LT3584B - Improved method for omeprazole synthesis - Google Patents

Improved method for omeprazole synthesis Download PDF

Info

Publication number
LT3584B
LT3584B LTIP1711A LTIP1711A LT3584B LT 3584 B LT3584 B LT 3584B LT IP1711 A LTIP1711 A LT IP1711A LT IP1711 A LTIP1711 A LT IP1711A LT 3584 B LT3584 B LT 3584B
Authority
LT
Lithuania
Prior art keywords
omeprazole
process according
aqueous phase
methoxy
naoh
Prior art date
Application number
LTIP1711A
Other languages
English (en)
Lithuanian (lt)
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 LTIP1711A publication Critical patent/LTIP1711A/xx
Publication of LT3584B publication Critical patent/LT3584B/lt

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)
LTIP1711A 1990-06-07 1993-12-30 Improved method for omeprazole synthesis LT3584B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE9002043A SE9002043D0 (sv) 1990-06-07 1990-06-07 Improved method for synthesis

Publications (2)

Publication Number Publication Date
LTIP1711A LTIP1711A (en) 1995-07-25
LT3584B true LT3584B (en) 1995-12-27

Family

ID=20379708

Family Applications (1)

Application Number Title Priority Date Filing Date
LTIP1711A LT3584B (en) 1990-06-07 1993-12-30 Improved method for omeprazole synthesis

Country Status (42)

Country Link
US (1) US5386032A (ja)
EP (1) EP0533752B1 (ja)
JP (1) JP2993122B2 (ja)
KR (1) KR0178045B1 (ja)
CN (1) CN1040536C (ja)
AP (1) AP216A (ja)
AT (1) ATE162790T1 (ja)
AU (1) AU640246B2 (ja)
BG (1) BG61265B1 (ja)
CA (1) CA2083605C (ja)
CZ (1) CZ279928B6 (ja)
DE (1) DE69128832T2 (ja)
DK (1) DK0533752T3 (ja)
DZ (1) DZ1504A1 (ja)
EG (1) EG19392A (ja)
ES (1) ES2113378T3 (ja)
FI (1) FI102967B1 (ja)
GR (1) GR3026642T3 (ja)
HK (1) HK1003831A1 (ja)
HR (1) HRP920770B1 (ja)
HU (1) HU214323B (ja)
IE (1) IE911845A1 (ja)
IL (1) IL98274A (ja)
IS (1) IS1752B (ja)
LT (1) LT3584B (ja)
LV (1) LV10271B (ja)
MA (1) MA22171A1 (ja)
NO (1) NO300541B1 (ja)
NZ (1) NZ238224A (ja)
PL (1) PL165433B1 (ja)
PT (1) PT97873B (ja)
RO (1) RO111366B1 (ja)
RU (1) RU2061693C1 (ja)
SA (1) SA91120027B1 (ja)
SE (1) SE9002043D0 (ja)
SG (1) SG48053A1 (ja)
SK (1) SK278505B6 (ja)
TN (1) TNSN91042A1 (ja)
UA (1) UA32524C2 (ja)
WO (1) WO1991018895A1 (ja)
YU (1) YU47570B (ja)
ZA (1) ZA913779B (ja)

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US6645988B2 (en) 1996-01-04 2003-11-11 Curators Of The University Of Missouri Substituted benzimidazole dosage forms and method 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
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US6437139B1 (en) 1997-05-06 2002-08-20 Pdi-Research Laboratories, Inc. Synthesis of pharmaceutically useful pyridine derivatives
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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
US6166213A (en) * 1998-08-11 2000-12-26 Merck & Co., Inc. Omeprazole process and compositions thereof
US6191148B1 (en) 1998-08-11 2001-02-20 Merck & Co., Inc. Omerazole 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
US6312712B1 (en) 1999-08-26 2001-11-06 Robert R. Whittle Method of improving bioavailability
US6262086B1 (en) 1999-08-26 2001-07-17 Robert R. Whittle Pharmaceutical unit dosage form
US6780880B1 (en) * 1999-08-26 2004-08-24 Robert R. Whittle FT-Raman spectroscopic measurement
US6268385B1 (en) 1999-08-26 2001-07-31 Robert R. Whittle Dry blend pharmaceutical formulations
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
US6316020B1 (en) 1999-08-26 2001-11-13 Robert R. Whittle 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
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
DE19951960C2 (de) * 1999-10-28 2002-06-27 Gruenenthal Gmbh Verfahren zur Herstellung als Ulkustherapeutika geeigneter Benzimidazol-Derivate
CN1876647A (zh) 2001-02-02 2006-12-13 特瓦制药工业有限公司 苯并咪唑化合物产品
KR100783020B1 (ko) * 2001-03-23 2007-12-07 동아제약주식회사 2-메틸클로라이드 피리딘 유도체 및 이를 이용한 벤즈이미다졸 유도체의 제조 방법
US6919459B2 (en) 2001-07-16 2005-07-19 Rudy Laurent Maria Broeckx Process for preparing benzimidazole-type compounds
JP2005521662A (ja) * 2002-01-25 2005-07-21 サンタラス インコーポレイティッド プロトンポンプ阻害剤の経粘膜送達
SE0203092D0 (en) 2002-10-18 2002-10-18 Astrazeneca Ab Method for the synthesis of a benzimidazole compound
WO2004073654A2 (en) * 2003-02-20 2004-09-02 Santarus, Inc. A novel formulation, omeprazole antacid complex-immediate release for rapid and sustained supression of gastric acid
AR045062A1 (es) * 2003-07-18 2005-10-12 Santarus Inc Formulaciones farmaceuticas para inhibir la secrecion de acido y metodos para preparar y utilizarlas
US8993599B2 (en) * 2003-07-18 2015-03-31 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
TWI337877B (en) * 2003-07-18 2011-03-01 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
CN102775388B (zh) * 2004-09-13 2016-01-20 武田药品工业株式会社 氧化化合物的制备方法和制备装置
WO2006040635A1 (en) * 2004-10-11 2006-04-20 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
HUE027865T2 (en) 2005-12-01 2016-11-28 Auspex Pharmaceuticals Inc Substituted phenyl ethylamines with serotonergic and / or norepinephrine activity
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
EP3103790B1 (en) 2007-03-15 2018-05-09 Auspex Pharmaceuticals, Inc. Substituted phenethylamine with serotoninergic and/or norepinephrinergic activity
US8513226B2 (en) * 2008-03-31 2013-08-20 Council Of Scientific And Industrial Research 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
WO2013108068A1 (en) 2012-01-21 2013-07-25 Jubilant Life Sciences Limited Process for the preparation of 2-pyridinylmethylsulfinyl benzimidazoles, their analogs and optically active enantiomers
KR20220066904A (ko) 2019-09-24 2022-05-24 프롤랙타 바이오사이언스, 인코포레이티드 염증 및 면역 질환의 치료용 조성물 및 방법

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4255431A (en) 1978-04-14 1981-03-10 Aktiebolaget Hassle Gastric acid secretion inhibiting substituted 2-(2-benzimidazolyl)-pyridines, pharmaceutical preparations containing same, and method for inhibiting gastric acid secretion

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IN148930B (ja) * 1977-09-19 1981-07-25 Hoffmann La Roche
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

Patent Citations (1)

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US4255431A (en) 1978-04-14 1981-03-10 Aktiebolaget Hassle Gastric acid secretion inhibiting substituted 2-(2-benzimidazolyl)-pyridines, pharmaceutical preparations containing same, and method for inhibiting gastric acid secretion

Also Published As

Publication number Publication date
HRP920770B1 (en) 2000-06-30
US5386032A (en) 1995-01-31
LTIP1711A (en) 1995-07-25
SK278505B6 (en) 1997-08-06
JP2993122B2 (ja) 1999-12-20
IS3711A7 (is) 1991-12-08
EG19392A (en) 1995-06-29
NO924682L (no) 1992-12-04
HRP920770A2 (en) 1995-12-31
CA2083605C (en) 1998-12-08
PT97873B (pt) 1998-10-30
AP9100274A0 (en) 1991-07-31
DK0533752T3 (da) 1998-06-02
BG61265B1 (en) 1997-04-30
DZ1504A1 (fr) 2004-09-13
RO111366B1 (ro) 1996-09-30
SG48053A1 (en) 1998-04-17
HK1003831A1 (en) 1998-11-06
EP0533752B1 (en) 1998-01-28
LV10271A (lv) 1994-10-20
FI102967B (fi) 1999-03-31
YU47570B (sh) 1995-10-03
FI102967B1 (fi) 1999-03-31
HUT63408A (en) 1993-08-30
LV10271B (en) 1995-04-20
RU2061693C1 (ru) 1996-06-10
HU214323B (hu) 1998-03-02
AP216A (en) 1992-09-02
FI925529A0 (fi) 1992-12-04
CS172691A3 (en) 1992-01-15
ATE162790T1 (de) 1998-02-15
SE9002043D0 (sv) 1990-06-07
ZA913779B (en) 1992-02-26
AU640246B2 (en) 1993-08-19
DE69128832D1 (de) 1998-03-05
GR3026642T3 (en) 1998-07-31
PL165433B1 (pl) 1994-12-30
FI925529A (fi) 1992-12-04
CA2083605A1 (en) 1991-12-08
NO924682D0 (no) 1992-12-04
WO1991018895A1 (en) 1991-12-12
JPH05507699A (ja) 1993-11-04
UA32524C2 (uk) 2001-02-15
YU99291A (sh) 1993-11-16
TNSN91042A1 (fr) 1992-10-25
IL98274A0 (en) 1992-06-21
IL98274A (en) 1995-03-30
MA22171A1 (fr) 1991-12-31
DE69128832T2 (de) 1998-05-28
ES2113378T3 (es) 1998-05-01
CZ279928B6 (cs) 1995-08-16
IE911845A1 (en) 1991-12-18
NZ238224A (en) 1993-11-25
NO300541B1 (no) 1997-06-16
HU9203855D0 (en) 1993-03-29
IS1752B (is) 2000-07-21
PT97873A (pt) 1992-04-30
EP0533752A1 (en) 1993-03-31
AU8080791A (en) 1991-12-31
CN1040536C (zh) 1998-11-04
KR0178045B1 (en) 1999-03-20
SA91120027B1 (ar) 2002-06-03
CN1058211A (zh) 1992-01-29

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