EE05402B1 - Meetod bensimidasooli-tüüpi ühendite valmistamiseks ning k?rvalsaadusena moodustunud sulfoonide eemaldamiseks - Google Patents

Meetod bensimidasooli-tüüpi ühendite valmistamiseks ning k?rvalsaadusena moodustunud sulfoonide eemaldamiseks

Info

Publication number
EE05402B1
EE05402B1 EEP200400052A EEP200400052A EE05402B1 EE 05402 B1 EE05402 B1 EE 05402B1 EE P200400052 A EEP200400052 A EE P200400052A EE P200400052 A EEP200400052 A EE P200400052A EE 05402 B1 EE05402 B1 EE 05402B1
Authority
EE
Estonia
Prior art keywords
benzimidazole
preparation
sulfones
removal
products
Prior art date
Application number
EEP200400052A
Other languages
English (en)
Estonian (et)
Inventor
Laurent Maria Broeckx Rudy
De Smaele Dirk
Marcel Herman Leurs Stefan
Original Assignee
Janssen Pharmaceutica N.V.
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 Janssen Pharmaceutica N.V. filed Critical Janssen Pharmaceutica N.V.
Publication of EE200400052A publication Critical patent/EE200400052A/xx
Publication of EE05402B1 publication Critical patent/EE05402B1/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Extraction Or Liquid Replacement (AREA)
EEP200400052A 2001-07-16 2002-07-09 Meetod bensimidasooli-tüüpi ühendite valmistamiseks ning k?rvalsaadusena moodustunud sulfoonide eemaldamiseks EE05402B1 (et)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01202696 2001-07-16
PCT/EP2002/007693 WO2003008406A1 (en) 2001-07-16 2002-07-09 Improved process for preparing benzimidazole-type compounds

Publications (2)

Publication Number Publication Date
EE200400052A EE200400052A (et) 2004-04-15
EE05402B1 true EE05402B1 (et) 2011-04-15

Family

ID=8180641

Family Applications (1)

Application Number Title Priority Date Filing Date
EEP200400052A EE05402B1 (et) 2001-07-16 2002-07-09 Meetod bensimidasooli-tüüpi ühendite valmistamiseks ning k?rvalsaadusena moodustunud sulfoonide eemaldamiseks

Country Status (23)

Country Link
US (1) US6919459B2 (cs)
EP (1) EP1409478B1 (cs)
JP (1) JP4320250B2 (cs)
KR (1) KR100914175B1 (cs)
CN (1) CN1235899C (cs)
AT (1) ATE321758T1 (cs)
AU (1) AU2002321204B2 (cs)
BR (1) BRPI0211101B8 (cs)
CA (1) CA2450433C (cs)
CZ (1) CZ304526B6 (cs)
DE (1) DE60210292T2 (cs)
EA (1) EA005773B1 (cs)
EE (1) EE05402B1 (cs)
ES (1) ES2261703T3 (cs)
HK (1) HK1069168A1 (cs)
HU (1) HU230155B1 (cs)
IL (2) IL159854A0 (cs)
MX (1) MXPA04000433A (cs)
NO (1) NO324257B1 (cs)
NZ (1) NZ530168A (cs)
PL (1) PL208291B1 (cs)
SK (1) SK287245B6 (cs)
WO (1) WO2003008406A1 (cs)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA200500673A1 (ru) * 2002-10-22 2005-12-29 Рэнбакси Лабораториз Лимитед Аморфная форма соли эзомепразола, способ ее получения и фармацевтическая композиция на её основе
US7683177B2 (en) 2003-06-10 2010-03-23 Teva Pharmaceutical Industries Ltd Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole
WO2006019151A1 (ja) * 2004-08-20 2006-02-23 Eisai R & D Management Co., Ltd. ベンズイミダゾール誘導体の製造方法
WO2006049486A1 (en) * 2004-11-08 2006-05-11 Dishman Pharmaceuticals And Chemicals Ltd. A PREPARATION METHOD FOR SUBSTITUTED 2-(2-PYRIDYLMETHOYLSULPHINYL)-l-H-BENZIMID AZOLES
EP1681056A1 (en) 2005-01-14 2006-07-19 Krka Tovarna Zdravil, D.D., Novo Mesto Process for preparing lansoprazole
GB0525710D0 (en) * 2005-12-17 2006-01-25 Pliva Hrvatska D O O An improved process for preparing of substituted 2-benzimidazolesulfoxide compounds
EP1801110A1 (en) 2005-12-22 2007-06-27 KRKA, tovarna zdravil, d.d., Novo mesto Esomeprazole arginine salt
EP1818331A1 (en) 2006-02-14 2007-08-15 EOS Eczacibasi Ozgun Kimyasal Urunler Sanayi Ve Ti Caret A.S. Process for the preparation of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole substantially free of sulfone impurity
WO2007129328A2 (en) * 2006-05-09 2007-11-15 Cadila Healthcare Limited Process for preparing 2-[pyridinyl]sulfinyl-substituted benzimidazoles
WO2007138468A2 (en) * 2006-06-01 2007-12-06 Wockhardt Ltd Processes for the preparation of lansoprazole
WO2008017020A2 (en) * 2006-08-03 2008-02-07 Dr. Reddy's Laboratories Limited Process for preparing proton pump inhibitors
EP2069329A4 (en) * 2006-10-06 2010-04-07 Reddys Lab Ltd Dr PROCESS FOR THE PREPARATION OF BENZIMIDAZOLE DERIVATIVES AND THEIR SALTS
EP1947099A1 (en) 2007-01-18 2008-07-23 LEK Pharmaceuticals D.D. Process for solvent removal from omeprazole salts
EA016297B1 (ru) * 2007-06-15 2012-03-30 Эмкьюр Фармасьютикалз Лимитед Способ сульфоксидирования биологически активных соединений
WO2008155780A2 (en) * 2007-06-21 2008-12-24 Matrix Laboratories Ltd Improved process for the preparation of pure rabeprazole
EP2022789A1 (en) * 2007-08-06 2009-02-11 Farmaprojects, S.A. Process for the preparation of a gastric acid secretion inhibitor
WO2009066317A2 (en) * 2007-08-20 2009-05-28 Macleods Pharmaceuticals Limited Process for the preparation of pantoprazole sodium
EP2030973A1 (en) * 2007-08-31 2009-03-04 KRKA, tovarna zdravil, d.d., Novo mesto Process for preparing 2-sulfinyl-1H-benzimidazoles
US8071781B2 (en) 2008-11-11 2011-12-06 Syn-Tech Chem. & Pharm. Co., Ltd. Process for preparing rabeprazole sodium
US9725500B2 (en) * 2010-03-02 2017-08-08 Seattle Genetics, Inc. Methods for screening antibodies
CN104418837A (zh) * 2013-08-19 2015-03-18 长沙市如虹医药科技有限公司 一种氧化硫醚成亚砜的方法
CN104402866A (zh) * 2014-11-07 2015-03-11 烟台万润精细化工股份有限公司 一种制备埃索美拉唑杂质j和k的方法
CN104402867A (zh) * 2014-11-07 2015-03-11 烟台万润精细化工股份有限公司 一种制备埃索美拉唑杂质h和b的方法
CN104530006B (zh) * 2015-01-06 2018-05-11 江苏奥赛康药业股份有限公司 兰索拉唑的制备方法
CN104744440B (zh) * 2015-03-12 2016-09-07 常州康丽制药有限公司 雷贝拉唑硫醚的回收方法
CN110487918B (zh) * 2018-05-14 2022-02-08 中国医学科学院药物研究所 泮托拉唑钠及其起始原料中基因毒性杂质的分析方法
CN109354587B (zh) * 2018-10-18 2020-09-18 成都天台山制药有限公司 泮托拉唑钠的制备方法和泮托拉唑钠

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE9002043D0 (sv) * 1990-06-07 1990-06-07 Astra Ab Improved method for synthesis
NZ244301A (en) * 1991-09-20 1994-08-26 Merck & Co Inc Preparation of 2-pyridylmethylsulphinylbenzimidazole and pyridoimidazole derivatives from the corresponding sulphenyl compounds
KR960002912B1 (ko) * 1993-02-19 1996-02-28 영진약품공업주식회사 신규한 벤즈이미다졸 유도체
ES2094694B1 (es) 1995-02-01 1997-12-16 Esteve Quimica Sa Nueva formulacion farmaceuticamente estable de un compuesto de bencimidazol y su proceso de obtencion.
CN1053444C (zh) * 1996-03-20 2000-06-14 常州市第四制药厂 奥美拉唑的一种精制方法
SK283805B6 (sk) * 1996-09-09 2004-02-03 Slovakofarma, A. S. Spôsob prípravy omeprazolu
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

Also Published As

Publication number Publication date
MXPA04000433A (es) 2004-03-18
HK1069168A1 (en) 2005-05-13
PL367006A1 (en) 2005-02-07
CN1525970A (zh) 2004-09-01
CZ304526B6 (cs) 2014-06-18
EE200400052A (et) 2004-04-15
PL208291B1 (pl) 2011-04-29
ES2261703T3 (es) 2006-11-16
JP2005500333A (ja) 2005-01-06
IL159854A0 (en) 2004-06-20
NO324257B1 (no) 2007-09-17
EP1409478A1 (en) 2004-04-21
JP4320250B2 (ja) 2009-08-26
BR0211101B1 (pt) 2013-12-17
EA005773B1 (ru) 2005-06-30
EP1409478B1 (en) 2006-03-29
KR100914175B1 (ko) 2009-08-27
AU2002321204B2 (en) 2008-05-08
KR20040016877A (ko) 2004-02-25
SK287245B6 (sk) 2010-04-07
BR0211101A (pt) 2004-06-22
HUP0400610A2 (hu) 2004-08-30
NZ530168A (en) 2004-08-27
ATE321758T1 (de) 2006-04-15
WO2003008406A1 (en) 2003-01-30
IL159854A (en) 2008-11-03
DE60210292D1 (de) 2006-05-18
BRPI0211101B8 (pt) 2021-05-25
CA2450433C (en) 2010-05-25
CA2450433A1 (en) 2003-01-30
CZ2004208A3 (cs) 2005-03-16
NO20040074L (no) 2004-01-08
HUP0400610A3 (en) 2012-09-28
DE60210292T2 (de) 2006-12-07
EA200400185A1 (ru) 2004-06-24
HU230155B1 (hu) 2015-09-28
CN1235899C (zh) 2006-01-11
US6919459B2 (en) 2005-07-19
US20040209918A1 (en) 2004-10-21
SK922004A3 (en) 2004-08-03

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