)
HU (1) HU227589B1 (hu)
ID (1) ID21850A (hu)
IL (1) IL130450A0 (hu)
IS (1) IS1981B (hu)
MY (1) MY117032A (hu)
NO (1) NO317191B1 (hu)
NZ (1) NZ336024A (hu)
PL (1) PL190377B1 (hu)
PT (1) PT946547E (hu)
RS (1) RS49685B (hu)
RU (1) RU2184734C2 (hu)
SA (1) SA97180739B1 (hu)
SE (1) SE510666C2 (hu)
SI (1) SI0946547T1 (hu)
SK (1) SK285151B6 (hu)
TR (1) TR199901410T2 (hu)
TW (1) TW538039B (hu)
UA (1) UA55436C2 (hu)
WO (1) WO1998028294A1 (hu)
ZA (1) ZA9711046B (hu)

Families Citing this family (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6699885B2 (en) 1996-01-04 2004-03-02 The Curators Of The University Of Missouri Substituted benzimidazole dosage forms and methods of using same
US6489346B1 (en) 1996-01-04 2002-12-03 The Curators Of The University Of Missouri Substituted benzimidazole dosage forms and method of using same
US5840737A (en) 1996-01-04 1998-11-24 The Curators Of The University Of Missouri Omeprazole solution and method for using same
US6645988B2 (en) 1996-01-04 2003-11-11 Curators Of The University Of Missouri Substituted benzimidazole dosage forms and method of using same
SI20019A (sl) * 1998-07-13 2000-02-29 LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. Izboljšan postopek sinteze 5-metoksi -2-/(4-metoksi-3,5-dimetil-2-piridil)metil/ sulfinil-1H-benzimidazola
IL142703A (en) 1998-11-10 2006-04-10 Astrazeneca Ab Crystalline form of omeprazole
UA72748C2 (en) * 1998-11-10 2005-04-15 Astrazeneca Ab A novel crystalline form of omeprazole
JP3926936B2 (ja) 1998-11-16 2007-06-06 エーザイ・アール・アンド・ディー・マネジメント株式会社 スルホキシド誘導体・アセトン錯体およびその製造法
SE9804003D0 (sv) 1998-11-23 1998-11-23 Astra Ab A method of producing drug particles
SE9900274D0 (sv) * 1999-01-28 1999-01-28 Astra Ab New compound
JP2000344739A (ja) * 1999-06-01 2000-12-12 Sumitomo Chem Co Ltd N−保護−アゼチジン−2−カルボン酸の製造方法
TWI289557B (en) 1999-06-17 2007-11-11 Takeda Chemical Industries Ltd A crystal of a hydrate of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole
SE0000773D0 (sv) * 2000-03-08 2000-03-08 Astrazeneca Ab New formulation
SE0000774D0 (sv) 2000-03-08 2000-03-08 Astrazeneca Ab New formulation
KR101035534B1 (ko) * 2000-05-15 2011-05-23 다케다 야쿠힌 고교 가부시키가이샤 결정의 제조방법
GB0016040D0 (en) * 2000-06-29 2000-08-23 Glaxo Group Ltd Novel process for preparing crystalline particles
CA2417311C (en) 2000-08-04 2012-07-10 Takeda Chemical Industries, Ltd. Crystalline alkali metal salts of lansoprazole and their production and use
SI20875A (sl) * 2001-04-25 2002-10-31 LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. Kristalna oblika omeprazola
US8206741B2 (en) 2001-06-01 2012-06-26 Pozen Inc. Pharmaceutical compositions for the coordinated delivery of NSAIDs
EP2163241A1 (en) 2001-06-01 2010-03-17 Pozen, Inc. Pharmaceutical compositions for the coordinated delivery of NSAIDs
GB2376231A (en) 2001-06-06 2002-12-11 Cipla Ltd Benzimidazole-cyclodextrin inclusion complex
SE0102993D0 (sv) 2001-09-07 2001-09-07 Astrazeneca Ab New self emulsifying drug delivery system
EP1515963B1 (en) 2002-06-27 2007-02-14 Dr. Reddy's Laboratories Ltd. A process for preparation of optically pure or optically enriched sulfoxide compounds, including amorphous esomeprazole and salts thereof
AU2003247729B2 (en) * 2002-06-27 2009-10-08 Dr. Reddy's Laboratories Limited A process for preparation of optically pure or optically enriched sulfoxide compounds, including amorphous esomeprazole and salts thereof
US7612098B2 (en) * 2002-08-30 2009-11-03 Dr. Reddy's Laboratories Limited Amorphous hydrous esomeprazole magnesium
EP2596792A1 (en) 2002-10-16 2013-05-29 Takeda Pharmaceutical Company Limited Stable solid preparations
US20040235903A1 (en) * 2002-10-22 2004-11-25 Khanna Mahavir Singh Amorphous form of esomeprazole salts
WO2004046134A2 (en) * 2002-11-18 2004-06-03 Dr. Reddy's Laboratories Limited Crystalline form ii of esomeprazole magnesium trihydrate and process for its preparation
CA2517714A1 (en) * 2003-02-28 2004-09-10 Ranbaxy Laboratories Limited Polymorphs of s-omeprazole
CN100364987C (zh) * 2003-03-24 2008-01-30 卫材R&D管理有限公司 亚砜衍生物或其盐的非定形态的制备方法
US20070060556A1 (en) * 2003-05-05 2007-03-15 Yatendra Kumar Barium salt of benzimidazole derivative
US8993599B2 (en) 2003-07-18 2015-03-31 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
SE0400410D0 (sv) 2004-02-20 2004-02-20 Astrazeneca Ab New compounds
US8815916B2 (en) 2004-05-25 2014-08-26 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
US8906940B2 (en) 2004-05-25 2014-12-09 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
AU2005264864B2 (en) 2004-06-16 2011-08-11 Takeda Pharmaceutical Company Limited Multiple PPI dosage form
NZ551970A (en) * 2004-06-24 2010-01-29 Astrazeneca Ab New process for the preparation of crystal modifications for use in the preparation of esomeprazole sodium salt
ES2246149B1 (es) * 2004-07-02 2007-06-01 Esteve Quimica, S.A. Formas solidas de la sal magnesica de s-omeprazol y procedimientos para su preparacion.
WO2006120520A1 (en) * 2005-05-06 2006-11-16 Glenmark Pharmaceuticals Limited Esomeprazole strontium salt, process for its preparation and pharmaceutical compositions containing same
EP1907375B1 (en) * 2005-06-08 2013-07-24 LEK Pharmaceuticals d.d. Crystalline solvate of omeprazole sodium
US7563812B2 (en) 2005-06-15 2009-07-21 Hetero Drugs Limited Amorphous esomeprazole hydrate
NL2000126C2 (nl) * 2005-07-15 2008-01-29 Solvay Werkwijze voor de vervaardiging van eptifibatide.
US20070043085A1 (en) * 2005-08-19 2007-02-22 Glenmark Pharmaceuticals Limited Process for the preparation of amorphous form of neutral esomeprazole
US7576219B2 (en) 2005-10-26 2009-08-18 Hanmi Pharm. Co., Ltd Crystalline S-omeprazole strontium hydrate, method for preparing same, and pharmaceutical composition containing same
EP1948637A4 (en) * 2005-11-14 2010-09-08 Hetero Drugs Ltd PROCESS FOR AMORPHES ESOMEPRAZOLE
JP2009518394A (ja) * 2005-12-05 2009-05-07 アストラゼネカ・アクチエボラーグ エソメプラゾールの非塩形態の新規の製造方法
EP1801110A1 (en) 2005-12-22 2007-06-27 KRKA, tovarna zdravil, d.d., Novo mesto Esomeprazole arginine salt
US7799925B2 (en) 2005-12-28 2010-09-21 Unión Químico Farmacéutica, S.A. Process for the preparation of the (S)-enantiomer of omeprazole
EP2000468A1 (en) * 2007-05-09 2008-12-10 Dr. Reddy's Laboratories Ltd. Esomeprazole salts and processes for preparation thereof
WO2009047775A2 (en) * 2007-10-08 2009-04-16 Hetero Drugs Limited Polymorphs of esomeprazole salts
NZ588379A (en) 2008-03-10 2012-07-27 Takeda Pharmaceutical Crystal of benzimidazole compound
EP2143722A1 (en) 2008-07-09 2010-01-13 Lek Pharmaceuticals D.D. Process for preparation of esomeprazole sodium of high chemical purity and new forms of esomeprazole sodium
AU2009290712A1 (en) * 2008-09-09 2010-03-18 Astrazeneca Ab Method for delivering a pharmaceutical composition to patient in need thereof
SG176724A1 (en) 2009-06-25 2012-01-30 Astrazeneca Ab Method for treating a patient at risk for developing an nsaid-associated ulcer
SG181535A1 (en) 2009-12-08 2012-07-30 Codexis Inc Synthesis of prazole compounds
EP2649187B1 (en) 2010-12-08 2017-11-22 Codexis, Inc. Biocatalysts and methods for the synthesis of armodafinil
EA028049B1 (ru) 2011-12-28 2017-10-31 Поузен Инк. Улучшенные композиции и способы доставки омепразола и ацетилсалициловой кислоты
RU2501549C1 (ru) 2012-08-30 2013-12-20 Авва Девелопмент Лтд Фармацевтическая композиция для лечения гастроэзофагеальной рефлюксной болезни
CN107043367A (zh) * 2017-05-26 2017-08-15 重庆莱美隆宇药业有限公司 一种中性s‑奥美拉唑的干燥工艺
WO2024075017A1 (en) 2022-10-04 2024-04-11 Zabirnyk Arsenii Inhibition of aortic valve calcification

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE7804231L (sv) * 1978-04-14 1979-10-15 Haessle Ab Magsyrasekretionsmedel
SE8301182D0 (sv) * 1983-03-04 1983-03-04 Haessle Ab Novel compounds
GB2189698A (en) * 1986-04-30 1987-11-04 Haessle Ab Coated omeprazole tablets
DE4035455A1 (de) * 1990-11-08 1992-05-14 Byk Gulden Lomberg Chem Fab Enantiomerentrennung
US5877192A (en) * 1993-05-28 1999-03-02 Astra Aktiebolag Method for the treatment of gastric acid-related diseases and production of medication using (-) enantiomer of omeprazole
SE9301830D0 (sv) * 1993-05-28 1993-05-28 Ab Astra New compounds
SE9302396D0 (sv) * 1993-07-09 1993-07-09 Ab Astra A novel compound form
HUT75775A (en) * 1994-07-08 1997-05-28 Astra Ab Medicament with multiple unit tablated dosage form containing omeprazole

Also Published As

Publication number Publication date
AU730129B2 (en) 2001-02-22
HK1022909A1 (en) 2000-08-25
BR9714059A (pt) 2000-05-09
ATE236898T1 (de) 2003-04-15
AU5502698A (en) 1998-07-17
RU2184734C2 (ru) 2002-07-10
HU227589B1 (en) 2011-09-28
SK76599A3 (en) 1999-12-10
WO1998028294A1 (en) 1998-07-02
KR20000069595A (ko) 2000-11-25
CZ220299A3 (cs) 2000-02-16
AR010361A1 (es) 2000-06-07
SE9604793D0 (sv) 1996-12-20
IS1981B (is) 2005-01-14
DK0946547T3 (da) 2003-06-30
HUP0001547A3 (en) 2002-06-28
CA2274076A1 (en) 1998-07-02
SA97180739B1 (ar) 2006-05-20
IS5070A (is) 1999-06-07
RS49685B (sr) 2007-11-15
TW538039B (en) 2003-06-21
CA2274076C (en) 2008-09-30
SE9604793L (sv) 1998-06-21
SK285151B6 (sk) 2006-07-07
EE03923B1 (et) 2002-12-16
NO317191B1 (no) 2004-09-13
EG24414A (en) 2009-05-25
NZ336024A (en) 2001-02-23
JP2001507025A (ja) 2001-05-29
IL130450A0 (en) 2000-06-01
UA55436C2 (uk) 2003-04-15
ES2194231T3 (es) 2003-11-16
ID21850A (id) 1999-08-05
ZA9711046B (en) 1998-06-22
NO993068L (no) 1999-06-21
JP4402174B2 (ja) 2010-01-20
CN1109684C (zh) 2003-05-28
NO993068D0 (no) 1999-06-21
CZ294784B6 (cs) 2005-03-16
SI0946547T1 (en) 2003-10-31
PL190377B1 (pl) 2005-12-30
CN1241183A (zh) 2000-01-12
EE9900259A (et) 2000-02-15
PT946547E (pt) 2003-07-31
DE69720774D1 (de) 2003-05-15
EP0946547B1 (en) 2003-04-09
HU0001547D0 (hu) 2002-05-29
SE510666C2 (sv) 1999-06-14
YU28199A (sh) 2002-03-18
TR199901410T2 (xx) 1999-08-23
DE69720774T2 (de) 2004-02-05
EP0946547A1 (en) 1999-10-06
MY117032A (en) 2004-04-30
PL334297A1 (en) 2000-02-14
US6162816A (en) 2000-12-19

Similar Documents

Publication Publication Date Title
HUP0001547A2 (hu) Az S-omeprazol új formája
NO2005025I1 (no) Krystalinsk ceftiofurfri syre, fremgangsmate for fremstilling av denne, og farmasoytisk preparat
RU99116303A (ru) Новая форма соединения
RU94031126A (ru) Циклические мочевины и их аналоги, пригодные в качестве ингибиторов протеазы ретровирусов, способ лечения вирусных инфекций, фармацевтическая композиция
BR9903984A (pt) Composição aquosa que contém peptìdio farmaceuticamente efetivo, utilização dessa composição, processo para a produção de uma composição farmacêutica para aplicação local e processo para aumentar a atividade de um polipeptìdio
DK0948527T3 (da) Cylosporinderivater, fremstilling af disse og farmaceutiske præparater indeholdende disse
ES2178268T3 (es) Formulaciones de liberacion controlada.
IT1254619B (it) Procedimento per la purificazione di acido ftalimmido-perossicaproico (pap) da impurezze di solventi clorurati
FI940806A (fi) Sykliset johdokset, näitä yhdisteitä sisältävät lääkeaineet ja menetelmä niiden valmistamiseksi
AU5669398A (en) Novel cyclosporin derivatives, method of preparation and pharmaceutical compositions containing them
HUP0400781A2 (hu) Eljárás (R)- vagy (S)-lansoprazol kristályosítására, az előállított kristályok, azokat tartalmazó gyógyszerkészítmények és alkalmazásuk
FI883249A (fi) Menetelmä terapeuttisesti käyttökelpoisten 3-desmetyylimevalonihappojohdannaisten valmistamiseksi
NO20012514D0 (no) Fremgangsmåte for fremstilling av partikler med en omdannet amorf og/eller meta-stabil krystallinsk region til krystallinsktilstand
RU94028888A (ru) Производные 1,3-замещенного циклоалкана и циклоалкена, смесь их изомеров или индивидуальные изомеры, их гидраты и соли, способ их получения и фармацевтическая композиция
HUP0302099A2 (hu) Az azithromicin monohidrátja, eljárás az előállítására és a monohidrátot tartalmazó gyógyszerkészítmény
MY126071A (en) Crystalline form ii of cabergoline.
HUP9901713A2 (hu) Eljárás enantiomer-tiszta 2-azetidinkarbonsav előállítására
CA2460970A1 (en) Processes for preparing crystalline and amorphous mupirocin calcium
ATE274513T1 (de) Verbindungen und verfahren zur behandlung von schmerz
Pincock et al. Spontaneous and induced generation of optical activity in racemic 1, 1′-Binaphthyl
ES2272198B1 (es) Procedimiento para la obtencion de hidrato de calcipotriol.
FI20001655A (fi) Kiteytysmenetelmõ
NO305658B1 (no) Termodynamisk stabil krystallform av 4"-deoksy-4"-epi-metylaminoavermektin-B1a/B1b-benzosyresalt og fremgangsmÕte for fremstilling av dette
HUP0004916A2 (hu) Eljárás 1,2,3,4-tetrahidroizokinolin-2,3-dikarbonsavanhidrid és felhasználásával (S)-N-terc-butil-1,2,3,4-tetrahidroizokinolin-3-karboxamid előállítására
Cuthbert et al. Cyclic sulphamidite analogues of penicillanic acid

Legal Events

Date Code Title Description
MM4A Lapse of definitive patent protection due to non-payment of fees