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LV10271A - Panemiens omeprazola iegusanai - Google Patents

Panemiens omeprazola iegusanai

Info

Publication number
LV10271A
LV10271A LV931020A LV931020A LV10271A LV 10271 A LV10271 A LV 10271A LV 931020 A LV931020 A LV 931020A LV 931020 A LV931020 A LV 931020A LV 10271 A LV10271 A LV 10271A
Authority
LV
Latvia
Prior art keywords
omeprazole
satisfaction
production
Prior art date
Application number
LV931020A
Other languages
English (en)
Other versions
LV10271B (en
Inventor
Arne Elof Braendstroem
Original Assignee
Astra Ab
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
Application filed by Astra Ab filed Critical Astra Ab
Publication of LV10271A publication Critical patent/LV10271A/lv
Publication of LV10271B publication Critical patent/LV10271B/xx

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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
LVP-93-1020A 1990-06-07 1993-08-10 Improved method for synthesis LV10271B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9002043A SE9002043D0 (sv) 1990-06-07 1990-06-07 Improved method for synthesis
PCT/SE1991/000402 WO1991018895A1 (en) 1990-06-07 1991-06-05 Improved method for synthesis

Publications (2)

Publication Number Publication Date
LV10271A true LV10271A (lv) 1994-10-20
LV10271B LV10271B (en) 1995-04-20

Family

ID=20379708

Family Applications (1)

Application Number Title Priority Date Filing Date
LVP-93-1020A LV10271B (en) 1990-06-07 1993-08-10 Improved method for synthesis

Country Status (42)

Country Link
US (1) US5386032A (lv)
EP (1) EP0533752B1 (lv)
JP (1) JP2993122B2 (lv)
KR (1) KR0178045B1 (lv)
CN (1) CN1040536C (lv)
AP (1) AP216A (lv)
AT (1) ATE162790T1 (lv)
AU (1) AU640246B2 (lv)
BG (1) BG61265B1 (lv)
CA (1) CA2083605C (lv)
CZ (1) CZ279928B6 (lv)
DE (1) DE69128832T2 (lv)
DK (1) DK0533752T3 (lv)
DZ (1) DZ1504A1 (lv)
EG (1) EG19392A (lv)
ES (1) ES2113378T3 (lv)
FI (1) FI102967B (lv)
GR (1) GR3026642T3 (lv)
HK (1) HK1003831A1 (lv)
HR (1) HRP920770B1 (lv)
HU (1) HU214323B (lv)
IE (1) IE911845A1 (lv)
IL (1) IL98274A (lv)
IS (1) IS1752B (lv)
LT (1) LT3584B (lv)
LV (1) LV10271B (lv)
MA (1) MA22171A1 (lv)
NO (1) NO300541B1 (lv)
NZ (1) NZ238224A (lv)
PL (1) PL165433B1 (lv)
PT (1) PT97873B (lv)
RO (1) RO111366B1 (lv)
RU (1) RU2061693C1 (lv)
SA (1) SA91120027B1 (lv)
SE (1) SE9002043D0 (lv)
SG (1) SG48053A1 (lv)
SK (1) SK278505B6 (lv)
TN (1) TNSN91042A1 (lv)
UA (1) UA32524C2 (lv)
WO (1) WO1991018895A1 (lv)
YU (1) YU47570B (lv)
ZA (1) ZA913779B (lv)

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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
US6645988B2 (en) * 1996-01-04 2003-11-11 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
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CA2204580A1 (en) * 1997-05-06 1998-11-06 Michel Zoghbi Synthesis of pharmaceutically useful pyridine derivatives
US6437139B1 (en) 1997-05-06 2002-08-20 Pdi-Research Laboratories, Inc. Synthesis of pharmaceutically useful pyridine derivatives
KR100463031B1 (ko) * 1997-05-26 2005-04-06 동아제약주식회사 5-메톡시-2-[3,5-디메틸-4-메톡시피리딜메틸)설피닐]-1h-벤즈이미다졸의신규제조방법
US6174548B1 (en) 1998-08-28 2001-01-16 Andrx Pharmaceuticals, Inc. Omeprazole formulation
SE9704183D0 (sv) 1997-11-14 1997-11-14 Astra Ab New process
US6096340A (en) 1997-11-14 2000-08-01 Andrx Pharmaceuticals, Inc. Omeprazole formulation
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
US6191148B1 (en) 1998-08-11 2001-02-20 Merck & Co., Inc. Omerazole process and compositions thereof
US6166213A (en) * 1998-08-11 2000-12-26 Merck & Co., Inc. Omeprazole process and compositions thereof
US6733778B1 (en) 1999-08-27 2004-05-11 Andrx Pharmaceuticals, Inc. Omeprazole formulation
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
US6353005B1 (en) 1999-03-02 2002-03-05 Sepracor, Inc. Method and compositions using (+) norcisapride in combination with proton pump inhibitors or H2 receptor antagonist
US6362202B1 (en) 1999-03-02 2002-03-26 Sepracor Inc. Methods and compositions using (−) norcisapride in combination with proton pump inhibitors or H2 receptor antagonists
US6780880B1 (en) 1999-08-26 2004-08-24 Robert R. Whittle FT-Raman spectroscopic measurement
US6312712B1 (en) 1999-08-26 2001-11-06 Robert R. Whittle Method of improving bioavailability
US6369087B1 (en) 1999-08-26 2002-04-09 Robert R. Whittle Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
US6316020B1 (en) 1999-08-26 2001-11-13 Robert R. Whittle Pharmaceutical formulations
US6268385B1 (en) 1999-08-26 2001-07-31 Robert R. Whittle Dry blend pharmaceutical formulations
US6312723B1 (en) 1999-08-26 2001-11-06 Robert R. Whittle Pharmaceutical unit dosage form
US6326384B1 (en) 1999-08-26 2001-12-04 Robert R. Whittle Dry blend pharmaceutical unit dosage form
US6262085B1 (en) 1999-08-26 2001-07-17 Robert R. Whittle Alkoxy substituted Benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
US6262086B1 (en) 1999-08-26 2001-07-17 Robert R. Whittle Pharmaceutical unit dosage form
DE19951960C2 (de) * 1999-10-28 2002-06-27 Gruenenthal Gmbh Verfahren zur Herstellung als Ulkustherapeutika geeigneter Benzimidazol-Derivate
CA2436467A1 (en) 2001-02-02 2002-08-15 Teva Pharmaceutical Industries Ltd. Processes for the production of substituted 2-(2-pyridylmethyl) sulfinyl-1h-benzimidazoles
KR100783020B1 (ko) * 2001-03-23 2007-12-07 동아제약주식회사 2-메틸클로라이드 피리딘 유도체 및 이를 이용한 벤즈이미다졸 유도체의 제조 방법
SK287245B6 (sk) * 2001-07-16 2010-04-07 Janssen Pharmaceutica N. V. Zlepšený spôsob prípravy zlúčenín benzimidazolového typu
EP1469839A2 (en) * 2002-01-25 2004-10-27 Santarus, Inc. Transmucosal delivery of proton pump inhibitors
SE0203092D0 (en) 2002-10-18 2002-10-18 Astrazeneca Ab Method for the synthesis of a benzimidazole compound
EP1603537A4 (en) * 2003-02-20 2009-11-04 Santarus Inc NOVEL FORMULATION, ANTICIPATED COMPLEX IMMEDIATE RELEASE FOR A FAST AND CONTINUOUS SUPPRESSION OF MAGIC ACID
US8993599B2 (en) * 2003-07-18 2015-03-31 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
US20050037070A1 (en) * 2003-07-18 2005-02-17 Santarus, Inc. Pharmaceutical formulatins useful for inhibiting acid secretion and methods for making and using them
CA2531566C (en) * 2003-07-18 2013-05-07 Santarus, Inc. Pharmaceutical formulation and method for treating acid-caused gastrointestinal disorders
US20070292498A1 (en) * 2003-11-05 2007-12-20 Warren Hall Combinations of proton pump inhibitors, sleep aids, buffers and pain relievers
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
ES2441970T3 (es) 2004-09-13 2014-02-07 Takeda Pharmaceutical Company Limited Método para producir lansoprazol
EP1802584B1 (en) * 2004-10-11 2009-09-16 Ranbaxy Laboratories Limited Processes for the preparation of substituted sulfoxides
KR100641534B1 (ko) 2005-07-28 2006-11-01 한미약품 주식회사 에스오메프라졸 및 그의 염의 제조방법
EA200801488A1 (ru) 2005-12-01 2010-02-26 Оспекс Фармасьютикалс, Инк. Замещенные фенетиламины, обладающие серотонинергической и/или норэпинефринергической активностью
EP1801110A1 (en) 2005-12-22 2007-06-27 KRKA, tovarna zdravil, d.d., Novo mesto Esomeprazole arginine salt
WO2007129328A2 (en) * 2006-05-09 2007-11-15 Cadila Healthcare Limited Process for preparing 2-[pyridinyl]sulfinyl-substituted benzimidazoles
US20090092658A1 (en) * 2007-10-05 2009-04-09 Santarus, Inc. Novel formulations of proton pump inhibitors and methods of using these formulations
WO2008092939A2 (en) 2007-01-31 2008-08-07 Krka, Tovarna Zdravil, D.D., Novo Mesto Process for the preparation of optically pure omeprazole via salt formation with a chiral amine or treatment with an entiomer converting enzyme and chromatographic separation
EP2125698B1 (en) 2007-03-15 2016-08-31 Auspex Pharmaceuticals, Inc. DEUTERATED d9-VENLAFAXINE
WO2009122435A2 (en) * 2008-03-31 2009-10-08 Council Of Scientific & Industrial Research A simultaneous method for the preparation of a mixture of 3- acetoxy-17-acetamido-16-formyl-androst-5,17-diene and 3- acetoxy-2'-chloro-5-androsteno[17,16-b]pyridine
WO2010134099A1 (en) 2009-05-21 2010-11-25 Cadila Healthcare Limited One pot process for preparing omeprazole and related compounds
CN102786513A (zh) * 2011-05-18 2012-11-21 中国医学科学院药物研究所 奥美拉唑晶e型物质及制备方法与在药品和保健品中应用
CN104203938A (zh) 2012-01-21 2014-12-10 朱比兰特生命科学有限公司 用于制备2-吡啶基甲基亚硫酰基苯并咪唑、它们的类似物和光学活性对映体的方法
CN114364389A (zh) 2019-09-24 2022-04-15 普罗莱克塔生物科学公司 用于治疗炎性和免疫疾病的组合物和方法

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IN148930B (lv) * 1977-09-19 1981-07-25 Hoffmann La Roche
SE7804231L (sv) * 1978-04-14 1979-10-15 Haessle Ab Magsyrasekretionsmedel
US4307102A (en) * 1981-02-19 1981-12-22 Sterling Drug Inc. Phenanthro[2,3-c]pyrazole
SE8300736D0 (sv) * 1983-02-11 1983-02-11 Haessle Ab Novel pharmacologically active compounds
ZW4585A1 (en) * 1984-04-19 1985-11-20 Hoffmann La Roche Imidazole derivatives
IL76839A (en) * 1984-10-31 1988-08-31 Byk Gulden Lomberg Chem Fab Picoline derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same
SE8500996D0 (sv) * 1985-03-01 1985-03-01 Haessle Ab Method of treatment
SE8600658D0 (sv) * 1986-02-14 1986-02-14 Haessle Ab Novel composition of matter
FI91754C (fi) * 1986-12-02 1994-08-10 Tanabe Seiyaku Co Analogiamenetelmä lääkeaineena käyttökelpoisen imidatsolijohdannaisen valmistamiseksi
DE3722810A1 (de) * 1987-07-10 1989-01-19 Hoechst Ag Substituierte benzimidazole, verfahren zu deren herstellung, diese enthaltende pharmazeutische zubereitungen und deren verwendung
SE9002206D0 (sv) * 1990-06-20 1990-06-20 Haessle Ab New compounds
NZ244301A (en) * 1991-09-20 1994-08-26 Merck & Co Inc Preparation of 2-pyridylmethylsulphinylbenzimidazole and pyridoimidazole derivatives from the corresponding sulphenyl compounds

Also Published As

Publication number Publication date
DE69128832T2 (de) 1998-05-28
HRP920770B1 (en) 2000-06-30
RO111366B1 (ro) 1996-09-30
PL165433B1 (pl) 1994-12-30
AU640246B2 (en) 1993-08-19
CN1040536C (zh) 1998-11-04
SK278505B6 (en) 1997-08-06
YU99291A (sh) 1993-11-16
AP9100274A0 (en) 1991-07-31
EP0533752B1 (en) 1998-01-28
FI102967B1 (fi) 1999-03-31
BG97146A (bg) 1993-12-24
SG48053A1 (en) 1998-04-17
KR0178045B1 (en) 1999-03-20
NZ238224A (en) 1993-11-25
IS1752B (is) 2000-07-21
HU214323B (hu) 1998-03-02
PT97873B (pt) 1998-10-30
IL98274A (en) 1995-03-30
EP0533752A1 (en) 1993-03-31
HK1003831A1 (en) 1998-11-06
TNSN91042A1 (fr) 1992-10-25
IL98274A0 (en) 1992-06-21
LTIP1711A (en) 1995-07-25
MA22171A1 (fr) 1991-12-31
PT97873A (pt) 1992-04-30
JPH05507699A (ja) 1993-11-04
ES2113378T3 (es) 1998-05-01
CN1058211A (zh) 1992-01-29
FI925529A0 (fi) 1992-12-04
LT3584B (en) 1995-12-27
DK0533752T3 (da) 1998-06-02
EG19392A (en) 1995-06-29
DZ1504A1 (fr) 2004-09-13
CA2083605C (en) 1998-12-08
NO924682D0 (no) 1992-12-04
DE69128832D1 (de) 1998-03-05
ATE162790T1 (de) 1998-02-15
ZA913779B (en) 1992-02-26
AP216A (en) 1992-09-02
HRP920770A2 (en) 1995-12-31
UA32524C2 (uk) 2001-02-15
SE9002043D0 (sv) 1990-06-07
NO300541B1 (no) 1997-06-16
BG61265B1 (en) 1997-04-30
WO1991018895A1 (en) 1991-12-12
SA91120027B1 (ar) 2002-06-03
CZ279928B6 (cs) 1995-08-16
NO924682L (no) 1992-12-04
IS3711A7 (is) 1991-12-08
FI102967B (fi) 1999-03-31
FI925529L (fi) 1992-12-04
LV10271B (en) 1995-04-20
RU2061693C1 (ru) 1996-06-10
CS172691A3 (en) 1992-01-15
HUT63408A (en) 1993-08-30
JP2993122B2 (ja) 1999-12-20
YU47570B (sh) 1995-10-03
HU9203855D0 (en) 1993-03-29
CA2083605A1 (en) 1991-12-08
GR3026642T3 (en) 1998-07-31
IE911845A1 (en) 1991-12-18
US5386032A (en) 1995-01-31
AU8080791A (en) 1991-12-31

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