DK1858881T3 - Fremgangsmåde til fremstilling af optisk aktive derivater af 2-2(pyridylmethylsulfinyl)-benzimidazol ved hjælp af et inklusionskompleks med 1,1'-binaphtalen-2,2'diol - Google Patents

Fremgangsmåde til fremstilling af optisk aktive derivater af 2-2(pyridylmethylsulfinyl)-benzimidazol ved hjælp af et inklusionskompleks med 1,1'-binaphtalen-2,2'diol

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Publication number
DK1858881T3
DK1858881T3 DK06708457T DK06708457T DK1858881T3 DK 1858881 T3 DK1858881 T3 DK 1858881T3 DK 06708457 T DK06708457 T DK 06708457T DK 06708457 T DK06708457 T DK 06708457T DK 1858881 T3 DK1858881 T3 DK 1858881T3
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DK
Denmark
Prior art keywords
benzimidazole
binaphthalene
diol
preparation
optically active
Prior art date
Application number
DK06708457T
Other languages
Danish (da)
English (en)
Inventor
Maime Ramon Berenguer
Guillen Yolanda Gasanz
Ruperez Jorge Medrano
Laura Coppi
Original Assignee
Esteve Quimica 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
Application filed by Esteve Quimica Sa filed Critical Esteve Quimica Sa
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Publication of DK1858881T3 publication Critical patent/DK1858881T3/da

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)
DK06708457T 2005-03-03 2006-02-22 Fremgangsmåde til fremstilling af optisk aktive derivater af 2-2(pyridylmethylsulfinyl)-benzimidazol ved hjælp af et inklusionskompleks med 1,1'-binaphtalen-2,2'diol DK1858881T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200500546A ES2259269B1 (es) 2005-03-03 2005-03-03 Procedimiento para la preparacion de derivados de 2-(2-piridilmetilsulfinil)-bencimidazol opticamente activos.
PCT/EP2006/060193 WO2006094904A1 (en) 2005-03-03 2006-02-22 Process for the preparation of optically active derivatives of 2-(2-pyridylmethylsulfinyl)-benzimidazole via inclusion complex with 1,1'-binaphthalene-2, 2'diol

Publications (1)

Publication Number Publication Date
DK1858881T3 true DK1858881T3 (da) 2008-12-01

Family

ID=36293310

Family Applications (1)

Application Number Title Priority Date Filing Date
DK06708457T DK1858881T3 (da) 2005-03-03 2006-02-22 Fremgangsmåde til fremstilling af optisk aktive derivater af 2-2(pyridylmethylsulfinyl)-benzimidazol ved hjælp af et inklusionskompleks med 1,1'-binaphtalen-2,2'diol

Country Status (19)

Country Link
US (1) US7777044B2 (es)
EP (1) EP1858881B1 (es)
JP (1) JP5097559B2 (es)
KR (1) KR101246479B1 (es)
CN (1) CN101133049B (es)
AT (1) ATE406362T1 (es)
AU (1) AU2006222032B2 (es)
CA (1) CA2598224C (es)
CY (1) CY1108491T1 (es)
DE (1) DE602006002495D1 (es)
DK (1) DK1858881T3 (es)
ES (2) ES2259269B1 (es)
HR (1) HRP20080510T3 (es)
MX (1) MX2007010705A (es)
NO (1) NO20074978L (es)
NZ (1) NZ561214A (es)
PT (1) PT1858881E (es)
WO (1) WO2006094904A1 (es)
ZA (1) ZA200707335B (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004056804A2 (en) * 2002-12-19 2004-07-08 Teva Pharmaceutical Industries Ltd. Solid states of pantoprazole sodium, processes for preparing them and processes for preparing known pantoprazole sodium hydrates
KR100641534B1 (ko) * 2005-07-28 2006-11-01 한미약품 주식회사 에스오메프라졸 및 그의 염의 제조방법
MX2008016196A (es) * 2006-07-05 2009-01-20 Lupin Ltd Proceso para la preparacion de enantiomeros opticamente puros u opticamente enriquecidos de compuestos de sulfoxido.
EP2152691B1 (en) * 2007-06-07 2011-11-23 Aurobindo Pharma Limited An improved process for preparing an optically active proton pump inhibitor
AU2008346115A1 (en) * 2007-12-18 2009-07-16 Watson Pharma Private Limited A process for preparation of stable amorphous R-lansoprazole
NZ589150A (en) * 2008-05-14 2012-03-30 Watson Pharma Private Ltd Stable r (+) -lansoprazole amine salt and a process for preparing the same
CN101391993B (zh) * 2008-10-28 2012-07-04 安徽美诺华药物化学有限公司 通过与(s)-(-)-1,1'-联萘-2,2'-二酚形成包合配合物制备s-奥美拉唑及其盐的方法
WO2010058409A2 (en) 2008-11-18 2010-05-27 Hetero Research Foundation Optical purification of esomeprazole
WO2010072759A1 (en) * 2008-12-24 2010-07-01 Krka, Tovarna Zdravil, D.D., Novo Mesto Process for the preparation of esomeprazole
EP2499125B1 (en) 2009-11-12 2016-01-27 Hetero Research Foundation Process for the resolution of omeprazole
CN102887885B (zh) * 2012-09-26 2014-12-10 江苏正大丰海制药有限公司 一种埃索美拉唑钠的制备方法
CN103483407B (zh) * 2013-10-10 2015-11-18 宁夏启元药业有限公司 一种硫氰酸红霉素萃取结晶用复合溶媒及萃取结晶方法
EP2980086B1 (en) 2014-07-29 2016-06-15 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Efficient process for the preparation of esomeprazole (S)-binol complex
CZ307419B6 (cs) * 2014-10-17 2018-08-08 Vysoká škola chemicko-technologická v Praze Způsob stanovení enantiomerní čistoty chirálních sulfoxidů pomocí 1H-NMR analýzy
CZ2014710A3 (cs) * 2014-10-17 2016-05-11 Vysoká škola chemicko - technologická v Praze Močovina na bázi binaftalenu pro stanovení enantiomerní čistoty chirálních sulfoxidů pomocí 1H-NMR analýzy
CN105294544B (zh) * 2015-11-30 2017-09-22 山东罗欣药业集团股份有限公司 一种高纯度匹可硫酸钠的制备方法

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4035455A1 (de) 1990-11-08 1992-05-14 Byk Gulden Lomberg Chem Fab Enantiomerentrennung
SE9301830D0 (sv) 1993-05-28 1993-05-28 Ab Astra New compounds
SE510650C2 (sv) 1997-05-30 1999-06-14 Astra Ab Ny förening
CN1087739C (zh) * 1998-12-28 2002-07-17 中国科学院成都有机化学研究所 光学纯的苯并咪唑类抗消化性溃疡药物的包结拆分制备法
SE9900274D0 (sv) 1999-01-28 1999-01-28 Astra Ab New compound
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
CN1117747C (zh) * 2000-06-19 2003-08-13 中国科学院成都有机化学研究所 光学纯兰索拉唑的制备方法
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
TW200410955A (en) 2002-07-29 2004-07-01 Altana Pharma Ag Novel salt of (S)-PANTOPRAZOLE
CN1223262C (zh) * 2003-08-07 2005-10-19 广水市东晨菌业科技有限公司 天麻有性繁殖同步栽培的方法
KR100641534B1 (ko) 2005-07-28 2006-11-01 한미약품 주식회사 에스오메프라졸 및 그의 염의 제조방법
EP1973896B1 (en) 2005-12-28 2009-04-15 Union Quimico-Farmaceutica, S.A. A process for the preparation of the (s)-enantiomer of omeprazole

Also Published As

Publication number Publication date
ES2259269B1 (es) 2007-11-01
CA2598224A1 (en) 2006-09-14
AU2006222032B2 (en) 2011-03-10
US7777044B2 (en) 2010-08-17
MX2007010705A (es) 2007-11-08
HRP20080510T3 (en) 2008-12-31
JP2008531641A (ja) 2008-08-14
NO20074978L (no) 2007-11-23
CN101133049B (zh) 2011-03-30
JP5097559B2 (ja) 2012-12-12
CN101133049A (zh) 2008-02-27
ZA200707335B (en) 2008-12-31
ATE406362T1 (de) 2008-09-15
DE602006002495D1 (de) 2008-10-09
ES2313617T3 (es) 2009-03-01
AU2006222032A1 (en) 2006-09-14
EP1858881B1 (en) 2008-08-27
PT1858881E (pt) 2008-10-08
ES2259269A1 (es) 2006-09-16
NZ561214A (en) 2009-09-25
CA2598224C (en) 2012-08-28
WO2006094904A1 (en) 2006-09-14
US20080167473A1 (en) 2008-07-10
CY1108491T1 (el) 2014-04-09
KR20070113212A (ko) 2007-11-28
EP1858881A1 (en) 2007-11-28
KR101246479B1 (ko) 2013-03-21

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